Cystic Fibrosis Tests & Cystic Fibrosis Treatments at University of Colorado Hospital

Tests for Cystic Fibrosis

Genetic Testing

Genetic testing is performed on adult patients suspected of having CF.

Sweat Tests

Sweat tests are performed at The Children's Hospital, and can help confirm the results of genetic testing.

Cystic Fibrosis Treatments

Airway Clearing Techniques

Patients with cystic fibrosis lung disease perform airway clearing techniques to help loosen and clear mucus from the lungs. In childhood, this can involve a friend or family member pounding on the patient’s back. Adult patients use a variety of methods, including a mechanical vest that shakes them and allows them to clear the mucus.

Inhaled Medications

Inhaled medications are used to help clear the airways, and include the enzyme DNase or concentrated saline.

Antibiotics

Antibiotics are used both on a chronic bases to suppress infection, and during periods of pulmonary exacerbations.

Pancreatic Replacement Enzymes

Pancreatic replacement enzymes are required to allow CF patients with pancreatic damage to digest food properly.

Insulin

Insulinis required by many adults with CF.

Bronchodilators

Most CF patients have a degree of "asthma," and require bronchodilators to keep their airway as clear as possible.