A reference to a diagnostic imaging service in an item in Part 2 includes a reference to the undertaking of the diagnostic imaging procedure used for rendering the service.
1.1.2 References in this Schedule to items include items determined under section 3C of the Act
A reference in this Schedule to an item includes a reference to an item relating to a health service that, under a determination in force under subsection 3C(1) of the Act, is treated as if there were an item in the table that relates to the service.
1.1.3 Dictionary
The Dictionary in Part 3 of this Schedule defines certain words and expressions that are used in this Schedule, and includes references to certain words and expressions that are defined elsewhere in this Schedule.
Division 1.2—General application provisions
Subdivision A—Capital sensitivity requirements
1.2.1 Restriction on items—services performed on aged equipment
(1) Subject to Subdivision B, an item in this Schedule does not apply to a service that is performed on diagnostic imaging equipment if the age of the equipment exceeds the applicable life age of the equipment.
(2) If reinstatement under clause 1.2.10B is granted in respect of diagnostic imaging equipment, an item in this Schedule does not apply to a service that is performed on that equipment on a day:
(a) that is before the day the reinstatement was granted; and
(b) on which the age of the equipment exceeded its new effective life age.
(3) If:
(a) reinstatement under clause 1.2.10B is granted in respect of diagnostic imaging equipment that has not been upgraded; and
(b) the equipment is not upgraded within 3 months after the end of the equipment’s new effective life age;
an item in this Schedule does not apply to a service that is performed on that equipment on a day that is after the end of 3 months after the end of the equipment’s new effective life age.
1.2.2 Age of equipment
Working out age of equipment
(1) The date from which the age of equipment is worked out for the purposes of this instrument is:
(a) the date the equipment was first installed in Australia; or
(b) if the equipment was imported as used equipment—the date of manufacture of the oldest component of the equipment.
(2) The applicable life age:
(a) for diagnostic imaging equipment that has not been upgraded—is the new effective life age of the equipment; and
(b) for diagnostic imaging equipment that has been upgraded—is the maximum extended life age of the equipment.
(3) The new effective life age and maximum extended life age for diagnostic imaging equipment are the periods set out in table 1.2.2 for that type of equipment. The type of equipment is defined by the type of service that is rendered using diagnostic imaging procedures carried out using the equipment:
Subdivision Subdivision A - Health Insurance (Diagnostic Imaging Services Table) Regulations (No. 2) 2020 - Capital sensitivity requirements | Zoe
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="5" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Table 1.2.2—Life ages</span></p></td></tr><tr><td style="width:8.54%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Item</span></p></td><td style="width:23.08%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Type of equipment</span></p></td><td style="width:34.6%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Definition of type of equipment</span></p></td><td style="width:16.14%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>New effective life age (years)</span></p></td><td style="width:17.64%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 4</span></p><p class="TableHeading" style="text-align:right"><span>Maximum extended life age (years)</span></p></td></tr></thead><tbody><tr><td style="width:8.54%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>1</span></p></td><td style="width:23.08%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Ultrasound equipment</span></p></td><td style="width:34.6%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Equipment primarily used in carrying out a diagnostic imaging procedure used in rendering a service to which an item in Group I1 applies</span></p></td><td style="width:16.14%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>10</span></p></td><td style="width:17.64%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>15</span></p></td></tr><tr><td style="width:8.54%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>2</span></p></td><td style="width:23.08%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>CT equipment</span></p></td><td style="width:34.6%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Equipment primarily used in carrying out a diagnostic imaging procedure used in rendering a service to which an item in Group I2 applies</span></p></td><td style="width:16.14%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>10</span></p></td><td style="width:17.64%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>15</span></p></td></tr><tr><td style="width:8.54%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>3</span></p></td><td style="width:23.08%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Mammography equipment</span></p></td><td style="width:34.6%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Equipment primarily used in carrying out a diagnostic imaging procedure used in rendering a service to which an item in Subgroup 10 of Group I3 applies</span></p></td><td style="width:16.14%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>10</span></p></td><td style="width:17.64%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>15</span></p></td></tr><tr><td style="width:8.54%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>4</span></p></td><td style="width:23.08%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Angiography equipment</span></p></td><td style="width:34.6%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Equipment primarily used in carrying out a diagnostic imaging procedure used in rendering a service to which an item in Subgroup 13 of Group I3 applies</span></p></td><td style="width:16.14%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>10</span></p></td><td style="width:17.64%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>15</span></p></td></tr><tr><td style="width:8.54%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>5</span></p></td><td style="width:23.08%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Other diagnostic radiology equipment</span></p></td><td style="width:34.6%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Equipment primarily used in carrying out a diagnostic imaging procedure used in rendering a service to which an item in Subgroups 1 to 9, 12, 14, 15 or 17 of Group I3 applies</span></p></td><td style="width:16.14%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>15</span></p></td><td style="width:17.64%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>20</span></p></td></tr><tr><td style="width:8.54%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>6</span></p></td><td style="width:23.08%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Nuclear medicine imaging equipment (other than for PET)</span></p></td><td style="width:34.6%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Equipment primarily used in carrying out a diagnostic imaging procedure used in rendering a service to which an item in Group I4 applies (other than items</span><span> </span><span>61523 to 61647)</span></p></td><td style="width:16.14%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>10</span></p></td><td style="width:17.64%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>15</span></p></td></tr><tr><td style="width:8.54%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>7</span></p></td><td style="width:23.08%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>MRI equipment</span></p></td><td style="width:34.6%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>Equipment primarily used in carrying out a diagnostic imaging procedure used in rendering a service to which an item in Group I5 applies</span></p></td><td style="width:16.14%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>10</span></p></td><td style="width:17.64%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>20</span></p></td></tr></tbody></table>
Upgrades
(4) Diagnostic imaging equipment has been upgraded if:
(a) an additional reasonable investment has been made, within the period mentioned in subclause (5), that improves the overall performance of the imaging system so that it is equivalent to new equipment supplied in Australia at the time of the improvement; or
(b) in the case of CT or angiography equipment that was not more than 15 years old on 1 January 2015—an additional reasonable investment has been made before 1 January 2016 that improves the overall performance of the imaging system so that it is equivalent to new equipment supplied in Australia at the time of the improvement; or
(c) the equipment has been accredited under The Royal Australian and New Zealand College of Radiologists’ Mammography Quality Assurance Program.
(5) For the purposes of paragraph (4)(a), the period is:
(a) the new effective life age for the equipment; or
(b) for equipment for which an exemption under clause 1.2.8 has been granted—the exemption period of the exemption; or
(c) for equipment for which reinstatement under clause 1.2.10B has been granted—3 months after the end of the equipment’s new effective life age.
1.2.4 Meaning of relevant proprietor
The relevant proprietor for diagnostic imaging equipment is:
(a) if the equipment is ordinarily located at diagnostic imaging premises—the proprietor of the premises; or
(b) if the equipment:
(i) is not ordinarily located at diagnostic imaging premises; and
(ii) is ordinarily located, when not in use, at a base for mobile diagnostic imaging equipment;
the proprietor of the base.
Subdivision B—Exemptions from capital sensitivity requirements
1.2.7 Equipment unable to be replaced etc. before end of applicable life age—applying for exemptions
Applying for exemption
(1) The relevant proprietor for diagnostic imaging equipment may apply to the Secretary for an exemption under clause 1.2.8 in respect of the equipment.
Note: For relevant proprietor, see clause 1.2.4.
(2) The application must:
(a) be in writing; and
(b) be made before the end of the equipment’s applicable life age; and
(c) set out:
(i) reasons why the proprietor is unable to replace the equipment (or upgrade the equipment, if it has not already been upgraded) before the end of the equipment’s applicable life age; and
(ii) the steps taken by the proprietor to replace the equipment (or upgrade the equipment, if it has not already been upgraded).
Notifying proprietor of receipt of application
(3) If:
(a) the Secretary receives an application under subclause (2) of this clause for an exemption in respect of the equipment; and
(b) the application complies with subclause (2);
the Secretary must notify the relevant proprietor for the equipment in writing that the Secretary has received the application.
Effect of application on capital sensitivity requirements
(4) Clause 1.2.1 does not apply to a service that is performed on the equipment during the period:
(a) starting when the Secretary notifies the relevant proprietor under subclause (3) of this clause that the Secretary has received an application in respect of the equipment; and
(b) ending when the Secretary makes a decision on the application under clause 1.2.8, or the application is withdrawn.
1.2.8 Equipment unable to be replaced etc. before end of applicable life age—granting exemptions
Scope of this clause
(1) This clause applies if, under subclause 1.2.7(3), the Secretary notifies the relevant proprietor for diagnostic imaging equipment that the Secretary has received an application for an exemption in respect of the equipment.
Granting exemption
(2) The Secretary must, by notice in writing given to the proprietor:
(a) subject to subclauses (3) and (4) of this clause, grant the exemption for a specified period; or
(b) refuse to grant the exemption.
(3) The Secretary must not grant the exemption unless the Secretary is satisfied that both of the following apply:
(a) due to circumstances beyond the control of the proprietor, the proprietor is unable to replace the equipment (or upgrade the equipment, if it has not already been upgraded) before the end of its applicable life age;
(b) the proprietor is taking reasonable steps to replace the equipment (or upgrade the equipment, if it has not already been upgraded) before the end of the period specified under paragraph (2)(a).
(4) The period specified under paragraph (2)(a) must end no later than 6 months after the end of the equipment’s applicable life age.
Note: The period specified under paragraph (2)(a) is the initial exemption period of the exemption: see clause 3.1. The exemption period can be extended or further extended under clause 1.2.10.
(5) The Secretary must make a decision on the application under subclause (2) within 28 days after notifying the proprietor as mentioned in subclause (1).
Effect of exemption or refusal on capital sensitivity requirements
(6) If the Secretary grants the exemption, clause 1.2.1 does not apply to a service that is performed on the equipment during the exemption period of the exemption (including the exemption period as extended or further extended under clause 1.2.10, if applicable).
(7) If the Secretary refuses to grant the exemption, clause 1.2.1 does not apply to a service that is performed on the equipment during the period:
(a) starting when the Secretary refuses to grant the exemption; and
(b) ending:
(i) when the relevant proprietor for the equipment applies under clause 1.2.11 for reconsideration of the decision to refuse to grant the exemption; or
(ii) if the relevant proprietor does not apply for such consideration—at the end of the period in which the proprietor could have applied for such reconsideration.
1.2.9 Equipment unable to be replaced etc. before end of applicable life age—applying for extensions of exemption periods
Scope of this clause
(1) This clause applies if an exemption under clause 1.2.8 in respect of diagnostic imaging equipment is in force.
Applying for extension of exemption period
(2) The relevant proprietor for the equipment may apply to the Secretary to extend or further extend under clause 1.2.10 the exemption period of the exemption.
Note: For relevant proprietor, see clause 1.2.4.
(3) The application must:
(a) be in writing; and
(b) be made before the end of the current exemption period of the exemption; and
(c) set out:
(i) reasons why the proprietor continues to be unable to replace or upgrade the equipment; and
(ii) the steps taken by the proprietor to replace the equipment (or upgrade the equipment, if it has not already been upgraded).
Notifying proprietor of receipt of application
(4) If:
(a) the Secretary receives an application under subclause (2) of this clause for an extension or further extension of the exemption; and
(b) the application complies with subclause (3);
the Secretary must notify the relevant proprietor for the equipment in writing that the Secretary has received the application.
Effect of application on capital sensitivity requirements
(5) Clause 1.2.1 does not apply to a service that is performed on the equipment during the period:
(a) starting when the Secretary notifies the relevant proprietor under subclause (4) of this clause that the Secretary has received an application in respect of the equipment; and
(b) ending when the Secretary makes a decision on the application under clause 1.2.10, or the application is withdrawn.
1.2.10 Equipment unable to be replaced etc. before end of applicable life age—extending exemption periods
Scope of this clause
(1) This clause applies if, under subclause 1.2.9(4), the Secretary notifies the relevant proprietor for diagnostic imaging equipment that the Secretary has received an application for an extension or further extension of the exemption period of an exemption in respect of the equipment.
Secretary may extend exemption period
(2) The Secretary must, by notice in writing given to the proprietor:
(a) subject to subclauses (3) and (4) of this clause, extend or further extend the exemption period for a specified period; or
(b) refuse to extend, or further extend, the exemption period.
(3) The Secretary must not extend or further extend the exemption period unless the Secretary is satisfied that both of the following apply:
(a) due to circumstances beyond the control of the proprietor, the proprietor is unable to replace the equipment (or upgrade the equipment, if it has not already been upgraded) before the end of the current exemption period of the exemption;
(b) the proprietor is taking reasonable steps to replace the equipment (or upgrade the equipment, if it has not already been upgraded) before the end of the exemption period as extended or further extended.
(4) The extension or further extension must be for no more than 3 months.
(5) The Secretary must make a decision on the application under subclause (2) within 28 days after notifying the proprietor as mentioned in subclause (1).
Effect of refusal on capital sensitivity requirements
(6) If the Secretary refuses to extend, or further extend, the exemption period, clause 1.2.1 does not apply to a service that is performed on the equipment during the period:
(a) starting when the Secretary refuses to extend, or further extend, the exemption period; and
(b) ending:
(i) when the relevant proprietor for the equipment applies under clause 1.2.11 for reconsideration of the decision to refuse to extend, or further extend, the exemption period; or
(ii) if the relevant proprietor does not apply for such consideration—at the end of the period in which the proprietor could have applied for such reconsideration.
Note: Clause 1.2.1 does not apply to a service provided using the equipment during the extended exemption period: see subclause 1.2.8(6).
Subdivision BA—Reinstatement for capital sensitivity requirements
1.2.10A Equipment not upgraded before end of new effective life age—applying for reinstatement of subsequently upgraded equipment
Applying for reinstatement
(1) The relevant proprietor for diagnostic imaging equipment may apply to the Secretary for reinstatement under clause 1.2.10B in respect of the equipment if:
(a) the equipment was not upgraded before the end of its new effective life age; and
(b) the relevant proprietor did not apply for an exemption under clause 1.2.8 in respect of the equipment before the end of its new effective life age.
Note: For relevant proprietor, see clause 1.2.4.
(2) The application must:
(a) be in writing; and
(b) be made within 3 months after the end of the equipment’s new effective life age; and
(c) set out:
(i) reasons why the proprietor was unable to upgrade the equipment before the end of its new effective life age; and
(ii) reasons why the proprietor was unable to apply for an exemption under clause 1.2.8 in respect of the equipment before the end of its new effective life age; and
(iii) an explanation of how the equipment has been, or will be, upgraded; and
(iv) if the equipment has not been upgraded—the steps taken by the proprietor to ensure that it will be upgraded within 3 months after the end of its new effective life age, and the date on which the upgrade will occur.
Notifying proprietor of receipt of application
(3) If:
(a) the Secretary receives an application under subclause (1) of this clause for reinstatement in respect of the equipment; and
(b) the application complies with subclause (2);
the Secretary must notify the relevant proprietor for the equipment in writing that the Secretary has received the application.
1.2.10B Equipment not upgraded before end of new effective life age—granting reinstatement of subsequently upgraded equipment
Scope of this clause
(1) This clause applies if, under subclause 1.2.10A(3), the Secretary notifies the relevant proprietor for diagnostic imaging equipment that the Secretary has received an application for reinstatement in respect of the equipment.
Granting reinstatement
(2) The Secretary must, by notice in writing given to the proprietor:
(a) subject to subclause (3) of this clause, grant the reinstatement; or
(b) refuse to grant the reinstatement.
(3) The Secretary must not grant the reinstatement unless the Secretary is satisfied that both of the following apply:
(a) the proprietor was unable to upgrade the equipment before the end of its new effective life age;
(b) the equipment has been or will be upgraded within 3 months after the end of its new effective life age.
(4) The Secretary must make a decision on the application under subclause (2) within 28 days after notifying the proprietor as mentioned in subclause (1).
Subdivision BB—Reconsideration and review of decisions
1.2.11 Reconsideration by Secretary—applying for reconsideration
Scope of this clause
(1) This clause applies to:
(a) a decision under clause 1.2.8 to refuse to grant an exemption in respect of diagnostic imaging equipment; or
(b) a decision under clause 1.2.10 to refuse to extend, or further extend, the exemption period of an exemption in respect of diagnostic imaging equipment; or
(c) a decision under clause 1.2.10B to refuse to grant reinstatement in respect of diagnostic imaging equipment.
Applying for reconsideration of decision
(2) The relevant proprietor for the equipment may apply to the Secretary for reconsideration of the decision under clause 1.2.12.
Note: For relevant proprietor, see clause 1.2.4.
(3) The application must:
(a) be in writing; and
(b) be made within:
(i) 28 days after the Secretary makes the decision; or
(ii) if the Secretary is satisfied that special circumstances exist—within such further period (if any) as the Secretary allows; and
(c) identify the decision for reconsideration; and
(d) set out the reasons for the application.
(4) The application may provide new material for the Secretary to consider.
Notifying proprietor of receipt of application
(5) If:
(a) the Secretary receives an application under subclause (2) of this clause for reconsideration of the decision; and
(b) the application complies with subclause (3);
the Secretary must notify the relevant proprietor for the equipment in writing that the Secretary has received the application.
Effect of application on capital sensitivity requirements—exemption decisions
(6) Clause 1.2.1 does not apply to a service that is performed on equipment to which a decision mentioned in paragraph (1)(a) or (b) relates during the period:
(a) starting when the Secretary notifies the relevant proprietor under subclause (5) of this clause that the Secretary has received an application in respect of the equipment; and
(b) ending when the Secretary makes a decision on the application under clause 1.2.12, or the application is withdrawn.
1.2.12 Reconsideration by Secretary—reconsidering decisions
Scope of this clause
(1) This clause applies if, under subclause 1.2.11(5), the Secretary notifies the relevant proprietor of diagnostic imaging equipment that the Secretary has received an application for reconsideration of a decision in respect of the equipment.
Reconsidering decisions
(2) The Secretary must:
(a) reconsider the decision; and
(b) by notice in writing given to the proprietor:
(i) affirm the decision; or
(ii) set aside the decision and make a decision in substitution for it.
(3) The Secretary must make a decision on the application under subclause (2) within 28 days after notifying the proprietor as mentioned in subclause (1).
Effect of affirmation of exemption decisions on capital sensitivity requirements
(4) If the Secretary affirms a decision mentioned in paragraph 1.2.11(1)(a) or (b), clause 1.2.1 does not apply to a service that is performed on equipment to which the decision relates during the period:
(a) starting when the Secretary affirms the decision; and
(b) ending:
(i) if an application for review of the decision to affirm is made under clause 1.2.13—when each party to the proceeding has been given a copy of the decision of the Administrative Review Tribunal on review; or
(ii) otherwise—when the time for making such an application for review expires.
Note: For the time for making an application for review, see section 18 of the Administrative Review Tribunal Act 2024.
1.2.13 Review by ART
Applications may be made to the Administrative Review Tribunal for review of decisions of the Secretary under clause 1.2.12.
Subdivision C—Other provisions
1.2.15 Meaning of symbols (R), (NR) and (H)
(1) A service corresponding to an item including the symbol (R) is an R‑type diagnostic imaging service.
(2) A service corresponding to an item including the symbol (NR) is an NR‑type diagnostic imaging service.
(3) An item in this Schedule including the symbol (H) applies only to a service performed or provided in a hospital.
1.2.16 Who may provide a diagnostic imaging service
Items in this Schedule relating to diagnostic imaging services apply whether the service is provided by:
(a) a medical practitioner; or
(b) a person, other than a medical practitioner, who provides the service under the supervision of a medical practitioner in accordance with accepted medical practice.
1.2.17 Restriction on items—report requirements for R‑type diagnostic imaging services
(1) An item relating to an R‑type diagnostic imaging service (except an item to which subclause (2) applies) applies only if the providing practitioner gives a report of the service performed to the practitioner, participating midwife or participating nurse practitioner who requested the service.
(2) This subclause applies to:
(a) items 55054, 55130, 55135, 55848, 57341, 59312, 59314, 60506, 60509 and 61109; and
(b) items 60918 and 60927.
Note: The items in paragraph (a) relate to services performed in conjunction with a surgical procedure. The items in paragraph (b) relate to services performed in preparation for a radiological procedure.
1.2.18 Bulk‑billing incentive
(1) This clause applies if:
(a) a service that is mentioned in an item in Divisions 2.1 to 2.5 of this Schedule is provided; and
(b) the service is not provided in a hospital; and
(c) the service is bulk‑billed.
(2) The fee for the service is 95% of the fee mentioned in this Schedule for the service.
Note: Under paragraph 10(2)(aa) of the Act and subsection 28(2) of the Health Insurance Regulations 2018, the medicare benefit payable is 100% of the fee for the service.
(3) This clause does not apply to the service specified in item 61369, 61466 or 61485.
1.2.21 Reduction in fees—multiple services on same day—general
(1) If a medical practitioner renders 2 or more diagnostic imaging services for the same patient on the same day, the fees set out in the items that apply to the services, other than the item with the highest fee, are reduced by $5.
(2) If a medical practitioner renders at least one R‑type diagnostic imaging service and at least one consultation service for the same patient on the same day, the highest fee, set out in the items that apply to diagnostic imaging services rendered by the practitioner for that patient on that day, is reduced:
(a) if the fee for the relevant consultation is at least $40—by $35; or
(b) if that fee is less than $40 but more than $15—by $15; or
(c) if that fee is less than $15—by the amount of that fee.
(3) For the purposes of subclause (2), if more than one consultation has occurred, the relevant consultation is the consultation having the highest fee set out in the items that apply to the consultation.
(4) If a medical practitioner renders at least one R‑type diagnostic imaging service and at least one non‑consultation service for the same patient on the same day, the highest fee that applies to any diagnostic imaging services performed by the medical practitioner for the same patient on the same day, is reduced by $5.
(5) If a medical practitioner renders an R‑type diagnostic imaging service, a consultation and a non‑consultation service for the same patient on the same day, the sum of the reductions under subclauses (2) and (4) must not exceed the highest fee that applies to any diagnostic imaging services rendered by the medical practitioner for the same patient on the same day.
(6) Clauses 2.1.2A, 2.1.17 and 2.5.8 apply, subject to subclauses (7), (8) and (8A), in addition to this clause.
(7) For the purposes of clause 2.1.2A, if a medical practitioner provides:
(a) 2 or more vascular ultrasound services for the same patient on the same day; and
(b) one or more other diagnostic imaging services for that patient on that day;
the amount of the fees payable for the vascular ultrasound services is taken, for this clause, to be an amount payable for one diagnostic imaging service.
(8) For the purposes of clause 2.5.8, if a medical practitioner provides:
(a) 2 or more MRI services mentioned in Subgroup 12 or 13 of Group I5 for the same patient on the same day; and
(b) one or more other diagnostic imaging services for that patient on that day;
the amount of the fees payable for the MRI services is taken, for this clause, to be an amount payable for one diagnostic imaging service.
(8A) For the purposes of clause 2.1.17, if a medical practitioner provides:
(a) 2 or more echocardiogram services mentioned in subclause 2.1.17(1) for the same patient on the same day; and
(b) one or more other diagnostic imaging services for that patient on that day;
the amount of the fees payable for the echocardiogram services is taken, for this clause, to be an amount payable for one diagnostic imaging service.
(9) This clause does not apply to diagnostic imaging services that are rendered in a remote area by a medical practitioner for whom a remote area exemption under section 23DX of the Act is in force for that area.
(10) This clause does not apply to the fee specified in item 59103, 64990, 64991, 64992, 64993, 64994 or 64995.
(11) In this Schedule:
consultation means a service under an item listed in Divisions 2.2 to 2.30 of the general medical services table.
highest fee means the highest fee specified for an item in the first claim submitted to the Chief Executive Medicare for the services provided.
non‑consultation service means a service under an item listed in the general medical services table, other than in Divisions 2.2 to 2.30 of the general medical services table.
1.2.22 Restriction on items—services provided with autologous injections of blood or blood products
An item in this Schedule does not apply to a service mentioned in the item if the service is provided to a patient at the same time as, or in connection with, an injection of blood or a blood product that is autologous.
1.2.23 Restriction on items—services provided with harvesting, storage, in vitro processing or injection of non‑haematopoietic stem cells
An item in this Schedule does not apply to a service mentioned in the item if the service is provided to a patient at the same time as, or in connection with, the harvesting, storage, in vitro processing or injection of non‑haematopoietic stem cells.
Part 2—Services and fees
Division 2.1—Group I1: ultrasound
Subdivision A—General
2.1.1 Restriction on items—ultrasound services
Items in this Division (except items 55600 and 55603) apply to an ultrasound service only if the diagnostic imaging procedure used in rendering the service is performed:
(a) by a medical practitioner; or
(b) on behalf of a medical practitioner by a person whose name is entered on the Register of Sonographers kept by the Chief Executive Medicare.
Note: Maintaining a register of sonographers is a function of the Chief Executive Medicare under section 32 of the Human Services (Medicare) Regulations 2017.
2.1.2 Restriction on items—R‑type ultrasound services
(1) Items in this Division (except items 55600 and 55603) marked with the symbol (R) apply to an ultrasound service (the eligible service) only if the service is performed:
(a) under the supervision of a specialist or a consultant physician in the practice of the specialist’s or consultant physician’s specialty who is available:
(i) to monitor and influence the conduct and diagnostic quality of the examination; and
(ii) if necessary, to attend on the patient personally; or
(b) under the supervision of a practitioner who:
(i) is not a specialist or consultant physician; and
(ii) meets the requirement of subclause (2); and
(iii) is available to monitor and influence the conduct and diagnostic quality of the examination and, if necessary, to attend on the patient personally; or
(c) in the circumstance mentioned in subclause (3), and under the supervision of a practitioner who is available:
(i) to monitor and influence the conduct and diagnostic quality of the examination; and
(ii) if necessary, to attend on the patient personally; or
(d) if paragraph (a), (b) or (c) cannot be complied with:
(i) in an emergency; or
(ii) in a location that is not less than 30 kilometres by the most direct road route from another practice where services that comply with paragraph (a) or (b) are available.
(2) For the purposes of subparagraph (1)(b)(ii), the requirement is that, between 1 September 1997 and 31 August 1999, at least 50 services were rendered by or on behalf of the practitioner at the location where the eligible service was rendered, and the rendering of those services entitled payment of medicare benefits.
(3) For the purposes of paragraph (1)(c), the circumstance is that, between 1 September 1997 and 31 August 1999, at least 50 services were rendered in nursing homes or patients’ residences by or on behalf of the practitioner, and the rendering of those services entitled payment of medicare benefits.
Subdivision B—Subgroups 1 to 4 of Group I1
2.1.2A Reduction in fees—multiple services on same day—vascular ultrasounds
(1) If a medical practitioner provides 2 or more vascular ultrasound services for the same patient on the same day, the fees specified for the items that apply to the services are reduced as follows:
(a) the second highest fee is reduced by 40%;
(b) any other fee, except the highest, is reduced by 50%.
(2) For the purposes of subclause (1):
(a) if 2 or more applicable fees are equally the highest:
(i) only one of those fees is taken to be the highest fee; and
(ii) the other, or another, highest fee is taken to be the second highest fee; and
(b) if 2 or more fees are equally second highest—any one of those fees may be taken to be the second highest for the purpose of paragraph (1)(b); and
(c) if a reduced fee calculated under subclause (1) is not a multiple of 5 cents—the reduced fee is taken to be the nearest amount that is a multiple of 5 cents.
(3) This clause does not apply to the fee specified in item 64990 or 64991.
2.1.3 Items in Subgroups 1 to 4 of Group I1
This clause sets out items in Subgroups 1 to 4 of Group I1.
