Suppr超能文献

脊髓性肌萎缩症(SMA)运动功能评估工具的最新技术。

State of the art for motor function assessment tools in spinal muscular atrophy (SMA).

机构信息

Service de Médecine Physique et Réadaptation Pédiatrique L'Escale, CHU Lyon, Université de Lyon, France; INMG, Inserm U1217, CNRS UMR5310, Université Lyon 1, Université de Lyon, Lyon, France.

出版信息

Arch Pediatr. 2020 Dec;27(7S):7S40-7S44. doi: 10.1016/S0929-693X(20)30276-1.

Abstract

Spinal muscular atrophy (SMA) is a progressive disease characterized by a degeneration of the spinal cord motor neurons. Many clinical trials - planned, in progress, or completed - have chosen motor function as the primary or secondary outcome because motor function assessment tools appeared to be more reliable than quantitative muscle testing in monitoring the course of the disease. Reliable, valid, and responsive outcome measures are needed to be able to capture the effectiveness of the therapeutic approach during clinical trials. Medical staff involved in neuromuscular diseases is faced with increasing pressure regarding the complex issue of choosing the right outcome measure for the objectives they have to assess. This paper provides a narrative literature review of available and validated motor function assessment tools in SMA population based on SMA subtypes, age and ambulant status. © 2020 French Society of Pediatrics. Published by Elsevier Masson SAS. All rights reserved.

摘要

脊髓性肌萎缩症(SMA)是一种进行性疾病,其特征是脊髓运动神经元的退化。许多临床试验 - 计划中、进行中或已完成 - 已选择运动功能作为主要或次要结局,因为运动功能评估工具在监测疾病过程方面似乎比定量肌肉测试更可靠。需要可靠、有效和敏感的结局测量来能够在临床试验中捕捉治疗方法的效果。涉及神经肌肉疾病的医务人员在选择适合他们评估目标的正确结局测量方面面临着越来越大的压力。本文基于 SMA 亚型、年龄和可移动状态,对 SMA 人群中可用的和经过验证的运动功能评估工具进行了叙述性文献回顾。© 2020 法国儿科学会。由 Elsevier Masson SAS 出版。保留所有权利。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验