Shin T W, Lee E J, Choi H W, Yoo Y M
Department of Pediatrics, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Department of Preventive Medicine, Yonsei University Wonju College of Medicine, Wonju, Republic of Korea.
Front Pediatr. 2025 Jun 19;13:1595348. doi: 10.3389/fped.2025.1595348. eCollection 2025.
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.
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.
After excluding infants with missing data ( = 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%, = 0.022) and became more pronounced in the second week after IPTW adjustment (8.206% vs. 22.888%, = 0.024).
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.
代谢性酸中毒在早产儿中较为常见;然而,其在支气管肺发育不良(BPD)发生发展中的独立作用仍不明确。在本研究中,我们调查了23⁺⁰至31⁺⁶周妊娠的早产儿代谢性酸中毒与中度/重度BPD发生或死亡之间的关联。
我们回顾性分析了2017年1月至2024年12月期间收治的254例孕周小于32周的早产儿的病历。主要结局是月经后36周前出现中度/重度BPD或死亡。在出生后的前14天内,每天分析血气参数,包括pH值、碱剩余、碳酸氢盐和乳酸。采用治疗权重的逆概率(IPTW)来调整诸如孕周、液体平衡、呼吸支持和动脉导管未闭(PDA)状态等混杂因素。
排除数据缺失的婴儿(n = 88)后,纳入168例婴儿,其中55例发生中度/重度BPD或死亡。经过IPTW调整后,出生后第6天(DOL 6)的代谢性酸中毒与中度/重度BPD或死亡显著相关(OR:1.369,95%CI:1.085 - 1.727)。在第一周,累积液体摄入量的差异具有统计学意义(7.365%对23.478%,P = 0.022),在IPTW调整后的第二周差异更加明显(8.206%对22.888%,P = 0.024)。
DOL 6时的代谢性酸中毒与中度/重度BPD或死亡风险增加相关,提示其作为一个可改变的风险因素的潜在作用。虽然过多的液体摄入与BPD有关,但我们的研究结果凸显了早产儿液体管理的复杂性。需要进一步研究来确定纠正代谢性酸中毒是否能改善呼吸结局。