Cystic fibrosis (CF) is an inherited disease that primarily affects the lungs and the digestive system, however, it also affects a number of other organs and systems. More than 90% of mortality of CF patients is due to lung complications. Healthy lungs are important for a long life for people with CF, We will discuss two important topics for maintaining respiratory health. Chronic use of drugs for maintaining respiratory health There are a number of drugs available to keep CF lungs healthy. We will discuss the science behind the recommendations for use of: Inhaled antibiotics Dornase alfa Azithromycin Hypertonic saline High-dose ibuprofen Ivacaftor CF Airway Clearance Therapies Airway Clearance therapy is very important to keeping CF lungs healthy. Our discussions cover the following topics such as the: Daily airway clearance Different techniques of airway clearance Effect of aerobic exercise on airway clearance
Modaresi, M. (2014). Maintaining Respiratory Health in Cystic Fibrosis Patients. Journal of Pediatric Perspectives, 2(2.1), 9–9. https://doi.org/10.22038/ijp.2014.2447
MLA
Modaresi, M. "Maintaining Respiratory Health in Cystic Fibrosis Patients", Journal of Pediatric Perspectives, 2, 2.1, 2014, 9–9. doi: 10.22038/ijp.2014.2447
HARVARD
Modaresi, M. (2014). 'Maintaining Respiratory Health in Cystic Fibrosis Patients', Journal of Pediatric Perspectives, 2(2.1), pp. 9–9. doi: 10.22038/ijp.2014.2447
CHICAGO
Modaresi, M., "Maintaining Respiratory Health in Cystic Fibrosis Patients." Journal of Pediatric Perspectives, 2 2.1 (2014): 9–9, doi: 10.22038/ijp.2014.2447
VANCOUVER
Modaresi M. Maintaining Respiratory Health in Cystic Fibrosis Patients. JPP; J Ped Perspect. 2014;2(2.1):9–9. doi: 10.22038/ijp.2014.2447