Thromb Haemost 2009; 102(02): 404-411
DOI: 10.1160/TH09-02-0126
New Technologies, Diagnostic Tools and Drugs
Schattauer GmbH

Response to aspirin in healthy individuals

Cross-comparison of light transmission aggregometry, VerifyNow system, platelet count drop, thromboelastography (TEG) and urinary 11-dehydrothromboxane B2
Normand Blais
1   Hematology and blood bank department, CHUM, Hôpital Notre Dame, Montréal, Québec, Canada
3   Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada
,
Chantal Pharand
2   Faculty of Pharmacy, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
4   Research Center, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
5   Department of Pharmacy, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
,
Marie Lordkipanidzé
2   Faculty of Pharmacy, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
4   Research Center, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
5   Department of Pharmacy, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
,
Ying K. Sia
4   Research Center, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
,
Yahye Merhi
7   Montreal Heart Institute Research Center, Montréal, Québec, Canada
,
Jean G. Diodati
3   Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada
4   Research Center, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
6   Division of Cardiology, Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada
› Author Affiliations
Financial support: This study was made possible through a grant from the Fondation de l’Hôpital du Sacré-Coeur de Montréal, Montréal, Canada. Normand Blais and Marie Lordkipanidzé are recipients of Training Awards from the Fonds de recherche en santé du Québec.
Further Information

Publication History

Received: 25 February 2009

Accepted after minor revision: 26 March 2009

Publication Date:
22 November 2017 (online)

Summary

Variable biological effect of aspirin is suggested to be related to pharmacological resistance. The incidence of this so-called “resistant” state varies with the study population and the assay used. We determined performance features of five assays used to assess aspirin effects in non-smoking healthy volunteers not taking any drug known to interfere with platelet function. Blood and urine samples were obtained immediately before and after 8–10 days of aspirin 80 mg intake. Forty-five participants 19–59 years old were enrolled. The sensitivity (SE), specificity (SP), and optimal cut-off (CO) value to detect the effect of aspirin were: light transmission aggregometry (LTA) with 1.6 mM arachidonic acid (AA) – SE 100%,SP 95.9%,CO 20%;LTA with adenosine diphosphate (ADP) 10 µM – SE 84.4%, SP 77.8%, CO 70%; Ver-

* Institution where work was carried out: Hôpital du Sacré-Cœur de Montréal, Montréal, Québec, Canada


 
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