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Influence of different antiplatelet treatment regimens for primary percutaneous coronary intervention on all-cause
Adam Witkowski1, Pawel Maciejewski, Wojciech Wasek
1Cardiac Catheterization Laboratory, Institute of Cardiology, 04-628 Warsaw, Poland. witkowski@hbz.pl
Insights
Aspirin alone was less effective than other antiplatelet regimens in reducing mortality after primary PCI for STEMI. Combination therapy with glycoprotein IIb/IIIa inhibitors and clopidogrel did not offer additional survival benefits over clopidogrel alone.
Area of Science:
- Cardiology
- Interventional Cardiology
- Pharmacology
Background:
- Primary percutaneous coronary intervention (PCI) is a key treatment for ST-segment elevation myocardial infarction (STEMI).
- Antiplatelet therapy is crucial in managing STEMI patients undergoing primary PCI.
- Different in-catheter laboratory antiplatelet regimens may impact patient outcomes.
Purpose of the Study:
- To evaluate the impact of various in-catheter laboratory antiplatelet strategies on 1-year all-cause mortality.
- To compare the effectiveness of glycoprotein IIb/IIIa inhibitors and clopidogrel, alone or in combination, versus aspirin alone in primary PCI for STEMI.
Main Methods:
- A large, multicenter registry analysis of 7193 patients undergoing primary PCI for STEMI.
- Patients were categorized based on their in-catheter laboratory antiplatelet treatment: aspirin alone, glycoprotein IIb/IIIa inhibitors alone, clopidogrel alone, or combination therapy.
- Propensity-adjusted survival analysis was used to compare 1-year all-cause mortality rates among the groups.
Main Results:
- One-year mortality rates varied across groups: aspirin alone (10.4%), GP IIb/IIIa inhibitors alone (9.0%), clopidogrel alone (9.7%), and combination therapy (15.3%).
- Propensity-adjusted analysis revealed significantly lower mortality with GP IIb/IIIa inhibitors alone, clopidogrel alone, and combination therapy compared to aspirin alone.
- No significant survival benefit was observed for combination therapy over clopidogrel monotherapy.
Conclusions:
- In primary PCI for STEMI, using glycoprotein IIb/IIIa inhibitors and clopidogrel, individually or combined, is associated with reduced 1-year all-cause mortality compared to aspirin alone.
- Adding glycoprotein IIb/IIIa inhibitors to a 300 mg loading dose of clopidogrel did not provide further mortality reduction.
Aims:
The aim of this analysis was to examine the influence of different in-cath-lab antiplatelet regimens for the primary percutaneous coronary intervention (PCI) on all-cause mortality.
Methods And Results:
The study group consisted of 7193 patients (pts) undergoing primary PCI in 38 centres in 2003 in Poland. All patients received pretreatment with 300 mg of aspirin, 992 pts (14%) received glycoprotein (GP) IIb/IIIa inhibitors, 2690 pts (37%) were treated with 300 mg loading dose of clopidogrel, and 1566 (22%) received combined antiplatelet treatment with both GP IIb/IIIa inhibitors and clopidogrel. Remaining 1945 patients (27%) did not receive GP IIb/IIIa inhibitors or clopidogrel. Primary endpoint of the study was all-cause mortality up to 1 year from ST-segment elevation myocardial infarction (STEMI). One year mortality rates in the four groups were: 10.4%, 9.0%, 9.7%, and 15.3%, respectively. Propensity-adjusted survival analysis showed significant reduction of mortality for combination therapy with GP IIb/IIIa inhibitors and clopidogrel, clopidogrel alone, and GP IIb/IIIa inhibitors alone over aspirin alone. No additive effect on survival was seen for a combination therapy with GP IIb/IIIa inhibitors and clopidogrel in comparison to treatment with clopidogrel alone.
Conclusion:
In this large cohort, multicentre STEMI registry in-cath-lab use of GP IIb/IIIa inhibitors and clopidogrel alone or in combination was associated with the reduction of 1 year all-cause mortality in the setting of primary PCI in comparison with aspirin only. However, the use of GP IIb/IIIa inhibitors on top of 300 mg loading dose of clopidogrel did not further reduce mortality.
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