Temporal trends in mortality and readmission after acute heart failure: a systematic review and meta‐regression in the past four decades
Aims Acute heart failure (AHF) is frequent and life‐threatening disease. However, innovative AHF therapies have remained limited, and care is based on experts' opinion. Temporal trends and benefits of long‐term oral cardiovascular medications on AHF outcomes remain uncertain. Methods and result...
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Veröffentlicht in: | European journal of heart failure 2021-03, Vol.23 (3), p.420-431 |
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creator | Kimmoun, Antoine Takagi, Koji Gall, Emmanuel Ishihara, Shiro Hammoum, Pierre El Bèze, Nathan Bourgeois, Alexandre Chassard, Guillaume Pegorer‐Sfes, Hugo Gayat, Etienne Solal, Alain C. Hollinger, Alexa Merkling, Thomas Mebazaa, Alexandre |
description | Aims
Acute heart failure (AHF) is frequent and life‐threatening disease. However, innovative AHF therapies have remained limited, and care is based on experts' opinion. Temporal trends and benefits of long‐term oral cardiovascular medications on AHF outcomes remain uncertain.
Methods and results
This study is registered with PROSPERO (CRD42018099885). A systematic review ranging from 1980 to 2017, searched AHF studies with more than 100 patients that reported death and/or readmission. Primary outcomes were temporal trends, assessed by meta‐regression, for 30‐day or 1‐year all‐cause death and/or readmission rates. Secondary outcomes were temporal trends of oral cardiovascular therapies and their influence on primary outcomes. Among the 45 143 studies screened, 285 were included, representing 15 million AHFs. In the past decades, though mortality and readmission remain high, there was a decline in 30‐day all‐cause death [odds ratio (OR) for a 10‐year increment: 0.74, 95% confidence interval (CI) 0.61–0.91; P = 0.004] that persisted at 1 year (OR 0.86, 95% CI 0.77–0.96; P = 0.007), while 30‐day and 1‐year all‐cause readmission rate remained roughly unchanged. Trends of primary outcomes were linear and did not differ among continents. Decline in 1‐year all‐cause death rate correlated with high proportions of oral or beta‐blockers, especially when combined with oral renin–angiotensin–aldosterone system inhibitors, but not with diuretics while trends in readmission remained unchanged with these therapies.
Conclusions
Although AHF outcomes remain poor, the present study revealed global favourable trends of survival after AHF episodes probably associated with greater use of oral neurohormonal antagonists. The present study urges to implement the combination of oral renin–angiotensin–aldosterone system inhibitors and beta‐blockers in patients at risk of AHF.
Over the last four decades, after an acute heart failure (AHF) episode, short and long‐term survival has improved markedly but short and long‐term all‐cause readmissions remain unacceptably high. Methodology, screening and main results are shown. For main results, upper panel 1: global and by continents odds ratios (OR) per decade for 1‐year all‐cause mortality. Lower panel 2: Combined effect of renin–angiotensin–aldosterone system inhibitors (RAASi) and beta‐blockers (BBs) at admission on 1‐year all‐cause death. For these analyses, a four‐class variable describing the combination of high and low (i.e. above an |
doi_str_mv | 10.1002/ejhf.2103 |
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Acute heart failure (AHF) is frequent and life‐threatening disease. However, innovative AHF therapies have remained limited, and care is based on experts' opinion. Temporal trends and benefits of long‐term oral cardiovascular medications on AHF outcomes remain uncertain.
Methods and results
This study is registered with PROSPERO (CRD42018099885). A systematic review ranging from 1980 to 2017, searched AHF studies with more than 100 patients that reported death and/or readmission. Primary outcomes were temporal trends, assessed by meta‐regression, for 30‐day or 1‐year all‐cause death and/or readmission rates. Secondary outcomes were temporal trends of oral cardiovascular therapies and their influence on primary outcomes. Among the 45 143 studies screened, 285 were included, representing 15 million AHFs. In the past decades, though mortality and readmission remain high, there was a decline in 30‐day all‐cause death [odds ratio (OR) for a 10‐year increment: 0.74, 95% confidence interval (CI) 0.61–0.91; P = 0.004] that persisted at 1 year (OR 0.86, 95% CI 0.77–0.96; P = 0.007), while 30‐day and 1‐year all‐cause readmission rate remained roughly unchanged. Trends of primary outcomes were linear and did not differ among continents. Decline in 1‐year all‐cause death rate correlated with high proportions of oral or beta‐blockers, especially when combined with oral renin–angiotensin–aldosterone system inhibitors, but not with diuretics while trends in readmission remained unchanged with these therapies.
