CF is a disease that causes mucus build-up in the lungs and other organs. It damages the lungs and makes it hard to breathe. It can also lead to frequent infections and malnutrition. CF is an inherited disease, which means it is passed down from your parents, through genes.
Genes are parts of DNA that carry information that determine your unique traits, such as height and eye color. Genes are also responsible for certain health problems. To have cystic fibrosis, you must have a CF gene from both your mother and your father. If only one parent has the gene, you will not get the disease.
Other names: sweat chloride test, cystic fibrosis sweat test, sweat electrolytes
A sweat test is used to diagnose cystic fibrosis.
A sweat test can diagnose cystic fibrosis (CF) in people of all ages, but it’s usually done on babies. Your baby may need a sweat test if he or she tested positive for CF on a routine newborn blood test. In the United States, new babies are usually tested for a variety of conditions including CF. Most sweat tests are done when babies are 2 to 4 weeks old.
An older child or adult who has never been tested for CF may need a cystic fibrosis sweat test if someone in the family has the disease and/or has symptoms of CF. These include:
Your health care provider will need to collect a sample of sweat for testing. The entire procedure will take about an hour and will probably include the following steps:
You don’t need any special preparations for a sweat test, but you should avoid applying any creams or lotions to the skin for 24 hours before the procedure.
There is no known risk to a sweat test. Your child may have a tingling or tickling sensation from the electric current, but should not feel any pain.
If the results show a high level of chloride, there is a good chance your child has cystic fibrosis. Your health care provider will probably order another sweat test and/or other tests to confirm or rule out a diagnosis. If you have questions about your child’s results, talk to your health care provider.
While there is no cure for cystic fibrosis (CF), there are treatments available that help reduce symptoms and improve quality of life. If your child was diagnosed with CF, talk with your health care provider about strategies and treatments to help manage the disease.