Duke Clinical Research Institute, Duke University Medical Center, Durham, North Carolina, USA.
Curr Opin Cardiol. 2010 Jul;25(4):312-20. doi: 10.1097/HCO.0b013e32833a524f.
Prevention of stroke and systemic emboli is paramount in the management of atrial fibrillation. Although warfarin is the predominant anticoagulant used in patients with atrial fibrillation, it has significant limitations that have impeded appropriate use of stroke prophylaxis in eligible patients with atrial fibrillation. Consequently, much research has been focused on finding an alternative to warfarin. We review the potential alternatives in development and evaluate the current evidence concerning their safety and efficacy.
Oral direct factor Xa inhibitors are potentially well tolerated and effective replacements for warfarin. These agents do not require cofactors and offer selective inhibition at a critical step of amplification in the coagulation cascade. Multiple direct anti-factor Xa agents are currently undergoing evaluation in phase I, II, and III trials. Early results suggest that these novel anticoagulants have favorable pharmacokinetic and pharmacodynamic profiles with minimal-to-no requirements for therapeutic monitoring. Two direct factor Xa inhibitors are emerging from phase II trials (betrixaban and YM150) and three are being evaluated in phase III trials (apixaban, edoxaban, and rivaroxaban) for the prevention of stroke and systemic emboli in patients with atrial fibrillation. The phase III trials of apixaban and rivaroxaban have completed enrollment and are in the follow-up phase.
Given the growing population of patients with atrial fibrillation, there is a great interest in finding new therapies for oral anticoagulation. The direct factor Xa inhibitors may offer several promising alternatives to warfarin therapy.
预防中风和全身栓塞是房颤管理的首要任务。尽管华法林是房颤患者中主要使用的抗凝药物,但它存在明显的局限性,这阻碍了在适合的房颤患者中进行适当的中风预防。因此,大量研究集中在寻找华法林的替代品上。我们综述了正在开发的潜在替代品,并评估了关于其安全性和有效性的当前证据。
口服直接因子 Xa 抑制剂可能具有良好的耐受性和有效性,可替代华法林。这些药物不需要辅助因子,并在凝血级联的放大关键步骤提供选择性抑制。多种直接抗因子 Xa 药物目前正在 I、II 和 III 期试验中进行评估。早期结果表明,这些新型抗凝剂具有良好的药代动力学和药效学特征,对治疗监测的要求最小化或无要求。两种直接因子 Xa 抑制剂(贝曲沙班和 YM150)已从 II 期试验中脱颖而出,三种(阿哌沙班、依度沙班和利伐沙班)正在 III 期试验中评估用于预防房颤患者的中风和全身栓塞。阿哌沙班和利伐沙班的 III 期试验已经完成入组,目前处于随访阶段。
鉴于房颤患者人数不断增加,人们对寻找新的口服抗凝治疗方法非常感兴趣。直接因子 Xa 抑制剂可能为华法林治疗提供几种有前途的替代方案。