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面肩肱型肌营养不良症患者的标准化临床评估:FSHD 临床评分。

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score.

机构信息

Department of Neurology, IRCCS Fondazione Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.

出版信息

Muscle Nerve. 2010 Aug;42(2):213-7. doi: 10.1002/mus.21671.

Abstract

To define numerically the clinical severity of facioscapulohumeral muscular dystrophy (FSHD), we developed a protocol that quantifies muscle weakness by combining the functional evaluation of six muscle groups affected in this disease. To validate reproducibility of the protocol, 69 patients were recruited. Each patient was evaluated by at least five neurologists, and an FSHD severity score was given by each examiner. The degree of agreement among clinicians' evaluations was measured by kappa-statistics. Nineteen subjects received a score between 0 and 1, 9 had a score between 2 and 4, 20 received a score between 5 and 10, and 8 had a score between 11 and 15. Of the 13 subjects with D4Z4 alleles within the normal range (ranging from 10 to 150 repeats), 12 obtained a score of 0 and only 1 had a score of 1. Kappa-statistics showed a very high concordance for all muscle groups. We developed a simple, reliable, easily used tool to define the clinical expression of FSHD. Longitudinal studies will assess its sensitivity and utility in measuring changes for widespread use.

摘要

为了对肌营养不良症(FSHD)的临床严重程度进行数值定义,我们开发了一种方案,通过合并受该病影响的六个肌肉群的功能评估来量化肌肉无力。为了验证方案的可重复性,我们招募了 69 名患者。每位患者都由至少五位神经科医生进行评估,每位检查者都会给出 FSHD 严重程度评分。通过kappa 统计测量临床医生评估结果的一致性程度。19 名患者的评分为 0-1,9 名患者的评分为 2-4,20 名患者的评分为 5-10,8 名患者的评分为 11-15。在 D4Z4 等位基因处于正常范围内(重复 10-150 次)的 13 名受试者中,12 名得分为 0,只有 1 名得分为 1。kappa 统计显示,所有肌肉群的一致性都非常高。我们开发了一种简单、可靠、易于使用的工具来定义 FSHD 的临床表达。纵向研究将评估其在广泛应用中测量变化的敏感性和实用性。

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