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比较美国和比利时早发性痴呆患者的预先护理计划:挑战部分与社会背景相关。

Comparing Advance Care Planning in Young-Onset Dementia in the USA vs Belgium: Challenges Partly Related to Societal Context.

作者信息

Van Rickstal Romy, De Vleminck Aline, Morrison Sean R, Koopmans Raymond T, van der Steen Jenny T, Engelborghs Sebastiaan, Neugroschl Judith, Aldridge Melissa D, Sano Mary, Van den Block Lieve

机构信息

Department of Family Medicine and Chronic Care, End-of-Life Care Research Group, Vrije Universiteit Brussel (VUB) and Ghent University, Belgium.

Department of Family Medicine and Chronic Care, End-of-Life Care Research Group, Vrije Universiteit Brussel (VUB) and Ghent University, Belgium.

出版信息

J Am Med Dir Assoc. 2020 Jun;21(6):851-857. doi: 10.1016/j.jamda.2020.01.007. Epub 2020 Mar 12.

Abstract

OBJECTIVES

Advance care planning in young-onset dementia largely remains a blind spot within current literature. This study aimed to explore the engagement in and the conceptualization of advance care planning from the perspective of family caregivers of persons with young-onset dementia and to identify potential similarities and differences in this area between American and Belgian persons with young-onset dementia and their family caregivers.

DESIGN

An exploratory qualitative study.

SETTING AND PARTICIPANTS

We purposively sampled adult family caregivers of persons with young-onset dementia; our respondents were 13 American and 15 Belgian caregivers with varying familial relationships to the patient.

METHODS

We conducted 28 semi-structured interviews, using the same interview guide for American and Belgian respondents. Verbatim transcripts were analysed through the method of constant comparative analysis.

RESULTS

Important similarities between American and Belgian respondents were restricted knowledge of advance care planning, limited communication about advance directives, and their recommendation for professionals to timely initiate advance care planning. Major differences were attention paid to those end-of-life decisions depicted in the legislature of their respective countries, American caregivers placed higher emphasis on financial planning than their Belgian peers, and, in the case of consulting professionals for advance directives, American caregivers turned to lawyers, whereas Belgian caregivers relied on physicians.

CONCLUSIONS AND IMPLICATIONS

Specific nuances and challenges in terms of advance care planning in young-onset dementia arise from a particular societal and legal context on the one hand, and from patients' and caregivers' younger age on the other. Professionals' awareness of and responsiveness to these specificities could facilitate the advance care planning process. Based on our interpretation of results, several recommendations for practice and policy are made.

摘要

目的

在当前文献中,早发性痴呆的预立医疗计划在很大程度上仍是一个盲点。本研究旨在从早发性痴呆患者家庭照料者的角度探讨预立医疗计划的参与情况和概念化,并确定美国和比利时早发性痴呆患者及其家庭照料者在这一领域的潜在异同。

设计

一项探索性定性研究。

背景与参与者

我们有目的地抽取了早发性痴呆患者的成年家庭照料者;我们的受访者包括13名美国照料者和15名比利时照料者,他们与患者的家庭关系各不相同。

方法

我们进行了28次半结构化访谈,对美国和比利时受访者使用相同的访谈指南。通过持续比较分析方法对逐字记录进行分析。

结果

美国和比利时受访者之间的重要相似之处在于对预立医疗计划的了解有限、关于预立医嘱的沟通有限,以及他们建议专业人员及时启动预立医疗计划。主要差异在于对各自国家立法中所描述的那些临终决定的关注、美国照料者比比利时同行更重视财务规划,以及在就预立医嘱咨询专业人员方面,美国照料者求助于律师,而比利时照料者依赖医生。

结论与启示

早发性痴呆预立医疗计划方面的特定细微差别和挑战一方面源于特定的社会和法律背景,另一方面源于患者和照料者年龄较轻。专业人员对这些特殊性的认识和应对能力有助于预立医疗计划过程。基于我们对结果的解读,提出了一些实践和政策建议。

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