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Predicting the risk of infant mortality for newborns operated for congenital heart defects: A population‐based cohort (EPICARD) study of two post‐operative predictive scores
Background Whereas no global severity score exists for congenital heart defects (CHD), risk (Risk Adjusted Cardiac Heart Surgery‐1: RACHS‐1) and/or complexity (Aristotle Basic Complexity: ABC) scores have been developed for those who undergo surgery. Population‐based studies for assessing the predic...
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Published in: | Health science reports 2021-06, Vol.4 (2), p.e300-n/a |
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creator | Lelong, Nathalie Tararbit, Karim Le Page‐Geniller, Lise‐Marie Cohen, Jérémie Kout, Souad Foix‐L'Hélias, Laurence Boileau, Pascal Chalumeau, Martin Goffinet, François Khoshnood, Babak Goffinet, François Khoshnood, Babak Bonnet, Damien Candilis, Drina Delezoide, Anne‐Lise Goffinet, François Houyel, Lucile Jouannic, Jean‐Marie Khoshnood, Babak Lelong, Nathalie Magnier, Suzel Magny, Jean‐François Rambaud, Caroline Salomon, Dominique Calderon, Johanna Goffinet, François Khoshnood, Babak Lelong, Nathalie Andrieu, Thibaut Thieulin, Anne‐Claire Vodovar, Véronique Bréart, Gérard Cabrol, Dominique Sérraf, Alain Sidi, Daniel Voyer, Marcel |
description | Background
Whereas no global severity score exists for congenital heart defects (CHD), risk (Risk Adjusted Cardiac Heart Surgery‐1: RACHS‐1) and/or complexity (Aristotle Basic Complexity: ABC) scores have been developed for those who undergo surgery. Population‐based studies for assessing the predictive ability of these scores are lacking.
Objective
To assess the predictive ability of RACHS‐1 and ABC scores for the risk of infant mortality using population‐based cohort (EPICARD) data for newborns with structural CHD.
Methods
The study population comprised 443 newborns who underwent curative surgery. We assessed the predictive ability of each score alone and in conjunction with an a priori selected set of predictors of infant mortality. Statistical analysis included logistic regression models for which we computed model calibration, discrimination (ROC), and a rarely used but clinically meaningful measure of variance explained (Tjur's coefficient of discrimination).
Results
The risk of mortality increased with increasing RACHS‐1 and the ABC scores and models based on both scores had adequate calibration. Model discrimination was higher for the RACHS‐1‐based model (ROC 0.68, 95% CI, 0.58‐0.79) than the ABC‐based one (ROC 0.59, 95% CI, 0.49‐0.69), P = 0.03. Neither score had the good predictive ability when this was assessed using Tjur's coefficient.
Conclusions
Even if the RACHS‐1 score had better predictive ability, both scores had low predictive ability using a variance‐explained measure. Because of this limitation and the fact that neither score can be used for newborns with CHD who do not undergo surgery, it is important to develop new predictive models that comprise all newborns with structural CHD. |
doi_str_mv | 10.1002/hsr2.300 |
format | article |
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Whereas no global severity score exists for congenital heart defects (CHD), risk (Risk Adjusted Cardiac Heart Surgery‐1: RACHS‐1) and/or complexity (Aristotle Basic Complexity: ABC) scores have been developed for those who undergo surgery. Population‐based studies for assessing the predictive ability of these scores are lacking.
Objective
To assess the predictive ability of RACHS‐1 and ABC scores for the risk of infant mortality using population‐based cohort (EPICARD) data for newborns with structural CHD.
Methods
The study population comprised 443 newborns who underwent curative surgery. We assessed the predictive ability of each score alone and in conjunction with an a priori selected set of predictors of infant mortality. Statistical analysis included logistic regression models for which we computed model calibration, discrimination (ROC), and a rarely used but clinically meaningful measure of variance explained (Tjur's coefficient of discrimination).
Results
The risk of mortality increased with increasing RACHS‐1 and the ABC scores and models based on both scores had adequate calibration. Model discrimination was higher for the RACHS‐1‐based model (ROC 0.68, 95% CI, 0.58‐0.79) than the ABC‐based one (ROC 0.59, 95% CI, 0.49‐0.69), P = 0.03. Neither score had the good predictive ability when this was assessed using Tjur's coefficient.
