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Optimal platelet inhibition in patients undergoing PCI: data from the Multicenter Registry of High-Risk Percutaneous
H M Mardikar1, M S Hiremath, David J Moliterno
1Spandan Heart Institute, Nagpur, India.
Insights
High-dose tirofiban achieved greater platelet inhibition than eptifibatide in high-risk PCI patients. Clopidogrel enhanced inhibition at 24 hours, not acutely with glycoprotein IIb/IIIa inhibitors.
Area of Science:
- Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Optimal platelet inhibition is crucial for preventing ischemic events during percutaneous coronary intervention (PCI).
- Comparing antiplatelet regimens is essential for high-risk PCI patients.
Purpose of the Study:
- To compare the efficacy of tirofiban and eptifibatide, with or without clopidogrel, in achieving optimal platelet inhibition.
- To evaluate different antiplatelet strategies in patients undergoing elective high-risk PCI.
Main Methods:
- A randomized open-label study involving 120 patients across 3 Indian heart centers.
- Patients were assigned to receive tirofiban, eptifibatide, tirofiban + clopidogrel, or eptifibatide + clopidogrel.
- Platelet aggregation inhibition (IPA) was the primary outcome, measured at 10 minutes, 6-8 hours, and 24 hours post-treatment.
Main Results:
- High-dose tirofiban demonstrated significantly higher IPA at 10 minutes (95.88% vs 91.22%) and 6-8 hours (93.11% vs 85.45%) compared to eptifibatide.
- More patients achieved >95% IPA with the high-dose tirofiban regimen.
- Clopidogrel addition did not acutely increase IPA from intravenous glycoprotein IIb/IIIa inhibitors but showed an effect at 24 hours.
Conclusions:
- High-dose tirofiban provides superior platelet inhibition compared to eptifibatide in high-risk PCI patients.
- The combination of clopidogrel with glycoprotein IIb/IIIa inhibitors shows a delayed benefit in platelet inhibition.
- These findings support optimizing antiplatelet therapy for improved outcomes in PCI procedures.
Background:
Optimal inhibition of platelet aggregation (IPA) may afford greater protection against ischemic events during percutaneous coronary intervention (PCI). The objective of this study was to test several antiplatelet regimens in elective high-risk PCI patients by comparing different combinations of glycoprotein IIb/IIIa inhibitors and clopidogrel.
Methods:
The study was a randomized open-label study at 3 heart centers in India. One hundred twenty patients were enrolled between July 2006 and September 2006. Patients were randomized to 1 of the 4 groups: group A--tirofiban, group B--eptifibatide, group C--tirofiban + clopidogrel 600-mg loading dose, and group D--eptifibatide + clopidogrel 600-mg loading dose. All patients received a clopidogrel maintenance dose after PCI. The primary outcome measure was the IPA assessed at 10 minutes, at 6 to 8 hours, and at 24 hours.
Results:
The IPA was higher with high-dose tirofiban compared with eptifibatide at 10 minutes (95.88 +/- 5.85% vs 91.22 +/- 7.52%, P = .003) and at 6 to 8 hours (93.11 +/- 7.6% vs 85.45 +/- 11.03, P < .001). Significantly more patients achieved >95% IPA with the high-dose tirofiban regimen.
Conclusions:
This head-to-head study comparing high-dose tirofiban with double-bolus eptifibatide demonstrated higher degree of platelet inhibition with high-dose tirofiban at 10 minutes and at 6 to 8 hours in patients undergoing elective high-risk PCI. The addition of clopidogrel did not acutely extend the IPA from intravenous glycoprotein IIb/IIIa inhibitors, but did so at 24 hours.
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