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The first Australian Capital Territory voluntary assisted dying bill in more than 25 years was tabled in parliament yesterday.

This was possible after the Commonwealth on territories making laws about assisted dying in December last year. This meant the ACT and Northern Territory could join the six Australian states which have now passed voluntary assisted dying laws.

As with all parliamentary debates about voluntary assisted dying in Australia, this will be a conscience vote. But what will ACT parliamentarians be voting on?

In some ways, the ACT bill reflects the :

• detailed eligibility criteria are reviewed by two independent and trained health practitioners
• patients need to make three requests at various points
• there is an oversight board scrutinising cases, along with offences, to protect patients
• health practitioners’ conscientious objection is protected.

But ACT bill has three new features:

• no specific timeframe until death
• nurse practitioners can be involved in assessing eligibility
• protections for patients in institutions that object to voluntary assisted dying.

No specific timeframe until death

Reflecting the , voluntary assisted would be available for adults living in the ACT with decision-making capacity who seek this choice voluntarily and without coercion. They must also be suffering intolerably.

But discussion will no doubt focus on the fact that the ACT bill does not contain an expected timeframe until death.

Australian states have normally required an expected death within six months, with an extension to 12 months for neurodegenerative conditions. Queensland has 12 months for all conditions.

But in the ACT, the relevant criteria is silent on time to death and requires only that the condition is “advanced, progressive and expected to cause death”.

Reasons for this policy choice include that a timeframe is arbitrary, it exacerbates suffering for terminally ill patients and was not supported in public consultation.

This new feature must be seen in context. Voluntary assisted dying so all of them must be satisfied before a person can access voluntary assisted dying.

The ACT bill requires the person’s condition be “advanced” and this is defined to include requiring that the person is in the “last stages of life”. Because this criterion must be satisfied too, just having an illness that will cause death is not enough to access the service.

Our that because eligibility criteria work together, removing the timeframe to death is unlikely to affect which conditions will allow people to access voluntary assisted dying.

Nurse practitioners can be involved in assessing eligibility

Australian voluntary assisted dying laws have to date required that both health practitioners assessing eligibility be doctors.

The ACT bill contemplates that one practitioner could be a nurse practitioner. When introducing the bill, Minister for Human Rights Tara Cheyne said nurse practitioners must have relevant experience and at least one year’s endorsement after qualifying before they can undertake that role.

Cheyne ; and of existing state voluntary assisted dying systems has been finding sufficient numbers of practitioners to assist patients.

Protecting patient access in objecting institutions

A third key difference is how the ACT bill deals with institutions which may object to voluntary assisted dying, such as faith-based hospitals.

There is this is a problem in the later states to pass voluntary assisted dying laws: South Australia, Queensland and New South Wales.

Those states generally protect access for permanent residents in facilities, such as aged care residents, but offer less protection for non-permanent residents, such as a patient in a hospital.

The ACT has opted for a simpler approach that does not distinguish between permanent and non-permanent residents, giving stronger protection for the latter.

The default is that voluntary assisted dying can be accessed in facilities unless that is not reasonably practicable.

The ACT bill also regulates this more robustly by requiring institutions to develop minimum standards for how they will comply with these laws and creating offences for non-compliance.

What happens next?

The bill was referred to a parliamentary committee for further consideration. This happened for Australian state voluntary assisted dying laws and provides opportunity for reflection on the bill.

Some will object to these features in the ACT bill because they are different from the Australian model. Such objections also arose when states after Victoria made decisions that their law would be different.

But it is difficult to argue the ACT should blindly follow what other states have done. There is evidence that and local considerations may also mean different approaches are needed.

We anticipate robust consideration of the bill by the committee and then parliament. If passed, the usual 18-month implementation period is proposed which means ACT residents could have access by 2025.

Ben White receives funding from the Australian Research Council, the ³Ô¹ÏÍøÕ¾ Health and Medical Research Council and Commonwealth and state governments for research and training about the law, policy and practice relating to end-of-life care. In relation to voluntary assisted dying, he (with colleagues) has been engaged by the Victorian, Western Australian and Queensland governments to design and provide the legislatively mandated training for health practitioners involved in voluntary assisted dying in those states. He (with Lindy Willmott) has also developed a model bill for voluntary assisted dying for parliaments to consider. He is a sessional member of the Queensland Civil and Administrative Tribunal, which has jurisdiction for some aspects of this state’s voluntary assisted dying legislation. Ben is a recipient of an Australian Research Council Future Fellowship (project number FT190100410: Enhancing End-of-Life Decision-Making: Optimal Regulation of Voluntary Assisted Dying) funded by the Australian government.

Lindy Willmott receives or has received funding from the Australian Research Council, the ³Ô¹ÏÍøÕ¾ Health and Medical Research Council and Commonwealth and state governments for research and training about the law, policy and practice relating to end-of-life care. In relation to voluntary assisted dying, she (with colleagues) has been engaged by the Victorian, Western Australian and Queensland governments to design and provide the legislatively mandated training for health practitioners involved in voluntary assisted dying in those states. She (with Ben White) has also developed a model Bill for voluntary assisted dying for parliaments to consider. Lindy Willmott is also a member of the Queensland Voluntary Assisted Dying Review Board, but writes this piece in her capacity as an academic researcher. She is a former board member of Palliative Care Australia.