Division of Cardiology and Duke Clinical Research Institute, Duke University, Durham, North Carolina 27710, USA; email:
Annu Rev Med. 2019 Jan 27;70:61-75. doi: 10.1146/annurev-med-042617-092334. Epub 2018 Nov 26.
Atrial fibrillation (AF) increases a patient's stroke risk four- to five-fold. Anticoagulation with the vitamin K antagonist (VKA) warfarin reduces the risk of stroke by 67%, but warfarin carries a significant risk of major bleeding and has unpredictable pharmacodynamics with a narrow therapeutic window, necessitating frequent monitoring of its anticoagulant effect. The non-vitamin K antagonist oral anticoagulants (NOACs) dabigatran, rivaroxaban, apixaban, and edoxaban provide more predictable anticoagulant activity than warfarin with a lower risk of major bleeding, and each is noninferior to warfarin for the prevention of stroke. All have earned regulatory approval in the past eight years. At least one of the NOACs is approved for use in all patients with AF, except those with mechanical valves and rheumatic mitral valve disease, for whom warfarin remains the only option. Recent clinical trials have shown that antithrombotic regimens including NOACs are safe and effective in patients with AF who need potent antiplatelet therapy.
心房颤动 (AF) 使患者的中风风险增加四到五倍。维生素 K 拮抗剂 (VKA) 华法林的抗凝治疗可将中风风险降低 67%,但华法林有发生大出血的显著风险,且药效动力学不可预测,治疗窗较窄,需要频繁监测其抗凝效果。非维生素 K 拮抗剂口服抗凝剂 (NOAC) 达比加群、利伐沙班、阿哌沙班和依度沙班的抗凝活性比华法林更可预测,且大出血风险更低,在预防中风方面均不劣于华法林。过去八年中,所有这些药物均获得了监管机构的批准。除了机械瓣膜和风湿性二尖瓣疾病的患者,至少有一种 NOAC 被批准用于所有 AF 患者,而对于这些患者,华法林仍然是唯一的选择。最近的临床试验表明,包括 NOAC 在内的抗血栓治疗方案在需要强效抗血小板治疗的 AF 患者中是安全有效的。