Congenital Adrenal Hyperplasia (CAH) by AutoDELFIA Neonatal 17 α-OH-progesterone Assay
Data | Value |
---|---|
Method | Solid Phase Two-Site Fluoroimmunometric Assay. |
CPT Code | 83516 |
Testing Scope | Detection of elevated levels of 17 α-OH-progesterone from clinical specimens. |
Preferred Specimen | Heel stick dried blood spots collected on FDA-approved filter paper (Perkin Elmer 226 Ahlstrom) at 24-48 hours of age and at 10-14 days of age. |
Specimen Container | Specimen collection kit comes with a biohazard flap to cover the blood when dried for about 4 hours and placed in an envelope for shipment. |
Specimen Identification | All information fields on the kit must be completely filled out. Each kit has a unique serial number and barcode. |
Special Instructions | After air-drying for 4 hours, send specimen for overnight delivery within 24 hours after collection. |
Shipping Requirements | Do not place specimen in a zipper bag without desiccant. Do not expose to direct sunlight, excessive humidity or high temperature. |
Note | Steroid and/or anticoagulant EDTA will interfere with the assay. |
Sample Rejection Criteria |
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Turnaround Time | Normal result within 24-36 hours. Presumptive positive result within 48-72 hours. |