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Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention

Potent antiplatelet therapy after primary percutaneous coronary intervention (PCI) has the potential to reduce infarct size. This study analyzed the association between on-treatment platelet reactivity and myocardial infarct size in patients with ST-segment elevation myocardial infarction (STEMI) un...

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Autores principales: Park, Seohwa, Yun, Kyeong Ho, Cho, Jae Young, Lee, Seung-Yul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chonnam National University Medical School 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485085/
https://www.ncbi.nlm.nih.gov/pubmed/34621641
http://dx.doi.org/10.4068/cmj.2021.57.3.204
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author Park, Seohwa
Yun, Kyeong Ho
Cho, Jae Young
Lee, Seung-Yul
author_facet Park, Seohwa
Yun, Kyeong Ho
Cho, Jae Young
Lee, Seung-Yul
author_sort Park, Seohwa
collection PubMed
description Potent antiplatelet therapy after primary percutaneous coronary intervention (PCI) has the potential to reduce infarct size. This study analyzed the association between on-treatment platelet reactivity and myocardial infarct size in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary PCI. In this single-center, retrospective study, 253 patients who underwent primary PCI for STEMI were divided into two groups according to platelet reactivity measurements (53 patients in the high platelet reactivity [HPR] group and 200 in the non-HPR group). Technetium Tc-99m tetrofosmin single-photon emission computed tomography (SPECT) was performed before hospital discharge. We measured the infarct size using SPECT imaging and serial cardiac biomarker levels, and compared the infarct sizes of each group. The patients with HPR were older (65.5±13.2 vs. 60.6±12.1 years, p=0.011) than the patients with non-HPR. On the other hand, the non-HPR group had a higher incidence of smoking (26.4% vs. 51.0%, p=0.001) than the HPR group. Infarct size was similar between the two groups (22.6±17.3% vs. 24.8±17.7%, p=0.416). Multivariate analysis revealed that onset to balloon time >240 min (odds ratio [OR]=1.92; 95% confidence interval [CI]=1.08–3.40; p=0.025) and anterior infarction (OR=5.28; 95% CI=3.05–9.14; p<0.001) were independent predictors of large (>22%) infarct size. HPR was not a predictor of infarct size assessed by SPECT. The two groups also showed analogous cumulative creatinine kinase-myocardial band and troponin T levels. In conclusion, compared to non-HPR, HPR showed no significant association with myocardial infarct size measured by SPECT imaging in early phase of MI.
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spelling pubmed-84850852021-10-06 Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention Park, Seohwa Yun, Kyeong Ho Cho, Jae Young Lee, Seung-Yul Chonnam Med J Original Article Potent antiplatelet therapy after primary percutaneous coronary intervention (PCI) has the potential to reduce infarct size. This study analyzed the association between on-treatment platelet reactivity and myocardial infarct size in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary PCI. In this single-center, retrospective study, 253 patients who underwent primary PCI for STEMI were divided into two groups according to platelet reactivity measurements (53 patients in the high platelet reactivity [HPR] group and 200 in the non-HPR group). Technetium Tc-99m tetrofosmin single-photon emission computed tomography (SPECT) was performed before hospital discharge. We measured the infarct size using SPECT imaging and serial cardiac biomarker levels, and compared the infarct sizes of each group. The patients with HPR were older (65.5±13.2 vs. 60.6±12.1 years, p=0.011) than the patients with non-HPR. On the other hand, the non-HPR group had a higher incidence of smoking (26.4% vs. 51.0%, p=0.001) than the HPR group. Infarct size was similar between the two groups (22.6±17.3% vs. 24.8±17.7%, p=0.416). Multivariate analysis revealed that onset to balloon time >240 min (odds ratio [OR]=1.92; 95% confidence interval [CI]=1.08–3.40; p=0.025) and anterior infarction (OR=5.28; 95% CI=3.05–9.14; p<0.001) were independent predictors of large (>22%) infarct size. HPR was not a predictor of infarct size assessed by SPECT. The two groups also showed analogous cumulative creatinine kinase-myocardial band and troponin T levels. In conclusion, compared to non-HPR, HPR showed no significant association with myocardial infarct size measured by SPECT imaging in early phase of MI. Chonnam National University Medical School 2021-09 2021-09-24 /pmc/articles/PMC8485085/ /pubmed/34621641 http://dx.doi.org/10.4068/cmj.2021.57.3.204 Text en © Chonnam Medical Journal, 2021 https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Seohwa
Yun, Kyeong Ho
Cho, Jae Young
Lee, Seung-Yul
Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention
title Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention
title_full Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention
title_fullStr Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention
title_full_unstemmed Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention
title_short Platelet Reactivity Was Not Associated with Infarct Size after Primary Percutaneous Coronary Intervention
title_sort platelet reactivity was not associated with infarct size after primary percutaneous coronary intervention
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8485085/
https://www.ncbi.nlm.nih.gov/pubmed/34621641
http://dx.doi.org/10.4068/cmj.2021.57.3.204
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