Oral treatment with nicorandil at discharge is associated with reduced mortality after acute myocardial infarction

Summary Background Previous studies showed that nicorandil can reduce coronary events in patients with coronary artery disease. However, it is unclear whether oral nicorandil treatment may reduce mortality following acute myocardial infarction (AMI). Methods and Results We examined the impact of ora...

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Veröffentlicht in:Journal of cardiology 2012-01, Vol.59 (1), p.14-21
Hauptverfasser: Sakata, Yasuhiko, MD, PhD, Nakatani, Daisaku, MD, PhD, Shimizu, Masahiko, MD, PhD, Suna, Shinichiro, MD, PhD, Usami, Masaya, MD, Matsumoto, Sen, MD, Hara, Masahiko, MD, Sumitsuji, Satoru, MD, Kawano, Shigeo, MD, Iwakura, Katsuomi, MD, Hamasaki, Toshimitsu, PhD, Sato, Hiroshi, MD, PhD, FJCC, Nanto, Shinsuke, MD, PhD, FJCC, Hori, Masatsugu, MD, PhD, FJCC, Komuro, Issei, MD, PhD, FJCC
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container_issue 1
container_start_page 14
container_title Journal of cardiology
container_volume 59
creator Sakata, Yasuhiko, MD, PhD
Nakatani, Daisaku, MD, PhD
Shimizu, Masahiko, MD, PhD
Suna, Shinichiro, MD, PhD
Usami, Masaya, MD
Matsumoto, Sen, MD
Hara, Masahiko, MD
Sumitsuji, Satoru, MD
Kawano, Shigeo, MD
Iwakura, Katsuomi, MD
Hamasaki, Toshimitsu, PhD
Sato, Hiroshi, MD, PhD, FJCC
Nanto, Shinsuke, MD, PhD, FJCC
Hori, Masatsugu, MD, PhD, FJCC
Komuro, Issei, MD, PhD, FJCC
description Summary Background Previous studies showed that nicorandil can reduce coronary events in patients with coronary artery disease. However, it is unclear whether oral nicorandil treatment may reduce mortality following acute myocardial infarction (AMI). Methods and Results We examined the impact of oral nicorandil treatment on cardiovascular events in 1846 AMI patients who were hospitalized within 24 h after AMI onset, treated with emergency percutaneous coronary intervention (PCI), and discharged alive. Patients were divided into those with (Group N, n = 535) and without (Group C, n = 1311) oral nicorandil treatment at discharge. No significant differences in age, gender, body mass index, prevalence of coronary risk factors, or history of myocardial infarction existed between the two groups; however, higher incidences of multi-vessel disease, and a lower rate of successful PCI were observed in Group N. During the median follow-up of 709 (340–1088) days, all-cause mortality rate was 43% lower in Group N compared with Group C (2.4% vs. 4.2%, stratified log-rank test: p = 0.0358). Multivariate Cox regression analysis revealed that nicorandil treatment was associated with all-cause death after discharge (Hazard ratio 0.495, 95% CI: 0.254–0.966, p = 0.0393), but not for other cardiovascular events such as re-infarction, admission for heart failure, stroke and arrhythmia. Conclusions The results suggest that oral administration of nicorandil is associated with reduced incidence of death in the setting of secondary prevention after AMI.
