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New Oral Anticoagulants for Stroke Prevention in Atrial Fibrillation: More Choices Bring More Challenges

机译:预防房颤卒中的新型口服抗凝剂:更多选择带来更多挑战

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Atrial fibrillation (AF) increases the risk of ischemic stroke approximately 5-fold.1 Whereas the average annual risk of stroke for AF patients averages 5%, the presence of additional risk factors such as heart failure, hypertension, diabetes, prior stroke, or age over 75 years increases this risk.2 To reduce this risk, guidelines from the American College of Chest Physicians for stroke prevention in AF strongly recommend an oral anticoagulant for patients at moderate to high risk for stroke .For decades warfarin has been the only available oral anticoagulant. An impressive body of clinical trial evidence has definitively shown that warfarin reduces the risk of ischemic stroke in AF patients by approximately two-thirds.2 However, long-term warfarin therapy also carries a substantial burden for the patient including a narrow therapeutic window, need for routine laboratory monitoring, and significant potential for drug and food interactions. These limitations likely account for the suboptimal utilization of warfarin in eligible patients with AF. For example, a recent population-based retrospective cohort study of 41,447 Medicare beneficiaries aged 66 years and older reported an overall warfarin use rate of 66.8%, a finding consistent with that of prior studies.Three novel oral anticoagulant drugs have been approved for stroke prevention in AF. Dabigatran,a direct thrombin inhibitor, and rivaroxaban, a factor Xa inhibitor, were approved in 2010 and 2011, respectively. In 2012, another factor Xa inhibitor, apixaban, received US Food and Drug Administration (FDA) approval. Although the availability of these newer oral anticoagulant drugs increases the therapeutic options for patients, it also presents challenges for clinicians who must now choose among the 4 agents. This article will discuss the advantages and disadvantages of these newer agents and their possible role in therapy.
机译:心房纤颤(AF)使缺血性中风的风险增加约5倍。1尽管AF患者的中风年平均风险为5%,但存在其他风险因素,如心力衰竭,高血压,糖尿病,既往中风或年龄超过75岁的人会增加这种风险。2为降低这种风险,美国胸外科医师学会预防房颤的指南强烈建议中度至高中风患者使用口服抗凝剂。数十年来,华法林一直是唯一可用的药物。口服抗凝药。大量令人印象深刻的临床试验证据明确表明,华法林将房颤患者的缺血性卒中风险降低了约三分之二。2然而,长期华法林治疗也给患者带来了沉重负担,包括狭窄的治疗窗口,需要用于常规实验室监测,以及药物和食物相互作用的巨大潜力。这些局限性可能是导致合格房颤患者使用华法林的次优原因。例如,最近一项针对41,447名66岁及以上的Medicare受益人的人群回顾性队列研究显示,华法林的总体使用率为66.8%,这一发现与之前的研究一致。三种新型口服抗凝药已被批准用于预防中风在AF中。直接凝血酶抑制剂达比加群和Xa因子抑制剂利伐沙班分别于2010年和2011年获得批准。 2012年,另一种Xa因子抑制剂apixaban获得了美国食品和药物管理局(FDA)的批准。尽管这些新型口服抗凝药的上市为患者提供了更多的治疗选择,但这也给现在必须在4种药物中进行选择的临床医生提出了挑战。本文将讨论这些新型药物的优缺点及其在治疗中的可能作用。

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