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Dabigatran etexilate for the prevention of stroke in patients with nonvalvular atrial fibrillation

机译:达比加群酯预防非瓣膜性房颤患者的中风

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For patients with nonvalvular atrial fibrillation, dabigatran etexilate is a new oral direct thrombin inhibitor to prevent stroke and systemic embolization. Dabigatran has few drug or food interactions, and has predictable pharmacokinetics that obviate the need for routine monitoring. The efficacy of dabigatran was established in the RELY trial, which found that dabigatran 150 mg twice-daily was superior to dose-Adjusted warfarin for the prevention of stroke in patients with nonvalvular atrial fibrillation, but with similar rates of bleeding. Dabigatran dosed at 110 mg twice-daily was noninferior to warfarin for the prevention of stroke, but had a lower risk of bleeding. There are few commercially available assays to monitor the effects of dabigatran and there is no known antidote that can complicate the management of emergent bleeding. For selected patients, dabigatran provides a net clinical benefit over warfarin, both in terms of morbidity, cost and patient satisfaction.
机译:对于非瓣膜性房颤患者,达比加群酯是一种新型口服直接凝血酶抑制剂,可预防中风和全身栓塞。达比加群几乎没有药物或食物相互作用,并且具有可预测的药代动力学,从而无需进行常规监测。达比加群的疗效在RELY试验中得到证实,该研究发现达比加群每天150 mg两次预防非瓣膜性房颤的卒中效果优于剂量调整的华法林,但出血率相似。达比加群每天两次服用110毫克,在预防中风方面不逊于华法林,但出血风险较低。几乎没有可商购的测定法来监测达比加群的作用,并且没有已知的解毒剂可使突发性出血的处理复杂化。对于选定的患者,达比加群在发病率,成本和患者满意度方面都比华法林提供了净的临床收益。

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