Quality of life of family caregivers of children and young adults with Down syndrome: A systematic review and meta-analysis.

IF 2.5 Q1 MEDICINE, GENERAL & INTERNAL Annals of the Academy of Medicine, Singapore Pub Date : 2024-08-19 DOI:10.47102/annals-acadmedsg.202420
Fergus Edward Cheok, Natania Rae Xiangqin Tan, Yu Yi Chan, Bryan Wei Zhi Wong, Gwyneth Kong, Zubair Amin, Yvonne Peng Mei Ng
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Abstract

Introduction: The aims of this systematic review and meta-analysis are to synthesise quality of life (QOL) of family caregivers of children and young adults with Down syndrome (DS) and determine factors affecting their QOL.

Method: This review was conducted as per Preferred Reporting Items for Systematic Reviews and Meta-Analyses guideline. Key search terms were "quality of life", "down syndrome" and "trisomy 21". Meta-analysis using random effect model was conducted where feasible. All studies underwent qualitative synthesis. The study protocol was registered with PROSPERO (CRD42023413532).

Results: Eighteen studies with 1956 caregivers were included. Of the 10 studies utilising the World Health Organization Quality of Life Instrument-Brief Version, 5 were included in the meta-analysis. Psychosocial domain had the highest score with mean (95% confidence interval [CI]) of 63.18 (39.10-87.25). Scores were poorer in physical, environmental and social domains: 59.36 (28.24-90.48), 59.82 (19.57-100.07) and 59.83 (44.24-75.41), respectively. Studies were heterogenous with I2 values ranging from 99-100% (P<0.01). The remaining 8 studies used 6 other instruments. Qualitative synthesis revealed that caregivers' QOL was adversely affected by child-related factors, such as level of functional independence, developmental delay, presence of multiple comorbidities, impaired activities of daily living and poor sleep quality. Environmental factors that adversely affected caregivers' QOL included number of children, housing and support from the family. Personal factors that affected caregivers' QOL included age, being a single mother, low education and low income.

Conclusion: QOL of caregivers of children with DS was lower than population reference data. Understand-ing the factors that influence family caregivers' QOL is an essential step towards improving the QOL of caregivers and their children with DS.

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唐氏综合症儿童和青少年家庭照顾者的生活质量:系统回顾和荟萃分析。
导言:本系统综述和荟萃分析旨在综合唐氏综合症(DS)儿童和年轻成人的家庭照顾者的生活质量(QOL),并确定影响其 QOL 的因素:本综述根据《系统综述和元分析首选报告项目》指南进行。关键词为 "生活质量"、"唐氏综合征 "和 "21 三体综合征"。在可行的情况下,采用随机效应模型进行 Meta 分析。所有研究均进行了定性综合。研究方案已在 PROSPERO 注册(CRD42023413532):共纳入了 18 项研究,涉及 1956 名护理人员。在采用世界卫生组织生活质量工具-简易版的 10 项研究中,有 5 项纳入了荟萃分析。心理社会领域得分最高,平均值(95% 置信区间 [CI])为 63.18(39.10-87.25)。身体、环境和社会领域的得分较低:分别为 59.36(28.24-90.48)、59.82(19.57-100.07)和 59.83(44.24-75.41)。研究结果不尽相同,I2 值介于 99%-100%(PC 结论:DS 儿童照顾者的 QOL 低于人口参考数据。了解影响家庭照顾者QOL的因素是改善照顾者及其DS患儿QOL的重要一步。
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