Return

Hepatitis A Antibody, IgM

Code:17010|CPT:86709|LOINC:13950-1

Synonyms
Антитела класса IgM к вирусу гепатита А.Anti-HAV, IgMAntibodies to Hepatitis A Virus, IgMAntibody to Hepatitis A Virus, IgMHAVAb, IgMHepatitis A Antibody, IgMHepatitis A virus IgM antibodiesViral Hepatitis A Antibody
IncludesHep A Ab, IgM

Analysis details

Methodology

  • Immunochemiluminometric assay (ICMA)
  • Electrochemiluminescence immunoassay (ECLIA)

Expected Turnaround Time

1 day

Special Instructions

  • Inform the laboratory about high-dose biotin use (vitamin B7/B8, vitamin H, coenzyme R) and stop it for at least 72 hours before collection.
  • Do not smoke during the 30 minutes prior to specimen collection.

How to use

Hepatitis A Antibody, IgM (anti-HAV IgM; HAVAb, IgM) is used to aid in diagnosing acute or recent hepatitis A virus infection by qualitatively detecting HAV-specific IgM. It is appropriate for patients with clinical signs or laboratory findings suggestive of acute hepatitis or following suspected exposure, and it is not intended for routine population screening. Restricting testing to patients with compatible symptoms or exposure history helps minimize false-positive results. IgM anti-HAV typically becomes detectable 2–3 weeks after infection and persists for several months (2–6 months). In contrast, IgG anti-HAV develops later and indicates past infection or immunity.

Limitations

Hepatitis A is acquired primarily through the fecal–oral route via contaminated food or water or through close contact with an infected person. The resulting hepatic inflammation disrupts bilirubin and nitrogenous waste handling, commonly producing increased serum bilirubin and elevated liver enzyme activities. IgM antibodies to HAV generally become detectable about 2–3 weeks after infection and remain present for 2–6 months, while IgG anti-HAV appears later and usually persists for life. This assay is not cleared or approved for screening blood or plasma donors. Performance characteristics have not been established for immunocompromised or immunosuppressed patients, cord blood, patients younger than 2 years, or cadaveric specimens.

Unitqualitative
Reference interval
IndicationsJaundice when acute viral hepatitis is suspected, Dark (tea-colored) urine or pale, acholic stools, Loss of appetite (anorexia), Marked fatigue, Nausea and vomiting, Abdominal pain, Fever, Arthralgia (joint pain), Cholestatic hepatitis presentation with malaise and fever, Unexplained elevations in total and direct bilirubin, alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase, or gamma-glutamyltransferase (GGT), Post-exposure assessment after contact with a person who has hepatitis A, regardless of symptoms

Possible Causes of Abnormal Results

Increased levels

  • autoimmune disease
  • hiv infection

Specimen Requirements

SpecimenSerum
ContainerGold/Tiger Top (SST, Gel Separator)
Volume1 mL (min 0.4 mL)
Storage InstructionsRoom temperature, Refrigerated, Frozen

References

Nelson NP, Weng MK, Hofmeister MG, et al. Prevention of Hepatitis A Virus Infection in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2020. MMWR Recomm Rep. 2020 Jul 3;69(5):1-38. PubMed 32614811.

Workowski KA, Bolan GA, Centers for Disease Control and Prevention. Sexually Transmitted Diseases Treatment Guidelines, 2015. MMWR Recomm Rep. 2015 Jun 5;64(RR-03):1-137. PubMed 26042815.

Chernecky & Berger: Laboratory Tests and Diagnostic Procedures, 5th ed.

Ferri: Ferri's Clinical Advisor 2009, 1st ed.

Fischbach, Frances Talaska: Manual of Laboratory & Diagnostic Tests, 7th Edition.

Keogh: Nursing laboratory and diagnostic tests (2011).

Moisio: Understanding Laboratory and Diagnostic Tests (1998).