[2020] QCAT 265
General information, not legal advice.
Queensland Civil and Administrative Tribunal
2020-07-28
Original judgment source is linked above.
PROFESSIONS AND TRADES - HEALTH CARE PROFESSIONALS - MEDICAL PRACTITIONERS - LICENCES AND REGISTRATION - where the applicant medical practitioner has applied for a review of the decision of the respondent pursuant to section 24 of the Health (Drugs and Poisons) Regulation 1996 to cancel the endorsements of the applicant in relation to Schedule 8 controlled drugs and Schedule 4 restricted drugs of dependency.
Health Act 1937 (Qld), s 5
(1) In deciding whether a person is a suitable person to hold, or to continue to hold, an endorsement the chief executive may have regard to, and may make inquiries about, the following -
(a) the person's knowledge and understanding of the person's obligations under this regulation;
(d) any previous convictions the person has under the Act or this regulation;
(e) whether the person engages, or has engaged, in conduct that risks, or is likely to risk, a controlled drug, a restricted drug or a poison being used for a purpose that is unlawful under a law of a State or the Commonwealth.
(2) Subsection (1) does not limit the matter to which the chief executive may have regard in considering the suitability of the person to hold an endorsement.
this regulation includes the Poisons Regulation 1973.
21 Holder of endorsement must comply with conditions
The holder of an endorsement must not contravene a condition of the endorsement. Maximum penalty - 80 penalty units.
23 Grounds for suspension or cancellation of endorsement
Each of the following is a ground for the suspension or cancellation of an endorsement -
(b) the holder of the endorsement is not a suitable person to hold the endorsement;
(d) the holder of the endorsement has breached a condition stated in the endorsement;
(e) the holder of the endorsement has contravened a provision of this regulation;
24 Procedure for suspension or cancellation of endorsement
(1) If the chief executive considers there is a ground to suspend or cancel an endorsement (the proposed action), the chief executive may give the holder of the endorsement (the endorsement holder) a written notice that -
(b) states the grounds for the proposed action; and
(c) outlines the facts and circumstances forming the basis for the grounds; and
(d) if the proposed action is suspension of the endorsement - states the proposed suspension period; and
(e) invites the endorsement holder to show, in writing and within a stated time of at least 28 days, why the proposed action should not be taken.
(2) The notice must state whether the proposed action relates to -
(a) all controlled drugs, restricted drugs, poisons or activities permitted under the endorsement; or
(b) a stated controlled drug, restricted drug or poison or a stated activity permitted under the endorsement.
(3) If, after considering all written representations made within the stated time, the chief executive still considers there is a ground to take the proposed action, the chief executive may -
(a) if the proposed action was to suspend the endorsement for all controlled drugs, restricted drugs, poisons or activities permitted under the endorsement for a stated period - suspend the endorsement, for not longer than the proposed suspension period, for -
(i) all controlled drugs, restricted drugs, poisons or activities permitted under the endorsement; or
(ii) a stated controlled drug, restricted drug or poison or a stated activity; or
(b) if the proposed action was to suspend the endorsement for a stated controlled drug, restricted drug or poison or a stated activity for a stated period - suspend the endorsement for the controlled drug, restricted drug, poison or activity for not longer than the proposed suspension period; or
(c) if the proposed action was to cancel the endorsement -
(i) for a stated controlled drug, restricted drug or poison or a stated activity - either cancel the endorsement, or suspend it for a stated period, for the controlled drug, restricted drug, poison or activity; or
(ii) if subparagraph (i) does not apply - either cancel the endorsement or suspend it for a stated period.
(4) Within 10 days after the chief executive makes the decision, the chief executive must give written notice of the decision to the endorsement holder.
(5) If the chief executive decides to suspend or cancel the endorsement, the notice must -
(a) be a QCAT information notice for the decision; and
(b) state the day before which the endorsement holder is not permitted to apply to the chief executive under section 26A.
(5A) The day mentioned in subsection (5)(b) must be a day the chief executive believes is reasonable having regard to the grounds for the suspension or cancellation.
