Ordering Recommendation

Can be ordered as part of the acute hepatitis panel, which includes HAV IgM, HBV core antibody IgM, HBV surface antigen, and HCV antibody to determine if patient has acute HBV infection; refer to Hepatitis Panel, Acute with Reflex to HBsAg Confirmation and Reflex to HCV by Quantitative NAAT (3002989).

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation
Collect

Serum separator tube.

Specimen Preparation

Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min: 0.5 mL) Also acceptable: K2EDTA plasma.

Storage/Transport Temperature

Refrigerated.

Unacceptable Conditions

Heparinized plasma. Specimens containing particulate material. Heat-inactivated, severely hemolyzed, or lipemic specimens.

Remarks
Stability

After separation from cells: Ambient: Unacceptable; Refrigerated: 1 week; Frozen: Indefinitely (avoid repeated freeze/thaw cycles)

Methodology

Qualitative Chemiluminescent Immunoassay

Performed

Sun-Sat

Reported

Within 24 hours

Reference Interval

Negative

Interpretive Data

This assay should not be used for blood donor screening, associated re-entry protocols, or for screening Human Cell, Tissues and Cellular Tissue-Based Products (HCT/P).

Compliance Category

FDA

Note

Hotline History

N/A

CPT Codes

86705

Components

Component Test Code* Component Chart Name LOINC
0020092 Hepatitis B Core Antibody, IgM 24113-3
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Anti Core IgM Antibody
  • Anti-Hepatitis Bc
  • Core Antibody IgM
  • HBV Core IgM
  • Hep B Core Ab IgM
  • Hep Bc Ab IgM
  • IgM Antibody to Hepatitis Bc
Hepatitis B Virus Core Antibody, IgM