Dhib M, Moulin B, Leroy A, Hameau B, Godin M, Johannides R, Fillastre J P
Department of Nephrology, C.H.U. de Rouen, France.
Eur J Clin Pharmacol. 1991;41(6):579-83. doi: 10.1007/BF00314988.
The pharmacokinetics of cefixime following a single oral dose of 200 mg have been investigated in 6 normal subjects and in 22 patients with various degrees of renal insufficiency. Serum and urine samples were collected between 0 and 72 h and were subjected to two methods of analysis: bioassay and HPLC. There was a linear relationship between the two sets of results from 228 samples. This result suggests that none of the metabolites, which may accumulate in uraemic patients, has antibacterial activity. In normal subjects, the peak serum level (Cmax) was 2.50 micrograms.ml-1 at 2.83 h (tmax); the apparent elimination half-life (t1/2) was 3.73 h; the apparent total body clearance (CL.f-1) was 154 ml.min-1, the mean renal clearance (CLR) was 39.1 ml.min-1 and the apparent fraction of the dose recovered in 24 h urine was 0.22. In uraemic patients, Cmax and tmax were slightly increased and t1/2 was increased to 12-14 h in patients with an endogenous creatinine clearance below 20 ml.min-1. The apparent volume of distribution was decreased. Apparent total and renal clearances were lower in proportion to the degree of renal insufficiency. Linear relationships were found between CL/f, CLR and creatinine clearance (CLCR). The findings suggest that the dose of cefixime needs to be reduced only in patients with severe renal failure.
对6名正常受试者和22名不同程度肾功能不全患者单次口服200mg头孢克肟后的药代动力学进行了研究。在0至72小时内收集血清和尿液样本,并采用两种分析方法:生物测定法和高效液相色谱法。来自228个样本的两组结果之间存在线性关系。该结果表明,可能在尿毒症患者体内蓄积的代谢产物均无抗菌活性。在正常受试者中,血清峰值水平(Cmax)在2.83小时(tmax)时为2.50μg/ml;表观消除半衰期(t1/2)为3.73小时;表观总体清除率(CL)为154ml/min,平均肾清除率(CLR)为39.1ml/min,24小时尿液中回收剂量的表观分数为0.22。在尿毒症患者中,内源性肌酐清除率低于20ml/min的患者,Cmax和tmax略有升高,t1/2增加至12 - 14小时。表观分布容积减小。表观总清除率和肾清除率与肾功能不全程度成比例降低。在CL、CLR和肌酐清除率(CLCR)之间发现了线性关系。研究结果表明,仅重度肾衰竭患者需要减少头孢克肟的剂量。