首页> 美国卫生研究院文献>European Journal of Heart Failure >Rationale and design of a randomized double‐blind event‐driven multicentre study comparing the efficacy and safety of oral rivaroxaban with placebo for reducing the risk of death myocardial infarction or stroke in subjects with heart failure and significant coronary artery disease following an exacerbation of heart failure: the COMMANDER HF trial
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Rationale and design of a randomized double‐blind event‐driven multicentre study comparing the efficacy and safety of oral rivaroxaban with placebo for reducing the risk of death myocardial infarction or stroke in subjects with heart failure and significant coronary artery disease following an exacerbation of heart failure: the COMMANDER HF trial

机译:一项随机双盲事件驱动多中心研究的理由和设计该研究比较了口服利伐沙班与安慰剂在降低心衰和严重冠状动脉疾病患者死亡发生心肌梗塞或中风的风险方面的功效和安全性。心力衰竭加重:COMMANDER HF试验

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摘要

AimsThrombin is a critical element of crosstalk between pathways contributing to worsening of established heart failure (HF). The aim of this study is to explore the efficacy and safety of rivaroxaban 2.5 mg bid compared with placebo (with standard care) after an exacerbation of HF in patients with reduced ejection fraction (HF‐rEF) and documented coronary artery disease.
机译:凝血酶是途径之间串扰的关键因素,会加剧已确立的心力衰竭(HF)。这项研究的目的是探讨在射血分数降低(HF-rEF)和有冠心病的患者中加重HF后利伐沙班2.5 mg mg bid与安慰剂(标准护理)相比的疗效和安全性。

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