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头孢曲松在腹膜透析期间的药代动力学。

Ceftriaxone pharmacokinetics during peritoneal dialysis.

作者信息

Koup J R, Keller E, Neumann H, Stoeckel K

出版信息

Eur J Clin Pharmacol. 1986;30(3):303-7. doi: 10.1007/BF00541533.

Abstract

The purpose of this study was to investigate the pharmacokinetics of intraperitoneally (IP) administered ceftriaxone (CRO) in patients maintained on chronic peritoneal dialysis. A single 2 g dose of CRO was administered IP to six adult patients who did not have peritonitis at the time of study. After a 5 hour dwell, the peritoneal fluid was exchanged with CRO-free fluid. Exchanges were carried out every 4 to 8 h, over a 24- to 28-h period. The peak total plasma CRO concentration was 104 micrograms/ml. An average of 74.1% of the IP dose of CRO was absorbed. Plasma protein binding was nonlinear; mean free fraction ranged from 12.8 to 17.9% at low and high concentrations. Dialysate concentrations at the end of subsequent exchanges ranged from means of 19.9 to 2.9 micrograms/ml. Total CRO clearance from plasma was 10.1 ml X kg-1 X h-1 and the mean terminal t 1/2 was 12.7 h. Dialytic clearance averaged 0.69 ml X kg-1 X h-1, only 6.9% of total clearance. A model which incorporates known characteristics of CRO binding and distribution in anuric patients was used to simulate plasma and peritoneal concentrations of CRO during multiple dose IP drug administration.

摘要

本研究的目的是调查在接受慢性腹膜透析的患者中腹腔内(IP)给予头孢曲松(CRO)的药代动力学。向6名在研究时未患腹膜炎的成年患者腹腔内给予单次2 g剂量的CRO。在留置5小时后,将腹腔液换成不含CRO的液体。在24至28小时内,每4至8小时进行一次更换。血浆中CRO的总浓度峰值为104微克/毫升。腹腔内给予的CRO剂量平均有74.1%被吸收。血浆蛋白结合呈非线性;在低浓度和高浓度下,平均游离分数范围为12.8%至17.9%。后续更换结束时透析液浓度范围为均值19.9至2.9微克/毫升。血浆中CRO的总清除率为10.1毫升×千克⁻¹×小时⁻¹,平均终末t 1/2为12.7小时。透析清除率平均为0.69毫升×千克⁻¹×小时⁻¹,仅占总清除率的6.9%。一个纳入了已知无尿患者中CRO结合和分布特征的模型被用于模拟多次腹腔内给药期间CRO的血浆和腹腔浓度。

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