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急性呼吸衰竭性神经病:危重病性多发性神经病的一种变体。

Acute respiratory failure neuropathy: a variant of critical illness polyneuropathy.

作者信息

Gorson K C, Ropper A H

机构信息

Neurology Service, St. Elizabeth's Hospital, Tufts University School of Medicine, Boston, MA 02135.

出版信息

Crit Care Med. 1993 Feb;21(2):267-71. doi: 10.1097/00003246-199302000-00020.

DOI:10.1097/00003246-199302000-00020
PMID:8428480
Abstract

OBJECTIVE

To describe a severe axonal polyneuropathy that follows acute respiratory failure and, in turn, causes continued ventilator dependence and paralysis after resolution of the primary illness.

DESIGN

Retrospective chart review of three patients and prospective analysis of two patients.

SETTING

Respiratory and neurologic ICUs of a general hospital.

PATIENTS

Five critically ill patients after an episode of acute respiratory failure. Neuromuscular blocking drugs were used in four patients, intermittently in two patients, high doses of corticosteroids were briefly administered in four, four patients had multiple organ failure, three patients had sepsis, but weakness preceded these complications in two patients.

INTERVENTIONS

None.

MAIN RESULTS

All patients had moderate-to-severe limb weakness with reduced or absent reflexes. Sensation was relatively preserved and the spinal fluid protein concentrations were normal. Electrophysiologic studies showed a severe, acute axonal motor neuropathy in four patients and normal studies in the fifth that later demonstrated denervation. Sensory potentials were mildly or not affected. Two quadriparetic patients died at 2.5 months, one remained weak and ventilator dependent several months after onset, and two patients recovered to walk in 4 to 6 months.

CONCLUSIONS

Severe axonal motor neuropathy after acute respiratory failure probably represents a variant of "critical illness polyneuropathy" that can be recognized from the temporal course of a conversion from primarily pulmonary to a pattern of neuromuscular ventilatory failure.

摘要

目的

描述一种继发于急性呼吸衰竭的严重轴索性多发性神经病,这种神经病继而导致在原发性疾病缓解后仍持续存在呼吸机依赖和瘫痪。

设计

对3例患者进行回顾性病历审查,并对2例患者进行前瞻性分析。

地点

一家综合医院的呼吸内科和神经科重症监护病房。

患者

5例急性呼吸衰竭发作后的重症患者。4例患者使用了神经肌肉阻滞剂,其中2例为间歇性使用;4例患者短期使用了高剂量皮质类固醇;4例患者出现多器官功能衰竭,3例患者发生脓毒症,但2例患者在这些并发症出现之前就已出现肌无力。

干预措施

无。

主要结果

所有患者均有中度至重度肢体无力,反射减弱或消失。感觉相对保留,脑脊液蛋白浓度正常。电生理研究显示,4例患者存在严重的急性轴索性运动神经病,第5例患者的研究结果正常,但后来显示有失神经改变。感觉电位轻度受影响或未受影响。2例四肢瘫患者在2.5个月时死亡,1例患者在发病后数月仍虚弱且依赖呼吸机,2例患者在4至6个月后恢复行走。

结论

急性呼吸衰竭后的严重轴索性运动神经病可能是“危重病性多发性神经病”的一种变体,可从主要由肺部疾病转变为神经肌肉通气衰竭模式的时间进程中识别出来。

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