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聚焦达比加群酯在预防房颤患者卒中及全身性栓塞事件中的应用。

Spotlight on dabigatran etexilate in the prevention of stroke and systemic embolism in patients with atrial fibrillation.

机构信息

Adis, a Wolters Kluwer Business, Auckland, New Zealand.

出版信息

Drugs Aging. 2011 May 1;28(5):415-9. doi: 10.2165/11207020-000000000-00000.

Abstract

The need for safe, effective and easily administered and monitored antithrombotic treatments that do not have the issues common to warfarin treatment has led to the development of new anticoagulant drugs. Dabigatran etexilate (Pradaxa®, Pradax™) is a prodrug of the direct thrombin inhibitor dabigatran, a direct, reversible, potent inhibitor of thrombin. Dabigatran does not interact with food, and is associated with very few known drug interactions. Dabigatran etexilate, at dosages of 110 and 150 mg twice daily, was shown to be noninferior to warfarin with regard to the incidence of stroke or systemic embolism in a large, randomized, partially blinded, multicentre study in a wide spectrum of patients with atrial fibrillation. Moreover, the higher dosage was associated with significantly greater efficacy than warfarin in this regard. These results were supported by secondary endpoints and subgroup analyses. In general, dabigatran etexilate is well tolerated, although it is associated with a higher rate of dyspepsia than warfarin. Major bleeding was as common in recipients of the higher dosage as, and less common in recipients of the lower dosage of dabigatran etexilate than, that in recipients of warfarin, and intracranial bleeding, life-threatening major bleeding and total bleeding were less common in recipients of either dabigatran etexilate dosage than in warfarin recipients. However, the higher dosage of dabigatran etexilate was associated with a higher rate of gastrointestinal bleeding than warfarin was. The incidence of hepatotoxicity did not significantly differ across treatment groups. In conclusion, dabigatran etexilate 150 mg twice daily is more effective than warfarin for the prevention of stroke and systemic embolism in patients with atrial fibrillation, and is generally well tolerated, particularly with regard to bleeding endpoints compared with warfarin. It requires more frequent administration than warfarin, but provides multiple improvements to various issues associated with warfarin administration. Direct comparisons with other new anticoagulant drugs would be beneficial, as would further investigation into the effects in different patient populations, long-term effects, and the gastrointestinal bleeding and dyspepsia observed with dabigatran etexilate treatment. Dabigatran etexilate is a promising new option for the prevention of stroke and systemic embolism in patients with atrial fibrillation.

摘要

达比加群酯(普伐他汀钠、普伐他汀)是直接凝血酶抑制剂达比加群的前体药物,是一种直接、可逆、强效的凝血酶抑制剂。达比加群酯与食物无相互作用,且与已知的药物相互作用很少。在一项大型、随机、部分盲、多中心研究中,达比加群酯 110mg 和 150mg,每日两次,与华法林比较,在预防房颤患者卒中或全身性栓塞方面非劣效。此外,该较高剂量在这方面显示出优于华法林的显著疗效。这些结果得到次要终点和亚组分析的支持。一般来说,达比加群酯耐受性良好,尽管其消化不良发生率高于华法林。大出血的发生率在较高剂量组与华法林组相似,而在较低剂量组则低于华法林组,颅内出血、危及生命的大出血和总出血的发生率在接受任何剂量达比加群酯治疗的患者中均低于华法林组。然而,达比加群酯较高剂量组的胃肠道出血发生率高于华法林组。各组的肝毒性发生率无显著差异。总之,与华法林相比,达比加群酯 150mg,每日两次,在预防房颤患者卒中或全身性栓塞方面更有效,且总体耐受性良好,特别是在出血终点方面优于华法林。与华法林相比,它需要更频繁的给药,但在与华法林给药相关的各种问题上提供了更多的改进。与其他新型抗凝药物进行直接比较将是有益的,进一步研究不同患者人群的长期效果、胃肠道出血和达比加群酯治疗相关的消化不良也将是有益的。达比加群酯是预防房颤患者卒中或全身性栓塞的一种很有前途的新选择。

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