Ohashi K, Tsunoo M, Tsuneoka K
J Antimicrob Chemother. 1986 Mar;17(3):347-51. doi: 10.1093/jac/17.3.347.
The effects of liver disease on the pharmacokinetics and protein binding of cefazolin and cephalothin were studied in patients with cirrhosis, chronic active hepatitis or normal liver function. The T1/2 and mean residence time of cefazolin were significantly shorter in cirrhosis. Cephalothin clearance was decreased by cirrhosis. Plasma protein binding of cefazolin, but not cephalothin was significantly reduced in cirrhosis. It is suggested that no dose reduction is necessary for either drug in severe hepatic impairment.
在肝硬化、慢性活动性肝炎或肝功能正常的患者中,研究了肝脏疾病对头孢唑林和头孢噻吩药代动力学及蛋白结合的影响。肝硬化患者中,头孢唑林的半衰期(T1/2)和平均驻留时间显著缩短。肝硬化会降低头孢噻吩的清除率。肝硬化患者中,头孢唑林的血浆蛋白结合率显著降低,而头孢噻吩则未降低。提示在严重肝功能损害时,两种药物均无需减量。