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阿米卡星在婴幼儿及学龄前儿童中的药代动力学

Pharmacokinetics of amikacin in infants and pre-school children.

作者信息

Kafetzis D A, Sinaniotis C A, Papadatos C J, Kosmidis J

出版信息

Acta Paediatr Scand. 1979 May;68(3):419-22. doi: 10.1111/j.1651-2227.1979.tb05030.x.

Abstract

The pharmacokinetic properties of amikacin sulfate in infants and children aged from three weeks to 6 years were studied during treatment with doses of 7.5 mg/kg every 12 hours using standard assay methods and technique of two compartment open model kinetic analysis. Peak serum concentrations of amikacin were measured 30 or 60 min after the first intramuscular injection. These ranged from 11.8 microgram/ml to 23 microgram/ml in infants and from 9.0 microgram/ml to 29 microgram/ml in children. Five minutes after the first intravenous bolous injection they varied from 16 microgram/ml to 29.8 microgram/ml in infants and from 34 microgram/ml to 42 microgram/ml in children. Twelve hours after injection serum concentrations were less than 0.8 microgram/ml in all patients. Mean serum half-lives of amikacin in infants and children were 2.1 hours and 2.0 hours after intramuscular, and 2.2 and 2.0 hours after intravenous administration respectively. No evidence of accumulation was observed after four days treatment. The amount of antibiotic recovered within 12 hours from the urine in all patients ranged from 34.5 to 65% of an intramuscular dose, and from 45.8 to 63.3% of an intravenous dose. The dosage regime of 7.5 mg/kg body weight given every 12 hours should be safe and effective for the treatment of infections in the age groups studied.

摘要

采用两室开放模型动力学分析的标准测定方法和技术,对3周龄至6岁婴幼儿及儿童在每12小时7.5mg/kg剂量治疗期间硫酸阿米卡星的药代动力学特性进行了研究。在首次肌肉注射后30或60分钟测定阿米卡星的血清峰值浓度。婴幼儿的峰值浓度范围为11.8微克/毫升至23微克/毫升,儿童为9.0微克/毫升至29微克/毫升。首次静脉推注后5分钟,婴幼儿的浓度在16微克/毫升至29.8微克/毫升之间,儿童在34微克/毫升至42微克/毫升之间。注射12小时后,所有患者的血清浓度均低于0.8微克/毫升。婴幼儿及儿童肌肉注射后阿米卡星的平均血清半衰期分别为2.1小时和2.0小时,静脉给药后分别为2.2小时和2.0小时。治疗4天后未观察到蓄积迹象。所有患者在12小时内从尿液中回收的抗生素量,肌肉注射剂量的范围为34.5%至65%,静脉注射剂量的范围为45.8%至63.3%。每12小时给予7.5mg/kg体重的给药方案对于所研究年龄组的感染治疗应是安全有效的。

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