Greaves W L, Kreeft J H, Ogilvie R I, Richards G K
Antimicrob Agents Chemother. 1981 Feb;19(2):253-5. doi: 10.1128/AAC.19.2.253.
The pharmacokinetic disposition of 2 g of cefoxitin administered intravenously over 30 min was determined in six patients undergoing continuous ambulatory peritoneal dialysis for chronic renal failure. During the 6-h dialysate dwell time after the drug infusion, the mean apparent volume of distribution for cefoxitin was 0.267 liter/kg (range, 0.201 to 0.325 liter/kg), and the mean elimination t1/2 from plasma was 7.8 h (range, 5.5 to 13.1 h). The peritoneal clearance, averaging 1.51 ml/min (range, 0.58 to 2.35 ml/min), was only 7.4% of the mean plasmas clearance of cefoxitin. Cefoxitin clearance was reduced in patients with renal failure and was not increased by peritoneal dialysis.
在6例因慢性肾衰竭接受持续性非卧床腹膜透析的患者中,测定了静脉注射2克头孢西丁历时30分钟的药代动力学情况。在药物输注后的6小时透析液驻留期内,头孢西丁的平均表观分布容积为0.267升/千克(范围为0.201至0.325升/千克),血浆平均消除半衰期为7.8小时(范围为5.5至13.1小时)。腹膜清除率平均为1.51毫升/分钟(范围为0.58至2.35毫升/分钟),仅为头孢西丁平均血浆清除率的7.4%。肾衰竭患者的头孢西丁清除率降低,腹膜透析未使其增加。