Risk Factors for Chronic Lung Disease and Mortality in Newborns with Congenital Diaphragmatic Hernia
Background: Congenital diaphragmatic hernia (CDH) is associated with a mortality rate of 10–35% in live-born infants. Moreover, CDH survivors have a substantial risk of developing long-term pulmonary sequelae, such as bronchopulmonary dysplasia (BPD). Objectives: This study aims to evaluate risk fac...
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Veröffentlicht in: | Neonatology (Basel, Switzerland) Switzerland), 2010-01, Vol.98 (4), p.370-380 |
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description | Background: Congenital diaphragmatic hernia (CDH) is associated with a mortality rate of 10–35% in live-born infants. Moreover, CDH survivors have a substantial risk of developing long-term pulmonary sequelae, such as bronchopulmonary dysplasia (BPD). Objectives: This study aims to evaluate risk factors associated with BPD and mortality in neonates with CDH, with particular focus on the initial ventilation mode. Methods: Eligible for inclusion were live-born infants with CDH born from 2001 through 2006 at the centers participating in the CDH Study Group. BPD (defined as oxygen dependency at day 30) and/or mortality by day 30 served as the primary endpoint. Results: A total of 2,078 neonates were included in the analysis. At day 30, 56% of the patients had either died or met the criteria for BPD. In infants who survived until day 30, the prevalence of BPD was 41%. The overall mortality rate was 31%. High-frequency oscillatory ventilation as initial ventilation mode, a right-sided defect, a prenatal diagnosis, a lower Apgar score at 5 min, a cardiac anomaly, a chromosomal anomaly and a lower gestational age were all associated with BPD and/or mortality by day 30. Conclusions: Despite improvements in neonatal care, the rates of BPD and early mortality in newborns with CDH are still considerable. Several important risk factors for a worse outcome are reported in this nonrandomized prospective observational study. |
doi_str_mv | 10.1159/000316974 |
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Moreover, CDH survivors have a substantial risk of developing long-term pulmonary sequelae, such as bronchopulmonary dysplasia (BPD). Objectives: This study aims to evaluate risk factors associated with BPD and mortality in neonates with CDH, with particular focus on the initial ventilation mode. Methods: Eligible for inclusion were live-born infants with CDH born from 2001 through 2006 at the centers participating in the CDH Study Group. BPD (defined as oxygen dependency at day 30) and/or mortality by day 30 served as the primary endpoint. Results: A total of 2,078 neonates were included in the analysis. At day 30, 56% of the patients had either died or met the criteria for BPD. In infants who survived until day 30, the prevalence of BPD was 41%. The overall mortality rate was 31%. High-frequency oscillatory ventilation as initial ventilation mode, a right-sided defect, a prenatal diagnosis, a lower Apgar score at 5 min, a cardiac anomaly, a chromosomal anomaly and a lower gestational age were all associated with BPD and/or mortality by day 30. Conclusions: Despite improvements in neonatal care, the rates of BPD and early mortality in newborns with CDH are still considerable. Several important risk factors for a worse outcome are reported in this nonrandomized prospective observational study.</description><identifier>ISSN: 1661-7800</identifier><identifier>EISSN: 1661-7819</identifier><identifier>DOI: 10.1159/000316974</identifier><identifier>PMID: 21042035</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Bronchopulmonary Dysplasia - mortality ; Chronic Disease ; Comorbidity ; Databases, Factual ; Female ; Hernia, Diaphragmatic - mortality ; Hernias, Diaphragmatic, Congenital ; High-Frequency Ventilation - adverse effects ; Humans ; Infant, Newborn ; International Cooperation ; Male ; Original Paper ; Prospective Studies ; Registries ; Respiratory Insufficiency - therapy ; Risk Factors ; Survival Rate</subject><ispartof>Neonatology (Basel, Switzerland), 2010-01, Vol.98 (4), p.370-380</ispartof><rights>2010 S. Karger AG, Basel</rights><rights>Copyright © 2010 S. Karger AG, Basel.