Cardiology Clinic, Thrombosis Centre, Department of Cardiac Thoracic and Vascular Sciences, and.
Rheumatology Unit, Department of Medicine, University of Padua, Padua, Italy.
Blood. 2018 Sep 27;132(13):1365-1371. doi: 10.1182/blood-2018-04-848333. Epub 2018 Jul 12.
Rivaroxaban is an effective and safe alternative to warfarin in patients with atrial fibrillation and venous thromboembolism. We tested the efficacy and safety of rivaroxaban compared with warfarin in high-risk patients with thrombotic antiphospholipid syndrome. This is a randomized open-label multicenter noninferiority study with blinded end point adjudication. Rivaroxaban, 20 mg once daily (15 mg once daily based on kidney function) was compared with warfarin (international normalized ratio target 2.5) for the prevention of thromboembolic events, major bleeding, and vascular death in patients with antiphospholipid syndrome. Only high-risk patients triple positive for lupus anticoagulant, anti-cardiolipin, and anti-β2-glycoprotein I antibodies of the same isotype (triple positivity) were included in the study. The trial was terminated prematurely after the enrollment of 120 patients (59 randomized to rivaroxaban and 61 to warfarin) because of an excess of events among patients in the rivaroxaban arm. Mean follow-up was 569 days. There were 11 (19%) events in the rivaroxaban group, and 2 (3%) events in the warfarin group. Thromboembolic events occurred in 7 (12%) patients randomized to rivaroxaban (4 ischemic stroke and 3 myocardial infarction), whereas no event was recorded in those randomized to warfarin. Major bleeding occurred in 6 patients: 4 (7%) in the rivaroxaban group and 2 (3%) in the warfarin group. No death was reported. The use of rivaroxaban in high-risk patients with antiphospholipid syndrome was associated with an increased rate of events compared with warfarin, thus showing no benefit and excess risk. This trial was registered at www.clinicaltrials.gov as #NCT02157272.
利伐沙班是房颤和静脉血栓栓塞患者中替代华法林的有效且安全的选择。我们检测了利伐沙班与华法林在血栓性抗磷脂综合征高危患者中的疗效和安全性。这是一项随机、开放标签、多中心非劣效性研究,终点评估设盲。利伐沙班 20mg 每日 1 次(肾功能不全者 15mg 每日 1 次)与华法林(国际标准化比值目标值 2.5)比较,用于预防抗磷脂综合征患者的血栓栓塞事件、大出血和血管性死亡。仅纳入狼疮抗凝物、抗心磷脂抗体和同种同型抗β2-糖蛋白 I 抗体三项均阳性(三重阳性)的高危患者。在招募了 120 例患者(利伐沙班组 59 例,华法林组 61 例)后,该试验因利伐沙班组事件过多而提前终止。平均随访 569 天。利伐沙班组有 11 例(19%)事件,华法林组有 2 例(3%)事件。利伐沙班组有 7 例(12%)患者发生血栓栓塞事件(4 例缺血性卒中和 3 例心肌梗死),而华法林组无事件发生。大出血发生在 6 例患者中:利伐沙班组 4 例(7%),华法林组 2 例(3%)。无死亡报告。与华法林相比,利伐沙班在抗磷脂综合征高危患者中的应用与事件发生率增加相关,因此没有获益且风险增加。该试验在 www.clinicaltrials.gov 注册,编号为 #NCT02157272。