在后maid时代改善临终对话

K. Serota, A. Ho
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引用次数: 0

摘要

临终医疗援助(MAiD)的合法化改变了姑息治疗和临终关怀提供者(phcp)与患者及其亲人进行临终对话的方式。我们目前还不知道多伦多地区的phcp是如何经历这种巨大的转变的,以及他们在转变实践以适应MAiD会话时面临的挑战。我们必须了解初级保健提供者面临的独特挑战,以便我们能够改善这些基本保健提供者的教育、资源和支持。我们还必须确保加拿大人在生命结束时得到最高质量的护理,无论他们是否选择医疗辅助死亡。为了研究这些独特的挑战,我采访了22位初级医师,记录了他们在后maid时代参与临终对话的经历。参与者包括医生、护士、社会工作者和其他受雇于宗教机构和世俗机构的专职卫生专业人员。他们对MAiD的个人看法差异很大;一些人被认定为出于良心拒服兵役者,而另一些人则积极参与评估和提供MAiD。初步专题分析显示,挑战包括将联邦立法转化为医疗实践;应对低效的制度政策和角色模糊;发展对话技巧,以平衡的方式与患者和家属分享MAiD信息,既提供信息,又不强制;并且,在能力下降的患者寻求MAiD时出现的道德和组织问题。最后,初级保健医师分享了个人倦怠、情绪负担和耻辱的经历。了解这些因素如何影响初级保健医生的工作和生活,使我们能够制定有针对性的策略,以改善围绕MAiD谈话、转诊和程序的制度政策,并减少在后MAiD时代参与临终谈话的负面个人和情感后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improving end-of-life conversations in the post-MAiD era
Legalizing medical assistance in dying (MAiD) has transformed how palliative and hospice care providers (PHCPs) engage in end of life conversations with patients and their loved ones. We do not currently know how PHCPs in the Toronto area have experienced this tremendous shift, and what challenges they have faced in transforming their practice to accommodate MAiD conversations. We must understand the unique challenges faced by PHCPs so that we can improve the education, resources, and supports available to these essential healthcare providers. We also must ensure that Canadians receive the highest quality care at the end of life, whether or not they choose to pursue a medically assisted death. To examine these unique challenges, I interviewed 22 PHCPs to document their experiences of engaging in end-of-life conversations in the post-MAiD era. Participants included physicians, nurses, social workers, and other allied health professionals employed in faith-based and secular institutions. Their personal beliefs about MAiD varied widely; some identified as conscientious objectors, while others actively engaged in MAiD assessment and provision. Initial thematic analysis revealed that challenges include translating the federal legislation into medical practice; navigating inefficient institutional policies and role ambiguity; developing conversation techniques to share MAiD information with patients and families in a balanced way that is informative yet uncoercive; and, navigating the ethical and organizational issues that arise when patients with declining capacity pursue MAiD. Finally, PHCPs shared personal experiences of burnout, emotional weight, and stigma. Understanding how these factors impact the work and lives of PHCPs allows us to develop targeted strategies to improve the institutional policies surrounding MAiD conversations, referrals, and procedures, as well as decrease the negative personal and emotional consequences of engaging in end-of-life conversations in the post-MAiD era.
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