Czerwinski A W, Pederson J A
Scand J Infect Dis Suppl. 1980;suppl 25:45-8.
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 +/- 1.9 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.
对24名肾功能稳定、肌酐清除率为0至139 ml/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 g头孢孟多后,1至2小时内达到血浆峰值浓度。随着肌酐清除率降低,最大血浆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±1.9小时。当肌酐清除率低于20 ml/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,头孢孟多的最大尿液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清除增加。