Ko R J, Sattler F R, Nichols S, Akriviadis E, Runyon B, Appleman M, Cohen J L, Koda R T
School of Pharmacy, University of Southern California, Los Angeles 90033.
Antimicrob Agents Chemother. 1991 Jul;35(7):1376-80. doi: 10.1128/AAC.35.7.1376.
The dispositions of cefotaxime and its metabolite desacetylcefotaxime were investigated in patients with different forms of chronic parenchymal liver disease (CPLD). A total of 31 subjects (27 patients and 4 controls) received a single 2-g dose of cefotaxime by infusion, and serial blood samples were drawn. The area under the concentration-time curve ranged from 176 to 241 micrograms.h/ml, the apparent half-life ranged from 1.49 to 2.42 h, and clearance ranged from 2.06 to 3.10 ml/min/kg in patients with four different forms of CPLD. The area under the concentration-time curve and the apparent half-life of desacetylcefotaxime ranged from 72 to 128 micrograms.h/ml and 7.1 to 13.4 h, respectively. Pharmacokinetic parameters were significantly different in patients with CPLD compared with those in control subjects and were related to clinical indices of hepatic impairment. Modest accumulation of cefotaxime in patients with severe hepatic impairment is unlikely to produce toxicity because of its high therapeutic index, and dosing modifications may not be required.
研究了不同类型慢性实质性肝病(CPLD)患者中头孢噻肟及其代谢产物去乙酰头孢噻肟的处置情况。共有31名受试者(27例患者和4名对照)通过静脉输注接受了单次2克剂量的头孢噻肟,并采集了系列血样。在四种不同类型CPLD的患者中,浓度-时间曲线下面积为176至241微克·小时/毫升,表观半衰期为1.49至2.42小时,清除率为2.06至3.10毫升/分钟/千克。去乙酰头孢噻肟的浓度-时间曲线下面积和表观半衰期分别为72至128微克·小时/毫升和7.1至13.4小时。与对照受试者相比,CPLD患者的药代动力学参数有显著差异,且与肝功能损害的临床指标相关。由于其高治疗指数,严重肝功能损害患者中头孢噻肟的适度蓄积不太可能产生毒性,可能不需要调整剂量。