Literature DB >> 30377217

Of dilemmas and tensions: a qualitative study of palliative care physicians' positions regarding voluntary active euthanasia in Quebec, Canada.

Emmanuelle Bélanger1, Anna Towers2, David Kenneth Wright3, Yuexi Chen4, Golda Tradounsky5, Mary Ellen Macdonald6.   

Abstract

OBJECTIVES: In 2015, the Province of Quebec, Canada passed a law that allowed voluntary active euthanasia (VAE). Palliative care stakeholders in Canada have been largely opposed to euthanasia, yet there is little research about their views. The research question guiding this study was the following: How do palliative care physicians in Quebec position themselves regarding the practice of VAE in the context of the new provincial legislation?
METHODS: We used interpretive description, an inductive methodology to answer research questions about clinical practice. A total of 18 palliative care physicians participated in semistructured interviews at two university-affiliated hospitals in Quebec.
RESULTS: Participants positioned themselves in opposition to euthanasia. Their justifications were framed within their professional commitment to not hasten death, which sat in tension with the value of patients' autonomy to choose how to die. Participants described VAE as unacceptable if it impeded opportunities to evaluate and alleviate suffering. Further, they contested government rhetoric that positioned VAE as a way to improve end-of-life care. Participants felt that VAE would diminish the potential of palliative care to relieve suffering. Dilemmas were apparent in their narratives, about reconciling respect for patient autonomy with broader palliative care values, and the value of accompanying and not abandoning patients who make requests for VAE while being committed to neither prolonging nor hastening death.
CONCLUSIONS: This study provides insight into nuanced positions of experienced palliative care physicians in Quebec and confirms expected tensions between an important stakeholder and the practice of VAE as guided by the new legislation. © Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Entities:  

Keywords:  euthanasia; palliative care

Mesh:

Year:  2018        PMID: 30377217     DOI: 10.1136/medethics-2017-104339

Source DB:  PubMed          Journal:  J Med Ethics        ISSN: 0306-6800            Impact factor:   2.903


  5 in total

1.  Emotional impact on healthcare providers involved in medical assistance in dying (MAiD): a systematic review and qualitative meta-synthesis.

Authors:  Saumil Yogendra Dholakia; Alireza Bagheri; Alexander Simpson
Journal:  BMJ Open       Date:  2022-07-15       Impact factor: 3.006

2.  Top Ten Tips Palliative Care Clinicians Should Know About Their Work's Intersection with Clinical Ethics.

Authors:  Meaghann S Weaver; Renee D Boss; Myra J Christopher; Tamryn F Gray; Stephanie Harman; Vanessa N Madrigal; Kelly N Michelson; Erin T Paquette; Rebecca D Pentz; Sara Scarlet; Connie M Ulrich; Jennifer K Walter
Journal:  J Palliat Med       Date:  2021-11-22       Impact factor: 2.947

3.  Introducing Medical Assistance in Dying in Canada: Lessons on Pragmatic Ethics and the Implementation of a Morally Contested Practice.

Authors:  Andrea Frolic; Allyson Oliphant
Journal:  HEC Forum       Date:  2022-09-02

4.  Experiences of healthcare providers with eligible patients' loss of decision-making capacity while awaiting medical assistance in dying.

Authors:  Caroline Variath; Elizabeth Peter; Lisa Cranley; Dianne Godkin
Journal:  Palliat Care Soc Pract       Date:  2022-10-14

Review 5.  Nurses' experiences of supporting patients requesting voluntary assisted dying: A qualitative meta-synthesis.

Authors:  Margaret Sandham; Melissa Carey; Emma Hedgecock; Rebecca Jarden
Journal:  J Adv Nurs       Date:  2022-06-24       Impact factor: 3.057

  5 in total

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