Limitations in activities of daily living in individuals with spinal muscular atrophy: A scoping review and multidisciplinary recommendations for clinical practice.

IF 3.5 4区 医学 Q2 CLINICAL NEUROLOGY
Journal of neuromuscular diseases Pub Date : 2026-07-01 Epub Date: 2025-11-26 DOI:10.1177/22143602251397438
Marta Ruggiero, Gabriele Giannotta, Giulia Morleo, Maria Carmela Oliva, Camilla Ferrante, Antonio Trabacca
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引用次数: 0

Abstract

Objective: This scoping review aims to explore and map the most frequently reported limitations in activities of daily living (ADLs) among individuals with spinal muscular atrophy (SMA), with the goal of informing clinical assessment and multidisciplinary care strategies.

Methods: The review followed the Joanna Briggs Institute (JBI) methodology for scoping reviews and adhered to the PRISMA-ScR reporting guidelines. A comprehensive search was conducted across PubMed, Scopus, Web of Science, and Embase up to December 2024. Eligible studies included qualitative, quantitative, and mixed-methods designs that reported ADL limitations in individuals with any SMA subtype. Data were extracted and descriptively synthesized, with additional input from a multidisciplinary rehabilitation team to provide practical clinical recommendations.

Results: Sixteen studies were included, encompassing a wide range of methodologies and SMA types. The most frequently reported ADL limitations included mobility (e.g., walking, transferring, climbing stairs) and self-care tasks (e.g., dressing, toileting, feeding). Upper limb function and instrumental ADLs, such as cooking, writing, and technology use, were less frequently assessed but emerged as important in maintaining autonomy, particularly in adults. Recent studies post-gene therapy demonstrates a broader focus on daily functioning and patient-reported outcomes. A multidisciplinary framework outlining domain-specific interventions and professional roles was developed based on the extracted data.

Conclusions: While mobility remains central to SMA-related disability, this review highlights the substantial burden of self-care and upper limb limitations. Findings support a shift toward more comprehensive, patient-centered assessment and rehabilitation approaches in SMA care.

脊髓性肌萎缩症患者日常生活活动的限制:临床实践的范围审查和多学科建议。
目的:本综述旨在探索和绘制脊髓性肌萎缩症(SMA)患者中最常报道的日常生活活动(adl)限制,目的是为临床评估和多学科护理策略提供信息。方法:回顾遵循乔安娜布里格斯研究所(JBI)的方法进行范围审查,并遵守PRISMA-ScR报告指南。在PubMed、Scopus、Web of Science和Embase上进行了全面的搜索,截止到2024年12月。合格的研究包括定性、定量和混合方法设计,报告了任何SMA亚型个体的ADL限制。数据提取和描述性合成,与额外的输入来自多学科康复团队提供实用的临床建议。结果:纳入了16项研究,涵盖了广泛的方法和SMA类型。最常见的ADL限制包括行动能力(如行走、移动、爬楼梯)和自我照顾任务(如穿衣、如厕、进食)。上肢功能和工具性adl(如烹饪、写作和技术使用)的评估频率较低,但在维持自主性方面表现出重要作用,尤其是在成年人中。最近的研究表明,后基因治疗更广泛地关注日常功能和患者报告的结果。根据提取的数据,制定了一个多学科框架,概述了特定领域的干预措施和专业角色。结论:虽然活动能力仍然是sma相关残疾的核心,但本综述强调了自我护理和上肢限制的实质性负担。研究结果支持在SMA护理中转向更全面、以患者为中心的评估和康复方法。
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
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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