(a) the day the notice is given to the endorsement holder; or
(1) Subject to section 74(3), a person must not dispense, obtain, prescribe, sell or use a specified condition drug unless the person -
(a) dispenses, obtains, prescribes, sells or uses the specified condition drug under an approval; or
(b) is a doctor and dispenses, obtains or prescribes the specified condition drug for the treatment of -
(iii) attention deficit disorder in a child at least 4 years; or
(2) The chief executive may give an approval mentioned in subsection (1)(a) only to -
(b) a person who satisfies the chief executive that the specified condition drug is to be used for a genuine analytical or research purpose.
specified condition drug means the following controlled drugs -
(1) A prescriber may give a dispenser an oral prescription for a controlled drug the prescriber is endorsed to prescribe.
(2) Within 24 hours after giving the oral prescription, the prescriber must ensure a paper prescription for the drug is sent by facsimile transmission to the dispenser.
(3) Within 7 days after giving the oral prescription, the prescriber must send a paper prescription by post or by hand or send an electronic prescription for the drug to the dispenser.
(4) If the dispenser does not receive a paper prescription or electronic prescription for the drug from the prescriber within 14 days after being given the oral prescription, the dispenser must immediately give a written report about the circumstances to the chief executive.
120 Notice required if lengthy treatment with controlled drug
(1) This section applies if a doctor or nurse practitioner -
(a) administers, dispenses, prescribes or supplies, or intends to administer, dispense, prescribe or supply, a controlled drug in the treatment of a patient for more than 2 months; or
(b) reasonably suspects a patient has been treated with a controlled drug by another doctor or nurse practitioner for more than 2 months and the doctor or nurse practitioner intends to administer, dispense, prescribe or supply a controlled drug in the treatment of the patient.
(2) The doctor or nurse practitioner must immediately give the chief executive a written report in the approved form about the circumstances of the patient's treatment.
(3) The chief executive may ask the doctor or nurse practitioner to give the chief executive additional information about the treatment of the patient within a stated reasonable time.
(4) The doctor or nurse practitioner must comply with the request, unless the doctor or nurse practitioner has a reasonable excuse for not complying with it.
(1) If a relevant practitioner reasonably believes a person is a drug dependent person, the relevant practitioner must not, without an approval -
(a) dispense or prescribe a controlled drug for the person; or
(b) administer or supply a controlled drug to or for the person; or
(c) give an oral or written instruction to supply a controlled drug to or for the person.
(2) If a relevant practitioner reasonably believes that it is necessary for the relevant practitioner to treat a drug dependent person, or the relevant practitioner proposes to treat a class of drug dependent persons, the relevant practitioner must give the chief executive a report in the approved form about -
(a) if the relevant practitioner reasonably believes that it is necessary to treat a drug dependent person - the circumstances of the person's treatment; or
(b) if the relevant practitioner proposes to treat a class of drug dependent persons - the class of drug dependent persons the relevant practitioner proposes to treat and the proposed treatment of the persons.
(3) The chief executive may ask the relevant practitioner to give the chief executive stated additional information about the treatment of the drug dependent person or class of persons within a stated reasonable time.
(4) The relevant practitioner must comply with the request, unless the relevant practitioner has a reasonable excuse for not complying with it.
(5) If the chief executive is reasonably satisfied that, for the welfare of the drug dependent person or class of drug dependent person, it is necessary for the relevant practitioner to treat the person or persons with a controlled drug, the chief executive may give the relevant practitioner written approval to administer, dispense, prescribe, supply or give an oral or written instruction to supply a stated quantity or volume of the controlled drug.
(6) Also, if the chief executive is reasonably satisfied that, for the welfare of the drug dependent person or class of drug dependent persons, it is necessary for the chief executive to give the relevant practitioner an oral approval to administer, dispense, prescribe, supply or give an oral or written instruction to supply a stated quantity or volume of the controlled drug to or for the person or persons, the chief executive may give the oral approval.
(7) However, if the chief executive gives the relevant practitioner an oral approval, the chief executive must give the relevant practitioner written confirmation of the approval as soon as possible after giving the oral approval.
(8) A relevant practitioner to whom a written or oral approval has been given under subsection (5) or (6) must not administer, dispense, prescribe, supply, or give an oral or written instruction to supply a controlled drug to the person or persons other than under the approval.
(9) An approval given under this section has effect for the period stated in the approval.
(10) This section does not apply to a relevant practitioner treating a drug dependent person as an inpatient in a hospital.
relevant practitioner means a doctor, nurse practitioner or surgical podiatrist.