Note: The fees in Group I1 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I1—Ultrasound</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 1—General</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55028</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Head, ultrasound scan of (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55029</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Head, ultrasound scan of (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55030</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Orbital contents, ultrasound scan of (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55031</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Orbital contents, ultrasound scan of (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55032</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Neck, one or more structures of, ultrasound scan of (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55033</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Neck, one or more structures of, ultrasound scan of (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="page-break-inside:avoid"><span>55036</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="page-break-inside:avoid"><span>Abdomen, ultrasound scan of (including scan of urinary tract when performed), for morphological assessment, if:</span></p><p class="Tablea"><span>(a) the service is not solely a transrectal ultrasonic examination of any of the following:</span></p><p class="Tablei"><span>(i) prostate gland;</span></p><p class="Tablei"><span>(ii) bladder base;</span></p><p class="Tablei"><span>(iii) urethra; and</span></p><p class="Tablea" style="page-break-inside:avoid"><span>(b) within 24 hours of the service, a service mentioned in item</span><span> </span><span>55038 is not performed on the same patient by the providing practitioner (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right; page-break-inside:avoid"><span>112.95</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55037</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Abdomen, ultrasound scan of (including scan of urinary tract when performed), for morphological assessment, if the service is not solely a transrectal ultrasonic examination of any of the following:</span></p><p class="Tablea"><span>(a) prostate gland;</span></p><p class="Tablea"><span>(b) bladder base;</span></p><p class="Tablea"><span>(c) urethra (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55038</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Urinary tract, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is not solely a transrectal ultrasonic examination of any of the following:</span></p><p class="Tablei"><span>(i) prostate gland;</span></p><p class="Tablei"><span>(ii) bladder base;</span></p><p class="Tablei"><span>(iii) urethra; and</span></p><p class="Tablea"><span>(b) within 24 hours of the service, a service mentioned in item</span><span> </span><span>55036 or 55065 is not performed on the same patient by the providing practitioner (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55039</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Urinary tract, ultrasound scan of, if the service is not solely a transrectal ultrasonic examination of any of the following:</span></p><p class="Tablea"><span>(a) prostate gland;</span></p><p class="Tablea"><span>(b) bladder base;</span></p><p class="Tablea"><span>(c) urethra (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55048</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Scrotum, ultrasound scan of (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>111.15</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55049</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Scrotum, ultrasound scan of (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55054</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Ultrasonic cross</span><span>‑</span><span>sectional echography, in conjunction with a surgical procedure (other than a procedure to which item</span><span> </span><span>55848 or 55850 applies) using interventional techniques, not being a service associated with a service to which any other item in this Group applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55065</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis, ultrasound scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the service is not solely a service to which an item (other than item</span><span> </span><span>55736 or 55739) in Subgroup 5 of this Group applies or a transrectal ultrasonic examination of any of the following:</span></p><p class="Tablei"><span>(i) prostate gland;</span></p><p class="Tablei"><span>(ii) bladder base;</span></p><p class="Tablei"><span>(iii) urethra; and</span></p><p class="Tablea"><span>(b) within 24 hours of the service, a service mentioned in item</span><span> </span><span>55038 is not performed on the same patient by the providing practitioner (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>99.70</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55066</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Breasts, both, ultrasound scan of, in conjunction with a surgical procedure using interventional techniques, if:</span></p><p class="Tablea"><span>(a) the request for the scan indicates that an ultrasound</span><span>‑</span><span>guided breast intervention be performed; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with any other item in this Group (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>221.45</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="page-break-inside:avoid; page-break-after:avoid"><span>55068</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis, ultrasound scan of, by any or all approaches, if the service is not solely a service to which an item (other than item</span><span> </span><span>55736 or 55739) in Subgroup 5 of this Group applies or a transrectal ultrasonic examination of any of the following:</span></p><p class="Tablea"><span>(a) prostate gland;</span></p><p class="Tablea"><span>(b) bladder base;</span></p><p class="Tablea"><span>(c) urethra (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right; page-break-inside:avoid; page-break-after:avoid"><span>35.50</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55070</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Breast, one, ultrasound scan of (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>99.70</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55071</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Breast, one, ultrasound scan of, in conjunction with a surgical procedure using interventional techniques, if:</span></p><p class="Tablea"><span>(a) the request for the scan indicates that an ultrasound</span><span>‑</span><span>guided breast intervention be performed; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with any other item in this group (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>210.45</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55073</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Breast, one, ultrasound scan of (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>34.55</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55076</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Breasts, both, ultrasound scan of (including an ultrasound scan for post mastectomy surveillance) (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55079</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Breasts, both, ultrasound scan of (including an ultrasound scan for post mastectomy surveillance) (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55084</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Urinary bladder, ultrasound scan of, by any or all approaches, if within 24 hours of the service, a service mentioned in item</span><span> </span><span>11917, 55036, 55038, 55065, 55600 or 55603 is not performed on the same patient by the providing practitioner (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>99.70</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55085</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Urinary bladder, ultrasound scan of, by any or all approaches, if within 24 hours of the service, a service mentioned in item</span><span> </span><span>11917, 55037, 55039, 55068, 55600 or 55603 is not performed on the same patient by the providing practitioner (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>34.55</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 2—Cardiac</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55118</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Heart, two</span><span>‑</span><span>dimensional or three</span><span>‑</span><span>dimensional real time transoesophageal examination of, from at least 2 levels, and in more than one plane at each level, if:</span></p><p class="Tablea"><span>(a) the service includes:</span></p><p class="Tablei"><span>(i) real time colour flow mapping and, if indicated, pulsed wave Doppler examination; and</span></p><p class="Tablei"><span>(ii) recordings on digital media; and</span></p><p class="Tablea"><span>(b) the service is not:</span></p><p class="Tablei"><span>(i) an intra</span><span>‑</span><span>operative service; or</span></p><p class="Tablei"><span>(ii) a service associated with a service to which an item in Subgroup 3 of this Group applies</span></p><p class="Tablea"><span>(R) (H) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>279.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55130</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><a id="_Hlk80178069"><span>Intraoperative two</span><span>‑</span><span>dimensional or three</span><span>‑</span><span>dimensional real time transoesophageal echocardiography, if the service:</span></a></p><p class="Tablea"><span>(a) includes Doppler techniques with colour flow mapping and recordings on digital media; and</span></p><p class="Tablea"><span>(b) is performed during cardiac surgery; and</span></p><p class="Tablea"><span>(c) incorporates sequential assessment of cardiac function before and after the surgical procedure; and</span></p><p class="Tablea"><span>(d) is not associated with a service to which item</span><span> </span><span>55135, or an item in Subgroup 3, applies</span></p><p class="Tablea"><span class="TabletextChar">(R) (H) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.55</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55135</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><a id="_Hlk80178864"><span>Intraoperative two</span><span>‑</span><span>dimensional or three</span><span>‑</span><span>dimensional real time transoesophageal echocardiography, if the service:</span></a></p><p class="Tablea"><span>(a) is provided on the same day as a service to which item</span><span> </span><span>38477, 38484, 38499, 38516 or 38517 applies; and</span></p><p class="Tablea"><span>(b) includes Doppler techniques with colour flow mapping and recordings on digital media; and</span></p><p class="Tablea"><span>(c) is performed during cardiac valve surgery (replacement or repair); and</span></p><p class="Tablea"><span>(d) incorporates sequential assessment of cardiac function and valve competence before and after the surgical procedure; and</span></p><p class="Tablea"><span>(e) is not associated with a service to which item</span><span> </span><span>22054,</span><span> </span><span>55130, or an item in Subgroup 3, applies</span></p><p class="Tablea"><span class="TabletextChar">(R) (H) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.90</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 3—Vascular</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55238</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, unilateral, involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of arteries or bypass grafts in the lower limb or of arteries and bypass grafts in the lower limb, below the inguinal ligament, not being a service associated with any of the following:</span></p><p class="Tablea"><span>(a) a service to which an item in Subgroup 4 applies;</span></p><p class="Tablea"><span>(b) a service to which item</span><span> </span><span>55880, 55881, 55882, 55883, 55884, 55885, 55886, 55887, 55888, 55889, 55890, 55891, 55892, 55893, 55894 or 55895 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55244</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, unilateral, involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of veins in the lower limb, below the inguinal ligament, for acute venous thrombosis, not being a service associated with any of the following:</span></p><p class="Tablea"><span>(a) a service to which item</span><span> </span><span>55246 applies;</span></p><p class="Tablea"><span>(b) a service to which an item in Subgroup 4 applies;</span></p><p class="Tablea"><span>(c) a service to which item</span><span> </span><span>55880, 55881, 55882, 55883, 55884, 55885, 55886, 55887, 55888, 55889, 55890, 55891, 55892, 55893, 55894 or 55895 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55246</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, unilateral, involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of veins in the lower limb, below the inguinal ligament, for chronic venous disease, not being a service associated with any of the following:</span></p><p class="Tablea"><span>(a) a service to which item</span><span> </span><span>55244 applies;</span></p><p class="Tablea"><span>(b) a service to which an item in Subgroup 4 applies;</span></p><p class="Tablea"><span>(c) a service to which item</span><span> </span><span>55880, 55881, 55882, 55883, 55884, 55885, 55886, 55887, 55888, 55889, 55890, 55891, 55892, 55893, 55894 or 55895 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55248</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, unilateral, involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of arteries or bypass grafts in the upper limb or of arteries and bypass grafts in the upper limb, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55252</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, unilateral, involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of veins in the upper limb, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55274</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, bilateral, involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of extra</span><span>‑</span><span>cranial bilateral carotid and vertebral vessels, with or without subclavian and innominate vessels, with or without oculoplethysmography or peri</span><span>‑</span><span>orbital Doppler examination, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55276</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of intra</span><span>‑</span><span>abdominal, aorta and iliac arteries or inferior vena cava and iliac veins or of intra</span><span>‑</span><span>abdominal, aorta and iliac arteries and inferior vena cava and iliac veins, excluding pregnancy related studies, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55278</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of renal or visceral vessels or of renal and visceral vessels, including aorta, inferior vena cava and iliac vessels as required excluding pregnancy related studies, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55280</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of intra</span><span>‑</span><span>cranial vessels, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55282</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning involving B mode ultrasound imaging and integrated Doppler flow measurements:</span></p><p class="Tablea"><span>(a) by spectral analysis of cavernosal artery of the penis following intracavernosal administration of a vasoactive agent; and</span></p><p class="Tablea"><span>(b) performed during the period of pharmacological activity of the injected agent, to confirm a diagnosis of vascular aetiology for impotence; and</span></p><p class="Tablea"><span>(c) if a specialist in diagnostic radiology, nuclear medicine, sexual health medicine, urology, general surgery (sub</span><span>‑</span><span>specialising in vascular surgery) or a consultant physician in nuclear medicine attends the patient in person at the practice location where the service is performed, immediately before or for a period during the performance of the service; and</span></p><p class="Tablea"><span>(d) if the specialist or consultant physician interprets the results and prepares a report, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55284</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning involving B mode ultrasound imaging and integrated Doppler flow measurements:</span></p><p class="Tablea"><span>(a) by spectral analysis of cavernosal tissue of the penis to confirm a diagnosis; and</span></p><p class="Tablea"><span>(b) if indicated, assess the progress and management of:</span></p><p class="Tablei"><span>(i) priapism; or</span></p><p class="Tablei"><span>(ii) fibrosis of any type; or</span></p><p class="Tablei"><span>(iii) fracture of the tunica; or</span></p><p class="Tablei"><span>(iv) arteriovenous malformations; and</span></p><p class="Tablea"><span>(c) if a specialist in diagnostic radiology, nuclear medicine, sexual health medicine, urology, general surgery (sub</span><span>‑</span><span>specialising in vascular surgery) or a consultant physician in nuclear medicine attends the patient in person at the practice location where the service is performed, immediately before or for a period during the performance of the service; and</span></p><p class="Tablea"><span>(d) if the specialist or consultant physician interprets the results and prepares a report, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55292</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, unilateral, involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of surgically created arteriovenous fistula or surgically created arteriovenous access grafts in the upper or lower limbs, not being a service associated with a service to which an item in Subgroup 4 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55294</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning involving B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of arteries or veins, or both, including any associated skin marking, for mapping of bypass conduit before vascular surgery, not being a service associated with any of the following:</span></p><p class="Tablea"><span>(a) a service to which an item in Subgroup 3 or 4 applies;</span></p><p class="Tablea"><span>(b) a service to which item</span><span> </span><span>55880, 55881, 55882, 55883, 55884, 55885, 55886, 55887, 55888, 55889, 55890, 55891, 55892, 55893, 55894 or 55895 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>172.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55296</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, unilateral, involving B mode ultrasound imaging and integrated Doppler flow spectral analysis and marking of veins in the lower limbs below the inguinal ligament before varicose vein surgery, including any associated skin marking, not being a service associated with any of the following:</span></p><p class="Tablea"><span>(a) a service to which an item in Subgroup 3 or 4 applies;</span></p><p class="Tablea"><span>(b) a service to which item</span><span> </span><span>55880, 55881, 55882, 55883, 55884, 55885, 55886, 55887, 55888, 55889, 55890, 55891, 55892, 55893, 55894 or 55895 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>112.70</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 4—Urological</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55600</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Prostate, bladder base and urethra, ultrasound scan of, if performed:</span></p><p class="Tablea"><span>(a) personally by a medical practitioner (not being the medical practitioner who assessed the patient as specified in paragraph</span><span> </span><span>(c)) using one or more transducer probes that can obtain both axial and sagittal scans in 2 planes at right angles; and</span></p><p class="Tablea"><span>(b) after a digital rectal examination of the prostate by that medical practitioner; and</span></p><p class="Tablea"><span>(c) on a patient who has been assessed by:</span></p><p class="Tablei"><span>(i) a specialist in urology, radiation oncology or medical oncology; or</span></p><p class="Tablei"><span>(ii) a consultant physician in medical oncology;</span></p><p class="Tablea"><span style="width:14.2pt; text-indent:0pt; display:inline-block"></span><span>who has:</span></p><p class="Tablei"><span>(iii) examined the patient in the 60 days before the scan; and</span></p><p class="Tablei"><span>(iv) recommended the scan for the management of the patient’s current prostatic disease (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55603</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Prostate, bladder base and urethra, ultrasound scan of, if performed:</span></p><p class="Tablea"><span>(a) personally by a medical practitioner who made the assessment mentioned in paragraph</span><span> </span><span>(c) using one or more transducer probes that can obtain both axial and sagittal scans in 2 planes at right angles; and</span></p><p class="Tablea"><span>(b) after a digital rectal examination of the prostate by that medical practitioner; and</span></p><p class="Tablea"><span>(c) on a patient who has been assessed by:</span></p><p class="Tablei"><span>(i) a specialist in urology, radiation oncology or medical oncology; or</span></p><p class="Tablei"><span>(ii) a consultant physician in medical oncology;</span></p><p class="Tablea"><span style="width:14.2pt; text-indent:0pt; display:inline-block"></span><span>who has:</span></p><p class="Tablei"><span>(iii) examined the patient in the 60 days before the scan; and</span></p><p class="Tablei"><span>(iv) recommended the scan for the management of the patient’s current prostatic disease (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr></tbody></table>
Subdivision C—Subgroup 5 of Group I1: obstetric and gynaecological
2.1.4 Obstetric and gynaecological ultrasound services—limits
(1) For NR‑type diagnostic imaging services mentioned in an item in this Subdivision (other than item 55758), the specified fee for no more than 3 services provided to the same patient in any one pregnancy applies.
(2) For any patient, items 55706, 55707, 55708, 55709, 55718, 55723, 55742, 55743, 55759, 55762, 55768 and 55770 are applicable only once in a pregnancy.
2.1.5 Obstetric and gynaecological services—referrals and clinical notes
(1) A referral for a service mentioned in item 55700, 55704, 55707, 55712, 55718, 55721, 55740, 55742, 55757, 55759, 55764, 55768 and 55772 must state the relevant condition or clinical indication for the service.
(2) If a referral for a service mentioned in item 55712, 55721, 55764 or 55772 is given by a medical practitioner who has obstetric privileges at a non‑metropolitan hospital, the referral must also state the words ‘non‑metropolitan obstetric privileges’.
(3) A medical practitioner’s clinical notes for a service mentioned in item 55703, 55705, 55708, 55715, 55723, 55725, 55741, 55743, 55758, 55762, 55766, 55770 or 55774 must state the relevant condition or clinical indication for the service.
2.1.6 Items in Subgroup 5 of Group I1
This clause sets out items in Subgroup 5 of Group I1.
Note: The fees in Group I1 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="page-break-inside:avoid"><span>Group I1—Ultrasound</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="page-break-inside:avoid"><span>Column 1</span></p><p class="TableHeading" style="page-break-inside:avoid"><span>Item</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="page-break-inside:avoid"><span>Column 2</span></p><p class="TableHeading" style="page-break-inside:avoid"><span>Diagnostic imaging service</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right; page-break-inside:avoid"><span>Column 3</span></p><p class="TableHeading" style="text-align:right; page-break-inside:avoid"><span>Fee ($)</span></p></td></tr></thead><tbody><tr style="height:3.5pt"><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="page-break-inside:avoid"><span>Subgroup 5—Obstetric and gynaecological</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="page-break-inside:avoid; page-break-after:avoid"><span>55700</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, for determining the gestation, location, viability or number of fetuses, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is less than 12 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55704, 55705, 55707, 55708, 55740, 55741, 55742 or 55743 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right; page-break-inside:avoid; page-break-after:avoid"><span>60.90</span></p></td></tr><tr style="height:1pt"><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55703</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, for determining the gestation, location, viability or number of fetuses, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is less than 12 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55704, 55705, 55707, 55708, 55740, 55741, 55742 or 55743 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>35.50</span></p></td></tr><tr style="height:1pt"><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55704</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, for determining the structure, gestation, location, viability or number of fetuses, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is 12 to 16 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>71.05</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55705</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, for determining the structure, gestation, location, viability or number of fetuses, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is 12 to 16 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>35.50</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55706</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, if:</span></p><p class="Tablea"><span>(a) the dating for the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound:</span></p><p class="Tablei"><span>(i) is not performed in the same pregnancy as item</span><span> </span><span>55709; and</span></p><p class="Tablei"><span>(ii) is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>101.50</span></p></td></tr><tr style="height:38.25pt"><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55707</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the pregnancy (as confirmed by the current ultrasound) is dated by a fetal crown rump length of 45 to 84 mm; and</span></p><p class="Tablea"><span>(b) nuchal translucency measurement is performed to assess the risk of fetal abnormality; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>71.05</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55708</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the pregnancy (as confirmed by the current ultrasound) is dated by a crown rump length of 45 to 84 mm; and</span></p><p class="Tablea"><span>(b) nuchal translucency measurement is performed to assess the risk of fetal abnormality; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>35.50</span></p></td></tr><tr style="height:10pt"><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55709</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound:</span></p><p class="Tablei"><span>(i) is not performed in the same pregnancy as item</span><span> </span><span>55706; and</span></p><p class="Tablei"><span>(ii) is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.55</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55712</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, if:</span></p><p class="Tablea"><span>(a) the current ultrasound is requested by a medical practitioner who:</span></p><p class="Tablei"><span>(i) is a Member or a Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists; or</span></p><p class="Tablei"><span>(ii) has a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iii) has a qualification recognised by the Royal Australian and New Zealand College of Obstetricians and Gynaecologists as being equivalent to a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iv) has obstetric privileges at a non</span><span>‑</span><span>metropolitan hospital; and</span></p><p class="Tablea"><span>(b) the dating of the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks of gestation; and</span></p><p class="Tablea"><span>(c) further examination is clinically indicated after performance, in the same pregnancy, of a scan mentioned in item</span><span> </span><span>55706 or 55709; and</span></p><p class="Tablea"><span>(d) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>116.70</span></p></td></tr><tr style="height:28.1pt"><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55715</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, performed by or on behalf of a medical practitioner who is a Member or a Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) further examination is clinically indicated after performance, in the same pregnancy, of a scan mentioned in item</span><span> </span><span>55706 or 55709; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>40.60</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55718</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound:</span></p><p class="Tablei"><span>(i) is not performed in the same pregnancy as item</span><span> </span><span>55723; and</span></p><p class="Tablei"><span>(ii) is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>101.50</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55721</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the current ultrasound is requested by a medical practitioner who:</span></p><p class="Tablei"><span>(i) is a Member or a Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists; or</span></p><p class="Tablei"><span>(ii) has a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iii) has a qualification recognised by the Royal Australian and New Zealand College of Obstetricians and Gynaecologists as being equivalent to a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iv) has obstetric privileges at a non</span><span>‑</span><span>metropolitan hospital; and</span></p><p class="Tablea"><span>(b) the dating of the pregnancy (as confirmed by current ultrasound) is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(c) further examination is clinically indicated in the same pregnancy to which item</span><span> </span><span>55718 or 55723 applies; and</span></p><p class="Tablea"><span>(d) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>116.70</span></p></td></tr><tr style="height:33.5pt"><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55723</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the current ultrasound:</span></p><p class="Tablei"><span>(i) is not performed in the same pregnancy as item</span><span> </span><span>55718; and</span></p><p class="Tablei"><span>(ii) is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.55</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55725</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, performed by or on behalf of a medical practitioner who is a Member or a Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) further examination is clinically indicated in the same pregnancy to which item</span><span> </span><span>55718 or 55723 applies; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>40.60</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55729</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Duplex scanning, if:</span></p><p class="Tablea"><span>(a) the service involves:</span></p><p class="Tablei"><span>(i) B mode ultrasound imaging and integrated Doppler flow measurements by spectral analysis of the umbilical artery; and</span></p><p class="Tablei"><span>(ii) measured assessment of amniotic fluid volume after the 24th week of gestation; and</span></p><p class="Tablea"><span>(b) there is reason to suspect intrauterine growth retardation or a significant risk of fetal death;</span></p><p class="Tabletext"><span>—examination and report (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>27.65</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55736</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis, ultrasound scan of, in association with saline infusion of the endometrial cavity, by any or all approaches, if a previous transvaginal ultrasound has revealed an abnormality of the uterus or fallopian tube (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>128.90</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55739</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis, ultrasound scan of, in association with saline infusion of the endometrial cavity, by any or all approaches, if a previous transvaginal ultrasound has revealed an abnormality of the uterus or fallopian tube (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>57.85</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55740</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, for determining the structure, gestation, location, viability or number of fetuses, if:</span></p><p class="Tablea"><span>(a) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(b) the dating of the pregnancy (as confirmed by the current ultrasound) is 12 to 16 weeks of gestation; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>108.30</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55741</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, for determining the structure, gestation, location, viability or number of fetuses, if:</span></p><p class="Tablea"><span>(a) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(b) the dating of the pregnancy (as confirmed by the current ultrasound) is 12 to 16 weeks of gestation; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>54.10</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55742</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(b) the pregnancy (as confirmed by the current ultrasound) is dated by a fetal crown rump length of 45 to 84 mm; and</span></p><p class="Tablea"><span>(c) nuchal translucency measurement is performed to assess the risk of fetal abnormality; and</span></p><p class="Tablea"><span>(d) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>108.30</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55743</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(b) the pregnancy (as confirmed by the current ultrasound) is dated by a fetal crown rump length of 45 to 84 mm; and</span></p><p class="Tablea"><span>(c) nuchal translucency measurement is performed to assess the risk of fetal abnormality; and</span></p><p class="Tablea"><span>(d) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>54.10</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55757</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, for cervical length assessment for risk of preterm labour, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is between 14 and 30 weeks of gestation; and</span></p><p class="Tablea"><span>(b) any of the following apply:</span></p><p class="Tablei"><span>(i) the patient has a history indicating high risk of preterm labour or birth or second trimester fetal loss;</span></p><p class="Tablei"><span>(ii) the patient has symptoms suggestive of threatened preterm labour or second trimester fetal loss;</span></p><p class="Tablei"><span>(iii) the patient’s cervical length is less than 25 mm on an ultrasound before 28 weeks gestation; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>51.55</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55758</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, for cervical length assessment for risk of preterm labour, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) the dating of the pregnancy (as confirmed by the current ultrasound) is between 14 and 30 weeks of gestation; and</span></p><p class="Tablea"><span>(b) any of the following apply:</span></p><p class="Tablei"><span>(i) the patient has a history indicating high risk of preterm labour or birth or second trimester fetal loss;</span></p><p class="Tablei"><span>(ii) the patient has symptoms suggestive of threatened preterm labour or second trimester fetal loss;</span></p><p class="Tablei"><span>(iii) the patient’s cervical length is less than 25 mm on an ultrasound before 28 weeks gestation; and</span></p><p class="Tablea"><span>(c) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in another item in this Subgroup (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>19.60</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>55759</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, if:</span></p><p class="Tablea"><span>(a) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(b) the dating of the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks gestation; and</span></p><p class="Tablea"><span>(c) the service mentioned in item</span><span> </span><span>55706, 55709, 55712, 55715 or 55762 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(d) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>152.25</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55762</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, if:</span></p><p class="Tablea"><span>(a) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(b) the dating of the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks gestation; and</span></p><p class="Tablea"><span>(c) the service mentioned in item</span><span> </span><span>55706, 55709, 55712, 55715 or 55759 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(d) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>60.90</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55764</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, if:</span></p><p class="Tablea"><span>(a) the service is requested by a medical practitioner who:</span></p><p class="Tablei"><span>(i) is a Member or Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists; or</span></p><p class="Tablei"><span>(ii) has a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iii) has a qualification recognised by the Royal Australian and New Zealand College of Obstetricians and Gynaecologists as equivalent to a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iv) has obstetric privileges at a non</span><span>‑</span><span>metropolitan hospital; and</span></p><p class="Tablea"><span>(b) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(c) the dating of the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks gestation; and</span></p><p class="Tablea"><span>(d) further examination is clinically indicated in the same pregnancy in which item</span><span> </span><span>55759 or 55762 has been performed; and</span></p><p class="Tablea"><span>(e) the service mentioned in item</span><span> </span><span>55706, 55709, 55712 or 55715 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(f) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R))</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>162.40</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55766</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, with measurement of all parameters for dating purposes, performed by or on behalf of a medical practitioner, who is a Member or Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists, if:</span></p><p class="Tablea"><span>(a) an ultrasound of the same pregnancy confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(b) the dating of the pregnancy (as confirmed by the current ultrasound) is 17 to 22 weeks of gestation; and</span></p><p class="Tablea"><span>(c) further examination is clinically indicated in the same pregnancy in which item</span><span> </span><span>55759 or 55762 has been performed; and</span></p><p class="Tablea"><span>(d) the service mentioned in item</span><span> </span><span>55706, 55709, 55712 or 55715 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(e) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>65.95</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55768</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) dating of the pregnancy (as confirmed by the current ultrasound) is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) an ultrasound confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(c) the service is not performed in the same pregnancy as item</span><span> </span><span>55770; and</span></p><p class="Tablea"><span>(d) the service mentioned in item</span><span> </span><span>55718, 55721, 55723 or 55725 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(e) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>152.25</span></p></td></tr><tr style="height:11.25pt"><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55770</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) dating of the pregnancy (as confirmed by the current ultrasound) is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) an ultrasound confirms a multiple pregnancy; and</span></p><p class="Tablea"><span>(c) the service is not performed in the same pregnancy as item</span><span> </span><span>55768; and</span></p><p class="Tablea"><span>(d) the service mentioned in item</span><span> </span><span>55718, 55721, 55723 or 55725 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(e) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>60.90</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55772</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, if:</span></p><p class="Tablea"><span>(a) dating of the pregnancy as confirmed by the current ultrasound is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) the service is requested by a medical practitioner who:</span></p><p class="Tablei"><span>(i) is a Member or Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists; or</span></p><p class="Tablei"><span>(ii) has a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iii) has a qualification recognised by the Royal Australian and New Zealand College of Obstetricians and Gynaecologists as equivalent to a Diploma of Obstetrics; or</span></p><p class="Tablei"><span>(iv) has obstetric privileges at a non</span><span>‑</span><span>metropolitan hospital; and</span></p><p class="Tablea"><span>(c) further examination is clinically indicated in the same pregnancy to which item</span><span> </span><span>55768 or 55770 has been performed; and</span></p><p class="Tablea"><span>(d) the pregnancy as confirmed by an ultrasound is a multiple pregnancy; and</span></p><p class="Tablea"><span>(e) the service mentioned in item</span><span> </span><span>55718, 55721, 55723 or 55725 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(f) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (R)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>162.40</span></p></td></tr><tr><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55774</span></p></td><td style="width:76.3%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Pelvis or abdomen, pregnancy</span><span>‑</span><span>related or pregnancy complication, fetal development and anatomy, ultrasound (the </span><span style="font-weight:bold; font-style:italic">current ultrasound</span><span>) scan of, by any or all approaches, performed by or on behalf of a medical practitioner who is a Member or a Fellow of the Royal Australian and New Zealand College of Obstetricians and Gynaecologists, if:</span></p><p class="Tablea"><span>(a) dating of the pregnancy as confirmed by the current ultrasound is after 22 weeks of gestation; and</span></p><p class="Tablea"><span>(b) further examination is clinically indicated in the same pregnancy to which item</span><span> </span><span>55768 or 55770 has been performed; and</span></p><p class="Tablea"><span>(c) the pregnancy as confirmed by an ultrasound is a multiple pregnancy; and</span></p><p class="Tablea"><span>(d) the service mentioned in item</span><span> </span><span>55718, 55721, 55723 or 55725 is not performed in conjunction with the current ultrasound during the same pregnancy; and</span></p><p class="Tablea"><span>(e) the current ultrasound is not performed on the same patient within 24 hours of a service mentioned in item</span><span> </span><span>55757 or 55758 (NR)</span></p></td><td style="width:11.74%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>65.95</span></p></td></tr></tbody></table>
Subdivision D—Subgroup 6 of Group I1: musculoskeletal ultrasound
2.1.8 Unilateral item cannot be claimed twice if bilateral item could have been claimed
If:
(a) 2 services (the unilateral services) to which an item listed in column 1 of an item of table 2.1.8 applies are provided in conjunction with each other; and
(b) a service to which an item in column 2 of the item applies could have been provided instead of the 2 unilateral services;
only one of the unilateral services may be claimed.
