Test Code Epic LAB3798 Hepatitis E Virus IgM Antibody Screen with Reflex to Confirmation, Serum
Additional Codes
SQ code HEVMM
Mayo code HEVM
Reporting Name
HEV IgM Ab Screen, SSpecimen Type
Serum SSTPerforming Laboratory
Mayo Clinic Laboratories in RochesterUseful For
Diagnosis of acute or recent (<6 months) hepatitis E infection
Testing Algorithm
If hepatitis E virus (HEV) IgM antibody screen is reactive or borderline, HEV IgM antibody confirmation will be performed at an additional charge.
For more information see Hepatitis E: Testing Algorithm for Diagnosis and Management.
Necessary Information
Date of collection is required.
Specimen Required
Collection Container/Tube: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL
Collection Instructions:
1. Centrifuge blood collection tube per collection tube manufacturer's instructions (eg, centrifuge within 2 hours of collection for BD Vacutainer tubes).
2. Aliquot serum into plastic vial.
Specimen Minimum Volume
See Specimen Required
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum SST | Frozen (preferred) | ||
Refrigerated | 24 hours |
Special Instructions
Reference Values
Negative
Day(s) Performed
Tuesday, Thursday
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
86790
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
HEVM | HEV IgM Ab Screen, S | 14212-5 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
86212 | HEV IgM Ab Screen, S | 14212-5 |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Gross icterus | Reject |
Method Name
Enzyme Immunoassay (EIA)
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
HEVML | HEV IgM Ab Confirmation, S | Yes | No |
Method Description
This is a qualitative, in vitro test for the detection and identification of IgM antibodies specifically against hepatitis E virus (HEV) in human serum. This assay is a screening test based on the principle of an indirect sandwich enzyme-linked immunosorbent assay.
Highly purified recombinant HEV-ORF2 viral antigens (specific for HEV genotypes 1 and 3) are fixed to microplate wells. Diluted patient serum specimens are incubated in the wells, in which antibodies bind specifically to the HEV recombinant antigens coating the surface of the wells. Unbound antibodies are then washed away. Anti-human immunoglobulin antibodies (IgM), which are coupled to horseradish peroxidase, are then added to the wells and incubated. Unbound conjugate antibodies are then washed away. Specifically, bound antibodies are detected by a peroxidase-catalyzed color reaction. Intensity of the color, as measured with a photometric analyzer, is proportionate to the quantity of bound HEV IgM antibodies present in the serum specimen.(Unpublished Mayo method)
Report Available
1 to 7 daysForms
If not ordering electronically, complete, print, and send 1 of the following:
-Gastroenterology and Hepatology Test Request (T728)
-Infectious Disease Serology Test Request (T916)
-Microbiology Test Request (T244)