ArticleFrontiers in pediatrics2025
Metabolic acidosis as a risk factor for bronchopulmonary dysplasia in preterm infants born between 23 + 0 and 31 + 6 weeks of gestation: a retrospective case-control study.
Article in Frontiers in pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- SIRT3 deficiency drives alveolar epithelial mitochondrial dysfunction in bronchopulmonary dysplasia via PDHA1 hyperacetylation.iScience · 2026Article
- Administration of Sodium Bicarbonate in Critically Ill Newborns: A Systematic Review and Meta-Analysis.Journal of personalized medicine · 2026Review
- A Predictive Model for Moderate or Severe Neonatal Acute Respiratory Distress Syndrome in Extremely Preterm Infants with Premature Rupture of Membranes: Development and Internal Validation.Journal of inflammation research · 2026Article
- EBNEO Commentary: Late Permissive Hypercapnia for Mechanically Ventilated Preterm Infants.Acta paediatrica (Oslo, Norway : 1992) · 2025Article
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Authors and funding
4 authors.
Funding
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Abstract
Background: Metabolic acidosis is a common condition in preterm infants; however, its independent role in the development of bronchopulmonary dysplasia (BPD) remains unclear. In this study, we examined the association between metabolic acidosis and the occurrence of moderate/severe BPD or mortality in preterm infants born between 23 + 0 and 31 + 6 weeks of gestation. Methods: We retrospectively reviewed the medical records of 254 preterm infants (<32 weeks gestation) admitted between January 2017 and December 2024. The primary outcome was moderate/severe BPD or mortality before 36 weeks of postmenstrual age. Blood gas parameters, including pH, base excess, bicarbonate, and lactate, were analyzed daily during the first 14 days of life. Inverse probability of treatment weighting (IPTW) was applied to adjust for confounders such as gestational age, fluid balance, respiratory support, and patent ductus arteriosus (PDA) status. Results: After excluding infants with missing data ( Conclusion: Metabolic acidosis on DOL 6 was associated with an increased risk of moderate/severe BPD or mortality, suggesting its potential role as a modifiable risk factor. While excessive fluid intake has been linked to BPD, our findings highlight the complexity of fluid management in preterm infants. Further research is needed to determine whether correcting metabolic acidosis could improve respiratory outcomes.
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