Conclusions
Even if the RACHS‐1 score had better predictive ability, both scores had low predictive ability using a variance‐explained measure. Because of this limitation and the fact that neither score can be used for newborns with CHD who do not undergo surgery, it is important to develop new predictive models that comprise all newborns with structural CHD.</description><identifier>ISSN: 2398-8835</identifier><identifier>EISSN: 2398-8835</identifier><identifier>DOI: 10.1002/hsr2.300</identifier><identifier>PMID: 34027127</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Births ; Cardiology ; congenital heart defects ; Infant mortality ; Life Sciences ; Newborn babies ; Pediatrics ; Population ; Population-based studies ; Probability ; severity scores ; Surgery ; thoracic surgery ; Variables</subject><ispartof>Health science reports, 2021-06, Vol.4 (2), p.e300-n/a</ispartof><rights>2021 The Authors. published by Wiley Periodicals LLC.</rights><rights>2021 The Authors. Health Science Reports published by Wiley Periodicals LLC.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</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-c6330-a7bb55aa54fba19937d2e54c72d1e23a0985fcb018e381ff844cc0aeb7fed4df3</citedby><cites>FETCH-LOGICAL-c6330-a7bb55aa54fba19937d2e54c72d1e23a0985fcb018e381ff844cc0aeb7fed4df3</cites><orcidid>0000-0002-3188-0536 ; 0000-0002-1772-2195 ; 0000-0002-8722-5805 ; 0000-0001-8175-3706 ; 0000-0002-2644-6858 ; 0000-0001-9755-6467 ; 0000-0002-7890-3790 ; 0000-0003-3572-8985</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2545615742/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2545615742?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,11543,25734,27905,27906,36993,36994,44571,46033,46457,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34027127$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.sorbonne-universite.fr/hal-03236338$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Lelong, Nathalie</creatorcontrib><creatorcontrib>Tararbit, Karim</creatorcontrib><creatorcontrib>Le Page‐Geniller, Lise‐Marie</creatorcontrib><creatorcontrib>Cohen, Jérémie</creatorcontrib><creatorcontrib>Kout, Souad</creatorcontrib><creatorcontrib>Foix‐L'Hélias, Laurence</creatorcontrib><creatorcontrib>Boileau, Pascal</creatorcontrib><creatorcontrib>Chalumeau, Martin</creatorcontrib><creatorcontrib>Goffinet, François</creatorcontrib><creatorcontrib>Khoshnood, Babak</creatorcontrib><creatorcontrib>Goffinet, François</creatorcontrib><creatorcontrib>Khoshnood, Babak</creatorcontrib><creatorcontrib>Bonnet, Damien</creatorcontrib><creatorcontrib>Candilis, Drina</creatorcontrib><creatorcontrib>Delezoide, Anne‐Lise</creatorcontrib><creatorcontrib>Goffinet, François</creatorcontrib><creatorcontrib>Houyel, Lucile</creatorcontrib><creatorcontrib>Jouannic, Jean‐Marie</creatorcontrib><creatorcontrib>Khoshnood, Babak</creatorcontrib><creatorcontrib>Lelong, Nathalie</creatorcontrib><creatorcontrib>Magnier, Suzel</creatorcontrib><creatorcontrib>Magny, Jean‐François</creatorcontrib><creatorcontrib>Rambaud, Caroline</creatorcontrib><creatorcontrib>Salomon, Dominique</creatorcontrib><creatorcontrib>Calderon, Johanna</creatorcontrib><creatorcontrib>Goffinet, François</creatorcontrib><creatorcontrib>Khoshnood, Babak</creatorcontrib><creatorcontrib>Lelong, Nathalie</creatorcontrib><creatorcontrib>Andrieu, Thibaut</creatorcontrib><creatorcontrib>Thieulin, Anne‐Claire</creatorcontrib><creatorcontrib>Vodovar, Véronique</creatorcontrib><creatorcontrib>Bréart, Gérard</creatorcontrib><creatorcontrib>Cabrol, Dominique</creatorcontrib><creatorcontrib>Sérraf, Alain</creatorcontrib><creatorcontrib>Sidi, Daniel</creatorcontrib><creatorcontrib>Voyer, Marcel</creatorcontrib><creatorcontrib>EPICARD Study Group</creatorcontrib><creatorcontrib>the EPICARD Study Group</creatorcontrib><title>Predicting the risk of infant mortality for newborns operated for congenital heart defects: A population‐based cohort (EPICARD) study of two post‐operative predictive scores</title><title>Health science reports</title><addtitle>Health Sci Rep</addtitle><description>Background
Whereas no global severity score exists for congenital heart defects (CHD), risk (Risk Adjusted Cardiac Heart Surgery‐1: RACHS‐1) and/or complexity (Aristotle Basic Complexity: ABC) scores have been developed for those who undergo surgery. Population‐based studies for assessing the predictive ability of these scores are lacking.
