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

机译:线粒体缺损儿童肌肉活检术后麻醉相关的发病率和死亡率。

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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.
机译:背景:线粒体缺陷(MD)患儿可能会因麻醉而增加发生心肺和神经系统并发症的风险。这项研究的目的是确定MD儿童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年间接受线粒体和肌肉疾病疑似诊断性手术穿刺活检的155名10岁以下儿童的麻醉,手术和医疗记录进行了回顾性研究。122例患者的数据确诊为MD发现诊断被分析。麻醉是根据参加人员的判断进行的。在患有MD的儿童中,测量了氧化磷酸化系统的不同复合物的活性。结果:从术前评估中,脑病的症状最常见(n = 93),其次是肌肉无力(n = 32),乳酸性酸中毒(n = 15),心肌病和/或传导缺陷(n = 10)和慢性呼吸问题(n = 7)。 MD儿童的平均年龄为32.4个月(SD = 26.9)。麻醉的平均持续时间为36.0分钟(标准差= 12.6),平均在恢复室的停留时间为33.0分钟(标准差= 24.0)。在麻醉或麻醉后监护病房(PACU)期间,没有需要药理干预的心率或血压的重大变化。在PACU中,发生了短暂的SpO2 <80%气道阻塞短发。患有MD的儿童的生化分析表明,有42名儿童孤立缺乏氧化磷酸化的5种蛋白质复合物之一,有41名儿童缺乏复合蛋白质,39名儿童没有明确的定位。结论:通过标准的术前评估,监测和麻醉管理,在接受MD诊断的手术肌肉活检的患儿中,没有重大的围手术期和术后麻醉相关并发症。

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