Test Code A Hepatitis A Antibody, Total
Useful For
In aiding in the diagnosis of previous or ongoing hepatitis A viral infection. Also useful for the determination of susceptibility to Hepatitis A.
Synonyms/Keywords
Anti-HAV, HAVAB, Hep A Virus Antibody
Specimen Requirements
| Fasting Required | Specimen Type | Preferred Container/Tube | Acceptable Container/Tube | Specimen Volume | Specimen Minimum Volume (allows for 1 repeat) |
Pediatric Minimum Volume (no repeat) |
|---|---|---|---|---|---|---|
| No | Serum | Serum Separator Tube (SST) | Red Top Tube (RTT) | 1 mL | 0.5 mL | 0.3 mL |
Collection/Processing Instructions
Separate serum from the blood within 60 minutes of venipuncture and transport in an aliquot tube. Specimen must be free of particulate matter including fibrin.
Regional/Outreach sites: Please send samples to Marshfield frozen.
High doses of exogenous biotin (also termed Vitamin B7, Vitamin H or Coenzyme R) may interfere with this assay. It is recommended that patients refrain from consuming any multivitamin or supplement containing biotin for at least 72 hours prior to collection of a blood sample.
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Ambient | <8 hours |
| Refrigerated | <48 hours | |
| Frozen at -20 C | 6 months | |
| Frozen at -70 C | >6 months |
Rejection Criteria
| Grossly hemolyzed |
|---|
| Grossly icteric |
| Specimens containing precipitate |
| Cadaver specimens |
| Heat-inactivated specimens |
| Body fluids other than serum |
Test Information
Hepatitis A virus (HAV) is endemic throughout the world, however, occurring most commonly in areas of poor hygiene and low socioeconomic conditions. The virus is transmitted primarily by the fecal-oral route, and it is spread by close person-to-person contact and by food- and water-borne epidemics. Viral spread by parenteral routes (e.g., exposure to blood) is possible but rare, because infected individuals are viremic for a short period of time (usually <3 weeks). There is little or no evidence of transplacental transmission from mother to fetus or transmission to newborn during delivery.
Limitations
- The results determined by different assays from different manufacturers can vary due to differences in assay specificities and cannot be used interchangeably.
- A nonreactive test result does not exclude the possibility of exposure to hepatitis A virus.
- HAV Total assay does not distinguish among different classes of antibodies. The assay cannot be used to determine if a reactive sample is due to an acute infection or is the result of a previous infection.
- Assay performance characteristics have not been evaluated for immunocompromised, immunosuppressed, cord blood and neonatal patients.
- A reactive or positive result does not exclude co-infection by another hepatitis virus.
Interferences
Heterophilic antibodies in human serum can react with the immunoglobulins included in the assay components causing interference with immunoassay. Patients receiving therapy with high doses of biotin (>5 mg/day), should be tested 8 hours after last biotin administration.
High doses of exogenous biotin (also termed Vitamin B7, Vitamin H or Coenzyme R) may interfere with this assay.
Interpretations
Antibodies to HAV (anti-HAV) are detectable by the time symptoms occur, usually 15 to 45 days after exposure. The early antibody response is largely comprised of the IgM antibody subclass. Anti-HAV IgM is detectable for 3 to 6 months after the onset of illness, whereas anti-HAV IgG can persist indefinitely. The specific determination of anti-HAV IgM is the most useful serological marker for diagnosing acute HAV infection. Total anti-HAV is used primarily for determination of previous exposure to Hepatitis A virus. The measurement of anti-HAV total activity is also used to identify HAV susceptible individuals for vaccination. Positive results should be correlated with the patients clinical history. A positive anti-HAV total result with a negative anti-HAV IgM result indicates probable immunity to hepatitis A from either natural infection or vaccination. However, this assay does not have FDA clearance for confirmation of immunity, whether by natural infection or vaccination.
Acute hepatitis A is a reportable disease in Wisconsin and other states.
Reference Range Information
| Performing Location | Reference Range |
|---|---|
| Marshfield | Reported as "Reactive" or "Non-reactive". |
Marshfield Labs Performing Department
Marshfield Labs Chemistry
Performing Information
| Performing Location | Day(s) Test Performed | Analytical Time | Methodology/Instrumentation |
|---|---|---|---|
| Marshfield | Monday through Friday | 1 day | Competitive Immunoassay using Direct Chemiluminescent Technology/Siemens Centaur |
CPT Codes
| CPT | Modifier (if needed) |
Quantity | Description | Comments |
|---|---|---|---|---|
| 86708 |
Outreach CPT Codes
| CPT | Modifier (if needed) |
Quantity | Description | Comments |
|---|---|---|---|---|
| 86708 |
Ordering Applications
| Ordering Application | Description |
|---|---|
| Cerner | Hepatitis A Antibody, Total |