Rainbow Babies and Children's Hospital, Case Western Reserve University, Cleveland, Ohio, USA.
Neonatology. 2012;101(4):345-52. doi: 10.1159/000337355. Epub 2012 Jun 1.
Despite changes in the epidemiology of bronchopulmonary dysplasia (BPD), longer-term morbidity, particularly in the form of airway dysfunction, remains a substantial problem in former preterm infants. The stage for this respiratory morbidity may begin as early as the transition from fetal to neonatal life. Newer therapeutic approaches for BPD should be directed toward minimizing this longer-term respiratory morbidity. Neonatal animal models focused primarily on hyperoxic exposure may provide important insights into the pathogenesis of longer-term airway hyperreactivity in this population.
尽管支气管肺发育不良 (BPD) 的流行病学发生了变化,但以前早产儿的长期发病率,特别是气道功能障碍的形式,仍然是一个严重的问题。这种呼吸系统发病率的阶段可能早在胎儿向新生儿生命的过渡时期就开始了。针对 BPD 的新治疗方法应该旨在最大限度地减少这种长期的呼吸发病率。主要关注高氧暴露的新生儿动物模型可能为该人群的长期气道高反应性的发病机制提供重要的见解。