利鲁唑
肌萎缩侧索硬化
医学
呼吸衰竭
呼吸系统
重症监护医学
缓和医疗
生活质量(医疗保健)
通风(建筑)
神经肌肉疾病
疾病
麻醉
内科学
机械工程
工程类
护理部
作者
Susana Pinto,Mamede de Carvalho
摘要
SUMMARY In the last three decades, improvements in respiratory management are responsible for increasing survival and improving quality of life for amyotrophic lateral sclerosis (ALS) patients. Nowadays, ALS patients with respiratory involvement are offered a support treatment other than the traditional respiratory palliative care. Knowledge about available respiratory support potentialities is essential for appropriate, customized and effective treatment of ALS, which should probably be started sooner than the conventional approach. There is evidence supporting that respiratory support has a larger impact than riluzole on survival. Noninvasive ventilation is essential in the treatment of ALS patients with respiratory involvement. In this article methods to determine respiratory failure in ALS, mechanical invasive and noninvasive ventilation, telemetry, diaphragm pacing, cough aids and respiratory exercise are reviewed, after a brief overlook of respiratory insufficiency in ALS.
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