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Strategies to optimize initial P2Y12 inhibitor therapy in STEMI patients
Alexandra C Millhuff1, James C Blankenship2
1Department of Internal Medicine, University of New Mexico, Albuquerque, NM, USA.
Insights
Dual antiplatelet therapy is standard for ST-elevation myocardial infarction (STEMI) patients undergoing percutaneous coronary intervention (PCI). Optimal P2Y12 inhibitor use, like ticagrelor and prasugrel, in STEMI is still evolving, with crushing/chewing as an alternative strategy.
Area of Science:
- Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 inhibitor is standard for ST-elevation myocardial infarction (STEMI) patients post-percutaneous coronary intervention (PCI).
- While DAPT reduces ischemic events, optimal P2Y12 inhibitor administration strategies in STEMI remain under investigation.
Purpose of the Study:
- This review summarizes current evidence on the optimal use of ticagrelor and prasugrel during the acute phase of STEMI.
Main Methods:
- Literature review of current evidence on ticagrelor and prasugrel use in STEMI.
- Analysis of strategies for rapid platelet inhibition in the acute STEMI setting.
Main Results:
- High platelet activity in acute STEMI and PCI necessitates rapid and adequate platelet inhibition.
- Increased ticagrelor/prasugrel loading doses or earlier administration have not fully bridged the platelet inhibition gap.
- Strategies like bridging with intravenous agents or crushing/chewing oral tablets are being explored to enhance early ticagrelor/prasugrel efficacy.
Conclusions:
- Oral ticagrelor/prasugrel before or immediately after STEMI PCI typically suffices to prevent thrombotic complications.
- Crushing or chewing ticagrelor/prasugrel tablets offers an alternative to intravenous P2Y12 inhibitors when faster inhibition is needed or oral administration is difficult.
Introduction:
Dual antiplatelet therapy (DAPT) with aspirin and a P2Y12 inhibitor is the standard of care for patients who undergo percutaneous coronary intervention (PCI) for ST elevation myocardial infarction (STEMI). Though this regimen reduces rates of ischemic events in patients with STEMI, the optimal strategy for P2Y12 administration in STEMI patients is still evolving.
Purpose:
The purpose of this review is to summarize current evidence on optimal use of ticagrelor and prasugrel in the acute phase of STEMI.
Summary:
Due to high platelet activity in the acute setting of STEMI and PCI, adequate and rapid platelet inhibition is important. Strategies of increased ticagrelor/prasugrel loading dose or earlier administration in STEMI have not been successful in closing this platelet inhibition gap. Potential strategies for improving ticagrelor/prasugrel use early in STEMI include bridging with intravenous antiplatelet agents or crushed or chewed administration.
Conclusion:
Oral ticagrelor/prasugrel given before or immediately after STEMI PCI is usually sufficient to prevent thrombotic complications. When faster platelet inhibition is desired, or oral administration is compromised by inability to swallow tablets, crushing/chewing ticagrelor/prasugrel tablets is an alternative to intravenous P2Y12 inhibitor therapy.
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