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头孢西丁在正常受试者和肾功能不全患者中的药代动力学。

Pharmacokinetics of cefoxitin in normal subjects and in patients with renal insufficiency.

作者信息

Humbert G, Fillastre J P, Leroy A, Godin M, Van Winzum C

机构信息

Tissue Physiopathology Group, University of Rouen, France.

出版信息

Rev Infect Dis. 1979 Jan-Feb;1(1):118-26. doi: 10.1093/clinids/1.1.118.

Abstract

The pharmacokinetics of a single intravenous dose of 30 mg of cefoxitin/kg given to normal subjects and to patients with various degrees of chronic renal insufficiency were studied. The serum half-life of cefoxitin was correlated inversely with the rate of creatinine clearance, and the half-life increased exponentially when the creatinine clearance rate fell below 30 ml/min per 1.73 m2. The elimination of cefoxitin into urine was rapid and extensive in patients whose creatinine clearance was greater than 30 ml/min per 1.73 m2. In patients with more severe degrees of renal impairment, renal clearance of drug was diminished markedly (less than 20% of the administered dose was excreted in 4 hr as compared with greater than 60% in the former group). The clearance of cefoxitin can be increased fivefold by hemodialysis in patients with end-stage renal disease.

摘要

对正常受试者以及不同程度慢性肾功能不全患者静脉注射单剂量30mg/kg头孢西丁后的药代动力学进行了研究。头孢西丁的血清半衰期与肌酐清除率呈负相关,当肌酐清除率低于每1.73m²每分钟30ml时,半衰期呈指数增加。肌酐清除率大于每1.73m²每分钟30ml的患者,头孢西丁经尿液的消除迅速且广泛。在肾功能损害更严重的患者中,药物的肾清除率显著降低(4小时内排泄的给药剂量少于20%,而前一组大于60%)。终末期肾病患者通过血液透析,头孢西丁的清除率可提高五倍。

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