安宁疗护中家属替代决策的经验:质性研究的系统回顾。

IF 7.5 1区 医学 Q1 NURSING
Ting Yu, Yijing Li, Ziyi Hu, Shanshan Liu, Cong Wang, Qian Chen, Yan Jiang
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引用次数: 0

摘要

背景:替代决策者在决定临终病人是否接受安宁疗护方面扮演关键角色。有必要更好地了解临终病人临终关怀中替代决策的家庭经验,为制定有针对性的干预措施提供基础,例如决策支持工具或咨询,以帮助家庭成员在决策过程中导航。目的:目的是分析和综合全球关于临终病人是否接受临终关怀的替代决策的家庭成员经验的定性数据。设计:这是一项定性研究的系统综述。数据来源:检索PubMed、Web of Science、Cochrane Library、Embase、护理与联合健康文献累积索引、中国生物医学文献服务系统、中国国家知识基础设施、万方、中国科技期刊数据库,检索时间为建库至2024年9月。研究包括家庭成员对是否接受临终关怀病人的替代决定。综述方法:本综述以乔安娜布里格斯研究所定性证据系统综述手册为指导。两名审稿人独立筛选研究并提取数据。合格的研究通过乔安娜布里格斯研究所的定性研究关键评估工具进行评估。主题合成以Thomas和Harden提出的方法为指导。结果:共纳入9项研究。综合定性数据得出三个主题:(1)理性与情感之间的决策动机。代理决策者考虑临终关怀的原因涉及多个方面,是客观和主观因素共同作用的结果。(2)决策准备源于知识和经验。需要以知识为基础和经验为基础,以确保代理决策者做出明智的决定。(3)回顾过去和展望未来的决策反思。代理决策者对病人选择临终关怀的决定表示满意,并认真考虑个人未来的临终决定。结论:决定临终病人是否接受安宁疗护对家属来说是件复杂的事。这个过程从理性与情感动机共存的决策开始,透过获取安宁疗护的知识与经验,为决策做准备,最后以反思整个决策过程而告终。这些发现强调了为家庭决策者提供足够的信息和情感支持的重要性,这可以改善决策并促进更富有同情心的临终关怀。未来的研究应侧重于制定有效的战略来加强这些支持系统。研究注册:在PROSPERO (CRD42024526197)上注册了一个协议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Family members' experiences of surrogate decision-making in hospice care: A systematic review of qualitative studies.

Background: Surrogate decision-makers play a key role in determining whether end-of-life patients receive hospice care. There is a need to better understand families' experiences of surrogate decision-making in hospice care for end-of-life patients to provide a basis for developing targeted interventions, such as decision support tools or counseling, to help family members navigate the decision-making process.

Aim: The aim was to analyze and synthesize global qualitative data on family members' experiences of surrogate decision-making regarding whether to receive hospice care for end-of-life patients.

Design: This was a systematic review of qualitative studies.

Data sources: The PubMed, Web of Science, Cochrane Library, Embase, Cumulated Index to Nursing and Allied Health Literature, Chinese Biomedical Literature Service System, China National Knowledge Infrastructure, WanFang and China Science and Technology Journal databases were searched from inception to September 2024. Studies related to family members making surrogate decisions about whether to receive hospice care for end-of-life patients were included.

Review methods: This review was guided by the Joanna Briggs Institute Manual for Systematic reviews of qualitative evidence. Two reviewers independently screened the studies and extracted the data. The eligible studies were assessed via the Joanna Briggs Institute critical appraisal instrument for qualitative research. Thematic synthesis was guided by the method developed by Thomas and Harden.

Results: A total of nine studies were included. The synthesis of qualitative data resulted in three themes: (1) Decision motivation between rationality and emotion. The reasons surrogate decision-makers considered hospice care for patients involved multiple aspects and were a result of both objective and subjective factors. (2) Decision preparation stemmed from knowledge and experience. A knowledge-based foundation and experiential grounding were needed to ensure that surrogate decision-makers make informed decision. (3) Decision reflection through looking back and forward. Surrogate decision-makers expressed satisfaction with the decision to choose hospice care for patients, coupled with serious consideration of personal future end-of-life decisions.

Conclusion: Determining whether patients receive hospice care at end of life is complex for family members. This process begins with the coexistence of rational and emotional motives for decision-making, involves preparation for decision-making through the acquisition of knowledge and experience about hospice care, and culminates in reflection on the entire decision-making process. These findings underscore the importance of providing sufficient informational and emotional support to family decision-makers, which can improve decision-making and promote more compassionate end-of-life care. Future research should focus on developing effective strategies to strengthen these support systems.

Study registration: A protocol was registered on the PROSPERO (CRD42024526197).

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来源期刊
CiteScore
15.00
自引率
2.50%
发文量
181
审稿时长
21 days
期刊介绍: The International Journal of Nursing Studies (IJNS) is a highly respected journal that has been publishing original peer-reviewed articles since 1963. It provides a forum for original research and scholarship about health care delivery, organisation, management, workforce, policy, and research methods relevant to nursing, midwifery, and other health related professions. The journal aims to support evidence informed policy and practice by publishing research, systematic and other scholarly reviews, critical discussion, and commentary of the highest standard. The IJNS is indexed in major databases including PubMed, Medline, Thomson Reuters - Science Citation Index, Scopus, Thomson Reuters - Social Science Citation Index, CINAHL, and the BNI (British Nursing Index).
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