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Published on: November 20, 2015
Gastrointestinal malformations: impact of prenatal diagnosis on gestational age at birth
Ester Garne1, Maria Loane, Helen Dolk
1Kolding Hospital, Kolding, Denmark. egarne@health.sdu.dk
Insights
Prenatal diagnosis of gastrointestinal malformations (GIM) may lead to earlier birth, increasing mortality risk. Balancing early delivery benefits against risks is crucial for managing GIM cases.
Area of Science:
- Perinatal Medicine
- Medical Genetics
- Public Health
Background:
- Prenatal diagnosis of congenital malformations aims to improve infant outcomes.
- The impact of prenatal diagnosis on gestational age (GA) at birth requires further investigation.
Purpose of the Study:
- To analyze the extent to which prenatal diagnosis of gastrointestinal malformations (GIM) shortens gestational age (GA) at birth.
- To evaluate the implications of reduced GA on infant mortality risk.
Main Methods:
- Utilized data from 14 population-based congenital malformation registries (EUROCAT) from 1997-2002.
- Included 1047 liveborn infants with GIMs (oesophageal atresia, duodenal atresia, omphalocele, gastroschisis, diaphragmatic hernia) and no chromosomal anomalies.
- Compared GA at birth between prenatally and postnatally diagnosed infants.
Main Results:
- Median GA at birth was lower in prenatally diagnosed GIM cases for four out of five malformations.
- The reduction in GA for prenatally diagnosed infants was sufficient to potentially increase mortality risk.
- Birthweight did not significantly differ based on GA between pre- and postnatally diagnosed groups.
Conclusions:
- Prenatal diagnosis of GIM may result in earlier delivery, potentially increasing infant mortality.
- Clinical management decisions must weigh the benefits of early delivery against potential risks.
- The benefits of prenatal diagnosis for liveborn infants may be negated by the adverse effects of a reduced gestational age at birth.
Abstract:
The aim of the study was to analyse the degree to which gestational age (GA) has been shortened due to prenatal diagnosis of gastrointestinal malformations (GIM). The data source for the study was 14 population-based registries of congenital malformations (EUROCAT). All liveborn infants with GIMs and without chromosomal anomalies, born 1997-2002, were included. The 14 registries identified 1047 liveborn infants with one or more GIMs (oesophageal atresia, duodenal atresia, omphalocele, gastroschisis and diaphragmatic hernia). Median GA at birth was lower in prenatally diagnosed cases for all five malformations, although not statistically significant for gastroschisis. There was little difference in median birthweight by GA for the pre- and postnatally diagnosed infants. The difference in GA at birth between prenatally and postnatally diagnosed infants with GIMs is enough to increase the risk of mortality for the prenatally diagnosed infants. Clinicians need to balance the risk of early delivery against the benefits of clinical convenience when making case management decisions after prenatal diagnosis. Very few studies have been able to show benefits of prenatal diagnosis of congenital malformations for liveborn infants. This may be because the benefits of prenatal diagnosis are outweighed by the problems arising from a lower GA at birth.
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