doi_str_mv 10.1016/j.jjcc.2011.08.001
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However, it is unclear whether oral nicorandil treatment may reduce mortality following acute myocardial infarction (AMI). Methods and Results We examined the impact of oral nicorandil treatment on cardiovascular events in 1846 AMI patients who were hospitalized within 24 h after AMI onset, treated with emergency percutaneous coronary intervention (PCI), and discharged alive. Patients were divided into those with (Group N, n = 535) and without (Group C, n = 1311) oral nicorandil treatment at discharge. No significant differences in age, gender, body mass index, prevalence of coronary risk factors, or history of myocardial infarction existed between the two groups; however, higher incidences of multi-vessel disease, and a lower rate of successful PCI were observed in Group N. During the median follow-up of 709 (340–1088) days, all-cause mortality rate was 43% lower in Group N compared with Group C (2.4% vs. 4.2%, stratified log-rank test: p = 0.0358). Multivariate Cox regression analysis revealed that nicorandil treatment was associated with all-cause death after discharge (Hazard ratio 0.495, 95% CI: 0.254–0.966, p = 0.0393), but not for other cardiovascular events such as re-infarction, admission for heart failure, stroke and arrhythmia. Conclusions The results suggest that oral administration of nicorandil is associated with reduced incidence of death in the setting of secondary prevention after AMI.</description><identifier>ISSN: 0914-5087</identifier><identifier>EISSN: 1876-4738</identifier><identifier>DOI: 10.1016/j.jjcc.2011.08.001</identifier><identifier>PMID: 21924584</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Acute myocardial infarction ; Administration, Oral ; Aged ; Angioplasty, Balloon, Coronary ; Cardiovascular ; Female ; Humans ; Male ; Mortality ; Myocardial Infarction - mortality ; Myocardial Infarction - prevention &amp; control ; Myocardial Infarction - therapy ; Nicorandil ; Nicorandil - administration &amp; dosage ; Patient Discharge ; Secondary prevention ; Vasodilator Agents - administration &amp; dosage</subject><ispartof>Journal of cardiology, 2012-01, Vol.59 (1), p.14-21</ispartof><rights>Japanese College of Cardiology</rights><rights>2011 Japanese College of Cardiology</rights><rights>Copyright © 2011 Japanese College of Cardiology. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-e4c6b9b20d02c3bc1297e3ced8d5a088aef25309d3ae433afb6a1488e224b3e3</citedby><cites>FETCH-LOGICAL-c478t-e4c6b9b20d02c3bc1297e3ced8d5a088aef25309d3ae433afb6a1488e224b3e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jjcc.2011.08.001$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21924584$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sakata, Yasuhiko, MD, PhD</creatorcontrib><creatorcontrib>Nakatani, Daisaku, MD, PhD</creatorcontrib><creatorcontrib>Shimizu, Masahiko, MD, PhD</creatorcontrib><creatorcontrib>Suna, Shinichiro, MD, PhD</creatorcontrib><creatorcontrib>Usami, Masaya, MD</creatorcontrib><creatorcontrib>Matsumoto, Sen, MD</creatorcontrib><creatorcontrib>Hara, Masahiko, MD</creatorcontrib><creatorcontrib>Sumitsuji, Satoru, MD</creatorcontrib><creatorcontrib>Kawano, Shigeo, MD</creatorcontrib><creatorcontrib>Iwakura, Katsuomi, MD</creatorcontrib><creatorcontrib>Hamasaki, Toshimitsu, PhD</creatorcontrib><creatorcontrib>Sato, Hiroshi, MD, PhD, FJCC</creatorcontrib><creatorcontrib>Nanto, Shinsuke, MD, PhD, FJCC</creatorcontrib><creatorcontrib>Hori, Masatsugu, MD, PhD, FJCC</creatorcontrib><creatorcontrib>Komuro, Issei, MD, PhD, FJCC</creatorcontrib><title>Oral treatment with nicorandil at discharge is associated with reduced mortality after acute myocardial infarction</title><title>Journal of cardiology</title><addtitle>J Cardiol</addtitle><description>Summary Background Previous studies showed that nicorandil can reduce coronary events in patients with coronary artery disease. However, it is unclear whether oral nicorandil treatment may reduce mortality following acute myocardial infarction (AMI). Methods and Results We examined the impact of oral nicorandil treatment on cardiovascular events in 1846 AMI patients who were hospitalized within 24 h after AMI onset, treated with emergency percutaneous coronary intervention (PCI), and discharged alive. Patients were divided into those with (Group N, n = 535) and without (Group C, n = 1311) oral nicorandil treatment at discharge. No significant differences in age, gender, body mass index, prevalence of coronary risk factors, or history of myocardial infarction existed between the two groups; however, higher incidences of multi-vessel disease, and a lower rate of successful PCI were observed in Group N. During the median follow-up of 709 (340–1088) days, all-cause mortality rate was 43% lower in Group N compared with Group C (2.4% vs. 4.2%, stratified log-rank test: p = 0.0358). Multivariate Cox regression analysis revealed that nicorandil treatment was associated with all-cause death after discharge (Hazard ratio 0.495, 95% CI: 0.254–0.966, p = 0.0393), but not for other cardiovascular events such as re-infarction, admission for heart failure, stroke and arrhythmia. 