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Ischemic Stroke Risk After Acute Coronary Syndrome

BACKGROUND: Prior studies show an increased risk of ischemic stroke (IS) after myocardial infarction; however, there is limited evidence on long‐term risk and whether it is directly related to cardiac injury. We hypothesized that the risk of IS after acute coronary syndrome is significantly higher i...

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Autores principales: Yaghi, Shadi, Pilot, Markeith, Song, Christopher, Blum, Christina A., Yakhkind, Aleksandra, Silver, Brian, Furie, Karen L., Elkind, Mitchell S. V., Sherzai, Dean, Sherzai, Ayesha Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015356/
https://www.ncbi.nlm.nih.gov/pubmed/27413043
http://dx.doi.org/10.1161/JAHA.115.002590
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author Yaghi, Shadi
Pilot, Markeith
Song, Christopher
Blum, Christina A.
Yakhkind, Aleksandra
Silver, Brian
Furie, Karen L.
Elkind, Mitchell S. V.
Sherzai, Dean
Sherzai, Ayesha Z.
author_facet Yaghi, Shadi
Pilot, Markeith
Song, Christopher
Blum, Christina A.
Yakhkind, Aleksandra
Silver, Brian
Furie, Karen L.
Elkind, Mitchell S. V.
Sherzai, Dean
Sherzai, Ayesha Z.
author_sort Yaghi, Shadi
collection PubMed
description BACKGROUND: Prior studies show an increased risk of ischemic stroke (IS) after myocardial infarction; however, there is limited evidence on long‐term risk and whether it is directly related to cardiac injury. We hypothesized that the risk of IS after acute coronary syndrome is significantly higher if there is evidence of cardiac injury, such as ST‐segment elevation myocardial infarction (STEMI) or non‐STEMI, than when there is no evidence of cardiac injury, such as in unstable angina. METHODS AND RESULTS: Administrative claims data were obtained from all emergency department encounters and hospitalizations at California's nonfederal acute care hospitals between 2008 and 2011. Patients with STEMI, non‐STEMI, and unstable angina were identified using appropriate International Classification of Diseases, Ninth Revision, Clinical Modification codes. The primary outcome was IS during 2 years of follow‐up. Unadjusted and adjusted Cox proportional hazards models were used to determine the association between acute coronary syndrome subtype and IS risk. We identified 73 059 patients with a diagnosis of STEMI (n=26 427), non‐STEMI (n=39 833), or unstable angina (n=6819) during the study period. In the fully adjusted models that included potential confounders such as atrial fibrillation and congestive heart failure, the risk of IS was higher with STEMI (hazard ratio 4.17, 95% CI 3.00–5.83; P<0.001) and non‐STEMI (hazard ratio 3.73, 95% CI 2.68–5.19, P<0.001) compared with unstable angina. CONCLUSIONS: Non‐STEMI and STEMI confer an equally increased risk of IS. Studies exploring IS mechanisms in cardiac patients are needed to improve and tailor stroke prevention strategies.
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spelling pubmed-50153562016-09-19 Ischemic Stroke Risk After Acute Coronary Syndrome Yaghi, Shadi Pilot, Markeith Song, Christopher Blum, Christina A. Yakhkind, Aleksandra Silver, Brian Furie, Karen L. Elkind, Mitchell S. V. Sherzai, Dean Sherzai, Ayesha Z. J Am Heart Assoc Original Research BACKGROUND: Prior studies show an increased risk of ischemic stroke (IS) after myocardial infarction; however, there is limited evidence on long‐term risk and whether it is directly related to cardiac injury. We hypothesized that the risk of IS after acute coronary syndrome is significantly higher if there is evidence of cardiac injury, such as ST‐segment elevation myocardial infarction (STEMI) or non‐STEMI, than when there is no evidence of cardiac injury, such as in unstable angina. METHODS AND RESULTS: Administrative claims data were obtained from all emergency department encounters and hospitalizations at California's nonfederal acute care hospitals between 2008 and 2011. Patients with STEMI, non‐STEMI, and unstable angina were identified using appropriate International Classification of Diseases, Ninth Revision, Clinical Modification codes. The primary outcome was IS during 2 years of follow‐up. Unadjusted and adjusted Cox proportional hazards models were used to determine the association between acute coronary syndrome subtype and IS risk. We identified 73 059 patients with a diagnosis of STEMI (n=26 427), non‐STEMI (n=39 833), or unstable angina (n=6819) during the study period. In the fully adjusted models that included potential confounders such as atrial fibrillation and congestive heart failure, the risk of IS was higher with STEMI (hazard ratio 4.17, 95% CI 3.00–5.83; P<0.001) and non‐STEMI (hazard ratio 3.73, 95% CI 2.68–5.19, P<0.001) compared with unstable angina. CONCLUSIONS: Non‐STEMI and STEMI confer an equally increased risk of IS. Studies exploring IS mechanisms in cardiac patients are needed to improve and tailor stroke prevention strategies. John Wiley and Sons Inc. 2016-07-13 /pmc/articles/PMC5015356/ /pubmed/27413043 http://dx.doi.org/10.1161/JAHA.115.002590 Text en © 2016 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley Blackwell. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Yaghi, Shadi
Pilot, Markeith
Song, Christopher
Blum, Christina A.
Yakhkind, Aleksandra
Silver, Brian
Furie, Karen L.
Elkind, Mitchell S. V.
Sherzai, Dean
Sherzai, Ayesha Z.
Ischemic Stroke Risk After Acute Coronary Syndrome
title Ischemic Stroke Risk After Acute Coronary Syndrome
title_full Ischemic Stroke Risk After Acute Coronary Syndrome
title_fullStr Ischemic Stroke Risk After Acute Coronary Syndrome
title_full_unstemmed Ischemic Stroke Risk After Acute Coronary Syndrome
title_short Ischemic Stroke Risk After Acute Coronary Syndrome
title_sort ischemic stroke risk after acute coronary syndrome
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015356/
https://www.ncbi.nlm.nih.gov/pubmed/27413043
http://dx.doi.org/10.1161/JAHA.115.002590
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