Maintaining Normal Lung Function In Children With Cystic Fibrosis Is Possible With Aggressive Treatment Regardless Of Pseudomonas Aeruginosa Infections

Cystic fibrosis (CF) is an orphan disease with increased morbidity and mortality, mainly due to chronic pulmonary infections. The symptoms and treatment are complex, and patients are followed at specialised CF centres. The exact treatment, and the segregation policies to avoid cross-infection from airway pathogens, vary between CF centres, including those in Scandinavian countries.