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Decreased cardiac mortality with nicorandil in patients with ischemic heart failure
BACKGROUND: Effective treatments in heart failure (HF) patients with ischemic etiology have not been fully established. Nicorandil, combination of nitrate component and sarcolemmal adenosine triphosphate-sensitive potassium channel opener, is a potent vasodilator of coronary and peripheral vessels a...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452293/ https://www.ncbi.nlm.nih.gov/pubmed/28569214 http://dx.doi.org/10.1186/s12872-017-0577-3 |
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author | Yoshihisa, Akiomi Sato, Yu Watanabe, Shunsuke Yokokawa, Tetsuro Sato, Takamasa Suzuki, Satoshi Oikawa, Masayoshi Kobayashi, Atsushi Takeishi, Yasuchika |
author_facet | Yoshihisa, Akiomi Sato, Yu Watanabe, Shunsuke Yokokawa, Tetsuro Sato, Takamasa Suzuki, Satoshi Oikawa, Masayoshi Kobayashi, Atsushi Takeishi, Yasuchika |
author_sort | Yoshihisa, Akiomi |
collection | PubMed |
description | BACKGROUND: Effective treatments in heart failure (HF) patients with ischemic etiology have not been fully established. Nicorandil, combination of nitrate component and sarcolemmal adenosine triphosphate-sensitive potassium channel opener, is a potent vasodilator of coronary and peripheral vessels and has been used as an antianginal agent. Therefore, we examined impacts of nicorandil on cardiac mortality in ischemic HF patients. METHODS: Consecutive 334 HF patients with ischemic etiology were retrospectively registered and divided into 2 groups based on oral administration of nicorandil: nicorandil group (n = 116) and non-nicorandil group (n = 218). We retrospectively examined cardiac mortality. RESULTS: In the Kaplan-Meier analysis (mean follow-up period 963 days), cardiac mortality was significantly lower in the nicorandil group than in the non-nicorandil group (11.2% vs. 19.7%, P = 0.032). In the Cox proportional hazard analysis, usage of nicorandil was a suppressor of cardiac mortality (hazard ratio 0.512, 95% confidence interval 0.275–0.953, P = 0.035), and this result was consistent in several subgroup analyses, such as left ventricular ejection fraction, percutaneous coronary intervention, coronary artery bypass graft, diabetes, β-blockers, and statins. CONCLUSION: Nicorandil is potentially effective for reducing mortality in patients with ischemic heart failure. TRIAL REGISTRATION: This was a retrospective study. |
format | Online Article Text |
id | pubmed-5452293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54522932017-06-01 Decreased cardiac mortality with nicorandil in patients with ischemic heart failure Yoshihisa, Akiomi Sato, Yu Watanabe, Shunsuke Yokokawa, Tetsuro Sato, Takamasa Suzuki, Satoshi Oikawa, Masayoshi Kobayashi, Atsushi Takeishi, Yasuchika BMC Cardiovasc Disord Research Article BACKGROUND: Effective treatments in heart failure (HF) patients with ischemic etiology have not been fully established. Nicorandil, combination of nitrate component and sarcolemmal adenosine triphosphate-sensitive potassium channel opener, is a potent vasodilator of coronary and peripheral vessels and has been used as an antianginal agent. Therefore, we examined impacts of nicorandil on cardiac mortality in ischemic HF patients. METHODS: Consecutive 334 HF patients with ischemic etiology were retrospectively registered and divided into 2 groups based on oral administration of nicorandil: nicorandil group (n = 116) and non-nicorandil group (n = 218). We retrospectively examined cardiac mortality. RESULTS: In the Kaplan-Meier analysis (mean follow-up period 963 days), cardiac mortality was significantly lower in the nicorandil group than in the non-nicorandil group (11.2% vs. 19.7%, P = 0.032). In the Cox proportional hazard analysis, usage of nicorandil was a suppressor of cardiac mortality (hazard ratio 0.512, 95% confidence interval 0.275–0.953, P = 0.035), and this result was consistent in several subgroup analyses, such as left ventricular ejection fraction, percutaneous coronary intervention, coronary artery bypass graft, diabetes, β-blockers, and statins. CONCLUSION: Nicorandil is potentially effective for reducing mortality in patients with ischemic heart failure. TRIAL REGISTRATION: This was a retrospective study. BioMed Central 2017-05-31 /pmc/articles/PMC5452293/ /pubmed/28569214 http://dx.doi.org/10.1186/s12872-017-0577-3 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Yoshihisa, Akiomi Sato, Yu Watanabe, Shunsuke Yokokawa, Tetsuro Sato, Takamasa Suzuki, Satoshi Oikawa, Masayoshi Kobayashi, Atsushi Takeishi, Yasuchika Decreased cardiac mortality with nicorandil in patients with ischemic heart failure |
title | Decreased cardiac mortality with nicorandil in patients with ischemic heart failure |
title_full | Decreased cardiac mortality with nicorandil in patients with ischemic heart failure |
title_fullStr | Decreased cardiac mortality with nicorandil in patients with ischemic heart failure |
title_full_unstemmed | Decreased cardiac mortality with nicorandil in patients with ischemic heart failure |
title_short | Decreased cardiac mortality with nicorandil in patients with ischemic heart failure |
title_sort | decreased cardiac mortality with nicorandil in patients with ischemic heart failure |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5452293/ https://www.ncbi.nlm.nih.gov/pubmed/28569214 http://dx.doi.org/10.1186/s12872-017-0577-3 |
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