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Synergistic influence of rivaroxaban on inflammation and coagulation biomarkers in patients with coronary artery disease and peripheral artery disease on aspirin therapy

机译:蓖麻毒素对冠状动脉疾病患者炎症和凝血生物标志物对阿司匹林疗法的协同影响

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摘要

COMPASS study demonstrated efficacy of dual pathway inhibition with 2.5 mg twice daily rivaroxaban and aspirin in patients with polyvascular disease (coronary artery disease, peripheral arterial disease or both), the underlying mechanism of which is not clearly understood. In this Phase IV, prospective, open-label and randomized study, we hypothesize that treatment with rivaroxaban is associated with a reduction in platelet activation and aggregation, inflammation and coagulation markers. 30 patients will be randomly treated with aspirin (81 mg q.d.) or aspirin plus rivaroxaban (2.5 mg b.i.d.) for 12 weeks. Platelet aggregation, platelet activation and inflammation markers, thrombin generation kinetics and tissue factor-induced platelet–fibrin clot strength will be measured at baseline, and 4 and 12 weeks after randomization.
机译:COMPACT研究证明了双途径抑制与每日蓖麻毒素(冠状动脉疾病,周围动脉疾病或两者)患者的每日蓖麻毒素和阿司匹林的疗效效果,其潜在机制也没有清楚地理解。 在这一阶段,前瞻性,开放标签和随机研究中,我们假设用蓖麻毒素的处理与血小板活化和聚集,炎症和凝血标志物的降低有关。 30名患者将随意处理阿司匹林(81mg Q.D.)或阿司匹林加里伐昔扎班(2.5mg B.I.D.)持续12周。 血小板聚集,血小板活化和炎症标志物,凝血酶产生动力学和组织因子诱导的血小板纤维蛋白凝块强度将在基线下测量,随机化后4和12周。

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