β Blockade after myocardial infarction: systematic review and meta regression analysis
Abstract Objectives: To assess the effectiveness of β blockers in short term treatment for acute myocardial infarction and in longer term secondary prevention; to examine predictive factors that may influence outcome and therefore choice of drug; and to examine the clinical importance of the results...
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Veröffentlicht in: | BMJ 1999-06, Vol.318 (7200), p.1730-1737 |
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description | Abstract Objectives: To assess the effectiveness of β blockers in short term treatment for acute myocardial infarction and in longer term secondary prevention; to examine predictive factors that may influence outcome and therefore choice of drug; and to examine the clinical importance of the results in the light of current treatment. Design:Systematic review of randomised controlled trials. Setting: Randomised controlled trials. Subjects: Patients with acute or past myocardial infarction. Intervention: βBlockers compared with control. Main:outcome measures All cause mortality and non-fatal reinfarction. Results: Overall, 5477 of 54 234 patients (10.1%) randomised to β blockers or control died. We identified a 23% reduction in the odds of death in long term trials (95% confidence interval 15% to 31%), but only a 4% reduction in the odds of death in short term trials (−8% to 15%). Meta regression in long term trials did not identify a significant reduction in effectiveness in drugs with cardioselectivity but did identify a near significant trend towards decreased benefit in drugs with intrinsic sympathomimetic activity. Most evidence is available for propranolol, timolol, and metoprolol. In long term trials, the number needed to treat for 2 years to avoid a death is 42, which compares favourably with other treatments for patients with acute or past myocardial infarction. Conclusions: β Blockers are effective in long term secondary prevention after myocardial infarction, but they are underused in such cases and lead to avoidable mortality and morbidity. |
doi_str_mv | 10.1136/bmj.318.7200.1730 |
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Design:Systematic review of randomised controlled trials. Setting: Randomised controlled trials. Subjects: Patients with acute or past myocardial infarction. Intervention: βBlockers compared with control. Main:outcome measures All cause mortality and non-fatal reinfarction. Results: Overall, 5477 of 54 234 patients (10.1%) randomised to β blockers or control died. We identified a 23% reduction in the odds of death in long term trials (95% confidence interval 15% to 31%), but only a 4% reduction in the odds of death in short term trials (−8% to 15%). Meta regression in long term trials did not identify a significant reduction in effectiveness in drugs with cardioselectivity but did identify a near significant trend towards decreased benefit in drugs with intrinsic sympathomimetic activity. Most evidence is available for propranolol, timolol, and metoprolol. In long term trials, the number needed to treat for 2 years to avoid a death is 42, which compares favourably with other treatments for patients with acute or past myocardial infarction. Conclusions: β Blockers are effective in long term secondary prevention after myocardial infarction, but they are underused in such cases and lead to avoidable mortality and morbidity.</description><identifier>ISSN: 0959-8138</identifier><identifier>EISSN: 1468-5833</identifier><identifier>EISSN: 1756-1833</identifier><identifier>DOI: 10.1136/bmj.318.7200.1730</identifier><identifier>PMID: 10381708</identifier><language>eng</language><publisher>England: British Medical Journal Publishing Group</publisher><subject>Adrenergic beta-Antagonists - therapeutic use ; Cardiovascular agents ; Death ; Estimation methods ; Experimentation ; Heart ; Humans ; International studies ; Mortality ; Myocardial infarction ; Myocardial Infarction - drug therapy ; Randomized Controlled Trials as Topic ; Regression Analysis ; Secondary prevention ; Sympathomimetics ; Treatment Outcome</subject><ispartof>BMJ, 1999-06, Vol.318 (7200), p.1730-1737</ispartof><rights>1999 BMJ Publishing Group Ltd.</rights><rights>Copyright 1999 BMJ</rights><rights>Copyright © 1999, British Medical Journal 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b488t-58ee5fe6017a4c855dc4d52a882679c9de5ed546acf6109bc05243a373ce2eec3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25185062$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25185062$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,778,782,801,883,27907,27908,58000,58233</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10381708$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Freemantle, Nick</creatorcontrib><creatorcontrib>Cleland, John</creatorcontrib><creatorcontrib>Young, Philip</creatorcontrib><creatorcontrib>Mason, James</creatorcontrib><creatorcontrib>Harrison, Jane</creatorcontrib><title>β Blockade after myocardial infarction: systematic review and meta regression analysis</title><title>BMJ</title><addtitle>BMJ</addtitle><description>Abstract Objectives: To assess the effectiveness of β blockers in short term treatment for acute myocardial infarction and in longer term secondary prevention; to examine predictive factors that may influence outcome and therefore choice of drug; and to examine the clinical importance of the results in the light of current treatment. Design:Systematic review of randomised controlled trials. Setting: Randomised controlled trials. Subjects: Patients with acute or past myocardial infarction. Intervention: βBlockers compared with control. Main:outcome measures All cause mortality and non-fatal reinfarction. Results: Overall, 5477 of 54 234 patients (10.1%) randomised to β blockers or control died. We identified a 23% reduction in the odds of death in long term trials (95% confidence interval 15% to 31%), but only a 4% reduction in the odds of death in short term trials (−8% to 15%). Meta regression in long term trials did not identify a significant reduction in effectiveness in drugs with cardioselectivity but did identify a near significant trend towards decreased benefit in drugs with intrinsic sympathomimetic activity. Most evidence is available for propranolol, timolol, and metoprolol. In long term trials, the number needed to treat for 2 years to avoid a death is 42, which compares favourably with other treatments for patients with acute or past myocardial infarction. Conclusions: β Blockers are effective in long term secondary prevention after myocardial infarction, but they are underused in such cases and lead to avoidable mortality and morbidity.