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氟康唑在持续非卧床腹膜透析患者中的药代动力学。

Pharmacokinetics of fluconazole in patients undergoing continuous ambulatory peritoneal dialysis.

作者信息

Debruyne D, Ryckelynck J P, Moulin M, Hurault de Ligny B, Levaltier B, Bigot M C

机构信息

Pharmacology Laboratory, University Hospital Centre of Caen, France.

出版信息

Clin Pharmacokinet. 1990 Jun;18(6):491-8. doi: 10.2165/00003088-199018060-00006.

Abstract

The pharmacokinetics of fluconazole given orally (100 mg) or intraperitoneally (50 and 150 mg) were determined in 15 patients with chronic renal failure who were undergoing continuous ambulatory peritoneal dialysis. The half-life (72 to 85 hours) was intermediate between values obtained in healthy volunteers and in patients with renal insufficiency studied during an interhaemodialysis period. The peritoneal clearance, 0.26 to 0.33 L/h, led to an 18% recovery of administered drug in the dialysates after 48 hours. The peritoneal absorption was slow (time to peak plasma concentration 7 hours) but the peritoneal bioavailability was excellent at 87 +/- 5%. The mean concentrations of fluconazole up to 24 hours were 770 and 1900 micrograms/L after single intraperitoneal doses of 50 and 150 mg, respectively. The volume of distribution (40 to 60 L) did not differ from that determined in patients with normal renal function. In the case of fungal peritonitis essentially attributed to Candida spp., a 6-hour intraperitoneal infusion of fluconazole 150 mg every 2 days appears to be a good regimen to rapidly exceed minimum inhibitory concentrations and treat infection without risk of systemic dissemination of fungi or toxicity.

摘要

对15例正在接受持续性非卧床腹膜透析的慢性肾衰竭患者测定了口服(100毫克)或腹腔注射(50毫克和150毫克)氟康唑后的药代动力学。半衰期(72至85小时)介于健康志愿者和血液透析间期研究的肾功能不全患者所测得的值之间。腹膜清除率为0.26至0.33升/小时,48小时后透析液中药物回收率为18%。腹膜吸收缓慢(血浆浓度达峰时间为7小时),但腹膜生物利用度极佳,为87±5%。单次腹腔注射50毫克和150毫克氟康唑后,24小时内氟康唑的平均浓度分别为770微克/升和1900微克/升。分布容积(40至60升)与肾功能正常患者所测得的无异。对于主要由念珠菌属引起的真菌性腹膜炎,每2天6小时腹腔输注150毫克氟康唑似乎是一种良好的给药方案,能迅速超过最低抑菌浓度并治疗感染,而无真菌全身播散或毒性风险。

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