A. Moore et al., PROGNOSIS OF CONGENITAL DIAPHRAGMATIC-HERNIA, Australian and New Zealand Journal of Obstetrics and Gynaecology, 38(1), 1998, pp. 16-21
Congenital diaphragmatic hernia (CDH) contributes significantly to per
inatal morbidity and mortality, This retrospective study examines the
experience of a major teaching hospital to establish survival rates an
d factors influencing outcome. Survival rates were found to relate clo
sely to the stage at which the diagnosis was made and the presence of
associated anomalies. Ultrasound diagnosis early in pregnancy is assoc
iated with a higher mortality rate than diagnosis made late in pregnan
cy or after delivery. Logistic regression analysis and chi-squared ana
lysis did not establish to a significant degree that any factor, alone
or in combination, was a reliable prognostic indicator, It is acknowl
edged, however, that figures in this series are small, Survival figure
s are presented to facilitate reliable parental counselling, In partic
ular, the presence of associated major anomalies and the gestational a
ge at which diagnosis is made are of critical importance in accurately
counselling parents regarding the prognosis for survival, In this stu
dy, excluding terminations, the mortality rate for isolated CDH diagno
sis before the 21st week was 45.5%, with a corresponding survival rate
of 54.5%. Once the infant was liveborn, however, the survival rate ro
se to 68.0%, and if the infant survived transfer to a paediatric surgi
cal unit, the survival rate in this study was 73.9%.