West Nile Virus by PCR
Ordering Recommendation
Use to confirm positive West Nile antibodies test or clarify equivocal serologic test results.
New York DOH Approval Status
Specimen Required
Lavender (EDTA), pink (K2EDTA) or serum separator tube. OR CSF.
Separate serum or plasma from cells.
Transfer 1 mL serum, plasma or CSF to a sterile container. (Min: 0.5 mL)
Frozen.
Heparinized specimens.
Specimen source required.
Ambient: 8 hours; Refrigerated: 24 hours; Frozen: 3 months
Methodology
Qualitative Polymerase Chain Reaction
Performed
Mon-Fri
Reported
1-4 days
Reference Interval
Interpretive Data
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
87798
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0050229 | West Nile Virus by PCR | 34892-0 |
0050242 | West Nile Virus Source | 31208-2 |
Aliases
- Arbovirus
- Flavivirus
- West Nile PCR
- WNV
- WNV Molecular Detection, PCR
- WNV PCR