Management of congenital diaphragmatic hernia with transposition of the great arteries

Hazumu Nagata; Kenichiro Yamamura; Kouji Nagata; Kiyoshi Uike; Eiji Morihana; Kenji Ihara; Yasuo Yumoto; Naoki Fusazaki; Hideaki Kado; Kiyoko Kato; Tomoaki Taguchi; Toshiro Hara

doi:10.1111/ped.12912

Management of congenital diaphragmatic hernia with transposition of the great arteries

Hazumu Nagata, Kenichiro Yamamura, Kouji Nagata, Kiyoshi Uike, Eiji Morihana, Kenji Ihara, Yasuo Yumoto, Naoki Fusazaki, Hideaki Kado, Kiyoko Kato, Tomoaki Taguchi, Toshiro Hara

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1 Citation (Scopus)

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.

Original language	English
Pages (from-to)	516-518
Number of pages	3
Journal	Pediatrics International
Volume	58
Issue number	6
DOIs	https://doi.org/10.1111/ped.12912
Publication status	Published - Jun 1 2016

All Science Journal Classification (ASJC) codes

Pediatrics, Perinatology, and Child Health

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10.1111/ped.12912

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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.",

author = "Hazumu Nagata and Kenichiro Yamamura and Kouji Nagata and Kiyoshi Uike and Eiji Morihana and Kenji Ihara and Yasuo Yumoto and Naoki Fusazaki and Hideaki Kado and Kiyoko Kato and Tomoaki Taguchi and Toshiro Hara",

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T1 - Management of congenital diaphragmatic hernia with transposition of the great arteries

AU - Nagata, Hazumu

AU - Yamamura, Kenichiro

AU - Nagata, Kouji

AU - Uike, Kiyoshi

AU - Morihana, Eiji

AU - Ihara, Kenji

AU - Yumoto, Yasuo

AU - Fusazaki, Naoki

AU - Kado, Hideaki

AU - Kato, Kiyoko

AU - Taguchi, Tomoaki

AU - Hara, Toshiro

PY - 2016/6/1

Y1 - 2016/6/1

N2 - 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.

AB - 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.

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Management of congenital diaphragmatic hernia with transposition of the great arteries

Abstract

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