Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia.
Respirology. 2010 Aug;15(6):1009-11. doi: 10.1111/j.1440-1843.2010.01765.x. Epub 2010 Apr 23.
There is emerging evidence that cystic fibrosis lung disease begins early in infancy. Newborn screening allows early detection and surveillance of pulmonary disease and the possibility of early intervention in this life-shortening condition. We report two children with cystic fibrosis who underwent a comprehensive assessment from diagnosis that included measurement of lung function, limited-slice high-resolution CT and BAL performed annually. Early aggressive surveillance enabled significant lung disease and bronchiectasis to be detected during the first few years of life and led to a change in management, highlighting a clinical role for CT scanning during the preschool years in children with cystic fibrosis.
有新的证据表明囊性纤维化肺病在婴儿期早期就开始了。新生儿筛查可以早期发现和监测肺部疾病,并有可能对这种缩短生命的疾病进行早期干预。我们报告了两名囊性纤维化患儿,他们从诊断开始就接受了全面评估,包括每年进行肺功能、有限切片高分辨率 CT 和 BAL 检测。早期积极的监测使得在生命的最初几年中能够检测到明显的肺部疾病和支气管扩张,并导致治疗方式的改变,这突出了 CT 扫描在学龄前儿童囊性纤维化患者中的临床作用。