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Abdominal wall defects in the era of prenatal diagnosis
O H Nielsen1, N Kvist, V Brocks
1Department of Paediatric Surgery, Juliane Marie Centre for Children, Women and Reproduction, National University Hospital, Rigshospitalet, DK-2100, Copenhagen Ø, Denmark.
Insights
Prenatal diagnosis of abdominal wall defects (AWD) did not improve outcomes for omphalocele, suggesting termination is a viable option. For gastroschisis, prenatal diagnosis and delivery method did not affect survival rates.
Area of Science:
- Perinatal Medicine
- Pediatric Surgery
- Medical Imaging
Background:
- Abdominal wall defects (AWD) are congenital anomalies requiring specialized care.
- Prenatal diagnosis allows for early identification and management planning.
Purpose of the Study:
- To evaluate the impact of prenatal diagnosis on outcomes for different types of AWD.
- To assess prognostic factors for omphalocele, cord hernia, and gastroschisis.
Main Methods:
- Retrospective review of 141 AWD cases from 1980-1994.
- Analysis of prenatal diagnosis rates, delivery methods, and patient outcomes.
- Categorization of AWD into omphalocele, cord hernia, and gastroschisis.
Main Results:
- Omphalocele has a poor prognosis, with prenatal diagnosis not improving survival; termination is a reasonable option.
- Gastroschisis outcomes (mortality, morbidity) were not significantly affected by prenatal diagnosis or delivery mode.
- Cord hernia generally has a good prognosis with primary closure, barring other severe anomalies.
Conclusions:
- Prenatal diagnosis does not improve outcomes for omphalocele.
- For gastroschisis, neither prenatal diagnosis nor delivery method impacts mortality or morbidity.
- Management strategies should consider the specific AWD type and associated anomalies.
Abstract:
In order to study the effects of prenatal diagnosis, we reviewed all 141 cases of abdominal wall defects (AWD) seen in our institution since 1980. In the period up to the end of 1994, 65 AWDs were diagnosed at the Department of Obstetric Ultrasound and another 76 infants were born with an AWD, 44 with omphalocele (prenatal diagnosis 29), 21 with a cord hernia (prenatal diagnosis 4), and 76 with gastroschisis (prenatal diagnosis 32). In the prenatal diagnosis group the frequency of cesarean section was 48%, in the postnatal diagnosis group 13%. In the omphalocele group, the pregnancy was terminated in 12 cases and there were 10 intrauterine deaths. A further 10 babies died in the first days of life, so that only 12 came to operation; 6 survived. At least 27 of the 44 infants had other severe anomalies. Omphalocele has a poor prognosis that is not improved by prenatal diagnosis, so that termination is a reasonable option. In the cord hernia group 1 patient died because of a cardiac anomaly; all the others had primary closure without complications. In the gastroschisis group, the pregnancy was terminated in 7 cases and there were 2 intrauterine and 2 neonatal deaths. Sixty-five infants were operated upon immediately after birth, 50 (77%) with primary closure and 15 in two stages. Four died after primary closure (8%) and 4 after a silastic silo (27%). The overall mortality was 12.3%. Postoperative intestinal morbidity was assessed by the period until total enteral nutrition could be established, which was from 8 to 185 days (median 17 days). The unfavorable prognostic factors were intestinal thickening and staged closure. Neither prenatal diagnosis nor mode of delivery could be shown to have any effect on mortality or morbidity.
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