CPC Clinical Research, Aurora, Colorado, USA; Division of Cardiology, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA. Electronic address: https://twitter.com/me_canonico.
CPC Clinical Research, Aurora, Colorado, USA; Division of Endocrinology, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado, USA.
J Am Coll Cardiol. 2024 Aug 27;84(9):801-811. doi: 10.1016/j.jacc.2024.05.060.
Rivaroxaban 2.5 mg plus aspirin reduced limb and cardiovascular events and increased bleeding in patients with symptomatic peripheral artery disease (PAD) after lower extremity revascularization in the VOYAGER PAD (Efficacy and Safety of Rivaroxaban in Reducing the Risk of Major Thrombotic Vascular Events in Subjects With Symptomatic Peripheral Artery Disease Undergoing Peripheral Revascularization Procedures of the Lower Extremities) study. Fragile patients are at heightened risk for ischemic and bleeding events.
The purpose of this study was to investigate the safety and efficacy of rivaroxaban 2.5 mg in fragile patients from VOYAGER PAD.
Patients were categorized as fragile based on prespecified criteria (age >75 years, weight ≤50 kg, or baseline estimated glomerular filtration rate <50 mL/min/1.73 m). The primary efficacy outcome was the composite of acute limb ischemia, major amputation of a vascular etiology, myocardial infarction, ischemic stroke, or cardiovascular death. The principal safety outcome was TIMI major bleeding.
Of 6,564 randomized patients, a total of 1,674 subjects were categorized as fragile at baseline. In the placebo arm, fragile patients were at higher risk of the primary outcome (HR: 1.34; 95% CI: 1.12-1.61) and TIMI major bleeding (HR: 1.57; 95% CI: 0.83-2.96), compared with nonfragile patients. The effect of rivaroxaban on the primary endpoint was not modified by frailty status (fragile HR: 0.93; 95% CI: 0.75-1.15; nonfragile HR: 0.83; 95% CI: 0.72-0.97; P interaction = 0.37). Rivaroxaban increased TIMI major bleeding in fragile (HR: 1.54; 95% CI: 0.82-2.91) and nonfragile patients (HR: 1.37; 95% CI: 0.84-2.23; P interaction = 0.65).
Patients with PAD after lower extremity revascularization meeting fragile criteria are at higher risk of ischemic complications and bleeding. Rivaroxaban reduces ischemic risk and increases bleeding regardless of frailty status. These data may assist in personalization of antithrombotic therapy in fragile population.
在下肢血运重建后,利伐沙班 2.5mg 加阿司匹林可降低有症状外周动脉疾病(PAD)患者的肢体和心血管事件,并增加出血。在 VOYAGER PAD(利伐沙班降低有症状外周动脉疾病患者下肢血运重建术后主要血栓血管事件风险的疗效和安全性)研究中。脆弱的患者发生缺血和出血事件的风险更高。
本研究旨在探讨 VOYAGER PAD 中利伐沙班 2.5mg 在脆弱患者中的安全性和疗效。
根据预先设定的标准(年龄>75 岁、体重≤50kg 或基线估算肾小球滤过率<50mL/min/1.73m),患者被归类为脆弱。主要疗效终点为急性肢体缺血、血管病因所致大截肢、心肌梗死、缺血性卒中和心血管死亡的复合终点。主要安全性终点为 TIMI 大出血。
在 6564 名随机患者中,共有 1674 名患者在基线时被归类为脆弱。在安慰剂组中,脆弱患者发生主要结局的风险较高(HR:1.34;95%CI:1.12-1.61)和 TIMI 大出血(HR:1.57;95%CI:0.83-2.96),与非脆弱患者相比。利伐沙班对主要终点的影响不受脆弱状态的影响(脆弱 HR:0.93;95%CI:0.75-1.15;非脆弱 HR:0.83;95%CI:0.72-0.97;P 交互=0.37)。利伐沙班增加了脆弱(HR:1.54;95%CI:0.82-2.91)和非脆弱患者(HR:1.37;95%CI:0.84-2.23;P 交互=0.65)的 TIMI 大出血。
下肢血运重建后患有 PAD 的患者符合脆弱标准,发生缺血并发症和出血的风险更高。利伐沙班可降低缺血风险并增加出血风险,无论脆弱状态如何。这些数据可能有助于个体化脆弱人群的抗血栓治疗。