Key result
Short-term dual antiplatelet therapy for 1 to 3 months is feasible for most patients following percutaneous coronary intervention, while long-term therapy may benefit those at high ischemic risk.
Why the study?
Optimal DAPT duration, selection of P2Y12 inhibitor, SAPT choice, and combining oral anticoagulation remain controversial challenges in balancing ischemic and bleeding risks after PCI.
What is the optimal antithrombotic therapy regimen to balance ischemic protection and bleeding risk in patients undergoing PCI?
What is the optimal antithrombotic therapy regimen to balance ischemic protection and bleeding risk in patients undergoing PCI?
Answers are grounded in this paper and cite their sources.
This review summarizes current evidence on optimizing antithrombotic therapy after PCI to balance the prevention of ischemic events with the risk of bleeding.
Percutaneous coronary intervention (PCI) has become a standard-of-care procedure in the setting of angina or acute coronary syndrome. Antithrombotic therapy is the cornerstone of pharmacological treatment aimed at preventing ischemic events following PCI. Dual antiplatelet therapy as the combination of aspirin and P2Y12 inhibitor has been proven to decrease stent-related thrombotic risks. However, the optimal duration of dual antiplatelet therapy, an appropriate P2Y12 inhibitor, and the choice of aspirin versus P2Y12 inhibitor as single antiplatelet therapy remain controversial. Furthermore, the combined use of oral anticoagulation in addition to antiplatelet therapy is a complex issue in clinical practice, such as in patients with atrial fibrillation. The key challenge concerning the optimal antithrombotic regimen is ensuring a balance between protection against thrombotic events and against excessive increases in bleeding risk. In this review article, we summarize the current evidence concerning antithrombotic therapy in patients with coronary artery disease undergoing PCI.
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Saito et al. (2019) conducted a review in Coronary artery disease undergoing percutaneous coronary intervention. Antithrombotic therapy was evaluated. Short-term dual antiplatelet therapy for 1 to 3 months is feasible for most patients following percutaneous coronary intervention, while long-term therapy may benefit those at high ischemic risk.
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