|
The following article is from the SAVES newsletter, The
VE Bulletin, Vol 16 No 1, Mar 99
The Darwin Experience with Voluntary
Euthanasia: Lessons to be Learnt
For the period of 9 months from July 96 to April 97 Marshall Perron's
"Rights of the Terminally Ill" Act was operating in the Northern Territory.
In that period, 4 of my terminally ill patients made use of the legislation
to end their lives at a time of their choosing. This is the only experience
of voluntary euthanasia in the Australian setting, and lessons can be learnt
that are of relevance to others contemplating such legislation.
The Darwin experience has been documented in The Lancet under
the title "Seven Deaths in Darwin: case studies under the Rights of
the Terminally Ill Act", which I co-authored with Kissane and Street
(1). This collaboration with academics known to be hostile to the Act was
carried out so that hitherto unpublished material could be put in the public
domain. It was also reasoned that criticism of the Northern Territory experience
by known opponents of the legislation would provide the most useful and
critical analysis of the data.
The following are the significant findings from that publication:
-
Throughout the two year period, 1996 to 1998, seven people sought to use
the Territory law. All had cancer, and one was ineligible because her disease
was not considered terminal. Three of the seven were from the NT. Far from
the predicted "rush" to die in the NT, numbers were modest, and the Act
excluded those found to be ineligible. Social isolation was noted, but
the authors differed in their assessment of this and the significance they
placed upon it.
-
Symptoms of depression were common. This is an expected finding, and the
authors (specifically Kissane v Nitschke) differed over the significance
they attached to this finding. My belief is that all people suffering from
major life limiting disease will show "symptoms of depression". Indeed,
it surprises me that there is not more evidence of this. Nevertheless,
none of the patients, when examined by qualified psychiatrists, were found
to be so depressed as to warrant further treatment, or to claim that they
were unable to give informed consent.
-
It was noted that those patients who qualified to use the Act commonly
deferred their decision to proceed. This is evidence of what I have called
the "euthanasia paradox" where the presence of legislation reduces the
levels of anxiety of the terminally ill and enables them to relax and lessens
the chance that they will act precipitously. There is evidence that legislation
allows the terminally ill to live longer and improves the quality of their
remaining lives.
-
Medical opinions about the nature of presenting illness differed (in one
case), and this difference of opinion presented problems for the patient
involved and her subsequent utilisation of the Act. Janet Mills' South
Australian oncologist stated clearly that he believed she had less than
six months to live. The NT oncologist refused to state this (but also signed
a public statement saying he would never participate in the ROTI Act).
In desperation, an orthopaedic surgeon distressed by what he saw as the
politicising of the medical role, signed her papers and allowed Janet to
proceed. Predicting the terminal nature of illness is notoriously difficult
and provided an excuse used by doctors who were hostile to the operation
of the Act.
-
The "gatekeeping" role of doctors was a source of difficulty, given the
profession's hostility to the concept of voluntary euthanasia. Perron was
wary of heavily medicalising the legislation, anticipating that there would
be problems that would develop with the medical profession controlling
access to the law, but this was forced upon him. There is evidence that,
given the "keys to the gate", some doctors acted to subvert and damage
the legislation, and strategies had to be developed to bypass these individuals.
Better legislation would place doctors in an advisory role only.
The most critical analysis of data from the NT experience fails to produce
any serious objections to the Territory's model of voluntary euthanasia
legislation. There were ways the legislation could have been improved, and there is evidence that the
legislation provided benefits to terminally ill patients.
Philip Nitschke, MMBS PhD
(1) Kissane DW, Street A, Nitschke P (1998). Seven Deaths in Darwin: case studies under the Rights of the Terminally Ill Act. The Lancet, 352 (9134), 1097- 1102.
|