Troy S M, Schultz R W, Parker V D, Chiang S T, Blum R A
Department of Medicine, Millard Fillmore Hospital, Buffalo, NY 14209-1194.
Clin Pharmacol Ther. 1994 Jul;56(1):14-21. doi: 10.1038/clpt.1994.95.
The pharmacokinetics of venlafaxine and its active metabolite O-desmethylvenlafaxine were studied in subjects with various degrees of renal dysfunction, including subjects requiring maintenance hemodialysis. Venlafaxine was administered as a single 50 mg dose, with blood and urine samples obtained at intervals up to 48 hours after administration for the subjects receiving dialysis or 72 hours for the subjects not receiving dialysis. Six subjects receiving dialysis also completed an intradialysis evaluation to estimate dialysis clearance. Concentrations of venlafaxine and O-desmethylvenlafaxine in plasma, urine, and dialysate fluid were determined by high-performance liquid chromatography. Apparent total clearance of venlafaxine and O-desmethylvenlafaxine were both significantly decreased by approximately 55% in the subjects receiving dialysis, and terminal disposition half-life was significantly prolonged for both compounds. Venlafaxine and O-desmethylvenlafaxine are poorly dialyzable. In conclusion, the disposition of venlafaxine and O-desmethylvenlafaxine is markedly altered in renal disease; therefore dosage adjustment is warranted for patients with creatinine clearance values below 30 ml/min.
在包括需要维持性血液透析的受试者在内的不同程度肾功能不全的受试者中研究了文拉法辛及其活性代谢物O-去甲文拉法辛的药代动力学。文拉法辛以50mg单剂量给药,对于接受透析的受试者,在给药后长达48小时的间隔时间采集血样和尿样,对于未接受透析的受试者则在72小时采集。6名接受透析的受试者还完成了透析内评估以估计透析清除率。通过高效液相色谱法测定血浆、尿液和透析液中文拉法辛和O-去甲文拉法辛的浓度。在接受透析的受试者中,文拉法辛和O-去甲文拉法辛的表观总清除率均显著降低约55%,并且两种化合物的终末处置半衰期均显著延长。文拉法辛和O-去甲文拉法辛的透析性较差。总之,肾病患者中文拉法辛和O-去甲文拉法辛的处置明显改变;因此,肌酐清除率低于30ml/min的患者需要调整剂量。