The fee applicable for items in this Subdivision includes any views of another part of the patient taken for comparison purposes.
2.1.10 Items in Subgroup 6 of Group I1
This clause sets out items in Subgroup 6 of Group I1.
Note: The fees in Group I1 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I1—Ultrasound</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 6—Musculoskeletal ultrasound</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55812</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Chest or abdominal wall, one or more areas, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55070, 55073, 55076 or 55079 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55814</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Chest or abdominal wall, one or more areas, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55070, 55073, 55076 or 55079 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55844</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Assessment of a mass associated with the skin or subcutaneous structures, not being a part of the musculoskeletal system, one or more areas, ultrasound scan of (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>88.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55846</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Assessment of a mass associated with the skin or subcutaneous structures, not being a part of the musculoskeletal system, one or more areas, ultrasound scan of (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55848</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Musculoskeletal ultrasound, in conjunction with a surgical procedure using interventional techniques, not being a service associated with a service to which any other item in this group applies, and not performed in conjunction with a service mentioned in item</span><span> </span><span>55054 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>138.65</span></p></td></tr><tr style="height:10pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55850</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Musculoskeletal ultrasound, in conjunction with a surgical procedure using interventional techniques, inclusive of a diagnostic musculoskeletal ultrasound service, if:</span></p><p class="Tablea"><span>(a) a medical practitioner or nurse practitioner has indicated on a referral for a musculoskeletal ultrasound that an ultrasound guided intervention be performed if clinically indicated; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55054 or any other item in this Subgroup (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>183.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55852</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Paediatric spine, spinal cord and overlying subcutaneous tissues, ultrasound scan of (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55854</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Paediatric spine, spinal cord and overlying subcutaneous tissues, ultrasound scan of (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55856</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hand or wrist, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55858 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55857</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hand or wrist, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55859 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55858</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hand or wrist, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55856 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55859</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hand or wrist, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55857 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55860</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Forearm or elbow, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55862 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55861</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Forearm or elbow, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55863 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55862</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Forearm or elbow, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55860 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55863</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Forearm or elbow, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55861 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55864</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Shoulder or upper arm, or both, left or right, ultrasound scan of, if</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) an injury to a muscle, tendon or muscle/tendon junction;</span></p><p class="Tablei"><span>(ii) rotator cuff tear, calcification or tendinosis (biceps, subscapular, supraspinatus or infraspinatus);</span></p><p class="Tablei"><span>(iii) biceps subluxation;</span></p><p class="Tablei"><span>(iv) capsulitis and bursitis;</span></p><p class="Tablei"><span>(v) a mass, including a ganglion;</span></p><p class="Tablei"><span>(vi) an occult fracture;</span></p><p class="Tablei"><span>(vii) acromioclavicular joint pathology; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55866 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55865</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Shoulder or upper arm, or both, left or right, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) an injury to a muscle, tendon or muscle/tendon junction;</span></p><p class="Tablei"><span>(ii) rotator cuff tear, calcification or tendinosis (biceps, subscapular, supraspinatus or infraspinatus);</span></p><p class="Tablei"><span>(iii) biceps subluxation;</span></p><p class="Tablei"><span>(iv) capsulitis and bursitis;</span></p><p class="Tablei"><span>(v) a mass, including a ganglion;</span></p><p class="Tablei"><span>(vi) an occult fracture;</span></p><p class="Tablei"><span>(vii) acromioclavicular joint pathology; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55867 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55866</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Shoulder or upper arm, or both, left and right, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) an injury to a muscle, tendon or muscle/tendon junction;</span></p><p class="Tablei"><span>(ii) rotator cuff tear, calcification or tendinosis (biceps, subscapular, supraspinatus or infraspinatus);</span></p><p class="Tablei"><span>(iii) biceps subluxation;</span></p><p class="Tablei"><span>(iv) capsulitis and bursitis;</span></p><p class="Tablei"><span>(v) a mass, including a ganglion;</span></p><p class="Tablei"><span>(vi) an occult fracture;</span></p><p class="Tablei"><span>(vii) acromioclavicular joint pathology; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55864 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55867</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Shoulder or upper arm, or both, left and right, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) an injury to a muscle, tendon or muscle/tendon junction;</span></p><p class="Tablei"><span>(ii) rotator cuff tear, calcification or tendinosis (biceps, subscapular, supraspinatus or infraspinatus);</span></p><p class="Tablei"><span>(iii) biceps subluxation;</span></p><p class="Tablei"><span>(iv) capsulitis and bursitis;</span></p><p class="Tablei"><span>(v) a mass, including a ganglion;</span></p><p class="Tablei"><span>(vi) an occult fracture;</span></p><p class="Tablei"><span>(vii) acromioclavicular joint pathology; and</span></p><p class="Tablea"><span>(c) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55865 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55868</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hip or groin, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55870 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55869</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hip or groin, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55871 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55870</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hip or groin, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55868 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55871</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Hip or groin, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55869 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55872</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Paediatric hip examination for dysplasia, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55874 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55873</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Paediatric hip examination for dysplasia, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55875 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55874</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Paediatric hip examination for dysplasia, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55872 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55875</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Paediatric hip examination for dysplasia, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55873 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55876</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Buttock or thigh, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55878 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55877</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Buttock or thigh or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55879 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55878</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Buttock or thigh, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55876 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55879</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Buttock or thigh, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55877 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55880</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Knee, left or right, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) abnormality of tendons or bursae about the knee;</span></p><p class="Tablei"><span>(ii) a meniscal cyst, popliteal fossa cyst, mass or pseudomass;</span></p><p class="Tablei"><span>(iii) a nerve entrapment or a nerve or nerve sheath tumour;</span></p><p class="Tablei"><span>(iv) an injury of collateral ligaments; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55882 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55881</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Knee, left or right, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) abnormality of tendons or bursae about the knee;</span></p><p class="Tablei"><span>(ii) a meniscal cyst, popliteal fossa cyst, mass or pseudomass;</span></p><p class="Tablei"><span>(iii) a nerve entrapment or a nerve or nerve sheath tumour;</span></p><p class="Tablei"><span>(iv) an injury of collateral ligaments; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55883 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55882</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Knee, left and right, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) abnormality of tendons or bursae about the knee;</span></p><p class="Tablei"><span>(ii) a meniscal cyst, popliteal fossa cyst, mass or pseudomass;</span></p><p class="Tablei"><span>(iii) a nerve entrapment or a nerve or nerve sheath tumour;</span></p><p class="Tablei"><span>(iv) an injury of collateral ligaments; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55880 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55883</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Knee, left and right, ultrasound scan of, if:</span></p><p class="Tablea"><span>(a) the service is used for the assessment of one or more of the following suspected or known conditions:</span></p><p class="Tablei"><span>(i) abnormality of tendons or bursae about the knee;</span></p><p class="Tablei"><span>(ii) a meniscal cyst, popliteal fossa cyst, mass or pseudomass;</span></p><p class="Tablei"><span>(iii) a nerve entrapment or a nerve or nerve sheath tumour;</span></p><p class="Tablei"><span>(iv) an injury of collateral ligaments; and</span></p><p class="Tablea"><span>(b) the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55881 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p style="text-align:right; line-height:normal; font-size:10pt"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55884</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Lower leg, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55886 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55885</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Lower leg, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55887 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55886</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Lower leg, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55884 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55887</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Lower leg, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55885 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55888</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Ankle or hind foot, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55890 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55889</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Ankle or hind foot, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55891 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55890</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Ankle or hind foot, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55888 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55891</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Ankle or hind foot, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55889 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55892</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Mid foot or fore foot, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55894 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>110.75</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55893</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Mid foot or fore foot, or both, left or right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55895 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>38.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55894</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Mid foot or fore foot, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55892 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>122.90</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>55895</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext"><span>Mid foot or fore foot, or both, left and right, ultrasound scan of, if the service is not performed in conjunction with a service mentioned in item</span><span> </span><span>55893 (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top; background-color:#ffffff"><p class="Tabletext" style="text-align:right"><span>42.65</span></p></td></tr></tbody></table>
Subdivision E—Subgroup 7 of Group I1: Transthoracic and stress echocardiograms
2.1.11 Restrictions on items for transthoracic echocardiograms—assessments
Items 55126, 55127, 55128, 55129, 55133 and 55134
(1) Items 55126, 55127, 55128, 55129, 55133 and 55134 apply to a service only if the service includes assessments of each of the following, to the extent possible:
(a) the left ventricular structure and function, including quantification of systolic function using M‑mode, 2‑dimensional or 3‑dimensional imaging and diastolic function;
(b) the right ventricular structure and function, with quantitative assessment;
(c) the left and right atrial structure, including quantification of atrial sizes;
(d) the vascular connections of the heart, including the great vessels and systemic venous structures;
(e) the pericardium and any haemodynamic consequences of pericardial abnormalities;
(f) all present valves, including structural assessment and measurement of blood flow velocities across the valves using pulsed wave and continuous wave Doppler techniques with quantification of stenosis or regurgitation;
(g) additional haemodynamic parameters, including the assessment of pulmonary pressures.
Item 55132
(2) Item 55132 applies to a service only if the service includes assessments of each of the following, to the extent possible:
(a) the ventricular structure and function, including quantification of systolic function (if the ventricular configuration allows accurate quantification) using at least one of M‑mode, 2‑dimensional or 3‑dimensional imaging;
(b) the diastolic function;
(c) the atrial structure, including quantification of atrial sizes;
(d) the vascular connections of the heart, including the great vessels and systemic venous structures;
(e) the pericardium and any haemodynamic consequences of pericardial abnormalities;
(f) all present valves, including structural assessment and measurement of blood flow velocities across the valves using relevant Doppler techniques with quantification;
(g) subxiphoid views where recommended for congenital heart lesions;
(h) additional haemodynamic parameters relevant to the clinical condition under review.
Item 55137
(3) Item 55137 applies to a service only if the service includes assessments of each of the following, to the extent possible:
(a) the ventricular structure and function;
(b) the atrial structure;
(c) the vascular connections of the heart, including the great vessels and systemic venous structures;
(d) the pericardium and any haemodynamic consequences of pericardial abnormalities;
(e) all present valves, including structural assessment and measurement of blood flow velocities across the valves using pulsed wave and continuous wave Doppler techniques with quantification of stenosis or regurgitation.
2.1.12 Restriction on item 55126—timing
Item 55126 does not apply to a service provided to a patient if, in the previous 24 months, a service associated with a service to which item 55127, 55128, 55129, 55132, 55133 or 55134 applies has been provided to the patient.
2.1.13 Restriction on items for stress echocardiograms—patients, requests and requirements
(1) Items 55141, 55143, 55145 and 55146 apply to a service performed on a patient only if:
(a) one or more of subclauses 2.1.14(1), (2) and (3) apply to the patient; and
(b) the request for the service identifies any symptoms or clinical indications mentioned in those subclauses that apply to the patient; and
(c) the service is performed in accordance with clause 2.1.15; and
(d) subclause (2) does not apply to the patient.
(2) This subclause applies to a patient if:
(a) stress echocardiography would not provide adequate information about the patient because of:
(i) the patient’s body habitus, or other physical conditions (including heart rhythm disturbance); or
(ii) the patient’s inability to exercise to the required extent; or
(b) the results of a previous imaging service indicate that a stress echocardiogram service would not provide adequate information.
2.1.14 Stress echocardiograms—patients
(1) This subclause applies to a patient if:
(a) the patient displays symptoms of typical or atypical angina, including constricting discomfort of one or more of the following:
(i) the front of the chest;
(ii) the neck;
(iii) the shoulders;
(iv) the jaw;
(v) the arms; or
(b) the patient’s symptoms are:
(i) precipitated by physical exertion; or
(ii) relieved within 5 minutes or less by rest or glyceryl trinitrate.
(2) This subclause applies to a patient if:
(a) the patient has known coronary artery disease; and
(b) the patient displays one or more symptoms that are suggestive of ischaemia; and
(c) the symptoms:
(i) are not adequately controlled with medical therapy; or
(ii) have evolved since the last functional study undertaken of the patient.
(3) This subclause applies to a patient if one or more of the following clinical indications apply to the patient:
(a) assessment of myocardial ischaemia with exercise is required because the patient has congenital heart lesions, has undergone surgery and reversal of ischemia is considered possible;
(b) the patient does not have a known coronary artery disease but assessment indicates that resting twelve‑lead electrocardiogram changes are consistent with coronary artery disease or ischaemia;
(c) coronary artery disease related lesions, of uncertain functional significance, have previously been identified on a computed tomography coronary angiography or invasive coronary angiography;
(d) an assessment by a specialist or consultant physician indicates that the patient has potential non‑coronary artery disease, where a stress echocardiography study is likely to assist the diagnosis;
(e) an assessment indicates that the patient has undue exertional dyspnoea of uncertain aetiology;
(f) a pre‑operative assessment of the patient, who has a functional capacity of less than 4 metabolic equivalents, confirms that surgery is an intermediate to high risk, and the patient also has at least one of the following conditions:
(i) ischaemic heart disease;
(ii) previous myocardial infarction;
(iii) heart failure;
(iv) stroke;
(v) transient ischaemic attack;
(vi) renal dysfunction (serum creatinine greater than 170umol/L or 2 mg/dL or a creatinine clearance of less than 60 mL/min);
(vii) diabetes mellitus requiring insulin therapy;
(g) assessment is required before cardiac surgery or catheter‑based interventions to:
(i) increase the cardiac output to assess the severity of aortic stenosis; or
(ii) determine whether valve regurgitation worsens with exercise or correlates with functional capacity; or
(iii) correlate functional capacity with the ischaemic threshold;
(h) either silent myocardial ischaemia is suspected or, due to the patient’s cognitive capacity or expressive language impairment, it is not possible to accurately assess symptom frequency based on medical history.
2.1.15 Stress echocardiograms—requirements
Safety requirements
(1) A stress echocardiogram service must be performed:
(a) on premises equipped with resuscitation equipment, including a defibrillator; and
(b) by a person trained in the matters mentioned in subclause (4) and cardiopulmonary resuscitation who is in continuous personal attendance during the procedure.
(2) At the time the service is performed, a second person trained in the matters mentioned in subclause (4) and cardiopulmonary resuscitation must be located at the premises, and must be immediately available to respond if required.
(3) One of the persons mentioned in subclauses (1) and (2) must be a medical practitioner.
(4) For the purposes of paragraph (1)(b) and subclause (2), the matters are:
(a) how to safely perform exercise or pharmacological stress monitoring and recording; and
(b) how to recognise the symptoms and signs of cardiac disease.
Other requirements
(5) A stress echocardiogram service must include all of the following:
(a) for an exercise stress echocardiogram:
(i) two‑dimensional recordings before exercise (baseline) from at least 2 acoustic windows; and
(ii) matching recordings at, or immediately after, peak exercise, including at least parasternal short and long axis views, and apical 4‑chamber and 2‑chamber views;
(b) for a pharmacological stress echocardiogram:
(i) two‑dimensional recordings before drug infusion (baseline) from at least 2 acoustic windows; and
(ii) at least 2 matching recordings during drug infusion (with one recording at the time of the peak drug dose), including at least parasternal short and long axis views, and apical 4‑chamber and 2‑chamber views;
(c) recordings on digital media with equipment permitting display of baseline and matching peak images on the same screen;
(d) resting electrocardiogram and continuous multi‑channel electrocardiogram monitoring and recording during stress;
(e) blood pressure monitoring and the recording of other parameters (including heart rate).
2.1.16 Restrictions on items for stress echocardiograms—timing
(1) Item 55141 does not apply to a service provided to a patient if, in the previous 24 months, a service associated with a service to which item 55143, 55145 or 55146 applies has been provided to the patient.
(2) Item 55145 does not apply to a service provided to a patient if, in the previous 24 months, a service associated with a service to which item 55141, 55143 or 55146 applies has been provided to the patient.
(3) Item 55146 does not apply to a service provided to a patient if, in the previous 24 months, a service associated with a service to which item 55143 or 55145 applies has been provided to the patient.
2.1.17 Reduction in fees—multiple services on same day—transthoracic and stress echocardiograms
(1) If a medical practitioner provides 2 or more echocardiogram services mentioned in items 55126, 55127, 55128, 55129, 55132, 55133, 55134, 55137, 55141, 55143, 55145 or 55146 for the same patient on the same day, any fees specified for the items that apply to the services, except the highest fee, are reduced by 40%.
(2) For the purposes of subclause (1):
(a) if 2 or more applicable fees are equally the highest—only one of those fees is taken to be the highest fee; and
(b) if a reduced fee calculated under subclause (1) is not a multiple of 5 cents—the reduced fee is taken to be the nearest amount that is a multiple of 5 cents.
2.1.18 Items in Subgroup 7 of Group I1
This clause sets out items in Subgroup 7 of Group I1.
Note: The fees in Group I1 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="TableHeading"><span>Group I1—Ultrasound</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 7—Transthoracic and stress echocardiograms</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55126</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Initial real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 3 acoustic windows, with recordings on digital media, if the service:</span></p><p class="Tablea"><span>(a) is for the investigation of any of the following:</span></p><p class="Tablei"><span>(i) symptoms or signs of cardiac failure;</span></p><p class="Tablei"><span>(ii) suspected or known ventricular hypertrophy or dysfunction;</span></p><p class="Tablei"><span>(iii) pulmonary hypertension;</span></p><p class="Tablei"><span>(iv) valvular, aortic, pericardial, thrombotic or embolic disease;</span></p><p class="Tablei"><span>(v) heart tumour;</span></p><p class="Tablei"><span>(vi) symptoms or signs of congenital heart disease;</span></p><p class="Tablei"><span>(vii) other rare indications; and</span></p><p class="Tablea"><span>(b) is not associated with a service to which:</span></p><p class="Tablei"><span>(i) another item in this Subgroup applies (except items</span><span> </span><span>55137, 55141, 55143, 55145 and 55146); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 2 applies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(iii) an item in Subgroup 3 applies</span></p><p class="Tabletext"><span>Applicable not more than once in a 24 month period (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>234.15</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55127</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Repeat serial real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 3 acoustic windows, with recordings on digital media, if the service:</span></p><p class="Tablea"><span>(a) is for the investigation of known valvular dysfunction; and</span></p><p class="Tablea"><span>(b) is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><span>(c) is not associated with a service to which:</span></p><p class="Tablei"><span>(i) another item in this Subgroup applies (except items</span><span> </span><span>55137, 55141, 55143, 55145 and 55146); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 2 applies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(iii) an item in Subgroup 3 applies (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>234.15</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55128</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Repeat serial real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 3 acoustic windows, with recordings on digital media, if the service:</span></p><p class="Tablea"><span>(a) is for the investigation of known valvular dysfunction; and</span></p><p class="Tablea"><span>(b) is requested by a medical practitioner (other than a specialist or consultant physician) at, or from, a practice located in a Modified Monash 3, 4, 5, 6 or 7 area; and</span></p><p class="Tablea"><span>(c) is not associated with a service to which:</span></p><p class="Tablei"><span>(i) another item in this Subgroup applies (except items</span><span> </span><span>55137, 55141, 55143, 55145 and 55146); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 2 applies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(iii) an item in Subgroup 3 applies (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>234.15</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55129</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Repeat serial real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 3 acoustic windows, with recordings on digital media, if:</span></p><p class="Tablea"><span>(a) valvular dysfunction is not the primary issue for the patient (although it may be a secondary issue); and</span></p><p class="Tablea"><span>(b) the service is for the investigation of any of the following:</span></p><p class="Tablei"><span>(i) symptoms or signs of cardiac failure;</span></p><p class="Tablei"><span>(ii) suspected or known ventricular hypertrophy or dysfunction;</span></p><p class="Tablei"><span>(iii) pulmonary hypertension;</span></p><p class="Tablei"><span>(iv) aortic, thrombotic, embolic disease or pericardial disease (excluding isolated pericardial effusion or pericarditis);</span></p><p class="Tablei"><span>(v) heart tumour;</span></p><p class="Tablei"><span>(vi) structural heart disease;</span></p><p class="Tablei"><span>(vii) other rare indications; and</span></p><p class="Tablea"><span>(c) the service is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><span>(d) the service is not associated with a service to which:</span></p><p class="Tablei"><span>(i) another item in this Subgroup applies (except items</span><span> </span><span>55137, 55141, 55143, 55145 and 55146); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 2 applies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(iii) an item in Subgroup 3 applies (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>234.15</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55132</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Serial real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 4 acoustic windows, with recordings on digital media, if the service:</span></p><p class="Tablea"><span>(a) is for the investigation of a patient who:</span></p><p class="Tablei"><span>(i) is under 17 years of age; or</span></p><p class="Tablei"><span>(ii) has complex congenital heart disease; and</span></p><p class="Tablea"><span>(b) is performed by a specialist or consultant physician practising in the speciality of cardiology; and</span></p><p class="Tablea"><span>(c) is not associated with a service to which:</span></p><p class="Tablei"><span>(i) another item in this Subgroup applies (except items</span><span> </span><span>55137, 55141, 55143, 55145 and 55146); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 2 applies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(iii) an item in Subgroup 3 applies (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>234.15</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55133</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Frequent repetition serial real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 3 acoustic windows, with recordings on digital media, if the service:</span></p><p class="Tablea"><span>(a) is for the investigation of a patient who:</span></p><p class="Tablei"><span>(i) has an isolated pericardial effusion or pericarditis; or</span></p><p class="Tablei"><span>(ii) has a normal baseline study, and has commenced medication for non</span><span>‑</span><span>cardiac purposes that has cardiotoxic side effects and is a pharmaceutical benefit (within the meaning of Part</span><span> </span><span>VII of the </span><span style="font-style:italic">National Health Act 1953</span><span>) for the writing of a prescription for the supply of which under that Part an echocardiogram is required; and</span></p><p class="Tablea"><span>(b) is not associated with a service to which:</span></p><p class="Tablei"><span>(i) another item in this Subgroup applies (except items</span><span> </span><span>55137, 55141, 55143, 55145 and 55146); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 2 ap</span><a id="opcCurrentPosition"></a><span>plies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(iii) an item in Subgroup 3 applies (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>210.75</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55134</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Repeat real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 3 acoustic windows, with recordings on digital media, for the investigation of rare cardiac pathologies, if the service:</span></p><p class="Tablea"><span>(a) is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><span>(b) is not associated with a service to which:</span></p><p class="Tablei"><span>(i) another item in this Subgroup applies (except items</span><span> </span><span>55137, 55141, 55143, 55145 and 55146); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 2 applies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(iii) an item in Subgroup 3 applies (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>234.15</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55137</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Serial real time transthoracic echocardiographic examination of the heart with real time colour flow mapping from at least 4 acoustic windows, with recordings on digital media, if the service:</span></p><p class="Tablea"><span>(a) is for the investigation of a fetus with suspected or confirmed:</span></p><p class="Tablei"><span>(i) complex congenital heart disease; or</span></p><p class="Tablei"><span>(ii) functional heart disease; or</span></p><p class="Tablei"><span>(iii) fetal cardiac arrhythmia; or</span></p><p class="Tablei"><span>(iv) cardiac structural abnormality requiring confirmation; and</span></p><p class="Tablea"><span>(b) is performed by a specialist or consultant physician practising in the speciality of cardiology with advanced training and expertise in fetal cardiac imaging; and</span></p><p class="Tablea"><a id="_Hlk80179257"><span>(c) is not associated with a service to which:</span></a></p><p class="Tablei"><span>(i) an item in Subgroup 2 applies (except items</span><span> </span><span>55118 and 55130); or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 3 applies (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>234.15</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55141</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Exercise stress echocardiography focused study, other than a service associated with a service to which:</span></p><p class="Tablea"><span>(a) item</span><span> </span><span>11704, 11705, 11707, 11714, 11729 or 11730 applies; or</span></p><p class="Tablea"><span>(b) an item in Subgroup 3 applies</span></p><p class="Tabletext"><span>Applicable not more than once in a 24 month period (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>417.45</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55143</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Repeat pharmacological or exercise stress echocardiography if:</span></p><p class="Tablea"><span>(a) a service to which item</span><span> </span><span>55141, 55145 or 55146, or this item, applies has been performed on the patient in the previous 24 months; and</span></p><p class="Tablea"><span>(b) the patient has symptoms of ischaemia that have evolved and are not adequately controlled with optimal medical therapy; and</span></p><p class="Tablea"><span>(c) the service is requested by a specialist or a consultant physician; and</span></p><p class="Tablea"><span>(d) the service is not associated with a service to which:</span></p><p class="Tablei"><span>(i) item</span><span> </span><span>11704, 11705, 11707, 11714, 11729 or 11730 applies; or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 3 applies</span></p><p class="Tabletext"><span>Applicable not more than once in a 12 month period (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>417.45</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55145</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Pharmacological stress echocardiography, other than a service associated with a service to which:</span></p><p class="Tablea"><span>(a) item</span><span> </span><span>11704, 11705, 11707, 11714, 11729 or 11730 applies; or</span></p><p class="Tablea"><span>(b) an item in Subgroup 3 applies</span></p><p class="Tabletext"><span>Applicable not more than once in a 24 month period (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>483.85</span></p></td></tr><tr><td style="width:13.9%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>55146</span></p></td><td style="width:72.84%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Pharmacological stress echocardiography if:</span></p><p class="Tablea"><span>(a) a service to which item</span><span> </span><span>55141 applies has been performed on the patient in the previous 4 weeks, and the test has failed due to an inadequate heart rate response; and</span></p><p class="Tablea"><span>(b) the service is not associated with a service to which:</span></p><p class="Tablei"><span>(i) item</span><span> </span><span>11704, 11705, 11707, 11714, 11729 or 11730 applies; or</span></p><p class="Tablei"><span>(ii) an item in Subgroup 3 applies</span></p><p class="Tabletext"><span>Applicable not more than once in a 24 month period (R)</span></p></td><td style="width:13.26%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>483.85</span></p></td></tr></tbody></table>
(1) Items in this Division (other than items 57360 and 57364) apply to a CT service that is:
(a) performed under the supervision of a specialist in the specialty of diagnostic radiology who is available:
(i) to monitor and influence the conduct and diagnostic quality of the examination; and
(ii) if necessary, to attend on the patient personally; and
(b) reported by a specialist in the specialty of diagnostic radiology.
