Disease Areas:
Cough,Cystic fibrosis,Primary ciliary dyskinesiaDevice Types:
In2itiveThis prospective study evaluated changes in airway remodeling in 83 children with cystic fibrosis, primary ciliary dyskinesia, or a history of recurrent infections and/or persistent or recurrent cough. Spirometry endpoints, which were collected pre-bronchoscopy, included FEV1 and FVC, and were measured using the Vitalograph In2itive spirometer.
