支气管肺发育不良
医学
坏死性小肠结肠炎
早产儿视网膜病变
脑室出血
儿科
妊娠期
室周白质软化
胎龄
回顾性队列研究
败血症
机械通风
出生体重
呼吸窘迫
入射(几何)
低出生体重
新生儿重症监护室
新生儿学
早产
重症监护
怀孕
外科
遗传学
物理
光学
生物
作者
Erik A. Jensen,Erika M. Edwards,Lucy T. Greenberg,Roger F. Soll,Danielle Ehret,Jeffrey D. Horbar
出处
期刊:Pediatrics
[American Academy of Pediatrics]
日期:2021-07-01
卷期号:148 (1)
被引量:59
标识
DOI:10.1542/peds.2020-030007
摘要
BACKGROUND AND OBJECTIVES The Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network recently proposed new, severity-based diagnostic criteria for bronchopulmonary dysplasia (BPD). This study provides the first benchmark epidemiological data applying this definition. METHODS Retrospective cohort study of infants born from 22 to 29 weeks’ gestation in 2018 at 715 US hospitals in the Vermont Oxford Network. Rates of BPD, major neonatal morbidities, and common respiratory therapies, stratified by BPD severity, were determined. RESULTS Among 24 896 infants, 2574 (10.3%) died before 36 weeks’ postmenstrual age (PMA), 12 198 (49.0%) did not develop BPD, 9192 (36.9%) developed grade 1 or 2 BPD, and 932 (3.7%) developed grade 3 BPD. Rates of mortality before 36 weeks’ PMA and grade 3 BPD decreased from 52.7% and 9.9%, respectively, among infants born at 22 weeks’ gestation to 17.3% and 0.8% among infants born at 29 weeks’ gestation. Grade 1 or 2 BPD peaked in incidence (51.8%) among infants born at 25 weeks’ gestation. The frequency of severe intraventricular hemorrhage or cystic periventricular leukomalacia increased from 4.8% among survivors without BPD to 23.4% among survivors with grade 3 BPD. Similar ranges were observed for late onset sepsis (4.8%–31.4%), surgically treated necrotizing enterocolitis (1.4%–17.1%), severe retinopathy of prematurity (1.2%–23.0%), and home oxygen therapy (2.0%–67.5%). CONCLUSIONS More than one-half of very preterm infants born in the United States died before 36 weeks’ PMA or developed BPD. Greater BPD severity was associated with more frequent development of major neonatal morbidities, in-hospital mortality, and use of supplemental respiratory support at discharge.
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