Kp. Vanmeurs et al., CONGENITAL DIAPHRAGMATIC-HERNIA - LONG-TERM OUTCOME IN NEONATES TREATED WITH EXTRACORPOREAL MEMBRANE-OXYGENATION, The Journal of pediatrics, 122(6), 1993, pp. 893-899
As more infants with congenital diaphragmatic hernia (CDH) survive wit
h extracorporeal membrane oxygenation (ECMO), it seems prudent to deta
il the long-term outcome in these medically complex infants. Eighteen
children with CDH treated with postoperative ECMO were recruited for p
articipation in this study. The mean duration of ECMO was 193 hours (r
ange 82 to 493 hours), mean time to extubation after ECMO was 142 hour
s (range 34 to 312 hours), and median duration of hospitalization was
46 days (range 30 to 181 days). Of the 18 infants, 4 (22%) were discha
rged home requiring oxygen therapy. At follow-up the notable findings
were a high incidence of gastroesophageal reflux and failure to thrive
. At both 1 and 2 years of age, 50% of infants were at less than the 5
th percentile for weight. At 1 and 2 years of age, 39% and 21%, respec
tively, were at less than the Sth percentile for weight/length ratio.
A total of 16 children (89%) had clinical evidence of reflux, and 8 (4
4%) were discharged home on a regimen of nasogastric feedings. Reherni
ation occurred in 4 children (22%) and was more frequent when a patch
was used. An electrocardiogram showed right ventricular hypertrophy in
6 (43%); oxygen saturation by pulse oximetry was >95% in all children
, and pulmonary artery pressure was estimated by Doppler echocardiogra
phy to be normal in 12 of 14 children examined. The neurodevelopmental
outcome (Bayley Scales or Stanford-Binet scale) at 1 to 4 years of ag
e was not dissimilar from that of other ECMO-treated children. Given t
he severity of illness in the neonatal period, the general health and
development of children with CDH surviving after ECMO are good. Surpri
singly few children have long-term respiratory complications related t
o pulmonary hypoplasia. Follow-up in the first few years should be aim
ed at aggressive nutritional intervention to prevent the growth failur
e that appears to be prevalent in these children.