Survival benefit with concomitant clopidogrel and glycoprotein IIb/IIIa inhibitor therapy at ad hoc percutaneous coronary intervention
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Published on: March 15, 2022
Richard J Gumina1, Eric H Yang, Gurpreet S Sandhu
1Ohio State University, Columbus, USA.
Insights
Combining glycoprotein (GP) IIb/IIIa inhibitors with clopidogrel during percutaneous coronary interventions (PCI) significantly lowers 30-day and long-term mortality. This dual antiplatelet therapy approach improves survival rates in patients undergoing PCI.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Glycoprotein (GP) IIb/IIIa inhibitors are potent antiplatelet agents used in percutaneous coronary interventions (PCI).
- Concomitant use with clopidogrel, a P2Y12 inhibitor, represents a dual antiplatelet therapy (DAPT) strategy.
- Understanding the clinical outcomes of this combined regimen in ad hoc PCI is crucial for optimizing patient management.
Purpose of the Study:
- To evaluate the impact of GP IIb/IIIa inhibitors combined with clopidogrel on clinical outcomes.
- To assess both short-term (30-day) and long-term mortality in patients undergoing ad hoc PCI.
Main Methods:
- A retrospective study of patients undergoing elective or urgent ad hoc PCI between March 1998 and December 2006.
- Stratification of patients based on the administration of GP IIb/IIIa inhibitors with concomitant clopidogrel.
- Propensity score analysis was employed to adjust for baseline differences and confounding factors.
Main Results:
- Long-term mortality was significantly lower in patients receiving GP IIb/IIIa inhibitors at the time of PCI (P<.001).
- After propensity adjustments, a significant reduction in 30-day mortality was observed (HR, 0.56; P=.01).
- Long-term survival significantly improved with GP IIb/IIIa inhibitor use, persisting after adjustments (HR, 0.88; P=.021).
- Patients treated with drug-eluting stents showed improved adjusted long-term mortality.
Conclusions:
- Coadministration of GP IIb/IIIa inhibitors and dual antiplatelet therapy is associated with reduced risk-adjusted mortality in ad hoc PCI.
- This combination therapy appears to be a safe and effective strategy for improving survival in this patient population.
Objective:
To study clinical outcomes in patients given glycoprotein (GP) IIb/IIIa inhibitors with concomitant clopidogrel at the time of ad hoc percutaneous coronary interventions (PCI).
Patients And Methods:
We studied 30-day and long-term outcomes of patients undergoing elective or urgent PCI from March 1, 1998, to December 31, 2006, stratified by administration of GP IIb/IIIa inhibitors with concomitant clopidogrel treatment at the time of ad hoc PCI.
Results:
The mean+/-SD age was 66.3+/-11.9 years in 5196 patients receiving compared with 67.8+/-11.8 years in 4681 patients not receiving a GP IIb/IIIa inhibitor (P<.001). Overall, 30-day unadjusted mortality was lower in patients who received a GP IIb/IIIa inhibitor (1.0% vs 1.2%; P=.22). Long-term mortality was significantly lower (P<.001) in patients receiving GP IIb/IIIa inhibitors at the time of PCI. After propensity analysis to adjust for the likelihood of receiving GP IIb/IIIa inhibitors on the basis of clinical, angiographic, and procedural characteristics, a significant reduction in 30-day mortality with GP IIb/IIIa inhibitor use was identified (hazard ratio, 0.56; 95% confidence interval, 0.36-0.87; P=.01). Kaplan-Meier analysis (median follow-up, 48 months) revealed a significant improvement in long-term survival in patients receiving a GP IIb/IIIa inhibitor at the time of ad hoc PCI that persisted after propensity adjustments (hazard ratio, 0.88; 95% confidence interval, 0.79-0.98; P=.021). Patients treated with drug-eluting stents showed a significant improvement in adjusted long-term mortality.
Conclusion:
In patients undergoing elective or urgent ad hoc PCI, coadministration of a GP IIb/IIIa inhibitor and dual antiplatelet therapy is associated with reduced risk-adjusted 30-day and long-term mortality.
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