Understanding health-related quality of life of informal carers in amyotrophic lateral sclerosis: a scoping review and conceptual framework.

IF 3.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Rosie Bamber, Jill Carlton, Christopher McDermott, Theocharis Stavroulakis
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引用次数: 0

Abstract

Background: Amyotrophic Lateral Sclerosis (ALS) is a rapidly progressive, life-limiting neurodegenerative disease. Informal carers provide extensive support, significantly impacting their health-related quality of life (HRQoL). Current HRQoL measurement using person-reported outcome measures (PROMs) in ALS carers lacks consistency and comprehensiveness, hindering robust assessment and synthesis. There is evident need for a comprehensive conceptual framework of HRQoL, to fully capture the multidimensional nature of caregiving in ALS. Such a framework is essential to inform research and clinical practice, ensuring relevant measurement and meaningful clinical discussions. This study aimed to develop this evidence-based framework.

Methods: This study comprised two stages. Firstly, a scoping review was undertaken in March 2024 using Medline, Embase, and CINAHL to identify primary articles exploring HRQoL in ALS carers. Qualitative, mixed methods and quantitative articles using multi-item PROMs to assess HRQoL in informal ALS carers were included. Relevant themes and subthemes were extracted from articles and PROMs and mapped onto an existing conceptual framework for people with ALS (Quality of Life in ALS, QuALS), which covers physical, psychological, and social HRQoL domains in people with ALS. The Carer-QuALS framework was subsequently developed and refined using existing literature and consultation with ALS carers. PROMs within this review were then indexed against the finalised Carer-QuALS framework.

Results: From 715 search results, 82 articles and 44 PROMs were eligible for inclusion. One new subtheme 'physical caring activities' emerged, while seven subthemes lacked support from the literature. In three structured consultation sessions, nine ALS carers, reviewed the draft Carer-QuALS framework (consisting of seven themes and 43 subthemes). Based on their input, one new subtheme 'privacy' was added, six subthemes were removed, and one was retained, despite lacking support from review literature. The final Carer-QuALS framework includes 37 subthemes: 8 physical, 6 social, and 23 psychological.

Conclusions: This review presents a comprehensive conceptual framework encompassing the multidimensional impact of ALS caregiving on the HRQoL of informal carers. The framework provides a resource that can be used by researchers, clinicians, and patient advocacy groups for multiple purposes (e.g., to support PROM selection to measure HRQoL, to guide future PROM development, and to facilitate discussions between informal carers and clinicians).

了解肌萎缩性侧索硬化症非正式护理人员的健康相关生活质量:范围审查和概念框架。
背景:肌萎缩性侧索硬化症(ALS)是一种快速进展的、限制生命的神经退行性疾病。非正式照护者提供广泛的支持,极大地影响了他们与健康有关的生活质量。目前在ALS护理人员中使用的个人报告结果测量(PROMs) HRQoL测量缺乏一致性和综合性,阻碍了可靠的评估和综合。显然需要一个全面的HRQoL概念框架,以充分捕捉ALS护理的多维性。这样的框架对于研究和临床实践至关重要,确保相关的测量和有意义的临床讨论。本研究旨在建立以证据为基础的框架。方法:本研究分为两个阶段。首先,在2024年3月使用Medline, Embase和CINAHL进行了范围审查,以确定探讨ALS护理人员HRQoL的主要文章。采用定性、混合方法和定量方法对非正式ALS照护者的HRQoL进行评估。从文章和论文中提取相关主题和子主题,并将其映射到ALS患者现有的概念框架(ALS患者的生活质量,QuALS)中,该框架涵盖了ALS患者的身体,心理和社会HRQoL领域。随后,利用现有文献和对渐冻症护理人员的咨询,开发和完善了护理人员-质量框架。然后根据最终的职业资格框架对该审查中的prom进行索引。结果:在715个检索结果中,有82篇文章和44篇论文符合纳入条件。一个新的子主题“身体护理活动”出现了,而七个子主题缺乏文献支持。在三次有组织的咨询会议中,9名渐冻症护理人员审查了由7个主题和43个副主题组成的渐冻症护理人员资格框架草案。根据他们的意见,增加了一个新的子主题“隐私”,删除了六个子主题,保留了一个子主题,尽管缺乏综述文献的支持。最终的职业资格框架包括37个子主题:8个身体,6个社会,23个心理。结论:本综述提出了一个全面的概念框架,涵盖了ALS护理对非正式照护者HRQoL的多维影响。该框架提供了一种可供研究人员、临床医生和患者权益团体用于多种目的的资源(例如,支持PROM的选择以衡量HRQoL,指导未来PROM的发展,并促进非正式护理人员和临床医生之间的讨论)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.30
自引率
2.80%
发文量
154
审稿时长
3-8 weeks
期刊介绍: Health and Quality of Life Outcomes is an open access, peer-reviewed, journal offering high quality articles, rapid publication and wide diffusion in the public domain. Health and Quality of Life Outcomes considers original manuscripts on the Health-Related Quality of Life (HRQOL) assessment for evaluation of medical and psychosocial interventions. It also considers approaches and studies on psychometric properties of HRQOL and patient reported outcome measures, including cultural validation of instruments if they provide information about the impact of interventions. The journal publishes study protocols and reviews summarising the present state of knowledge concerning a particular aspect of HRQOL and patient reported outcome measures. Reviews should generally follow systematic review methodology. Comments on articles and letters to the editor are welcome.
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