Conclusions
Although AHF outcomes remain poor, the present study revealed global favourable trends of survival after AHF episodes probably associated with greater use of oral neurohormonal antagonists. The present study urges to implement the combination of oral renin–angiotensin–aldosterone system inhibitors and beta‐blockers in patients at risk of AHF.
Over the last four decades, after an acute heart failure (AHF) episode, short and long‐term survival has improved markedly but short and long‐term all‐cause readmissions remain unacceptably high. Methodology, screening and main results are shown. For main results, upper panel 1: global and by continents odds ratios (OR) per decade for 1‐year all‐cause mortality. Lower panel 2: Combined effect of renin–angiotensin–aldosterone system inhibitors (RAASi) and beta‐blockers (BBs) at admission on 1‐year all‐cause death. For these analyses, a four‐class variable describing the combination of high and low (i.e. above and below the median, respectively) percentages of prescription of RAASi and BBs was created. ORs and 95% confidence interval (CI) are represented. CV, cardiovascular; ER, emergency room.</description><identifier>ISSN: 1388-9842</identifier><identifier>EISSN: 1879-0844</identifier><identifier>DOI: 10.1002/ejhf.2103</identifier><identifier>PMID: 33443295</identifier><language>eng</language><publisher>Oxford, UK: John Wiley & Sons, Ltd</publisher><subject>Acute heart failure ; Cardiology and cardiovascular system ; Human health and pathology ; Life Sciences ; Meta‐analysis ; Outcomes ; Systematic review</subject><ispartof>European journal of heart failure, 2021-03, Vol.23 (3), p.420-431</ispartof><rights>2021 European Society of Cardiology.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3943-a7d8925c452a3227c636335007b958c8d6acaad5ff61ae88e656d07d5fd1b4b53</citedby><cites>FETCH-LOGICAL-c3943-a7d8925c452a3227c636335007b958c8d6acaad5ff61ae88e656d07d5fd1b4b53</cites><orcidid>0000-0001-8715-7753</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fejhf.2103$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fejhf.2103$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,1427,27903,27904,45553,45554,46387,46811</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33443295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.univ-lorraine.fr/hal-03114734$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Kimmoun, Antoine</creatorcontrib><creatorcontrib>Takagi, Koji</creatorcontrib><creatorcontrib>Gall, Emmanuel</creatorcontrib><creatorcontrib>Ishihara, Shiro</creatorcontrib><creatorcontrib>Hammoum, Pierre</creatorcontrib><creatorcontrib>El Bèze, Nathan</creatorcontrib><creatorcontrib>Bourgeois, Alexandre</creatorcontrib><creatorcontrib>Chassard, Guillaume</creatorcontrib><creatorcontrib>Pegorer‐Sfes, Hugo</creatorcontrib><creatorcontrib>Gayat, Etienne</creatorcontrib><creatorcontrib>Solal, Alain C.</creatorcontrib><creatorcontrib>Hollinger, Alexa</creatorcontrib><creatorcontrib>Merkling, Thomas</creatorcontrib><creatorcontrib>Mebazaa, Alexandre</creatorcontrib><creatorcontrib>METAHF Team</creatorcontrib><title>Temporal trends in mortality and readmission after acute heart failure: a systematic review and meta‐regression in the past four decades</title><title>European journal of heart failure</title><addtitle>Eur J Heart Fail</addtitle><description>Aims
Acute heart failure (AHF) is frequent and life‐threatening disease. However, innovative AHF therapies have remained limited, and care is based on experts' opinion. Temporal trends and benefits of long‐term oral cardiovascular medications on AHF outcomes remain uncertain.
Methods and results
This study is registered with PROSPERO (CRD42018099885). A systematic review ranging from 1980 to 2017, searched AHF studies with more than 100 patients that reported death and/or readmission. Primary outcomes were temporal trends, assessed by meta‐regression, for 30‐day or 1‐year all‐cause death and/or readmission rates. Secondary outcomes were temporal trends of oral cardiovascular therapies and their influence on primary outcomes. Among the 45 143 studies screened, 285 were included, representing 15 million AHFs. In the past decades, though mortality and readmission remain high, there was a decline in 30‐day all‐cause death [odds ratio (OR) for a 10‐year increment: 0.74, 95% confidence interval (CI) 0.61–0.91; P = 0.004] that persisted at 1 year (OR 0.86, 95% CI 0.77–0.96; P = 0.007), while 30‐day and 1‐year all‐cause readmission rate remained roughly unchanged. Trends of primary outcomes were linear and did not differ among continents. Decline in 1‐year all‐cause death rate correlated with high proportions of oral or beta‐blockers, especially when combined with oral renin–angiotensin–aldosterone system inhibitors, but not with diuretics while trends in readmission remained unchanged with these therapies.