</rights><rights>Copyright (c) 2010 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-eeb191a01dad2b88863deb8594ced019e371f50cedb2eeace53ac2f446b109b33</citedby><cites>FETCH-LOGICAL-c367t-eeb191a01dad2b88863deb8594ced019e371f50cedb2eeace53ac2f446b109b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,2425,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21042035$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van den Hout, L.</creatorcontrib><creatorcontrib>Reiss, I.</creatorcontrib><creatorcontrib>Felix, J.F.</creatorcontrib><creatorcontrib>Hop, W.C.J.</creatorcontrib><creatorcontrib>Lally, Pamela A.</creatorcontrib><creatorcontrib>Lally, Kevin P.</creatorcontrib><creatorcontrib>Tibboel, D.</creatorcontrib><creatorcontrib>Congenital Diaphragmatic Hernia Study Group</creatorcontrib><creatorcontrib>for the Congenital Diaphragmatic Hernia Study Group</creatorcontrib><title>Risk Factors for Chronic Lung Disease and Mortality in Newborns with Congenital Diaphragmatic Hernia</title><title>Neonatology (Basel, Switzerland)</title><addtitle>Neonatology</addtitle><description>Background: Congenital diaphragmatic hernia (CDH) is associated with a mortality rate of 10–35% in live-born infants. Moreover, CDH survivors have a substantial risk of developing long-term pulmonary sequelae, such as bronchopulmonary dysplasia (BPD). Objectives: This study aims to evaluate risk factors associated with BPD and mortality in neonates with CDH, with particular focus on the initial ventilation mode. Methods: Eligible for inclusion were live-born infants with CDH born from 2001 through 2006 at the centers participating in the CDH Study Group. BPD (defined as oxygen dependency at day 30) and/or mortality by day 30 served as the primary endpoint. Results: A total of 2,078 neonates were included in the analysis. At day 30, 56% of the patients had either died or met the criteria for BPD. In infants who survived until day 30, the prevalence of BPD was 41%. The overall mortality rate was 31%. High-frequency oscillatory ventilation as initial ventilation mode, a right-sided defect, a prenatal diagnosis, a lower Apgar score at 5 min, a cardiac anomaly, a chromosomal anomaly and a lower gestational age were all associated with BPD and/or mortality by day 30. Conclusions: Despite improvements in neonatal care, the rates of BPD and early mortality in newborns with CDH are still considerable. Several important risk factors for a worse outcome are reported in this nonrandomized prospective observational study.</description><subject>Bronchopulmonary Dysplasia - mortality</subject><subject>Chronic Disease</subject><subject>Comorbidity</subject><subject>Databases, Factual</subject><subject>Female</subject><subject>Hernia, Diaphragmatic - mortality</subject><subject>Hernias, Diaphragmatic, Congenital</subject><subject>High-Frequency Ventilation - adverse effects</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>International Cooperation</subject><subject>Male</subject><subject>Original Paper</subject><subject>Prospective Studies</subject><subject>Registries</subject><subject>Respiratory Insufficiency - therapy</subject><subject>Risk Factors</subject><subject>Survival Rate</subject><issn>1661-7800</issn><issn>1661-7819</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpd0M9LwzAUB_AgitPpwbtI8CIeqnlt0x9Hqc4JU0H0XNL2tcvWJTNpGfvvjWz24CkJ-bwvjy8hF8DuAHh6zxgLIErj8ICcQBSBFyeQHg53xkbk1NoFY5zzyD8mIx9Y6LOAn5DqQ9olnYiy08bSWhuazY1WsqSzXjX0UVoUFqlQFX3VphOt7LZUKvqGm0IbZelGdnOaadWgku7bTYj13IhmJToXMkWjpDgjR7VoLZ7vzzH5mjx9ZlNv9v78kj3MvDKI4s5DLCAFwaASlV8kSRIFFRYJT8MSKwYpBjHUnLlH4SOKEnkgSr8Ow6gAlhZBMCY3u9y10d892i5fSVti2wqFurd5wpKQpzHnTl7_kwvdG-WWyxMIXWNxCA7d7lBptLUG63xt5EqYbQ4s_y0-H4p39mof2BcrrAb517QDlzuwFKZBM4D9_A8CUoap</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>van den Hout, L.</creator><creator>Reiss, I.</creator><creator>Felix, J.F.</creator><creator>Hop, W.C.J.</creator><creator>Lally, Pamela A.</creator><creator>Lally, Kevin P.</creator><creator>Tibboel, D.</creator><general>S. 