Biological efficacy of a 600 mg loading dose of clopidogrel in ST-elevation myocardial infarction

Optimal platelet reactivity (PR) inhibition is critical to prevent thrombotic events in primary percutaneous coronary intervention (PCI). We aimed to determine the relationship between high on-treatment platelet reactivity (HTPR) and ST-elevation myocardial infarction (STEMI) following a 600 mg load...

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Veröffentlicht in:Thrombosis and haemostasis 2012-07, Vol.108 (1), p.101-106
Hauptverfasser: Bonello, Laurent, Berbis, Julie, Laine, Marc, Armero, Sébastien, Bessereau, Jacques, Jacquin, Laurent, Bonello, Caroline, Camillieri, Elise, Barragan, Paul, Dignat-George, Françoise, Paganelli, Franck, Camoin-Jau, Laurence
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Sprache:eng
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Zusammenfassung:Optimal platelet reactivity (PR) inhibition is critical to prevent thrombotic events in primary percutaneous coronary intervention (PCI). We aimed to determine the relationship between high on-treatment platelet reactivity (HTPR) and ST-elevation myocardial infarction (STEMI) following a 600 mg loading dose (LD) of clopidogrel. We performed a prospective monocentre study enrolling patients on clopidogrel undergoing PCI. The VASP index was used to assess PR inhibition after clopidogrel LD. HTPR was defined according to the consensus as a VASP index ≥50%. The present study included 833 patients undergoing PCI. Most patients had PCI for an acute coronary syndrome (58.7%). The mean VASP index was 50 ± 23% with a large inter-individual variability (range: 1–94%). Patients with a VASP index ≥50% were significantly older (p= 0.03), with a higher body mass index (BMI) (p
ISSN:0340-6245
2567-689X
DOI:10.1160/TH12-02-0125