(1) A relevant practitioner must not, without an approval -
(a) dispense or prescribe a restricted drug of dependency for a person the relevant practitioner reasonably believes is a drug dependent person; or
(b) administer or supply a restricted drug of dependency to or for a drug dependent person.
(2) If a relevant practitioner reasonably believes it is necessary for the relevant practitioner to treat a drug dependent person, or the relevant practitioner proposes to treat a class of drug dependent persons, with a restricted drug of dependency, the relevant practitioner must give the chief executive a report in the approved form about -
(a) if the relevant practitioner reasonably believes it is necessary to treat a drug dependent person - the circumstances of the person's treatment; or
(b) if the relevant practitioner proposes to treat a class of drug dependent persons - the class of drug dependent persons the relevant practitioner proposes to treat and the proposed treatment of the persons.
(3) The chief executive may ask the relevant practitioner to give the chief executive stated additional information about the treatment of the drug dependent person, or class of drug dependent persons, within a stated reasonable time.
(4) The relevant practitioner must comply with the request, unless the relevant practitioner has a reasonable excuse for not complying with it.
(5) If the chief executive is reasonably satisfied that, for the welfare of the drug dependent person, or class of drug dependent persons, it is necessary for the relevant practitioner to treat the person, or class of persons, with a restricted drug of dependency, the chief executive may give the relevant practitioner a written approval to administer, dispense, prescribe, supply or use a stated quantity or volume of the restricted drug.
(6) Also, if the chief executive is reasonably satisfied that, for the welfare of the drug dependent person, or class of drug dependent persons, it is necessary for the chief executive to give the relevant practitioner an oral approval to administer, dispense, prescribe, supply or use a stated quantity or volume of the restricted drug of dependency to or for the person or persons, the chief executive may give the oral approval.
(7) However, if the chief executive gives the relevant practitioner an oral approval, the chief executive must give the relevant practitioner written confirmation of the approval as soon as possible after giving the oral approval.
(8) A relevant practitioner to whom an approval has been given about a restricted drug of dependency for a drug dependent person, or class of drug dependent persons, must not administer, dispense, prescribe or supply a restricted drug of dependency to, or use a restricted drug of dependency on, the person or persons other than under the approval.
(9) This section does not apply to a relevant practitioner treating a drug dependent person as an inpatient in a hospital.
relevant practitioner means a doctor, nurse practitioner or surgical podiatrist.
drug dependent person means a person -
(a) who, as a result of repeated administration to the person of controlled or restricted drugs or poisons -
(ii) exhibits drug-seeking behaviour that suggests impaired control;
over the person's continued use of controlled or restricted drugs or poisons; and
(b) who, when the administration to the person of controlled or restricted drugs or poisons ceases, suffers or is likely to suffer mental or physical distress or disorder.
Patient Treatment Class Approval for the treatment of persons on the Opioid Treatment Program for drug dependence with controlled drug methadone syrup/liquid or buprenorphine tablets/film
Please find attached your amended Patient Class Approval to treat persons on the Opioid Treatment Program for drug dependence with controlled drugs methadone syrup/liquid or buprenorphine tablets/film to 100 in total. In accordance with section 18 of the Health (Drugs and Poisons) Regulation 1996, please find attached your Patient Treatment Class Approval.
Your Patient Treatment Class Approval has been granted for two years and is due to expire on 30 June 2018. As MRQ[9] does not send out reminders, you will need to seek further approval to continue prescribing after this date.
Date of Effect: This approval takes effect as of 1st July 2017[10]
Please find attached your treatment approval for prescribing to drug dependent patients on the ...QOTP.
This approval is valid for four (4) weeks only and has stated conditions which you are legally required to adhere to. Over the next four weeks Medicines Regulation and Quality will be reviewing your prescribing for the QOTP with a view to determining if an extension to the approval will be provided.
In addition, please note that you are not able to register any further patients on the QOTP at this time.
Date of Effect: This approval takes effect on 30 June 2018
Date of Expiry: This approval expires on 31 July 2018 unless it otherwise expires immediately upon your notification to Medicines Regulation and Quality that you have ceased prescribing for persons on the Queensland Opioid Treatment Program.
Am I able to take this patient on in the month of July 2018?