Objective
To assess the predictive ability of RACHS‐1 and ABC scores for the risk of infant mortality using population‐based cohort (EPICARD) data for newborns with structural CHD.
Methods
The study population comprised 443 newborns who underwent curative surgery. We assessed the predictive ability of each score alone and in conjunction with an a priori selected set of predictors of infant mortality. Statistical analysis included logistic regression models for which we computed model calibration, discrimination (ROC), and a rarely used but clinically meaningful measure of variance explained (Tjur's coefficient of discrimination).
Results
The risk of mortality increased with increasing RACHS‐1 and the ABC scores and models based on both scores had adequate calibration. Model discrimination was higher for the RACHS‐1‐based model (ROC 0.68, 95% CI, 0.58‐0.79) than the ABC‐based one (ROC 0.59, 95% CI, 0.49‐0.69), P = 0.03. Neither score had the good predictive ability when this was assessed using Tjur's coefficient.
Conclusions
Even if the RACHS‐1 score had better predictive ability, both scores had low predictive ability using a variance‐explained measure. Because of this limitation and the fact that neither score can be used for newborns with CHD who do not undergo surgery, it is important to develop new predictive models that comprise all newborns with structural CHD.</description><subject>Births</subject><subject>Cardiology</subject><subject>congenital heart defects</subject><subject>Infant mortality</subject><subject>Life Sciences</subject><subject>Newborn babies</subject><subject>Pediatrics</subject><subject>Population</subject><subject>Population-based studies</subject><subject>Probability</subject><subject>severity scores</subject><subject>Surgery</subject><subject>thoracic surgery</subject><subject>Variables</subject><issn>2398-8835</issn><issn>2398-8835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkk9uEzEUh0cIRKtSiRMgS2zaRYr_jDMzLJCiUkilSFQF1pbtec44TMZT25MoO47AVbgSJ8FpQmkrIVa2nr_3_WzrZdlLgs8IxvRNEzw9Yxg_yQ4pq8pRWTL-9N7-IDsOYYETimnOy-p5dsByTAtCi8Ps55WH2upouzmKDSBvwzfkDLKdkV1ES-ejbG3cIOM86mCtnO8Ccj14GaG-rWrXzaGziUMNSB9RDQZ0DG_RBPWuH1oZret-ff-hZEgt2jVJik4uri7PJ9fvT1GIQ73ZZsa1Sw0hJnQXYFeA-v390jZo5yG8yJ4Z2QY43q9H2dcPF1_Op6PZp4_JOBvpMWN4JAulOJeS50ZJUlWsqCnwXBe0JkCZxFXJjVaYlMBKYkyZ51pjCaowUOe1YUfZ5c5bO7kQvbdL6TfCSStuC87PRXqs1S0IqYAqppWqUlwNUhasGsvSsIIQRZROrnc7Vz-oJdQauuhl-0D68KSzjZi7lSgJYyXLk-B0J2getU0nM7GtYUZZene5Iok92Yd5dzNAiGJpg4a2lR24IQjKGeE5K2iR0NeP0IUbfJe-NVGcjauC4_9QOR8TXuT0b6z2LgQP5u6eBIvtoIrtoIo0qAl9df877sA_Y5mA0Q5Y2xY2_xSJ6edruhX-BqUA9sg</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>Lelong, Nathalie</creator><creator>Tararbit, Karim</creator><creator>Le Page‐Geniller, Lise‐Marie</creator><creator>Cohen, Jérémie</creator><creator>Kout, Souad</creator><creator>Foix‐L'Hélias, Laurence</creator><creator>Boileau, Pascal</creator><creator>Chalumeau, Martin</creator><creator>Goffinet, François</creator><creator>Khoshnood, Babak</creator><creator>Goffinet, François</creator><creator>Khoshnood, Babak</creator><creator>Bonnet, Damien</creator><creator>Candilis, Drina</creator><creator>Delezoide, Anne‐Lise</creator><creator>Goffinet, François</creator><creator>Houyel, Lucile</creator><creator>Jouannic, Jean‐Marie</creator><creator>Khoshnood, Babak</creator><creator>Lelong, Nathalie</creator><creator>Magnier, Suzel</creator><creator>Magny, Jean‐François</creator><creator>Rambaud, Caroline</creator><creator>Salomon, Dominique</creator><creator>Calderon, Johanna</creator><creator>Goffinet, François</creator><creator>Khoshnood, Babak</creator><creator>Lelong, 