Test ID: HAIGM Hepatitis A IgM Antibody, Serum
Necessary Information
Date of draw is required.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Centrifuge blood collection tube per collection tube manufacturer's instructions (eg, centrifuge and aliquot within 2 hours of collection for BD Vacutainer tubes).
2. Aliquot serum into plastic vial.
Useful For
Diagnosis of acute or recent hepatitis A infection
Special Instructions
Method Name
Chemiluminescent Microparticle Immunoassay (CMIA)
Reporting Name
Hepatitis A IgM Ab, SSpecimen Type
SerumSpecimen Minimum Volume
0.4 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Refrigerated (preferred) | 7 days | |
Ambient | 72 hours |
Clinical Information
Hepatitis A virus (HAV) is endemic throughout the world, occurring most commonly, however, 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. Outbreaks frequently occur in overcrowded situations and in high-density institutions and centers, such as prisons and health care or day care centers. Viral spread by parenteral routes (eg, 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.
Serological diagnosis of acute viral hepatitis A depends on the detection of specific anti-HAV IgM. Its presence in the patient's serum indicates a recent exposure to HAV. HAV-specific IgM antibody level becomes detectable in the blood by 4 weeks after infection, persisting at elevated levels for about 2 months before declining to undetectable levels by 6 months. They rarely persist beyond 12 months after infection.
Interpretation
This assay detects the presence of hepatitis A virus (HAV)-specific IgM antibody in serum.
Negative results indicate either 1) inadequate or delayed anti-HAV IgM response after known exposure to HAV, or 2) absence of acute or recent hepatitis A.
Equivocal results may be seen in early acute hepatitis A associated with rising anti-HAV IgM levels or recent hepatitis A infection associated with declining anti-HAV IgM levels. Retesting for both anti-HAV IgM (HAIGM / Hepatitis A IgM Antibody, Serum) and anti-HAV IgG (HAIGG / Hepatitis A IgG Antibody, Serum) in 2 to 4 weeks is recommended to determine the definitive HAV infection status.
Positive results indicate acute or recent (<6 months) hepatitis A infection. As required by laws in almost all states, positive anti-HAV IgM test results must be urgently reported to state health departments for epidemiologic investigations of possible outbreak transmission.
Clinical Reference
1. Centers for Disease Control and Prevention: Prevention of hepatitis A through active or passive immunization: Recommendations of the Advisory Committee on Immunization Practices (ACIP). MMWR Morb Mortal Wkly Rep. 2006;55(RR7):1-23
2. Nainan OV, Xia G, Vaughan G, Margolis HS: Diagnosis of hepatitis A infection: a molecular approach. Clin Microbiol. Rev 2006;19:63-79
3. de Paula VS: Laboratory diagnosis of hepatitis A. Future Virology. 2012;7(5):461-472
Day(s) and Time(s) Performed
Monday through Saturday; Varies
Analytic Time
1 dayTest Classification
This test has been cleared, approved or is exempt by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86709
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
HAIGM | Hepatitis A IgM Ab, S | 13950-1 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
HAIGM | Hepatitis A IgM Ab, S | 13950-1 |
Forms
If not ordering electronically, complete, print, and send a Gastroenterology and Hepatology Client Test Request (T728) with the specimen.
mml-gi-liver-hepatitis