Management of congenital diaphragmatic hernia with transposition of the great arteries
Congenital diaphragmatic hernia (CDH) is a relatively rare malformation, but it has a high mortality rate. Its association with congenital heart disease lowers survival rate due to severe acidosis and desaturation caused by persistent pulmonary hypertension of the neonate. We describe herein a case...
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Veröffentlicht in: | Pediatrics international 2016-06, Vol.58 (6), p.516-518 |
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creator | Nagata, Hazumu Yamamura, Kenichiro Nagata, Kouji Uike, Kiyoshi Morihana, Eiji Ihara, Kenji Yumoto, Yasuo Fusazaki, Naoki Kado, Hideaki Kato, Kiyoko Taguchi, Tomoaki Hara, Toshiro |
description | Congenital diaphragmatic hernia (CDH) is a relatively rare malformation, but it has a high mortality rate. Its association with congenital heart disease lowers survival rate due to severe acidosis and desaturation caused by persistent pulmonary hypertension of the neonate. We describe herein a case of CDH with transposition of the great arteries and intact ventricular septum, in a patient who was prenatally diagnosed, managed with extracorporeal oxygenation (ECMO) support and successfully treated with both CDH repair and Jatene procedure, with no respiratory or circulatory sequelae. In conclusion, precise prenatal estimation is essential, and ECMO is a useful therapeutic option in these complex cases. |
doi_str_mv | 10.1111/ped.12912 |
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Its association with congenital heart disease lowers survival rate due to severe acidosis and desaturation caused by persistent pulmonary hypertension of the neonate. We describe herein a case of CDH with transposition of the great arteries and intact ventricular septum, in a patient who was prenatally diagnosed, managed with extracorporeal oxygenation (ECMO) support and successfully treated with both CDH repair and Jatene procedure, with no respiratory or circulatory sequelae. In conclusion, precise prenatal estimation is essential, and ECMO is a useful therapeutic option in these complex cases.</description><identifier>ISSN: 1328-8067</identifier><identifier>EISSN: 1442-200X</identifier><identifier>DOI: 10.1111/ped.12912</identifier><identifier>PMID: 27073102</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject>Acidosis ; Arteries ; Cardiovascular disease ; Complications ; congenital diaphragmatic hernia ; Congenital diseases ; Coronary artery disease ; Desaturation ; extracorporeal oxygenation ; Heart diseases ; Heart rate ; Hernia ; Hernias ; Mortality ; Oxygenation ; Pediatrics ; persistent pulmonary hypertension of the neonate ; Prenatal development ; pulmonary hypoplasia ; Septum ; Transposition ; transposition of the great arteries and intact ventricular septum ; Ventricle</subject><ispartof>Pediatrics international, 2016-06, Vol.58 (6), p.516-518</ispartof><rights>2016 Japan Pediatric Society</rights><rights>2016 Japan Pediatric Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4752-3ea276419a3f4d86ed5562896281e25456464d0be23cdc3f6ac804e9c018191c3</citedby><cites>FETCH-LOGICAL-c4752-3ea276419a3f4d86ed5562896281e25456464d0be23cdc3f6ac804e9c018191c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fped.12912$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fped.12912$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27073102$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nagata, Hazumu</creatorcontrib><creatorcontrib>Yamamura, Kenichiro</creatorcontrib><creatorcontrib>Nagata, Kouji</creatorcontrib><creatorcontrib>Uike, Kiyoshi</creatorcontrib><creatorcontrib>Morihana, Eiji</creatorcontrib><creatorcontrib>Ihara, Kenji</creatorcontrib><creatorcontrib>Yumoto, Yasuo</creatorcontrib><creatorcontrib>Fusazaki, Naoki</creatorcontrib><creatorcontrib>Kado, Hideaki</creatorcontrib><creatorcontrib>Kato, Kiyoko</creatorcontrib><creatorcontrib>Taguchi, Tomoaki</creatorcontrib><creatorcontrib>Hara, Toshiro</creatorcontrib><title>Management of congenital diaphragmatic hernia with transposition of the great arteries</title><title>Pediatrics international</title><addtitle>Pediatr Int</addtitle><description>Congenital diaphragmatic hernia (CDH) is a relatively rare malformation, but it has a high mortality rate. Its association with congenital heart disease lowers survival rate due to severe acidosis and desaturation caused by persistent pulmonary hypertension of the neonate. We describe herein a case of CDH with transposition of the great arteries and intact ventricular septum, in a patient who was prenatally diagnosed, managed with extracorporeal oxygenation (ECMO) support and successfully treated with both CDH repair and Jatene procedure, with no respiratory or circulatory sequelae. In conclusion, precise prenatal estimation is essential, and ECMO is a useful therapeutic option in these complex cases.