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the risk of infant mortality for newborns operated for congenital heart defects: A population‐based cohort (EPICARD) study of two post‐operative predictive scores</title><author>Lelong, Nathalie ; Tararbit, Karim ; Le Page‐Geniller, Lise‐Marie ; Cohen, Jérémie ; Kout, Souad ; Foix‐L'Hélias, Laurence ; Boileau, Pascal ; Chalumeau, Martin ; Goffinet, François ; Khoshnood, Babak ; Goffinet, François ; Khoshnood, Babak ; Bonnet, Damien ; Candilis, Drina ; Delezoide, Anne‐Lise ; Goffinet, François ; Houyel, Lucile ; Jouannic, Jean‐Marie ; Khoshnood, Babak ; Lelong, Nathalie ; Magnier, Suzel ; Magny, Jean‐François ; Rambaud, Caroline ; Salomon, Dominique ; Calderon, Johanna ; Goffinet, François ; Khoshnood, Babak ; Lelong, Nathalie ; Andrieu, Thibaut ; Thieulin, Anne‐Claire ; Vodovar, Véronique ; Bréart, Gérard ; Cabrol, Dominique ; Sérraf, Alain ; Sidi, Daniel ; Voyer, Marcel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6330-a7bb55aa54fba19937d2e54c72d1e23a0985fcb018e381ff844cc0aeb7fed4df3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Births</topic><topic>Cardiology</topic><topic>congenital heart defects</topic><topic>Infant mortality</topic><topic>Life Sciences</topic><topic>Newborn babies</topic><topic>Pediatrics</topic><topic>Population</topic><topic>Population-based studies</topic><topic>Probability</topic><topic>severity scores</topic><topic>Surgery</topic><topic>thoracic surgery</topic><topic>Variables</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lelong, Nathalie</creatorcontrib><creatorcontrib>Tararbit, Karim</creatorcontrib><creatorcontrib>Le Page‐Geniller, Lise‐Marie</creatorcontrib><creatorcontrib>Cohen, Jérémie</creatorcontrib><creatorcontrib>Kout, 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Johanna</creatorcontrib><creatorcontrib>Goffinet, François</creatorcontrib><creatorcontrib>Khoshnood, Babak</creatorcontrib><creatorcontrib>Lelong, Nathalie</creatorcontrib><creatorcontrib>Andrieu, Thibaut</creatorcontrib><creatorcontrib>Thieulin, Anne‐Claire</creatorcontrib><creatorcontrib>Vodovar, Véronique</creatorcontrib><creatorcontrib>Bréart, Gérard</creatorcontrib><creatorcontrib>Cabrol, Dominique</creatorcontrib><creatorcontrib>Sérraf, Alain</creatorcontrib><creatorcontrib>Sidi, Daniel</creatorcontrib><creatorcontrib>Voyer, Marcel</creatorcontrib><creatorcontrib>EPICARD Study Group</creatorcontrib><creatorcontrib>the EPICARD Study Group</creatorcontrib><collection>Wiley Open Access Journals</collection><collection>Wiley-Blackwell Free Backfiles(OpenAccess)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals(OpenAccess)</collection><jtitle>Health science reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lelong, Nathalie</au><au>Tararbit, Karim</au><au>Le Page‐Geniller, Lise‐Marie</au><au>Cohen, Jérémie</au><au>Kout, Souad</au><au>Foix‐L'Hélias, Laurence</au><au>Boileau, Pascal</au><au>Chalumeau, Martin</au><au>Goffinet, François</au><au>Khoshnood, Babak</au><au>Goffinet, François</au><au>Khoshnood, Babak</au><au>Bonnet, Damien</au><au>Candilis, Drina</au><au>Delezoide, Anne‐Lise</au><au>Goffinet, François</au><au>Houyel, Lucile</au><au>Jouannic, Jean‐Marie</au><au>Khoshnood, Babak</au><au>Lelong, Nathalie</au><au>Magnier, Suzel</au><au>Magny, Jean‐François</au><au>Rambaud, Caroline</au><au>Salomon, Dominique</au><au>Calderon, Johanna</au><au>Goffinet, François</au><au>Khoshnood, Babak</au><au>Lelong, Nathalie</au><au>Andrieu, Thibaut</au><au>Thieulin, Anne‐Claire</au><au>Vodovar, Véronique</au><au>Bréart, Gérard</au><au>Cabrol, Dominique</au><au>Sérraf, Alain</au><au>Sidi, Daniel</au><au>Voyer, Marcel</au><aucorp>EPICARD