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Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA
Data are scarce on long-term outcomes after ischemic stroke (IS) or transient ischemic attack (TIA). In this prospective cohort study, we examined the cumulative incidence of major adverse cardiovascular events (MACE) after IS and TIA using a competing risk model and factors associated with new even...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206105/ https://www.ncbi.nlm.nih.gov/pubmed/37221291 http://dx.doi.org/10.1038/s41598-023-35601-x |
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author | Carlsson, Andreas Irewall, Anna-Lotta Graipe, Anna Ulvenstam, Anders Mooe, Thomas Ögren, Joachim |
author_facet | Carlsson, Andreas Irewall, Anna-Lotta Graipe, Anna Ulvenstam, Anders Mooe, Thomas Ögren, Joachim |
author_sort | Carlsson, Andreas |
collection | PubMed |
description | Data are scarce on long-term outcomes after ischemic stroke (IS) or transient ischemic attack (TIA). In this prospective cohort study, we examined the cumulative incidence of major adverse cardiovascular events (MACE) after IS and TIA using a competing risk model and factors associated with new events using a Cox-proportional hazard regression model. All patients discharged alive from Östersund Hospital with IS or TIA between 2010 and 2013 (n = 1535) were followed until 31 December 2017. The primary endpoint was a composite of IS, type 1 acute myocardial infarction (AMI), and cardiovascular (CV) death. Secondary endpoints were the individual components of the primary endpoint, in all patients and separated in IS and TIA subgroups. The cumulative incidence of MACE (median follow-up: 4.4 years) was 12.8% (95% CI: 11.2–14.6) within 1 year after discharge and 35.6% (95% CI: 31.8–39.4) by the end of follow-up. The risk of MACE and CV death was significantly increased in IS compared to TIA (p-values < 0.05), but not the risk of IS or type 1 AMI. Age, kidney failure, prior IS, prior AMI, congestive heart failure, atrial fibrillation, and impaired functional status, were associated with an increased risk of MACE. The risk of recurring events after IS and TIA is high. IS patients have a higher risk of MACE and CV death than TIA patients. |
format | Online Article Text |
id | pubmed-10206105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102061052023-05-25 Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA Carlsson, Andreas Irewall, Anna-Lotta Graipe, Anna Ulvenstam, Anders Mooe, Thomas Ögren, Joachim Sci Rep Article Data are scarce on long-term outcomes after ischemic stroke (IS) or transient ischemic attack (TIA). In this prospective cohort study, we examined the cumulative incidence of major adverse cardiovascular events (MACE) after IS and TIA using a competing risk model and factors associated with new events using a Cox-proportional hazard regression model. All patients discharged alive from Östersund Hospital with IS or TIA between 2010 and 2013 (n = 1535) were followed until 31 December 2017. The primary endpoint was a composite of IS, type 1 acute myocardial infarction (AMI), and cardiovascular (CV) death. Secondary endpoints were the individual components of the primary endpoint, in all patients and separated in IS and TIA subgroups. The cumulative incidence of MACE (median follow-up: 4.4 years) was 12.8% (95% CI: 11.2–14.6) within 1 year after discharge and 35.6% (95% CI: 31.8–39.4) by the end of follow-up. The risk of MACE and CV death was significantly increased in IS compared to TIA (p-values < 0.05), but not the risk of IS or type 1 AMI. Age, kidney failure, prior IS, prior AMI, congestive heart failure, atrial fibrillation, and impaired functional status, were associated with an increased risk of MACE. The risk of recurring events after IS and TIA is high. IS patients have a higher risk of MACE and CV death than TIA patients. Nature Publishing Group UK 2023-05-23 /pmc/articles/PMC10206105/ /pubmed/37221291 http://dx.doi.org/10.1038/s41598-023-35601-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Carlsson, Andreas Irewall, Anna-Lotta Graipe, Anna Ulvenstam, Anders Mooe, Thomas Ögren, Joachim Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA |
title | Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA |
title_full | Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA |
title_fullStr | Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA |
title_full_unstemmed | Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA |
title_short | Long-term risk of major adverse cardiovascular events following ischemic stroke or TIA |
title_sort | long-term risk of major adverse cardiovascular events following ischemic stroke or tia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206105/ https://www.ncbi.nlm.nih.gov/pubmed/37221291 http://dx.doi.org/10.1038/s41598-023-35601-x |
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