(2) Items 57360 and 57364 apply to a CT service that is:
(a) performed under the supervision of a specialist or consultant physician who is recognised by the Conjoint Committee for the Recognition of Training in CT Coronary Angiography and available:
(i) to monitor and influence the conduct and diagnostic quality of the examination; and
(ii) if necessary, to attend on the patient personally; and
(b) reported by a specialist or consultant physician who is recognised by the Conjoint Committee for the Recognition of Training in CT Coronary Angiography.
(3) However, items in this Division apply to a CT service that does not comply with the requirements mentioned in subclause (1) or (2) if the service is performed:
(a) in an emergency; or
(b) because of medical necessity, in a remote location.
2.2.2 Restriction on items—attenuation correction and anatomical correlation
Items in this Division do not apply to a CT service that is performed for the purpose of attenuation correction or anatomical correlation of another diagnostic imaging procedure.
2.2.3 Application of items 56001 and 56007 if axial scan performed for exclusion of acoustic neuroma
If an axial scan is performed for the exclusion of acoustic neuroma, item 56001 or 56007 applies instead of any other item in this Schedule that might be taken to apply to the service.
2.2.4 CT services—assessment of headache
(1) If the service mentioned in item 56007 or 56036 is used for the assessment of a headache of a patient to whom this clause applies, the fee mentioned in the item applies only if:
(a) a scan without intravenous contrast medium has been performed on the patient; and
(b) the service is required because the result of the scan is abnormal.
(2) This clause applies to a patient who:
(a) is under 50 years; and
(b) is (apart from the headache) otherwise well; and
(c) has no localising symptoms or signs; and
(d) has no history of malignancy or immunosuppression.
2.2.5 CT services—number of services
Items 56220 to 56238 and 56620 to 56630 apply once only for a service mentioned in any of those items, regardless of the number of patient attendances required to complete the service.
2.2.5A Restriction on item 57360—patients
Item 57360 does not apply to a service provided to a patient if:
(a) in the previous 5 years, a service to which item 57360 or 57364 applies has been provided to the patient; and
(b) no obstructive coronary artery disease was detected as part of that service;
unless the patient is:
(c) eligible, under clause 5.10.17A of the general medical services table, for a service to which item 38244 or 38247 applies; or
(d) eligible, under clause 5.10.17B of the general medical services table, for a service to which item 38248 or 38249 applies.
Subdivision B—Subgroups 1 to 13 of Group I2
2.2.6 Items in Subgroups 1 to 13 of Group I2
This clause sets out items in Subgroups 1 to 13 of Group I2.
Note: The fees in Group I2 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:99.98%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I2—Computed tomography—examination</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 1—Head</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56001</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of brain without intravenous contrast medium, not being a service to which item</span><span> </span><span>57001 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>214.35</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56007</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of brain with intravenous contrast medium and with any scans of the brain before intravenous contrast injection, when performed, not being a service to which item</span><span> </span><span>57007 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>274.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56010</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of pituitary fossa with or without intravenous contrast medium and with or without brain scan when performed (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>277.05</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56013</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of orbits with or without intravenous contrast medium and with or without brain scan when performed (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>274.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56016</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of petrous bones in axial and coronal planes in 1 mm or 2 mm sections, with or without intravenous contrast medium, with or without scan of brain (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>318.65</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56022</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of facial bones, para nasal sinuses or both without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>247.25</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56028</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of facial bones, para nasal sinuses or both with intravenous contrast medium and with any scans of the facial bones, para nasal sinuses or both before intravenous contrast injection, when performed (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>370.05</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56030</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of facial bones, para nasal sinuses or both, with scan of brain, without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>247.25</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56036</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of facial bones, para nasal sinuses or both, with scan of brain, with intravenous contrast medium, if:</span></p><p class="Tablea"><span>(a) a scan without intravenous contrast medium has been performed; and</span></p><p class="Tablea"><span>(b) the service is required because the result of the scan mentioned in paragraph</span><span> </span><span>(a) is abnormal (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>370.05</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 2—Neck</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56101</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of soft tissues of neck, including larynx, pharynx, upper oesophagus and salivary glands (not associated with cervical spine) without intravenous contrast medium, not being a service to which item</span><span> </span><span>56801 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>252.70</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56107</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of soft tissues of neck, including larynx, pharynx, upper oesophagus and salivary glands (not associated with cervical spine)—with intravenous contrast medium and with any scans of soft tissues of neck, including larynx, pharynx, upper oesophagus and salivary glands (not associated with cervical spine) before intravenous contrast injection, when undertaken, not being a service associated with a service to which item</span><span> </span><span>56807 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>373.60</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 3—Spine</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56219</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, one or more regions with intrathecal contrast medium, including the preparation for intrathecal injection of contrast medium and any associated plain X</span><span>‑</span><span>rays, not being a service to which item</span><span> </span><span>59724 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.45</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56220</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, cervical region, without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>263.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56221</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, thoracic region, without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>263.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56223</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, lumbosacral region, without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>263.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56224</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, cervical region, with intravenous contrast medium and with any scans of the cervical region of the spine before intravenous contrast injection when undertaken (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>386.05</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56225</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, thoracic region, with intravenous contrast medium and with any scans of the thoracic region of the spine before intravenous contrast injection when undertaken (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>386.05</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56226</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, lumbosacral region, with intravenous contrast medium and with any scans of the lumbosacral region of the spine prior to intravenous contrast injection when undertaken (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>386.05</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56233</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, 2 examinations of the kind referred to in items</span><span> </span><span>56220, 56221 and 56223, without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>263.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56234</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, 2 examinations of the kind referred to in items</span><span> </span><span>56224, 56225 and 56226, with intravenous contrast medium and with any scans of these regions of the spine before intravenous contrast injection when undertaken (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>386.05</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56237</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, 3 regions cervical, thoracic and lumbosacral, without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>263.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56238</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of spine, 3 regions, cervical, thoracic and lumbosacral, with intravenous contrast medium and with any scans of these regions of the spine before intravenous contrast injection when undertaken (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>386.05</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 4—Chest and upper abdomen</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56301</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of chest, including lungs, mediastinum, chest wall and pleura, with or without scans of the upper abdomen, without intravenous contrast medium, not being a service to which item</span><span> </span><span>56801 or 57001 applies and not including a study performed to exclude coronary artery calcification or image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>324.20</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56307</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of chest, including lungs, mediastinum, chest wall and pleura, with or without scans of the upper abdomen, with intravenous contrast medium and with any scans of the chest, including lungs, mediastinum, chest wall or pleura and upper abdomen before intravenous contrast injection, when undertaken, not being a service to which item</span><span> </span><span>56807 or 57007 applies and not including a study performed to exclude coronary artery calcification or image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>439.55</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 5—Upper abdomen only</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56401</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper abdomen only (diaphragm to iliac crest) without intravenous contrast medium, not being a service to which item</span><span> </span><span>56301, 56501, 56801 or 57001 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>274.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56407</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper abdomen only (diaphragm to iliac crest), with intravenous contrast medium, and with any scans of upper abdomen (diaphragm to iliac crest) before intravenous contrast injection, when undertaken, not being a service to which item</span><span> </span><span>56307, 56507, 56807 or 57007 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>395.65</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56409</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of pelvis only (iliac crest to pubic symphysis) without intravenous contrast medium not being a service associated with a service to which item</span><span> </span><span>56401 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>274.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56412</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of pelvis only (iliac crest to pubic symphysis), with intravenous contrast medium and with any scans of pelvis (iliac crest to pubic symphysis) before intravenous contrast injection, when undertaken, not being a service to which item</span><span> </span><span>56407 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>395.65</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 6—Upper abdomen and pelvis</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56501</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper abdomen and pelvis without intravenous contrast medium, not for the purposes of virtual colonoscopy and not being a service to which item</span><span> </span><span>56801 or 57001 applies(R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>422.95</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56507</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper abdomen and pelvis with intravenous contrast medium and with any scans of upper abdomen and pelvis before intravenous contrast injection, when performed, not for the purposes of virtual colonoscopy and not being a service to which item</span><span> </span><span>56807 or 57007 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>527.55</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56553</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of colon for exclusion or diagnosis of colorectal neoplasia in a symptomatic or high risk patient if:</span></p><p class="Tablea"><span>(a) one or more of the following applies:</span></p><p class="Tablei"><span>(i) the patient has had an incomplete colonoscopy in the 3 months before the scan;</span></p><p class="Tablei"><span>(ii) there is a high</span><span>‑</span><span>grade colonic obstruction;</span></p><p class="Tablei"><span>(iii) the service is requested by a specialist or consultant physician who performs colonoscopies in the practice of the specialist’s or consultant physician’s speciality; and</span></p><p class="Tablea"><span>(b) the service is not a service to which item</span><span> </span><span>56301, 56307, 56401, 56407, 56409, 56412, 56501, 56507, 56801, 56807 or 57001 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>571.40</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 7—Extremities</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56620</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of knee, without intravenous contrast medium, not being a service to which item</span><span> </span><span>56622 or 56629 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>241.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56622</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of lower limb, left or right or both, one region (other than knee), or more than one region (which may include knee), without intravenous contrast medium, not being a service to which item</span><span> </span><span>56620 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>241.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56623</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of lower limb, left or right or both, one region (other than knee), or more than one region (which may include knee), with intravenous contrast medium and with any scans of the lower limb before intravenous contrast injection, when performed, not being a service to which item</span><span> </span><span>56626 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>367.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56626</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of knee, with intravenous contrast medium and with any scans of the knee before intravenous contrast injection, when performed, not being a service to which to which item</span><span> </span><span>56623 or 56630 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>367.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56627</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper limb, left or right or both, any one region, or more than one region, without intravenous contrast medium (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>241.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56628</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper limb, left or right or both, any one region, or more than one region, with intravenous contrast medium and with any scans of the upper limb before intravenous contrast injection, when performed (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>367.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56629</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper limb and lower limb, left or right or both, any one region (other than knee), or more than one region (which may include knee) without intravenous contrast medium not being a service to which item</span><span> </span><span>56620 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>241.75</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>56630</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of upper limb and lower limb, left or right or both, any one region (other than knee), or more than one region (which may include knee) with intravenous contrast medium with any scans of the limbs before intravenous contrast injection, when performed, not being a service to which item</span><span> </span><span>56626 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>367.75</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 8—Chest, abdomen, pelvis and neck</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56801</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of chest, abdomen and pelvis with or without scans of soft tissues of neck without intravenous contrast medium, not including a study performed to exclude coronary artery calcification or image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>512.70</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>56807</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of chest, abdomen and pelvis with or without scans of soft tissues of neck with intravenous contrast medium and with any scans of chest, abdomen and pelvis with or without scans of soft tissue of neck before intravenous contrast injection, when performed, not including a study performed to exclude coronary artery calcification or image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>615.40</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 9—Brain, chest and upper abdomen</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57001</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of brain and chest with or without scans of upper abdomen without intravenous contrast medium, not including a study performed to exclude coronary artery calcification or image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>512.80</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57007</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—scan of brain and chest with or without scans of upper abdomen with intravenous contrast medium and with any scans of brain and chest and upper abdomen before intravenous contrast injection, when performed, not including a study performed to exclude coronary artery calcification or image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>623.85</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 10—Pelvimetry</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57201</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—pelvimetry (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>170.55</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 11—Interventional techniques</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57341</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography, in conjunction with a surgical procedure using interventional techniques (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>516.45</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 12—Angiography</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57352</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—angiography with intravenous contrast medium of any or all, or any part, of:</span></p><p class="Tablea"><span>(a) the arch of the aorta; or</span></p><p class="Tablea"><span>(b) the carotid arteries; or</span></p><p class="Tablea"><span>(c) the vertebral arteries and their branches (head and neck);</span></p><p class="Tabletext"><span>including any scans performed before intravenous contrast injection—one or more data acquisitions, including image editing, and maximum intensity projections or 3 dimensional surface shaded display, with hardcopy or digital recording of multiple projections, if:</span></p><p class="Tablea"><span>(d) either:</span></p><p class="Tablei"><span>(i) the service is requested by a specialist or consultant physician; or</span></p><p class="Tablei"><span>(ii) the service is requested by a medical practitioner (other than a specialist or consultant physician) and the request indicates that the patient’s case has been discussed with a specialist or consultant physician; and</span></p><p class="Tablea"><span>(e) the service is not a service to which another item in this group applies; and</span></p><p class="Tablea"><span>(f) the service is performed for the exclusion of arterial stenosis, occlusion, aneurysm or embolism; and</span></p><p class="Tablea"><span>(g) the service is not a study performed to image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p style="text-align:right; line-height:normal"><span>560.40</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57353</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—angiography with intravenous contrast medium of any or all, or any part, of:</span></p><p class="Tablea"><span>(a) the ascending and descending aorta; or</span></p><p class="Tablea"><span>(b) the common iliac and abdominal branches including upper limbs (chest, abdomen and upper limbs);</span></p><p class="Tabletext"><span>including any scans performed before intravenous contrast injection—one or more data acquisitions, including image editing, and maximum intensity projections or 3 dimensional surface shaded display, with hardcopy or digital recording of multiple projections, if:</span></p><p class="Tablea"><span>(c) either:</span></p><p class="Tablei"><span>(i) the service is requested by a specialist or consultant physician; or</span></p><p class="Tablei"><span>(ii) the service is requested by a medical practitioner (other than a specialist or consultant physician) and the request indicates that the patient’s case has been discussed with a specialist or consultant physician; and</span></p><p class="Tablea"><span>(d) the service is not a service to which another item in this group applies; and</span></p><p class="Tablea"><span>(e) the service is performed for the exclusion of arterial stenosis, occlusion, aneurysm or embolism; and</span></p><p class="Tablea"><span>(f) the service is not a study performed to image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>560.40</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57354</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—angiography with intravenous contrast medium of any or all, or any part, of:</span></p><p class="Tablea"><span>(a) the descending aorta; or</span></p><p class="Tablea"><span>(b) the pelvic vessels (aorto</span><span>‑</span><span>iliac segment) and lower limbs;</span></p><p class="Tabletext"><span>including any scans performed before intravenous contrast injection—one or more data acquisitions, including image editing, and maximum intensity projections or 3 dimensional surface shaded display, with hardcopy or digital recording of multiple projections, if:</span></p><p class="Tablea"><span>(c) either:</span></p><p class="Tablei"><span>(i) the service is requested by a specialist or consultant physician; or</span></p><p class="Tablei"><span>(ii) the service is requested by a medical practitioner (other than a specialist or consultant physician) and the request indicates that the patient’s case has been discussed with a specialist or consultant physician; and</span></p><p class="Tablea"><span>(d) the service is not a service to which another item in this group applies; and</span></p><p class="Tablea"><span>(e) the service is performed for the exclusion of arterial stenosis, occlusion, aneurysm or embolism; and</span></p><p class="Tablea"><span>(f) the service is not a study performed to image the coronary arteries (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>560.40</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><a id="_Hlk66699338"><span>57357</span></a></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography—angiography with intravenous contrast medium of any or all, or any part, of the pulmonary arteries and their branches, including any scans performed before intravenous contrast injection—one or more data acquisitions, including image editing, and maximum intensity projections or 3 dimensional surface shaded display, with hardcopy or digital recording of multiple projections, if:</span></p><p class="Tablea"><span>(a) the service is:</span></p><p class="Tablei"><span>(i) performed for the exclusion of pulmonary arterial stenosis, occlusion, aneurysm or embolism and is requested by a specialist or consultant physician; or</span></p><p class="Tablei"><span>(ii) performed for the exclusion of pulmonary arterial stenosis, occlusion or aneurysm, is requested by a medical practitioner (other than a specialist or consultant physician) and the request indicates that the patient’s case has been discussed with a specialist or consultant physician; or</span></p><p class="Tablei"><span>(iii) performed for the exclusion of pulmonary embolism and is requested by a medical practitioner (other than a specialist or consultant physician); and</span></p><p class="Tablea"><span>(b) the service is not:</span></p><p class="Tablei"><span>(i) a service to which another item in this group applies; or</span></p><p class="Tablei"><span>(ii) a study performed to image the coronary arteries (R) (Anaes)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>560.40</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57360</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography of the coronary arteries performed on a minimum of a 64 slice (or equivalent) scanner if:</span></p><p class="Tablea"><span>(a) the request is made by a specialist or consultant physician; and</span></p><p class="Tablea"><span>(b) the patient has stable or acute symptoms consistent with coronary ischaemia; and</span></p><p class="Tablea"><span>(c) the patient is at low to intermediate risk of an acute coronary event, including having no significant cardiac biomarker elevation and no electrocardiogram changes indicating acute ischaemia (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>769.15</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><a id="_Hlk80184688"><span>57364</span></a></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Computed tomography of the coronary arteries performed on a minimum of a 64 slice (or equivalent) scanner, if:</span></p><p class="Tablea"><span>(a) the service is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><span>(b) at least one of the following apply to the patient:</span></p><p class="Tablei"><span>(i) the patient has stable symptoms and newly recognised left ventricular systolic dysfunction of unknown aetiology;</span></p><p class="Tablei"><span>(ii) the patient requires exclusion of coronary artery anomaly or fistula;</span></p><p class="Tablei"><span>(iii) the patient will be undergoing non</span><span>‑</span><span>coronary cardiac surgery;</span></p><p class="Tablei"><span>(iv) the patient meets the criteria to be eligible for a service to which item</span><span> </span><span>38247, 38249 or 38252 applies, but as an alternative to selective coronary angiography will require an assessment of the patency of one or more</span><span style="font-style:italic"> </span><span>bypass grafts</span></p><p class="Tabletext"><span>(R) (Anaes)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>769.15</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 13—Cone beam computed tomography</span></p></td></tr><tr><td style="width:12.22%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57362</span></p></td><td style="width:75.82%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cone beam computed tomography—dental and temporo</span><span>‑</span><span>mandibular joint imaging (without contrast medium) for diagnosis and management of any of the following:</span></p><p class="Tablea"><span>(a) mandibular and dento</span><span>‑</span><span>alveolar fractures;</span></p><p class="Tablea"><span>(b) dental implant planning;</span></p><p class="Tablea"><span>(c) orthodontics;</span></p><p class="Tablea"><span>(d) endodontic conditions;</span></p><p class="Tablea"><span>(e) periodontal conditions;</span></p><p class="Tablea"><span>(f) temporo</span><span>‑</span><span>mandibular joint conditions</span></p><p class="Tabletext"><span>Applicable once per patient per day, not being for a service to which any of items</span><span> </span><span>57960 to 57969 apply, and not being a service associated with another service in Group I2 (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>124.35</span></p></td></tr></tbody></table>
Division 2.3—Group I3: diagnostic radiology
Subdivision A—General
2.3.1 Application of items in Subdivision B, D, E or G to services rendered using diagnostic imaging procedures carried out in metropolitan areas and certain inner regional areas
(1) This clause applies to a service described in an item in Subdivision B, D, E or G if the diagnostic imaging procedure used to render the service is carried out in an area other than area that is:
(a) both:
(i) Inner Regional Australia; and
(ii) RRMA4 or RRMA5; or
(b) Outer Regional Australia; or
(c) Remote Australia; or
(d) Very Remote Australia; or
(e) Norfolk Island.
(2) The item applies to the service only if the procedure is carried out as permitted by subclause (3) or (4).
(3) For the purposes of subclause (2), the procedure used to render a service described in an item in Subdivision B, D, E or G may be carried out:
(a) by a medical practitioner; or
(b) by a person who is registered as a medical radiation practitioner under a law of a State or Territory, if the person carries out the procedure under the supervision of a medical practitioner in accordance with accepted medical practice.
(4) For the purposes of subclause (2), the procedure used to render a service described in an item in Subgroup 3 of Group I3 may also be carried out by a dental practitioner if the dental practitioner carries out the procedure under the supervision of a medical practitioner in accordance with accepted medical practice.
2.3.2 Restriction on items—certain services requested by chiropractors, osteopaths and physiotherapists
For any particular patient, if the service mentioned in any of the following items is requested more than once on the same day by the same chiropractor, physiotherapist, or osteopath, the item applies to the service only once on that day:
(a) items 58100 to 58106;
(b) items 58109 and 58112.
2.3.3 Increased fees for certain diagnostic radiology services carried out at residential aged care facilities
(1) This clause applies to a service to which item 57509, 57515, 57521, 57527, 57703, 57709, 57712, 57715, 58503, 58521, 58524, 58527 or 58903 applies.
(2) If:
(a) a providing practitioner renders a service to a care recipient of a residential aged care facility during an attendance at the facility; and
(b) subclause (3) does not apply in relation to that attendance; and
(c) the service was requested during a personal attendance on the care recipient at the facility by the requesting practitioner; and
(d) subclause (4) applies to the service;
the fee for the service is the amount listed in the item that applies to the service plus $74.75.
(3) If:
(a) a providing practitioner renders 2 or more services to one or more care recipients of a residential aged care facility during an attendance at the facility; and
(b) the services were requested during personal attendances on the care recipients by one or more requesting practitioners at the facility; and
(c) subclause (4) applies to at least one of the services;
the fee for the first service carried out during the attendance by the providing practitioner is the amount listed in the item that applies to the service plus $74.75.
(4) This subclause applies to a service if the service is requested because a care recipient of a residential aged care facility:
(a) for a service to which item 57509, 57515, 57521, 57527, 57703, 57709, 57712, 57715, 58521, 58524 or 58527 applies—has had a fall; and
(b) for a service to which item 58503 applies—is suspected of having pneumonia or heart failure; and
(c) for a service to which item 58903 applies—is suspected of having an acute abdomen or bowel obstruction.
Subdivision B—Subgroups 1 to 9 of Group I3
2.3.4 Items in Subgroups 1 to 9 of Group I3
This clause sets out items in Subgroups 1 to 9 of Group I3.
Note: The fees in Group I3 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I3—Diagnostic radiology</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 1—Radiographic examination of extremities</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57506</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hand, wrist, forearm, elbow or humerus (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>30.20</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57509</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hand, wrist, forearm, elbow or humerus (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>40.35</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57512</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hand and wrist, or hand, wrist and forearm, or wrist and forearm, or forearm and elbow, or elbow and humerus (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>41.10</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57515</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hand and wrist, or hand, wrist and forearm, or wrist and forearm, or forearm and elbow, or elbow and humerus (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>54.80</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57518</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Foot, ankle, leg or femur (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>33.00</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57521</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Foot, ankle, leg or femur (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.05</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>57522</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Knee (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>33.00</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>57523</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>Knee (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.05</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57524</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Foot and ankle, or ankle and leg, or leg and knee, or knee and femur (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>50.15</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57527</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Foot and ankle, or ankle and leg, or leg and knee, or knee and femur (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>66.75</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 2—Radiographic examination of shoulder or pelvis</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57700</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Shoulder or scapula (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>41.10</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57703</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Shoulder or scapula (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>54.80</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57706</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Clavicle (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>33.00</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57709</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Clavicle (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.05</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57712</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hip joint (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.85</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57715</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Pelvic girdle (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>61.80</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57721</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Femur, internal fixation of neck or intertrochanteric (pertrochanteric) fracture (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>100.75</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 3—Radiographic examination of head</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57901</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Skull, not in association with item</span><span> </span><span>57902 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>65.45</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57902</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cephalometry, not in association with item</span><span> </span><span>57901 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>65.45</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57905</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Mastoids or petrous temporal bones (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>65.45</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57907</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Sinuses, or facial bones—orbit, maxilla or malar, any or all (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>48.00</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57915</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Mandible, not by orthopantomography technique (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.85</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57918</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Salivary calculus (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.85</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57921</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Nose (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.85</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57924</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Eye (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.85</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57927</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Temporo</span><span>‑</span><span>mandibular joints (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>50.40</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57930</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Teeth—single area (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>33.40</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57933</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Teeth—full mouth (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>79.40</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57939</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Palato</span><span>‑</span><span>pharyngeal studies with fluoroscopic screening (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>65.45</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57942</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Palato</span><span>‑</span><span>pharyngeal studies without fluoroscopic screening (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>50.40</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57945</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Larynx, lateral airways and soft tissues of the neck, not being a service associated with a service to which item</span><span> </span><span>57939 or 57942 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.05</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57960</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Orthopantomography for diagnosis or management (or both) of trauma, infection, tumour or a congenital or surgical condition of the teeth or maxillofacial region (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>48.10</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57963</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Orthopantomography for diagnosis or management (or both) of any of the following conditions, if the signs and symptoms of the condition is present:</span></p><p class="Tablea"><span>(a) impacted teeth;</span></p><p class="Tablea"><span>(b) caries;</span></p><p class="Tablea"><span>(c) periodontal pathology;</span></p><p class="Tablea"><span>(d) periapical pathology (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>48.10</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57966</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Orthopantomography for diagnosis or management (or both) of missing or crowded teeth, or developmental anomalies of the teeth or jaws (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>48.10</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>57969</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Orthopantomography for diagnosis or management (or both) of temporo</span><span>‑</span><span>mandibular joint arthroses or dysfunction (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>48.10</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 4—Radiographic examination of spine</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58100</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—cervical (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>68.15</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58103</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—thoracic (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>55.95</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58106</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—lumbosacral (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>78.15</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58108</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—4 regions, cervical, thoracic, lumbosacral and sacrococcygeal (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>111.65</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58109</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—sacrococcygeal (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.70</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58112</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—2 examinations of the kind mentioned in items</span><span> </span><span>58100, 58103, 58106 and 58109 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>98.70</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58115</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—3 examinations of the kind mentioned in items</span><span> </span><span>58100, 58103, 58106 and 58109 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>111.65</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58120</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—4 regions, cervical, thoracic, lumbosacral and sacrococcygeal, if the service to which item</span><span> </span><span>58120 or 58121 applies has not been performed on the same patient within the same calendar year (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>111.65</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58121</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Spine—3 examinations of the kind mentioned in items</span><span> </span><span>58100, 58103, 58106 and 58109, if the service to which item</span><span> </span><span>58120 or 58121 applies has not been performed on the same patient within the same calendar year (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>111.65</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 5—Bone age study and skeletal survey</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58300</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Bone age study (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>40.70</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58306</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Skeletal survey (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>90.75</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 6—Radiographic examination of thoracic region</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58500</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Chest (lung fields) by direct radiography (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>35.90</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58503</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Chest (lung fields) by direct radiography (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.85</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58506</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Chest (lung fields) by direct radiography with fluoroscopic screening (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>61.65</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58509</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Thoracic inlet or trachea (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>40.35</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58521</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Left ribs, right ribs or sternum (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.05</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58524</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Left and right ribs, left ribs and sternum, or right ribs and sternum (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>57.35</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58527</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Left ribs, right ribs and sternum (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>70.45</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 7—Radiographic examination of urinary tract</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58700</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Plain renal only (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>46.75</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58706</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Intravenous pyelography, with or without preliminary plain films and with or without tomography (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>160.25</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58715</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Antegrade or retrograde pyelography with or without preliminary plain films and with preparation and contrast injection, one side (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>153.80</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58718</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Retrograde cystography or retrograde urethrography with or without preliminary plain films and with preparation and contrast injection (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>128.00</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58721</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Retrograde micturating cysto</span><span>‑</span><span>urethrography, with preparation and contrast injection (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>140.30</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 8—Radiographic examination of alimentary tract and biliary system</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58900</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Plain abdominal only, not being a service associated with a service to which item</span><span> </span><span>58909, 58912 or 58915 applies (NR)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>36.25</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58903</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Plain abdominal only, not being a service associated with a service to which item</span><span> </span><span>58909, 58912 or 58915 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>48.30</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58909</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Barium or other opaque meal of one or more of pharynx, oesophagus, stomach or duodenum, with or without preliminary plain films of pharynx, chest or duodenum, not being a service associated with a service to which item</span><span> </span><span>57939, 57942 or 57945 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>91.30</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58912</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Barium or other opaque meal of oesophagus, stomach, duodenum and follow through to colon, with or without screening of chest and with or without preliminary plain film (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>111.90</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58915</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Barium or other opaque meal, small bowel series only, with or without preliminary plain film (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>80.15</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58916</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Small bowel enema, barium or other opaque study of the small bowel, including duodenal intubation, with or without preliminary plain films, not being a service associated with a service to which item</span><span> </span><span>30488 applies (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>140.60</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58921</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Opaque enema, with or without air contrast study and with or without preliminary plain films (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>137.30</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58927</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cholegraphy direct, with or without preliminary plain films and with preparation and contrast injection, not being a service associated with a service to which item</span><span> </span><span>30439 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>77.60</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58933</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cholegraphy, percutaneous transhepatic, with or without preliminary plain films and with preparation and contrast injection (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>208.70</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58936</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cholegraphy, drip infusion, with or without preliminary plain films, with preparation and contrast injection and with or without tomography (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>198.90</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>58939</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Defaecogram (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>141.40</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 9—Radiographic examination for localisation of foreign bodies</span></p></td></tr><tr><td style="width:12.2%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59103</span></p></td><td style="width:75.84%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Localisation of foreign body, if provided in conjunction with a service mentioned in Subgroups 1 to 12 of Group I3 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>21.60</span></p></td></tr></tbody></table>
Subdivision C—Subgroup 10 of Group I3: radiographic examination of breasts
2.3.5 Mammography services—eligible services
Items in this Subdivision apply only to a mammography service performed:
(a) under the supervision of a specialist in the specialty of diagnostic radiology who is available:
(i) to monitor and influence the conduct and diagnostic quality of the examination; and
(ii) if necessary, to attend on the patient personally; or
(b) if paragraph (a) cannot be complied with:
(i) in an emergency; or
(ii) because of medical necessity, in a remote location.