Conclusions
Although AHF outcomes remain poor, the present study revealed global favourable trends of survival after AHF episodes probably associated with greater use of oral neurohormonal antagonists. The present study urges to implement the combination of oral renin–angiotensin–aldosterone system inhibitors and beta‐blockers in patients at risk of AHF.
Over the last four decades, after an acute heart failure (AHF) episode, short and long‐term survival has improved markedly but short and long‐term all‐cause readmissions remain unacceptably high. Methodology, screening and main results are shown. For main results, upper panel 1: global and by continents odds ratios (OR) per decade for 1‐year all‐cause mortality. Lower panel 2: Combined effect of renin–angiotensin–aldosterone system inhibitors (RAASi) and beta‐blockers (BBs) at admission on 1‐year all‐cause death. For these analyses, a four‐class variable describing the combination of high and low (i.e. above and below the median, respectively) percentages of prescription of RAASi and BBs was created. ORs and 95% confidence interval (CI) are represented. CV, cardiovascular; ER, emergency room.</description><subject>Acute heart failure</subject><subject>Cardiology and cardiovascular system</subject><subject>Human health and pathology</subject><subject>Life Sciences</subject><subject>Meta‐analysis</subject><subject>Outcomes</subject><subject>Systematic review</subject><issn>1388-9842</issn><issn>1879-0844</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kbtOHDEUhq0oCAihyAtELkMx4NvMeNIhBNmglWhIbZ21z2SN5rKxPaDtqKl4Rp4kXpZLRXWso-__juSfkG-cHXPGxAneLNtjwZn8RPa5rpuCaaU-57fUumi0EnvkS4w3jPE647tkT0qlpGjKffJwjf1qDNDRFHBwkfqB9mNI0Pm0pjA4GhBc72P040ChTRgo2CkhXSKERFvw3RTwJwUa1zFhD8nbnLn1ePcc7zHB0_1jwL8Bt5J8IS2RriDm-DgF6tCCw_iV7LTQRTx8mQfkz8X59dmsmF_9-n12Oi-sbJQsoHa6EaVVpQApRG0rWUlZMlYvmlJb7SqwAK5s24oDao1VWTlW54XjC7Uo5QE52nqX0JlV8D2EtRnBm9np3Gx2THKuaqlueWZ_bNlVGP9NGJPJX2Gx62DAcYpGqFozxbWu3rU2jDEGbN_cnJlNTWZTk9nUlNnvL9pp0aN7I197ycDJFrjzHa4_Npnzy9nFs_I_-HOe4g</recordid><startdate>202103</startdate><enddate>202103</enddate><creator>Kimmoun, Antoine</creator><creator>Takagi, Koji</creator><creator>Gall, Emmanuel</creator><creator>Ishihara, Shiro</creator><creator>Hammoum, Pierre</creator><creator>El Bèze, Nathan</creator><creator>Bourgeois, Alexandre</creator><creator>Chassard, Guillaume</creator><creator>Pegorer‐Sfes, Hugo</creator><creator>Gayat, Etienne</creator><creator>Solal, Alain C.</creator><creator>Hollinger, Alexa</creator><creator>Merkling, Thomas</creator><creator>Mebazaa, Alexandre</creator><general>John Wiley & Sons, Ltd</general><general>European Society of Cardiology (Wiley)</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-8715-7753</orcidid></search><sort><creationdate>202103</creationdate><title>Temporal trends in mortality and readmission after acute heart failure: a systematic review and meta‐regression in the past four decades</title><author>Kimmoun, Antoine ; Takagi, Koji ; Gall, Emmanuel ; Ishihara, Shiro ; Hammoum, Pierre ; El Bèze, Nathan ; Bourgeois, Alexandre ; Chassard, Guillaume ; Pegorer‐Sfes, Hugo ; Gayat, Etienne ; Solal, Alain C. ; Hollinger, Alexa ; Merkling, Thomas ; Mebazaa, Alexandre</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3943-a7d8925c452a3227c636335007b958c8d6acaad5ff61ae88e656d07d5fd1b4b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acute heart failure</topic><topic>Cardiology and cardiovascular system</topic><topic>Human health and pathology</topic><topic>Life Sciences</topic><topic>Meta‐analysis</topic><topic>Outcomes</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kimmoun, Antoine</creatorcontrib><creatorcontrib>Takagi, Koji</creatorcontrib><creatorcontrib>Gall, Emmanuel</creatorcontrib><creatorcontrib>Ishihara, Shiro</creatorcontrib><creatorcontrib>Hammoum, Pierre</creatorcontrib><creatorcontrib>El Bèze, Nathan</creatorcontrib><creatorcontrib>Bourgeois, Alexandre</creatorcontrib><creatorcontrib>Chassard, Guillaume</creatorcontrib><creatorcontrib>Pegorer‐Sfes, Hugo</creatorcontrib><creatorcontrib>Gayat, Etienne</creatorcontrib><creatorcontrib>Solal, Alain C.