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Prevention of bronchopulmonary dysplasia in extremely low gestational age neonates: current evidence
Christian F Poets1, Laila Lorenz1
1Department of Neonatology, University Children's Hospital, Tübingen, Germany.
Insights
Preventing bronchopulmonary dysplasia (BPD) in premature infants involves non-invasive respiratory support, surfactant, and caffeine. Dexamethasone and azithromycin show promise, but careful consideration of side effects is crucial for reducing BPD rates.
Area of Science:
- Neonatal Medicine
- Respiratory Medicine
- Pediatric Critical Care
Background:
- Bronchopulmonary dysplasia (BPD) is a common complication in extremely premature infants, with persistent high rates.
- Effective prevention strategies are crucial for improving outcomes in this vulnerable population.
Purpose of the Study:
- To review recent meta-analyses on interventions for preventing bronchopulmonary dysplasia (BPD).
- To identify evidence-based strategies for reducing BPD incidence in neonates.
Main Methods:
- Systematic review of recent meta-analyses focusing on BPD prevention.
- Analysis of interventions including respiratory support, surfactant, ventilation strategies, and pharmacotherapy.
Main Results:
- Non-invasive respiratory support, surfactant without intubation, and volume-targeted ventilation are effective.
- Synchronized nasal ventilation post-extubation and early caffeine citrate administration improve outcomes.
- Intramuscular vitamin A and low-dose hydrocortisone show benefit but have limitations (cost, pain, sepsis risk).
- Dexamethasone offers a potential balance of efficacy and risk, while azithromycin for Ureaplasma colonization is promising.
- Exclusive breastfeeding and infection control require further study.
Conclusions:
- Multiple non-pharmacological and pharmacological interventions can effectively reduce BPD.
- Optimizing respiratory support, early caffeine, and judicious steroid use are key strategies.
- Targeted antibiotic therapy and supportive care like breastfeeding warrant further investigation for BPD prevention.
Abstract:
Bronchopulmonary dysplasia (BPD) is one of the most frequent complications in extremely low gestational age neonates, but has remained largely unchanged in rate. We reviewed data on BPD prevention focusing on recent meta-analyses. Interventions with proven effectiveness in reducing BPD include the primary use of non-invasive respiratory support, the application of surfactant without endotracheal ventilation and the use of volume-targeted ventilation in infants requiring endotracheal intubation. Following extubation, synchronised nasal ventilation is more effective than continuous positive airway pressure in reducing BPD. Pharmacologically, commencing caffeine citrate on postnatal day 1 or 2 seems more effective than a later start. Applying intramuscular vitamin A for the first 4 weeks reduces BPD, but is expensive and painful and thus not widely used. Low-dose hydrocortisone for the first 10 days prevents BPD, but was associated with almost twice as many cases of late-onset sepsis in infants born at 24-25 weeks' gestation. Inhaled corticosteroids, despite reducing BPD, were associated with a higher mortality rate. Administering dexamethasone to infants still requiring mechanical ventilation around postnatal weeks 2-3 may represent the best trade-off between restricting steroids to infants at risk of BPD while still affording high efficacy. Finally, identifying infants colonised with ureaplasma and treating those requiring intubation and mechanical ventilation with azithromycin is another promising approach to BPD prevention. Further interventions yet only backed by cohort studies include exclusive breastmilk feeding and a better prevention of nosocomial infections.
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