Colorado Prevention Center Clinical Research, Aurora, Colorado, USA.
Divisions of Cardiology and Hematology, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA.
J Thromb Haemost. 2022 May;20(5):1193-1205. doi: 10.1111/jth.15673. Epub 2022 Mar 7.
Vascular disease burden after lower extremity revascularization (LER) comprises more than the first event, more vascular beds than the local arteries, and more than one clinical event type.
Assess total arterial and venous thrombotic burden after LER for symptomatic peripheral artery disease (PAD) and effect of low-dose anticoagulation added to low-dose antiplatelet therapy.
PATIENTS/METHODS: VOYAGER PAD randomized 6564 symptomatic PAD patients undergoing LER to rivaroxaban 2.5 mg twice-daily or placebo on aspirin background. Marginal proportional-hazards models used to generate treatment hazard ratios and associated 95% CIs for first and total events; non-thrombotic deaths treated as competing terminal events. Incidence rates calculated as number of events per 100 patient-years follow-up.
Over 2.5 years (median), first and total thrombotic event rates: 7.1 and 10.3 events/100 patient-years, respectively, in placebo group. Two-thirds (925/1372) of total thrombotic events (arterial 95%, venous 5%) were nonfatal first events. Nearly one-third of patients with first event had a second arterial or venous thrombotic event. Rivaroxaban plus aspirin reduced first and total arterial and venous thrombotic events to 5.4 and 7.9 events/100 patient-years, respectively, a reduction in total thrombotic events over aspirin of 23% (HR: 0.77, 95%CI: 0.67-0.89, p = .0005), preventing 6.1 total arterial and venous thrombotic events at 3 years.
Assessing total arterial and venous thrombotic events, not just first events, provides more complete information about disease burden and absolute on-treatment impact. Following LER, judicious modulation of more than one coagulation pathway can provide broader benefit than intensifying inhibition of one hemostatic system component.
下肢血运重建(LER)后的血管疾病负担不仅包括首次事件,还包括多个血管床和多种临床事件类型。
评估下肢动脉疾病(PAD)症状患者接受 LER 治疗后总的动脉和静脉血栓形成负担,以及低剂量抗凝治疗联合低剂量抗血小板治疗的效果。
患者/方法:VOYAGER PAD 研究纳入 6564 例行 LER 的症状性 PAD 患者,随机接受利伐沙班 2.5mg 每日两次或安慰剂联合阿司匹林治疗。采用边缘比例风险模型生成首次和总事件的治疗风险比及其 95%置信区间;非血栓性死亡视为竞争终末事件。发生率以每 100 患者-年随访事件数计算。
在 2.5 年(中位数)的随访期间,安慰剂组的首次和总血栓事件发生率分别为 7.1 和 10.3 事件/100 患者-年。三分之二(925/1372)的总血栓事件(动脉 95%,静脉 5%)为非致命性首次事件。近三分之一的首次事件患者发生了第二次动脉或静脉血栓事件。利伐沙班联合阿司匹林使首次和总动脉及静脉血栓事件分别减少至 5.4 和 7.9 事件/100 患者-年,总血栓事件较阿司匹林降低 23%(风险比:0.77,95%置信区间:0.67-0.89,p=0.0005),3 年时可预防 6.1 例总动脉和静脉血栓事件。
评估总的动脉和静脉血栓事件,而不仅仅是首次事件,可提供更全面的疾病负担和治疗中绝对影响的信息。在 LER 后,明智地调节多个凝血途径的活性可能比强化一种止血系统成分的抑制作用带来更广泛的获益。