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Fetal Echocardiography and Pulsed-wave Doppler Ultrasound in a Rabbit Model of Intrauterine Growth Restriction
Published on: June 29, 2013
Fetal growth restriction is worse than extreme prematurity for the developing lung
Sophie Soudée1, Lucie Vuillemin, Corinne Alberti
1Neonatal Intensive Care Unit, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Université Paris Diderot, Sorbonne Paris Cité, Paris France.
Insights
Very preterm infants with intrauterine growth restriction (IUGR) face higher risks of neonatal mortality and chronic lung disease (CLD). This risk is greater than for extremely low gestational age (ELGA) infants or those appropriate for gestational age (AGA).
Area of Science:
- Neonatal Medicine
- Perinatal Research
- Pediatric Pulmonology
Background:
- Perinatal lung development is sensitive to inflammation and intrauterine growth restriction (IUGR), key risk factors for chronic lung disease (CLD) in preterm infants.
- The comparative impact of extremely low gestational age (ELGA) versus IUGR on CLD and co-morbidities in very preterm infants requires further investigation.
Purpose of the Study:
- To compare neonatal morbidity, including CLD, and mortality among three groups of very preterm infants.
- Groups included: ELGA infants with normal birth weight (ELGA-AGA), very preterm infants with IUGR (<3rd percentile) (VLGA-IUGR), and very preterm infants appropriate for gestational age (VLGA-AGA) matched with VLGA-IUGR.
Main Methods:
- Retrospective comparison of perinatal and neonatal characteristics across the three infant groups.
- Exclusion of infants with major congenital anomalies.
- Chronic lung disease (CLD) diagnosis based on supplemental oxygen or non-invasive ventilation at 36 weeks postmenstrual age.
Main Results:
- Neonatal mortality was 35% higher in very preterm infants with IUGR (VLGA-IUGR) compared to ELGA-AGA infants, despite a 3-week difference in gestational age.
- Very preterm infants with IUGR (VLGA-IUGR) were five times more likely to develop CLD than ELGA-AGA infants.
- These associations remained significant after adjusting for antenatal steroids, gender, and respiratory distress syndrome.
Conclusions:
- Very preterm infants with IUGR (VLGA-IUGR) exhibit increased risks for neonatal mortality and CLD.
- These risks are elevated compared to both extremely low gestational age infants appropriate for gestational age (ELGA-AGA) and very preterm infants appropriate for gestational age (VLGA-AGA).
Background:
Perinatal lung growth is highly vulnerable to inflammation and intrauterine growth restriction (IUGR), two major risk factors for chronic lung disease (CLD) in preterm neonates. However, the balance between extremely low gestational age (ELGA) and IUGR in very preterm infants as risk factors for CLD and co-morbidities remains poorly explored.
Objectives:
This single-center study aims to compare neonatal morbidity (including CLD) and mortality among ELGA infants with normal birth weight (ELGA-AGA), very preterm infants with IUGR <3rd percentile (VLGA-IUGR) and very preterm infants with a birth weight appropriate for gestational age (VLGA-AGA), matched with VLGA-IUGR infants.
Methods:
Selected characteristics of the perinatal and neonatal periods were recorded and retrospectively compared among the three groups. Infants with major congenital anomalies were excluded. The diagnosis of CLD was based on whether the infant was receiving supplemental oxygen and/or non-invasive ventilation at a postmenstrual age of 36 weeks.
Results:
We found that, despite a median difference of 3 weeks in gestational age at birth between VLGA-IUGR and ELGA-AGA infants, neonatal mortality was 35% higher in neonates who had experienced fetal growth restriction, and that VLGA- IUGR was five times more predictive of CLD than was ELGA-AGA. These differences persisted after adjustment for confounding factors such as antenatal steroids, gender and respiratory distress syndrome.
Conclusions:
This study reports that VLGA-IUGR infants are at higher risk of neonatal mortality and CLD than both ELGA-AGA and VLGA-AGA infants.
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