Anesthesia for a child with complex I respiratory chain enzyme deficiency
Publication in refereed journal


香港中文大学研究人员 ( 现职)

郭志德教授 (麻醉及深切治疗学系)

全文

数位物件识别号 (DOI) http://dx.doi.org/10.1016/S0952-8180(98)00074-9

引用次数
Web of Sciencehttp://aims.cuhk.edu.hk/converis/portal/Publication/19WOS source URL

其它资讯

摘要The mitochondrial myopathies are a rare group of conditions affecting the respiratory chain and oxidative phosphorylation. The anesthetic management of a 6-year-old girl with complex I respiratory chain deficiency requiring surgery for a fractured hip is presented and discussed. Potential problems were masseter spasm, tendency to develop lactate acidosis, and malignant hyperthermia susceptibility. These problem; were avoided by the use of a laryngeal mash airway, allowing the patient to spontaneously ventilate; caudal analgesia; and maintenance of anesthesia with a proprofol infusion. (C) http://aims.cuhk.edu.hk/converis/portal/Publication/1998 by Elsevier Science Inc.

着者Cheam EWS, Critchley LAH
期刊名称Journal of Clinical Anesthesia
出版年份http://aims.cuhk.edu.hk/converis/portal/Publication/1998
月份9
日期1
卷号10
期次6
出版社ELSEVIER SCIENCE INC
页次524 - 527
国际标準期刊号0952-8180
语言英式英语

关键词analgesia, caudal; anesthesia, intravenous; complex I respiratory chain deficiency; malignant hyperthermia; mitochondrial myopathy; propofol
Web of Science 学科类别Anesthesiology; ANESTHESIOLOGY