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

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)


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 languageEnglish
Pages (from-to)516-518
Number of pages3
JournalPediatrics International
Issue number6
Publication statusPublished - Jun 1 2016

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health


Dive into the research topics of 'Management of congenital diaphragmatic hernia with transposition of the great arteries'. Together they form a unique fingerprint.

Cite this