South Australian Health and Medical Research Institute, PO Box 11060, Adelaide, SA, 5001, Australia.
Monash Cardiovascular Research Centre, Monash University, Clayton, Melbourne, VIC, Australia.
Am J Cardiovasc Drugs. 2019 Aug;19(4):343-348. doi: 10.1007/s40256-018-00322-4.
The COMPASS trial compared the impact of the selective direct factor Xa inhibitor, rivaroxaban, as monotherapy or in combination with aspirin on major adverse cardiovascular events (MACE) in patients with stable atherosclerotic disease. Patients treated with rivaroxaban 2.5 mg twice daily in combination with aspirin experienced fewer cardiovascular events but more bleeding complications than those who received aspirin monotherapy. In contrast, a higher dose of rivaroxaban (5 mg twice daily) and aspirin produced no clinical benefit and continued to be associated with greater bleeding rates than aspirin. Examining this study in the context of other trials of anticoagulant therapy in atherosclerotic vascular disease, this review attempts to place the role of very low-dose rivaroxaban in clinical context and highlights areas for future research.
COMPASS 试验比较了选择性直接因子 Xa 抑制剂利伐沙班单药治疗或与阿司匹林联合治疗对稳定动脉粥样硬化疾病患者主要不良心血管事件(MACE)的影响。与阿司匹林单药治疗相比,接受每日两次 2.5 毫克利伐沙班联合阿司匹林治疗的患者发生心血管事件的次数更少,但出血并发症更多。相比之下,更高剂量的利伐沙班(每日两次 5 毫克)和阿司匹林并未带来临床获益,且出血率仍高于阿司匹林。在其他抗栓治疗在动脉粥样硬化血管疾病中的试验背景下对该研究进行考察,本综述尝试将极低剂量利伐沙班的作用置于临床背景下,并强调未来研究的领域。