神经肌肉疾病患者的呼吸管理:当前观点

Degenerative Neurological and Neuromuscular Disease Pub Date : 2016-11-18 eCollection Date: 2016-01-01 DOI:10.2147/DNND.S87323
Gerald Pfeffer, Marcus Povitz
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引用次数: 25

摘要

神经肌肉呼吸性无力难以识别,因为症状可能发生在夜间,非特异性或归因于其他条件。呼吸肌无力的出现提示多种可能的异质性疾病,包括神经退行性、自身免疫性和遗传性神经肌肉疾病。在某些情况下,存在疾病改善管理,但在没有这种干预的情况下,支持呼吸治疗可以改善生活质量和生存率。在这篇综述中,我们讨论慢性神经肌肉呼吸无力的鉴别诊断和诊断方法。我们也回顾了在这些条件下呼吸衰竭的临床评估和管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Respiratory management of patients with neuromuscular disease: current perspectives.

Neuromuscular ventilatory weakness can be difficult to recognize because the symptoms can be nocturnal, nonspecific, or attributed to other conditions. The presence of respiratory muscle weakness suggests a number of possible heterogeneous conditions, including neurodegenerative, autoimmune, and genetic neuromuscular diseases. In some conditions, disease-modifying management exists, but in the absence of such intervention, supportive respiratory therapy can improve quality of life and survival. In this review, we discuss the differential diagnosis and diagnostic approach to chronic neuromuscular respiratory weakness. We also review the clinical assessment and management of respiratory failure in these conditions.

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