2.3.6 Items in Subgroup 10 of Group I3
This clause sets out items in Subgroup 10 of Group I3.
Note: The fees in Group I3 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I3—Diagnostic radiography</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 10—Radiographic examination of breasts</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59300</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Mammography of both breasts if there is reason to suspect the presence of malignancy because of:</span></p><p class="Tablea"><span>(a) the past occurrence of breast malignancy in the patient; or</span></p><p class="Tablea"><span>(b) significant history of breast or ovarian malignancy in the patient’s family; or</span></p><p class="Tablea"><span>(c) symptoms or indications of breast disease found on examination of the patient by a medical practitioner (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>90.85</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59302</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Three dimensional tomosynthesis of both breasts, if there is reason to suspect the presence of breast malignancy because of:</span></p><p class="Tablea"><span>(a) the past occurrence of breast malignancy in the patient; or</span></p><p class="Tablea"><span>(b) significant history of breast or ovarian malignancy in the patient’s family; or</span></p><p class="Tablea"><span>(c) symptoms or signs found on examination of the patient by a medical practitioner;</span></p><p class="Tabletext"><span>not being a service to which item</span><span> </span><span>59300 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>217.75</span></p></td></tr><tr style="height:28.6pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59303</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Mammography of one breast if:</span></p><p class="Tablea"><span>(a) the service is specifically requested for a unilateral mammogram; and</span></p><p class="Tablea"><span>(b) there is reason to suspect the presence of malignancy because of:</span></p><p class="Tablei"><span>(i) the past occurrence of breast malignancy in the patient; or</span></p><p class="Tablei"><span>(ii) significant history of breast or ovarian malignancy in the patient’s family; or</span></p><p class="Tablei"><span>(iii) symptoms or indications of breast disease found on examination of the patient by a medical practitioner (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>54.75</span></p></td></tr><tr style="height:52.55pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59305</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Three dimensional tomosynthesis of one breast, if there is reason to suspect the presence of breast malignancy because of:</span></p><p class="Tablea"><span>(a) the past occurrence of breast malignancy in the patient; or</span></p><p class="Tablea"><span>(b) significant history of breast or ovarian malignancy in the patient’s family; or</span></p><p class="Tablea"><span>(c) symptoms or signs found on examination of the patient by a medical practitioner;</span></p><p class="Tabletext"><span>not being a service to which item</span><span> </span><span>59303 applies (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>122.85</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59312</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Radiographic examination of both breasts, in conjunction with a surgical procedure on each breast, using interventional techniques (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>88.30</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59314</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Radiographic examination of one breast, in conjunction with a surgical procedure using interventional techniques (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>53.30</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59318</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Radiographic examination of excised breast tissue to confirm satisfactory excision of one or more lesions in one breast or both following pre</span><span>‑</span><span>operative localisation in conjunction with a service under item</span><span> </span><span>31536 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.75</span></p></td></tr></tbody></table>
Subdivision D—Subgroups 12 and 13 of Group I3
2.3.7 Items in Subgroups 12 and 13 of Group I3
This clause sets out items in Subgroups 12 and 13 of Group I3.
Note: The fees in Group I3 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I3—Diagnostic radiography</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 12—Radiographic examination with opaque or contrast media</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59700</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Discography, each disc, with or without preliminary plain films and with preparation and contrast injection (R) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>98.00</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59703</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Dacryocystography, one side, with or without preliminary plain film and with preparation and contrast injection (R)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>77.05</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59712</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hysterosalpingography, with or without preliminary plain films and with preparation and contrast injection (R)(Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>115.40</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59715</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Bronchography, one side, with or without preliminary plain films and with preparation and contrast injection, on a person under 16 years of age (R) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>145.70</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59718</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Phlebography, one side, with or without preliminary plain films and with preparation and contrast injection (R) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>136.65</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59724</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Myelography, one or more regions, with or without preliminary plain films and with preparation and contrast injection, not being a service associated with a service to which item</span><span> </span><span>56219 applies (R)(Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>229.85</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59733</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Sialography, one side, with preparation and contrast injection, not being a service associated with a service to which item</span><span> </span><span>57918 applies (R)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>109.30</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59739</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Sinogram or fistulogram, one or more regions, with or without preliminary plain films and with preparation and contrast injection (R))</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>74.85</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59751</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Arthrography, each joint, excluding the facet (zygapophyseal) joints of the spine, single or double contrast study, with or without preliminary plain films and with preparation and contrast injection (R)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>141.25</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59754</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Lymphangiography, one or both sides, with preliminary plain films and follow</span><span>‑</span><span>up radiography and with preparation and contrast injection (R)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>222.65</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59763</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Air insufflation during video—fluoroscopic imaging including associated consultation (R)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>135.90</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 13—Angiography</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>59970</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Angiography or digital subtraction angiography, or both, with fluoroscopy and image acquisition, using a mobile image intensifier, including any preliminary plain films, preparation and contrast injection—one or more regions (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>170.80</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60000</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of head and neck with or without arch aortography—1 to 3 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>572.45</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60003</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of head and neck with or without arch aortography—4 to 6 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>839.50</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60006</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of head and neck with or without arch aortography—7 to 9 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,193.75</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60009</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of head and neck with or without arch aortography—10 or more data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,396.95</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60012</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of thorax—1 to 3 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>572.45</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60015</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of thorax—4 to 6 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>839.50</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60018</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of thorax—7 to 9 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,193.75</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60021</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of thorax—10 or more data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,396.95</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60024</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of abdomen—1 to 3 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>572.45</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60027</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of abdomen—4 to 6 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>839.50</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60030</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of abdomen—7 to 9 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,193.75</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60033</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of abdomen—10 or more data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,396.95</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60036</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of upper limb or limbs—1 to 3 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>572.45</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60039</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of upper limb or limbs—4 to 6 data acquisition runs(R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>839.50</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60042</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of upper limb or limbs—7 to 9 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,193.75</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60045</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of upper limb or limbs—10 or more data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,396.95</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60048</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of lower limb or limbs—1 to 3 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>572.45</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60051</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of lower limb or limbs—4 to 6 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>839.50</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60054</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of lower limb or limbs—7 to 9 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,193.75</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60057</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of lower limb or limbs—10 or more data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,396.95</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60060</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of aorta and lower limb or limbs—1 to 3 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>572.45</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60063</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of aorta and lower limb or limbs—4 to 6 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>839.50</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60066</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of aorta and lower limb or limbs—7 to 9 data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,193.75</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60069</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Digital subtraction angiography, examination of aorta and lower limb or limbs—10 or more data acquisition runs (R) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,396.95</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60072</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Selective arteriography or selective venography by digital subtraction angiography technique—one vessel (NR) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>48.80</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60075</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Selective arteriography or selective venography by digital subtraction angiography technique—2 vessels (NR) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>97.55</span></p></td></tr><tr><td style="width:12.3%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60078</span></p></td><td style="width:74.48%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Selective arteriography or selective venography by digital subtraction angiography technique—3 or more vessels (NR) (H) (Anaes.)</span></p></td><td style="width:13.22%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>146.40</span></p></td></tr></tbody></table>
Subdivision E—Subgroup 15 of Group I3: fluoroscopic examination
2.3.8 Items in Subgroup 15 of Group I3
This clause sets out items in Subgroup 15 of Group I3.
Note: The fees in Group I3 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I3—Diagnostic radiography</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 15—Fluoroscopic examination</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60500</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Fluoroscopy, with general anaesthesia (not being a service associated with a radiographic examination) (R) (H) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.05</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60503</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Fluoroscopy, without general anaesthesia (not being a service associated with a radiographic examination) (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>30.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60506</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Fluoroscopy, using a mobile image intensifier, that:</span></p><p class="Tablea"><span>(a) lasts less than 1 hour; and</span></p><p class="Tablea"><span>(b) is in conjunction with a surgical procedure;</span></p><p class="Tabletext"><span>not being a service associated with a service to which another item in this Group applies (R) (H)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>64.70</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60509</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="margin-right:1.6pt"><span>Fluoroscopy, using a mobile image intensifier, that:</span></p><p class="Tablea" style="margin-right:1.6pt"><span>(a) lasts 1 hour or more; and</span></p><p class="Tablea" style="margin-right:1.6pt"><span>(b) is in conjunction with a surgical procedure;</span></p><p class="Tabletext"><span>not being a service associated with a service to which another item in this Group applies (R) (H)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>100.40</span></p></td></tr></tbody></table>
Subdivision F—Subgroup 16 of Group I3: preparation for radiological procedure
2.3.9 Preparation of patients for radiological procedures
Items in this Subdivision apply only to the preparation of a patient for a radiological procedure for a service to which item 59970 applies by:
(a) injecting opaque or contrast media; or
(b) removing fluid and replacing it with air, oxygen or other contrast media; or
(c) a similar method.
2.3.10 Items in Subgroup 16 of Group I3
This clause sets out items in Subgroup 16 of Group I3.
Note: The fees in Group I3 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I3—Diagnostic radiography</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 16—Preparation for radiological procedure</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60918</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Arteriography (peripheral) or phlebography—one vessel, when used in association with a service to which item</span><span> </span><span>59970 applies, not being a service associated with a service to which any of items</span><span> </span><span>60000 to 60078 apply (NR) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.85</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>60927</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Selective arteriogram or phlebogram, when used in association with a service to which item</span><span> </span><span>59970 applies, not being a service associated with a service to which any of items</span><span> </span><span>60000 to 60078 apply (NR) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>38.60</span></p></td></tr></tbody></table>
Subdivision G—Subgroup 17 of Group I3: interventional techniques
2.3.11 Meaning of angiography suite
In this Schedule:
angiography suite means a room that contains only equipment designed for angiography that is able to perform digital subtraction or rapid‑sequence film angiography.
2.3.12 Items in Subgroup 17 of Group I3
This clause sets out items in Subgroup 17 of Group I3.
Note: The fees in Group I3 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I3—Diagnostic radiography</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 17—Interventional techniques</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61109</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Fluoroscopy in an angiography suite with image intensification, in conjunction with a surgical procedure using interventional techniques, not being a service associated with a service to which another item in this Group applies (R) (H)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>262.80</span></p></td></tr></tbody></table>
Division 2.4—Group I4: nuclear medicine imaging
Subdivision A—General
2.4.1 Nuclear scanning services (other than PET nuclear scanning services) and adjunctive services
(1) An item in Subgroup 1 or 3 of Group I4 applies only if:
(a) the performance of the service does not involve the use of positron‑emission radio‑isotopes or a PET scanner; and
(b) the service is performed under the supervision of a nuclear medicine credentialled specialist who is available to monitor and influence the conduct and diagnostic quality of the examination; and
(c) a nuclear medicine credentialled specialist or a specialist in the specialty of diagnostic radiology is available, if necessary, to attend on the patient personally; and
(d) the service is reported by a nuclear medicine credentialled specialist.
(2) Paragraphs (1)(a) to (c) do not apply if the service is performed:
(a) in an emergency; or
(b) because of medical necessity, in a remote location.
2.4.1A Restriction on items for stress myocardial perfusion studies—patients, requests and requirements
Items 61324, 61329, 61345, 61349, 61357, 61394, 61398, 61406, 61410 and 61414 apply to a service performed on a patient only if:
(a) one or more of subclauses 2.4.1B(1), (2) and (3) apply to the patient; and
(b) the request for the service identifies any symptoms or clinical indications mentioned in those subclauses that apply to the patient; and
(c) the service is performed in accordance with clause 2.4.1C.
(1) This subclause applies to a patient if:
(a) the patient displays symptoms of typical or atypical angina, including constricting discomfort of one or more of the following:
(i) the front of the chest;
(ii) the neck;
(iii) the shoulders;
(iv) the jaw;
(v) the arms; or
(b) the patient’s symptoms are:
(i) precipitated by physical exertion; or
(ii) relieved within 5 minutes or less by rest or glyceryl trinitrate.
(2) This subclause applies to a patient if:
(a) the patient has known coronary artery disease; and
(b) the patient displays one or more symptoms that are suggestive of ischaemia; and
(c) the symptoms:
(i) are not adequately controlled with medical therapy; or
(ii) have evolved since the last functional study undertaken of the patient.
(3) This subclause applies to a patient if one or more of the following clinical indications apply to the patient:
(a) the patient does not have a known coronary artery disease but assessment indicates that resting twelve‑lead electrocardiogram changes are consistent with coronary artery disease or ischaemia;
(b) coronary artery disease related lesions, of uncertain functional significance, have previously been identified on a computed tomography coronary angiography or invasive coronary angiography;
(c) an assessment by a specialist or consultant physician indicates that the patient has possible painless myocardial ischaemia, where a stress myocardial perfusion study is likely to assist the diagnosis;
(d) an assessment indicates that the patient has undue exertional dyspnoea of uncertain aetiology;
(e) a pre‑operative assessment of the patient, who has a functional capacity of less than 4 metabolic equivalents, confirms that surgery is an intermediate to high risk, and the patient also has at least one of the following conditions:
(i) ischaemic heart disease;
(ii) previous myocardial infarction;
(iii) heart failure;
(iv) stroke;
(v) transient ischaemic attack;
(vi) renal dysfunction (serum creatinine greater than 170umol/L or 2 mg/dL or a creatinine clearance of less than 60 mL/min);
(vii) diabetes mellitus requiring insulin therapy;
(f) assessment, including quantification, is required before either percutaneous coronary intervention or coronary bypass surgery to quantify the extent and severity of myocardial ischaemia, and to ensure the criteria for intervention are met;
(g) assessment is required of relative amounts of ischaemic viable myocardium and non‑viable (infarcted) myocardium because the patient has a previous myocardial infarction;
(h) assessment of myocardial ischaemia with exercise is required because the patient has congenital heart lesions, has undergone surgery and ischemia is considered possible;
(i) the patient is under 17 years old, with coronary anomalies, and assessment of myocardial perfusion is required before and after cardiac surgery:
(i) for congenital heart disease; or
(ii) where there is a probable or confirmed coronary artery abnormality;
(j) myocardial perfusion abnormality is suspected but, due to the patient’s cognitive capacity or expressive language impairment, it is not possible to accurately assess symptom frequency based on medical history.
(1) A stress myocardial perfusion study must be performed:
(a) on premises equipped with resuscitation equipment, including a defibrillator; and
(b) by a person trained in cardiopulmonary resuscitation who is in continuous personal attendance during the procedure.
(2) At the time the service is performed, a second person trained in the matters mentioned in subclause (4) and cardiopulmonary resuscitation must be located at the premises while the exercise test is performed, and must be immediately available to respond if required.
(3) One of the persons mentioned in subclauses (1) and (2) must be a medical practitioner.
(4) For the purposes of subclause (2), the matters are:
(a) how to safely perform exercise or pharmacological stress monitoring and recording; and
(b) how to recognise the symptoms and signs of cardiac disease.
2.4.2 PET nuclear scanning services
An item in Subgroup 2 of Group I4 applies only if the service is performed on a person:
(a) at the written request of a specialist or consultant physician (the requesting practitioner) if:
(i) the person is the requesting practitioner’s patient; and
(ii) the requesting practitioner decides that the service is necessary; and
(b) at the premises of a comprehensive practice; and
(c) in accordance with clauses 2.4.3 and 2.4.4.
2.4.3 PET nuclear scanning services—performance under supervision
For the purposes of paragraph 2.4.2(c), the service is performed in accordance with this clause if:
(a) all of the following subparagraphs apply:
(i) the service is performed under the supervision of a PET credentialled specialist who is available to monitor and influence the conduct and diagnostic quality of the examination;
(ii) a PET credentialled specialist, a nuclear medicine credentialled specialist or a specialist in the specialty of diagnostic radiology is available, if necessary, to attend on the patient personally;
(iii) the service is reported by a PET credentialled specialist; or
(b) the service is performed:
(i) in an emergency; or
(ii) because of medical necessity, in a remote location.
2.4.4 PET nuclear scanning services—equipment
For the purposes of paragraph 2.4.2(c), the service is performed in accordance with this clause if the service is performed on a person using equipment that meets the requirements set out in Requirements for PET Accreditation (Instrumentation & Radiation Safety) 3rd Edition (2017), issued by the Australian and New Zealand Society of Nuclear Medicine Inc, as existing on 1 July 2020.
Note: The Requirements for PET Accreditation (Instrumentation & Radiation Safety) 3rd Edition (2017) could in 2020 be viewed on the website of the Society (https://www.anzsnm.org.au).
Subdivision B—Subgroups 1, 2 and 3 of Group I4
2.4.6 Items in Subgroups 1, 2 and 3 of Group I4
This clause sets out items in Subgroups 1, 2 and 3 of Group I4.
