Diaz-Abad Montserrat, Todd Nevins, Zilliox Lindsay, Sanchez Ana, Hafer-Macho Charlene
Dr. Diaz-Abad and Dr. Todd are with the Department of Medicine, University of Maryland School of Medicine in Baltimore, Maryland.
Drs. Zilliox, Sanchez, and Hafer-Macko are with the Department of Neurology, University of Maryland School of Medicine in Baltimore, Maryland.
Innov Clin Neurosci. 2019 Nov 1;16(11-12):11-13.
Stepwise approach to therapy and increasing use of immunosuppressive agents have led to increasingly good prognosis and survival in myasthenia gravis (MG). However, there is a small subset of patients with treatment-refractory disease who experience a higher disease burden and increased rates of myasthenic crises and exacerbations, including respiratory failure. A 54-year-old man with treatment-refractory MG on chronic plasma exchange therapy had rapidly fluctuating weakness, poor sleep quality, and worsening respiratory symptoms in between treatments. He was started on home nocturnal noninvasive ventilation with volume-assured pressure support mode and experienced marked improvement in sleep quality, dyspnea, fatigue, and daytime sleepiness.
逐步治疗方法以及免疫抑制剂使用的增加,已使重症肌无力(MG)患者的预后和生存率越来越好。然而,有一小部分难治性疾病患者疾病负担更高,肌无力危象和病情加重(包括呼吸衰竭)的发生率增加。一名54岁接受慢性血浆置换治疗的难治性MG男性患者,在治疗期间肌无力迅速波动、睡眠质量差且呼吸症状恶化。他开始接受家庭夜间无创通气,采用容量保证压力支持模式,睡眠质量、呼吸困难、疲劳和日间嗜睡情况均有显著改善。