Cardiovascular Division, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
J Am Coll Cardiol. 2013 Jul 23;62(4):286-90. doi: 10.1016/j.jacc.2013.03.041. Epub 2013 Apr 16.
The aim of this study was to determine if rivaroxaban is associated with a reduction in stent thrombosis among patients with acute coronary syndromes (ACS) in the ATLAS-ACS 2 TIMI 51 (Anti-Xa Therapy to Lower Cardiovascular Events in Addition to Standard Therapy in Subjects With Acute Coronary Syndrome-Thrombolysis in Myocardial Infarction 51) trial.
Dual antiplatelet therapy (DAPT) has been the mainstay of efforts to prevent stent thrombosis. Because thrombin is a potent stimulant of platelet activation, we hypothesized that inhibition of thrombin generation via factor Xa inhibition may further reduce the risk of stent thrombosis.
The ATLAS-ACS 2 TIMI 51 study was a placebo-controlled trial that randomly assigned 15,526 patients with recent ACS to receive twice-daily doses of either 2.5 mg or 5 mg of rivaroxaban or placebo for a mean of 13 months and up to 31 months.
Among patients who had a stent placed before or at the time of the index event, rivaroxaban significantly reduced independently adjudicated Academic Research Consortium definite and probable stent thrombosis in the pooled (1.9% vs. 1.5%; hazard ratio [HR]: 0.65; p = 0.017) and the 2.5 mg twice-daily (1.9% vs. 1.5%; HR: 0.61; p = 0.023) treatment groups when compared with placebo, with a trend toward a reduction in the 5 mg twice-daily treatment group (1.9% vs. 1.5%; HR: 0.70; p = 0.089). Among patients who received both aspirin and a thienopyridine (stratum 2), the benefit of rivaroxaban emerged during the period of active treatment with DAPT (HR: 0.68; 95% CI: 0.50 to 0.92, combined rivaroxaban group vs. placebo). Among stented patients who were treated with dual antiplatelet therapy, there was a mortality reduction among those treated with twice-daily rivaroxaban 2.5 mg (HR: 0.56; 95% CI: 0.35 to 0.89; p = 0.014).
Among stented patients with ACS treated with DAPT, the administration of twice-daily rivaroxaban 2.5 mg was associated with a reduction in stent thrombosis and mortality. (An Efficacy and Safety Study for Rivaroxaban in Patients With Acute Coronary Syndrome; NCT00809965).
本研究旨在确定在 ATLAS-ACS 2 TIMI 51(急性冠脉综合征患者加用抗 Xa 治疗以降低心血管事件-血栓溶解 51)试验中,利伐沙班是否与急性冠脉综合征(ACS)患者的支架血栓形成减少相关。
双联抗血小板治疗(DAPT)一直是预防支架血栓形成的主要方法。由于凝血酶是血小板激活的有效刺激物,我们假设通过因子 Xa 抑制抑制凝血酶生成可能会进一步降低支架血栓形成的风险。
ATLAS-ACS 2 TIMI 51 研究是一项安慰剂对照试验,纳入了 15526 例近期 ACS 患者,随机接受每日两次 2.5 mg 或 5 mg 利伐沙班或安慰剂治疗,平均随访 13 个月,最长随访 31 个月。
在索引事件前或同时置入支架的患者中,与安慰剂相比,利伐沙班显著降低了经独立评估的学术研究联合会(Academic Research Consortium)明确和可能的支架血栓形成(1.9%比 1.5%;风险比[HR]:0.65;p=0.017)和每日两次 2.5 mg 利伐沙班组(1.9%比 1.5%;HR:0.61;p=0.023),而每日两次 5 mg 利伐沙班组则呈降低趋势(1.9%比 1.5%;HR:0.70;p=0.089)。在接受阿司匹林和噻吩吡啶的患者(分层 2)中,DAPT 治疗期间,利伐沙班的获益出现(HR:0.68;95%CI:0.50 至 0.92,联合利伐沙班组与安慰剂组)。在接受 DAPT 治疗的支架置入 ACS 患者中,每日两次 2.5 mg 利伐沙班治疗组的死亡率降低(HR:0.56;95%CI:0.35 至 0.89;p=0.014)。
在接受 DAPT 治疗的 ACS 支架置入患者中,每日两次 2.5 mg 利伐沙班可降低支架血栓形成和死亡率。(急性冠脉综合征患者使用利伐沙班的疗效和安全性研究;NCT00809965)。