Adopted by the 35th World Medical Assembly
Venice, Italy, October 1983
and Revised by the WMA General Assembly, Pilanesberg, South Africa,
October 2006
Preface
- When addressing the ethical issues associated with end-of-life
care, questions regarding euthanasia and physician-assisted
suicide inevitably arise. The World Medical Association condemns
as unethical both euthanasia and physician-assisted suicide.
It should be understood that WMA policy on these issues is fully
applicable in the context of this Statement on Terminal Illness.
Preamble
- When a patient's medical diagnosis precludes the hope of
health being restored or maintained, and the death of the patient
is inevitable, the physician and the patient are often faced
with a complex set of decisions regarding medical interventions.
Advances in medical science have improved the ability of physicians
to address many issues associated with end-of-life care. However,
it is an area of medicine that historically has not received
the attention it deserves. While the priority of research to
cure disease should not be compromised, more attention must
be paid to developing palliative treatments and improving the
ability of physicians to assess and address the medical and
psychological components of symptoms in terminal illness. The
dying phase must be recognized and respected as an important
part of a person's life. As public pressure increases in many
countries to consider physician assisted suicide and euthanasia
as acceptable options to end suffering in terminal patients,
the ethical imperative to improve palliative treatment in the
terminal phase of life comes into sharp focus.
- The World Medical Association recognizes that attitudes and
beliefs toward death and dying vary widely from culture to culture
and among different religions. In addition, many palliative
and life-sustaining measures require technologies and/or financial
resources that are simply not available in many places. The
approach to medical care of the terminally ill will be influenced
significantly by these factors, and thus attempting to developing
detailed guidelines on terminal care that can be universally
applied is neither practical nor wise. Therefore, the World
Medical Association articulates the following core principles
to assist physicians and National Medical Associations with
decision-making related to terminal care.
Principles
- The duty of physicians is to heal, where possible, to relieve
suffering and to protect the best interests of their patients.
There shall be no exception to this principle even in the case
of incurable disease.
- In the care of terminal patients, the primary responsibilities
of the physician are to assist the patient in maintaining an
optimal quality of life through controlling symptoms and addressing
psychosocial needs, and to enable the patient to die with dignity
and in comfort. Physicians should inform patients of the availability,
benefits and other potential effects of palliative care.
- The patient's right to autonomy in decision-making must be
respected with regard to decisions in the terminal phase of
life. This includes the right to refuse treatment and to request
palliative measures to relieve suffering but which may have
the additional effect of accelerating the dying process. However,
physicians are ethically prohibited from actively assisting
patients in suicide. This includes administering any treatments
whose palliative benefits, in the opinion of the physician,
do not justify the additional effects.
- The physician must not employ any means that would provide
no benefit for the patient.
- . Physicians should recognise the right of patients to develop
written advance directives that describe their wishes regarding
care in the event that they are unable to communicate and that
designate a substitute decision-maker to make decisions that
are not expressed in the advance directive. In particular, physicians
should discuss the patient's wishes regarding the approach to
life-sustaining interventions as well as palliative measures
that might have the additional effect of accelerating death.
Whenever possible, the patient's substitute decision-maker should
be included in these conversations.
- Physicians should endeavour to understand and address the
psychosocial needs of their patients, especially as they relate
to patients' physical symptoms. Physicians should try to ensure
that psychological and spiritual resources are available to
patients and their families to help them deal with the anxiety,
fear and grief associated with terminal illness.
- The clinical management of pain in terminal patients is of
paramount importance in terms of alleviating suffering. Physicians
and National Medical Associations should promote the dissemination
and sharing of information regarding pain management to ensure
that all physicians involved in terminal care have access to
best practice guidelines and the most current treatments and
methods available. Physicians should be able to pursue clinically
appropriate aggressive pain management without undue fear of
regulatory or legal repercussions.
- National Medical Associations should encourage governments
and research institutions to invest additional resources in
developing treatments to improve end-of-life care. Medical school
curricula should include the teaching of palliative medical
care. Where it does not exist, the establishment of palliative
medicine as a medical specialty should be considered.
- National Medical Associations should advocate for the development
of networks among institutions and organizations involved in
palliative care in order to foster communication and collaboration
- Physicians may, when the patient cannot reverse the final
process of cessation of vital functions, apply such artificial
means as are necessary to keep organs active for transplantation
provided that they act in accordance with the ethical guidelines
established in the World Medical Association Declaration of
Sydney on the Determination of Death and the Recovery of Organs.
14.10.2006
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