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头孢孟多在肾功能损害患者中的药代动力学。

Pharmacokinetics of cefamandole in patients with renal impairment.

作者信息

Czerwinski A W, Pederson J A

出版信息

Antimicrob Agents Chemother. 1979 Feb;15(2):161-4. doi: 10.1128/AAC.15.2.161.

Abstract

Cefamandole pharmacokinetics were investigated in 24 adult males with stable renal function and creatinine clearances of 0 to 139 ml/min. After intramuscular injection of 1.0 g of cefamandole, peak plasma concentrations were achieved between 1 and 2 h. Maximum plasma concentration and drug half-life increased as creatinine clearance decreased; i.e., with normal renal function the half-life was 1.49 +/- 0.10 h, and in anephrics the half-life was 11.48 +/- 1.91 h. The greatest increase in half-life occurred when the creatinine clearance was less than 20 ml/min. At these levels of renal impairment, there was significant variance in calculated half-life among patients. The maximum urine concentration and rate of cefamandole urinary excretion decreased as renal function declined. Evidence suggesting renal and nonrenal methods of drug elimination is presented. Hemodialysis resulted in increased cefamandole elimination.

摘要

对24名肾功能稳定、肌酐清除率为0至139毫升/分钟的成年男性进行了头孢孟多的药代动力学研究。肌肉注射1.0克头孢孟多后,血浆浓度在1至2小时内达到峰值。随着肌酐清除率的降低,血浆最大浓度和药物半衰期增加;即,肾功能正常时半衰期为1.49±0.10小时,无肾者半衰期为11.48±1.91小时。当肌酐清除率低于20毫升/分钟时,半衰期增加最为显著。在这些肾功能损害水平下,患者之间计算出的半衰期存在显著差异。随着肾功能下降,头孢孟多的最大尿浓度和尿排泄率降低。提出了提示药物经肾和非肾途径消除的证据。血液透析导致头孢孟多的清除增加。

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