As explained, your current approval does not allow you to take on any new patients onto the QOTP.
Date of Effect: This approval takes effect on 01 August 2018
Date of Expiry: This approval expires on 31 October 2018 unless it otherwise expires immediately upon your notification to Medicines Regulation and Quality that you have ceased prescribing for persons on the Queensland Opioid Treatment Program.
Thank you for your time in discussing this matter on the phone today.
Based on our discussion, I confirm the following matters that I discussed with you.
Your current approval (see attached) to treat drug dependent persons with methadone and buprenorphine under the Queensland Opioid Treatment Program [QOTP] expires tomorrow, Wednesday 31 October 2018.
This means that from after that date you cannot lawfully, act as a treatment provider under the QOTP and you cannot:
I acknowledge the email content below by you. There will be a few extra QOTP patients admitted today that I have to submit shortly. This action contravenes my current approval attached by you.
I advise that you should refer to the copy of the approval I have attached and that this is a legal instrument under the provisions of the Health (Drugs & Poisons) Regulation, 1996.
You are lawfully required to comply with the conditions of this approval.
Any actions you take that are potentially in breach of those conditions on this approval could result in actions by the Department against you.
I have not in anyway given you authorisation to not comply with the conditions set out in this approval.
In exercising its review jurisdiction, the tribunal -
(a) must decide the review in accordance with this Act and the enabling Act under which the reviewable decision being reviewed was made; and
(b) may perform the functions conferred on the tribunal by this Act or the enabling Act under which the reviewable decision being reviewed was made; and
(c) has all the functions of the decision-maker for the reviewable decision being reviewed.
(1) The purpose of the review of a reviewable decision is to produce the correct and preferable decision.
(2) The tribunal must hear and decide a review of a reviewable decision by way of a fresh hearing on the merits.
The respondent's grounds for cancellation and reasons for decision
(a) admitting patients to the QOTP contrary to the conditions of the approval dated 1 August 2018 in contravention of section 21 of the Regulation;
(b) prescribing specific condition drugs in contravention of section 78 of the Regulation;
(c) failing to provide requisite treatment reports to the Chief Executive in contravention of section 120 of the Regulation;
(d) failing to endorse scripts with collection conditions as required by an approval in contravention of section 122(8) of the Regulation;
(e) prescribing drugs to drug dependent persons without written approval of the Chief Executive, contrary to section 122(1) of the Regulation;
(f) prescribing restricted drugs of dependency to drug dependent persons without approval in contravention of section 213 of the Regulation;
(g) failing to provide paper prescriptions after giving oral prescriptions in contravention of section 81 of the Regulation.
(a) the applicant's knowledge of the telephone enquiry service provided by MRQ whereby prescribers can seek patient histories and identify issues with persons seeking schedule 8 controlled drugs evidenced by the applicant's use of that service on occasions in 2016 to 2018;
(b) notifications sent to the applicant during the previous five years about prescribing schedule 8 controlled drugs in contravention of sections 78, 120, 121 and 122 of the Regulation;
(c) concerns regarding the number of drug dependent persons for whom the applicant had prescribed schedule 8 controlled drugs and/or schedule 4 restricted drugs of dependency and his apparent lack of compliance with his legislative obligations under the Regulation;
(d) some of the contents of the applicant's submissions in the emails of 3 and 4 November 2018 indicating further non-compliance with the Regulation, including as follows:
(i) further instances of admitting patients to the QOTP contrary to the conditions of the approval dated 1 August 2018, contrary to section 21 of the Regulation;
(ii) further instances of prescribing drugs to drug dependent persons without written approval of the Chief Executive, contrary to section 122(1) of the Regulation;
(iii) further instances of prescribing restricted drugs of dependency to drug dependent persons without approval in contravention of section 213 of the Regulation.
I have made the decision to cancel your endorsements pursuant to s 24 of the Regulation based on the evidence and other material before me, and I am also satisfied:
Date cancellation takes effect
The cancellation of your endorsements takes immediate effect on the day notice is given to you, or your legal representative.
In accordance with ss 24(5)(p) and 24(5A) of the Regulation, you are not permitted to apply to the Chief Executive under s 26A of the Regulation for an amendment or appeal of the decision to cancel your endorsements, until close of business on 8 February 2021.
