多重先天性关节挛缩活动度测量的内容有效性:参与临床医生和有生活经验的人。

IF 1.9 Q3 REHABILITATION
Frontiers in rehabilitation sciences Pub Date : 2025-08-04 eCollection Date: 2025-01-01 DOI:10.3389/fresc.2025.1576267
Ahlam Zidan, Laurie Snider, Jaclyn Sions, Kristen Donlevie, Alexa Cirillo, Verity Pacey, Noémi Dahan-Oliel
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引用次数: 0

摘要

摘要:下肢损伤在先天性多发性关节挛缩症(AMC)患儿中很常见,经常导致活动受限。由于缺乏针对AMC的评估工具,临床医生和研究人员经常使用尚未对AMC人群进行正式验证的工具。本研究旨在根据基于共识的健康测量工具标准(COSMIN)和国际功能、残疾和健康分类(ICF)框架,建立AMC儿童常用活动能力测量的内容效度。方法:将“功能活动能力量表(FMS)”、“吉列功能评估问卷(FAQ)”、“儿童功能独立性量表(WeeFIM)”和“患者报告的结果测量信息系统(PROMIS)”中的项目使用ICF的精炼链接规则与ICF类别进行链接。三个评价者进行独立联结,用Kappa系数计算评价者间信度。由有生活经验的人、临床医生和研究人员组成的专家小组审查了评分者确定的ICF代码,并使用COSMIN标准评估了四项措施的可理解性、相关性和全面性。计算内容效度指数(CVI)和修正Kappa (k*)。结果:评分间一致性显著[κ = 0.79, (95% CI: 0.78-0.84)]。大多数概念(84.4%)与“活动及参与”范畴有关,“环境因素”(8.9%)及“身体功能”(6.7%)则占少数。大多数测量的CVI和k*值显示极好的内容效度(0.91至1),除了PROMIS青年运动(≤0.82)。专家小组发现,这些措施具有高度的可理解性和相关性,但全面性不够。大多数研究的活动测量遗漏了诸如疼痛、疲劳、活动辅助和补偿策略等概念。结论:FMS、FAQ、WeeFIM和PROMIS(家长代理/儿童)具有良好的内容效度。然而,这些措施都不能完全解决AMC儿童的全部活动体验。将缺失的概念(如环境挑战、补偿策略和疼痛)纳入现有或新开发的评估工具中,对于提供更全面的功能灵活性评估至关重要。这样做将支持更全面的临床评估,改善结果跟踪,并加强对患有AMC的儿童的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Content validity of mobility measures in arthrogryposis multiplex congenita: engaging clinicians and people with lived experience.

Content validity of mobility measures in arthrogryposis multiplex congenita: engaging clinicians and people with lived experience.

Content validity of mobility measures in arthrogryposis multiplex congenita: engaging clinicians and people with lived experience.

Content validity of mobility measures in arthrogryposis multiplex congenita: engaging clinicians and people with lived experience.

Introduction: Lower-extremity impairment is prevalent in children with Arthrogryposis multiplex congenita (AMC), frequently leading to mobility limitations. Without AMC-specific assessment tools, clinicians and researchers often employ tools that have not been formally validated for the AMC population. This study aims to establish the content validity of commonly used mobility measures in children with AMC following the COnsensus-based Standards for health Measurement INstruments (COSMIN) and the International Classification of Functioning, Disability, and Health (ICF) framework.

Methods: Items from the measures "Functional Mobility Scale (FMS), Gillette Functional Assessment Questionnaire (FAQ), Functional Independence Measure for Children (WeeFIM), and Patient-Reported Outcomes Measurement Information System (PROMIS)" were linked to the ICF categories using the refined linking rules of the ICF. Three raters conducted independent linking, and inter-rater reliability was calculated using the Kappa coefficient. An expert panel consisting of people with lived experience, clinicians and researchers reviewed the ICF codes identified by the raters and evaluated the comprehensibility, relevance, and comprehensiveness of the four measures using the COSMIN standards. The Content Validity Index (CVI) and modified Kappa (k*) were calculated.

Results: Inter-rater agreement was substantial [κ = 0.79, (95% CI: 0.78-0.84)]. Most concepts (84.4%) were linked to the "Activities and Participation" domain, with a limited representation of "Environmental Factors" (8.9%) and "Body Functions" (6.7%). The CVI and k* values for most measures indicated excellent content validity (0.91 to 1), except for the PROMIS Mobility Young Adult (≤0.82). The expert panel found that measures exhibited high comprehensibility and relevance, but comprehensiveness was insufficient. Most studied mobility measures missed concepts such as pain, fatigue, mobility aids, and compensatory strategies.

Conclusions: FMS, FAQ, WeeFIM, and PROMIS (Parent Proxy/Pediatric) demonstrated good content validity. However, none of these measures fully address the full spectrum of mobility experiences in children with AMC. Incorporating missing concepts, such as environmental challenges, compensatory strategies, and pain, into existing or newly developed assessment tools is essential for providing a more holistic evaluation of functional mobility. Doing so will support more comprehensive clinical assessment, improve outcome tracking, and enhance care for children living with AMC.

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