Update on cystic fibrosis

Abstract

Over the past year, research in cystic fibrosis (CF) has focused upon methods to diagnose CF more quickly and more accurately, assess lung function and lung infection in infants with CF, and improve the use of existing therapies for CF. The new application of growth hormone to patients with CF to improve growth and nutrition has been investigated. There has also been research into psychosocial aspects of CF care, including evaluation of coping mechanisms, genetic counseling, and transition to adult care. Research also suggests a predisposition to chronic rhinosinusitis in CF carriers.