IMPROVED SURVIVAL FOR CONGENITAL DIAPHRAGMATIC-HERNIA, BASED ON PRENATAL ULTRASOUND DIAGNOSIS AND REFERRAL TO A COMBINED OBSTETRIC-PEDIATRIC SURGICAL CENTER
Ks. Shaw et al., IMPROVED SURVIVAL FOR CONGENITAL DIAPHRAGMATIC-HERNIA, BASED ON PRENATAL ULTRASOUND DIAGNOSIS AND REFERRAL TO A COMBINED OBSTETRIC-PEDIATRIC SURGICAL CENTER, Journal of pediatric surgery, 29(9), 1994, pp. 1268-1269
Between January 1990 and January 1993, 36 patients with antenatal ultr
asound (US) diagnosis and/or postnatal diagnosis of congenital diaphra
gmatic hernia (CDH) were referred to the authors' high-risk obstetric
and pediatric hospital. Among the 36, there were four spontaneous abor
tions (11%). five deaths after live births (14%), one false-positive U
S examination, and 26 patients who underwent surgery, 23 of whom survi
ved (66% overall, 74% of live births, and 89% postoperatively). Only o
ne survivor had extracorporeal membrane oxygenation (ECMO). Thirty-fiv
e ultrasound examinations were performed in 24 patients; there were 18
true-positives results (51%), one false-positive (3%), and 16 false-n
egatives (46%). In this series, there were 25 left-sided CDHs, eight r
ight-sided, one bilateral, and one central. Of the four right-sided he
rnias having antenatal US, only one was diagnosed prenatally; 15 of th
e 17 left-sided CDHs were diagnosed correctly (88%). All 19 babies wit
h the prenatal diagnosis were born at the authors' institution. US dia
gnosis before 25 weeks' gestation and polyhydramnios separately result
ed in a mortality rate of only 50%. Patients born at this institution
tend to be sicker than those transferred from elsewhere, as reflected
by the lower 1- and 5-minute Apgar scores (3.7 v 6.9, P < .001, and 5.
4 v 6.9, P < .16, respectively), lower gestational ages (37.0 v 39.2 w
eeks, P < .007), and lower birth weights (2,525 v 3,049 g, P < .02). N
evertheless, transferred patients had a mortality rate (3 of 15 patien
ts, 20%) similar to that of nontransferred patients (5 of 20 patients,
25%). The authors conclude that (1) systematic prenatal US can diagno
se CDH and enable referral to a center that provides high risk obstetr
ic and pediatric surgical care, thus providing optimal postnatal treat
ment, and (2) contrary to other reports, antenatal diagnosis of CDH di
d not presage a high mortality rate. Copyright (C) 1994 by W.B. Saunde
rs Company