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Updated: Jul 20, 2025

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Published on: March 15, 2022
Antithrombotic treatment following percutaneous coronary intervention in patients with high bleeding risk
Zaid I Almarzooq1,2,3,4, Nora M Al-Roub4, Scott Kinlay1,2,3
1Veterans Affairs Boston Healthcare System, West Roxbury.
Insights
For patients with high bleeding risk (HBR) after percutaneous coronary intervention (PCI), shorter dual antiplatelet therapy (DAPT) durations (1-3 months) reduce bleeding events without increasing ischemic risks. This review examines antithrombotic strategies for HBR patients post-PCI.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Medicine
Background:
- Patients with high bleeding risk (HBR) after percutaneous coronary intervention (PCI) often present with advanced age, prior bleeding history, anemia, chronic kidney disease, or require long-term anticoagulation.
- Managing antithrombotic therapy in HBR patients post-PCI is crucial to balance ischemic event prevention and bleeding complications.
Conclusions:
- Shorter DAPT durations (1-3 months) are effective in reducing bleeding events in HBR patients post-PCI.
- Antithrombotic de-escalation and timely switching strategies offer viable options for mitigating bleeding risk in this population.
- Further research is needed to establish long-term efficacy and safety profiles of these strategies.
Purpose Of Review:
Review the clinical outcomes of different antithrombotic strategies in patients with high bleeding risk (HBR) after percutaneous coronary intervention (PCI).
Recent Findings:
Patients with HBR after PCI include those with advanced age (e.g. >75 years of age), a prior history of major bleeding, anemia, chronic kidney disease, and those with indications for long-term anticoagulation. Strategies that successfully decrease bleeding risk in this population include shorter durations of dual antiplatelet therapy (DAPT; of 1-3 months) followed by single antiplatelet therapy with aspirin or a P2Y 12 inhibitor, or de-escalating from a more potent P2Y 12 inhibitor (prasugrel or ticagrelor) to less potent antiplatelet regimens (aspirin with clopidogrel or half-dose ticagrelor or half-dose prasugrel). Patients on DAPT, and a full dose anticoagulation for other indications, have a lower risk of major bleeding without an increase in 1-2-year adverse ischemic events, when rapidly switched from DAPT to a single antiplatelet therapy (within a week after PCI) with aspirin or clopidogrel. Longer term data on the benefits and risks of these strategies is lacking.
Summary:
In patients with HBR after PCI, shorter durations of DAPT (1-3 months) decrease the risk of major bleeding without increasing the risk of adverse ischemic events.
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