How is CF diagnosed?
Parents of all newborn babies in Australia are offered bloodspot screening (the heel prick test) for their babies. This test identifies those who have rare, but serious, medical conditions including cystic fibrosis. The benefit of this test is early detection.
Usually, a blood sample is taken between 48 and 72 hours after birth by pricking the baby’s heel and placing a few drops of blood onto a screening card. The blood sample is examined in a laboratory. If a baby is confirmed as having a medical condition, the parents will be contacted.
If a baby is thought to have CF, a sweat test may be performed to confirm or exclude the diagnosis. People with CF have a problem with their cells transporting salt (chloride), which results in higher concentrations salt in the sweat. The sweat test measures this by collecting a small amount of sweat for analysis.
There are also ways to test for CF during pregnancy which are only usually only carried out in pregnancies with a high chance of cystic fibrosis, such as when both parents are known to be carriers of the CF gene change.
Occasionally CF may not be diagnosed until later in life. Some children are diagnosed later in childhood, whether it be weeks after birth or even years, and sometimes CF is not diagnosed until adulthood.
One reason for this is that CF can vary widely in its severity and symptoms, and can resemble other lung conditions such as asthma or bronchitis which makes diagnosis challenging. Another reason is that there are around 2,000 different gene changes that cause CF and some gene changes are harder to detect.