Boelaert J, Schurgers M, Matthys E, Daneels R, van Peer A, De Beule K, Woestenborghs R, Heykants J
Renal Unit, Algemeen Ziekenhuis St. Jan, Brugge, Belgium.
Antimicrob Agents Chemother. 1988 Oct;32(10):1595-7. doi: 10.1128/AAC.32.10.1595.
The single-dose pharmacokinetics of 200 mg of oral itraconazole were studied in seven uremic patients, seven patients treated by hemodialysis, and five patients treated by continuous ambulatory peritoneal dialysis. Plasma concentration-versus-time profiles showed wide intersubject variation. This study could not demonstrate any significant effect of renal dysfunction and hemodialysis or continuous ambulatory peritoneal dialysis treatment upon the pharmacokinetics of itraconazole, and firm conclusions concerning dosing in such patients should await confirmation of our data in a larger patient population.
对7名尿毒症患者、7名接受血液透析治疗的患者和5名接受持续性非卧床腹膜透析治疗的患者,研究了口服200毫克伊曲康唑的单剂量药代动力学。血浆浓度-时间曲线显示个体间差异很大。本研究未能证明肾功能不全、血液透析或持续性非卧床腹膜透析治疗对伊曲康唑药代动力学有任何显著影响,关于此类患者给药的明确结论有待在更大患者群体中对我们的数据进行确认。