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丁咯地尔在血液透析患者中的透析清除率

Dialysis clearance of buflomedil in hemodialysed patients.

作者信息

Rey E, Moynot A, d'Athis P, Pello J Y, Maurel A, Frydman M O, Buisson C, Olive G

机构信息

Pharmacologie clinique, Hôpital Saint-Vincent de Paul, Paris, France.

出版信息

Arzneimittelforschung. 1996 May;46(5):492-5.

PMID:8737633
Abstract

Buflomedil (CAS 55837-25-7, Fonzylane) is a peripherally vasoactive drug which improves nutritional blood flow in ischaemic tissue of patients with peripheral vascular disease by the way of an increase of perfusion in the microcirculation. Ten hemodialysed patients with chronic renal failure treated with intravenous infusion of 400 mg of buflomedil during 4 h of dialysis were included in the first study. This study was carried out to determine the dialysis plasma clearance and the amount of drug dialysed during the first intravenous administration of buflomedil. The dialysis clearance calculated from the amount recovered in dialysate was (mean +/- SD) 25.4 +/- 25.6 ml/min. The drug recovery resulting from hemodialysis represented a small fraction of the dose (< or = 5%). A second study was carried out to determine the accumulation of buflomedil in chronic hemodialysed patient. The drug concentration were measured before and at the end (4 h) of the infusion of buflomedil in six other patients maintained on intermittent hemodialysis (3 per week) for 4 weeks. The average Cmin and Cmax were stable during the 12 successive dialyses (mean +/- SD intervals were between 0.36 +/- 0.53 and 0.66 +/- 0.79 microgram/ml for Cmin and between 5.15 +/- 2.19 and 7.37 +/- 1.76 micrograms/ml for Cmax), showing no trend of accumulation of buflomedil. These results agree with the pharmacokinetics of the drug which is mainly metabolised in the liver and has a low renal clearance. Dialysis is unable to modify significantly the plasma concentration of the drug in regularly dialysed patients.

摘要

丁咯地尔(CAS 55837-25-7,福辛普利)是一种外周血管活性药物,它通过增加微循环灌注来改善外周血管疾病患者缺血组织的营养血流。第一项研究纳入了10名接受血液透析的慢性肾衰竭患者,在透析4小时期间静脉输注400毫克丁咯地尔。这项研究旨在确定丁咯地尔首次静脉给药期间的透析血浆清除率和透析药物量。根据透析液中回收量计算的透析清除率为(平均值±标准差)25.4±25.6毫升/分钟。血液透析导致的药物回收量占剂量的一小部分(≤5%)。第二项研究旨在确定丁咯地尔在慢性血液透析患者中的蓄积情况。在另外6名维持间歇性血液透析(每周3次)4周的患者中,在丁咯地尔输注前和结束时(4小时)测量药物浓度。在连续12次透析期间,平均最低浓度(Cmin)和最高浓度(Cmax)保持稳定(Cmin的平均值±标准差区间在0.36±0.53至0.66±0.79微克/毫升之间,Cmax在5.15±2.19至7.37±1.76微克/毫升之间),表明没有丁咯地尔蓄积的趋势。这些结果与该药物的药代动力学一致,该药物主要在肝脏代谢,肾清除率较低。透析不能显著改变定期透析患者的药物血浆浓度。

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