Restricting conversations about voluntary assisted dying: implications for clinical practice.


Journal

BMJ supportive & palliative care
ISSN: 2045-4368
Titre abrégé: BMJ Support Palliat Care
Pays: England
ID NLM: 101565123

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 13 05 2019
revised: 18 06 2019
accepted: 26 06 2019
pubmed: 9 8 2019
medline: 25 8 2020
entrez: 9 8 2019
Statut: ppublish

Résumé

On 19 June 2019, assisted dying became lawful in Victoria, the second most populous state in Australia. Section 8 of the The authors reviewed and analysed literature on the importance of communication at the EOL including the need to understand and appropriately respond to Desire to Die or Desire to Hasten Death statements. A legal critique of section 8 of the Victorian Contemporary literature suggests that open and honest communication between doctor and patient including the provision of information about all EOL options when sought by the patient represents good clinical practice and will lead to optimal EOL care. The provision of such information also reflects professional, ethical and legal norms. Despite (arguably) promoting an appropriate policy objective, the legislative prohibition on health professionals initiating conversations about voluntary assisted dying may, in cases where patients seek information about all EOL options, lead to less optimal patient outcomes.

Identifiants

pubmed: 31391175
pii: bmjspcare-2019-001887
doi: 10.1136/bmjspcare-2019-001887
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

105-110

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: LW has been engaged by the Victorian Government to design and provide the legislatively mandated training for doctors involved in voluntary assisted dying. LW is also a member of the board of Palliative Care Australia (but this article only represents her views not those of Palliative Care Australia). BW has been engaged by the Victorian Government to design and provide the legislatively mandated training for doctors involved in voluntary assisted dying. DK is on the Voluntary Assisted Dying Review Board (but this article represents her views only). JD is a former member of the Physicians’ Advisory Committee for Dying with Dignity Canada, a group that advocated for the legalisation of voluntary assisted dying in Canada. He currently works at Bruyere Continuing Care, a Catholic healthcare facility. This article does not represent the views of either Dying with Dignity Canada or Bruyere Continuing Care. LD has no competing interests.

Auteurs

Lindy Willmott (L)

Australian Centre for Health Law Research, Faculty of Law, Queensland University of Technology, Brisbane, Queensland, Australia l.willmott@qut.edu.au.

Ben White (B)

Australian Centre for Health Law Research, Faculty of Law, Queensland University of Technology, Brisbane, Queensland, Australia.

Danielle Ko (D)

Austin Health, Heidelberg, Victoria, Australia.

James Downar (J)

Division of Palliative Care, Department of Medicine, University of Ottawa, Ottawa, Ontario, Canada.

Luc Deliens (L)

End of Life Care Research Group, Vrije Universiteit Brussel, Brussels, Belgium.
Department of Public Health and Primary Care, Ghent University, Ghent, Belgium.

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