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Chronic lung disease and developmental delay at 2 years of age in children born before 28 weeks' gestation
Matthew Laughon1, Michael T O'Shea, Elizabeth N Allred
1Division of Neonatal-Perinatal Medicine, School of Medicine, University of North Carolina, Chapel Hill, North Carolina 27599-7596, USA. matt_laughon@med.unc.edu
Insights
Extremely low gestational age newborns (ELGANs) with chronic lung disease (CLD) did not show increased developmental delay risk when other factors were considered. However, severe CLD may still be linked to poorer psychomotor development in ELGANs.
Area of Science:
- Neonatalogy
- Developmental Pediatrics
- Pulmonology
Background:
- Extremely low gestational age newborns (ELGANs) face heightened risks for chronic lung disease (CLD) and developmental delays.
- Existing research suggests a potential link between CLD and impaired neurodevelopment in ELGANs.
Purpose of the Study:
- To investigate the association between CLD and developmental outcomes in ELGANs at 24 months corrected age.
- To identify risk factors contributing to developmental delay in this vulnerable population.
Main Methods:
- Prospective cohort study of 915 infants born before 28 weeks gestation.
- Developmental assessment using Bayley Scales and Vineland Adaptive Behavior Scales at 24 months.
- CLD defined by oxygen use at 36 weeks postmenstrual age; stratified by mechanical ventilation (MV) use.
Main Results:
- 49% of ELGANs developed CLD, with 14% requiring MV.
- After accounting for other risk factors, CLD (with or without MV) was not significantly associated with low Mental Developmental Index (MDI) or Psychomotor Developmental Index (PDI).
- Severe CLD requiring MV showed a trend towards increased risk for low PDI, but did not reach statistical significance.
Conclusions:
- The association between CLD and developmental delay in ELGANs appears mediated by other risk factors.
- Once adjusted for confounding variables, CLD itself does not significantly increase the risk of low MDI or PDI.
- Severe CLD may warrant closer monitoring for potential impacts on psychomotor development.
Introduction:
Extremely low gestational age newborns (ELGANs) are at increased risk of chronic lung disease (CLD) and of developmental delay. Some studies have suggested that CLD contributes to developmental delay.
Patients And Methods:
We examined data collected prospectively on 915 infants born before the 28th week of gestation in 2002-2004 who were assessed at 24 months of age with the Bayley Scales of Infant Development-2nd Edition or the Vineland Adaptive Behavior Scales. We excluded infants who were not able to walk independently (Gross Motor Function Classification System score < 1) and, therefore, more likely to have functionally important fine motor impairments. We defined CLD as receipt of oxygen at 36 weeks' postmenstrual age and classified infants as either not receiving mechanical ventilation (MV) (CLD without MV) or receiving MV (CLD with MV).
Results:
Forty-nine percent of ELGANs had CLD; of these, 14% were receiving MV at 36 weeks' postmenstrual age. ELGANs without CLD had the lowest risk of a Mental Developmental Index (MDI) or a Psychomotor Developmental Index (PDI) of <55, followed by ELGANs with CLD not receiving MV, and ELGANs with CLD receiving MV (9%, 12%, and 18% for the MDI and 7%, 10%, and 20% for the PDI, respectively). In time-oriented multivariate models, the risk of an MDI of <55 was associated with the following variables: gestational age of <25 weeks; single mother; late bacteremia; pneumothorax; and necrotizing enterocolitis. The risk of a PDI of <55 was associated with variables such as single mother, a complete course of antenatal corticosteroids, early and persistent pulmonary dysfunction, pulmonary deterioration during the second postnatal week, pneumothorax, and pulmonary interstitial emphysema. CLD, without or with MV, was not associated with the risk of either a low MDI or a low PDI. However, CLD with MV approached, but did not achieve, nominal statistical significance (odds ratio: 1.9 [95% confidence interval: 0.97-3.9]) for the association with a PDI of <55.
Conclusions:
Among children without severe gross motor delays, risk factors for CLD account for the association between CLD and developmental delay. Once those factors are considered in time-oriented risk models, CLD does not seem to increase the risk of either a low MDI or a low PDI. However, severe CLD might increase the risk of a low PDI.
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