Cystic fibrosis (CF) is a genetic disorder that affects various body systems, leading to premature death. Newborn screening in all states has helped identify those who have this disorder and allows for earlier interventions. Although traditionally viewed as a pulmonary disorder, treatments are available to address the various manifestations of CF. Airway clearance, nutritional support, pancreatic-enzyme replacement, and chronic antibiotic therapy are among the current recommended treatments. The most recent development involves the use of cystic fibrosis transmembrane conductance regulators that help to correct the underlying problem rather than just treat the symptoms. Pharmacists can serve an important role in the proper treatment of primary and secondary symptoms of CF.
|Original language||English (US)|
|Number of pages||6|
|Specialist publication||U.S. Pharmacist|
|Publication status||Published - May 1 2018|
All Science Journal Classification (ASJC) codes
- Pharmaceutical Science