3.8 Article

The natural history of ALS is changing: Improved survival

期刊

AMYOTROPHIC LATERAL SCLEROSIS
卷 10, 期 5-6, 页码 324-331

出版社

INFORMA HEALTHCARE
DOI: 10.3109/17482960903009054

关键词

Amyotrophic lateral sclerosis; neuromuscular disease; motor neuron disease; natural history; epidemiology

资金

  1. Northeast ALS (NEALS) Consortium
  2. Digiovanni Fund

向作者/读者索取更多资源

In the past two decades new practice parameters for clinical care in ALS were developed and several clinical trials were performed. We sought to review information in these prospective datasets and assess whether natural history of ALS has changed over time. Survival and the rate of functional decline were compared across the placebo arms of efficacy trials conducted from 1999 to 2005 by the Northeast ALS Consortium (NEALS). Similar data from the placebo arms of 12 other published efficacy ALS trials conducted between 1990 and 2008 were compared descriptively. In the three NEALS clinical trials, survival improved over time in the placebo cohort (p = 0.05) while the rate of change in maximum voluntary isometric contraction (MVIC) (p = 0.15), ALS Functional Rating Scale (ALSFRS) (p = 0.6) and vital capacity (%VC) (p = 0.5) was unchanged. No differences were observed in the mean rates of decline of these outcome measures in the published clinical trials. However, survival improved in the more recently conducted trials. Survival improved over time in placebo controlled participants enrolled in clinical trials in ALS since 1990. However, the decline in measures of function appears unchanged since then. These changes in natural history reflect improvements in symptomatic care of ALS.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据