17182 ANDROSTENEDIONE

Test Code
ANDROST


Preferred Specimen
1 mL serum collected in a red-top tube (no gel)


Patient Preparation
An early morning specimen is preferred.

Minimum Volume
0.25 mL


Other Acceptable Specimens
Plasma collected in: EDTA (lavender-top) tube, EDTA (royal blue-top) tube, sodium heparin (green-top) tube or lithium heparin (green-top) tube


Instructions
Draw blood in a red-top tube (no gel). Separate serum after clotting. Do not submit glass tubes.


Transport Container
Transport tube


Transport Temperature
Refrigerated (cold packs)


Specimen Stability
Room temperature: 72 hours
Refrigerated: 28 days
Frozen: 2 years


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Gross hemolysis • Samples collected in serum separator tubes (SST)


Methodology
Chromatography/Mass Spectrometry

Setup Schedule
Set up: Daily; Report available: 2-5 days


Clinical Significance
Androstenedione may be useful in evaluating patients with androgen excess and managing patients with congenital adrenal hyperplasia (CAH).




The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.