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Dual pathway inhibition for atherosclerotic cardiovascular disease: Recent advances

期刊

KARDIOLOGIA POLSKA
卷 80, 期 12, 页码 1200-1210

出版社

POLISH CARDIAC SOC
DOI: 10.33963/KP.a2022.0283

关键词

atherosclerosis; cerebrovascular disease; coronary artery disease; peripheral arterial disease; rivaroxaban

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Atherosclerotic cardiovascular disease (ASCVD) is a serious condition that is associated with significant morbidity, mortality, and healthcare costs. Antiplatelet therapy, especially the dual pathway inhibition (DPI) strategy of combining aspirin and low-dose rivaroxaban, has shown benefits and cost-effectiveness in preventing ASCVD events. The absolute benefits of DPI therapy vary depending on the type and history of the disease. Additional trials are being conducted to assess the impact of DPI therapy in other populations of interest.
Atherosclerotic cardiovascular disease (ASCVD), which includes coronary artery disease (CAD), cerebrovascular disease, and peripheral arterial disease (PAD) is associated with significant morbidity, mortality, and healthcare costs. Antiplatelet therapy has long been the mainstay of antithrombotic therapy for the prevention of first-ever and recurrent ASCVD events. More recently, however, randomized trials have demonstrated the benefits and cost-effectiveness of a dual pathway inhibition (DPI) strategy in acute and chronic ASCVD. When used in combination, aspirin and low-dose rivaroxaban work synergistically to inhibit platelet activation and thrombin generation, thereby preventing thrombus formation. Among patients with recent acute coronary syndrome (ACS), those with positive cardiac biomarkers or ST-segment elevation myocardial infarction, or a history of heart failure derive the greatest absolute benefits. Among patients with chronic ASCVD, those with involvement of two or more vascular beds, heart failure, chronic kidney disease, or diabetes derive the greatest absolute benefits. Additional trials are underway to assess the impact of DPI therapy in other populations of interest, including patients with ACS at high risk of left ventricular thrombus formation, intracranial atherosclerotic disease with recent transient ischemic attack or stroke, peripheral arterial disease with limiting claudication or post lower extremity revascularization, and advanced chronic kidney disease with ASCVD or risk factors for ASCVD. Further work is required to assess the possible added benefit of combining rivaroxaban with clopidogrel or ticagrelor instead of aspirin.

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