Hyaluronic Acid, Serum
Ordering Recommendation
Noninvasive assessment of liver status.
New York DOH Approval Status
Specimen Required
Serum separator tube. Also acceptable: Green (sodium or lithium heparin), lavender (EDTA), or pink (K2EDTA).
Allow serum specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 2 hours of collection. Transfer 2 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)
Refrigerated.
Specimens exposed to repeated freeze/thaw cycles.
Ambient: 24 hours; Refrigerated: 2 weeks; Frozen: 1 year
Methodology
Quantitative Enzyme-Linked Immunosorbent Assay
Performed
Tue
Reported
1-9 days
Reference Interval
0-54 ng/mL
Interpretive Data
This test is performed using the Corgenix Hyaluronic Acid test kit. Results obtained with different assay methods or kits cannot be used interchangeably.
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
Note
Hotline History
CPT Codes
83520
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0081138 | Hyaluronic Acid, Serum | 12736-5 |
Aliases
- HA
- Hyaluronate