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Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors

BACKGROUND: Data are lacking on the risk and impact of a serious hemorrhage on the prognosis after ischemic stroke (IS) or transient ischemic attack (TIA). We aimed to estimate the incidence of serious hemorrhage, analyze the impact on mortality, and identify predictors of hemorrhage after discharge...

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Autores principales: Ögren, Joachim, Irewall, Anna-Lotta, Söderström, Lars, Mooe, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886551/
https://www.ncbi.nlm.nih.gov/pubmed/29621285
http://dx.doi.org/10.1371/journal.pone.0195324
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author Ögren, Joachim
Irewall, Anna-Lotta
Söderström, Lars
Mooe, Thomas
author_facet Ögren, Joachim
Irewall, Anna-Lotta
Söderström, Lars
Mooe, Thomas
author_sort Ögren, Joachim
collection PubMed
description BACKGROUND: Data are lacking on the risk and impact of a serious hemorrhage on the prognosis after ischemic stroke (IS) or transient ischemic attack (TIA). We aimed to estimate the incidence of serious hemorrhage, analyze the impact on mortality, and identify predictors of hemorrhage after discharge from IS or TIA. METHODS AND FINDINGS: All patients admitted to Östersund Hospital for an IS or TIA in 2010–2013 were included (n = 1528, mean age: 75.1 years). Serious hemorrhages were identified until 31(st) December 2015. Incidence rates were calculated. The impact on mortality (stratified by functional level) was determined with Kaplan-Meier analysis. Non-parametric estimation under the assumption of competing risk was performed to assess the cumulative incidence and predictors of serious hemorrhages. The incidence rates of serious (n = 113) and intracranial hemorrhages (n = 45) after discharge from IS and TIA were 2.48% and 0.96% per year at risk, respectively. Patients with modified Rankin Scale (mRS) scores of 3–5 exhibited 58.9% mortality during follow-up and those with mRS scores of 0–2 exhibited 18.4% mortality. A serious hemorrhage did not affect mortality in patients with impaired functional status, but it increased the risk of death in patients with mRS scores of 0–2. Hypertension was associated with increased risk of serious hemorrhage. CONCLUSIONS: We found that, after discharge from an IS or TIA, serious hemorrhages were fairly common. Impairments in function were associated with high mortality, but serious hemorrhages only increased the risk of mortality in patients with no or slight disability. Improved hypertension treatment may decrease the risk of serious hemorrhage, but in patients with low functional status, poor survival makes secondary prevention challenging.
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spelling pubmed-58865512018-04-20 Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors Ögren, Joachim Irewall, Anna-Lotta Söderström, Lars Mooe, Thomas PLoS One Research Article BACKGROUND: Data are lacking on the risk and impact of a serious hemorrhage on the prognosis after ischemic stroke (IS) or transient ischemic attack (TIA). We aimed to estimate the incidence of serious hemorrhage, analyze the impact on mortality, and identify predictors of hemorrhage after discharge from IS or TIA. METHODS AND FINDINGS: All patients admitted to Östersund Hospital for an IS or TIA in 2010–2013 were included (n = 1528, mean age: 75.1 years). Serious hemorrhages were identified until 31(st) December 2015. Incidence rates were calculated. The impact on mortality (stratified by functional level) was determined with Kaplan-Meier analysis. Non-parametric estimation under the assumption of competing risk was performed to assess the cumulative incidence and predictors of serious hemorrhages. The incidence rates of serious (n = 113) and intracranial hemorrhages (n = 45) after discharge from IS and TIA were 2.48% and 0.96% per year at risk, respectively. Patients with modified Rankin Scale (mRS) scores of 3–5 exhibited 58.9% mortality during follow-up and those with mRS scores of 0–2 exhibited 18.4% mortality. A serious hemorrhage did not affect mortality in patients with impaired functional status, but it increased the risk of death in patients with mRS scores of 0–2. Hypertension was associated with increased risk of serious hemorrhage. CONCLUSIONS: We found that, after discharge from an IS or TIA, serious hemorrhages were fairly common. Impairments in function were associated with high mortality, but serious hemorrhages only increased the risk of mortality in patients with no or slight disability. Improved hypertension treatment may decrease the risk of serious hemorrhage, but in patients with low functional status, poor survival makes secondary prevention challenging. Public Library of Science 2018-04-05 /pmc/articles/PMC5886551/ /pubmed/29621285 http://dx.doi.org/10.1371/journal.pone.0195324 Text en © 2018 Ögren et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Ögren, Joachim
Irewall, Anna-Lotta
Söderström, Lars
Mooe, Thomas
Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors
title Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors
title_full Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors
title_fullStr Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors
title_full_unstemmed Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors
title_short Serious hemorrhages after ischemic stroke or TIA – Incidence, mortality, and predictors
title_sort serious hemorrhages after ischemic stroke or tia – incidence, mortality, and predictors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886551/
https://www.ncbi.nlm.nih.gov/pubmed/29621285
http://dx.doi.org/10.1371/journal.pone.0195324
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