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Updated: Jun 18, 2026

Interventional Diagnostic Procedure: A Practical Guide for the Assessment of Coronary Vascular Function
Published on: March 15, 2022
Are glycoprotein inhibitors safe during percutaneous coronary intervention in patients on chronic warfarin treatment?
Heli Lahtela1, Pasi P Karjalainen, Matti Niemelä
1Department of Medicine, Turku University Hospital, Turku, Finland.
Insights
Glycoprotein IIb/IIIa inhibitors (GPIs) significantly increase major bleeding risk in atrial fibrillation patients undergoing percutaneous coronary intervention (PCI) on warfarin. Caution is advised when using GPIs in this high-risk population.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Atrial fibrillation (AF) patients often require anticoagulation with warfarin.
- Percutaneous coronary intervention (PCI) is a common procedure for coronary artery disease.
- The safety of glycoprotein IIb/IIIa inhibitors (GPIs) in AF patients on warfarin undergoing PCI is not well-established.
Purpose of the Study:
- To evaluate the safety of using GPIs during PCI in patients with AF on chronic warfarin therapy.
- To identify risk factors for major bleeding in this patient cohort.
Main Methods:
- Retrospective analysis of 377 AF patients on warfarin undergoing PCI across seven centers.
- Data collection included periprocedural GPI use, bleeding events, access site complications, and major adverse cardiovascular events.
- Multivariable analysis and propensity score adjustment were used to assess the impact of GPIs on bleeding risk.
Main Results:
- 29% of patients received periprocedural GPIs, with significant inter-hospital variation.
- GPI use was higher in patients with ST-elevation myocardial infarction.
- Major bleeding occurred more frequently in patients treated with GPIs (9.0% vs. 1.5%, p=0.001).
- GPI use (OR 5.1) and older age (OR 1.2) were independent predictors of major bleeding.
- GPIs remained a significant predictor of major bleeding even after propensity score adjustment (OR 3.8).
- Periprocedural INR levels and warfarin pause did not predict major bleeding in the GPI group.
Conclusions:
- GPIs significantly increase the risk of major bleeding in AF patients on warfarin undergoing PCI.
- The increased bleeding risk associated with GPIs is independent of periprocedural INR levels.
- GPIs should be used with caution in this fragile patient population due to elevated bleeding risk.
Abstract:
The aim of this study was to evaluate the safety of glycoprotein IIb/IIIa inhibitors (GPIs) during percutaneous coronary intervention (PCI) in patients on chronic warfarin therapy due to atrial fibrillation (AF). We analysed all consecutive AF patients (N = 377, mean age 70 years, male 71%) on warfarin therapy referred for PCI in seven centres. Major bleeding, access site complications and major adverse cardiovascular events were recorded during hospitalisation. A total of 111 patients (29%) received periprocedural GPIs with a wide inter-hospital variation in their use (range 3-68%). The use of GPIs increased with the severity of the disease presentation and 49% of patients with ST-elevation myocardial infarction received GPIs. Mean periprocedural international normalised ratio (INR) of patients who received GPIs was 1.89 (range 1.1-3.3). Major bleeding was more common in the patients treated with GPIs (9.0% vs. 1.5%, p = 0.001) than in those without GPIs, but there was no difference in major adverse cardiovascular events between the groups. In multivariable analysis, use of GPIs (odds ratio [OR] 5.1, 95% confidence interval [CI] 1.3-20.6, p = 0.02) and old age (OR 1.2, 95% CI 1.0-1.3, p= 0.02) remained as the only independent predictors of major bleeding. Also after adjusting for propensity score, GPIs remained as a significant predictor of major bleeding (OR 3.8, 95% CI 1.03-14.1, p = 0.045). In the GPI group, major bleeding was not predicted by INR level or warfarin pause. GPIs increase the risk of major bleeding events irrespective of periprocedural INR levels and should be used with caution in this fragile patient group.
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