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Switch from abciximab to eptifibatide during percutaneous coronary intervention
Magnus Wahlin1, Per Albertsson, Thomas Karlsson
1The Department of Molecular and Clinical Medicine/Cardiology, Sahlgrenska University Hospital and Gothenburg University, Sweden.
Insights
Switching from abciximab to eptifibatide for glycoprotein IIb/IIIa inhibition during percutaneous coronary intervention (PCI) did not show significant clinical outcome differences up to six months. Further studies are needed to confirm if eptifibatide is a safe alternative to abciximab in PCI.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Pharmacology
Background:
- Glycoprotein (GP) IIb/IIIa inhibitors are crucial for reducing ischemic complications during percutaneous coronary intervention (PCI).
- Abciximab is well-documented but more expensive than eptifibatide.
- This study investigates the clinical outcomes following a switch from abciximab to eptifibatide.
Purpose of the Study:
- To evaluate the clinical outcomes up to six months after switching from abciximab to eptifibatide for GPIIb/IIIa inhibition during PCI.
- To compare the safety and efficacy of eptifibatide versus abciximab in a real-world clinical setting.
Main Methods:
- A cohort study followed 660 patients undergoing de novo PCI.
- Patients received either abciximab (n=310) or eptifibatide (n=350) for GPIIb/IIIa inhibition.
- Clinical outcomes were assessed up to six months post-PCI, comparing patients before and after the drug switch.
Main Results:
- Baseline characteristics were similar between the abciximab and eptifibatide groups.
- Trends suggested lower in-hospital (0.6% vs 2.0%) and six-month mortality (2.3% vs 3.7%) with abciximab, though not statistically significant (NS).
- The combined endpoint of death, myocardial infarction, stroke, revascularization, and bleeding occurred in 14.9% (abciximab) vs 16.8% (eptifibatide) (NS).
Conclusions:
- No significant clinical outcome deterioration was observed after switching from abciximab to eptifibatide for routine GPIIb/IIIa inhibition during PCI.
- A clinically significant difference between the two agents cannot be excluded due to the limited sample size.
- Eptifibatide appears to be a viable alternative to abciximab in this patient population.
Background:
Treatment with glycoprotein (GP) IIb/IIIa inhibitors during percutaneous coronary intervention (PCI) reduce ischemic complications and improve outcome. Of the GPIIb/IIIa inhibitors abciximab is better documented than eptifibatide, but the former is more expensive. The aim of this study was to monitor a switch from abciximab to eptifibatide with respect to clinical outcome up to six months after PCI.
Methods:
All consecutive patients that six months before and six months after a switch from abciximab to eptifibatide received GPIIb/IIIa inhibitors during and after de novo PCIs were followed for six months with respect to clinical outcome.
Results:
310 patients received abciximab and 350 eptifibatide. Baseline characteristics were similar in the two groups. 55% of the patients underwent PCI for acute ST-elevation myocardial infarction and 41% for unstable coronary artery disease. There were trends for lower mortality among abciximab-treated than among the eptifibatide-treated patients during in-hospital stay (0.6% vs 2.0%:NS) as well as during the six month follow up (2.3% vs 3.7%:NS). The combined endpoint of death, myocardial infarction, stroke, repeated revascularisation and serious bleeding occurred in 14.9% in the abciximab group vs 16.8% in the eptifibatide group (NS).
Conclusion:
The study could not demonstrate any significant deterioration of clinical results after a switch from abciximab to eptifibatide as routine GPIIb/IIIa inhibition during PCI. With respect to the limited number of patients a clinical significant difference between the two GPIIb/IIIa inhibitors cannot, however, be excluded.
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