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High on-treatment platelet reactivity to aspirin in patients after myocardial infarction.

Authors :
Stolarek, Wioleta
Kasprzak, Michał
Sikora, Joanna
Siemińska, Emilia
Grześk, Grzegorz
Source :
Biomedicine & Pharmacotherapy. Mar2022, Vol. 147, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Aspirin (ASA) is widely used as an antiplatelet therapeutic drug in secondary prevention. Last years brought many reports on ASA resistance or high on-treatment platelet reactivity (HTPR) to aspirin.This study is a post-hoc prospective analysis with 30 patients evaluated during follow up on average of 6.3 years after hospitalization from myocardial infarction. The examined population was divided into two subgroups according to the response to ASA. In order to estimate the function of blood platelets and their responsiveness to acetylsalicylic acid therapy, ASPI-test was used. The measurements were performed by the method of whole blood impedance aggregometry. During long-term follow up significantly higher percentage of high platelet reactivity was observed, compared with previous visits (p = 0.00001). Considering clinical endpoints of the research that were connected with coronary disease, no differences were obtained.The frequency of HTPR to aspirin in this study was higher than data reported in literature among subjects with CV diseases. In long-term observation the highest percentage of ASA non-responders was reported (58.6%). HTPR to aspirin did not affect the presence of the clinical endpoints for the study. [Display omitted] • The frequency of ASA resistance was higher than data reported in literature among subjects with cardiovascular diseases. • In long-term observation the highest percentage of ASA non-responders was reported. • The presence of ASA resistance did not affect the presence of the clinical endpoints for the study. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07533322
Volume :
147
Database :
Academic Search Index
Journal :
Biomedicine & Pharmacotherapy
Publication Type :
Academic Journal
Accession number :
155208107
Full Text :
https://doi.org/10.1016/j.biopha.2022.112618