脑损伤后家庭生活质量:基于家庭成员视角的定性研究。

IF 3.3 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
José Luis Castillo, Alba Aza, María Fernández, Mari Storli Rasmussen, Nada Andelic, Miguel Ángel Verdugo
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引用次数: 0

摘要

目的:探讨获得性脑损伤(ABI)后家庭成员对其家庭生活质量(FQoL)的看法,对于制定旨在促进康复和改善家庭福祉的干预措施至关重要。本研究的目的是了解他们对家庭生活质量的看法,根据他们在家庭中的角色,确定其组成部分,以及不同家庭成员对ABI患者家庭生活质量的差异。方法:对ABI幸存者以及ABI成人的主要(PCs)和非主要家庭照顾者(npc)进行定性研究。通过西班牙脑损伤联合会招募了来自不同家庭的24名幸存者,22名PCs和14名npc。就家庭福祉进行了八个角色特定的焦点小组。在逐字抄写之后,进行了主题分析(Braun和Clarke, 2006),以确定FQoL的主要领域及其指标。对比分析检查了三组参与者之间的差异。结果:确定了ABI家庭生活质量的主题、副主题和指标,包括个人幸福感、家庭关系、家庭资源、社区关系和社区资源五个领域。此外,还报告了家庭成员角色之间的差异。结论:这些发现强调了通过承认不同家庭成员的经历来解决家庭生活质量问题的重要性。从以家庭为中心的方法出发,专业人员应根据不同家庭成员的目标和需求提供适当的支持,旨在提高受ABI影响家庭的整体生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Family quality of life after brain injuries: a qualitative study on the perspectives of family members.

Purpose: Exploring the perceptions of family members after an acquired brain injury (ABI) regarding their family quality of life (FQoL) is essential for tailoring interventions aimed at promoting recovery and improving family well-being. The aim of this study was to understand their perspectives on FQoL, identify its components, and differences among different family members of people with ABI according to their role within families.

Methods: A qualitative study was conducted with ABI survivors and both primary (PCs) and non-primary family caregivers (NPCs) of adults with ABI. A total of 24 survivors, 22 PCs and 14 NPCs from different families were recruited through Spanish Brain Injury Federation. Eight role-specific focus groups on family well-being were conducted. Following verbatim transcription, a thematic analysis (Braun and Clarke, 2006) was performed to identify main domains of FQoL and their indicators. Comparative analyses examined differences among the three groups of participants.

Results: Themes, subthemes and indicators of FQoL for ABI families were identified, encompassing five domains-individual well-being, family relationships, family resources, community relationships and community resources-. Also, differences between family members' roles were reported.

Conclusion: These findings highlight the importance of addressing FQoL by acknowledging the different family members' experiences. From a family-centered approach, professionals should align to the goals and needs of different family members to provide appropriate support, aiming at enhancing the overall quality of life for families affected by ABI.

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来源期刊
Quality of Life Research
Quality of Life Research 医学-公共卫生、环境卫生与职业卫生
CiteScore
6.50
自引率
8.60%
发文量
224
审稿时长
3-8 weeks
期刊介绍: Quality of Life Research is an international, multidisciplinary journal devoted to the rapid communication of original research, theoretical articles and methodological reports related to the field of quality of life, in all the health sciences. The journal also offers editorials, literature, book and software reviews, correspondence and abstracts of conferences. Quality of life has become a prominent issue in biometry, philosophy, social science, clinical medicine, health services and outcomes research. The journal''s scope reflects the wide application of quality of life assessment and research in the biological and social sciences. All original work is subject to peer review for originality, scientific quality and relevance to a broad readership. This is an official journal of the International Society of Quality of Life Research.
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