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血液透析后氨基糖苷类药物的再分布现象:奈替米星和妥布霉素

Aminoglycoside redistribution phenomenon after hemodialysis: netilmicin and tobramycin.

作者信息

Halstenson C E, Berkseth R O, Mann H J, Matzke G R

出版信息

Int J Clin Pharmacol Ther Toxicol. 1987 Jan;25(1):50-5.

PMID:3557729
Abstract

The serum concentration time profile of netilmicin and tobramycin before, during, and after hemodialysis was assessed in 5 noninfected adult chronic hemodialysis patients. The pharmacokinetic profile was biexponential for both agents in the pre-hemodialysis period. The total body clearance of netilmicin was significantly greater than that of tobramycin (5.32 +/- 0.75 ml/min vs 3.66 +/- 1.00 ml/min; p less than 0.05). The hemodialysis clearances of netilmicin and tobramycin were similar (60.8 +/- 16.6 ml/min and 54.7 +/- 18.8 ml/min, respectively). Netilmicin and tobramycin serum concentrations increased significantly 10 minutes after cessation of hemodialysis and maximally rebounded to 38.3 +/- 16.2% and 18.3 +/- 3.0% at 1.7 +/- 0.3 hours and 1.9 +/- 0.7 hours, respectively. This phenomenon may be a primary contributor to the marked variability observed in the clinical pharmacokinetics of these agents in hemodialysis patients. These data suggest that clinical serum concentrations should not be drawn until two hours after hemodialysis.

摘要

对5例未感染的成年慢性血液透析患者在血液透析前、透析期间和透析后的奈替米星和妥布霉素血清浓度-时间曲线进行了评估。在血液透析前期,两种药物的药代动力学曲线均为双指数型。奈替米星的总体清除率显著高于妥布霉素(5.32±0.75 ml/min对3.66±1.00 ml/min;p<0.05)。奈替米星和妥布霉素的血液透析清除率相似(分别为60.8±16.6 ml/min和54.7±18.8 ml/min)。血液透析停止10分钟后,奈替米星和妥布霉素的血清浓度显著升高,在1.7±0.3小时和1.9±0.7小时时分别最大反弹至38.3±16.2%和18.3±3.0%。这种现象可能是血液透析患者中这些药物临床药代动力学观察到显著变异性的主要原因。这些数据表明,血液透析后两小时内不应采集临床血清浓度样本。

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