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非裔美国痴呆症患者替代决策者的经历。

Experience of African American Surrogate Decision Makers of Patients With Dementia.

作者信息

Hart Alysha S, Matthews Alicia K, Arslanian-Engoren Cynthia, Patil Crystal L, Krassa Teresa J, Bonner Gloria J

出版信息

J Hosp Palliat Nurs. 2022 Feb 1;24(1):84-94. doi: 10.1097/NJH.0000000000000822.

Abstract

Dementia cases are expected to grow for African Americans and surrogate decision makers (SDMs) will have a significant role at the end of life (EOL). This qualitative exploratory case study used Cognitive Task Analysis and an integrated conceptual framework to understand the EOL decision experience of African American SDMs for patients with advanced dementia. Using a holistic multiple-case design, 8 African American SDMs were interviewed about their experiences with the decision-making process, including role acceptance, role enactment, and emotional outcomes of decision making. Thirteen themes germane to understanding the EOL decision experience of African American SDMs were identified. Findings suggest African American SDMs often lack sufficient knowledge of disease prognosis and intervention options to make informed treatment choices at EOL. In particular, African Americans extend the caregiver role to SDM for patients with dementia at EOL without being fully aware of the role and decision-making responsibilities. Surrogates lacked a general understanding of EOL options resulting in underutilization of hospice and palliative care and subsequent regret, and few interventions exist to improve the uptake of EOL care services. There is a need to develop culturally appropriate role preparation, education, and decision support to improve EOL treatment decisions and emotional adjustment of surrogates of patients with advanced dementia, which should be rendered early and throughout the illness trajectory.

摘要

预计非裔美国人的痴呆症病例将会增加,而替代决策者(SDM)在生命末期(EOL)将发挥重要作用。本定性探索性案例研究采用认知任务分析和综合概念框架,以了解非裔美国替代决策者在晚期痴呆症患者生命末期的决策经历。采用整体多案例设计,对8名非裔美国替代决策者进行了访谈,了解他们在决策过程中的经历,包括角色接受、角色履行以及决策的情感结果。确定了13个与理解非裔美国替代决策者生命末期决策经历相关的主题。研究结果表明,非裔美国替代决策者往往缺乏足够的疾病预后和干预选择知识,无法在生命末期做出明智的治疗选择。特别是,非裔美国人在生命末期将照顾者角色扩展到痴呆症患者的替代决策者,却没有充分意识到该角色和决策责任。替代决策者对生命末期的选择缺乏全面了解,导致临终关怀和姑息治疗利用不足并随后产生遗憾,而且几乎没有干预措施来提高生命末期护理服务的利用率。有必要制定符合文化背景的角色准备、教育和决策支持措施,以改善晚期痴呆症患者替代决策者的生命末期治疗决策和情感调适,这些措施应在疾病轨迹的早期及整个过程中提供。

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