Test Code LAB551 Acute Hepatitis Panel
Additional Codes
AHP
Includes:
Hepatitis A Antibody IgM, Hepatitis B Core Antibody IgM, Hepatitis B Surface Antigen Screen and Hepatitis C Virus Antibody Screen
Collection:
Specimen: Blood
Container: Serum Separator or Plain Red Tube
Volume: 7 mL; Minimum 3 mL
Pediatric Collection:
Three Gold or Red microtainers filled to 600 uL.
Stability:
Once serum is separated from cells:
Ambient: 8 Hours
Refrigerated (preferred): 1 Week
Frozen: 2 Weeks
Turn Around Time (TAT):
STAT: 2 HOURS
Routine: 3 HOURS
Test Availability:
24 hours a day / 7 Days a week
Performing Laboratory Section:
Chemistry / UMC MAIN LABORATORY
Reference Interval:
Hepatitis A Antibody IgM: Non-reactive
Hepatitis B Core Antibody IgM: Non-reactive
Hepatitis B Surface Antigen Screen: Non-reactive
Hepatitis C Virus Antibody Screen: Non-reactive
Interpretive Data:
Hepatitis A Antibody, IgM | |
---|---|
Patients with positive test results are reported by the Laboratory to the local Health Dept. Interpretation information is based on the Abbott product literature. Results by other assay methods cannot be used interchangeably with the Abbott assay values. |
|
Result | Interpretation |
Nonreactive | IgM anti-HAV not detected. Does not exclude the possibility of exposure to or infection with HAV. Levels of IgM anti-HAV may be below the cut-off in early infection. |
Grayzone | IgM antibodies to HAV may or may not be present. Patients exhibiting grayzone test results should be closely monitored by redrawing and retesting at approximately one week intervals.† |
Reactive | IgM anti-HAV detected. Presumptive evidence of HAV infection. A reactive IgM anti-HAV result does not rule out other hepatitis infections. |
† Monitoring the level of IgM anti-HAV by redrawing and retesting at approximately one week intervals will distinguish rapidly rising IgM anti-HAV levels associated with early acute hepatitis A infection from gradually decreasing or unchanging IgM anti-HAV levels often associated with late acute stage of HAV infection.
Hepatitis B Core Antibody, IgM | |
---|---|
Patients with positive test results are reported by the Laboratory to the local Health Dept. Interpretation information is based on the Abbott product literature. Results by other assay methods cannot be used interchangeably with the Abbott assay values. |
|
Result | Interpretation |
Nonreactive | IgM anti-HBc antibodies not detected. Does not exclude the possibility of expsoure to infection with HBV. |
Grayzone | Antibodies to IgM Anti-HBc may or may not be present. Patients with specimens exhibiting grayzone test results should be retested at approximately one-week intervals.* |
Reactive | Presumptive evidence of IgM anti-HBc. |
*Monitoring the level of IgM anti-HBc by retesting at approximately one week intervals will distinguish rapidly rising IgM anti-HBc levels associated with early acute hepatitis B infection from gradually decreasing or unchanging IgM anti-HBc levels often associated with late acute stage of HBV infection, six to nine months from the appearance of HBsAg.
Hepatitis B Surface Antigen Screen | |
---|---|
Interpretation information is based on the Abbott product literature. Results by other assay methods cannot be used interchangeably with the Abbott assay values. |
|
Result | Interpretation |
Nonreactive | Specimen considered negative for HBsAg. |
Reactive | Specimen considered repeatedly reactive; will be confirmed using the ALINITY HBsAg Qualitative Confirmatory assay. |
Hepatitis C Virus Antibody Screen | |
---|---|
Interpretation information is based on the Abbott product literature. Results by other assay methods cannot be used interchangeably with the Abbott assay values. |
|
Result | Interpretation |
Nonreactive | Antibodies to HCV not detected; does not exclude the possibility of exposure to HCV. |
Equivocal | Antibodies to HCV may or may not be present; a reflexive HCV RNA test will be performed on the specimen to determine infection status (current or resolved). |
Reactive | Presumptive evidence of antibodies to HCV; a reflexive HCV RNA test will be performed on the specimen to determine infection status (current or resolved). |