阿米卡星(BB-K8)在血液透析患者中的药代动力学。

J M Lanao, A Dominguez-Gil, J M Tabernero, J A Sanchez Tomero
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引用次数: 0

摘要

对10例透析6小时的终末期肾功能损害患者静脉注射阿米卡星(BB-K8) 7.5 mg/kg后的药代动力学进行了研究。双室动力学模型已被用于描述抗生素血浆浓度的双相下降,从而确定抗生素在中央和外周室的量,其消除主要通过肾脏。血液透析期间阿米卡星平均药代动力学参数为:α = 3.422 h-1 β = 0.176 h-1 K12 = 1.820 h-1 K21 = 1.327 h-1, K13 = 0.450 h-1, Vc = 9.242 l Vp = 11.455 l Vdss = 20.697 l, δ = 0.377 l/kg。为终末期肾损害患者建立了一种药代动力学参数的给药方案,以保证抗生素的安全和有效浓度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics of amikacin (BB-K8) in patients undergoing hemodialysis.

The pharmacokinetics of Amikacin (BB-K8) was studied after administration in an i.v. bolus injection of 7.5 mg/kg to 10 patients with terminal renal impairment undergoing dialysis sessions of 6 hours. A two-compartment kinetic model has been used to describe the bi-phasic decrease of the plasma concentrations of the antibiotic thus establishing the amounts of the antibiotic in the central and peripheral compartments, its elimination being principally through the kidney. During the hemodialysis sessions the average pharmacokinetic parameters of the Amikacin were: alpha = 3.422 h-1 beta = 0.176 h-1 K12 = 1.820 h-1 K21 = 1.327 H-1, K13 = 0.450 h-1, Vc = 9.242 l Vp = 11.455 l Vdss = 20.697 l and delta = 0.377 l/kg. A dosage regimen as a function of the pharmacokinetic parameters is established for patients with terminal renal impairment which guarantees safe and efficient concentrations of the antibiotic.

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