</creatorcontrib><creatorcontrib>Hollinger, Alexa</creatorcontrib><creatorcontrib>Merkling, Thomas</creatorcontrib><creatorcontrib>Mebazaa, Alexandre</creatorcontrib><creatorcontrib>METAHF Team</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>European journal of heart failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kimmoun, Antoine</au><au>Takagi, Koji</au><au>Gall, Emmanuel</au><au>Ishihara, Shiro</au><au>Hammoum, Pierre</au><au>El Bèze, Nathan</au><au>Bourgeois, Alexandre</au><au>Chassard, Guillaume</au><au>Pegorer‐Sfes, Hugo</au><au>Gayat, Etienne</au><au>Solal, Alain C.</au><au>Hollinger, Alexa</au><au>Merkling, Thomas</au><au>Mebazaa, Alexandre</au><aucorp>METAHF Team</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Temporal trends in mortality and readmission after acute heart failure: a systematic review and meta‐regression in the past four decades</atitle><jtitle>European journal of heart failure</jtitle><addtitle>Eur J Heart Fail</addtitle><date>2021-03</date><risdate>2021</risdate><volume>23</volume><issue>3</issue><spage>420</spage><epage>431</epage><pages>420-431</pages><issn>1388-9842</issn><eissn>1879-0844</eissn><abstract>Aims
Acute heart failure (AHF) is frequent and life‐threatening disease. However, innovative AHF therapies have remained limited, and care is based on experts' opinion. Temporal trends and benefits of long‐term oral cardiovascular medications on AHF outcomes remain uncertain.
Methods and results
This study is registered with PROSPERO (CRD42018099885). A systematic review ranging from 1980 to 2017, searched AHF studies with more than 100 patients that reported death and/or readmission. Primary outcomes were temporal trends, assessed by meta‐regression, for 30‐day or 1‐year all‐cause death and/or readmission rates. Secondary outcomes were temporal trends of oral cardiovascular therapies and their influence on primary outcomes. Among the 45 143 studies screened, 285 were included, representing 15 million AHFs. In the past decades, though mortality and readmission remain high, there was a decline in 30‐day all‐cause death [odds ratio (OR) for a 10‐year increment: 0.74, 95% confidence interval (CI) 0.61–0.91; P = 0.004] that persisted at 1 year (OR 0.86, 95% CI 0.77–0.96; P = 0.007), while 30‐day and 1‐year all‐cause readmission rate remained roughly unchanged. Trends of primary outcomes were linear and did not differ among continents. Decline in 1‐year all‐cause death rate correlated with high proportions of oral or beta‐blockers, especially when combined with oral renin–angiotensin–aldosterone system inhibitors, but not with diuretics while trends in readmission remained unchanged with these therapies.
Conclusions
Although AHF outcomes remain poor, the present study revealed global favourable trends of survival after AHF episodes probably associated with greater use of oral neurohormonal antagonists. The present study urges to implement the combination of oral renin–angiotensin–aldosterone system inhibitors and beta‐blockers in patients at risk of AHF.
Over the last four decades, after an acute heart failure (AHF) episode, short and long‐term survival has improved markedly but short and long‐term all‐cause readmissions remain unacceptably high. Methodology, screening and main results are shown. For main results, upper panel 1: global and by continents odds ratios (OR) per decade for 1‐year all‐cause mortality. Lower panel 2: Combined effect of renin–angiotensin–aldosterone system inhibitors (RAASi) and beta‐blockers (BBs) at admission on 1‐year all‐cause death. For these analyses, a four‐class variable describing the combination of high and low (i.e. above and below the median, respectively) percentages of prescription of RAASi and BBs was created. ORs and 95% confidence interval (CI) are represented. CV, cardiovascular; ER, emergency room.</abstract><cop>Oxford, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>33443295</pmid><doi>10.1002/ejhf.2103</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8715-7753</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute heart failure Cardiology and cardiovascular system Human health and pathology Life Sciences Meta‐analysis Outcomes Systematic review |
title | Temporal trends in mortality and readmission after acute heart failure: a systematic review and meta‐regression in the past four decades |
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