Abstract | AIMS: METHODS AND RESULTS: This retrospective observational study involves 3047 patients receiving dual-antiplatelet therapy who underwent PCI for NSTEMI. Primary outcome was all-cause mortality. Major adverse cardiac events ( MACE) were a secondary outcome. Mean follow-up was 4.6 years. Patients treated with GP IIb/IIIa inhibitors were younger with fewer comorbidities. Although the unadjusted Kaplan-Meier analysis suggested that GP IIb/IIIa inhibitor use was associated with improved outcomes, multivariate analysis (including propensity scoring) showed no benefit for either survival (P = 0.136) or MACE (P = 0.614). GP IIb/IIIa inhibitor use was associated with an increased risk of major bleeding (P = 0.021). CONCLUSION: Although GP IIb/IIIa inhibitor use appeared to improve outcomes after PCI for NSTEMI, patients who received GP IIb/IIIa inhibitors tended to be at lower risk. After multivariate adjustment we observed no improvement in MACE or survival and an increased risk of major bleeding.
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Authors | J P Howard, D A Jones, S Gallagher, K Rathod, S Antoniou, P Wright, C Knight, A Mathur, R Weerackody, A Wragg |
Journal | BioMed research international
(Biomed Res Int)
Vol. 2014
Pg. 643981
( 2014)
ISSN: 2314-6141 [Electronic] United States |
PMID | 24895595
(Publication Type: Journal Article, Observational Study)
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Chemical References |
- Platelet Aggregation Inhibitors
- Platelet Glycoprotein GPIIb-IIIa Complex
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Topics |
- Aged
- Electrocardiography
- Female
- Humans
- Kaplan-Meier Estimate
- Male
- Middle Aged
- Multivariate Analysis
- Myocardial Infarction
(drug therapy, mortality, physiopathology)
- Percutaneous Coronary Intervention
- Platelet Aggregation Inhibitors
(adverse effects, therapeutic use)
- Platelet Glycoprotein GPIIb-IIIa Complex
(antagonists & inhibitors, metabolism)
- Proportional Hazards Models
- Time Factors
- Treatment Outcome
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