Further matters referred to on behalf of the respondent at hearing
(a) the applicant's conviction of a criminal offence in 1996- I have disregarded this matter for reasons expressed earlier;
(b) consequent findings and orders of the Medicare Participation Review Committee in 1997 and of the Medical Assessment Tribunal in 1997 and 1999- I have only had regard to the orders made as part of the timeline of the applicant's practice relevant to the extent of his experience;
(c) regulatory action by the Medical Board of Australia in 2017 after a finding of unsatisfactory professional performance- I do not consider this matter to have substantial relevance to the matters in issue in this review and have disregarded it;
(d) investigations and regulatory action by AHPRA and the Board in 2018 and 2019 in relation to the applicant's clinical performance- I do not consider the other matters regarding clinical performance to have substantial relevance to the matters in issue in this review, note that they are the subject of dispute in other proceedings before the Tribunal, and have chosen to disregard them.
You received MCHTU's Notice of Cancellation at 3pm on 12 February 2019. You understood that it meant stop using relevant schedule 4 and schedule 8 drugs immediately. Your goal was to rapidly comply with the Notice in a clinically safe manner over the following one to two weeks. You intended to rapidly wean and stop schedule 4 restricted drugs and schedule 8 controlled drug use and replace them with alternative medication such as Tramadol. You are aware that this will breach the Notice. You also intended to ask other doctors to take over the care or consult of patients needing to continue those drugs, including medicinal cannabis.[46]
In regards to I carrying out unlawful activities or breaches by writing S4 and S8 scripts between 12/2/2019 to 7/3/2019, I agree that Cancellation of S4/S8 legislatively meant "effective immediately" but I advocate to view those unlawful activities or breaches more in an "EBP[47] manner" rather than purely legislative manner "wean/ stop S4 and S8 drug use in my attempt to 'safely' deal with the S4 and S8 cancellation" vs "delay and applying for S4/S8 reinstatement before I return to work had I have the knowledge of Cancellation on 8/2/2019" vs "seeing selective patients".[48]
The Board were concerned that 'rapidly weaning' a patient off medication which they have previously required is a potentially unsafe method of taking steps to comply with restrictions and your submission in this regard is a further indication that you lack insight into the serious risk posed by your unsafe prescribing.[49]
I have had many conversations to MRQ and Dr. Bill Loveday with regard to and in support of your situation, particularly with reference to my observation of so many people now who I have observed to now go off the programme and turn back to illicit drugs as a result of your suspension. While some patients may well have taken advantage of your busyness, I firmly believe that patients seeing you benefited enormously from your personal care and attention albeit possibly at the cost of your paperwork.
I personally cannot recall any non-compliance issues with the Poisons and Drugs regulation as with every issue I observed, you provided me with the respect of immediate consultation via phone to correct any outstanding issues. I am aware however of the fact that due to the sensitivity of the nature of the comments you may need to put in a patients file during a consultation, that in doing so has been logistically challenging for you especially due to the relative busyness of your work and the seemingly urgent demands of the next patient preventing you from writing up the necessary patient notes and documentation of your previous consultation. Surely with a minor structural workplace change, these logistical and practical issues could be easily implemented without the need for an ongoing continuance of suspension.
I will put these thoughts in writing as you have my utmost support as a physician and friend.[52]
I accept that Mr Flavel genuinely holds the opinions expressed in his email, based upon such knowledge he has of the applicant's prescribing practices in his role as a prescriber. I have taken his views into account, particularly insofar as they support the applicant's contention that his contraventions of the Regulation occurred in the context of a heavy workload and time constraints.
In my experience, Dr Ting has been able to provide an exceptional level of care to some of the most difficult cases I work with, bringing expertise while successfully engaging them in the process. Colleagues have relied on Dr Ting over the past year to help provide intervention for transient young people, young mothers and numerous clients seeking treatment for their mental health.
Although I work within a mental health outreach program, it is my personal experience as a patient of Dr Ting that has led me to appreciate his knowledge of pharmacology and desire to see people achieve their best quality of life. Having accessed Dr Ting more than 12 times in the last 18 months, I cannot emphasize enough the important role he has played in allowing me to manage my own mental health symptoms and medications. Dr Ting's background working with drugs of dependence has been invaluable in my treatment and he has been the only health practitioner in the last 17 years who would assist me in reducing my medications safely and gradually removing those of dependence from my life as we searched for appropriate replacements. This was a challenging and difficult process for me, and I have a profound appreciation for his responsiveness and support throughout this time.
