Walking test outcomes in adults with genetic neuromuscular diseases: a systematic literature review of their measurement properties.

IF 3.3 3区 医学 Q1 REHABILITATION
Nawale Hadouiri, Isabelle Fournel, Christel Thauvin-Robinet, Agnès Jacquin-Piques, Paul Ornetti, Mathieu Gueugnon
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引用次数: 0

Abstract

Introduction: Neuromuscular diseases (NMDs) include a large group of heterogeneous diseases. NMDs frequently involve gait disorders, which affect quality of life. Several walking tests and tools have been described in the literature, but there is no consensus regarding the use of walking tests and tools in NMDs or of their measurement properties for walking outcomes. The aim of this review is to present an overview of walking tests, including their measurement properties when used in adults with inherited or genetic NMDs. The aim is to help clinicians and researchers choose the most appropriate test for their objective.

Evidence acquisition: A systematic review was conducted after consulting MEDLINE (via PubMed), EMBASE, Science direct, Google Scholar and Cochrane Central Register of Controlled Trials databases for published studies in which walking outcome measurement properties were assessed. The validity, reliability, measurement error and responsiveness properties were evaluated in terms of statistical methods and methodological design qualities using the COnsensus-based Standards for the selection of health Measurement Instruments (COSMIN) guidelines.

Evidence synthesis: We included 46 studies in NMDs. These studies included 15 different walking tests and a wide variety of walking outcomes, assessed with six types of walking tools. Overall, the 6MWT was the most studied test in terms of measurement properties. The methodological design and statistical methods of most studies evaluating construct validity, reliability and measurement error were "very good." The majority of outcome measurements were valid and reliable. However, studies on responsiveness as minimal important difference or minimal important change were lacking or were found to have inadequate methodological and statistical methods according to the COSMIN guidelines.

Conclusions: Most walking outcomes were found to be valid and reliable in NMDs. However, in view of the growing number of clinical trials, further studies are needed to clarify additional measurement properties.

遗传性神经肌肉疾病成年患者的步行测试结果:关于其测量特性的系统性文献综述。
导言:神经肌肉疾病(NMD)包括一大类异质性疾病。NMD 经常会出现步态障碍,影响生活质量。文献中介绍了几种步行测试和工具,但对于步行测试和工具在 NMDs 中的应用或其对步行结果的测量特性尚未达成共识。本综述旨在概述步行测试,包括其在遗传性或基因性 NMDs 成人患者中的测量特性。目的是帮助临床医生和研究人员根据其目标选择最合适的测试:我们查阅了 MEDLINE(通过 PubMed)、EMBASE、Science direct、Google Scholar 和 Cochrane Central Register of Controlled Trials 数据库中已发表的评估步行结果测量特性的研究,然后进行了系统性综述。根据基于共识的健康测量工具选择标准(COSMIN)指南,从统计方法和方法设计质量方面对有效性、可靠性、测量误差和响应性进行了评估:我们纳入了 46 项关于 NMD 的研究。这些研究包括 15 种不同的步行测试和多种步行结果,使用六种步行工具进行评估。总体而言,就测量特性而言,6MWT 是研究最多的测试。大多数评估构建有效性、可靠性和测量误差的研究的方法设计和统计方法都 "非常好"。大多数结果测量是有效和可靠的。然而,根据 COSMIN 准则,缺乏关于最小重要差异或最小重要变化的响应性的研究,或研究发现方法和统计方法不足:结论:大多数步行结果在 NMDs 中都是有效和可靠的。然而,鉴于临床试验的数量不断增加,还需要进一步的研究来明确更多的测量属性。
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
8.50
自引率
4.40%
发文量
162
审稿时长
6-12 weeks
期刊介绍: The European Journal of Physical and Rehabilitation Medicine publishes papers of clinical interest in physical and rehabilitation medicine.
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