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Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study

INTRODUCTION: Although statin therapy is beneficial to patients with ischemic stroke, statin use, and intracerebral hemorrhage (ICH) remain a concern. ICH survivors commonly have comorbid cardiovascular risk factors that would otherwise warrant cholesterol‐lowering medication, thus emphasizing the i...

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Autores principales: Tai, Shu‐Yu, Lin, Feng‐Cheng, Lee, Chung‐Yin, Chang, Chai‐Jan, Wu, Ming‐Tsang, Chien, Chen‐Yu
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/PMC4867570/
https://www.ncbi.nlm.nih.gov/pubmed/27247857
http://dx.doi.org/10.1002/brb3.487
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author Tai, Shu‐Yu
Lin, Feng‐Cheng
Lee, Chung‐Yin
Chang, Chai‐Jan
Wu, Ming‐Tsang
Chien, Chen‐Yu
author_facet Tai, Shu‐Yu
Lin, Feng‐Cheng
Lee, Chung‐Yin
Chang, Chai‐Jan
Wu, Ming‐Tsang
Chien, Chen‐Yu
author_sort Tai, Shu‐Yu
collection PubMed
description INTRODUCTION: Although statin therapy is beneficial to patients with ischemic stroke, statin use, and intracerebral hemorrhage (ICH) remain a concern. ICH survivors commonly have comorbid cardiovascular risk factors that would otherwise warrant cholesterol‐lowering medication, thus emphasizing the importance of assessing the characteristics of statin therapy in this population. METHODS: We performed a cohort study by using 10 years of data collected from the National Health Insurance Research Database in Taiwan. We enrolled 726 patients admitted for newly diagnosed ICH from January 1, 2001 to December 31, 2010. The patients were categorized into high‐ (92), moderate‐ (545), and low‐intensity (89) statin groups, and into hydrophilic (295) and lipophilic (431) statin groups. The composite outcomes included all‐cause mortality, recurrent ICH, ischemic stroke, transient ischemic attack, and acute coronary events. RESULTS: The patients in the low‐intensity group did not differ significantly from the patients in the high‐intensity group in risk of all‐cause mortality (adjusted hazard ratio [aHR] = 0.65, 95% confidence interval [CI] = 0.28–1.55) and recurrent ICH (aHR = 0.66, 95% CI = 0.30–1.44). In contrast, the patients in the hydrophilic group had a significantly lower risk of recurrent ICH than did those in the lipophilic group (aHR = 0.69, 95% CI = 0.48–0.99). We determined no significant differences in other composite endpoints between hydrophilic and lipophilic statin use. CONCLUSION: Hydrophilic statin therapy is associated with a reduced risk of recurrent ICH in post‐ICH patients. The intensity of statin use had no significant effect on recurrent ICH or other components of the composite outcome. Additional studies are required to clarify the biological mechanisms underlying these observations.
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spelling pubmed-48675702016-05-31 Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study Tai, Shu‐Yu Lin, Feng‐Cheng Lee, Chung‐Yin Chang, Chai‐Jan Wu, Ming‐Tsang Chien, Chen‐Yu Brain Behav Original Research INTRODUCTION: Although statin therapy is beneficial to patients with ischemic stroke, statin use, and intracerebral hemorrhage (ICH) remain a concern. ICH survivors commonly have comorbid cardiovascular risk factors that would otherwise warrant cholesterol‐lowering medication, thus emphasizing the importance of assessing the characteristics of statin therapy in this population. METHODS: We performed a cohort study by using 10 years of data collected from the National Health Insurance Research Database in Taiwan. We enrolled 726 patients admitted for newly diagnosed ICH from January 1, 2001 to December 31, 2010. The patients were categorized into high‐ (92), moderate‐ (545), and low‐intensity (89) statin groups, and into hydrophilic (295) and lipophilic (431) statin groups. The composite outcomes included all‐cause mortality, recurrent ICH, ischemic stroke, transient ischemic attack, and acute coronary events. RESULTS: The patients in the low‐intensity group did not differ significantly from the patients in the high‐intensity group in risk of all‐cause mortality (adjusted hazard ratio [aHR] = 0.65, 95% confidence interval [CI] = 0.28–1.55) and recurrent ICH (aHR = 0.66, 95% CI = 0.30–1.44). In contrast, the patients in the hydrophilic group had a significantly lower risk of recurrent ICH than did those in the lipophilic group (aHR = 0.69, 95% CI = 0.48–0.99). We determined no significant differences in other composite endpoints between hydrophilic and lipophilic statin use. CONCLUSION: Hydrophilic statin therapy is associated with a reduced risk of recurrent ICH in post‐ICH patients. The intensity of statin use had no significant effect on recurrent ICH or other components of the composite outcome. Additional studies are required to clarify the biological mechanisms underlying these observations. John Wiley and Sons Inc. 2016-05-13 /pmc/articles/PMC4867570/ /pubmed/27247857 http://dx.doi.org/10.1002/brb3.487 Text en © 2016 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Tai, Shu‐Yu
Lin, Feng‐Cheng
Lee, Chung‐Yin
Chang, Chai‐Jan
Wu, Ming‐Tsang
Chien, Chen‐Yu
Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study
title Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study
title_full Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study
title_fullStr Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study
title_full_unstemmed Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study
title_short Statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study
title_sort statin use after intracerebral hemorrhage: a 10‐year nationwide cohort study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867570/
https://www.ncbi.nlm.nih.gov/pubmed/27247857
http://dx.doi.org/10.1002/brb3.487
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