Treatment for Cystic Fibrosis
Treatment for cystic fibrosis (CF) will depend on your child’s symptoms, age, and general health. It will also depend on how severe the condition is.
There is no cure for CF. But research in gene therapy is being done. The gene that causes CF has been found. This may lead to a better understanding of the disease. Over time, gene therapy research may cure, prevent, or slow the disease's progress. Goals of treatment are to ease severity of symptoms and slow the progress of the disease. Treatment may include:
CFTR modulator therapies. CFTR (cystic fibrosis transmembrane regulator) is the protein that is not formed correctly in people with CF. There are new CFTR modulator therapies that are designed to correct the function of the defective protein made by the CF gene. These proteins are only appropriate for certain people with CF. They only help people with certain genetic abnormalities.
Managing problems that cause lung obstruction, such as:
Chest physical therapy. This helps loosen and clear lung secretions. Treatment may include postural drainage. It may also include devices that vibrate the chest wall and loosen secretions. Chest physical therapy can be done using the hands. Or it can done mechanically with a vest.
Exercise. This helps loosen mucus, stimulate coughing, and improve overall physical condition.
Medicines, such as bronchodilators and anti-inflammatories. These are used to decrease inflammation and swelling, thin the mucus, open airways, and help breathing.
Antibiotics. These treat infections.
Managing digestive problems, which may include:
Changing your child's diet
Pancreatic enzymes to help digestion
Treatments for intestinal blockages
Psychosocial support. Provides help in dealing with coping, independence, sterility, sex issues, money issues, and relationships.
As lung disease gets near the end stage, a lung transplant may be an option. The type of transplant done is often a double lung transplant. That’s because leaving the other, sicker lung in place puts it at risk for infection and damage. Not everyone is a candidate for a lung transplant. Ask your child's healthcare provider for more information.
With medical and psychosocial support, many children and teens with CF can cope well and lead a productive life.
Online Medical Reviewer: Alan J Blaivas DODaphne Pierce-Smith RN MSN CCRCPaula Goode RN BSN MSN
Date Last Reviewed: 3/1/2019
© 2000-2019 The StayWell Company, LLC. 800 Township Line Road, Yardley, PA 19067. All rights reserved. This information is not intended as a substitute for professional medical care. Always follow your healthcare professional's instructions.
- Autosomal Recessive: Cystic Fibrosis, Sickle Cell Anemia, Tay Sachs Disease
- Chronic Respiratory Disorders
- Cystic Fibrosis and the Digestive System
- Cystic Fibrosis and the Reproductive System
- Cystic Fibrosis and the Respiratory System
- Cystic Fibrosis in Children
- Cystic Fibrosis Overview
- Diagnosis of Cystic Fibrosis
- Feeding Your Child with Cystic Fibrosis
- Symptoms of Cystic Fibrosis
- The Genetics of Cystic Fibrosis
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