What is the Sweat Test?|
The sweat test is called a “diagnostic test.” It is the most accurate way to tell whether or not your baby has CF. It is sometimes called the “gold standard” test for CF. The sweat test measures how much salt is in your baby’s sweat. Remember, most babies who need to have a sweat test because of an abnormal newborn screen do not have CF. But it is important to be sure that they do not.
Yes. If your baby’s screening test was “abnormal” or “positive” for CF, the baby needs to have a sweat test to find out if she or he has CF.back to top
When I was pregnant, I had a blood test to see if I was a CF carrier and it was negative. Now my baby has a positive (abnormal) screen for CF. Does my baby still need a sweat test?
Yes. Any baby who had a positive (abnormal) newborn screen for CF should have a sweat test. Standard prenatal genetic screening tests look for only the most common CF gene mutations, not all of them.
You could carry a gene mutation that was not included in the test you had when you were pregnant. Remember, most babies who have a positive (abnormal) screen for CF do not have CF. But, it is important to be sure that they do not have CF. This is true regardless of whether your test for being a CF carrier was negative.
The sweat test should be done at a CF Foundation-accredited care center. This test can usually be done within the first few weeks of your baby’s life. If you have questions about or need help scheduling the sweat test, talk with your baby’s doctor.
On the day of the sweat test, do not use any lotions, creams or moisturizing soaps on your baby’s arms or legs. Bring an extra blanket or sweater and hat to keep your baby warm so he or she will sweat during the test. Be sure your baby has been fed. Doing so may help your baby sweat more. Your baby also may be able to feed during the test.
The sweat test does not hurt. You can stay with your baby throughout the procedure. A special gel is put on your baby’s skin on an arm or leg. Small patches with wires cover the gel for about 5 minutes. This causes your baby to sweat. The skin may feel warm and tingly while the patches are in place, but it is not painful. The sweat is collected on a gauze pad or disk. After about 30 minutes, the gauze or disk is removed and taken to a laboratory to measure the salt. The sweat test takes about one hour from start to finish.
It would be helpful if your spouse/partner comes with you to the appointment. Many CF care centers also offer parents genetic counseling at the time of the sweat test. This counseling can help you understand the genetics of CF and what it means for you and your partner as well as for your baby in the future.
If you have other young children, it might be best to leave them with a babysitter or bring someone to watch them at the appointment. This will allow you to talk with the genetic counselor or health care provider with fewer distractions.
We recognize that it can be very stressful for parents to wait for the sweat test. Therefore, staff at CF care centers make every effort to schedule sweat tests as quickly as possible. While even a few days' wait can add to your worry and anxiety, your baby is not in any immediate danger. Call your baby's doctor if you have any concerns about your baby's health or well-being while you are waiting for the sweat test.
If you have questions or concerns while you are waiting for the sweat test appointment, we encourage you to call the CF Foundation-accredited care center and ask to speak with a nurse or genetic counselor who can answer your questions.
Results of the sweat test should be available to you and your doctor within a few days.
The sweat test looks at how much salt is in your baby’s sweat. Salt is made up of two parts — sodium and chloride. The sweat test measures the amount of chloride (Cl-) in a person’s sweat.
There are four possible results of a sweat chloride test:
This sometimes happens because young infants have immature sweat glands. It has nothing to do with whether or not your baby has CF. You will need to talk to your baby’s health care provider to see what next step he or she recommends.
Depending on the results of the newborn screen, your provider might say it’s okay to wait to do the sweat test later.
Or, your provider might suggest other tests such as DNA or genetic testing. It can be very frustrating for parents when the first tests do not answer the question of whether their baby has CF.
It is important for you to know that the amount of sweat a baby produces has no bearing on whether or not the child has CF.
The sweat test is recommended as the first diagnostic test for CF. But sometimes a sweat test cannot be done successfully or in a timely manner. Reasons include an infant’s premature birth; a hospital or clinic that does not routinely perform sweat tests; not enough sweat collected during the sweat test; or intermediate (borderline) results from the sweat test.
In these cases, the baby’s doctor or the CF care center staff might suggest a genetic test instead of, or in addition to, the sweat test. Genetic testing can be done by collecting a small amount of blood from the baby and sending it to a special lab to check for CF gene mutations. It can take several weeks before the results are available.
If your health insurance does not cover genetic testing, a member of the CF care center can talk with you about your options. For more on the guidelines for diagnosing CF, see the CF Foundation’s consensus report, “Guidelines for Diagnosis of Cystic Fibrosis in Newborns through Older Adults.”
If your baby’s newborn screen for CF was abnormal but the baby’s diagnostic test (sweat test) was normal, your child does not have CF. We call this situation a “false positive” newborn screen. Reasons for false positives can include prematurity and a lot of stress during delivery. Babies who have one CF gene mutation may also have a positive newborn screen but not have cystic fibrosis. Anyone with one CF gene mutation is said to be a "carrier of CF."
It is important to remember that newborn screening is done to make sure that all babies with CF are found as soon as possible. It also finds babies who do not have CF. It is a good thing that your baby doesn't have CF, but a positive newborn screen also causes a lot of stress for many parents.
Some babies with an abnormal newborn screening result do not have CF but are carriers of one CF gene mutation. People who carry only one CF gene mutation do not have CF. They are fine and usually do not know they are CF carriers.If your baby is a carrier of CF, it also means that at least one parent is a CF carrier and both parents could be carriers. If you are both CF carriers and you plan to have more children, there is a chance that you could have a child with CF in the future. In time, your child should learn about what it means to be a CF carrier (especially in terms of childbearing).
To learn more about being a CF carrier and what you can do, see the "What does it mean to be a carrier?" section.back to top