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重症脓毒症患者中危重病性肌病和神经病的早期发展

Early development of critical illness myopathy and neuropathy in patients with severe sepsis.

作者信息

Khan Jaffar, Harrison Taylor B, Rich Mark M, Moss Marc

机构信息

Department of Neurology, Division of Pulmonary, Allergy, and Critical Care Medicine, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

Neurology. 2006 Oct 24;67(8):1421-5. doi: 10.1212/01.wnl.0000239826.63523.8e.

DOI:10.1212/01.wnl.0000239826.63523.8e
PMID:17060568
Abstract

OBJECTIVES

To characterize the prevalence, time of onset, and cause of neuromuscular dysfunction in patients with severe sepsis.

METHODS

We conducted a prospective cohort study in which participants with severe sepsis underwent weekly neurologic examinations and nerve conduction studies (NCSs) within 72 hours of developing severe sepsis until intensive care unit (ICU) discharge. Electromyography was preformed if clinical weakness developed or if there was a significant reduction in nerve conduction response amplitudes.

RESULTS

Abnormal NCS were present upon enrollment in 63% of patients (31/48). The presence of abnormal baseline NCS was predictive of hospital mortality (55% vs 0% for patients with normal baseline NCS; p < 0.001). Development of acquired neuromuscular dysfunction could be predicted by NCS done on day 7. Twenty patients remained in the ICU long enough to have serial NCSs; 50% of these patients developed acquired neuromuscular dysfunction. Most patients with acquired neuromuscular dysfunction had electrophysiologic evidence of both critical illness myopathy and critical illness neuropathy.

CONCLUSION

Changes in nerve conduction studies occur in the majority of patients early in the course of severe sepsis and predict the development of acquired neuromuscular dysfunction and mortality in intensive care unit patients. Most patients with acquired neuromuscular dysfunction after sepsis have both critical illness myopathy and critical illness neuropathy.

摘要

目的

描述严重脓毒症患者神经肌肉功能障碍的患病率、发病时间及病因。

方法

我们进行了一项前瞻性队列研究,严重脓毒症参与者在发生严重脓毒症72小时内至重症监护病房(ICU)出院期间,每周接受一次神经学检查和神经传导研究(NCS)。如果出现临床肌无力或神经传导反应幅度显著降低,则进行肌电图检查。

结果

63%的患者(31/48)在入组时NCS异常。基线NCS异常可预测医院死亡率(基线NCS正常的患者为0%,异常的患者为55%;p<0.001)。第7天进行的NCS可预测获得性神经肌肉功能障碍的发生。20名患者在ICU停留时间足够长,得以进行系列NCS;其中50%的患者发生了获得性神经肌肉功能障碍。大多数获得性神经肌肉功能障碍患者同时有危重病性肌病和危重病性神经病的电生理证据。

结论

大多数严重脓毒症患者在病程早期神经传导研究就会出现变化,这可预测ICU患者获得性神经肌肉功能障碍的发生及死亡率。脓毒症后大多数获得性神经肌肉功能障碍患者同时有危重病性肌病和危重病性神经病。

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