Department of Pediatrics, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA.
Department of Pediatrics, Northwestern University Feinberg School of Medicine, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, IL.
J Pediatr. 2024 Dec;275:114252. doi: 10.1016/j.jpeds.2024.114252. Epub 2024 Aug 22.
To evaluate associations between neonatal risk factors and pulmonary vein stenosis (PVS) among infants born preterm with severe bronchopulmonary dysplasia (sBPD).
We performed a case-control study of infants born from 2010 to 2022 at <32 weeks' gestation with sBPD among 46 neonatal intensive care units in the Children's Hospitals Neonatal Consortium. Cases with PVS were matched to controls using epoch of diagnosis (2010-2016; 2017-2022) and hospital. Multivariable logistic regression analyses were utilized to evaluate PVS association with neonatal risk factors.
From 10 171 preterm infants with sBPD, we identified 109 cases with PVS and matched those to 327 controls. The prevalence of PVS (1.07%) rose between epochs (0.8% in 2010-2016 to 1.2% in 2017-2022). Relative to controls, infants with PVS were more likely to be <500 g at birth, to be small for gestational age <10th%ile, or have surgical necrotizing enterocolitis, atrial septal defects, or pulmonary hypertension. In multivariable models, these associations persisted, and small for gestational age, surgical necrotizing enterocolitis, atrial septal defects, and pulmonary hypertension were each independently associated with PVS. Among infants on respiratory support at 36 weeks' postmenstrual age, infants with PVS had 4.3-fold higher odds of receiving mechanical ventilation at 36 weeks' postmenstrual age. Infants with PVS also had 3.6-fold higher odds of in-hospital mortality relative to controls.
In a large cohort of preterm infants with sBPD, multiple independent, neonatal risk factors are associated with PVS. These results lay important groundwork for the development of targeted screening to guide the diagnosis and management of PVS in preterm infants with sBPD.
评估新生儿危险因素与极早早产且患有严重支气管肺发育不良(sBPD)婴儿的肺静脉狭窄(PVS)之间的相关性。
我们对 2010 年至 2022 年间在儿童医院新生儿联盟的 46 个新生儿重症监护病房中出生胎龄<32 周且患有 sBPD 的婴儿进行了一项病例对照研究。使用诊断时的时期(2010-2016 年;2017-2022 年)和医院将 PVS 病例与对照进行匹配。利用多变量逻辑回归分析评估 PVS 与新生儿危险因素的相关性。
在 10171 例患有 sBPD 的早产儿中,我们发现了 109 例 PVS 病例,并将这些病例与 327 例对照进行了匹配。PVS 的患病率(1.07%)在两个时期之间上升(2010-2016 年为 0.8%,2017-2022 年为 1.2%)。与对照组相比,患有 PVS 的婴儿出生体重<500 克、小于胎龄<10%或患有手术性坏死性小肠结肠炎、房间隔缺损或肺动脉高压的可能性更大。在多变量模型中,这些相关性仍然存在,并且小于胎龄、手术性坏死性小肠结肠炎、房间隔缺损和肺动脉高压均与 PVS 独立相关。在出生后 36 周时接受呼吸支持的婴儿中,患有 PVS 的婴儿在 36 周时接受机械通气的可能性是对照组的 4.3 倍。与对照组相比,患有 PVS 的婴儿住院死亡率也高出 3.6 倍。
在一项患有严重支气管肺发育不良的大量早产儿队列中,多个独立的新生儿危险因素与 PVS 相关。这些结果为针对患有严重支气管肺发育不良的早产儿的 PVS 进行有针对性的筛查以指导其诊断和管理奠定了重要基础。