"Walk me through the final day": A thematic analysis study on the family caregiver experience of the Medical Assistance in Dying procedure day.

IF 3.6 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Palliative Medicine Pub Date : 2024-06-01 Epub Date: 2024-05-09 DOI:10.1177/02692163241248725
Rinat Nissim, Paige Chu, Alison Stere, Eryn Tong, Ekaterina An, Debbie Selby, Sally Bean, Elie Isenberg-Grzeda, Gary Rodin, Madeline Li, Sarah Hales
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Abstract

Background: Legalization of assisted dying is progressively expanding worldwide. In Canada, the Medical Assistance in Dying Act became law in 2016. As assisted dying regulations evolve worldwide, comprehending its subjective impact and broader consequences, especially on family members, becomes pivotal for shaping practice, policy, and training.

Aim: The goal of this study is to understand the experience of family caregivers on the assisted dying procedure day.

Design: Qualitative, thematic analysis, research using semi-structured interviews.

Setting/participants: Family caregivers of patients who received assisted dying in two hospitals in Canada were recruited. Interviews were conducted at least 6 months after patient death. Conceptual saturation was achieved after analyzing 18 interviews.

Results: While caregivers expressed gratitude for the availability of Medical Assistance in Dying, they also described the procedure day as potentially jarring and unsettling. We identified five aspects that shaped their experience: attuned support from the clinical team; preparation for clinical details; congruence between the setting and the importance of the event; active participation and ceremony; and pacing and timing of the procedure. Together, these aspects impacted the level of uneasiness felt by caregivers on the procedure day.

Conclusions: This study emphasized the importance of a family-centered approach to delivering Medical Assistance in Dying. It underscored recognizing the needs of family caregivers during the procedure day and offering strategies to ease their experience. Healthcare providers in jurisdictions where assisted dying is legal or deliberated should consider the applicability of these findings to their unique context.

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"陪我走过最后一天":关于临终医疗协助程序日家庭照顾者体验的主题分析研究。
背景:协助死亡合法化正在全球范围内逐步扩大。在加拿大,《临终医疗协助法案》于 2016 年成为法律。随着协助死亡法规在全球范围内的发展,理解其主观影响和更广泛的后果,尤其是对家庭成员的影响,对于形成实践、政策和培训至关重要。Aim: The goal of this study is to understand the experience of family caregivers on the assisted dying procedure day.Design.设计:设计:采用半结构式访谈进行定性、主题分析研究:在加拿大的两家医院招募了接受协助死亡病人的家庭护理人员。访谈在患者死亡至少 6 个月后进行。在对 18 个访谈进行分析后,达到了概念饱和:结果:虽然护理人员对临终医疗协助的可用性表示感谢,但他们也将程序当天描述为潜在的刺痛和不安。我们发现有五个方面影响了他们的体验:临床团队的贴心支持;临床细节的准备;环境与事件重要性之间的一致性;积极参与和仪式;程序的节奏和时间安排。这些方面共同影响了护理人员在手术当天的不安程度:本研究强调了以家庭为中心的临终医疗协助方法的重要性。它强调要认识到家庭照护者在手术当天的需求,并提供策略来缓解他们的体验。在临终医疗协助合法或经过审议的司法管辖区,医疗服务提供者应考虑这些研究结果在其独特环境中的适用性。
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来源期刊
Palliative Medicine
Palliative Medicine 医学-公共卫生、环境卫生与职业卫生
CiteScore
7.60
自引率
9.10%
发文量
125
审稿时长
6-12 weeks
期刊介绍: Palliative Medicine is a highly ranked, peer reviewed scholarly journal dedicated to improving knowledge and clinical practice in the palliative care of patients with far advanced disease. This outstanding journal features editorials, original papers, review articles, case reports, correspondence and book reviews. Essential reading for all members of the palliative care team. This journal is a member of the Committee on Publication Ethics (COPE).
期刊最新文献
Utilizing intricate care networks: An ethnography of patients and families navigating palliative care in a resource-limited setting. Definition and recommendations of advance care planning: A Delphi study in five Asian sectors. Pharmacological treatment of pain, dyspnea, death rattle, fever, nausea, and vomiting in the last days of life in older people: A systematic review. A pragmatic approach to selecting a grading system for clinical practice recommendations in palliative care. 'A good ending but not the end': Exploring family preparations surrounding a relative's death and the Afterlife - A qualitative study.
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