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Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients

BACKGROUND: Mortality after myocardial infarction (MI) among patients undergoing dialysis is high. However, studies investigating the use of secondary prevention medications after MI and clinical outcomes in dialysis patients are lacking. This study aimed to examine the association of the number of...

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Autores principales: Lin, Ting-Yun, Hsieh, Tsung-Han, Hung, Szu-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613425/
https://www.ncbi.nlm.nih.gov/pubmed/36325012
http://dx.doi.org/10.1093/ckj/sfac170
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author Lin, Ting-Yun
Hsieh, Tsung-Han
Hung, Szu-Chun
author_facet Lin, Ting-Yun
Hsieh, Tsung-Han
Hung, Szu-Chun
author_sort Lin, Ting-Yun
collection PubMed
description BACKGROUND: Mortality after myocardial infarction (MI) among patients undergoing dialysis is high. However, studies investigating the use of secondary prevention medications after MI and clinical outcomes in dialysis patients are lacking. This study aimed to examine the association of the number of guideline-recommended medications (antiplatelets, β-blockers, statins and renin–angiotensin–aldosterone system inhibitors) with all-cause mortality after MI in hemodialysis (HD) patients. METHODS: We conducted a nationwide cohort study of incident HD patients who were admitted for MI between 1 January 2010 and 31 December 2014 and were followed up until 31 December 2015, using Taiwan's national health insurance research database. RESULTS: Of 1471 patients (mean age 68 years, 41.9% women) included in the analysis, 281 (19.1%) were treated with one cardioprotective medication, 406 (27.6%) with two, 490 (33.3%) with three and 294 (20%) with four. During a median follow-up of 1.0 years, 458 (31.1%) patients died. In a multivariable Cox model, each additional use of guideline-recommended therapies was associated with a significant 12% reduction in the risk of mortality {hazard ratio [HR] 0.88 [95% confidence interval (CI) 0.80–0.97]}. Similar results were obtained in the analysis with the inverse probability of treatment weighting [HR 0.84 (95% CI 0.77–0.92)] and in the propensity score–matched subcohort [HR 0.87 (95% CI 0.77–0.98)]. The decreased mortality risk was consistently observed across all subgroups. CONCLUSIONS: The use of more evidence-based medications for secondary prevention after MI was associated with a lower risk of all-cause mortality in HD patients.
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spelling pubmed-96134252022-11-01 Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients Lin, Ting-Yun Hsieh, Tsung-Han Hung, Szu-Chun Clin Kidney J Original Article BACKGROUND: Mortality after myocardial infarction (MI) among patients undergoing dialysis is high. However, studies investigating the use of secondary prevention medications after MI and clinical outcomes in dialysis patients are lacking. This study aimed to examine the association of the number of guideline-recommended medications (antiplatelets, β-blockers, statins and renin–angiotensin–aldosterone system inhibitors) with all-cause mortality after MI in hemodialysis (HD) patients. METHODS: We conducted a nationwide cohort study of incident HD patients who were admitted for MI between 1 January 2010 and 31 December 2014 and were followed up until 31 December 2015, using Taiwan's national health insurance research database. RESULTS: Of 1471 patients (mean age 68 years, 41.9% women) included in the analysis, 281 (19.1%) were treated with one cardioprotective medication, 406 (27.6%) with two, 490 (33.3%) with three and 294 (20%) with four. During a median follow-up of 1.0 years, 458 (31.1%) patients died. In a multivariable Cox model, each additional use of guideline-recommended therapies was associated with a significant 12% reduction in the risk of mortality {hazard ratio [HR] 0.88 [95% confidence interval (CI) 0.80–0.97]}. Similar results were obtained in the analysis with the inverse probability of treatment weighting [HR 0.84 (95% CI 0.77–0.92)] and in the propensity score–matched subcohort [HR 0.87 (95% CI 0.77–0.98)]. The decreased mortality risk was consistently observed across all subgroups. CONCLUSIONS: The use of more evidence-based medications for secondary prevention after MI was associated with a lower risk of all-cause mortality in HD patients. Oxford University Press 2022-07-23 /pmc/articles/PMC9613425/ /pubmed/36325012 http://dx.doi.org/10.1093/ckj/sfac170 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the ERA. 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
Lin, Ting-Yun
Hsieh, Tsung-Han
Hung, Szu-Chun
Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients
title Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients
title_full Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients
title_fullStr Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients
title_full_unstemmed Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients
title_short Association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients
title_sort association of secondary prevention medication use after myocardial infarction with mortality in hemodialysis patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9613425/
https://www.ncbi.nlm.nih.gov/pubmed/36325012
http://dx.doi.org/10.1093/ckj/sfac170
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