Hirsutism Evaluation Panel
Also known as: HIRSUTISM
Use
This panel aids in the detection and subclassification of hyperandrogenism, which is most useful in women and children with moderate to severe hirsutism or hirsutism of any degree when it is sudden in onset or rapidly progressive. It provides valuable insights by quantifying hormone levels that could indicate androgen excess, helping in the identification and management of conditions that result in hirsutism.
Special Instructions
Collect serum or plasma between 6-10 a.m. to ensure accurate measurement, as hormone levels can fluctuate throughout the day. Separate serum from cells as soon as possible or within 2 hours of collection to maintain sample integrity.
Limitations
The test is performed in a CLIA certified laboratory but has not been cleared or approved by the FDA, which may impact its acceptance in certain regulatory environments. Hemolyzed specimens are unacceptable, which could lead to the need for repeat collections. The long-term stability of serum at room temperature is limited to 2 hours, which necessitates prompt processing and freezing for accurate results.
New York Approved
Methodology
Immunoassay (CLIA/ECLIA)
Biomarkers
LOINC Codes
- 2191-5
- 2986-8
- 49042-5
- 13967-5
- 1854-9
Result Turnaround Time
1-5 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
2.5 mL
Minimum Volume
1.5 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Collect in a serum separator tube or serum from plain red tube between 6-10 a.m. Separate serum from cells ASAP or within 2 hours of collection.
Storage Instructions
Store and transport frozen.
Causes for Rejection
Hemolyzed specimens
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 2 hours |
| Refrigerated | 48 hours |
| Frozen | 2 months |
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