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线粒体缺陷患儿肌肉活检术后与麻醉相关的发病率和死亡率。

Anesthesia-related morbidity and mortality after surgery for muscle biopsy in children with mitochondrial defects.

作者信息

Driessen Jacques, Willems Simone, Dercksen Sander, Giele Janneke, van der Staak Frans, Smeitink Jan

机构信息

Department of Anesthesiology, Radboud University Medical Center, Nijmegen, The Netherlands.

出版信息

Paediatr Anaesth. 2007 Jan;17(1):16-21. doi: 10.1111/j.1460-9592.2006.02043.x.

Abstract

BACKGROUND

Children with mitochondrial defects (MD) may have an increased risk for cardiorespiratory and neurological complications from anesthesia. The aim of this study was to determine the incidence of perioperative complications and adverse events in children with MD.

METHODS

We performed a retrospective review of the anesthesia, surgical and medical records of 155 children up to 10 years who underwent a diagnostic surgical muscle biopsy for suspected mitochondrial and muscle disorders between 1999 and 2003. The data of the 122 patients where a definite MD diagnosis was found were analyzed. Anesthesia was conducted according to the discretion of the attending staff. In children with MD the activity of the different complexes of the oxidative phosphorylation system was measured.

RESULTS

From the preoperative assessment, signs of encephalopathy were most frequent (n = 93), followed by muscle weakness (n = 32), lactic acidosis (n = 15), cardiomyopathy and/or conduction defects (n = 10) and chronic respiratory problems (n = 7). The mean age of the children with MD was 32.4 months (SD = 26.9). The mean duration of anesthesia was 36.0 min (SD = 12.6) and the mean length of stay in the recovery room was 33.0 min (SD = 24.0). There were no major changes in heart rate or blood pressure which required pharmacological intervention during anesthesia or postanesthesia care unit (PACU) stay. A short episode of SpO2 <80% with airway obstruction occurred once in the PACU. Biochemical analysis in the children with a MD showed an isolated deficiency of one of the five protein complexes of oxidative phosphorylation in 42 children, a combination of complex deficiencies in 41 and no definite localization in 39 children.

CONCLUSION

With standard preoperative assessment, monitoring and anesthesia management, there were no major peroperative and postoperative anesthesia-related complications in children undergoing surgical muscle biopsy with a MD diagnosis.

摘要

背景

线粒体缺陷(MD)患儿麻醉后发生心肺和神经并发症的风险可能增加。本研究旨在确定MD患儿围手术期并发症和不良事件的发生率。

方法

我们对1999年至2003年间155名10岁以下因疑似线粒体和肌肉疾病接受诊断性手术肌肉活检的患儿的麻醉、手术和医疗记录进行了回顾性分析。对确诊为MD的122例患者的数据进行了分析。麻醉由主治医护人员酌情进行。对MD患儿测定氧化磷酸化系统不同复合体的活性。

结果

术前评估显示,脑病体征最为常见(n = 93),其次是肌肉无力(n = 32)、乳酸酸中毒(n = 15)、心肌病和/或传导缺陷(n = 10)以及慢性呼吸问题(n = 7)。MD患儿的平均年龄为32.4个月(标准差 = 26.9)。平均麻醉时间为36.0分钟(标准差 = 12.6),在恢复室的平均停留时间为33.0分钟(标准差 = 24.0)。麻醉期间或在麻醉后护理单元(PACU)停留期间,心率或血压没有发生需要药物干预的重大变化。在PACU发生过一次因气道阻塞导致SpO2<80%的短暂情况。对MD患儿的生化分析显示,42名患儿氧化磷酸化的五种蛋白质复合体之一存在单独缺陷,41名患儿存在复合体缺陷组合,39名患儿没有明确的定位。

结论

通过标准的术前评估、监测和麻醉管理,诊断为MD的患儿在接受手术肌肉活检时,围手术期和术后未发生与麻醉相关的重大并发症。

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