Judemann K, Lunz D, Zausig Y A, Graf B M, Zink W
Klinik für Anästhesiologie, Universitätsklinikum Regensburg, Deutschland.
Anaesthesist. 2011 Oct;60(10):887-901. doi: 10.1007/s00101-011-1951-7.
Intensive care unit-acquired weakness (ICUAW) is a severe complication in critically ill patients which has been increasingly recognized over the last two decades. By definition ICUAW is caused by distinct neuromuscular disorders, namely critical illness polyneuropathy (CIP) and critical illness myopathy (CIM). Both CIP and CIM can affect limb and respiratory muscles and thus complicate weaning from a ventilator, increase the length of stay in the intensive care unit and delay mobilization and physical rehabilitation. It is controversially discussed whether CIP and CIM are distinct entities or whether they just represent different organ manifestations with common pathomechanisms. These basic pathomechanisms, however, are complex and still not completely understood but metabolic, inflammatory and bioenergetic alterations seem to play a crucial role. In this respect several risk factors have recently been revealed: in addition to the administration of glucocorticoids and non-depolarizing muscle relaxants, sepsis and multi-organ failure per se as well as elevated levels of blood glucose and muscular immobilization have been shown to have a profound impact on the occurrence of CIP and CIM. For the diagnosis, careful physical and neurological examinations, electrophysiological testing and in rare cases nerve and muscle biopsies are recommended. Nevertheless, it appears to be difficult to clearly distinguish between CIM and CIP in a clinical setting. At present no specific therapy for these neuromuscular disorders has been established but recent data suggest that in addition to avoidance of risk factors early active mobilization of critically ill patients may be beneficial.
重症监护病房获得性肌无力(ICUAW)是危重症患者的一种严重并发症,在过去二十年中越来越受到关注。根据定义,ICUAW由特定的神经肌肉疾病引起,即危重病性多发性神经病(CIP)和危重病性肌病(CIM)。CIP和CIM均可影响肢体和呼吸肌,从而使机械通气撤机复杂化,增加重症监护病房的住院时间,并延迟活动和身体康复。CIP和CIM是不同的实体,还是仅仅代表具有共同发病机制的不同器官表现,目前仍存在争议。然而,这些基本的发病机制很复杂,仍未完全明确,但代谢、炎症和生物能量改变似乎起着关键作用。在这方面,最近发现了几个危险因素:除了使用糖皮质激素和非去极化肌松剂外,脓毒症和多器官功能衰竭本身以及血糖水平升高和肌肉制动已被证明对CIP和CIM的发生有深远影响。对于诊断,建议进行仔细的体格和神经检查、电生理测试,在罕见情况下进行神经和肌肉活检。然而,在临床环境中似乎很难清楚地区分CIM和CIP。目前尚未确立针对这些神经肌肉疾病的特异性治疗方法,但最近的数据表明,除了避免危险因素外,危重症患者早期积极活动可能有益。