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氨曲南在儿科患者中的单剂量药代动力学。

Single-dose pharmacokinetics of aztreonam in pediatric patients.

作者信息

Stutman H R, Marks M I, Swabb E A

出版信息

Antimicrob Agents Chemother. 1984 Aug;26(2):196-9. doi: 10.1128/AAC.26.2.196.

Abstract

Single intravenous doses (30 mg/kg) of aztreonam, a novel monobactam antibiotic, were administered to 29 children from 2 days to 11 years old. Serum, urine, and, when possible, cerebrospinal fluid samples were analyzed by high-pressure liquid chromatography and microbiological methods. The concentration of aztreonam in serum 15 min after drug administration was approximately 100 micrograms/ml in all age groups. The elimination half-life varied inversely, and the clearance from serum varied directly, with age. Aztreonam pharmacokinetics in 2- to 12-year-olds were similar to those in adults. The concentration in urine was high and prolonged, with potentially therapeutic concentrations still present 12 to 24 h after infusion in all age groups. Penetration into cerebrospinal fluid averaged 17.3% in children with inflamed meninges. Standard clinical and laboratory measurements revealed no untoward reactions. The 30-mg/kg dose of aztreonam produced potentially therapeutic concentrations in serum, urine, and cerebrospinal fluid. A dosage schedule of every 6 to 8 h in older children and every 8 to 12 h in neonates is suggested for multiple-dose clinical trials.

摘要

对29名年龄从2天至11岁的儿童静脉注射单剂量(30毫克/千克)的新型单环β-内酰胺类抗生素氨曲南。通过高压液相色谱法和微生物学方法分析血清、尿液样本,如有可能还分析脑脊液样本。给药后15分钟,所有年龄组血清中氨曲南的浓度约为100微克/毫升。消除半衰期与年龄成反比,血清清除率与年龄成正比。2至12岁儿童的氨曲南药代动力学与成人相似。尿液中的浓度较高且持续时间长,所有年龄组在输注后12至24小时仍存在潜在治疗浓度。脑膜发炎儿童脑脊液中的渗透率平均为17.3%。标准的临床和实验室检查未发现不良反应。30毫克/千克剂量的氨曲南在血清、尿液和脑脊液中产生了潜在治疗浓度。建议在多剂量临床试验中,大龄儿童每6至8小时给药一次,新生儿每8至12小时给药一次。

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