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. doi: 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
M. Modaresi, "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. Journal of Pediatric Perspectives, 2014; 2(2.1): 9-9. doi: 10.22038/ijp.2014.2447