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Metabolic acidosis as a risk factor for bronchopulmonary dysplasia in preterm infants born between 23 + 0 and 31 + 6
T W Shin1, E J Lee1, H W Choi2
1Department of Pediatrics, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Insights
Metabolic acidosis in preterm infants on day 6 of life is linked to increased risk of bronchopulmonary dysplasia (BPD) or death. This finding suggests metabolic acidosis may be a modifiable risk factor for BPD in premature infants.
Area of Science:
- Neonatology
- Pediatric Pulmonology
- Neonatal Intensive Care
Background:
- Metabolic acidosis is common in preterm infants but its role in bronchopulmonary dysplasia (BPD) is unclear.
- Preterm infants born between 23 + 0 and 31 + 6 weeks gestation are at risk for BPD.
- Understanding risk factors for BPD is crucial for improving outcomes in premature infants.
Purpose of the Study:
- To investigate the association between metabolic acidosis and moderate/severe BPD or mortality in preterm infants.
- To determine if metabolic acidosis is an independent risk factor for BPD in premature infants.
- To explore the relationship between fluid balance and metabolic acidosis in the context of BPD.
Main Methods:
- Retrospective review of 168 preterm infants (<32 weeks gestation) with complete data.
- Analysis of daily blood gas parameters (pH, base excess, bicarbonate, lactate) during the first 14 days of life.
- Inverse probability of treatment weighting (IPTW) used to adjust for confounders like gestational age, fluid balance, and respiratory support.
Main Results:
- Metabolic acidosis on day 6 of life (DOL 6) was significantly associated with moderate/severe BPD or mortality (OR: 1.369).
- Infants who developed BPD or died had significantly different cumulative fluid intake during the first and second weeks.
- IPTW adjustment confirmed the association between DOL 6 metabolic acidosis and adverse outcomes.
Conclusions:
- Metabolic acidosis on DOL 6 is associated with an increased risk of moderate/severe BPD or mortality in preterm infants.
- Metabolic acidosis may represent a modifiable risk factor for BPD, warranting further investigation.
- Fluid management in preterm infants is complex, and its interaction with metabolic acidosis requires further study to improve respiratory outcomes.
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 (n = 88), 168 infants were included, of whom 55 developed moderate/severe BPD or died. Following IPTW adjustment, metabolic acidosis on day 6 of life (DOL 6) was significantly associated with moderate/severe BPD or mortality (OR: 1.369, 95% CI: 1.085-1.727). Differences in cumulative fluid intake were statistically significant during the first week (7.365% vs. 23.478%, p = 0.022) and became more pronounced in the second week after IPTW adjustment (8.206% vs. 22.888%, p = 0.024).
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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