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The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction

Left ventricular (LV) apical thrombus formation is a well described and clinically important complication of acute myocardial infarction (MI) with a substantial risk of thromboembolism. Alterations in the inflammatory status may contribute to this complication. The aim of this study was to evaluate...

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Autores principales: Tok, Derya, Ekizler, Firdevs Aysenur, Tak, Bahar Tekin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771313/
https://www.ncbi.nlm.nih.gov/pubmed/36550886
http://dx.doi.org/10.1097/MD.0000000000032215
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author Tok, Derya
Ekizler, Firdevs Aysenur
Tak, Bahar Tekin
author_facet Tok, Derya
Ekizler, Firdevs Aysenur
Tak, Bahar Tekin
author_sort Tok, Derya
collection PubMed
description Left ventricular (LV) apical thrombus formation is a well described and clinically important complication of acute myocardial infarction (MI) with a substantial risk of thromboembolism. Alterations in the inflammatory status may contribute to this complication. The aim of this study was to evaluate the predictive role of the systemic immune-inflammation index (SII) in identifying high risk patients who will develop an apical thrombus formation during the acute phase of anterior transmural infarction. Consecutive 1753 patients (mean age: 61.5 ± 9.6 years; male: 63.8 %) with first acute anterior MI who underwent primary percutaneous coronary intervention were assessed. Patients were divided into 2 groups according to the presence of apical thrombus. SII was calculated using the following equation: neutrophil (N) × platelet (P) ÷ lymphocyte (L). LV apical thrombus was detected on transthoracic echocardiogram in 99 patients (5.6%). Patients with an apical thrombus had lower LV ejection fraction, prolonged time from symptoms to treatment, higher rate of post-percutaneous coronary intervention thrombolysis in myocardial infarction flow ≤1 and significantly higher mean high-sensitivity C-reactive protein, and SII values and lower lymphocyte than those without an apical thrombus. Admission SII level was found to be a significant predictor for early LV apical thrombus formation complicating a first-ever anterior MI. This simple calculated tool may be used to identify high-risk patients for LV thrombus and individualization of targeted therapy.
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spelling pubmed-97713132022-12-23 The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction Tok, Derya Ekizler, Firdevs Aysenur Tak, Bahar Tekin Medicine (Baltimore) 3400 Left ventricular (LV) apical thrombus formation is a well described and clinically important complication of acute myocardial infarction (MI) with a substantial risk of thromboembolism. Alterations in the inflammatory status may contribute to this complication. The aim of this study was to evaluate the predictive role of the systemic immune-inflammation index (SII) in identifying high risk patients who will develop an apical thrombus formation during the acute phase of anterior transmural infarction. Consecutive 1753 patients (mean age: 61.5 ± 9.6 years; male: 63.8 %) with first acute anterior MI who underwent primary percutaneous coronary intervention were assessed. Patients were divided into 2 groups according to the presence of apical thrombus. SII was calculated using the following equation: neutrophil (N) × platelet (P) ÷ lymphocyte (L). LV apical thrombus was detected on transthoracic echocardiogram in 99 patients (5.6%). Patients with an apical thrombus had lower LV ejection fraction, prolonged time from symptoms to treatment, higher rate of post-percutaneous coronary intervention thrombolysis in myocardial infarction flow ≤1 and significantly higher mean high-sensitivity C-reactive protein, and SII values and lower lymphocyte than those without an apical thrombus. Admission SII level was found to be a significant predictor for early LV apical thrombus formation complicating a first-ever anterior MI. This simple calculated tool may be used to identify high-risk patients for LV thrombus and individualization of targeted therapy. Lippincott Williams & Wilkins 2022-12-16 /pmc/articles/PMC9771313/ /pubmed/36550886 http://dx.doi.org/10.1097/MD.0000000000032215 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. 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 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle 3400
Tok, Derya
Ekizler, Firdevs Aysenur
Tak, Bahar Tekin
The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction
title The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction
title_full The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction
title_fullStr The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction
title_full_unstemmed The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction
title_short The relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction
title_sort relation between apical thrombus formation and systemic immune-inflammation index in patients with acute anterior myocardial infarction
topic 3400
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771313/
https://www.ncbi.nlm.nih.gov/pubmed/36550886
http://dx.doi.org/10.1097/MD.0000000000032215
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