Test Code Sweat CL Sweat Chloride
Performing Laboratory
Women and Children Hospital Laboratory | 304-388-2385 |
Specimen Requirements
Sweat-Macroduct Sweat Collection Device
50 uL (minimum 15uL from each site)
The collection and the analysis be performed in duplicate.
A suitable site on the patient’s lower arm or upper leg only, should be selected for the attachment of electrodes for the iotophoresis procedure. The selected site must be free of breaks, fissures, or any other abnormality in the skin. There should be no sign of inflammation, rash, or eczematous lesion, due to the likelihood of contamination by serous fluid. The area must be wrinkle-free and hairless as possible.
Do not attempt iontophoresis on a patient who is receiving oxygen-enriched respiratory therapy in an enclosed space. The possibility of an explosion due to the generation of an electrical spark cannot be discounted. With medical approval, it is often possible to remove the patient form such an environment for the duration of the iontophoresis, perhaps with the temporary support of a respiratory facemask.
Sweat MUST NOT be stimulated or collected from the head or the trunk. The electrodes used for stimulation must be placed such that iontophoretic current NEVER crosses the patient’s trunk, to avoid the possibility of current crossing the heart, resulting in cardiac depolarization.
Storage and Stability
Not acceptable to refrigerate or freeze specimens
Reference Values
<30 mmol/L | Newborns with positive newborn screen; CF unlikely | Other population;CF unlikely |
30-59 mmol/L | All populations; intermediate range | Needs further study to rule out CF as a diagnosis |
> 60 mmol/L | All populations; indicative of CF | For individuals presenting with a postive newborn screen or clinical features or family history |
Methodology
Stimulation iontophoresis -Collection
Choridometer-Analysis
Days Test Set Up and Turnaround
Monday through Friday, 8:00 AM- 4:00 PM
Results available within 72 hours
CPT Coding
89230-Collection
82438- Analysis
Additional Information
All positve tests must be repeated at a different collection time. The techologist will notify the patient's physcian and document the date and time the physician was notified of the positive result.
Use: The sweat test with iontophoretic stimulation is considered the most reliable single test in the doagnosis of cystic fibrosis. Test becomes positive between 3 and 5 weeks of age in most affected infants.