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不同程度肾功能患者的头孢磺啶药代动力学

Cefsulodin pharmacokinetics in patients with various degrees of renal function.

作者信息

Matzke G R, Keane W F

出版信息

Antimicrob Agents Chemother. 1983 Mar;23(3):369-73. doi: 10.1128/AAC.23.3.369.

Abstract

The pharmacokinetics of cefsulodin were characterized in 19 patients with different degrees of renal function after a single 500-mg, 30-min intravenous infusion. Six subjects had a creatinine clearance (Clcr) of greater than 100 ml min-1 (group I), eight had a Clcr of between 12 and 42 ml min-1 (group II), and five had a Clcr of less than 10 ml min-1 (group III). Nine plasma and four urine samples were collected in the first 36 h. The plasma concentration-time data were fitted to a two-compartment open model. The mean beta-phase half-life was 1.77, 6.37, and 10.12 h in groups I, II, and III, respectively. A significant decline in plasma clearance (Clp) was also noted between the three groups: 136 to 49.6 to 27.2 ml min-1 in groups I, II, and III, respectively. Steady-state volume of distribution was 0.26 liter kg-1, regardless of renal function. The observed linear relationship between Clp and Clcr (Clp = 24.09 + 0.765 Clcr; r = 0.9566) can be utilized to revise dosage schedules for patients with any degree of renal impairment. The nonrenal clearance of cefsulodin was also noted to be significantly lower in groups II and III than in group I. Further investigations will be necessary to elucidate the mechanism(s) responsible for the decrease in the nonrenal clearance of cefsulodin.

摘要

对19例不同程度肾功能的患者进行单次500毫克、30分钟静脉输注后,对头孢磺啶的药代动力学进行了研究。6名受试者的肌酐清除率(Clcr)大于100毫升/分钟(I组),8名受试者的Clcr在12至42毫升/分钟之间(II组),5名受试者的Clcr小于10毫升/分钟(III组)。在最初的36小时内收集了9份血浆样本和4份尿液样本。血浆浓度-时间数据拟合为二室开放模型。I组、II组和III组的平均β相半衰期分别为1.77小时、6.37小时和10.12小时。三组之间的血浆清除率(Clp)也有显著下降:I组、II组和III组分别从136降至49.6再降至27.2毫升/分钟。无论肾功能如何,稳态分布容积均为0.26升/千克。观察到的Clp与Clcr之间的线性关系(Clp = 24.09 + 0.765 Clcr;r = 0.9566)可用于调整任何程度肾功能损害患者的给药方案。还发现II组和III组头孢磺啶的非肾清除率明显低于I组。有必要进一步研究以阐明导致头孢磺啶非肾清除率降低的机制。

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