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Old and new oral anticoagulants for secondary stroke prevention in atrial fibrillation

机译:新旧口服抗凝药可预防房颤继发性卒中

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Vitamin K antagonists, such as warfarin, used in oral anticoagulation therapy currently represent the standard drugs for the primary and secondary prevention of stroke in non-valvular atrial fibrillation (AF), with a relative risk reduction close to 70%. Newer oral anticoagulants, such as direct thrombin inhibitors ( i.e ., dabigatran) and direct factor Xa inhibitors ( i.e ., apixaban and rivaroxaban) have been recently compared with warfarin in large randomized trials for stroke prevention in AF. The new oral anticoagulants showed, compared with warfarin, no statistically significant difference in the rate of stroke or systemic embolism in secondary prevention (patients with previous transient ischemic attack or stroke) subgroups. With regard to safety, the risk of intracranial bleeding was reduced with new anticoagulants compared with warfarin. Indirect treatment comparisons of clinical trials on secondary prevention cohorts showed no significant difference in efficacy among apixaban, rivaroxaban, and dabigatran; but dabigatran 110 mg was associated with less intracranial bleedings than rivaroxaban.
机译:口服抗凝治疗中使用的维生素K拮抗剂(如华法林)目前是非瓣膜性心房颤动(AF)中一级和二级预防中风的标准药物,相对危险度降低了近70%。最近在大型随机试验中,较新的口服抗凝剂(如直接凝血酶抑制剂(即达比加群)和直接因子Xa抑制剂(即阿哌沙班和利伐沙班))与华法林进行了比较,以预防房颤。与华法林相比,新的口服抗凝剂在二级预防(先前有短暂性脑缺血发作或中风的患者)亚组中,中风或全身性栓塞的发生率无统计学差异。在安全性方面,与华法林相比,新型抗凝剂降低了颅内出血的风险。二级预防队列临床试验的间接治疗比较显示,阿哌沙班,利伐沙班和达比加群的疗效无显着差异。但达比加群110 mg的颅内出血量比利伐沙班低。

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