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Prognosis in fetal diaphragmatic hernia
G K Sharland1, S M Lockhart, A J Heward
1Department of Perinatal Cardiology, Guy's Hospital, London, England.
American Journal of Obstetrics and Gynecology
|January 1, 1992
Summary
Congenital diaphragmatic hernia diagnosed prenatally has high mortality. Early diagnosis before 25 weeks
Area of Science:
- Perinatal medicine
- Fetal surgery
- Pediatric surgery
Background:
- Congenital diaphragmatic hernia (CDH) presents a significant challenge in perinatal care.
- High mortality rates are associated with prenatally detected CDH.
- Early presentation and polyhydramnios are suspected adverse prognostic factors.
Purpose of the Study:
- To retrospectively analyze outcomes of prenatally diagnosed congenital diaphragmatic hernia.
- To evaluate the impact of gestational age at diagnosis on mortality.
- To identify reliable prognostic indicators for fetal CDH.
Main Methods:
- Retrospective review of 55 cases of prenatally diagnosed CDH.
- Analysis of mortality rates based on gestational age at diagnosis.
- Assessment of factors including polyhydramnios, cardiac development, chromosomal anomalies, and heart disease.
Main Results:
- Overall mortality for prenatally detected CDH was 73%.
- Mortality was 74% for diagnosis before 25 weeks' gestation (excluding terminations) versus 60% after 25 weeks.
- Underdevelopment of left-sided cardiac structures was a significant prognostic factor; polyhydramnios was not confirmed as predictive.
Conclusions:
- While diagnosis before 25 weeks' gestation is linked to higher mortality, it is not universally fatal.
- Exclusion of congenital heart disease, chromosomal anomalies, and severe left heart underdevelopment improves survival odds.
- Prognostic factors must be considered in the management planning for fetal CDH.