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dosage</topic><topic>Patient Discharge</topic><topic>Secondary prevention</topic><topic>Vasodilator Agents - administration &amp; dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sakata, Yasuhiko, MD, PhD</creatorcontrib><creatorcontrib>Nakatani, Daisaku, MD, PhD</creatorcontrib><creatorcontrib>Shimizu, Masahiko, MD, PhD</creatorcontrib><creatorcontrib>Suna, Shinichiro, MD, PhD</creatorcontrib><creatorcontrib>Usami, Masaya, MD</creatorcontrib><creatorcontrib>Matsumoto, Sen, MD</creatorcontrib><creatorcontrib>Hara, Masahiko, MD</creatorcontrib><creatorcontrib>Sumitsuji, Satoru, MD</creatorcontrib><creatorcontrib>Kawano, Shigeo, MD</creatorcontrib><creatorcontrib>Iwakura, Katsuomi, MD</creatorcontrib><creatorcontrib>Hamasaki, Toshimitsu, PhD</creatorcontrib><creatorcontrib>Sato, Hiroshi, MD, PhD, FJCC</creatorcontrib><creatorcontrib>Nanto, Shinsuke, MD, PhD, FJCC</creatorcontrib><creatorcontrib>Hori, Masatsugu, MD, PhD, FJCC</creatorcontrib><creatorcontrib>Komuro, Issei, MD, PhD, FJCC</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sakata, Yasuhiko, MD, PhD</au><au>Nakatani, Daisaku, MD, PhD</au><au>Shimizu, Masahiko, MD, PhD</au><au>Suna, Shinichiro, MD, PhD</au><au>Usami, Masaya, MD</au><au>Matsumoto, Sen, MD</au><au>Hara, Masahiko, MD</au><au>Sumitsuji, Satoru, MD</au><au>Kawano, Shigeo, MD</au><au>Iwakura, Katsuomi, MD</au><au>Hamasaki, Toshimitsu, PhD</au><au>Sato, Hiroshi, MD, PhD, FJCC</au><au>Nanto, Shinsuke, MD, PhD, FJCC</au><au>Hori, Masatsugu, MD, PhD, FJCC</au><au>Komuro, Issei, MD, PhD, FJCC</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral treatment with nicorandil at discharge is associated with reduced mortality after acute myocardial infarction</atitle><jtitle>Journal of cardiology</jtitle><addtitle>J Cardiol</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>59</volume><issue>1</issue><spage>14</spage><epage>21</epage><pages>14-21</pages><issn>0914-5087</issn><eissn>1876-4738</eissn><abstract>Summary Background Previous studies showed that nicorandil can reduce coronary events in patients with coronary artery disease. However, it is unclear whether oral nicorandil treatment may reduce mortality following acute myocardial infarction (AMI). Methods and Results We examined the impact of oral nicorandil treatment on cardiovascular events in 1846 AMI patients who were hospitalized within 24 h after AMI onset, treated with emergency percutaneous coronary intervention (PCI), and discharged alive. Patients were divided into those with (Group N, n = 535) and without (Group C, n = 1311) oral nicorandil treatment at discharge. No significant differences in age, gender, body mass index, prevalence of coronary risk factors, or history of myocardial infarction existed between the two groups; however, higher incidences of multi-vessel disease, and a lower rate of successful PCI were observed in Group N. During the median follow-up of 709 (340–1088) days, all-cause mortality rate was 43% lower in Group N compared with Group C (2.4% vs. 4.2%, stratified log-rank test: p = 0.0358). Multivariate Cox regression analysis revealed that nicorandil treatment was associated with all-cause death after discharge (Hazard ratio 0.495, 95% CI: 0.254–0.966, p = 0.0393), but not for other cardiovascular events such as re-infarction, admission for heart failure, stroke and arrhythmia. Conclusions The results suggest that oral administration of nicorandil is associated with reduced incidence of death in the setting of secondary prevention after AMI.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>21924584</pmid><doi>10.1016/j.jjcc.2011.08.001</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Acute myocardial infarction
Administration, Oral
Aged
Angioplasty, Balloon, Coronary
Cardiovascular
Female
Humans
Male
Mortality
Myocardial Infarction - mortality
Myocardial Infarction - prevention & control
Myocardial Infarction - therapy
Nicorandil
Nicorandil - administration & dosage
Patient Discharge
Secondary prevention
Vasodilator Agents - administration & dosage
title Oral treatment with nicorandil at discharge is associated with reduced mortality after acute myocardial infarction
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