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Association between early postnatal antibiotic exposure and bronchopulmonary dysplasia in very preterm infants: a
Cheng Min1, Ying Sui1, Qu Chen1
1Neonatal Intensive Care Unit, Huzhou Maternity & Child Healthcare Hospital, Huzhou, Zhejiang, China.
Insights
Early antibiotic exposure in very preterm infants increases risks for bronchopulmonary dysplasia (BPD) and mortality. Optimizing antibiotic use is crucial for improving long-term outcomes in these vulnerable infants.
Area of Science:
- Neonatal Medicine
- Pediatric Pharmacology
- Infectious Diseases
Background:
- Very preterm infants have immature immune systems, increasing infection risk.
- Empirical antibiotic therapy is common but may have adverse effects.
- Understanding antibiotic impact on infant outcomes is vital for neonatal care.
Purpose of the Study:
- To systematically evaluate the association between early postnatal antibiotic exposure and bronchopulmonary dysplasia (BPD) in very preterm infants.
- To assess the link between early antibiotic use and other adverse outcomes like necrotizing enterocolitis (NEC), mortality, and late-onset sepsis (LOS).
- To provide evidence for optimizing antibiotic stewardship in neonatal intensive care units.
Main Methods:
- Systematic literature search of PubMed, Embase, Wiley, and Cochrane Library databases up to March 2026.
- Inclusion of observational cohort studies comparing early vs. no/short-term antibiotic exposure.
- Meta-analysis of primary outcome (BPD) and secondary outcomes (NEC, mortality, LOS) using fixed/random-effects models; sensitivity and bias analyses performed.
Main Results:
- Eleven studies included; early antibiotic exposure significantly increased BPD risk (OR 1.44, 95% CI: 1.12-1.85).
- Increased risks observed for NEC (OR 1.18, 95% CI: 1.09-1.28) and mortality (OR 1.19, 95% CI: 1.05-1.35).
- No significant association found for late-onset sepsis; results remained stable after sensitivity analysis, though mortality interpretation requires caution due to publication bias.
Conclusions:
- Early postnatal antibiotic exposure is linked to higher risks of BPD and mortality in very preterm infants.
- Careful assessment of infection risk and optimized antibiotic strategies are essential.
- Improving antibiotic stewardship can enhance long-term outcomes for vulnerable preterm neonates.
Objective:
Very preterm infants are at high risk of infection due to their immature immune systems, and empirical antibiotic therapy is commonly initiated shortly after birth. However, excessive or unnecessary antibiotic exposure may adversely affect organ development and long-term outcomes. This study aimed to systematically evaluate the association between early postnatal antibiotic exposure and bronchopulmonary dysplasia (BPD) as well as other adverse outcomes in very preterm infants, to provide evidence for optimizing antibiotic stewardship in neonatal care.
Methods:
PubMed, Embase, Wiley Online Library, and the Cochrane Library database were systematically searched from inception to March 2026. Observational cohort studies comparing early postnatal antibiotic exposure with no exposure or short-term exposure were included. The primary outcome was bronchopulmonary dysplasia (BPD), and secondary outcomes included necrotizing enterocolitis (NEC), mortality, and late-onset sepsis (LOS). Meta-analysis was performed using fixed-effects or random-effects models to calculate pooled odds ratios (ORs) with 95% confidence intervals (CIs). Sensitivity analysis and Egger's test were conducted to assess the robustness of the results and potential publication bias. For outcomes with significant publication bias, the trim-and-fill method was applied.
Results:
A total of 11 studies was included. Pooled analysis showed that early postnatal antibiotic exposure was associated with an increased risk of BPD (OR = 1.44, 95% CI: 1.12-1.85). In addition, the risks of NEC (OR = 1.18, 95% CI: 1.09-1.28) and mortality (OR = 1.19, 95% CI: 1.05-1.35) were significantly increased, while no statistically significant association was observed for late-onset sepsis (OR = 0.98, 95% CI: 0.71-1.34). Sensitivity analyses indicated that the results were stable. Publication bias was detected for BPD and mortality; after trim-and-fill correction, the BPD result remained robust, whereas the mortality result warrants cautious interpretation.
Conclusion:
Early postnatal antibiotic exposure is associated with an increased risk of BPD and several adverse outcomes in very preterm infants. Careful assessment of infection risk and optimization of antibiotic initiation and discontinuation strategies may help improve long-term outcomes in this population.
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