Note: The fees in Subgroup 1 of Group I4 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100.16%; border-collapse:collapse"><thead><tr><td colspan="4" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I4—Nuclear medicine imaging</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="4" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 1—Nuclear medicine—non PET</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61310</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Myocardial infarct avid study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>380.15</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61313</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Gated cardiac blood pool study, (equilibrium) (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>313.95</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61314</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Gated cardiac blood pool study, with or without intervention, and first pass blood flow or cardiac shunt study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>434.70</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><a id="_Hlk66698828"><span>61321</span></a></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Single rest myocardial perfusion study for the assessment of the extent and severity of viable and non</span><span>‑</span><span>viable myocardium, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has left ventricular systolic dysfunction and probable or confirmed coronary artery disease; and</span></p><p class="Tablea"><span>(b) the service uses a single rest technetium</span><span>‑</span><span>99m (Tc</span><span>‑</span><span>99m) protocol; and</span></p><p class="Tablea"><span>(c) the service is requested by a specialist or a consultant physician; and</span></p><p class="Tablea"><a id="_Hlk80179931"><span>(d) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61325, 61329, 61345, 61398 or 61406 applies; and</span></a></p><p class="Tablea"><span>(e) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61325, 61329, 61345, 61398 or 61406, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>340.50</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61324</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Single stress myocardial perfusion study, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) at least one of the following applies:</span></p><p class="Tablei"><span>(i) the patient has body habitus or other physical conditions (including heart rhythm disturbance) to the extent that a stress echocardiography would not provide adequate information;</span></p><p class="Tablei"><span>(ii) the patient is unable to exercise to the extent required for a stress echocardiography to provide adequate information;</span></p><p class="Tablei"><span>(iii) the patient has had a failed stress echocardiography provided in a service to which item</span><span> </span><span>55141, 55143, 55145 or 55146 applies; and</span></p><p class="Tablea"><span>(c) the service includes resting ECG, continuous ECG monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(d) the service is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><a id="_Hlk80179988"><span>(e) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61325, 61329, 61345, 61357, 61394, 61398, 61406 or 61414 applies; and</span></a></p><p class="Tablea"><span>(f) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61329, 61345, 61357, 61394, 61398, 61406 or 61414, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>675.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61325</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Single rest myocardial perfusion study for the assessment of the extent and severity of viable and non</span><span>‑</span><span>viable myocardium, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has left ventricular systolic dysfunction and probable or confirmed coronary artery disease; and</span></p><p class="Tablea"><span>(b) the service uses:</span></p><p class="Tablei"><span>(i) an initial rest study followed by a redistribution study on the same day; and</span></p><p class="Tablei"><span>(ii) a thallous chloride</span><span>‑</span><span>201 (Tl</span><span>‑</span><span>201) protocol; and</span></p><p class="Tablea"><span>(c) the service is requested by a specialist or a consultant physician; and</span></p><p class="Tablea"><a id="_Hlk80180082"><span>(d) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61329, 61345, 61398 or 61406 applies; and</span></a></p><p class="Tablea"><span>(e) if the patient is 17 years or older:</span></p><p class="Tablei"><span>(i) a service to which item</span><span> </span><span>61321, 61329, 61345, 61398 or 61406 applies has not been provided to the patient in the previous 24 months; and</span></p><p class="Tablei"><span>(ii) the service is applicable only twice each 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>340.50</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61328</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Lung perfusion study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>235.60</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61329</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Combined stress and rest, stress and re</span><span>‑</span><span>injection or rest and redistribution myocardial perfusion study, including delayed imaging or re</span><span>‑</span><span>injection protocol on a subsequent occasion, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) at least one of the following applies:</span></p><p class="Tablei"><span>(i) the patient has body habitus or other physical conditions (including heart rhythm disturbance) to the extent that a stress echocardiography would not provide adequate information;</span></p><p class="Tablei"><span>(ii) the patient is unable to exercise to the extent required for a stress echocardiography to provide adequate information;</span></p><p class="Tablei"><span>(iii) the patient has had a failed stress echocardiography provided in a service to which item</span><span> </span><span>55141, 55143, 55145 or 55146 applies; and</span></p><p class="Tablea"><span>(c) the service includes resting electrocardiograph, continuous electrocardiograph monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(d) the service is requested by a medical practitioner (other than a specialist or consultant physician); and</span></p><p class="Tablea"><a id="_Hlk80180157"><span>(e) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61324, 61325, 61345, 61357, 61394, 61398, 61406 or 61414 applies; and</span></a></p><p class="Tablea"><span>(f) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61321, 61324, 61325, 61345, 61357, 61394, 61398, 61406 or 61414, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,016.40</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61340</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Lung ventilation study using aerosol, technegas or xenon gas (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>261.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61345</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Combined stress and rest, stress and re</span><span>‑</span><span>injection or rest and redistribution myocardial perfusion study, including delayed imaging or re</span><span>‑</span><span>injection protocol on a subsequent occasion, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) at least one of the following applies:</span></p><p class="Tablei"><span>(i) the patient has body habitus or other physical conditions (including heart rhythm disturbance) to the extent that a stress echocardiography would not provide adequate information;</span></p><p class="Tablei"><span>(ii) the patient is unable to exercise to the extent required for a stress echocardiography to provide adequate information;</span></p><p class="Tablei"><span>(iii) the patient has had a failed stress echocardiography provided in a service to which item</span><span> </span><span>55141, 55143, 55145 or 55146 applies; and</span></p><p class="Tablea"><span>(c) the service includes resting electrocardiograph, continuous electrocardiograph monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(d) the service is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><a id="_Hlk80181069"><span>(e) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61324, 61325, 61329, 61357, 61394, 61398, 61406 or 61414 applies; and</span></a></p><p class="Tablea"><span>(f) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61321, 61324, 61325, 61329, 61357, 61394, 61398, 61406 or 61414, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,016.40</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61348</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Lung perfusion study and lung ventilation study using aerosol, technegas or xenon gas (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>458.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61349</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Repeat combined stress and rest, stress and re</span><span>‑</span><span>injection or rest and redistribution myocardial perfusion study, including delayed imaging or re</span><span>‑</span><span>injection protocol on a subsequent occasion, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><a id="_Hlk80181289"><span>(a) both:</span></a></p><p class="Tablei"><span>(i) a service has been provided to the patient in the previous 24 months to which this item, or item</span><span> </span><span>61324, 61329, 61345, 61357, 61394, 61398, 61406, 61410 or 61414, applies; and</span></p><p class="Tablei"><span>(ii) the patient has subsequently</span><span style="font-style:italic"> </span><span>undergone a revascularisation procedure; and</span></p><p class="Tablea"><span>(b) the patient has one or more symptoms of cardiac ischaemia that have evolved and are not adequately controlled with optimal medical therapy; and</span></p><p class="Tablea"><span>(c) at least one of the following applies:</span></p><p class="Tablei"><span>(i) the patient has body habitus or other physical conditions (including heart rhythm disturbance) to the extent that a stress echocardiography would not provide adequate information;</span></p><p class="Tablei"><span>(ii) the patient is unable to exercise to the extent required for a stress echocardiography to provide adequate information;</span></p><p class="Tablei"><span>(iii) the patient has had a failed stress echocardiography provided in a service to which item</span><span> </span><span>55141, 55143, 55145 or 55146 applies; and</span></p><p class="Tablea"><span>(d) the service is requested by a specialist or a consultant physician; and</span></p><p class="Tablea"><a id="_Hlk80181344"><span>(e) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730 or 61410 applies; and</span></a></p><p class="Tablea"><span>(f) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61410, applies has not been provided to the patient in the previous 12 months</span></p><p class="Tabletext"><span>Applicable not more than once in 12 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,016.40</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61353</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Liver and spleen study (colloid) (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>400.15</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61356</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Red blood cell spleen or liver study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>406.55</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61357</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Single stress myocardial perfusion study, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) at least one of the following applies:</span></p><p class="Tablei"><span>(i) the patient has body habitus or other physical conditions (including heart rhythm disturbance) to the extent that a stress echocardiography would not provide adequate information;</span></p><p class="Tablei"><span>(ii) the patient is unable to exercise to the extent required for a stress echocardiography to provide adequate information;</span></p><p class="Tablei"><span>(iii) the patient has had a failed stress echocardiography provided in a service to which items</span><span> </span><span>55141, 55143, 55145 or 55146 applies; and</span></p><p class="Tablea"><span>(c) the service includes resting electrocardiograph, continuous electrocardiograph monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(d) the service is requested by a medical practitioner (other than a specialist or consultant physician); and</span></p><p class="Tablea"><a id="_Hlk80181424"><span>(e) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61324, 61325, 61329, 61345, 61394, 61398, 61406 or 61414 applies; and</span></a></p><p class="Tablea"><span>(f) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61324, 61329, 61345, 61394, 61398, 61406, or 61414, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>675.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61360</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hepatobiliary study, including morphine administration or pre</span><span>‑</span><span>treatment with a cholagogue when performed (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>417.45</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61361</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Hepatobiliary study with formal quantification following baseline imaging, using a cholagogue (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>477.55</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61364</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Bowel haemorrhage study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>514.35</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61368</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Meckel’s diverticulum study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>230.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61369</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Indium</span><span>‑</span><span>labelled octreotide study (including single photon emission tomography when undertaken), if:</span></p><p class="Tablea"><span>(a) a gastro</span><span>‑</span><span>entero</span><span>‑</span><span>pancreatic endocrine tumour is suspected on the basis of biochemical evidence with negative or equivocal conventional imaging; or</span></p><p class="Tablea"><span>(b) both:</span></p><p class="Tablei"><span>(i) a surgically amenable gastro</span><span>‑</span><span>entero</span><span>‑</span><span>pancreatic endocrine tumour has been identified on the basis of conventional techniques; and</span></p><p class="Tablei"><span>(ii) the study is to exclude additional disease sites (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>2,086.30</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61372</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Salivary study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>230.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61373</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Gastro</span><span>‑</span><span>oesophageal reflux study, including delayed imaging on a separate occasion when performed (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>506.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61376</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Oesophageal clearance study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>148.35</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61381</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Gastric emptying study, using single tracer (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>594.45</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61383</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Combined solid and liquid gastric emptying study using dual isotope technique or the same isotope on separate days (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>646.80</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61384</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Radionuclide colonic transit study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>711.75</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61386</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Renal study, including perfusion and renogram images and computer analysis or cortical study with planar imaging (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>344.15</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61387</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Renal cortical study, with single photon emission tomography and planar quantification (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>445.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61389</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Single renal study with pre</span><span>‑</span><span>procedural administration of a diuretic or angiotensin converting enzyme (ACE) inhibitor (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>383.50</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61390</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Renal study with diuretic administration after a baseline study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>424.30</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61393</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Combined examination involving a renal study following angiotensin converting enzyme (ACE) inhibitor provocation and a baseline study, in either order and related to a single referral episode (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>626.70</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61394</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Single stress myocardial perfusion study, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) the service is provided at, or from, a practice located in a Modified Monash 3, 4, 5, 6 or 7 area; and</span></p><p class="Tablea"><span>(c) a stress echocardiography service is not available in the Modified Monash area where the service is provided; and</span></p><p class="Tablea"><span>(d) the service includes resting electrocardiograph, continuous electrocardiograph monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(e) the service is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><a id="_Hlk80181468"><span>(f) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61324, 61325, 61329, 61345, 61357, 61398, 61406 or 61414 applies; and</span></a></p><p class="Tablea"><span>(g) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61324, 61329, 61345, 61357, 61398, 61406 or 61414, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>675.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61397</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cystoureterogram (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>255.50</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61398</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Combined stress and rest, stress and re</span><span>‑</span><span>injection or rest and redistribution myocardial perfusion study, including delayed imaging or re</span><span>‑</span><span>injection protocol on a subsequent occasion, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) the service is provided at, or from, a practice located in a Modified Monash 3, 4, 5, 6 or 7 area; and</span></p><p class="Tablea"><span>(c) a stress echocardiography service is not available in the Modified Monash area where the services is provided; and</span></p><p class="Tablea"><span>(d) the service includes resting electrocardiograph, continuous electrocardiograph monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(e) the service is requested by a medical practitioner (other than a specialist or consultant physician); and</span></p><p class="Tablea"><a id="_Hlk80181519"><span>(f) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61324, 61325, 61329, 61345, 61357, 61394, 61406 or 61414 applies; and</span></a></p><p class="Tablea"><span>(g) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61321, 61324, 61325, 61329, 61345, 61357, 61394, 61406 or 61414, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,016.40</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61402</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cerebral perfusion study, with single photon emission tomography and with planar imaging when performed (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>626.25</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61406</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Combined stress and rest, stress and re</span><span>‑</span><span>injection or rest and redistribution myocardial perfusion study, including delayed imaging or re</span><span>‑</span><span>injection protocol on a subsequent occasion, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) the service is provided at, or from, a practice located in a Modified Monash 3, 4, 5, 6 or 7 area; and</span></p><p class="Tablea"><span>(c) a stress echocardiography service is not available in the Modified Monash area where the service is provided; and</span></p><p class="Tablea"><span>(d) the service includes resting electrocardiograph, continuous electrocardiograph monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(e) the service is requested by a specialist or consultant physician; and</span></p><p class="Tablea"><a id="_Hlk80181565"><span>(f) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61324, 61325, 61329, 61345, 61357, 61394, 61398 or 61414 applies; and</span></a></p><p class="Tablea"><span>(g) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61321, 61324, 61325, 61329, 61345, 61357, 61394, 61398 or 61414, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,016.40</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61409</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cerebro</span><span>‑</span><span>spinal fluid transport study using technetium 99m, with imaging on 2 or more separate occasions (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>904.05</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61410</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Repeat combined stress and rest, stress and re</span><span>‑</span><span>injection or rest and redistribution myocardial perfusion study, including delayed imaging or re</span><span>‑</span><span>injection protocol on a subsequent occasion, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><a id="_Hlk80181614"><span>(a) both:</span></a></p><p class="Tablei"><span>(i) a service has been provided to the patient in the previous 24 months to which this item, or item</span><span> </span><span>61324, 61329, 61345, 61349, 61357, 61394, 61398, 61406 or 61414, applies; and</span></p><p class="Tablei"><span>(ii) the patient has subsequently</span><span style="font-style:italic"> </span><span>undergone a revascularisation procedure; and</span></p><p class="Tablea"><span>(b) the patient has one or more symptoms of cardiac ischaemia that have evolved and are not adequately controlled with optimal medical therapy; and</span></p><p class="Tablea"><span>(c) the service is provided at, or from, a practice located in a Modified Monash 3, 4, 5, 6 or 7 area; and</span></p><p class="Tablea"><span>(d) a stress echocardiography service is not available in the Modified Monash area where the service is provided; and</span></p><p class="Tablea"><a id="_Hlk80181648"><span>(e) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729 or 11730 applies; and</span></a></p><p class="Tablea"><span>(f) if the patient is 17 years or older—a service to which item</span><span> </span><span>61349 applies has not been provided to the patient in the previous 12 months</span></p><p class="Tabletext"><span>Applicable not more than once in 12 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,016.40</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61413</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cerebro</span><span>‑</span><span>spinal fluid shunt patency study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>233.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61414</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Single stress myocardial perfusion study, with single photon emission tomography, with or without planar imaging, if:</span></p><p class="Tablea"><span>(a) the patient has symptoms of cardiac ischaemia; and</span></p><p class="Tablea"><span>(b) the service is provided at, or from, a practice located in a Modified Monash 3, 4, 5, 6 or 7 area; and</span></p><p class="Tablea"><span>(c) a stress echocardiography service is not available in the Modified Monash area where the service is provided; and</span></p><p class="Tablea"><span>(d) the service includes resting electrocardiograph, continuous electrocardiograph monitoring during exercise (with recording), blood pressure monitoring and the recording of other parameters (including heart rate); and</span></p><p class="Tablea"><span>(e) the service is requested by a medical practitioner (other than a specialist or consultant physician); and</span></p><p class="Tablea"><a id="_Hlk80181688"><span>(f) the service is not associated with a service to which item</span><span> </span><span>11704, 11705, 11707, 11714, 11729, 11730, 61321, 61324, 61325, 61329, 61345, 61357, 61394, 61398 or 61406 applies; and</span></a></p><p class="Tablea"><span>(g) if the patient is 17 years or older—a service to which this item, or item</span><span> </span><span>61324, 61329, 61345, 61357, 61398 or 61406, applies has not been provided to the patient in the previous 24 months (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>675.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61421</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Bone study—whole body, with, when undertaken, blood flow, blood pool and delayed imaging on a separate occasion (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>496.60</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61425</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Bone study—whole body and single photon emission tomography, with, when undertaken, blood flow, blood pool and delayed imaging on a separate occasion (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>621.70</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61426</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body study using iodine (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>574.20</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61429</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body study using gallium (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>562.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61430</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body study using gallium, with single photon emission tomography (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>682.55</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61433</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body study using cells labelled with technetium (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>514.35</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61434</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body study using cells labelled with technetium, with single photon emission tomography (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>636.95</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61438</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body study using thallium (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>696.50</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61441</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Bone marrow study—whole body using technetium labelled bone marrow agents (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>506.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61442</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body study, using gallium—with single photon emission tomography of 2 or more body regions acquired separately (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>778.70</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61445</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Bone marrow study—localised using technetium labelled agent (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>296.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61446</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Regional scintigraphic study using an approved bone scanning agent, including, when undertaken, blood flow imaging, blood pool imaging and repeat imaging on a separate occasion (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>345.20</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61449</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Regional scintigraphic study and single photon emission tomography, using an approved bone scanning agent, including, when undertaken, blood flow imaging, blood pool imaging and repeat imaging on a separate occasion (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>472.15</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61450</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Localised study using gallium (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>411.45</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61453</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Localised study using gallium, with single photon emission tomography (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>532.70</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61454</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Localised study using cells labelled with technetium (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>360.30</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61457</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Localised study using cells labelled with technetium, with single photon emission tomography (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>486.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61461</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Localised study using thallium (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>546.30</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61462</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Repeat planar and single photon emission tomography imaging, or repeat planar imaging or single photon emission tomography imaging on an occasion subsequent to the performance of item</span><span> </span><span>61364, 61426, 61429, 61430, 61442, 61450, 61453, 61469 or 61485, if there is no additional administration of radiopharmaceutical and if the previous radionuclide scan was abnormal or equivocal (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>133.50</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61466</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Cerebro</span><span>‑</span><span>spinal fluid transport study using indium</span><span>‑</span><span>111, with imaging on 2 or more separate occasions (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>4,855.10</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61469</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Lymphoscintigraphy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>360.30</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61473</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Thyroid study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>181.55</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61480</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Parathyroid study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>400.40</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61485</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Adrenal study, with single photon emission tomography (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>3,481.75</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61495</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Tear duct study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>230.90</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61499</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Particle perfusion study (infra</span><span>‑</span><span>arterial) or Le Veen shunt study (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>261.85</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61650</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>LeukoScan study of the long bones and feet for suspected osteomyelitis, if:</span></p><p class="Tablea"><span>(a) the patient does not have access to ex</span><span>‑</span><span>vivo white blood cell scanning; and</span></p><p class="Tabletext"><span>(b) the patient is not being investigated for other sites of infection (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>909.45</span></p></td></tr><tr><td colspan="4" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 2—PET</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61523</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, performed for evaluation of a solitary pulmonary nodule, if:</span></p><p class="Tablea"><span>(a) the nodule is considered unsuitable for transthoracic fine needle aspiration biopsy; or</span></p><p class="Tablea"><span>(b) an attempt at pathological characterisation has failed (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61524</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, performed for the staging of locally advanced (Stage III) breast cancer, for a patient who is considered suitable for active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61525</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, performed for the evaluation of suspected metastatic or suspected locally or regionally recurrent breast carcinoma, for a patient who is considered suitable for active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61529</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, performed for the staging of proven non</span><span>‑</span><span>small cell lung cancer, if curative surgery or radiotherapy is planned (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61538</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>FDG PET study of the brain for evaluation of suspected residual or recurrent malignant brain tumour based on anatomical imaging findings, after definitive therapy (or during ongoing chemotherapy) in patients who are considered suitable for further active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>901.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61541</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, following initial therapy, performed for the evaluation of suspected residual, metastatic or recurrent colorectal carcinoma in a patient considered suitable for active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61553</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, following initial therapy, performed for the evaluation of suspected metastatic or recurrent malignant melanoma in a patient considered suitable for active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>999.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61559</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>FDG PET study of the brain, performed for the evaluation of refractory epilepsy, that is being evaluated for surgery (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>918.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61560</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>FDG PET study of the brain, performed for the diagnosis of Alzheimer’s disease, if:</span></p><p class="Tablea"><span>(a) clinical evaluation of the patient by a specialist, or in consultation with a specialist, is equivocal; and</span></p><p class="Tablea"><span>(b) the service includes a quantitative comparison of the results of the study with the results of an FDG PET study of a normal brain from a reference database; and</span></p><p class="Tablea"><span>(c) a service to which this item applies has not been performed on the patient in the previous 12 months; and</span></p><p class="Tablea"><span>(d) a service to which item</span><span> </span><span>61402 applies has not been performed on the patient in the previous 12 months for the diagnosis or management of Alzheimer’s disease</span></p><p class="Tabletext"><span>Applicable not more than 3 times per lifetime (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>605.05</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61563</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body prostate</span><span>‑</span><span>specific membrane antigen PET study performed for the initial staging of intermediate to high</span><span>‑</span><span>risk prostate adenocarcinoma, for a previously untreated patient who is considered suitable for locoregional therapy with curative intent</span></p><p class="Tabletext"><span>Applicable once per lifetime (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,300.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61564</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body prostate</span><span>‑</span><span>specific membrane antigen PET study performed for the restaging of recurrent prostate adenocarcinoma, for a patient who:</span></p><p class="Tablea"><span>(a) has undergone prior locoregional therapy; and</span></p><p class="Tablea"><span>(b) is considered suitable for further locoregional therapy to determine appropriate therapeutic pathways and timing of treatment initiation</span></p><p class="Tabletext"><span>Applicable twice per lifetime (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,300.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61565</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, following initial therapy, performed for the evaluation of suspected residual, metastatic or recurrent ovarian carcinoma in a patient considered suitable for active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61571</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study for the further primary staging of patients with histologically proven carcinoma of the uterine cervix, at FIGO stage IB2 or greater by conventional staging, prior to planned radical radiation therapy or combined modality therapy with curative intent (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61575</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study for the further staging of patients with confirmed local recurrence of carcinoma of the uterine cervix considered suitable for salvage pelvic chemoradiotherapy or pelvic exenteration with curative intent (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61577</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, performed for the staging of proven oesophageal or gastro</span><span>‑</span><span>oesophageal junction carcinoma, in a patient considered suitable for active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61598</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study performed for the staging of biopsy</span><span>‑</span><span>proven, newly</span><span>‑</span><span>diagnosed or recurrent head and neck cancer (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61604</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study performed for the evaluation of a patient with suspected residual head and neck cancer after definitive treatment, and who is suitable for active therapy (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61610</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study performed for the evaluation of metastatic squamous cell carcinoma of unknown primary site involving cervical nodes (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61612</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study for the initial staging of cancer, for a patient who is considered suitable for active therapy, if:</span></p><p class="Tablea"><span>(a) the cancer is a typically FDG</span><span>‑</span><span>avid cancer; and</span></p><p class="Tablea"><span>(b) there is at least a 10% likelihood that the PET study result will inform a significant change in management for the patient</span></p><p class="Tabletext"><span>Applicable once per cancer diagnosis (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61614</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study, following initial therapy, performed for the evaluation of suspected residual, metastatic or recurrent cancer in a patient who is undergoing, or is suitable for, active therapy, if the cancer is a typically FDG</span><span>‑</span><span>avid cancer (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61620</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study for the initial staging of newly diagnosed or previously untreated Hodgkin or non</span><span>‑</span><span>Hodgkin lymphoma (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61622</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study to assess response to first line therapy either during treatment or within 3 months of completing definitive first line treatment for Hodgkin or non</span><span>‑</span><span>Hodgkin lymphoma (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61628</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study for restaging following confirmation of recurrence of Hodgkin or non</span><span>‑</span><span>Hodgkin lymphoma (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61632</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study to assess response to second</span><span>‑</span><span>line chemotherapy if haemopoietic stem cell transplantation is being considered for Hodgkin or non</span><span>‑</span><span>Hodgkin lymphoma (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61640</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study for initial staging of a patient with biopsy</span><span>‑</span><span>proven bone or soft tissue sarcoma (excluding gastrointestinal stromal tumour) considered by conventional staging to be potentially curable (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>999.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61646</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body FDG PET study for the evaluation of patients with suspected residual or recurrent sarcoma (excluding gastrointestinal stromal tumour) after the initial course of definitive therapy to determine suitability for subsequent therapy with curative intent (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>999.00</span></p></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61647</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Whole body </span><span style="font-size:6.67pt; vertical-align:super">68</span><span>Ga</span><span>‑</span><span>DOTA</span><span>‑</span><span>peptide PET study, if:</span></p><p class="Tablea"><span>(a) a gastro</span><span>‑</span><span>entero</span><span>‑</span><span>pancreatic neuroendocrine tumour is suspected on the basis of biochemical evidence with negative or equivocal conventional imaging; or</span></p><p class="Tablea"><span>(b) both:</span></p><p class="Tablei"><span>(i) a surgically amenable gastro</span><span>‑</span><span>entero</span><span>‑</span><span>pancreatic neuroendocrine tumour has been identified on the basis of conventional techniques; and</span></p><p class="Tablei"><span>(ii) the study is for excluding additional disease sites (R)</span></p></td><td colspan="2" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>953.00</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 3—Adjunctive services</span></p></td><td style="border-top:0.75pt solid #000000; vertical-align:top"></td></tr><tr><td style="width:12.26%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>61505</span></p></td><td style="width:74.42%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>CT scan:</span></p><p class="Tablea"><span>(a) performed at the same time as, and covering the same body area as, single photon emission tomography or positron emission tomography; and</span></p><p class="Tablea"><span>(b) performed for the purpose of anatomic localisation or attenuation correction; and</span></p><p class="Tablea"><span>(c) performed in association with a service to which an item in Subgroup 1 or 2 of Group I4 applies;</span></p><p class="Tabletext"><span>if no separate diagnostic CT report is issued (R)</span></p></td><td style="width:13.2%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>100.00</span></p></td><td style="vertical-align:top"></td></tr><tr style="height:0pt"><td style="width:51.45pt"></td><td style="width:312.1pt"></td><td style="width:55.35pt"></td><td style="width:0.5pt"></td></tr></tbody></table>
Division 2.5—Group I5: magnetic resonance imaging
Subdivision A—General
2.5.1 Application of items to certain MRI and MRA services
(1) The items in Subgroups 1 to 21 apply to an MRI or MRA service performed:
(a) at the request of a specialist or consultant physician in accordance with clause 2.5.2; and
(b) in a permissible circumstance mentioned in clause 2.5.3; and
(c) using equipment that is:
(i) located at the premises of a comprehensive practice; and
(ii) if the equipment is located in a Modified Monash 1 area—eligible equipment mentioned in clause 2.5.5.
(3) The items in Subgroups 22 and 32 apply to an MRI or MRA service performed:
(a) at the request of a medical practitioner in accordance with clause 2.5.2; and
(b) in a permissible circumstance mentioned in clause 2.5.3; and
(c) using equipment that is:
(i) located at the premises of a comprehensive practice; and
(ii) if the equipment is located in a Modified Monash 1 area—eligible equipment mentioned in clause 2.5.5.
(4) The items in Subgroups 33 and 34 apply to an MRI service performed:
(a) at the request of a medical practitioner other than a specialist or consultant physician in accordance with clause 2.5.2; and
(b) in a permissible circumstance mentioned in clause 2.5.3; and
(c) using equipment that is:
(i) located at the premises of a comprehensive practice; and
(ii) if the equipment is located in a Modified Monash 1 area—eligible equipment mentioned in clause 2.5.5.
2.5.2 MRI and MRA services—request
For the purposes of clause 2.5.1, a request must:
(a) be made in writing; and
(b) identify the clinical indications for the service.
2.5.3 MRI and MRA services—permissible circumstances for performance
For the purposes of clause 2.5.1, a service is performed in a permissible circumstance only if it is:
(a) both:
(i) performed under the supervision of an eligible provider who is available to monitor and influence the conduct and diagnostic quality of the examination, including, if necessary, by personal attendance on the patient; and
(ii) reported by an eligible provider; or
(b) performed in an emergency; or
(c) performed because of medical necessity, in a remote location.
2.5.4 MRI and MRA services—eligible provider
A person mentioned in column 2 of an item of table 2.5.4 is an eligible provider for an MRI or MRA service mentioned in column 1 of the item.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Table 2.5.4—Eligible providers</span></p></td></tr><tr><td style="width:8.58%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Item</span></p></td><td style="width:30.48%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>MRI or MRA service</span></p></td><td style="width:60.94%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Person</span></p></td></tr></thead><tbody><tr><td style="width:8.58%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>1</span></p></td><td style="width:30.48%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>A service to which none of items</span><span> </span><span>63390 and 63395 to 63397 apply</span></p></td><td style="width:60.94%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tablea"><span>A person who is a specialist in diagnostic radiology</span></p></td></tr><tr><td style="width:8.58%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>2</span></p></td><td style="width:30.48%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>A service to which any of items</span><span> </span><span>63395 to 63397 apply</span></p></td><td style="width:60.94%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>A person who is:</span></p><p class="Tablea"><span>(a) a specialist in diagnostic radiology or a consultant physician; and</span></p><p class="Tablea"><span>(b) recognised by the Conjoint Committee for Certification in Cardiac MRI</span></p></td></tr><tr><td style="width:8.58%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>3</span></p></td><td style="width:30.48%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>A service to which item</span><span> </span><span>63390 applies</span></p></td><td style="width:60.94%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.4pt; padding-left:5.4pt; vertical-align:top"><p class="Tabletext"><span>A person who is:</span></p><p class="Tablea"><span>(a) a specialist in diagnostic radiology; or</span></p><p class="Tablea"><span>(b) a consultant physician who is recognised by the Conjoint Committee for Certification in Cardiac MRI</span></p></td></tr></tbody></table>
2.5.5 MRI and MRA services—eligible equipment
For the purposes of clause 2.5.1, equipment is eligible equipment if it is:
(a) included on the Diagnostic Imaging Register in relation to the location specific practice number for the comprehensive practice at which it is located; and
(b) made available to the practice by a person who is subject to a current deed with the Commonwealth that relates to the equipment so included on the Register.
2.5.7 MRI and MRA services—meaning of scan
In items 63001 to 63563 and 63740 to 63743:
scan means a minimum of 3 sequences.
2.5.8 Restriction on items—multiple services in certain subgroups on a day
If an MRI service described in an item in Subgroup 1, 2, 4, 5 or 14 of Group I5, and an MRA service described in an item in Subgroup 3 or 15 of Group I5, are provided to the same patient on the same day, the item in Subgroup 3 or 15 of Group I5 does not apply to the MRA service.
2.5.8A Restriction on items—multiple services in certain subgroups in an attendance
Multiple services in subgroups 1 to 5
(1) If more than one service described in an item in Subgroup 1, 2, 3, 4 or 5 of Group I5 is provided to a patient in a single attendance, only the following items apply to the services:
(a) the item that describes the service with the highest fee;
(b) each item that describes a service to which subclause (4) applies (if any).
Multiple services in subgroups 6 to 10
(2) If more than one service described in an item in Subgroup 6, 7, 8, 9 or 10 of Group I5 is provided to a patient in a single attendance, only the following items apply to the services:
(a) the item that describes the service with the highest fee;
(b) each item that describes a service to which subclause (4) applies (if any).
Multiple services with same highest fee
(3) For the purposes of paragraphs (1)(a) and (2)(a), if 2 or more applicable fees are equally the highest, only one of those fees is taken to be the highest fee.
Services with documented clinical need
(4) For the purposes of paragraphs (1)(b) and (2)(b), this subclause applies to a service provided to a person in an attendance if the clinical need for the service is:
(a) stated in the request for the service; and
(b) appropriately documented in the record of the service.
2.5.8B Reduction in fees—multiple services on same day—Subgroups 12 and 13
(1) If a medical practitioner provides 2 or more MRI services described in Subgroup 12 or 13 of Group I5 for the same person on the same day, the fees specified for the items that apply to the services, other than the item with the highest fee, are reduced by 50%.
(2) For the purposes of subclause (1):
(a) if 2 or more applicable fees are equally the highest, only one of those fees is taken to be the highest fee; and
(b) if a reduced fee calculated under subclause (1) is not a multiple of 5 cents, the reduced fee is taken to be the nearest amount that is a multiple of 5 cents.
2.5.9 Restriction on items—related MRI or MRA services
An MRI or MRA item does not apply to a service provided to a person if:
(a) the MRI or MRA item is specified in column 1 of an item (the table item) of table 2.5.9; and
(b) during the period (the limitation period):
(i) specified in column 2 of the table item; and
(ii) ending immediately before the service is provided;
the person was provided with one or more services (the earlier services) to which any of the MRI or MRA items mentioned in the table item applied; and
(c) the number of earlier services provided to the person in the limitation period was equal to the maximum number specified in column 3 of the table item.
2.5.9A Circumstances for suspecting prostate cancer for item 63541
(1) For the purposes of subparagraph (a)(ii) of item 63541, the circumstances for suspecting a patient of developing prostate cancer are that:
(a) 2 PSA quantitation tests have been performed for the patient, with an interval between the tests of at least 1 month but not more than 3 months; and
(b) subclause (2), (3), (4), (5) or (6) applies to the patient.
Patients at least 70 years of age
(2) This subclause applies to a patient if:
(a) the patient is at least 70 years of age; and
(b) both PSA quantitation tests showed a PSA concentration of greater than 5.5 µg/L; and
(c) a free/total PSA ratio test performed for the patient at least 1 month but not more than 3 months after the first PSA quantitation test showed a free/total PSA ratio of less than 25%.
Patients under 70 years of age without increased risk due to family history
(3) This subclause applies to a patient if:
(a) the patient is under 70 years of age; and
(b) both PSA quantitation tests showed a PSA concentration of greater than 3 µg/L; and
(c) a free/total PSA ratio test performed for the patient at least 1 month but not more than 3 months after the first PSA quantitation test showed a free/total PSA ratio of less than 25%.
(4) This subclause applies to a patient if:
(a) the patient is under 70 years of age; and
(b) the first PSA quantitation test showed a PSA concentration of greater than 3 µg/L; and
(c) the second PSA quantitation test showed a PSA concentration of greater than 5.5 µg/L.
Patients under 70 years of age with increased risk due to family history
(5) This subclause applies to a patient if:
(a) the patient is under 70 years of age; and
(b) both PSA quantitation tests showed a PSA concentration of greater than 2 µg/L; and
(c) a free/total PSA ratio test performed for the patient at least 1 month but not more than 3 months after the first PSA quantitation test showed a free/total PSA ratio of less than 25%; and
(d) the patient has a first‑degree biological relative:
(i) who has, or has had, prostate cancer; or
(ii) who is suspected of carrying a BRCA 1 or BRCA 2 mutation.
