Ja. Dagostino et al., OUTCOME FOR INFANTS WITH CONGENITAL DIAPHRAGMATIC-HERNIA REQUIRING EXTRACORPOREAL MEMBRANE-OXYGENATION - THE FIRST YEAR, Journal of pediatric surgery, 30(1), 1995, pp. 10-15
Congenital diaphragmatic hernia (CDH) has been associated with a high
mortality rate. The purposes of this study were to determine the impac
t of extracorporeal membrane oxygenation (ECMO) on the survival of inf
ants with CDH and to document the sequelae and 1-year neurodevelopment
al outcome for CDH infants who required ECMO. Thirty neonates with CDH
were admitted between May 7, 1990 and October 1, 1992. Twenty require
d ECMO and were enrolled in our neonatal follow-up program. Informatio
n about the infants' neonatal course was obtained from chart review, a
nd the infants were seen at 3, 6, and 12 months of age for medical and
neurodevelopmental follow-up. Primary diaphragmatic repair was perfor
med in 13 infants. Five required Goretex graft reconstruction (GGR), a
nd two did not have repair. Sixteen (80%) of the 20 infants who requir
ed ECMO survived. The overall survival rate increased from 31% (10 of
32) in the 5 years previous to the start of the ECMO program to 63% (1
9 of 30) since then (P = .01). The most common sequelae noted by the t
ime of discharge included gastroesophageal reflux (GER; 81%), the need
for tube feeding (69%), and chronic lung disease (CLD; 62%). At 1 yea
r of age, mean cognitive skills were average (87 +/- 23) and motor ski
lls were borderline (75 +/- 24) according to the Bayley Scales of Infa
nt Development. Hypotonia was present in 10 of 13 patients. GER remain
ed in 6 of 13 and CLD in 3 of 13. There were differences in the mean c
ognitive (65 +/- 28 v 97 +/- 13; P = .07) and motor skills (51 +/- 3 v
85 +/- 21; P = .01) between infants requiring (GGR) and those in whom
primary reduction was possible. Furthermore, those with GGR required
significantly prolonged durations of ECMO bypass, mechanical ventilati
on, oxygen therapy, sedation, hospitalization, and tube feedings. Thes
e results suggest that ECMO improved survival for infants with CDH; ho
wever, sequelae were frequently seen. At 1 year of age, those with the
largest diaphragmatic defects fared worse than those with smaller def
ects. Copyright (C) 1995 by W.B. Saunders Company