I believe Dr Ting provides a unique and important service to the community.
I have taken into account this genuine and eloquent accolade of the applicant. It is consistent with my own conclusion that the applicant genuinely cares for his patients. He meant no harm to his patients by his breaches. Indeed, his regulatory failures seem to stem from his prioritisation of what he believes to be in the best interests of his patients over, and sometimes to the exclusion of, regulatory requirements.
DR TING: So, basically, my argument is, yes, that twice-weekly conditions stated on that was - is a breach. So, if you don't put that on the script, it's a breach. So there was a phone call with - MMU in regarding as to whether that should be relaxed. So, essentially, what I've done in that [indistinct] instead of making it twice weekly, I make it weekly on the clinical grounds that it's a complex patient and there was, you know, financial and transport problems. So the description is that this patient and the wife - what they are telling me is that they have only 5 like 10 or $20 petrol money to get to chemist for [indistinct]
So, in that scenario, I was - my justification for - I guess you can call it "breach of the condition" - instead of twice weekly, I make it weekly is because, look, you have to cater to the patient clinical situation. So it's not a wilful - you know, instead of twice weekly, you make it weekly. It's more to cater them. And the other counter submission to the MMU is that, if the patient needs to be, you know - if you make it weekly and if the patient somehow misbehave or financially got better, then we can always go back to twice weekly. So [indistinct] I call it "evidence best practice" in the sense that, you know, you have to adjust condition. Sure, the condition are for safety of patient, but sometimes you have to cater for the specific situation. So the specific situation in this [indistinct] is financial. Patient are well-behave and so forth. So I - I just want to take that into consideration for that section that I was talking about. So section 122(8) for that counter-argument to the respondent argument.[55]
DR TING: So, basically, this email - look, what Susan Ballantyne is implying, if you read through the email, I think she's - she's saying that twice weekly is safer for the patient which makes sense in the [indistinct] or clinical reasoning. But, if you read through the - the email, is that, you know, I talked to her about this patient and I got support from the pharmacist as well. If you read through the second 5 page - first page, second page, there was correspondence between the pharmacist, Steven Flavel, supporting what we're doing. So what the pharmacist and I were saying is that, you know, this patient situation is such that there is financial difficulty and a lot of complex issue and, in this specific circumstances, there is a rationale for relaxing the - the number of times he had to collect the medication.[56]
DEPUTY PRESIDENT: Okay. So what has happened is you've advocated for the patient, but Dr Ballantyne has said twice weekly.
DR TING: Yes, your Honour.
DEPUTY PRESIDENT: That's a condition of the approval which is later given on the 24th, but you haven't, in fact, written that on the script.
DR TING: Correct, your Honour. I think that's what's happening.
DEPUTY PRESIDENT: And you've done that because you don't agree with Dr Ballantyne.
DR TING: I'm not sure - look, like, your Honour was trying to say whether it's - whether there's an intentional sort of - I don't agree. I can't quite recollect. So, basically, the approval was - I think it's a lead up to the approval basically, I think is the best way to describe it. So there was, you know, discussion between Dr Ballantyne and myself, you know, what to do and so forth. So my advocate was for - instead of twice weekly, it was for weekly, I guess, and then it can be, you know - - -
DEPUTY PRESIDENT: But you didn't take the decision for an answer.
DR TING: The person who give the approval - I mean, it's a complex Queensland Health system. So, even though my discussion is with Dr Ballantyne, the approval subsequently meant, if you look - if you manage to hunt it down, is not Dr Ballantyne herself that wrote that approval. I think Margo Hickman would be the person or another person who wrote that approval. So it's quite - - -
DEPUTY PRESIDENT: But the approval was consistent with the opinion that she had expressed - - -
DR TING: Yes. No. I'm not - - -
DEPUTY PRESIDENT: - - - in her email.
DR TING: Sorry?
DEPUTY PRESIDENT: The approval was consistent with the opinion she had expressed. It wasn't inconsistent with it.
DR TING: No. It was consistent with the - yes. The approval was consistent with the opinion that she said.