(6) This subclause applies to a patient if:
(a) the patient is under 70 years of age; and
(b) the first PSA quantitation test showed a PSA concentration of greater than 2 µg/L; and
(c) the second PSA quantitation test showed a PSA concentration of greater than 5.5 µg/L; and
(d) the patient has a first‑degree biological relative:
(i) who has, or has had, prostate cancer; or
(ii) who is suspected of carrying a BRCA 1 or BRCA 2 mutation.
2.5.9B Restriction on item 63543—timing and purpose
(1) Subject to subclauses (2) and (3), item 63543 is applicable to a service described in that item for a patient with a diagnosis of prostate cancer if it is:
(a) the first service provided after the date of the diagnosis; or
(b) the first service provided after 12 months after the date of the service mentioned in paragraph (a); or
(c) the first service provided after 3 years after the date of a service to which item 63543 applied under paragraph (b) or this paragraph.
(2) Subject to subclause (3), item 63543 is also applicable to a service described in that item if the clinical need for the service is:
(a) stated in the request for the service; and
(b) appropriately documented in the record of the service.
(3) Item 63543 is not applicable to a service provided for the purposes of:
(a) treatment planning; or
(b) monitoring after treatment of prostate cancer.
Subdivision B—Subgroups 1 to 19 of Group I5
2.5.10 Items in Subgroups 1 to 19 of Group I5
This clause sets out items in Subgroups 1 to 19 of Group I5.
Note: The fees in Group I5 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I5—Magnetic resonance imaging</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 1—Scan of head—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63001</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for tumour of the brain or meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63004</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for inflammation of brain or meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63007</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for skull base or orbital tumour (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63010</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for stereotactic scan of brain, with fiducials in place, for the sole purpose of allowing planning for stereotactic neurosurgery (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>336.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63019</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA if performed) for the assessment of suitability for the treatment of medically refractory essential tremor with magnetic resonance imaging</span><span>‑</span><span>guided focused ultrasound</span></p><p class="Tabletext"><span>Applicable once per patient per lifetime (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>426.50</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63020</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA if performed) for the post</span><span>‑</span><span>procedure assessment of the patient following magnetic resonance imaging</span><span>‑</span><span>guided focused ultrasound for the treatment of medically refractory essential tremor</span></p><p class="Tabletext"><span>Applicable once per patient per lifetime (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>426.50</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 2—Scan of head—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63040</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for acoustic neuroma (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>336.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63043</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for pituitary tumour (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63046</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for toxic or metabolic or ischaemic encephalopathy (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63049</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for demyelinating disease of the brain (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63052</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for congenital malformation of the brain or meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63055</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for venous sinus thrombosis (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63058</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for head trauma (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63061</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for epilepsy (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63064</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for stroke (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63067</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for carotid or vertebral artery dissection (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63070</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for intracranial aneurysm (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63073</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head (including MRA, if performed) for intracranial arteriovenous malformation (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 3—Scan of head and neck vessels—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63101</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI and MRA of extracranial or intracranial circulation (or both)—scan of head and neck vessels for stroke (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="page-break-inside:avoid"><span>Subgroup 4—Scan of head and cervical spine—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="page-break-inside:avoid; page-break-after:avoid"><span>63111</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="page-break-inside:avoid; page-break-after:avoid"><span>MRI—scan of head and cervical spine (including MRA, if performed) for tumour of the central nervous system or meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right; page-break-inside:avoid; page-break-after:avoid"><span>492.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63114</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head and cervical spine (including MRA, if performed) for inflammation of the central nervous system or meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 5—Scan of head and cervical spine—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63125</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head and cervical spine (including MRA, if performed) for demyelinating disease of the central nervous system (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63128</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head and cervical spine (including MRA, if performed) for congenital malformation of the central nervous system or meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63131</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head and cervical spine (including MRA, if performed) for syrinx (congenital or acquired) (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 6—Scan of spine—one region or 2 contiguous regions—for infection or tumour</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63151</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for infection (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63154</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for tumour (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 7—Scan of spine—one region or 2 contiguous regions—for other conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63161</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for demyelinating disease (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63164</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for congenital malformation of the spinal cord or the cauda equina or the meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63167</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for myelopathy (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63170</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for syrinx (congenital or acquired) (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63173</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for cervical radiculopathy (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63176</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for sciatica (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63179</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for spinal canal stenosis (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63182</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for previous spinal surgery (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63185</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one region or 2 contiguous regions of the spine for trauma (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 8—Scan of spine—3 contiguous or 2 non</span><span>‑</span><span>contiguous regions—for infection or tumour</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63201</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for infection (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63204</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for tumour (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 9—Scan of spine—3 contiguous or 2 non</span><span>‑</span><span>contiguous regions—for other conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63219</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for demyelinating disease (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63222</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for congenital malformation of the spinal cord or the cauda equina or the meninges (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63225</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for myelopathy (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63228</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for syrinx (congenital or acquired) (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63231</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for cervical radiculopathy (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63234</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for sciatica (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63237</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for spinal canal stenosis (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63240</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for previous spinal surgery (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63243</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of 3 contiguous or 2 non</span><span>‑</span><span>contiguous regions of the spine for trauma (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 10—Scan of cervical spine and brachial plexus—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63271</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cervical spine and brachial plexus for tumour (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63274</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cervical spine and brachial plexus for trauma (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63277</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cervical spine and brachial plexus for cervical radiculopathy (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63280</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cervical spine and brachial plexus for previous surgery (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 11—Scan of musculoskeletal system—for tumour, infection or osteonecrosis</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63301</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for tumour arising in bone or musculoskeletal system, excluding tumours arising in breast, prostate or rectum (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>380.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63304</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for infection arising in bone or musculoskeletal system, excluding infection arising in breast, prostate or rectum (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>380.80</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63307</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for osteonecrosis (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>380.80</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 12—Scan of musculoskeletal system—for joint derangement</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63322</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for derangement of hip or its supporting structures (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63325</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for derangement of shoulder or its supporting structures (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63328</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for derangement of knee or its supporting structures (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63331</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for derangement of ankle or foot (or both) or its supporting structures (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63334</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for derangement of one or both temporomandibular joints or their supporting structures (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>336.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63337</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for derangement of wrist or hand (or both) or its supporting structures (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63340</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for derangement of elbow or its supporting structures (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 13—Scan of musculoskeletal system—for Gaucher disease</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63361</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of musculoskeletal system for Gaucher disease (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 14—Scan of cardiovascular system—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63385</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cardiovascular system for congenital disease of the heart or a great vessel (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63388</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cardiovascular system for tumour of the heart or a great vessel (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.68%; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63390</span></p></td><td style="width:69.86%; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cardiovascular system for assessment of myocardial structure, function and</span><span style="font-style:italic"> </span><span>characterisation, if the request for the scan indicates that the patient has:</span></p><p class="Tablea"><span>(a) acute onset (less than 3 months) heart failure caused by suspected myocarditis which would otherwise require endomyocardial biopsy to confirm the diagnosis of myocarditis; or</span></p><p class="Tablea"><span>(b) unexplained arrhythmia caused by suspected myocarditis which would otherwise require endomyocardial biopsy to confirm the diagnosis of myocarditis; or</span></p><p class="Tablea"><span>(c) suspected drug</span><span>‑</span><span>induced myocarditis, if the results from all of the following examinations are inconclusive to form a diagnosis:</span></p><p class="Tablei"><span>(i) troponin;</span></p><p class="Tablei"><span>(ii) chest X</span><span>‑</span><span>ray;</span></p><p class="Tablei"><span>(iii) transthoracic echocardiogram</span></p><p class="Tabletext"><span>(R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>616.60</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63391</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cardiovascular system for abnormality of thoracic aorta (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63395</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cardiovascular system for assessment of myocardial structure and function involving:</span></p><p class="Tablea"><span>(a) dedicated right ventricular views; and</span></p><p class="Tablea"><span>(b) 3D volumetric assessment of the right ventricle; and</span></p><p class="Tablea"><span>(c) reporting of end</span><span>‑</span><span>diastolic and end</span><span>‑</span><span>systolic volumes, ejection fraction and BSA</span><span>‑</span><span>indexed values;</span></p><p class="Tabletext"><span>if the request for the scan indicates that:</span></p><p class="Tablea"><span>(d) the patient presented with symptoms consistent with arrhythmogenic right ventricular cardiomyopathy (ARVC); or</span></p><p class="Tablea"><span>(e) investigative findings in relation to the patient are consistent with ARVC</span></p><p class="Tabletext"><span>(R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>855.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63397</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of cardiovascular system for assessment of myocardial structure and function involving:</span></p><p class="Tablea"><span>(a) dedicated right ventricular views; and</span></p><p class="Tablea"><span>(b) 3D volumetric assessment of the right ventricle; and</span></p><p class="Tablea"><span>(c) reporting of end</span><span>‑</span><span>diastolic and end</span><span>‑</span><span>systolic volumes, ejection fraction and BSA</span><span>‑</span><span>indexed values;</span></p><p class="Tabletext"><span>if the request for the scan indicates that the patient:</span></p><p class="Tablea"><span>(d) is asymptomatic; and</span></p><p class="Tablea"><span>(e) has one or more first degree relatives diagnosed with confirmed arrhythmogenic right ventricular cardiomyopathy (ARVC)</span></p><p class="Tabletext"><span>(R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>855.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 15—Magnetic resonance angiography—scan of cardiovascular system—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63401</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRA—if the request for the scan specifically identifies the clinical indication for the scan—scan of cardiovascular system for vascular abnormality in a patient with a previous anaphylactic reaction to an iodinated contrast medium (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63404</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRA—if the request for the scan specifically identifies the clinical indication for the scan—scan of cardiovascular system for obstruction of the superior vena cava, inferior vena cava or a major pelvic vein (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 16—Magnetic resonance angiography—for specified conditions—person under the age of 16 years</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63416</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRA—scan of person under the age of 16 for the vasculature of limbs prior to limb or digit transfer surgery in congenital limb deficiency syndrome (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 17—Magnetic resonance imaging—person under the age of 16 years—for physeal fusion or Gaucher disease</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63425</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of person under the age of 16 for post</span><span>‑</span><span>inflammatory or post</span><span>‑</span><span>traumatic physeal fusion (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63428</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of person under the age of 16 for Gaucher disease (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 18—Magnetic resonance imaging—person under the age of 16 years—for other conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63440</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of person under the age of 16 for pelvic or abdominal mass (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63443</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of person under the age of 16 for mediastinal mass (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63446</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of person under the age of 16 for congenital uterine or anorectal abnormality (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 19—Scan of body—for specified conditions</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63461</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the body for adrenal mass in a patient with a malignancy that is otherwise resectable (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63464</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of both breasts for the detection of cancer in a patient, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that the patient is asymptomatic and is younger than 60 years of age; and</span></p><p class="Tablea"><span>(c) the request for the scan identifies that the patient is at high risk of developing breast cancer due to one or more of the following:</span></p><p class="Tablei"><span>(i) genetic testing has identified the presence of a high risk breast cancer gene mutation in the patient or in a first degree relative of the patient;</span></p><p class="Tablei"><span>(ii) both:</span></p><p class="TableAA"><span>(A) one of the patient’s first or second degree relatives was diagnosed with breast cancer at age 45 years or younger; and</span></p><p class="TableAA"><span>(B) another first or second degree relative on the same side of the patient’s family was diagnosed with bone or soft tissue sarcoma at age 45 years or younger;</span></p><p class="Tablei"><span>(iii) the patient has a personal history of breast cancer before the age of 50 years;</span></p><p class="Tablei"><span>(iv) the patient has a personal history of mantle radiation therapy;</span></p><p class="Tablei"><span>(v) the patient has a lifetime risk estimation greater than 30% or a 10 year absolute risk estimation greater than 5% using a clinically relevant risk evaluation algorithm; and</span></p><p class="Tablea"><span>(d) the service is not performed in conjunction with item</span><span> </span><span>55076 or 55079</span></p><p class="Tabletext"><span>Applicable not more than once in a 12 month period (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>690.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63467</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of both breasts for the detection of cancer, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the person has had an abnormality detected as a result of a service mentioned in item</span><span> </span><span>63464 performed in the previous 12 months (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>690.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63487</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of both breasts, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that:</span></p><p class="Tablei"><span>(i) the patient has been diagnosed with metastatic cancer restricted to the regional lymph nodes; and</span></p><p class="Tablei"><span>(ii) clinical examination and conventional imaging have failed to identify the primary cancer (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>690.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63489</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one breast, performed in conjunction with a biopsy procedure on that breast and an ultrasound scan of that breast, if:</span></p><p class="Tablea"><span>(a) the request for the MRI scan identifies that the patient has a suspicious lesion seen on MRI but not on conventional imaging; and</span></p><p class="Tablea"><span>(b) the ultrasound scan is performed immediately before the MRI scan and confirms that the lesion is not amenable to biopsy guided by conventional imaging; and</span></p><p class="Tablea"><span>(c) a dedicated breast coil is used (R) (Anaes.)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,008.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63531</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of both breasts, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that:</span></p><p class="Tablei"><span>(i) the patient has a breast lesion; and</span></p><p class="Tablei"><span>(ii) the results of</span><span style="font-style:italic"> </span><span>conventional</span><span style="font-style:italic"> </span><span>imaging are inconclusive for the presence of breast cancer; and</span></p><p class="Tablei"><span>(iii) biopsy has not been possible (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>690.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63533</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of both breasts, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that:</span></p><p class="Tablei"><span>(i) the patient has been diagnosed with a breast cancer; and</span></p><p class="Tablei"><span>(ii) there is a discrepancy between the clinical assessment and the conventional imaging assessment of the extent of the malignancy; and</span></p><p class="Tablea"><span>(c) the results of breast MRI imaging may alter treatment planning (R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>690.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63541</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Multiparametric MRI—scan of the prostate for the detection of cancer, requested by a specialist in the speciality of urology, radiation oncology or medical oncology:</span></p><p class="Tablea"><span>(a) if the request for the scan identifies that the patient is suspected of developing prostate cancer:</span></p><p class="Tablei"><span>(i) on the basis of a digital rectal examination; or</span></p><p class="Tablei"><span>(ii) in the circumstances mentioned in clause</span><span> </span><span>2.5.9A; and</span></p><p class="Tablea"><span>(b) using a standardised image acquisition protocol involving:</span></p><p class="Tablei"><span>(i) T2</span><span>‑</span><span>weighted imaging; and</span></p><p class="Tablei"><span>(ii) diffusion</span><span>‑</span><span>weighted imaging; and</span></p><p class="Tablei"><span>(iii) (unless contraindicated) dynamic contrast enhancement</span></p><p class="Tabletext"><span>(R) (Anaes)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>450.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63543</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Multiparametric MRI—scan of the prostate for the assessment of cancer, requested by a specialist in the speciality of urology, radiation oncology or medical oncology:</span></p><p class="Tablea"><span>(a) if the request for the scan identifies that the patient:</span></p><p class="Tablei"><span>(i) is under active surveillance following a confirmed diagnosis of prostate cancer by biopsy histopathology; and</span></p><p class="Tablei"><span>(ii) is not undergoing, or planning to undergo, treatment for prostate cancer; and</span></p><p class="Tablea"><span>(b) using a standardised image acquisition protocol involving:</span></p><p class="Tablei"><span>(i) T2</span><span>‑</span><span>weighted imaging; and</span></p><p class="Tablei"><span>(ii) diffusion</span><span>‑</span><span>weighted imaging; and</span></p><p class="Tablei"><span>(iii) (unless contraindicated) dynamic contrast enhancement</span></p><p class="Tabletext"><span>(R) (Anaes)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>450.00</span></p></td></tr><tr><td style="width:12.68%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63547</span></p></td><td style="width:69.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of both breasts for the detection of cancer, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that:</span></p><p class="Tablei"><span>(i) the patient has a breast implant in situ; and</span></p><p class="Tablei"><span>(ii) anaplastic large cell lymphoma has been diagnosed</span></p><p class="Tabletext"><span>(R) (Anaes.) (Contrast)</span></p></td><td style="width:17.46%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>690.00</span></p></td></tr></tbody></table>
Subdivision C—Subgroup 20 of Group I5: scans of pelvis and upper abdomen for specified conditions
2.5.11 Restriction on items 63470, 63473, 63740 and 63743
(1) Item 63470 does not apply to the service mentioned in that item if the person to whom the service is provided has previously been provided with that service or a service mentioned in item 63473.
(2) Item 63473 does not apply to the service mentioned in that item if the person to whom the service is provided has previously been provided with that service or a service mentioned in item 63470.
(3) For any patient, if the service mentioned in item 63740 is provided for assessment of change to therapy in a patient with small bowel Crohn’s disease, the item applies to that service only once in a 12 month period.
(4) For any patient, if the service mentioned in item 63743 is provided for assessment of change to therapy of pelvis sepsis and fistulas from Crohn’s disease, the item applies to that service only once in a 12 month period.
2.5.13 Items in Subgroup 20 of Group I5
This clause sets out items in Subgroup 20 of Group I5.
Note: The fees in Group I5 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I5—Magnetic resonance imaging</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 20—Scan of pelvis and upper abdomen—for specified conditions</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><a id="_Hlk80184934"><span>63454</span></a></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the pelvis or abdomen, for a patient who is pregnant, if:</span></p><p class="Tablea"><span>(a) the pregnancy is at, or after, 18 weeks gestation; and</span></p><p class="Tablea"><span>(b) fetal abnormality is suspected; and</span></p><p class="Tablea"><span>(c) an ultrasound has been performed and is provided by, or on behalf of, or at the request of, a specialist who is practising in the specialty of obstetrics; and</span></p><p class="Tablea"><span>(d) the diagnosis of fetal abnormality as a result of the ultrasound is indeterminate or requires further examination; and</span></p><p class="Tablea"><span>(e) the MRI service is requested by a specialist practising in the specialty of obstetrics</span></p><p class="Tablea"><span>(R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,200.00</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63470</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the pelvis for the staging of histologically diagnosed cervical cancer at FIGO stage 1B or greater, if the request for scan identifies that:</span></p><p class="Tablea"><span>(a) a histological diagnosis of carcinoma of the cervix has been made; and</span></p><p class="Tablea"><span>(b) the patient has been diagnosed with cervical cancer at FIGO stage 1B or greater (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63473</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the pelvis and upper abdomen, in a single examination, for the staging of histologically diagnosed cervical cancer at FIGO stage 1B or greater, if the request for the scan identifies that:</span></p><p class="Tablea"><span>(a) a histological diagnosis of carcinoma of the cervix has been made; and</span></p><p class="Tablea"><span>(b) the patient has been diagnosed with cervical cancer at FIGO stage 1B or greater (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>627.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63476</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the pelvis for the initial staging, restaging or follow up of rectal cancer, if:</span></p><p class="Tablea"><span>(a) a high resolution T2 technique is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that the indication is for:</span></p><p class="Tablei"><span>(i) the initial staging of rectal cancer (including cancer of the rectosigmoid and anorectum); or</span></p><p class="Tablei"><span>(ii) the initial assessment of response to chemotherapy or chemoradiotherapy; or</span></p><p class="Tablei"><span>(iii) the assessment of possible recurrent tumour after complete response to neoadjuvant therapy, within an active surveillance program; or</span></p><p class="Tablei"><span>(iv) the assessment of recurrent disease prior to treatment planning</span></p><p class="Tablea"><span>(R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63539</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the abdomen, requested by a specialist or consultant physician, to assess the development or growth of renal tumours in a patient with a confirmed clinical or molecular diagnosis of a genetic disorder associated with an increased risk of developing renal tumours, other than a service to which item</span><span> </span><span>63540 applies</span></p><p class="Tabletext"><span>Applicable once in any 12 month period</span></p><p class="Tabletext"><span>(R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>686.70</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63540</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the abdomen, requested by a specialist or consultant physician, to assess a patient with one or more known renal tumours and with a confirmed clinical or molecular diagnosis of a genetic disorder associated with an increased risk of developing renal tumours, if the service is performed:</span></p><p class="Tablea"><span>(a) to evaluate changes in clinical condition or suspected complications of the known renal tumours; or</span></p><p class="Tablea"><span>(b) where a disease specific line of treatment has been initiated and an assessment of patient responsiveness to the treatment is required</span></p><p class="Tabletext"><span>Applicable once in any 3 month period</span></p><p class="Tabletext"><span>(R) (Anaes) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>686.70</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63549</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the pelvis or abdomen, for a patient with a multiple pregnancy, if:</span></p><p class="Tablea"><span>(a) the multiple pregnancy is at, or after, 18 weeks gestation; and</span></p><p class="Tablea"><span>(b) fetal abnormality is suspected; and</span></p><p class="Tablea"><span>(c) an ultrasound has been performed and is provided by, or on behalf of, or at the request of, a specialist who is practising in the specialty of obstetrics; and</span></p><p class="Tablea"><span>(d) the diagnosis of fetal abnormality as a result of the ultrasound is indeterminate or requires further examination; and</span></p><p class="Tablea"><span>(e) the MRI service is requested by a specialist practising in the specialty of obstetrics (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>1,828.80</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63563</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of the pelvis or abdomen, if the request for the scan identifies that the investigation is for:</span></p><p class="Tablea"><span>(a) sub</span><span>‑</span><span>fertility that requires one or more of the following:</span></p><p class="Tablei"><span>(i) an investigation of suspected Mullerian duct anomaly seen in pelvic ultrasound or hysterosalpingogram;</span></p><p class="Tablei"><span>(ii) an assessment of uterine mass identified on pelvic ultrasound before consideration of surgery;</span></p><p class="Tablei"><span>(iii) an investigation of recurrent implantation failure in IVF (2 or more embryo transfer cycles without viable pregnancy); or</span></p><p class="Tablea"><span>(b) surgical planning of a patient with known or suspected deep endometriosis involving the bowel, bladder or ureter (or any combination of the bowel, bladder or ureter), where the results of pelvic ultrasound are inconclusive</span></p><p class="Tabletext"><span>Applicable not more than once in a 2 year period (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>409.65</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63740</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan to evaluate small bowel Crohn’s disease if the service is provided to a patient for:</span></p><p class="Tablea"><span>(a) evaluation of disease extent at time of initial diagnosis of Crohn’s disease; or</span></p><p class="Tablea"><span>(b) evaluation of exacerbation, or suspected complications, of known Crohn’s disease; or</span></p><p class="Tablea"><span>(c) evaluation of known or suspected Crohn’s disease in pregnancy; or</span></p><p class="Tablea"><span>(d) assessment of change to therapy in a patient with small bowel Crohn’s disease (R) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>457.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63741</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan with enteroclysis for Crohn’s disease if the service is related to item</span><span> </span><span>63740 (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>265.25</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63743</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan for fistulising perianal Crohn’s disease if the service is provided to a patient for:</span></p><p class="Tablea"><span>(a) evaluation of pelvic sepsis and fistulas associated with established or suspected Crohn’s disease; or</span></p><p class="Tablea"><span>(b) assessment of change to therapy of pelvis sepsis and fistulas from Crohn’s disease (R) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr></tbody></table>
Subdivision D—Subgroups 21 and 22 of Group I5
2.5.13A MRI and MRA services—modifying items
(1) Subject to subclauses (2) to (7), if item 63491, 63494, 63497, 63498 or 63499 applies to an MRI or MRA service, the fee specified in that item applies in addition to the fee specified in the other item in Group I5 that applies to the service.
(2) If 2 or more MRI or MRA services mentioned in item 63494 are performed for a person on the same day, the fee specified in that item applies to one of those services only.
(3) If 2 or more MRI or MRA services mentioned in item 63497 are performed for a person on the same day, the fee specified in that item applies to one of those services only.
(4) If:
(a) one or more MRI or MRA services mentioned in item 63494; and
(b) one or more MRI or MRA services mentioned in item 63497;
are performed for a person on the same day, the fee specified in item 63494 or 63497, but not both those items, applies to one of those services only.
(5) If 2 or more MRI services mentioned in item 63498 are performed for a person on the same day, the fee specified in that item applies to one of those services only.
(6) If 2 or more MRI services mentioned in item 63499 are performed for a person on the same day, the fee specified in that item applies to one of those services only.
(7) If:
(a) one or more services mentioned in item 63498; and
(b) one or more services mentioned in item 63499;
are performed for a person on the same day, the fee specified in item 63498 or item 63499, but not both those items, applies to one of those services only.
2.5.14 Items in Subgroups 21, 22 and 32 of Group I5
This clause sets out items in Subgroups 21, 22 and 32 of Group I5.
Note: The fees in Group I5 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I5—Magnetic resonance imaging</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 21—Scan of body—for suspected hepato</span><span>‑</span><span>biliary or pancreatic pathology</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63482</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of pancreas and biliary tree for suspected biliary or pancreatic pathology (R) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63545</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—multiphase scans of liver (including delayed imaging, if performed) with a contrast agent, for characterisation, or staging where surgical resection or interventional techniques are under consideration, if:</span></p><p class="Tablea"><span>(a) the patient has a confirmed extra</span><span>‑</span><span>hepatic primary malignancy (other than hepatocellular carcinoma); and</span></p><p class="Tablea"><span>(b) computed tomography is negative or inconclusive for hepatic metastatic disease; and</span></p><p class="Tablea"><span>(c) the identification of liver metastases would change the patient’s treatment planning</span></p><p class="Tabletext"><span>Applicable not more than once in a 12 month period (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>550.00</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63546</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—multiphase scans of the liver (including delayed imaging, if performed) with a contrast agent, for diagnosis or staging, if:</span></p><p class="Tablea"><span>(a) the patient has:</span></p><p class="Tablei"><span>(i) known or suspected hepatocellular carcinoma; and</span></p><p class="Tablei"><span>(ii) chronic liver disease that has been confirmed by a specialist or consultant physician; and</span></p><p class="Tablea"><span>(b) the patient’s liver function has been identified as Child</span><span>‑</span><span>Pugh class A or B; and</span></p><p class="Tablea"><span>(c) the patient has an identified hepatic lesion over 10 mm in diameter</span></p><p class="Tabletext"><span>For any particular patient—applicable not more than once in a 12 month period (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>550.00</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 22—Modifying items</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63491</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI or MRA service to which an item in this Group (other than an item in this Subgroup) applies if:</span></p><p class="Tablea"><span>(a) the service is performed in accordance with clause</span><span> </span><span>2.5.1; and</span></p><p class="Tablea"><span>(b) the item for the service includes in its description ‘(Contrast)’; and</span></p><p class="Tablea"><span>(c) the service is performed using a contrast agent</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.80</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63494</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI or MRA service to which an item in this Group (other than an item in this Subgroup) applies if:</span></p><p class="Tablea"><span>(a) the service is performed in accordance with clause</span><span> </span><span>2.5.1; and</span></p><p class="Tablea"><span>(b) the service is performed using intravenous or intra muscular sedation</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>44.80</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63496</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI service to which item</span><span> </span><span>63545 or 63546 applies if:</span></p><p class="Tablea"><span>(a) the service is performed under the supervision of an eligible provider; and</span></p><p class="Tablea"><span>(b)the service is performed using an hepatobiliary</span><span>‑</span><span>specific contrast agent</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>250.00</span></p></td></tr><tr style="height:4.35pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63497</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI or MRA service to which an item in this Group (other than an item in this Subgroup) applies if:</span></p><p class="Tablea"><span>(a) the service is performed in accordance with clause</span><span> </span><span>2.5.1; and</span></p><p class="Tablea"><span>(b) the service is performed under anaesthetic in the presence of a medical practitioner who is qualified to perform an anaesthetic</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>156.80</span></p></td></tr><tr style="height:4.35pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63498</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI service to which item</span><span> </span><span>63501, 63502, 63504 or 63505 applies, if the service is performed on a person using intravenous or intra muscular sedation</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>47.15</span></p></td></tr><tr style="height:4.35pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63499</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI service to which item</span><span> </span><span>63501, 63502, 63504 or 63505 applies, if the service is performed on a person under anaesthetic in the presence of a medical practitioner who is qualified to perform an anaesthetic (H)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>165.05</span></p></td></tr><tr><td colspan="3" style="border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 32—Magnetic resonance imaging—PIP breast implant</span></p></td></tr><tr style="height:4.35pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63501</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one or both breasts for the evaluation of implant integrity, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that the patient:</span></p><p class="Tablei"><span>(i) has or is suspected of having a silicone breast implant manufactured by Poly Implant Prosthese (PIP); and</span></p><p class="Tablei"><span>(ii) the result of the scan confirms a loss of integrity of the implant (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>526.30</span></p></td></tr><tr style="height:4.35pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63502</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one or both breasts for the evaluation of implant integrity, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that the patient:</span></p><p class="Tablei"><span>(i) has or is suspected of having a silicone breast implant manufactured by Poly Implant Prosthese (PIP); and</span></p><p class="Tablei"><span>(ii) the result of the scan does not demonstrate a loss of integrity of the implant (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>526.30</span></p></td></tr><tr style="height:4.35pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63504</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one or both breasts for the evaluation of implant integrity, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that the patient:</span></p><p class="Tablei"><span>(i) has or is suspected of having a silicone breast implant manufactured by Poly Implant Prosthese (PIP); and</span></p><p class="Tablei"><span>(ii) presents with symptoms where implant rupture is suspected; and</span></p><p class="Tablei"><span>(iii) the result of the scan confirms a loss of integrity of the implant (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>526.30</span></p></td></tr><tr style="height:4.35pt"><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63505</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of one or both breasts for the evaluation of implant integrity, if:</span></p><p class="Tablea"><span>(a) a dedicated breast coil is used; and</span></p><p class="Tablea"><span>(b) the request for the scan identifies that the patient:</span></p><p class="Tablei"><span>(i) has or is suspected of having a silicone breast implant manufactured by Poly Implant Prosthese (PIP); and</span></p><p class="Tablei"><span>(ii) presents with symptoms where implant rupture is suspected; and</span></p><p class="Tablei"><span>(iii) the result of the scan does not demonstrate a loss of integrity of the implant (R)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>526.30</span></p></td></tr></tbody></table>
Subdivision E—Subgroup 33 of Group I5
2.5.15 Items in Subgroup 33 of Group I5
This clause sets out items in Subgroup 33 of Group I5.
