TY - JOUR
T1 - Extracorporeal membrane oxygenation for congenital diaphragmatic hernia in Japan
AU - Inamura, Noboru
AU - Usui, Noriaki
AU - Okuyama, Hiroomi
AU - Nagata, Kouji
AU - Kanamori, Yutaka
AU - Fujino, Yuji
AU - Takahashi, Shigehiro
AU - Hayakawa, Masahiro
AU - Taguchi, Tomoaki
N1 - Publisher Copyright:
© 2014 Japan Pediatric Society.
PY - 2015/8/1
Y1 - 2015/8/1
N2 - Background The aim of this study was to clarify how extracorporeal membrane oxygenation (ECMO) is used to treat congenital diaphragmatic hernia (CDH) in Japan. Methods We completed a nationwide survey of CDH involving 614 infants. The subjects included 43 patients who underwent ECMO. We compared the clinical data of the patients who did and did not survive ≥90 days, and analyzed the 24 h blood gas data in isolated CDH cases in both groups. Results Of the 43 CDH patients, non-isolated CDH associated with other life-threatening or chromosomal anomalies was diagnosed in six patients. Only one of these six patients was able to discontinue ECMO and survived, and the other five died shortly after birth. The other 37 patients all had isolated CDH. The reason for initiating ECMO in 31 of these patients was persistent pulmonary hypertension of the newborn (PPHN). In the 37 patients with isolated CDH, ECMO was initiated within 24 h after birth. Sixteen patients (37%) survived ≥90 days, and intact discharge was possible in eight cases. Among the isolated CDH patients, on ROC analysis of the lowest oxygenation index (OI) to predict 90 day survival, the cut-off was 15. Conclusions ECMO is used to treat PPHN starting from an early period after birth, but the mortality and morbidity are not favorable. For lowest OI, the index used to predict survival following ECMO, the cut-off was 15.
AB - Background The aim of this study was to clarify how extracorporeal membrane oxygenation (ECMO) is used to treat congenital diaphragmatic hernia (CDH) in Japan. Methods We completed a nationwide survey of CDH involving 614 infants. The subjects included 43 patients who underwent ECMO. We compared the clinical data of the patients who did and did not survive ≥90 days, and analyzed the 24 h blood gas data in isolated CDH cases in both groups. Results Of the 43 CDH patients, non-isolated CDH associated with other life-threatening or chromosomal anomalies was diagnosed in six patients. Only one of these six patients was able to discontinue ECMO and survived, and the other five died shortly after birth. The other 37 patients all had isolated CDH. The reason for initiating ECMO in 31 of these patients was persistent pulmonary hypertension of the newborn (PPHN). In the 37 patients with isolated CDH, ECMO was initiated within 24 h after birth. Sixteen patients (37%) survived ≥90 days, and intact discharge was possible in eight cases. Among the isolated CDH patients, on ROC analysis of the lowest oxygenation index (OI) to predict 90 day survival, the cut-off was 15. Conclusions ECMO is used to treat PPHN starting from an early period after birth, but the mortality and morbidity are not favorable. For lowest OI, the index used to predict survival following ECMO, the cut-off was 15.
UR - http://www.scopus.com/inward/record.url?scp=84940535002&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84940535002&partnerID=8YFLogxK
U2 - 10.1111/ped.12554
DO - 10.1111/ped.12554
M3 - Article
C2 - 25488275
AN - SCOPUS:84940535002
SN - 1328-8067
VL - 57
SP - 682
EP - 686
JO - Pediatrics International
JF - Pediatrics International
IS - 4
ER -