DEPUTY PRESIDENT: Yes. But you decided you didn't agree. So you do otherwise.
DR TING: Look, you can look at it in that matter, but, look, I - what I'm trying to make a point - you know, whether it's a wilful - what you call "wilful". Look, I do not recall whether - you know, when approval is and so forth. So my rationale of what I'm doing there essentially is that for the patient interest and based on clinical grounds, you know, just to - you know, just the best outcome because the patient can't afford to travel and so forth. So, look, the main point is I agree it's a breach. So, you know, if you don't write twice weekly, like what approval says, it's a definite breach. So I'm not arguing against that, but what I'm advocating is in the clinical manner, sometime - you know, you have to bend the rules, I guess, or, you know, change the condition to suit - suit the patient, basically.[57]
DR TING: Like, the example we give for [redacted], the case that we mentioned about. Look, it's a difficult situation. The chemist and I, we held a meeting about that patient and we decide, "Look, hang on. Sure, the regulation - the - in those conditions say it has to be twice weekly, and so forth." But if the patient doesn't have money sometime you just have to adjust that breach. I mean, the better option in that situation would be, in my opinion - I mean, it's a respectful opinion - you can give a patient some leeway. And I just say weekly collection and not get me into trouble, in the sense that you will breach. But my counter-argument with Dr Ballantyne, or part of it, is, it will not be a breach. So if the endorsement say once a week, if I change that to twice a week for a good reason you wouldn't call that a breach, even though it doesn't strictly, you know, comply exactly as it is.
So if you have a patient, your Honour, and if the endorsements say once a week, okay, and if I decide that you, as a patient, is misbehaving or misusing the drugs, if I change your endorsement to instead of once a week to twice a week, then if Queensland Health discover that issue I'm pretty sure they won't say, "Look, hang on. This is a breach." So sometime endorsement is there to serve that purpose, but sometimes it's also there that the doctor, it's not a given right, but it's - you have - sometime you have to form a judgment and to say, "Look, for this patient it's more beneficial, in one sense, to relax that, or change the condition until perhaps if she's got more money and so forth, if she can go to - to the chemist twice a week if she have money for the petrol", and so forth.[58]
Controlled drugs and drugs of dependence must be strictly managed and administered. They are dangerous and there is an inherent risk of injury, addiction or death in circumstances where they are prescribed outside of the regulatory regime, ie (the Regulations)
The Regulations are designed to protect public health and safety by regulating and restricting the prescribing of certain substances. The approval system stipulated within the Regulations is intended to enable appropriate treatment with these substances to be co-ordinated and monitored. The purpose of this is to reduce the possibility of adverse events occurring from poly-pharmacy and/or drug interactions, deliberate or accidental misuse or overdose, the risk of trafficking and death. Your circumvention of the Regulations and the system that underpins it therefore puts patients at risk of these serious adverse events.[60]
(a) the applicant's knowledge and understanding of his obligations under the Regulation: Whilst I am satisfied that the applicant has knowledge and understanding of his obligations under the Regulation at such a level that he is aware of the terms of those obligations and understands that failure to observe such obligations amounts to contravention of the Regulation, I am not satisfied that the applicant truly understands the importance of complying strictly with the terms of the Regulation. The lack of true understanding by the applicant of the importance of regulatory compliance is a factor weighing against his suitability;
(b) the applicant's qualifications and experience: The applicant holds requisite qualifications and registration (albeit currently suspended) as a medical practitioner. I have not regarded the current suspension of the applicant's registration as a medical practitioner as a factor weighing against his suitability. The applicant is an experienced general practitioner. The applicant's qualifications and experience is a factor in favour of his suitability;
(c) the applicant's character and standing, which I consider to be a neutral factor;
(d) the applicant's lack of any previous convictions under the Health Act or the Regulation, a factor in favour of his suitability;
(e) whether the applicant has engaged in conduct that risks, or is likely to risk, a controlled drug, a restricted drug or a poison being used for a purpose that is unlawful under a law of a State or the Commonwealth: I find that the number and type of the contraventions by the applicant of the Regulation constitutes a course of conduct engaged in by the applicant that risked, or was likely to risk, controlled and restricted drugs being obtained by persons in excess of proper therapeutic amounts and/or frequency, thus risking abuse of those drugs by the persons to whom they were prescribed and/or diversion to others to whom they were not prescribed, and thus risking such drugs being used contrary to applicable legislation, a factor weighing against his suitability.
