West Nile Virus, IgM
Label Mnemonic: | ARBWNV |
Epic code: | LAB7533 |
Downtime form: | Doctor/Provider Orders - Pathology Core and Specialty Care Nursery |
Commercial Mailout Laboratory
6240-8 RCP
356-8593
6240-8 RCP
356-8593
Specimen(s):
Serum
Specimen
Instructions:
Acute and convalescent specimens must be labeled as such; parallel
testing is preferred and convalescent specimens must be received within
30 days from receipt of the acute specimens. Please mark
specimen plainly as "acute" or "convalescent."
Collection Medium:
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Red top tube 5 mL (Clot Activator) |
Minimum:
Preferred Minimum: 1 mL serum in a red top tube
Absolute Minimum: 0.15 mL serum in a red top tube
Absolute Minimum: 0.15 mL serum in a red top tube
Rejection Criteria:
Plasma. Contaminated, hemolyzed, heat-inactivated, or severely lipemic
specimens.
Turn Around
Time:
1-8 days upon receipt at reference laboratory
Reference Range:
0.89 IV or less: Negative - No significant level of West Nile virus IgM
antibody detected.
0.90-1.10 IV: Equivocal - Questionable presence of West Nile virus IgM antibody detected. Repeat testing in 10-14 days may be helpful.
1.11 IV or greater: Positive - Presence of IgM antibody to West Nile virus detected, suggestive of current or recent infection.
0.90-1.10 IV: Equivocal - Questionable presence of West Nile virus IgM antibody detected. Repeat testing in 10-14 days may be helpful.
1.11 IV or greater: Positive - Presence of IgM antibody to West Nile virus detected, suggestive of current or recent infection.
Interpretive Data:
This test is intended to be used as a semi-quantitative means of
detecting West Nile virus-specific IgM in serum specimens in which
there is a clinical suspicion of West Nile virus infection. This test
should not be used solely for quantitative purposes, nor should the
results be used without correlation to clinical history or other data.
Because other members of the Flaviviridae family, such as St. Louis
encephalitis virus, show extensive cross-reactivity with West Nile
virus, serologic testing specific for these species should be
considered.
Seroconversion between acute and convalescent sera is considered strong evidence of current or recent infection. The best evidence for infection is a significant change on two appropriately timed specimens, where both tests are done in the same laboratory at the same time.
Seroconversion between acute and convalescent sera is considered strong evidence of current or recent infection. The best evidence for infection is a significant change on two appropriately timed specimens, where both tests are done in the same laboratory at the same time.
Methodology:
Semi-Quantitative Enzyme-Linked Immunosorbent Assay
CPT Code:
86788