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Initial statin dose after myocardial infarction and long-term cardiovascular outcomes

AIMS: Effective statin therapy is a cornerstone of secondary prevention after myocardial infarction (MI). Real-life statin dosing is nevertheless suboptimal and largely determined early after MI. We studied long-term outcome impact of initial statin dose after MI. METHODS AND RESULTS: Consecutive MI...

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Autores principales: Kytö, Ville, Rautava, Päivi, Tornio, Aleksi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892868/
https://www.ncbi.nlm.nih.gov/pubmed/36385668
http://dx.doi.org/10.1093/ehjcvp/pvac064
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author Kytö, Ville
Rautava, Päivi
Tornio, Aleksi
author_facet Kytö, Ville
Rautava, Päivi
Tornio, Aleksi
author_sort Kytö, Ville
collection PubMed
description AIMS: Effective statin therapy is a cornerstone of secondary prevention after myocardial infarction (MI). Real-life statin dosing is nevertheless suboptimal and largely determined early after MI. We studied long-term outcome impact of initial statin dose after MI. METHODS AND RESULTS: Consecutive MI patients treated in Finland who used statins early after index event were retrospectively studied (N = 72 401; 67% men; mean age 68 years) using national registries. High-dose statin therapy was used by 26.3%, moderate dose by 69.2%, and low dose by 4.5%. Differences in baseline features, comorbidities, revascularisation, and usage of other evidence-based medications were adjusted for with multivariable regression. The primary outcome was major adverse cardiovascular or cerebrovascular event (MACCE) within 10 years. Median follow-up was 4.9 years. MACCE was less frequent in high-dose group compared with moderate dose [adjusted hazard ratio (HR) 0.92; P < 0.0001; number needed to treat (NNT) 34.1] and to low dose [adj.HR 0.81; P < 0.001; NNT 13.4] as well as in moderate-dose group compared with low dose (adj.HR 0.88; P < 0.0001; NNT 23.4). Death (adj.HR 0.87; P < 0.0001; NNT 23.6), recurrent MI (adj.sHR 0.91; P = 0.0001), and stroke (adj.sHR 0.86; P < 0.0001) were less frequent with a high- vs. moderate-dose statin. Higher initial statin dose after MI was associated with better long-term outcomes in subgroups by age, sex, atrial fibrillation, dementia, diabetes, heart failure, revascularisation, prior statin usage, or usage of other evidence-based medications. CONCLUSION: Higher initial statin dose after MI is dose-dependently associated with better long-term cardiovascular outcomes. These results underline the importance of using a high statin dose early after MI.
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spelling pubmed-98928682023-02-02 Initial statin dose after myocardial infarction and long-term cardiovascular outcomes Kytö, Ville Rautava, Päivi Tornio, Aleksi Eur Heart J Cardiovasc Pharmacother Original Article AIMS: Effective statin therapy is a cornerstone of secondary prevention after myocardial infarction (MI). Real-life statin dosing is nevertheless suboptimal and largely determined early after MI. We studied long-term outcome impact of initial statin dose after MI. METHODS AND RESULTS: Consecutive MI patients treated in Finland who used statins early after index event were retrospectively studied (N = 72 401; 67% men; mean age 68 years) using national registries. High-dose statin therapy was used by 26.3%, moderate dose by 69.2%, and low dose by 4.5%. Differences in baseline features, comorbidities, revascularisation, and usage of other evidence-based medications were adjusted for with multivariable regression. The primary outcome was major adverse cardiovascular or cerebrovascular event (MACCE) within 10 years. Median follow-up was 4.9 years. MACCE was less frequent in high-dose group compared with moderate dose [adjusted hazard ratio (HR) 0.92; P < 0.0001; number needed to treat (NNT) 34.1] and to low dose [adj.HR 0.81; P < 0.001; NNT 13.4] as well as in moderate-dose group compared with low dose (adj.HR 0.88; P < 0.0001; NNT 23.4). Death (adj.HR 0.87; P < 0.0001; NNT 23.6), recurrent MI (adj.sHR 0.91; P = 0.0001), and stroke (adj.sHR 0.86; P < 0.0001) were less frequent with a high- vs. moderate-dose statin. Higher initial statin dose after MI was associated with better long-term outcomes in subgroups by age, sex, atrial fibrillation, dementia, diabetes, heart failure, revascularisation, prior statin usage, or usage of other evidence-based medications. CONCLUSION: Higher initial statin dose after MI is dose-dependently associated with better long-term cardiovascular outcomes. These results underline the importance of using a high statin dose early after MI. Oxford University Press 2022-11-16 /pmc/articles/PMC9892868/ /pubmed/36385668 http://dx.doi.org/10.1093/ehjcvp/pvac064 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Article
Kytö, Ville
Rautava, Päivi
Tornio, Aleksi
Initial statin dose after myocardial infarction and long-term cardiovascular outcomes
title Initial statin dose after myocardial infarction and long-term cardiovascular outcomes
title_full Initial statin dose after myocardial infarction and long-term cardiovascular outcomes
title_fullStr Initial statin dose after myocardial infarction and long-term cardiovascular outcomes
title_full_unstemmed Initial statin dose after myocardial infarction and long-term cardiovascular outcomes
title_short Initial statin dose after myocardial infarction and long-term cardiovascular outcomes
title_sort initial statin dose after myocardial infarction and long-term cardiovascular outcomes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9892868/
https://www.ncbi.nlm.nih.gov/pubmed/36385668
http://dx.doi.org/10.1093/ehjcvp/pvac064
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