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重症监护病房中不可兴奋的肌细胞膜患者的早期 II 型纤维萎缩。

Early type II fiber atrophy in intensive care unit patients with nonexcitable muscle membrane.

机构信息

Department of Anesthesiology and Operative Intensive Care Medicine, Campus Virchow-Klinikum & Campus Mitte, Charité University Medicine, Berlin, Germany.

出版信息

Crit Care Med. 2012 Feb;40(2):647-50. doi: 10.1097/CCM.0b013e31823295e6.

DOI:10.1097/CCM.0b013e31823295e6
PMID:21963579
Abstract

OBJECTIVE

Intensive care unit-acquired weakness indicates increased morbidity and mortality. Nonexcitable muscle membrane after direct muscle stimulation develops early and predicts intensive care unit-acquired weakness in sedated, mechanically ventilated patients. A comparison of muscle histology at an early stage in intensive care unit-acquired weakness has not been done. We investigated whether nonexcitable muscle membrane indicates fast-twitch myofiber atrophy during the early course of critical illness.

DESIGN

Prospective observational study.

SETTING

Two intensive care units at Charité University Medicine, Berlin.

PATIENTS

Patients at increased risk for development of intensive care unit-acquired weakness, indicated by Sepsis-related Organ Failure Assessment scores ≥8 on 3 of 5 consecutive days within their first week in the intensive care unit.

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

Electrophysiological compound muscle action potentials after direct muscle stimulation and muscle biopsies were obtained at median days 7 and 5, respectively. Patients with nonexcitable muscle membranes (n = 15) showed smaller median type II cross-sectional areas (p < .05), whereas type I muscle fibers did not compared with patients with preserved muscle membrane excitability (compound muscle action potentials after direct muscle stimulation ≥3.0 mV; n = 9). We also observed decreased mRNA transcription levels of myosin heavy chain isoform IIa and a lower densitometric ratio of fast-to-slow myosin heavy chain protein content.

CONCLUSION

We suggest that electrophysiological nonexcitable muscle membrane predicts preferential type II fiber atrophy in intensive care unit patients during early critical illness.

摘要

目的

重症监护病房获得性肌无力表明发病率和死亡率增加。直接肌肉刺激后无兴奋性肌膜在镇静、机械通气患者中早期出现,并预测重症监护病房获得性肌无力。尚未对重症监护病房获得性肌无力早期的肌肉组织学进行比较。我们研究了在危重病早期,无兴奋性肌膜是否表明快肌纤维萎缩。

设计

前瞻性观察研究。

地点

柏林夏洛蒂医科大学的两个重症监护病房。

患者

重症监护病房获得性肌无力风险增加的患者,其在重症监护病房的第一周内连续 5 天中有 3 天的 Sepsis-related Organ Failure Assessment 评分≥8。

干预

无。

测量和主要结果

直接肌肉刺激后的电生理学复合肌肉动作电位和肌肉活检分别在中位数第 7 天和第 5 天获得。无兴奋性肌膜的患者(n=15)的 II 型肌纤维横截面积中位数较小(p<0.05),而与肌肉膜兴奋性正常(直接肌肉刺激后的复合肌肉动作电位≥3.0 mV;n=9)的患者相比,I 型肌纤维则没有。我们还观察到肌球蛋白重链同工型 IIa 的 mRNA 转录水平降低,以及快肌与慢肌肌球蛋白重链蛋白含量的密度比降低。

结论

我们认为电生理学无兴奋性肌膜预测重症监护病房患者在早期危重病期间优先发生 II 型纤维萎缩。

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Crit Care Med. 2012 Feb;40(2):647-50. doi: 10.1097/CCM.0b013e31823295e6.
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