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家庭成员在日本养老院参与临终关怀讨论的体验:对家庭成员叙述的定性描述性研究。

Family Members' Experience of Discussions on End-of-Life Care in Nursing Homes in Japan: A Qualitative Descriptive Study of Family Members' Narratives.

出版信息

J Hosp Palliat Nurs. 2020 Oct;22(5):401-406. doi: 10.1097/NJH.0000000000000677.

Abstract

In nursing homes, discussions between family members and staff regarding the end of life for residents with cognitive impairment are crucial to the choice of treatment and care consistent with residents' wishes. However, family members experience burden in such discussions, and communication with staff remains inadequate. The purpose of this qualitative descriptive study was to elucidate the meaning of continuous end-of-life discussion for family members. Data were collected using semistructured individual interviews. Thirteen family members of residents from 3 nursing homes in Kyoto, Japan, participated in the study. Data were analyzed using thematic analysis, which focused on both explicit and implicit meanings. Four themes emerged regarding the experience of end-of-life discussion: "the end of life soaking in," "hardship of making the decision to end my family member's life," "wavering thoughts about decisions made and actions taken," and "feeling a sense of participation about the care." Family members had come to accept the deaths of residents through continuous discussion and experienced strong conflict in facing the death of their family members. Moreover, staff members should understand family members' beliefs and the burden they experience in facing residents' death.

摘要

在养老院中,家属和工作人员就认知障碍居民的生命末期进行讨论,对于选择符合居民意愿的治疗和护理方案至关重要。然而,家属在这些讨论中感到负担沉重,与工作人员的沟通仍然不足。本定性描述性研究旨在阐明家属持续进行生命末期讨论的意义。使用半结构式个人访谈收集数据。来自日本京都 3 家养老院的 13 名居民的家属参与了这项研究。使用主题分析对数据进行分析,重点关注明确和隐含的意义。关于生命末期讨论的体验出现了 4 个主题:“生命末期的浸润”、“决定结束我家人生命的艰难”、“对做出的决定和采取的行动犹豫不决”和“对护理感到参与感”。家属通过持续的讨论已经接受了居民的死亡,并在面对家人的死亡时经历了强烈的冲突。此外,工作人员应该理解家属的信仰和他们在面对居民死亡时所承受的负担。

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