[1] The application to review a decision filed 5 March 2019 states that the decision to be reviewed is "Notice of Urgent Cancellation of Approvals dated 19/2/2019" and annexes a copy of a notice of urgent cancellation of approvals pursuant to s 25A of the Regulation by which the delegate of the
Chief Executive gave the applicant notice of cancellations of approvals previously granted under sections 78, 122 and 213 of the Regulation to treat specified patients with schedule 4 and schedule 8 drugs. Such notice stated that the ground for such cancellation was the cancellation, pursuant to section 24 of the Regulation, of the applicant's endorsements under section 58 of the Regulation in relation to Schedule 8 controlled drugs and under section 161 of the Regulation in relation to Schedule 4 restricted drugs of dependency. Notwithstanding the terms of the application to review a decision, the parties' conduct of the litigation, including the material filed by the parties and the parties' submissions, written and oral, make it clear that it is the decision of 8 February 2019 that is in fact the subject of application to review: see T1-9:15-25.
[2] See section 36 and definitions of "medical practitioner" and "doctor" in Schedule 1 of the Acts Interpretation Act 1954 and sections 14(1) and 17 of the Statutory Instruments Act 1992.
[3] See definitions of "endorsement" and "authority" in appendix 9 of the Regulation.
[4] See definition of "controlled drug" in appendix 9 of the Regulation and Schedule 8 of the Poisons Standard (Cth).
[5] See definition of "restricted drug" in appendix 9 of the Regulation and Schedule 4 of the Poisons Standard (Cth).
[6] See definition of "restricted drug of dependency" in appendix 9 of the Regulation and Appendix 8 of the Regulation.
[7] Criminal Law (Rehabilitation of Offenders) Act 1986, s 9, and see definition of "criminal history" in appendix 9 of the Regulation.
[8] The apparent discrepancy in the dates of his approval to do so (3 May 2017) with his qualification to do so (10 May 2017 as per paragraph [12]) was the subject of submissions by the applicant: Hearing Document 2, index details re Document No 3; T1-26:37-42.
[9] Medicines Regulation & Quality - an Office within Queensland Health.
[10] The applicant made submissions as to the apparent back-dating of the approval from 19 October 2017 to 1 July 2017: HD 2, index details re Document No 5; HD 4 Chronology, 1 July 2017 entry; T1-28-35.
[11] See HD 6b, page 1267; HD 4 Chronology, 1 July 2017 entry; T1-22 and T1-28:20-40.
[12] See HD 2, index details re Document No 10.
[13] See HD 2, index details re Document No 10; HD 4 Chronology, 4 December 2017 entry; HD 6b, page 607.
[26] Ting v Medical Board of Australia, OCR076-19.
[27] Ting v Medical Board of Australia; Ting v Queensland Health [2019] QCAT 192.
[33] HD 2, index details re Document No 10; HD 4 Chronology, 4 December 2017 entry; HD 6a, page 1375; HD 6b, pages 540, 548 and 607.
[34] HD 2, Document No 38, pages 5-6; HD 6b, pages 540 and 548; T1-110:15-25.
[35] HD 2, index details re Documents Nos 20 and 23; HD 3, page 94; T1-10-11; T1-17-19; T2-24-29.
[37] HD 2, index details re Document No 24; T2-35-63.
[38] T2-36-37; T2-40; the S8INFO telephone enquiry service referred to in the respondent's reasons for decision, as to which see further the submissions on behalf of the respondent at T2-6.
[39] HD 2, index details re Documents Nos 7 and 10, Document No 45, and Document No 47, pages 2 and 4-5.
[40] T1-22-23; T1-33-35; T1-40-48; T1-71-72; T1-75-76;
[41] HD 2, index details re Document No 31, Document No 36, pages 1-3, and Document No 47, pages 3-4 and 6-10.
[47] "Evidence-based Practice": HD 2, page 1, paragraph 5.
[54] HD 2, index details re Document No 15.
[60] HD 6b, page 549, paragraphs 20-21.
Ting
Chief Executive, Queensland Health [2020] QCAT 265