重症监护患者多发神经病的电生理研究。

B J Ebeling, K Rommelsheim, H Stoeckel
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摘要

近年来,危重病人的多发性神经病变已引起人们的关注。肌肉无力和体感知觉受损的症状对于观察者来说更为明显,对于有意识的患者来说,如果避免长期的大量镇静,则可以识别。多神经病变的病因尚不清楚,诊断结果仍然罕见且部分有争议。我们对5例以肌肉无力为临床症状的多器官功能衰竭患者,在刺激混合周围神经后同时记录皮层体感诱发电位(SEP)和诱发肌电图(EMG),以检测传出和传入神经元通路的功能完整性。我们观察到不同程度的SEP和EMG改变,下肢比上肢更明显,这可能与轴突变性有关。这一过程可能是由多种因素和病理生理机制引起的。未发现新斯的明对肌电反应降低的影响。
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[Electrophysiologic studies in polyneuropathy of intensive care patients].

Polyneuropathy of the critically ill patient has gained attention in recent years. The symptoms of muscle weakness and impaired somatosensory perception are more obvious for the observer and recognizable for the conscious patient, if heavy long-term sedation is avoided. The cause of polyneuropathy remains unclear and diagnostic findings are still rare and partly controversial. In five of our patients with multiorgan failure and clinical signs of muscle weakness, cortical somatosensory evoked potentials (SEP) and the evoked electromyogram (EMG) were recorded simultaneously after the stimulation of mixed peripheral nerves to test the functional integrity of the efferent and afferent neuronal pathways. We observed different degrees of SEP and EMG alterations, which were more pronounced in the lower than in the upper extremities and which may be explained by an axonal degeneration. Such a process may be caused by multiple factors and pathophysiological mechanisms. An influence of neostigmine on a reduced EMG response could not be found.

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