The report reveals 52 people legally ended their lives from the time voluntary assisted dying became legal on June 19 last year to the end of December.
While the Victorian government is hailing the report as an indicator the law is operating successfully, some questions remain.
Notably, the report only documents people who have accessed the legislation. It doesn’t tell us about those who may have wanted to be assessed for voluntary assisted dying, but not been able to.
What the report tells us
The Voluntary Assisted Dying Review Board will report on the operation of voluntary assisted dying in Victoria every six months for the first two years, and then annually.
The review board’s first report was tabled in parliament on August 27 2019. As this initial report only covered the law in effect from June 19 to June 30, this second report, tabled in parliament on Wednesday, is the first to provide any real detail about voluntary assisted dying in practice.
The report gives us a snapshot of the number of patients progressing through various stages of the assessment and approval process. In brief:
- 136 patients had completed a “first assessment”
- 102 patients had completed a “consulting assessment” (this is a second assessment to confirm a person’s eligibility, performed by a different doctor)
- 81 voluntary assisted dying permits had been approved
- 52 deaths had been confirmed. Some 43 people self-administered the lethal substance, while nine required a practitioner to administer it for them.
The review board concludes these figures demonstrate “the Act has struck a balance between being strict with compliance, while still accessible to those who want this choice”.
The Victorian government estimated about a dozen patients would access voluntary assisted dying in the first year, so the number of reported deaths already well exceeds this.
The Chair of the review board, Justice Betty King QC, said the number of patients accessing voluntary assisted dying shows this is something Victorians wanted, and now it’s available, they’re using it.
Victorian Minister for Health Jenny Mikakos said the report indicates the legislation “is working well and as intended”.
What the report doesn’t tell us
Importantly, the report doesn’t provide any information about patients requesting access to voluntary assisted dying prior to the formal first assessment.
This means we don’t have any data at this stage about patients who may have wanted to access voluntary assisted dying but were not able to, or the reasons why this may have been the case.
For example, we’ve seen anecdotal reports of people unable to find a doctor willing or qualified to assess them for voluntary assisted dying.
Patients in regional or rural Victoria have also reportedly had difficulties accessing voluntary assisted dying due to a federal law prohibiting doctors from discussing it with patients over the phone or online.
These issues are in addition to the “gag clause” feature of the Victorian legislation, which prohibits all health practitioners from initiating a discussion about voluntary assisted dying with their patients.
The review board said it has recently started collecting data on terminally ill people who were unable to access the laws. But it’s an oversight that systematic processes to collect this information weren’t in place from the beginning.
In regards to those assessed for voluntary assisted dying, the report doesn’t explain the differences in reported numbers at each stage of the assessment and approval process. While some of the discrepancies are likely explained by the time it takes people to move through the steps, it’s unclear whether some patients decided not to proceed, or died during the process.
The report also doesn’t detail how long it takes patients to progress from a first assessment through to the permit application stage, though the review board noted the process can take several weeks.
Further, the report doesn’t provide any demographic detail about the patients who have accessed voluntary assisted dying, such as their age, sex, level of education or income. While the review board receives information on demographics, and acknowledges this is important, it didn’t report this data.
The limited information reported by the review board should be interpreted with caution, particularly in terms of understanding community access (and potential inaccess) to voluntary assisted dying in Victoria.
Without further detail, it’s premature to conclude the voluntary assisted dying legislation is “working well”.
Other jurisdictions considering or implementing voluntary assisted dying have an opportunity to learn from the initial period of operation as well as data collection and reporting in Victoria.
Western Australia passed similar voluntary assisted dying legislation in 2019, which will come into effect in 2021. Meanwhile, Queensland, South Australia and Tasmania are also exploring legalising voluntary assisted dying.
The report offers a useful snapshot of the initial uptake of voluntary assisted dying in Victoria. But we need more detailed data to better assess the operation of the legislation, including whether or not access is equitable, and “accessible to those who want this choice”, as the review board has suggested.
Courtney Hempton’s doctoral research was funded by the Australian Government (Research Training Program Scholarship), and she is currently engaged on a project funded by the Australian Research Council. She has previously been affiliated with the Monash Health Voluntary Assisted Dying Working Group and Voluntary Assisted Dying Steering Committee. Courtney is also grateful to Nia Sims, for insightful and ongoing conversations regarding the implementation and oversight of voluntary assisted dying in Victoria and beyond.