Test Code LAB0298869 West Nile Virus Antibody, IgG and IgM, Spinal Fluid
Additional Codes
Mayo Test ID |
---|
WNC |
Performing Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Aiding in diagnosis of central nervous system infection with West Nile virus
Special Instructions
Method Name
Enzyme-Linked Immunosorbent Assay (ELISA)
Reporting Name
West Nile Virus Ab, IgG and IgM,CSFSpecimen Type
CSFSpecimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube: Sterile vial
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Specimen Minimum Volume
0.8 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
CSF | Refrigerated (preferred) | 7 days | |
Frozen | 30 days |
Reject Due To
Gross hemolysis | Reject |
Reference Values
IgG: Negative
IgM: Negative
Reference values apply to all ages.
Interpretation
Presence of specific IgM-class antibodies to West Nile virus (WNV)is consistent with the acute phase of WNV meningitis or encephalitis. In the very early stages of acute WNV infection, IgM may be detectable in cerebrospinal fluid (CSF) before it becomes detectable in serum.
The absence of IgM antibodies to WNV may indicate absence of disease. However, specimens collected too early in the acute phase may be negative for IgM-class antibodies to WNV. If WNV central nervous system infection is suspected, a second specimen should be collected in 1 to 2 weeks and tested.
The presence of IgG-class antibodies to WNV may indicate recent or past central nervous system (CNS) infection with WNV. Clinical correlation is necessary.
This assay is unable to distinguish between intrathecal antibody synthesis and serum antibodies introduced into the CSF at the time of lumbar puncture or from a breakdown in the blood-brain barrier. Positive results should be interpreted with other laboratory and clinical data prior to a diagnosis of CNS infection.
Day(s) Performed
Monday, Wednesday, Friday
Report Available
Same day/1 to 4 daysSpecimen Retention Time
14 daysTest Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
86789
86788
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
WNC | West Nile Virus Ab, IgG and IgM,CSF | 94853-9 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
WNGC | West Nile Virus Ab, IgG, CSF | 77953-8 |
WNMC | West Nile Virus Ab, IgM, CSF | 29569-1 |
WNVCI | West Nile CSF Interpretation | 69048-7 |
Profile Information
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
WNGC | West Nile Virus Ab, IgG, CSF | No | Yes |
WNMC | West Nile Virus Ab, IgM, CSF | No | Yes |
WNVCI | West Nile CSF Interpretation | No | Yes |
Forms
If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.