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危重病相关无力与相关运动障碍。

Critical illness-associated weakness and related motor disorders.

机构信息

Department of Clinical Medicine and Neuroscience, CUNY School of Medicine, New York, NY, United States; Department of Medicine, Section of Internal Medicine and Neurology, White Plains Hospital, White Plains, NY, United States.

出版信息

Handb Clin Neurol. 2023;195:707-777. doi: 10.1016/B978-0-323-98818-6.00031-5.

Abstract

Weakness of limb and respiratory muscles that occurs in the course of critical illness has become an increasingly common and serious complication of adult and pediatric intensive care unit patients and a cause of prolonged ventilatory support, morbidity, and prolonged hospitalization. Two motor disorders that occur singly or together, namely critical illness polyneuropathy and critical illness myopathy, cause weakness of limb and of breathing muscles, making it difficult to be weaned from ventilatory support, commencing rehabilitation, and extending the length of stay in the intensive care unit, with higher rates of morbidity and mortality. Recovery can take weeks or months and in severe cases, and may be incomplete or absent. Recent findings suggest an improved prognosis of critical illness myopathy compared to polyneuropathy. Prevention and treatment are therefore very important. Its management requires an integrated team approach commencing with neurologic consultation, creatine kinase (CK) measurement, detailed electrodiagnostic, respiratory and neuroimaging studies, and potentially muscle biopsy to elucidate the etiopathogenesis of the weakness in the peripheral and/or central nervous system, for which there may be a variety of causes. These tenets of care are being applied to new cases and survivors of the coronavirus-2 disease pandemic of 2019. This chapter provides an update to the understanding and approach to critical illness motor disorders.

摘要

在危重病病程中发生的肢体和呼吸肌无力,已成为成人和儿科重症监护病房患者日益常见且严重的并发症,并导致需要长时间通气支持、发病率增加和住院时间延长。两种单独或同时发生的运动障碍,即危重病性多发性神经病和危重病性肌病,导致肢体和呼吸肌无力,使患者难以脱离通气支持、开始康复,并且延长重症监护病房的住院时间,导致发病率和死亡率更高。恢复可能需要数周或数月,在严重的情况下,可能不完全或不存在。最近的研究结果表明,与多发性神经病相比,危重病性肌病的预后有所改善。因此,预防和治疗非常重要。其管理需要采用多学科团队方法,从神经科会诊、肌酸激酶(CK)测量、详细的电诊断、呼吸和神经影像学研究以及可能的肌肉活检开始,以阐明外周和/或中枢神经系统无力的病因发病机制,其可能有多种原因。这些护理原则适用于 2019 年冠状病毒 2 型疾病大流行的新病例和幸存者。本章提供了对危重病运动障碍的理解和处理方法的更新。

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