Fernández-Lorente José, Esteban Angel, Salinero Emilio, Traba Alfredo, Prieto Julio, Palencia Eduardo
Servicio de Neurofisiología Clínica, Hospital General Universitario Gregorio Marañón, Madrid, España.
Rev Neurol. 2010 Jun 16;50(12):718-26.
Critical illness patients may show marked weakness acquired in the Intensive Care Unit (ICU). There are some disagreements about the myopathic versus neuropathic damage in this condition, presumably due to the lack of reliable diagnostic criteria.
To report the neurophysiological findings in critical patients, to classify them in groups according to the electro-physiological data of myopathy, and to ascertain the rapport between the neurophysiological classification of myopathy and the muscle biopsy results.
A prospective assessment of 33 ICU patients with marked weakness by means of needle electro-myography, electroneurography, and percutaneous muscle biopsy was carried out. Direct muscle stimulation was performed in 9 patients and repetitive nerve stimulation in 14 cases. RESULTS. According to neurophysiological criteria, patients were classified in 3 groups: definite (33%), probable (46%), and uncertain (21%) myopathy. The most conspicuous myopathic pathological findings including fibrillar atrophy and necrosis, vacuoles, and myosin and mitochondrial anomalies, were observed in both, definite and probable groups (26 patients). In 17 of these cases, low amplitude of the compound motor action potentials and normal sensory nerve action potentials were found. Axonal sensory-motor neuropathy was present in 11 patients, concomitant with neurophysiological data of myopathy in 7 cases.
Based on the neurophysiological criteria for the assessment and classification of acquired weakness in critically ill patients, myopathy is highly predominant over the neuropathic impairment. Histopathological findings are closely related to the electrophysiological diagnosis of myopathy. Neither neurophysiological nor pathological data support a hypothetic motor axonal neuropathy in this series.
危重症患者可能会出现因重症监护病房(ICU)获得性的明显肌无力。关于这种情况下的肌病性损伤与神经病性损伤存在一些分歧,推测是由于缺乏可靠的诊断标准。
报告危重症患者的神经生理学发现,根据肌病的电生理数据将他们分组,并确定肌病的神经生理学分类与肌肉活检结果之间的关系。
对33例有明显肌无力的ICU患者进行前瞻性评估,采用针极肌电图、神经电图和经皮肌肉活检。9例患者进行了直接肌肉刺激,14例进行了重复神经刺激。结果:根据神经生理学标准,患者分为3组:确诊(33%)、可能(46%)和不确定(21%)肌病。在确诊组和可能组(共26例患者)中均观察到最明显的肌病病理表现,包括纤维萎缩和坏死、空泡以及肌球蛋白和线粒体异常。在其中17例患者中,复合运动动作电位波幅降低而感觉神经动作电位正常。11例患者存在轴索性感觉运动神经病,其中7例伴有肌病的神经生理学数据。
基于评估和分类危重症患者获得性肌无力的神经生理学标准,肌病比神经病性损伤更为常见。组织病理学发现与肌病的电生理诊断密切相关。本系列研究中,神经生理学和病理学数据均不支持假设的运动轴索性神经病。