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727 Circadian variations of platelet reactivity on Clopidogrel in patients treated with elective percutaneous coronary intervention
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Abstract
Aims
The potential diurnal variations of platelet reactivity in patients on clopidogrel treated with elective percutaneous coronary intervention (PCI) for stable coronary artery disease (CAD) are currently unknown.
Methods and results
We prospectively enrolled 15 patients with stable CAD treated PCI and on clopidogrel therapy for at least eight days. All patients received their maintenance 75-mg clopidogrel dose at 8 AM. Platelet reactivity was assessed with the Verifynow P2Y12 assay at three different time points (10 AM, 6 PM, and 6 AM). Platelet reactivity is expressed as P2Y12 reaction units (PRU) and PRU thresholds ≥208 and ≥240 were used to define high platelet reactivity (HPR). A significant heterogeneity in diurnal levels of platelet reactivity was found (P = 0.0004), with a peak occurring at the 6 AM assessment. In addition, at the 6 AM evaluation patients showed the highest prevalence of HPR (53.3% of patients with PRU ≥240, 66.7% of patients with PRU ≥208).
Conclusions
Platelet reactivity in patients with stable CAD treated with PCI and taking clopidogrel in the morning follows a circadian rhythm, thus suggesting that platelet inhibition may not be constant and sufficient throughout the day. Whether an evening or a bis in die administration of clopidogrel may result in a constant and more reliable antiplatelet inhibition, should be investigated in dedicated studies.
Title: 727 Circadian variations of platelet reactivity on Clopidogrel in patients treated with elective percutaneous coronary intervention
Description:
Abstract
Aims
The potential diurnal variations of platelet reactivity in patients on clopidogrel treated with elective percutaneous coronary intervention (PCI) for stable coronary artery disease (CAD) are currently unknown.
Methods and results
We prospectively enrolled 15 patients with stable CAD treated PCI and on clopidogrel therapy for at least eight days.
All patients received their maintenance 75-mg clopidogrel dose at 8 AM.
Platelet reactivity was assessed with the Verifynow P2Y12 assay at three different time points (10 AM, 6 PM, and 6 AM).
Platelet reactivity is expressed as P2Y12 reaction units (PRU) and PRU thresholds ≥208 and ≥240 were used to define high platelet reactivity (HPR).
A significant heterogeneity in diurnal levels of platelet reactivity was found (P = 0.
0004), with a peak occurring at the 6 AM assessment.
In addition, at the 6 AM evaluation patients showed the highest prevalence of HPR (53.
3% of patients with PRU ≥240, 66.
7% of patients with PRU ≥208).
Conclusions
Platelet reactivity in patients with stable CAD treated with PCI and taking clopidogrel in the morning follows a circadian rhythm, thus suggesting that platelet inhibition may not be constant and sufficient throughout the day.
Whether an evening or a bis in die administration of clopidogrel may result in a constant and more reliable antiplatelet inhibition, should be investigated in dedicated studies.
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