</description><subject>Acidosis</subject><subject>Arteries</subject><subject>Cardiovascular disease</subject><subject>Complications</subject><subject>congenital diaphragmatic hernia</subject><subject>Congenital diseases</subject><subject>Coronary artery disease</subject><subject>Desaturation</subject><subject>extracorporeal oxygenation</subject><subject>Heart diseases</subject><subject>Heart rate</subject><subject>Hernia</subject><subject>Hernias</subject><subject>Mortality</subject><subject>Oxygenation</subject><subject>Pediatrics</subject><subject>persistent pulmonary hypertension of the neonate</subject><subject>Prenatal development</subject><subject>pulmonary hypoplasia</subject><subject>Septum</subject><subject>Transposition</subject><subject>transposition of the great arteries and intact ventricular septum</subject><subject>Ventricle</subject><issn>1328-8067</issn><issn>1442-200X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNp90ctKxDAUBuAgiveFLyAFN7qo5tYkXcp4BUUXKu5CTE9nIm1akwzi25txdCNoIOQQvvwEfoT2CD4meZ2M0BwTWhO6gjYJ57SkGD-v5plRVSos5AbaivEVY6yk4utog0osGcF0Ez3dGm-m0INPxdAWdvBT8C6ZrmicGWfBTHuTnC1mELwzxbtLsyIF4-M4RJfc4Bev0gyKaQCTChMSBAdxB621pouw-31uo8eL84fJVXlzd3k9Ob0pLZcVLRkYKgUntWEtb5SApqoEVXXeBGjFK8EFb_ALUGYby1phrMIcaouJIjWxbBsdLnPHMLzNISbdu2ih64yHYR41UVgJzghjmR78oq_DPPj8O02JEEIyWlX_KSJrhVkl2UIdLZUNQ4wBWj0G15vwoQnWi0p0rkR_VZLt_nfi_KXPtz_yp4MMTpbg3XXw8XeSvj8_W0Z-ArV0k1U</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Nagata, Hazumu</creator><creator>Yamamura, Kenichiro</creator><creator>Nagata, Kouji</creator><creator>Uike, Kiyoshi</creator><creator>Morihana, Eiji</creator><creator>Ihara, Kenji</creator><creator>Yumoto, Yasuo</creator><creator>Fusazaki, Naoki</creator><creator>Kado, Hideaki</creator><creator>Kato, Kiyoko</creator><creator>Taguchi, Tomoaki</creator><creator>Hara, Toshiro</creator><general>Blackwell Publishing Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope></search><sort><creationdate>201606</creationdate><title>Management of congenital diaphragmatic hernia with transposition of the great arteries</title><author>Nagata, Hazumu ; Yamamura, Kenichiro ; Nagata, Kouji ; Uike, Kiyoshi ; Morihana, Eiji ; Ihara, Kenji ; Yumoto, Yasuo ; Fusazaki, Naoki ; Kado, Hideaki ; Kato, Kiyoko ; Taguchi, Tomoaki ; Hara, Toshiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4752-3ea276419a3f4d86ed5562896281e25456464d0be23cdc3f6ac804e9c018191c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acidosis</topic><topic>Arteries</topic><topic>Cardiovascular disease</topic><topic>Complications</topic><topic>congenital diaphragmatic hernia</topic><topic>Congenital diseases</topic><topic>Coronary artery disease</topic><topic>Desaturation</topic><topic>extracorporeal oxygenation</topic><topic>Heart diseases</topic><topic>Heart rate</topic><topic>Hernia</topic><topic>Hernias</topic><topic>Mortality</topic><topic>Oxygenation</topic><topic>Pediatrics</topic><topic>persistent pulmonary hypertension of the neonate</topic><topic>Prenatal development</topic><topic>pulmonary hypoplasia</topic><topic>Septum</topic><topic>Transposition</topic><topic>transposition of the great arteries and intact ventricular septum</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nagata, Hazumu</creatorcontrib><creatorcontrib>Yamamura, Kenichiro</creatorcontrib><creatorcontrib>Nagata, Kouji</creatorcontrib><creatorcontrib>Uike, Kiyoshi</creatorcontrib><creatorcontrib>Morihana, Eiji</creatorcontrib><creatorcontrib>Ihara, Kenji</creatorcontrib><creatorcontrib>Yumoto, Yasuo</creatorcontrib><creatorcontrib>Fusazaki, Naoki</creatorcontrib><creatorcontrib>Kado, Hideaki</creatorcontrib><creatorcontrib>Kato, Kiyoko</creatorcontrib><creatorcontrib>Taguchi, Tomoaki</creatorcontrib><creatorcontrib>Hara, Toshiro</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Pediatrics international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nagata, Hazumu</au><au>Yamamura, Kenichiro</au><au>Nagata, Kouji</au><au>Uike, Kiyoshi</au><au>Morihana, Eiji</au><au>Ihara, Kenji</au><au>Yumoto, Yasuo</au><au>Fusazaki, Naoki</au><au>Kado, Hideaki</au><au>Kato, Kiyoko</au><au>Taguchi, Tomoaki</au><au>Hara, Toshiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management of congenital diaphragmatic hernia with transposition of the great arteries</atitle><jtitle>Pediatrics international</jtitle><addtitle>Pediatr Int</addtitle><date>2016-06</date><risdate>2016</risdate><volume>58</volume><issue>6</issue><spage>516</spage><epage>518</epage><pages>516-518</pages><issn>1328-8067</issn><eissn>1442-200X</eissn><abstract>Congenital diaphragmatic hernia (CDH) is a relatively rare malformation, but it has a high mortality rate. Its association with congenital heart disease lowers survival rate due to severe acidosis and desaturation caused by persistent pulmonary hypertension of the neonate. We describe herein a case of CDH with transposition of the great arteries and intact ventricular septum, in a patient who was prenatally diagnosed, managed with extracorporeal oxygenation (ECMO) support and successfully treated with both CDH repair and Jatene procedure, with no respiratory or circulatory sequelae. In conclusion, precise prenatal estimation is essential, and ECMO is a useful therapeutic option in these complex cases.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>27073102</pmid><doi>10.1111/ped.12912</doi><tpages>3</tpages></addata></record> |
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subjects | Acidosis Arteries Cardiovascular disease Complications congenital diaphragmatic hernia Congenital diseases Coronary artery disease Desaturation extracorporeal oxygenation Heart diseases Heart rate Hernia Hernias Mortality Oxygenation Pediatrics persistent pulmonary hypertension of the neonate Prenatal development pulmonary hypoplasia Septum Transposition transposition of the great arteries and intact ventricular septum Ventricle |
title | Management of congenital diaphragmatic hernia with transposition of the great arteries |
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