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Published on: February 5, 2021
Growth trajectory and neurodevelopmental outcome in infants with congenital diaphragmatic hernia
Ryan M Antiel1, Nan Lin1, Daniel J Licht1
1The Center for Fetal Diagnosis and Treatment, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Insights
Congenital diaphragmatic hernia (CDH) survivors often experience mild developmental delays by one year. Impaired growth, particularly low head circumference trajectory, is linked to poorer neurodevelopmental outcomes in these infants.
Area of Science:
- Pediatric Medicine
- Developmental Pediatrics
- Neonatology
Background:
- Congenital diaphragmatic hernia (CDH) is a serious birth defect impacting lung development.
- Neurodevelopmental (ND) outcomes in CDH survivors are a significant concern.
- Early identification of factors influencing ND outcomes is crucial for timely intervention.
Purpose of the Study:
- To assess the relationship between impaired growth and short-term neurodevelopmental outcomes in CDH survivors.
- To identify specific growth parameters associated with developmental trajectories.
- To evaluate the impact of neonatal intensive care unit (NICU) stay on neurodevelopment.
Main Methods:
- Retrospective analysis of 84 CDH survivors assessed at 12 months using the Bayley Scales of Infant Development-III (BSID-III).
- Group-based trajectory analysis to categorize growth patterns (weight, length, head circumference - HC).
- Multivariate analysis to determine predictors of neurodevelopmental scores.
Main Results:
- 51% of CDH survivors showed at least one mild developmental delay (1 SD below mean).
- Lower cognitive scores correlated with longer NICU stays.
- A 'high' head circumference (HC) trajectory group had significantly better motor scores compared to the 'low' HC group.
Conclusions:
- Approximately half of CDH survivors exhibit mild developmental delays at one year of age.
- Impaired head circumference growth trajectory is associated with worse neurodevelopmental outcomes.
- Longer NICU stays negatively impact cognitive and motor development in CDH survivors.
Purpose:
The purpose of this study was to evaluate the impact of impaired growth on short-term neurodevelopmental (ND) outcomes in CDH survivors.
Methods:
Between 9/2005-12/2014, 84 of 215 (39%) CDH survivors underwent ND assessment at 12months of age using the BSID-III.
Results:
Mean cognitive, language, and motor scores were 92.6±13.5, 87.1±11.6, and 87.0±14.4, respectively (normal 100±15). 51% of patients scored 1 SD below the population mean in at least one domain, and 13% scored 2 SD below the population mean. Group-based trajectory analysis identified two trajectory groups ('high' and 'low') for weight, length, and head circumference (HC) z-scores. (Fig. 1) 74% of the subjects were assigned to the 'high' trajectory group for weight, 77% to the 'high' height group, and 87% to the 'high' HC group, respectively. In multivariate analysis, longer NICU stay (p<0.01) was associated with lower cognitive scores. Motor scores were 11 points higher in the 'high' HC group compared to the 'low' HC group (p=0.05). Motor scores were lower in patients with longer NICU length of stay (p<0.001).
Conclusions:
At 1 year, half of CDH survivors had a mild delay in at least one developmental domain. Low HC trajectory was associated with worse neurodevelopmental outcomes.
Type Of Study:
Prognosis Study/Retrospective Study.
Level Of Evidence:
Level II.
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