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mortality</topic><topic>Chronic Disease</topic><topic>Comorbidity</topic><topic>Databases, Factual</topic><topic>Female</topic><topic>Hernia, Diaphragmatic - mortality</topic><topic>Hernias, Diaphragmatic, Congenital</topic><topic>High-Frequency Ventilation - adverse effects</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>International Cooperation</topic><topic>Male</topic><topic>Original Paper</topic><topic>Prospective Studies</topic><topic>Registries</topic><topic>Respiratory Insufficiency - therapy</topic><topic>Risk Factors</topic><topic>Survival Rate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van den Hout, L.</creatorcontrib><creatorcontrib>Reiss, I.</creatorcontrib><creatorcontrib>Felix, J.F.</creatorcontrib><creatorcontrib>Hop, W.C.J.</creatorcontrib><creatorcontrib>Lally, Pamela A.</creatorcontrib><creatorcontrib>Lally, Kevin P.</creatorcontrib><creatorcontrib>Tibboel, D.</creatorcontrib><creatorcontrib>Congenital Diaphragmatic Hernia Study Group</creatorcontrib><creatorcontrib>for the Congenital Diaphragmatic Hernia Study Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</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>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</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 Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database (ProQuest)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Neonatology (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van den Hout, L.</au><au>Reiss, I.</au><au>Felix, J.F.</au><au>Hop, W.C.J.</au><au>Lally, Pamela A.</au><au>Lally, Kevin P.</au><au>Tibboel, D.</au><aucorp>Congenital Diaphragmatic Hernia Study Group</aucorp><aucorp>for the Congenital Diaphragmatic Hernia Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk Factors for Chronic Lung Disease and Mortality in Newborns with Congenital Diaphragmatic Hernia</atitle><jtitle>Neonatology (Basel, Switzerland)</jtitle><addtitle>Neonatology</addtitle><date>2010-01-01</date><risdate>2010</risdate><volume>98</volume><issue>4</issue><spage>370</spage><epage>380</epage><pages>370-380</pages><issn>1661-7800</issn><eissn>1661-7819</eissn><abstract>Background: Congenital diaphragmatic hernia (CDH) is associated with a mortality rate of 10–35% in live-born infants. Moreover, CDH survivors have a substantial risk of developing long-term pulmonary sequelae, such as bronchopulmonary dysplasia (BPD). Objectives: This study aims to evaluate risk factors associated with BPD and mortality in neonates with CDH, with particular focus on the initial ventilation mode. Methods: Eligible for inclusion were live-born infants with CDH born from 2001 through 2006 at the centers participating in the CDH Study Group. BPD (defined as oxygen dependency at day 30) and/or mortality by day 30 served as the primary endpoint. Results: A total of 2,078 neonates were included in the analysis. At day 30, 56% of the patients had either died or met the criteria for BPD. In infants who survived until day 30, the prevalence of BPD was 41%. The overall mortality rate was 31%. High-frequency oscillatory ventilation as initial ventilation mode, a right-sided defect, a prenatal diagnosis, a lower Apgar score at 5 min, a cardiac anomaly, a chromosomal anomaly and a lower gestational age were all associated with BPD and/or mortality by day 30. Conclusions: Despite improvements in neonatal care, the rates of BPD and early mortality in newborns with CDH are still considerable. Several important risk factors for a worse outcome are reported in this nonrandomized prospective observational study.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>21042035</pmid><doi>10.1159/000316974</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bronchopulmonary Dysplasia - mortality Chronic Disease Comorbidity Databases, Factual Female Hernia, Diaphragmatic - mortality Hernias, Diaphragmatic, Congenital High-Frequency Ventilation - adverse effects Humans Infant, Newborn International Cooperation Male Original Paper Prospective Studies Registries Respiratory Insufficiency - therapy Risk Factors Survival Rate |
title | Risk Factors for Chronic Lung Disease and Mortality in Newborns with Congenital Diaphragmatic Hernia |
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