The Australian Health Practitioner Regulation Agency (AHPRA) has announced it will expand its “” on the cosmetic surgery industry. As the agency responsible for registering, accrediting and disciplining health practitioners, AHPRA is well placed to reshape conduct in what sociologists once called the .
Author
Christopher Rudge
Law lecturer, University of Sydney
It plans to develop stricter guidelines for non-surgical cosmetic procedures – especially advertising practices, consent procedures and pre-procedure suitability screening.
The regulator’s primary targets are health practitioners authorised to prescribe restricted drugs (schedule 4 medicines) to patients for aesthetic enhancement. The compounds are across each state and territory, but they are generally restricted to medical and nursing practitioners or people directly supervised by them.
But how does the regulator propose to make aesthetic medicine safer for patients, and what problems might lie beyond its reach?
Safe and effective … in skilled hands
AHPRA’s sets out a range of treatments it hopes to make safer for patients. Among them is the cosmetic procedure in the world: botulinum toxin type A, commonly known as Botox.
Widely to reduce wrinkles, Botox is also the and was first proposed as a . It’s also to treat eyelid spasms, excessive sweating, some bladder disorders and migraine.
Botox functions only at extremely low doses and has been approved for since the early 2000s. demonstrates it is safe and effective for cosmetic purposes. But a comprehensive study from the United Kingdom found about including bruising, headache and paresis (muscle weakness or paralysis).
One critical aspect of its safety is the injector’s skill. The Nursing and Midwifery Board of Australia recently updated its , underlining the skills expected.
The other injectables to be reviewed – dermal fillers, such as the hyaluronic acid and fat-dissolving agents like – present their own safety issues. The death of a given fillers in Sydney drew attention to the risks of these treatments and the importance of oversight.
Body image: a hidden source of harm
As AHPRA acknowledges, a different kind of risk is presented by the connection between Botox and body image disorders. One recent study found recipients of Botox reported than a control group. Others have shown patients with histories of body image distress tend to express and their mental health may worsen after treatment.
But the prospect of a patient with body dysmorphia also raises important legal questions for the law of medical consent and the practitioner’s duty to warn a patient of relevant harms.
The of medical consent, established in 1991, requires a practitioner to warn the patient of all “material” risks – those that the specific patient does or would consider significant – posed by the treatment or procedure. The same principle was adopted by the .
For patients with mental health issues, a practitioner would usually identify the likelihood of increased mental distress as a material risk. Valid consent would therefore entail discussion of the psychological risks of treatment.
The review will also home in on the risks of “thread lifting”, where are threaded under the skin to pull it into a certain position, and intense pulsed light (IPL) treatments .
Vulnerable patients and the media
Manipulative media environments can exacerbate patients’ vulnerability.
While some doctors may seek to , other promotions might normalise interventions and understate the .
COVID lockdowns and the closure of clinics reportedly increased for patients seeking cosmetic procedures. Others expressed increased concern about their facial appearance due to the apparently unflattering light of .
A recent tagged with #dermalfillers found most videos, many of which were promotions, lacked any reference to the risks of treatments.
AHPRA proposes to address these issues by reformulating the guidelines for advertising, introducing stricter rules to control “before and after” images, social media influencing and reinforcing the for health services.
A long time coming
Almost exactly a year ago, AHPRA published an into doctors who performed cosmetic surgery. The report followed widely reported cases of resulting in terrible patient outcomes.
As a result, the medical regulator created and a for complaints.
At the same time, an was reached between Australia’s health ministers that the title “cosmetic surgeon” – virtually unregulated for 20 years – would become restricted. The is expected to pass and will mean no medical practitioner can call themselves a surgeon without meeting a new .
Yet said the reforms had neglected non-surgical procedures.
Regulating modern cosmetics: it’s complicated
There are multiple centres of regulatory enforcement for cosmetic procedures.
While AHPRA and its national boards regulate health practitioners and the advertising of health services, other agencies co-regulate.
The Therapeutic Goods Administration (TGA) reviews and approves all injectable products for market supply. While it has approved many products for cosmetic injection, the TGA identifies such interventions as .
And while AHPRA deals with the advertising of health services, the TGA will prosecute while will control .
Mind the gaps
Because AHPRA has no real authority to regulate the actions of those who are not health practitioners, the reforms are unlikely to affect those operating outside a medical setting, such as or people who go to so-called ““.
Still, state laws will make the unauthorised use of schedule 4 drugs an in .
While it is too early to tell if the proposed reforms will improve patient outcomes dramatically, reforms like this play a critical role in setting standards and clarifying patient expectations.
Christopher Rudge has received research funding from the Commonwealth Medical Research Future Fund for a project about improving patients’ decision-making for stem cell therapies.
