脊髓性肌萎缩
弱点
萎缩
医学
物理医学与康复
进行性肌萎缩
肌肉萎缩
神经肌肉疾病
重症监护医学
病理
生物信息学
物理疗法
生物
外科
疾病
肌萎缩侧索硬化
作者
Molly McPheron,Marcia V. Felker
标识
DOI:10.1016/j.ymthe.2024.06.020
摘要
Spinal muscular atrophy is a rare and progressive neuromuscular disease that, without treatment, leads to progressive weakness and often death. A plethora of studies have led to the approval of three high-cost and effective treatments since 2016. These treatments, nusinersen, onasemnogene abeparvovec and risdiplam, have not been directly compared and have varying challenges in administration. In this review, we discuss the evidence supporting the use of these medications, the process of treatment selection, monitoring after treatment, the limited data comparing treatments, as well as future directions for investigation and therapy.
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