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High on-treatment platelet reactivity and outcome in elderly with non ST-segment elevation acute coronary syndrome - Insight from the GEPRESS study.
- Source :
-
International journal of cardiology [Int J Cardiol] 2018 May 15; Vol. 259, pp. 20-25. - Publication Year :
- 2018
-
Abstract
- Background: Elderly treated with dual antiplatelet therapy after percutaneous coronary intervention (PCI) represent a challenging population because of increased risk of both ischemic and bleeding events. We aimed to investigate the association between high on-treatment platelet reactivity (HPR) and long-term outcome in elderly with non-ST-elevated acute coronary syndromes (NSTE-ACS) undergoing PCI.<br />Methods: Platelet reactivity was measured by vasodilator-stimulated phosphoprotein (VASP) assay at three time-points (baseline, discharge, 1 month after PCI) in 1053 NSTE-ACS patients (311 elderly) treated with clopidogrel. Major adverse cardiac events (MACE) were assessed up to 1 year-follow-up.<br />Results: Elderly with HPR at discharge showed a significantly higher incidence of overall MACE (13 vs 4%, p = .006), cardiac death (6 vs 0.7%, p = .020), myocardial infarction (MI, 12 vs 4%, p = .031) and a trend for higher stent-thrombosis (5 vs 0.7%, p = .068). Similarly, elderly with 1-month-HPR showed between 1 month and 1 year significantly higher incidence of MACE (10 vs 4%, p = .012), cardiac death (6 vs 0.7%, p = .019) and composite cardiac death/MI (11 vs 4%, p = .014). Up to 1 year, elderly with HPR showed a 4-fold increased risk of MACE compared to both elderly without HPR (for discharge-HPR: p = .005; for 1-month-HPR: p = .01) and non-elderly with HPR (for discharge-HPR: p < .001; for 1-month-HPR: p < .0001). At multivariable analysis, HPR could independently predict 1-year-MACE in elderly (for discharge-HPR: HR = 3.191, CI: 1.373-7.417, p = .007; for 1-month-HPR: HR = 3.542, CI: 1.373-9.137, p = .009).<br />Conclusions: In elderly with NSTE-ACS undergoing PCI and treated with clopidogrel, HPR was independently associated with an increased risk of MACE up to 1 year.<br /> (Copyright © 2018 Elsevier B.V. All rights reserved.)
- Subjects :
- Acute Coronary Syndrome blood
Acute Coronary Syndrome genetics
Aged
Aged, 80 and over
Female
Humans
Male
Middle Aged
Non-ST Elevated Myocardial Infarction blood
Non-ST Elevated Myocardial Infarction genetics
Platelet Activation drug effects
Platelet Aggregation Inhibitors pharmacology
Prospective Studies
Treatment Outcome
Acute Coronary Syndrome therapy
Non-ST Elevated Myocardial Infarction therapy
Percutaneous Coronary Intervention trends
Platelet Activation physiology
Platelet Aggregation Inhibitors therapeutic use
Polymorphism, Genetic genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1874-1754
- Volume :
- 259
- Database :
- MEDLINE
- Journal :
- International journal of cardiology
- Publication Type :
- Academic Journal
- Accession number :
- 29579602
- Full Text :
- https://doi.org/10.1016/j.ijcard.2018.01.057