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西多福韦在连续性静脉-静脉血液滤过中的单剂量药代动力学

Single-dose pharmacokinetics of cidofovir in continuous venovenous hemofiltration.

作者信息

Vossen Matthias G, Gattringer Klaus-Bernhard, Jäger Walter, Kraff Stefanie, Thalhammer Florian

机构信息

Department of Internal Medicine I, Division of Infectious Diseases and Tropical Medicine, Medical University of Vienna, Vienna, Austria.

出版信息

Antimicrob Agents Chemother. 2014;58(4):1952-5. doi: 10.1128/AAC.01343-13. Epub 2014 Jan 13.

Abstract

Dosage recommendations for cidofovir are available for renally competent as well as impaired patients; however, there are no data for patients undergoing continuous renal replacement therapy. We determined the single-dose concentration-versus-time profile of cidofovir in a critically ill patient undergoing continuous venovenous hemofiltration (CVVH). One dose of 450 mg cidofovir (5 mg/kg) was administered intravenously due to a proven cytomegalovirus (CMV) infection and failure of first-line antiviral therapy. Additionally, 2 g of probenecid was administered orally 3 h prior to and 1 g was administered 2 h as well as 8 h after completion of the infusion. The concentrations of cidofovir in serum and ultrafiltrate were assessed by high-performance liquid chromatography. The peak serum concentration measured at 60 min postinfusion was 28.01 mg/liter at the arterial port. The trough serum level was 19.33 mg/liter at the arterial port after 24 h. The value of the area under the concentration-versus-time curve from 0 to 24 h was 543.8 mg·h/liter. The total body clearance was 2.46 ml/h/kg, and the elimination half-life time was 53.32 h. The sieving coefficient was 0.138±0.022. Total removal of the drug was 30.99% after 24 h. Because of these data, which give us a rough idea of the concentration profile of cidofovir in patients undergoing CVVH, a toxic accumulation of the drug following repeated doses may be expected. Further trials have to be done to determine the right dosage of cidofovir in patients undergoing CVVH to avoid toxic accumulation of the drug.

摘要

西多福韦的剂量推荐适用于肾功能正常以及肾功能受损的患者;然而,对于接受持续肾脏替代治疗的患者尚无相关数据。我们测定了一名接受持续静静脉血液滤过(CVVH)的重症患者中西多福韦的单剂量浓度-时间曲线。由于已证实的巨细胞病毒(CMV)感染及一线抗病毒治疗失败,静脉给予一剂450mg西多福韦(5mg/kg)。此外,在输注前3小时口服2g丙磺舒,输注结束后2小时及8小时分别口服1g丙磺舒。采用高效液相色谱法评估血清和超滤液中西多福韦的浓度。输注后60分钟在动脉端口测得的血清峰浓度为28.01mg/升。24小时后动脉端口的血清谷浓度为19.33mg/升。0至24小时浓度-时间曲线下面积值为543.8mg·h/升。总体清除率为2.46ml/h/kg,消除半衰期为53.32小时。筛滤系数为0.138±0.022。24小时后药物的总清除率为30.99%。基于这些数据,我们对CVVH患者中西多福韦的浓度曲线有了大致了解,预计重复给药后药物可能会发生毒性蓄积。必须开展进一步试验以确定CVVH患者中西多福韦的合适剂量,避免药物的毒性蓄积。

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