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P2Y12 Inhibitor Monotherapy: Considerations for Acute and Long-Term Secondary Prevention Post-PCI
Antonio Greco1, Maria Sara Mauro1, Davide Capodanno1
1Division of Cardiology, Azienda Ospedaliero-Universitaria Policlinico "G. Rodolico - San Marco", 95125 Catania, Italy.
Insights
Dual antiplatelet therapy (DAPT) after PCI may transition to P2Y12 inhibitor monotherapy. This approach reduces bleeding risk without increasing ischemic events, offering a safer alternative for secondary prevention in PCI patients.
Area of Science:
- Cardiology and Interventional Cardiology
- Pharmacology and Therapeutics
- Clinical Evidence and Guideline Updates
Background:
- Dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 inhibitor is standard after percutaneous coronary intervention (PCI).
- Long-term secondary prevention typically involves aspirin monotherapy post-DAPT.
- Emerging evidence supports P2Y12 inhibitor monotherapy in both acute and chronic settings post-PCI.
Purpose of the Study:
- To review current evidence on P2Y12 inhibitor monotherapy for secondary prevention after PCI.
- To assess the efficacy and safety of P2Y12 inhibitor monotherapy versus standard antiplatelet strategies.
- To explore the role of P2Y12 inhibitor monotherapy in patients requiring oral anticoagulation.
Main Methods:
- Review of accumulating evidence from clinical studies and randomized trials on P2Y12 inhibitor monotherapy.
- Analysis of outcomes including thrombotic complications, bleeding events, and net clinical benefit.
- Consideration of recent European and American guideline updates regarding antithrombotic therapy.
Main Results:
- Short-term DAPT followed by P2Y12 inhibitor monotherapy shows reduced bleeding without increased ischemic events compared to standard DAPT.
- Limited data on long-term P2Y12 inhibitor monotherapy suggests potential benefits over aspirin monotherapy.
- Guidelines now incorporate P2Y12 inhibitor monotherapy in specific post-PCI scenarios.
Conclusions:
- P2Y12 inhibitor monotherapy is a viable option for early and long-term secondary prevention post-PCI, particularly for reducing bleeding risk.
- Further research is needed to address remaining uncertainties and optimize antithrombotic strategies.
- Ongoing randomized trials aim to provide more definitive evidence on P2Y12 inhibitor monotherapy.
Abstract:
Following percutaneous coronary intervention (PCI), an initial course of dual antiplatelet therapy (DAPT) with aspirin and a inhibitor ( -i) is recommended to minimize the risk of thrombotic complications. After the initial period of DAPT, antiplatelet monotherapy, usually consisting of aspirin, is administered for long-term secondary prevention. However, over the last few years there has been accruing evidence on -i monotherapy, both in the acute (i.e., post-PCI; after a brief period of DAPT, transitioning to monotherapy before six or 12 months in patients with chronic or acute coronary syndrome, respectively) and chronic (i.e., long-term secondary prevention; after completion of six or 12 months of DAPT, in patients with chronic or acute coronary syndrome, respectively) settings. In aggregate, most studies of short DAPT with transition to -i monotherapy showed a reduced risk of bleeding complications, without any significant increase in ischemic events as compared to standard DAPT. On the other hand, the evidence on long-term -i monotherapy is scarce, but results from a randomized trial showed that clopidogrel monotherapy outperformed aspirin monotherapy in terms of net benefit, ischemic events and bleeding. Antiplatelet therapy is also recommended for patients undergoing PCI and with an established indication for long-term oral anticoagulation (OAC). In this scenario, a brief period of triple therapy (i.e., aspirin, -i and OAC) is followed by a course of dual antithrombotic therapy (usually with -i and OAC) and ultimately by lifelong OAC alone. European and American guidelines have been recently updated to provide new recommendations on antithrombotic therapy, including the endorsement of -i monotherapy in different settings. However, some areas of uncertainty still remain and further randomized investigations are ongoing to fulfil current gaps in knowledge. In this review, we assess the current knowledge and evidence on -i monotherapy for the early and long-term secondary prevention in patients undergoing PCI, and explore upcoming research and future directions in the field.
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