Your browser doesn't support javascript.
loading
How does Medical Assistance in Dying affect end-of-life care planning discussions? Experiences of Canadian multidisciplinary palliative care providers.
Ho, Anita; Norman, Joshua S; Joolaee, Soodabeh; Serota, Kristie; Twells, Louise; William, Leeroy.
Afiliação
  • Ho A; Centre for Applied Ethics, The University of British Columbia, 227 - 6356 Agricultural Road, Vancouver, BC V6T 1Z2, Canada.
  • Norman JS; School of Medicine, University of California, San Francisco, San Francisco, CA, USA.
  • Joolaee S; Department of Pediatrics, The University of British Columbia, Vancouver, BC, Canada; Nursing Care Research Center, Iran University of Medical Sciences, Tehran, Iran.
  • Serota K; Dalla Lana School of Public Health, University of Toronto, Toronto, ON, Canada.
  • Twells L; Faculty of Medicine, The University of British Columbia, Vancouver, BC, Canada.
  • William L; Supportive & Palliative Care Unit, Eastern Health, Melbourne, VIC, Australia.
Palliat Care Soc Pract ; 15: 26323524211045996, 2021.
Article em En | MEDLINE | ID: mdl-34568826
ABSTRACT

BACKGROUND:

More than a dozen countries have now legalized some form of assisted dying, and additional jurisdictions are considering similar legislations or expanding eligibility criteria. Despite the persistent controversies about the relationship between medicine, palliative care, and assisted dying, many people are interested in assisted dying. Understanding how end-of-life care discussions between patients and specialist palliative care providers may be affected by such legislation can inform end-of-life care delivery in the evolving socio-cultural and legal environment.

AIM:

To explore how the Canadian Medical Assistance in Dying legislation affects end-of-life care discussions between patients and multidisciplinary specialist palliative care providers.

DESIGN:

Qualitative thematic analysis of semi-structured interviews.

PARTICIPANTS:

Forty-eight specialist palliative care providers from Vancouver (n = 26) and Toronto (n = 22) were interviewed in person or by phone. Participants included physicians (n = 22), nurses (n = 15), social workers (n = 7), and allied health professionals (n = 4).

RESULTS:

Qualitative thematic analysis identified five notable considerations associated with Medical Assistance in Dying affecting end-of-life care discussions (1) concerns over having proactive conversations about the desire to hasten death, (2) uncertainties regarding wish-to-die statements, (3) conversation complexities around procedural matters, (4) shifting discussions about suffering and quality of life, and (5) the need and challenges of promoting open-ended discussions.

CONCLUSION:

Medical Assistance in Dying challenges end-of-life care discussions and requires education and support for all concerned to enable compassionate health professional communication. It remains essential to address psychosocial and existential suffering in medicine, but also to provide timely palliative care to ensure suffering is addressed before it is deemed irremediable. Hence, clarification is required regarding assisted dying as an intervention of last resort. Furthermore, professional and institutional guidance needs to better support palliative care providers in maintaining their holistic standard of care.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Qualitative_research Aspecto: Patient_preference Idioma: En Revista: Palliat Care Soc Pract Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Qualitative_research Aspecto: Patient_preference Idioma: En Revista: Palliat Care Soc Pract Ano de publicação: 2021 Tipo de documento: Article