Cystic fibrosis (CF) is an inherited disease. It causes a defect in certain cells of the lung and digestive systems. The defect makes the cells produce a thick, sticky mucus. This mucus can cause:
- Blockages in the lungs and airways
- Problems digesting and absorbing nutrients
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CF is a serious life-long condition, but the severity of the illness can vary greatly. The average life expectancy for someone with CF is about 35 years. Although, some with mild forms of CF can live to age 60 or beyond.
CF is a genetic disorder. A child with CF inherits defective genes from each parent. Parents who have the gene, but do not have CF, are called carriers.
Factors that increase your chance of CF include:
- Parents who are known carriers of the CF gene
- Siblings with CF
- Parents with CF—more often the mother since men with CF may be sterile
The abnormally thick mucus of CF blocks certain organs. This causes many of the symptoms of CF.
Symptoms in infants may include:
- Difficulty passing the first stool
- Salty sweat
- Intestinal obstruction, sometimes requiring surgery
Mucus that causes blockages in the lungs may lead to:
- Coughing and wheezing
- Shortness of breath
- Difficulty with exercise
- Abnormally shaped clubbed finger tips
- Malformed chest
Mucus can also block the pancreas. This can block enzymes used to help you digest food. This can lead to:
- Bulky, bad-smelling, floating stools, due to poor digestion of fats
- Trouble gaining weight
- Poor growth
Failure to thrive
Other symptoms may include:
Jaundice or other symptoms of liver disease
- Chronic nasal congestion from chronic sinus infections
- Nasal polyps
- Excessive thirst or urination that may indicate diabetes mellitus type 2
- Stomach pain or swelling from intestinal blockage
- Prevention of sperm production in males
- Mildly decreased fertility in females
Overall, girls are affected more severely than boys.
The doctor will ask about symptoms and medical history. A physical exam will be done. CF is suspected in a child with classic symptoms, especially if a sibling has CF.
CF is often diagnosed by symptoms, family history of CF, or a positive screening test in newborns. The diagnosis may be confirmed with genetic testing. Other lab tests that may be used to confirm CF include:
- Sweat chloride testing
- Transepithelial nasal potential difference measurement
Your doctor may need to check your lungs. This may be done to look for symptoms or to determine treatment. Tests may include:
Tests may also be needed to check the pancreas. These tests may be done to assess symptoms or determine treatment.
There is no cure for CF. Treatment is aimed at:
- Improving the amount of nutrition your body receives
- Preventing and treating lung and sinus infections
- Keeping the airways and lungs as clear as possible
Treatment for CF includes:
Better nutrition will help improve overall health. It will also improve growth and development in children. Children who have returned to normal weight within 2 years of the diagnosis have fewer coughing episodes and better lung function. Some nutritional steps that may help include:
- A high-calorie diet planned by a registered dietitian
- Nutritional supplements, including fat-soluble vitamins
- Pancreatic enzyme tablets with meals to improve digestion and absorption of nutrients
- Drinking lots of fluids and salt replacement, especially in hot weather or during illnesses
Managing Lung Infections
Thick mucus in the airways increases the risk of respiratory infections. The infection can also be more severe because of the mucus. Treatment of a current infection often requires antibiotics. Prevention of new infections may be done with:
- Antibiotics (usually inhaled)
Lung and Airway Support
Medications help keep the airways clear. Most will be delivered through an inhaler or nebulizer. Medications may include:
- Bronchodilators—to relax muscles and open the airway
- Mucolytic agents—to reduce mucus and help it move out of the lung
- Steroid inhalers—to decrease swelling and irritation (only when necessary)
Other steps that may help clear mucus from the lungs include:
- Hypertonic saline is a special type of salt water. A nebulizer machine creates a mist of this saline, which is inhaled. The mist may help thin out the mucus in the lungs.
is rhythmic clapping over the chest. They may help clear mucus from airways.
It is most helpful if done at least twice per day.
may be required as the disease progresses. Ventilation may also be needed.
Talk to your doctor about whether these are options for you.
Surgery may be required to treat blockages in the intestine.
may also be considered.
Support is important for those with CF and their families. Ask you doctor about local support groups or counseling options.
If you have the defective genes, there is no way to prevent CF.
Adults can be tested to see if they carry the genes before having children.
can determine if a baby will have CF.
American Lung Association
Cystic Fibrosis Foundation
About Kids Health—The Hospital for Sick Children
The Lung Association
About cystic fibrosis: what you need to know. Cystic Fibrosis Foundation website. Available at:
Accessed February 12, 2016.
Cystic fibrosis. American Academy of Pediatrics Healthy Children website. Available at:
Updated November 21, 2015. Accessed February 12, 2016.
Cystic fibrosis (CF). EBSCO DynaMed Plus website. Available at:
http://www.dynamed.com/topics/dmp~AN~T116913/Cystic-fibrosis-CF. Updated September 20, 2016. Accessed September 29, 2016.
Genetic testing. American Medical Association website. Available at:
Accessed February 12, 2016.
4/16/2009 DynaMed Plus Systematic Literature Surveillance
http://www.dynamed.com/topics/dmp~AN~T116913/Cystic-fibrosis-CF: Lai HJ, Shoff SM, Farrell PM, Wisconsin Cystic Fibrosis Neonatal Screening Group. Recovery of birth weight z score within 2 years of diagnosis is positively associated with pulmonary status at 6 years of age in children with cystic fibrosis.
10/1/2013 DynaMed Plus Systematic Literature Surveillance
http://www.dynamed.com/topics/dmp~AN~T116913/Cystic-fibrosis-CF: Elphick HE, Mallory G. Oxygen therapy for cystic fibrosis. Cochrane Database Syst Rev. 2013;7:CD003884.