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Postnatal dexamethasone, respiratory and neurodevelopmental outcomes at two years in babies born extremely preterm
Gordon Qin1,2, Jessica W Lo1,3, Neil Marlow4
1Division of Health and Social Care Research, King's College London, London, United Kingdom.
Insights
Postnatal dexamethasone in extremely preterm infants increased respiratory hospital admissions and neurodevelopmental impairment risks. These findings highlight potential long-term adverse effects despite short-term benefits for bronchopulmonary dysplasia.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Developmental Pediatrics
Background:
- Postnatal dexamethasone is used to reduce bronchopulmonary dysplasia in preterm infants.
- Concerns exist regarding potential long-term adverse neurodevelopmental outcomes associated with its use.
Purpose of the Study:
- To evaluate the impact of postnatal dexamethasone on respiratory and neurodevelopmental outcomes at two years of age.
- To adjust for various neonatal and infant risk factors in the analysis.
Main Methods:
- A cohort of 412 infants born between 23-28 weeks of gestation was studied.
- Logistic regression analysis was used to assess respiratory hospital admissions and neurodevelopmental impairment.
- Adjustments were made for multiple confounding variables including sex, birthweight, gestation, and neonatal morbidities.
Main Results:
- Postnatal dexamethasone use was significantly associated with increased respiratory hospital readmissions (0.35 vs 0.15).
- A higher proportion of infants receiving dexamethasone experienced neurodevelopmental impairment (0.59 vs 0.45).
- These associations persisted after adjusting for neonatal morbidities.
Conclusions:
- Postnatal dexamethasone administration in extremely preterm infants is linked to elevated risks of respiratory hospital admissions.
- The study also found an association between postnatal dexamethasone and increased neurodevelopmental impairment.
- These adverse outcomes were not attributable to increased neonatal complications.
Importance:
Postnatal dexamethasone is associated with reduction in bronchopulmonary dysplasia. There remains, however, concern that its short-term benefits are accompanied by long-term adverse effects e.g. poorer neurodevelopmental outcomes.
Objective:
Our aim was to determine the effects of administration of postnatal dexamethasone on respiratory and neurodevelopmental outcome at two years of age after adjusting for neonatal and infant risk factors.
Materials And Methods:
The study included 412 infants born at 23-28 weeks of gestation, 29% had received postnatal dexamethasone. Two outcomes were examined, respiratory hospital admissions in the past 12 months and neurodevelopmental impairment. Logistic regression, adjusted for sex, birthweight z-score, gestation, maternal smoking, oxygen dependency at 36 weeks, airleak, patent ductus arteriosus, pulmonary haemorrhage, major ultrasound abnormality, mode of ventilation and age at assessment, was undertaken.
Results:
After adjustment, postnatal dexamethasone was associated with significantly increased proportions of both respiratory hospital readmission: (0.35 vs 0.15, difference = 0.20; 95% CI: 0.08, 0.31) and neurodevelopmental impairment (0.59 vs 0.45, difference = 0.14; 95% CI: 0.02, 0.26).
Conclusions:
Postnatal dexamethasone use in extremely preterm infants is associated with increased risks of respiratory hospital admissions and neurodevelopmental impairment. These associations were not explained by excess neonatal morbidities.
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