</description><subject>Adrenergic beta-Antagonists - therapeutic use</subject><subject>Cardiovascular agents</subject><subject>Death</subject><subject>Estimation methods</subject><subject>Experimentation</subject><subject>Heart</subject><subject>Humans</subject><subject>International studies</subject><subject>Mortality</subject><subject>Myocardial infarction</subject><subject>Myocardial Infarction - drug therapy</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Regression Analysis</subject><subject>Secondary prevention</subject><subject>Sympathomimetics</subject><subject>Treatment Outcome</subject><issn>0959-8138</issn><issn>1468-5833</issn><issn>1756-1833</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhS0EoqPSB2AByooVGew4_gliU4byI41AiAJL645zUzxN4mJ7Wua1eBCeCUepRmXFyrLPd66P7iHkMaNLxrh8sRm2S870UlU0vyhO75EFq6Uuheb8PlnQRjSlZlwfkZMYt5TSiivdSPGQHDHKNVNUL8j3P7-L1723l9BiAV3CUAx7byG0DvrCjR0Em5wfXxZxHxMOkJwtAl47vClgbIsBE-T7RcAYM5bfoN9HFx-RBx30EU9uz2Py9e3Z-ep9uf707sPqdF1uaq1TzoooOpSUKaitFqK1dSsq0LqSqrFNiwJbUUuwnWS02VgqqpoDV9xihWj5MXk1z73abQZsLY4pQG-ughsg7I0HZ_5VRvfDXPhrwxmjLNuf3dqD_7nDmMzgosW-hxH9LhrZ6JyznkA2gzb4GAN2hy8YNVMfJveRh2oz9WGmPrLn6d1sdxzz9jPwZAa2Mflw0CvBtKCyyno56y6v_tdBh3BppOJKmI_fVmal3qz5uf5iPmf--cxPWf6f7y-OL7Bb</recordid><startdate>19990626</startdate><enddate>19990626</enddate><creator>Freemantle, Nick</creator><creator>Cleland, John</creator><creator>Young, Philip</creator><creator>Mason, James</creator><creator>Harrison, Jane</creator><general>British Medical Journal Publishing Group</general><general>British Medical Association</general><general>British Medical Journal</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19990626</creationdate><title>β Blockade after myocardial infarction: systematic review and meta regression analysis</title><author>Freemantle, Nick ; Cleland, John ; Young, Philip ; Mason, James ; Harrison, Jane</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b488t-58ee5fe6017a4c855dc4d52a882679c9de5ed546acf6109bc05243a373ce2eec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adrenergic beta-Antagonists - therapeutic use</topic><topic>Cardiovascular agents</topic><topic>Death</topic><topic>Estimation methods</topic><topic>Experimentation</topic><topic>Heart</topic><topic>Humans</topic><topic>International studies</topic><topic>Mortality</topic><topic>Myocardial infarction</topic><topic>Myocardial Infarction - drug therapy</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Regression Analysis</topic><topic>Secondary prevention</topic><topic>Sympathomimetics</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Freemantle, Nick</creatorcontrib><creatorcontrib>Cleland, John</creatorcontrib><creatorcontrib>Young, Philip</creatorcontrib><creatorcontrib>Mason, James</creatorcontrib><creatorcontrib>Harrison, Jane</creatorcontrib><collection>Istex</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMJ</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Freemantle, Nick</au><au>Cleland, John</au><au>Young, Philip</au><au>Mason, James</au><au>Harrison, Jane</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>β Blockade after myocardial infarction: systematic review and meta regression analysis</atitle><jtitle>BMJ</jtitle><addtitle>BMJ</addtitle><date>1999-06-26</date><risdate>1999</risdate><volume>318</volume><issue>7200</issue><spage>1730</spage><epage>1737</epage><pages>1730-1737</pages><issn>0959-8138</issn><eissn>1468-5833</eissn><eissn>1756-1833</eissn><abstract>Abstract Objectives: To assess the effectiveness of β blockers in short term treatment for acute myocardial infarction and in longer term secondary prevention; to examine predictive factors that may influence outcome and therefore choice of drug; and to examine the clinical importance of the results in the light of current treatment. Design:Systematic review of randomised controlled trials. Setting: Randomised controlled trials. Subjects: Patients with acute or past myocardial infarction. Intervention: βBlockers compared with control. Main:outcome measures All cause mortality and non-fatal reinfarction. Results: Overall, 5477 of 54 234 patients (10.1%) randomised to β blockers or control died. We identified a 23% reduction in the odds of death in long term trials (95% confidence interval 15% to 31%), but only a 4% reduction in the odds of death in short term trials (−8% to 15%). Meta regression in long term trials did not identify a significant reduction in effectiveness in drugs with cardioselectivity but did identify a near significant trend towards decreased benefit in drugs with intrinsic sympathomimetic activity. Most evidence is available for propranolol, timolol, and metoprolol. In long term trials, the number needed to treat for 2 years to avoid a death is 42, which compares favourably with other treatments for patients with acute or past myocardial infarction. Conclusions: β Blockers are effective in long term secondary prevention after myocardial infarction, but they are underused in such cases and lead to avoidable mortality and morbidity.</abstract><cop>England</cop><pub>British Medical Journal Publishing Group</pub><pmid>10381708</pmid><doi>10.1136/bmj.318.7200.1730</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adrenergic beta-Antagonists - therapeutic use Cardiovascular agents Death Estimation methods Experimentation Heart Humans International studies Mortality Myocardial infarction Myocardial Infarction - drug therapy Randomized Controlled Trials as Topic Regression Analysis Secondary prevention Sympathomimetics Treatment Outcome |
title | β Blockade after myocardial infarction: systematic review and meta regression analysis |
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