Study Group</aucorp><aucorp>the EPICARD Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predicting the risk of infant mortality for newborns operated for congenital heart defects: A population‐based cohort (EPICARD) study of two post‐operative predictive scores</atitle><jtitle>Health science reports</jtitle><addtitle>Health Sci Rep</addtitle><date>2021-06</date><risdate>2021</risdate><volume>4</volume><issue>2</issue><spage>e300</spage><epage>n/a</epage><pages>e300-n/a</pages><issn>2398-8835</issn><eissn>2398-8835</eissn><abstract>Background
Whereas no global severity score exists for congenital heart defects (CHD), risk (Risk Adjusted Cardiac Heart Surgery‐1: RACHS‐1) and/or complexity (Aristotle Basic Complexity: ABC) scores have been developed for those who undergo surgery. Population‐based studies for assessing the predictive ability of these scores are lacking.
Objective
To assess the predictive ability of RACHS‐1 and ABC scores for the risk of infant mortality using population‐based cohort (EPICARD) data for newborns with structural CHD.
Methods
The study population comprised 443 newborns who underwent curative surgery. We assessed the predictive ability of each score alone and in conjunction with an a priori selected set of predictors of infant mortality. Statistical analysis included logistic regression models for which we computed model calibration, discrimination (ROC), and a rarely used but clinically meaningful measure of variance explained (Tjur's coefficient of discrimination).
Results
The risk of mortality increased with increasing RACHS‐1 and the ABC scores and models based on both scores had adequate calibration. Model discrimination was higher for the RACHS‐1‐based model (ROC 0.68, 95% CI, 0.58‐0.79) than the ABC‐based one (ROC 0.59, 95% CI, 0.49‐0.69), P = 0.03. Neither score had the good predictive ability when this was assessed using Tjur's coefficient.
Conclusions
Even if the RACHS‐1 score had better predictive ability, both scores had low predictive ability using a variance‐explained measure. Because of this limitation and the fact that neither score can be used for newborns with CHD who do not undergo surgery, it is important to develop new predictive models that comprise all newborns with structural CHD.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>34027127</pmid><doi>10.1002/hsr2.300</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3188-0536</orcidid><orcidid>https://orcid.org/0000-0002-1772-2195</orcidid><orcidid>https://orcid.org/0000-0002-8722-5805</orcidid><orcidid>https://orcid.org/0000-0001-8175-3706</orcidid><orcidid>https://orcid.org/0000-0002-2644-6858</orcidid><orcidid>https://orcid.org/0000-0001-9755-6467</orcidid><orcidid>https://orcid.org/0000-0002-7890-3790</orcidid><orcidid>https://orcid.org/0000-0003-3572-8985</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2398-8835 |
ispartof | Health science reports, 2021-06, Vol.4 (2), p.e300-n/a |
issn | 2398-8835 2398-8835 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_abe2b3cbb9a54deaa7396a8f3711b1bc |
source | Publicly Available Content Database; PubMed Central(OpenAccess); Wiley Open Access Journals |
subjects | Births Cardiology congenital heart defects Infant mortality Life Sciences Newborn babies Pediatrics Population Population-based studies Probability severity scores Surgery thoracic surgery Variables |
title | Predicting the risk of infant mortality for newborns operated for congenital heart defects: A population‐based cohort (EPICARD) study of two post‐operative predictive scores |
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