Note: The fees in Group I5 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I5—Magnetic resonance imaging</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 33—Scan of body—person under the age of 16 years—general practice requests</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63507</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of head for a patient under 16 years if the service is for:</span></p><p class="Tablea"><span>(a) an unexplained seizure; or</span></p><p class="Tablea"><span>(b) an unexplained headache if significant pathology is suspected; or</span></p><p class="Tablea"><span>(c) paranasal sinus pathology that has not responded to conservative therapy (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63510</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of spine following radiographic examination for a patient under 16 years if the service is for:</span></p><p class="Tablea"><span>(a) significant trauma; or</span></p><p class="Tablea"><span>(b) unexplained neck or back pain with associated neurological signs; or</span></p><p class="Tablea"><span>(c) unexplained back pain if significant pathology is suspected (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63513</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of knee for internal joint derangement for a patient under 16 years (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63516</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of hip following radiographic examination for a patient under 16 years if any of the following is suspected:</span></p><p class="Tablea"><span>(a) septic arthritis;</span></p><p class="Tablea"><span>(b) slipped capital femoral epiphysis;</span></p><p class="Tablea"><span>(c) Perthes disease (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63519</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of elbow following radiographic examination for a patient under 16 years if a significant fracture or avulsion injury, which would change the way in which the patient is managed, is suspected (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63522</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>MRI—scan of wrist following radiographic examination for a patient under 16 years if a scaphoid fracture is suspected (R) (Anaes.) (Contrast)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>448.00</span></p></td></tr></tbody></table>
Subdivision F—Subgroup 34 of Group I5
2.5.16 Items in Subgroup 34 of Group I5
This clause sets out items in Subgroup 34 of Group I5.
Note: The fees in Group I5 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I5—Magnetic resonance imaging</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Subgroup 34—Scan of body—person over the age of 16 years—general practice requests</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63551</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Scan of head for a patient 16 years or older, after a request by a medical practitioner (other than a specialist or consultant physician), for any of the following:</span></p><p class="Tablea"><span>(a) unexplained seizure(s);</span></p><p class="Tablea"><span>(b) unexplained chronic headache with suspected intracranial pathology (R) (Contrast) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63554</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Scan of spine for a patient 16 years or older, after referral by a medical practitioner (other than a specialist or consultant physician), for suspected cervical radiculopathy (R) (Contrast) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>358.40</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63557</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Scan of spine for a patient 16 years or older, after referral by a medical practitioner (other than a specialist or consultant physician), for suspected cervical spinal trauma (R) (Contrast) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>492.80</span></p></td></tr><tr><td style="width:12.18%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>63560</span></p></td><td style="width:75.86%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext"><span>Scan of knee following acute knee trauma, after referral by a medical practitioner (other than a specialist or consultant physician), for a patient 16 to 49 years with:</span></p><p class="Tablea"><span>(a) inability to extend the knee suggesting the possibility of acute meniscal tear; or</span></p><p class="Tablea"><span>(b) clinical findings suggesting acute anterior cruciate ligament tear (R) (Contrast) (Anaes.)</span></p></td><td style="width:11.96%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>403.20</span></p></td></tr></tbody></table>
Division 2.6—Group I6: management of bulk‑billed services
2.6.1 Application of items 64990, 64991, 64992, 64993, 64994 and 64995
(2) If item 64990, 64991, 64992, 64993, 64994 or 64995 applies to a diagnostic imaging service, the fee specified in that item applies in addition to the fee specified in any other item in this Schedule that applies to the service.
(3) In this Schedule:
Commonwealth concession card holder has the same meaning as concessional beneficiary has for the purposes of Part VII of the National Health Act 1953.
practice location, for the provision of a diagnostic imaging service, means the place of practice for which the medical practitioner by whom, or on whose behalf, the service is provided, has been allocated a provider number by the Chief Executive Medicare.
unreferred service means a diagnostic imaging service that:
(a) is provided to a person by, or on behalf of, a medical practitioner, being a medical practitioner who is not a consultant physician, or specialist, in any speciality (other than a medical practitioner who is, for the Act, both a general practitioner and a consultant physician, or specialist, in a particular speciality); and
(b) has not been referred to the medical practitioner by another medical practitioner or person with referring rights.
2.6.2 Items in Group I6
This clause sets out items in Group I6.
Note: The fees in Group I6 are indexed in accordance with clause 2.7.1.
<table cellspacing="0" cellpadding="0" style="width:100%; border-collapse:collapse"><thead><tr><td colspan="3" style="border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Group I6—Management of bulk</span><span>‑</span><span>billed services</span></p></td></tr><tr><td style="width:12%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 1</span></p><p class="TableHeading"><span>Item</span></p></td><td style="width:75.98%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading"><span>Column 2</span></p><p class="TableHeading"><span>Description</span></p></td><td style="width:12.02%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:1.55pt; padding-left:1.55pt; vertical-align:top"><p class="TableHeading" style="text-align:right"><span>Column 3</span></p><p class="TableHeading" style="text-align:right"><span>Fee ($)</span></p></td></tr></thead><tbody><tr style="height:27.6pt"><td style="width:12%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>64990</span></p></td><td style="width:75.98%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>A diagnostic imaging service to which an item in this Schedule (other than this item or item</span><span> </span><span>64991, 64992, 64993, 64994 or 64995) applies if:</span></p><p class="Tablea"><span>(a) the service is an unreferred service; and</span></p><p class="Tablea"><span>(b) the service is provided to a person who is under the age of 16 or is a Commonwealth concession card holder; and</span></p><p class="Tablea"><span>(c) the person is not an admitted patient of a hospital; and</span></p><p class="Tablea"><span>(d) the service is bulk</span><span>‑</span><span>billed for the fees for:</span></p><p class="Tablei"><span>(i) this item; and</span></p><p class="Tablei"><span>(ii) the other item in this Schedule applying to the service</span></p></td><td style="width:12.02%; border-top:1.5pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>7.15</span></p></td></tr><tr><td style="width:12%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>64991</span></p></td><td style="width:75.98%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>A diagnostic imaging service to which an item in this Schedule (other than this item or item</span><span> </span><span>64990, 64992, 64993, 64994 or 64995) applies if:</span></p><p class="Tablea"><span>(a) the service is an unreferred service; and</span></p><p class="Tablea"><span>(b) the service is provided to a person who is under the age of 16 or is a Commonwealth concession card holder; and</span></p><p class="Tablea"><span>(c) the person is not an admitted patient of a hospital; and</span></p><p class="Tablea"><span>(d) the service is bulk</span><span>‑</span><span>billed for the fees for:</span></p><p class="Tablei"><span>(i) this item; and</span></p><p class="Tablei"><span>(ii) the other item in this Schedule applying to the service; and</span></p><p class="Tablea"><span>(e) the service is provided at, or from, a practice location in a Modified Monash 2 area</span></p></td><td style="width:12.02%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>10.80</span></p></td></tr><tr><td style="width:12%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>64992</span></p></td><td style="width:75.98%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>A diagnostic imaging service to which an item in this Schedule (other than this item or item</span><span> </span><span>64990, 64991, 64993, 64994 or 64995) applies if:</span></p><p class="Tablea"><span>(a) the service is an unreferred service; and</span></p><p class="Tablea"><span>(b) the service is provided to a person who is under the age of 16 or is a Commonwealth concession card holder; and</span></p><p class="Tablea"><span>(c) the person is not an admitted patient of a hospital; and</span></p><p class="Tablea"><span>(d) the service is bulk</span><span>‑</span><span>billed in relation to the fees for:</span></p><p class="Tablei"><span>(i) this item; and</span></p><p class="Tablei"><span>(ii) the other item in this Schedule applying to the service; and</span></p><p class="Tablea"><span>(e) the service is provided at, or from, a practice location in:</span></p><p class="Tablei"><span>(i) a Modified Monash 3 area; or</span></p><p class="Tablei"><span>(ii) a Modified Monash 4 area</span></p></td><td style="width:12.02%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>11.55</span></p></td></tr><tr><td style="width:12%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>64993</span></p></td><td style="width:75.98%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>A diagnostic imaging service to which an item in this Schedule (other than this item or item</span><span> </span><span>64990, 64991, 64992, 64994 or 64995) applies if:</span></p><p class="Tablea"><span>(a) the service is an unreferred service; and</span></p><p class="Tablea"><span>(b) the service is provided to a person who is under the age of 16 or is a Commonwealth concession card holder; and</span></p><p class="Tablea"><span>(c) the person is not an admitted patient of a hospital; and</span></p><p class="Tablea"><span>(d) the service is bulk</span><span>‑</span><span>billed in relation to the fees for:</span></p><p class="Tablei"><span>(i) this item; and</span></p><p class="Tablei"><span>(ii) the other item in this Schedule applying to the service; and</span></p><p class="Tablea"><span>(e) the service is provided at, or from, a practice location in a Modified Monash 5 area</span></p></td><td style="width:12.02%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>12.25</span></p></td></tr><tr><td style="width:12%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>64994</span></p></td><td style="width:75.98%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>A diagnostic imaging service to which an item in this Schedule (other than this item or item</span><span> </span><span>64990, 64991, 64992, 64993 or 64995) applies if:</span></p><p class="Tablea"><span>(a) the service is an unreferred service; and</span></p><p class="Tablea"><span>(b) the service is provided to a person who is under the age of 16 or is a Commonwealth concession card holder; and</span></p><p class="Tablea"><span>(c) the person is not an admitted patient of a hospital; and</span></p><p class="Tablea"><span>(d) the service is bulk</span><span>‑</span><span>billed in relation to the fees for:</span></p><p class="Tablei"><span>(i) this item; and</span></p><p class="Tablei"><span>(ii) the other item in this Schedule applying to the service; and</span></p><p class="Tablea"><span>(e) the service is provided at, or from, a practice location in a Modified Monash 6 area</span></p></td><td style="width:12.02%; border-top:0.75pt solid #000000; border-bottom:0.75pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>13.00</span></p></td></tr><tr><td style="width:12%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>64995</span></p></td><td style="width:75.98%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext"><span>A diagnostic imaging service to which an item in this Schedule (other than this item or item</span><span> </span><span>64990, 64991, 64992, 64993 or 64994) applies if:</span></p><p class="Tablea"><span>(a) the service is an unreferred service; and</span></p><p class="Tablea"><span>(b) the service is provided to a person who is under the age of 16 or is a Commonwealth concession card holder; and</span></p><p class="Tablea"><span>(c) the person is not an admitted patient of a hospital; and</span></p><p class="Tablea"><span>(d) the service is bulk</span><span>‑</span><span>billed in relation to the fees for:</span></p><p class="Tablei"><span>(i) this item; and</span></p><p class="Tablei"><span>(ii) the other item in this Schedule applying to the service; and</span></p><p class="Tablea"><span>(e) the service is provided at, or from, a practice location in a Modified Monash 7 area</span></p></td><td style="width:12.02%; border-top:0.75pt solid #000000; border-bottom:1.5pt solid #000000; padding-right:5.35pt; padding-left:5.35pt; vertical-align:top"><p class="Tabletext" style="text-align:right"><span>14.25</span></p></td></tr></tbody></table>
Division 2.7—Indexation of fees
2.7.1 Indexation—1 July 2025
(1) At the start of 1 July 2025 (the indexation time), each amount covered by subclause (2) is replaced by the amount worked out using the following formula:
Start formula 1.024 times the amount immediately before the indexation time end formula
Note: The indexed fees could in 2025 be viewed on the Department’s MBS Online website (http://www.health.gov.au).
(2) The amounts covered by this subclause are the following:
(a) the fee for each item in the following:
(i) Group I1 (ultrasound services);
(ii) Group I2 (computer tomography services);
(iii) Group I3 (diagnostic radiology services);
(iiia) Subgroup 1 of Group I4 (nuclear medicine imaging services—non PET);
(iv) Group I5 (magnetic resonance imaging services);
(v) Group I6 (bulk‑billed services);
(b) the amount mentioned in each of subclauses 2.3.3(2) and (3) (increased fee for certain diagnostic radiology services carried out at residential aged care facilities).
(3) An amount worked out under subclause (1) is to be rounded up or down to the nearest 5 cents (rounding down if the amount is an exact multiple of 2.5 cents).
Part 3—Dictionary
3.1 Dictionary
Note 1: All references in this clause to a provision are references to a provision in this Schedule, unless otherwise indicated.
Note 2: A number of expressions used in this Schedule are defined in subsection 3(1) of the Act, including the following:
(a) diagnostic imaging service;
(b) general medical services table;
(c) practitioner;
(d) Secretary;
(e) specialist.
Note 3: For the effect of the term (Anaes.) used in items in this Schedule, see subclause 5.9.4(1) of the general medical services table.
In this Schedule:
Act means the Health Insurance Act 1973.
angiography suite has the meaning given by clause 2.3.11.
applicable life age has the meaning given by subclause 1.2.2(2).
ASGC 2006 means the July 2006 edition of Statistical Geography Volume 1 ‑ Australian Standard Geographical Classification (ASGC) (ABS catalogue number 1216.0), published by the Australian Statistician, as existing on 1 July 2020.
ASGC 2010 means the July 2010 edition of the Australian Standard Geographical Classification (ASGC) (ABS catalogue number 1216.0), published by the Australian Statistician, as existing on 1 July 2020.
bulk‑billed: a diagnostic imaging service is bulk‑billed if:
(a) a medicare benefit is payable to a person in relation to the service; and
(b) under an agreement entered into under section 20A of the Act:
(i) the person assigns to the medical practitioner by whom, or on whose behalf, the service is provided, the person’s right to the payment of the medicare benefit; and
(ii) the medical practitioner accepts the assignment in full payment of the medical practitioner’s fee for the service provided.
care recipient has the meaning given by the general medical services table.
Commonwealth concession card holder has the meaning given by clause 2.6.1.
comprehensive practice means a medical practice, or a radiology department of a hospital, that provides X‑ray, ultrasound and computed tomography services (whether or not it provides other services).
computed tomography or CT means a service performed (with or without intravenous contrast) using a detector:
(a) that is coupled to an X‑ray tube that emits a finely collimated X‑ray beam as it rotates within a gantry around a patient either in incremental or helical manner; and
(b) that receives a series of data profiles depicting the degree of absorption of the X‑ray beam, which are transformed into a cross‑sectional image after the application of complex algorithms.
cone beam computed tomography means a service performed on a rotating gantry to which an X‑ray source and a 2‑dimensional flat panel detector are fixed that produces multiple sequential planar projection images in a single revolution around the patient, which are reconstructed into a 3‑dimensional image.
consultation has the meaning given by clause 1.2.21.
CT: see computed tomography.
eligible provider, for an MRI or MRA service, has the meaning given by clause 2.5.4.
exemption period of an exemption means the period mentioned in paragraph 1.2.8(2)(a) (as extended or further extended under clause 1.2.10 if applicable).
FDG means 18F‑fluorodeoxyglucose.
(H) has the meaning given by subclause 1.2.15(3).
highest fee has the meaning given by clause 1.2.21.
Inner Regional Australia means a Remoteness Area classified as Inner Regional Australia under the ASGC 2006.
JNMCAC means the Joint Nuclear Medicine Credentialling and Accreditation Committee of the RACP and RANZCR.
maximum extended life age has the meaning given by subclause 1.2.2(3).
Modified Monash 1 area means an area that is not a Modified Monash 2 to 7 area.
Modified Monash 2 area has the meaning given by the general medical services table.
Modified Monash 3 area has the meaning given by the general medical services table.
Modified Monash 4 area has the meaning given by the general medical services table.
Modified Monash 5 area has the meaning given by the general medical services table.
Modified Monash 6 area has the meaning given by the general medical services table.
Modified Monash 7 area has the meaning given by the general medical services table.
MRA means magnetic resonance angiography.
MRI means magnetic resonance imaging.
new effective life age has the meaning given by subclause 1.2.2(3).
non‑consultation service has the meaning given by clause 1.2.21.
non‑metropolitan hospital means a hospital that is located outside the Sydney, Melbourne, Brisbane, Adelaide, Perth, Greater Hobart, Darwin and Canberra statistical divisions, as defined in the ASGC 2010.
(NR) has the meaning given by clause 1.2.15.
nuclear medicine credentialled specialist means a specialist or consultant physician whose name is included in a register, given to the Chief Executive Medicare by the JNMCAC, of participants in the Joint Nuclear Medicine Specialist Credentialling Program of the JNMCAC.
Outer Regional Australia means a Remoteness Area classified as Outer Regional Australia under the ASGC 2006.
PET means positron emission tomography.
PET credentialled specialist means:
(a) a specialist or consultant physician who is credentialled under the Joint Nuclear Medicine Specialist Credentialling Program for the Recognition of the Credentials of Nuclear Medicine Specialists for Positron Emission Tomography overseen by the JNMCAC; or
(b) a specialist or consultant physician who:
(i) is a Fellow of the RACP or RANZCR; and
(ii) has reported 400 or more studies forming part of PET services for which a Medicare benefit was payable; and
(iii) is authorised under State or Territory law to prescribe and administer to humans the PET radiopharmaceuticals that are to be administered to a person; and
(iv) met the requirements of subparagraphs (i), (ii) and (iii) before 1 November 2011.
practice location has the meaning given by clause 2.6.1.
providing practitioner has the same meaning as in subsection 16B(1) of the Act.
PSA is short for prostate specific antigen.
(R) has the meaning given by clause 1.2.15.
RACP means The Royal Australasian College of Physicians (ABN 90 270 343 237).
RANZCR means The Royal Australian and New Zealand College of Radiologists (ABN 37 000 029 863).
relevant proprietor has the meaning given by clause 1.2.4.
Remote Australia means a Remoteness Area classified as Remote Australia under the ASGC 2006.
remote location means a place within Australia that is more than 30 kilometres by road from:
(a) a hospital that provides a radiology or computed tomography service under the direction of a specialist in the specialty of diagnostic radiology; or
(b) a free‑standing radiology or computed tomography facility under the direction of a specialist in the specialty of diagnostic radiology.
report means a report prepared by a medical practitioner.
residential aged care facility has the meaning given by the general medical services table.
RRMA4 means a small rural centre as classified by the Rural, Remote and Metropolitan Areas Classification.
RRMA5 means a rural centre with an urban centre population of less than 10,000 persons as classified by the Rural, Remote and Metropolitan Areas Classification.
Rural, Remote and Metropolitan Areas Classification has the meaning given by the general medical services table.
scan, for items 63001 to 63563 and 63740 to 63743, has the meaning given by clause 2.5.7.
sequence, for a scan, means a series of images collected at the same time with similar image parameters (not including images designed to establish patient position and subsequently used to plan other scans).
unreferred service has the meaning given by clause 2.6.1.
upgraded has the meaning given by subclause 1.2.2(4).
Very Remote Australia means a Remoteness Area classified as Very Remote Australia under the ASGC 2006.
Part 4—Application, saving and transitional provisions
amending instrument means the Health Insurance (Diagnostic Imaging Services Table) Amendment (Equipment Capital Sensitivity) Regulations 2022.
commencement day means the day the amending instrument commences.
4.2 Application of amendments
The amendments of clauses 1.2.8 and 1.2.10 of this instrument made by the amending instrument apply in relation to a decision on an application made by the Secretary on or after the commencement day, regardless of when the application was made.
amending instrument means the Health Insurance Legislation Amendment (2024 Measures No. 2) Regulations 2024.
4.4 Exemptions from capital sensitivity requirements
(1) The amendments of this instrument made by items 2 to 4 and 6 to 14 of Part 1 of Schedule 2 to the amending instrument apply in relation to a decision on an application made by the Secretary on or after 1 July 2024, regardless of when the application was made.
(2) The amendments of this instrument made by items 1 and 5 of Part 1 of Schedule 2 to the amending instrument apply in relation to applications made on or after 1 July 2024.
amending instrument means the Health Insurance Legislation Amendment (2025 Measures No. 2) Regulations 2025.
commencement day means the day the amending instrument commences.
pre‑commencement period, for relevant MRI equipment, means the period:
(a) that begins on the date from which the age of the equipment is worked out under subclause 1.2.2(1); and
(b) that ends immediately before the commencement day.
relevant MRI equipment means MRI equipment, in relation to which:
(a) immediately before the commencement day, both of the following apply:
(i) the equipment is located at the premises of a comprehensive practice located in a Modified Monash 1 area;
(ii) the equipment is neither eligible equipment nor partial eligible equipment (within the meaning of this instrument as in force immediately before the commencement day); and
(b) on and after the commencement day, all of the following apply:
(i) the equipment continues to be located at the premises of, and is included on the Diagnostic Imaging Register in relation to the location specific practice number for, the comprehensive practice;
(ii) the equipment is made available to the comprehensive practice by a person who is subject to a current deed with the Commonwealth that relates to the equipment so included on the Diagnostic Imaging Register;
(iii) the age of the equipment exceeds the new effective life age for MRI equipment.
Subdivision B—Capital sensitivity requirements for relevant MRI equipment
4.7 Applicable life age and restriction on items for relevant MRI equipment
Applicable life age
(1) Despite subclause 1.2.2(2), the applicable life age for relevant MRI equipment is the maximum extended life age of the equipment if subclause (2) or (3) of this clause applies.
(2) This subclause applies to relevant MRI equipment if:
(a) an additional reasonable investment has been made during the pre‑commencement period for the equipment; and
(b) the investment improves the overall performance of the equipment so that it is equivalent to new MRI equipment supplied in Australia at the time of the improvement.
(3) This subclause applies to relevant MRI equipment if:
(a) the Secretary grants a validation under subclause 4.9(2) in respect of the equipment; and
(b) before the end of the period of 12 months beginning on the day the validation is granted, the equipment is improved such that its overall performance is equivalent to new MRI equipment supplied in Australia at the time of the improvement.
Restriction on items—services performed on validated relevant MRI equipment
(4) If the Secretary grants a validation under subclause 4.9(2) in respect of relevant MRI equipment, an item in this Schedule does not apply to a service that is performed on that equipment on a day that is before the day the validation was granted.
Subdivision C—Validation of relevant MRI equipment subsequently meeting capital sensitivity requirements
4.8 Equipment unable to be improved before commencement day—applying for validation of subsequently improved equipment
Applying for validation
(1) The relevant proprietor for relevant MRI equipment may apply to the Secretary for validation under clause 4.9 in respect of the equipment if:
(a) during the pre‑commencement period for the equipment, the relevant proprietor took steps to make an additional reasonable investment that would improve the overall performance of the equipment so that it would be equivalent to new MRI equipment supplied in Australia at the time of the improvement; and
(b) the improvement is not completed before the commencement day.
Note: For relevant proprietor, see clause 1.2.4.
(2) The application must:
(a) be in writing; and
(b) be made within the period of 3 months beginning on the commencement day; and
(c) set out:
(i) reasons why the proprietor was unable to complete the improvement before the commencement day; and
(ii) an explanation of how the equipment has been, or will be, improved; and
(iii) if the improvement has not been completed—the steps taken by the proprietor to ensure that it will be completed before the end of the period of 12 months beginning on the day the validation is granted, and the date on which it will be completed.
Notifying proprietor of receipt of application
(3) If:
(a) the Secretary receives an application under subclause (1) for a validation in respect of the equipment; and
(b) the application complies with subclause (2);
the Secretary must notify the relevant proprietor for the equipment in writing that the Secretary has received the application.
4.9 Equipment unable to be improved before commencement day—granting validation of subsequently improved equipment
Scope of this clause
(1) This clause applies if, under subclause 4.8(3), the Secretary notifies the relevant proprietor for relevant MRI equipment that the Secretary has received an application for validation of the equipment.
Granting validation
(2) The Secretary must, by notice in writing given to the proprietor:
(a) subject to subclause (3) of this clause, grant the validation; or
(b) refuse to grant the validation.
(3) The Secretary must not grant the validation unless the Secretary is satisfied that both of the following apply:
(a) due to circumstances beyond the control of the proprietor, the proprietor was unable to complete the improvement before the commencement day;
(b) the improvement has been or will be completed before the end of the period of 12 months beginning on the day the validation is granted.
(4) The Secretary must make a decision on the application under subclause (2) within 28 days after notifying the proprietor as mentioned in subclause (1).
Effect of validation on capital sensitivity requirements
(5) If the Secretary grants a validation in relation to equipment that is still to be improved, clause 1.2.1 does not apply to a service that is performed on the equipment during the period:
(a) starting when the Secretary grants the validation; and
(b) ending on the earliest of the following:
(i) the day the improvement is completed;
(ii) the day that is 12 months after the day the validation is granted.
Note: If the improvement is completed as proposed within the period of 12 months beginning on the day the validation is granted, then the applicable life age of the equipment is the maximum extended life age of MRI equipment: see clause 4.7.
Subdivision D—Modified application of Subdivision BB of Division 1.2
4.10 Reconsideration by Secretary—refusal to validate relevant MRI equipment
(1) For the purposes of a decision under clause 4.9 to refuse to grant a validation in respect of relevant MRI equipment, clauses 1.2.11 and 1.2.12 are modified as set out in this clause.
(2) Subclause 1.2.11(1) is modified by adding at the end of the subclause:
“; or (d) a decision under clause 4.9 to refuse to grant a validation in respect of relevant MRI equipment.”
(3) Clause 1.2.11 is modified by omitting subclause (6).
(4) Clause 1.2.12 is modified by omitting subclause (4).