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[危重病性肌病。33例患者的神经生理学和肌肉活检评估]

[Critical illness myopathy. Neurophysiological and muscular biopsy assessment in 33 patients].

作者信息

Fernández-Lorente José, Esteban Angel, Salinero Emilio, Traba Alfredo, Prieto Julio, Palencia Eduardo

机构信息

Servicio de Neurofisiología Clínica, Hospital General Universitario Gregorio Marañón, Madrid, España.

出版信息

Rev Neurol. 2010 Jun 16;50(12):718-26.

PMID:20533250
Abstract

INTRODUCTION

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.

AIMS

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.

PATIENTS AND METHODS

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.

CONCLUSIONS

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.

摘要

引言

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。

目的

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。

患者和方法

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。

结论

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。

相似文献

1
[Critical illness myopathy. Neurophysiological and muscular biopsy assessment in 33 patients].[危重病性肌病。33例患者的神经生理学和肌肉活检评估]
Rev Neurol. 2010 Jun 16;50(12):718-26.
2
Signs of critical illness polyneuropathy and myopathy can be seen early in the ICU course.危重病性多发性神经病和肌病的体征在重症监护病房病程早期即可出现。
Acta Anaesthesiol Scand. 2009 Jul;53(6):717-23. doi: 10.1111/j.1399-6576.2009.01952.x. Epub 2009 Apr 14.
3
Clinical approach to the weak patient in the intensive care unit.重症监护病房中虚弱患者的临床处理方法
Respir Care. 2006 Sep;51(9):1024-40; discussion 1040-1.
4
[Neuromuscular manifestations in critically ill patients].[危重症患者的神经肌肉表现]
Ugeskr Laeger. 2007 Jun 4;169(23):2216-9.
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[Acquired neuromuscular syndrome in critically ill patients].[危重症患者获得性神经肌肉综合征]
Rev Neurol. 2006;42(11):674-80.
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Critical illness myopathy and neuropathy.危重病性肌病和神经病
Minerva Anestesiol. 2008 Jun;74(6):319-23.
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Critical illness myopathy: further evidence from muscle-fiber excitability studies of an acquired channelopathy.危重病性肌病:来自获得性离子通道病肌纤维兴奋性研究的进一步证据。
Muscle Nerve. 2008 Jan;37(1):14-22. doi: 10.1002/mus.20884.
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Persistent neuromuscular and neurophysiologic abnormalities in long-term survivors of prolonged critical illness.长期危重症幸存者存在持续的神经肌肉和神经生理异常。
Crit Care Med. 2003 Apr;31(4):1012-6. doi: 10.1097/01.CCM.0000053651.38421.D9.
9
Origin of ICU acquired paresis determined by direct muscle stimulation.通过直接肌肉刺激确定重症监护病房获得性麻痹的起源。
J Neurol Neurosurg Psychiatry. 2006 Apr;77(4):500-6. doi: 10.1136/jnnp.2005.070813. Epub 2005 Nov 23.
10
Neuromuscular manifestations of critical illness.危重症的神经肌肉表现
Muscle Nerve. 2005 Aug;32(2):140-63. doi: 10.1002/mus.20304.

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