Providing medically assisted dying in Canada: a qualitative study of emotional and moral impact

被引:0
|
作者
Winters, Janine Penfield [1 ]
Jaye, Chrystal [2 ]
Pickering, Neil John [1 ]
Walker, Simon [1 ]
机构
[1] Univ Otago, Bioeth Ctr, Dunedin 9016, New Zealand
[2] Univ Otago, Dunedin Sch Med, Gen Practice & Rural Hlth, Dunedin, New Zealand
关键词
Euthanasia; Health Workforce; Personal Autonomy; Ethics-; Medical; EUTHANASIA-RELATED STRAIN; PHYSICIANS EXPERIENCES; INNER LIFE; SUICIDE; CARE; DEATH; DOCTORS; OREGON;
D O I
10.1136/jme-2024-110137
中图分类号
B82 [伦理学(道德学)];
学科分类号
摘要
Purpose Medical assistance in dying (MAiD) in Canada places the medical provider at the centre of the process. The MAiD provider holds primary responsibility for determining eligibility and becomes acquainted with patients' inner desires and expressions of suffering. This is followed by the MAiD procedure of administering the lethal agent and being present at the death of eligible patients. We report participants' perceptions of the emotional and moral impacts of this role.Methodology Two years after MAiD was legalised in Canada, 22 early-adopting physician providers were interviewed. Data were examined using both phenomenological analysis and a novel ChatGPT-enhanced analysis of an anonymised subset of interview excerpts.Findings Participants described MAiD as emotionally provocative with both challenges and rewards. Providers expressed a positive moral impact when helping to optimise a patient's autonomy and moral comfort with their role in relieving suffering. Providers experienced tensions around professional duty and balancing self with service to others. Personal choice and patient gratitude enhanced the provider experience, while uncertainty and conflict added difficulty.Conclusions Participants described MAiD provision as strongly aligned with a patient-centred ethos of practice. This study suggests that, despite challenges, providing MAiD can be a meaningful and satisfying practice for physicians. Understanding the emotional and moral impact and factors that enhance or detract from the providers' experience allows future stakeholders to design and regulate assisted dying in ways congruent with the interests of patients, providers, families and society.
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页数:11
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