Nakanishi Hidehiko, Ito Masato, Kato Shin, Saito Makoto, Miyahara Naoyuki, Arai Hirokazu, Ota Erika, Namba Fumihiko
Division of Neonatal Intensive Care Medicine, Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Japan.
Department of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan.
Neonatology. 2025;122(3):339-349. doi: 10.1159/000543810. Epub 2025 Jan 27.
A recent scoping review identified histological chorioamnionitis (HCA), small for gestational age (SGA), and bubbly/cystic appearance on chest X-ray (bubbly/cystic CXR) as risk factors for severe bronchopulmonary dysplasia (BPD). To further validate these results, a large-scale database was analyzed.
This retrospective multicenter cohort study included infants born at <28 weeks' gestational age between 2003 and 2016. The validated risk factors identified from the scoping review were analyzed for independent associations with severe BPD using multivariable logistic regression. Additionally, the association of these factors with long-term outcomes at 3 years, including home oxygen therapy (HOT) and neurodevelopmental impairments (NDIs), was analyzed.
Among 15,834 extremely preterm infants, HCA, SGA, and bubbly/cystic CXR on postnatal day 28 were significantly and independently associated with severe BPD (adjusted odds ratio, 1.20; 95% confidence interval, 1.06-1.36) (1.73; 1.51-1.98) (1.79; 1.60-2.01), respectively. These three factors were also linked to HOT at 3 years (1.54; 1.14-2.08) (1.70; 1.21-2.39) (2.63; 1.94-3.56), respectively. Their combination significantly increased the prevalence of severe BPD and HOT at 3 years, particularly with bubbly/cystic CXR. Only SGA was independently associated with NDIs in BPD infants (1.55; 1.32-1.83).
HCA, SGA, and bubbly/cystic CXR on postnatal day 28 were identified as important risk factors for severe BPD and long-term respiratory outcomes. While further research is needed to validate their role in endotype-specific classification of BPD, these findings may contribute to early prognostic strategies and targeted interventions before 36 weeks' postmenstrual age.
最近一项范围综述确定组织学绒毛膜羊膜炎(HCA)、小于胎龄儿(SGA)以及胸部X线片上的气泡样/囊样表现(气泡样/囊样CXR)为重度支气管肺发育不良(BPD)的危险因素。为进一步验证这些结果,我们分析了一个大型数据库。
这项回顾性多中心队列研究纳入了2003年至2016年间出生时孕周小于28周的婴儿。使用多变量逻辑回归分析从范围综述中确定的经过验证的危险因素与重度BPD的独立关联。此外,还分析了这些因素与3岁时长期结局的关联,包括家庭氧疗(HOT)和神经发育障碍(NDI)。
在15834例极早产儿中,出生后第28天的HCA、SGA和气泡样/囊样CXR分别与重度BPD显著且独立相关(调整优势比分别为1.20;95%置信区间为1.06 - 1.36)(1.73;1.51 - 1.98)(1.79;1.60 - 2.01)。这三个因素也分别与3岁时的HOT相关(1.54;1.14 - 2.08)(1.70;1.21 - 2.39)(2.63;1.94 - 3.56)。它们的组合显著增加了3岁时重度BPD和HOT的患病率,尤其是伴有气泡样/囊样CXR时。在BPD婴儿中,只有SGA与NDI独立相关(1.55;1.32 - 1.83)。
出生后第28天的HCA、SGA和气泡样/囊样CXR被确定为重度BPD和长期呼吸结局的重要危险因素。虽然需要进一步研究来验证它们在BPD内型特异性分类中的作用,但这些发现可能有助于在月经龄36周前制定早期预后策略和针对性干预措施。