首页> 外文期刊>British Journal of Clinical Pharmacology >Effect of oseltamivir treatment on anticoagulation: a cross-over study in warfarinized patients.
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Effect of oseltamivir treatment on anticoagulation: a cross-over study in warfarinized patients.

机译:Oseltamivir治疗对抗凝的影响:Warfarinized患者的交叉研究。

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AIM: To investigate whether oseltamivir enhances the anticoagulant effect of warfarin and to evaluate any pharmacokinetic (PK) interaction between the agents. METHODS: Twenty volunteers (mean age 62 years) receiving daily warfarin and with INR values of 2.0-3.5 during the previous 2 weeks were randomized to concomitant oseltamivir 75 mg twice daily for 4.5 days or warfarin alone in a two-way cross-over design with a 4-8 day wash-out. Anticoagulant effects were assessed by calculating overall [AUEC(0,96 h)] and observed maximum effect (E(max) ) increase from baseline in INR, decrease from baseline in factor VIIa, and change in vitamin K concentrations. Plasma pharmacokinetics of (R)- and (S)-warfarin and oseltamivir were also assessed. RESULTS: For both treatments, changes in INR and factor VIIa during treatment were small; for net AUEC(0,96 h), least square mean values were -9.53 (oseltamivir + warfarin) and -1.69 h (warfarin alone) for INR (difference -7.84 h, 90% CI -18.86, 3.17 h), and 1.56 and 0.54 kIU l(1) h, respectively, for factor VIIa (difference, 1.01 kIU l(1) h; 90% CI -1.18, 3.21). Differences between the treatments in E(max) increase from baseline for INR, decrease from baseline for factor VIIa and change from baseline in vitamin K concentration were not statistically significant. Oseltamivir did not alter warfarin pharmacokinetics. Oseltamivir was well tolerated in this study with no clinically significant adverse safety findings. CONCLUSION: Concomitant administration of oseltamivir for 4.5 days to volunteers on daily warfarin had little or no effect on warfarin pharmacokinetics and no effect on pharmacodynamics.
机译:目的:研究奥司他韦是否能增强华法林的抗凝作用,并评估两种药物之间的药代动力学(PK)相互作用。方法:20名志愿者(平均年龄62岁)在前2周每天服用华法林,INR值为2.0-3.5,随机分为两组,分别服用奥司他韦75mg,每天两次,持续4.5天,或采用双向交叉设计,单独服用华法林,持续4-8天。通过计算总[AUEC(0,96 h)]和观察到的最大效应(E(max))来评估抗凝效果,INR比基线增加,因子VIIa比基线减少,维生素K浓度变化。还评估了(R)-和(S)-华法林和奥司他韦的血浆药代动力学。结果:对于两种治疗,INR和因子VIIa在治疗期间的变化都很小;对于净AUEC(0,96小时),INR的最小均方值分别为-9.53(奥司他韦+华法林)和-1.69小时(单独使用华法林)(差值-7.84小时,90%可信区间-18.86,3.17小时),因子VIIa的最小均方值分别为1.56和0.54千欧(1)小时;90%可信区间-1.18,3.21)。治疗组之间的E(max)差异在INR方面比基线检查时增加,在VIIa因子方面比基线检查时减少,在维生素K浓度方面比基线检查时变化无统计学意义。奥司他韦并没有改变华法林的药代动力学。在这项研究中,奥司他韦耐受性良好,没有临床上显著的不良安全性发现。结论:志愿者每天服用奥司他韦4.5天,对华法林的药代动力学几乎没有影响,对药效学也没有影响。

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