SWEAT CHLORIDE TEST
Sweat Chloride Test is essential for the diagnosis of cystic fibrosis (CF). Cystic fibrosis is a genetic disorder that affects the lungs and digestive system, leading to suppurative lung disease and other serious complications. Our state-of-the-art testing services help provide accurate diagnoses for children suspected of having cystic fibrosis.
What is the Sweat Chloride Test?
The Sweat Chloride Test is a key diagnostic procedure for cystic fibrosis. It measures the level of chloride (salt) in a child’s sweat. High levels of chloride in the sweat are indicative of cystic fibrosis, as the disorder affects the transport of salt in and out of cells. This test is non-invasive and is performed by stimulating sweat production, collecting the sweat, and analyzing the chloride content.
Why is the Sweat Chloride Test Important for Diagnosing Cystic Fibrosis?
What Role Does the Sweat Chloride Test Play in the Diagnosis of Cystic Fibrosis?
How is Sweat Chloride test performed?
Sweat chloride test is done in the hospital and it does not require any admission. The sweat glands on the arm of the child are stimulated using electrical signals and some chemicals, then the area of the arm is wrapped and child is allowed to sweat for around 30 minutes. After 30 minutes, sweat is collected and sent for analysis in biochemistry lab.
Understanding results of Sweat Chloride Test
Children with cystic fibrosis have high chloride content than children who don’t have cystic fibrosis. To understand what the sweat test results mean, a chloride level of:
When sweat chloride test results fall between the range of 30-59 mmol/L, the sweat test is usually repeated. If it remains intermediate the second time, genetic testing is advised.