Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Neurology, Curaçao Medical Center, Willemstad, Curaçao.
Eur J Neurol. 2021 Jul;28(7):2339-2348. doi: 10.1111/ene.14863. Epub 2021 May 2.
Facioscapulohumeral muscular dystrophy (FHSD) is a debilitating inherited muscle disease for which various therapeutic strategies are being investigated. Thus far, little attention has been given in FSHD to the development of scientifically sound outcome measures fulfilling regulatory authority requirements. The aim of this study was to design a patient-reported Rasch-built interval scale on activity and participation for FSHD.
A pre-phase FSHD-Rasch-built overall disability scale (pre-FSHD-RODS; consisting of 159 activity/participation items), based on the World Health Organization international classification of disease-related functional consequences was completed by 762 FSHD patients (Netherlands: n = 171; UK: n = 287; United States: n = 221; France: n = 52; Australia: n = 32). A proportion of the patient cohort completed it twice (n = 230; interval 2-4 weeks; reliability studies). The pre-FSHD-RODS was subjected to Rasch analyses to create a model fulfilling its requirements. Validity studies were performed through correlation with the motor function measure.
The pre-FSHD-RODS did not meet the Rasch model expectations. Based on determinants such as misfit statistics and misfit residuals, differential item functioning, and local dependency, we systematically removed items until a final 38-inquiry (originating from 32 items; six items split) FSHD-RODS was constructed achieving Rasch model expectations. Adequate test-retest reliability and (cross-cultural and external) validity scores were obtained.
The FSHD-RODS is a disease-specific interval measure suitable for detecting activity and participation restrictions in patients with FSHD with good item/person reliability and validity scores. The use of this scale is recommended in the near future, to determine the functional deterioration slope in FSHD per year as a preparation for the upcoming clinical intervention trials in FSHD.
面肩肱型肌营养不良症(FHSD)是一种使人衰弱的遗传性肌肉疾病,目前正在研究各种治疗策略。迄今为止,在 FSHD 中,很少关注满足监管机构要求的科学合理的结果测量方法的开发。本研究的目的是设计一种用于 FSHD 的基于患者报告的 Rasch 构建的活动和参与间隔量表。
根据世界卫生组织疾病相关功能后果的国际分类,基于 762 名 FSHD 患者(荷兰:n=171;英国:n=287;美国:n=221;法国:n=52;澳大利亚:n=32)完成了一个预先的 FSHD-Rasch 构建的总体残疾量表(预 FSHD-RODS;由 159 个活动/参与项目组成)。一部分患者队列(n=230)完成了两次(间隔 2-4 周;可靠性研究)。对预 FSHD-RODS 进行了 Rasch 分析,以创建符合其要求的模型。通过与运动功能测量相关的相关性进行有效性研究。
预 FSHD-RODS 不符合 Rasch 模型的预期。基于拟合统计和拟合残差、差异项目功能和局部依赖性等决定因素,我们系统地删除项目,直到构建最终的 38 项(源自 32 项;6 项拆分)FSHD-RODS,达到 Rasch 模型的预期。获得了足够的测试重测信度和(跨文化和外部)有效性评分。
FSHD-RODS 是一种适合检测 FSHD 患者活动和参与受限的疾病特异性间隔测量工具,具有良好的项目/个体可靠性和有效性评分。建议在不久的将来使用该量表,以确定 FSHD 每年的功能恶化斜率,为即将进行的 FSHD 临床干预试验做准备。