Histoplasma and Blastomyces Antigen, Serum (Sendout)
General Information
- Lab Name
- Histoplasma and Blastomyces Antigen, Serum (Sendout)
- Lab Code
- RHIBAG
- Epic Ordering
- Histoplasma and Blastomyces Antigen, Serum (Sendout)
- External Test Id
- HIBAG
- Description
Useful For:
- Diagnosing Histoplasma capsulatum or Blastomyces dermatitidis infection without differentiation between the organisms
- Monitoring antigen levels following initiation of antifungal treatment
Test Highlights:
- This test detects Histoplasma and Blastomyces antigen in serum, without differentiation between the 2 fungal pathogens.
- It aids in the diagnosis of histoplasmosis or blastomycosis alongside other routine methods, including culture, molecular testing, and serology.
- This test can be used to monitor response to antifungal therapy.
- References
- Mayo Clinical & Interpretive Information: Histoplasma and Blastomyces Antigen, Enzyme Immunoassay, Serum
- Synonyms
- Blastomyces dermatitidis antigen, HIBAG, Histoplasma Antigen, Histoplasma capsulatum Antigen, Histoplasma Polysaccharide Antigen, RHISTO
- Components
-
Code Name RHIBAR Histoplasma and Blastomyces Antigen Result RHIBAV Histoplasma and Blastomyces Antigen Value
Interpretation
- Method
Enzyme Immunoassay (EIA)
- Reference Range
- See individual components
- Ref. Range Notes
Reference Values:
Histoplasma/Blastomyces Antigen Result: Not Detected Histoplasma/Blastomyces Antigen Value: Not Detected Interpretation:
Not detected: No antigen from Histoplasma or Blastomyces detected. False-negative results may occur depending on extent of disease or site of infection. Repeat testing on a new specimen if clinically indicated.
Detected, <1.5 ng/mL: Antigen from Histoplasma or Blastomyces (unable to differentiate) was detected, below the limit of quantification (<1.5 ng/mL). Result should be correlated with clinical presentation, exposure history, and other diagnostic procedures, such as culture, serology, histopathology, and radiographic findings to aid in the differentiation between histoplasmosis or blastomycosis.
Detected, 1.5-25.0 ng/mL: Antigen from Histoplasma or Blastomyces (unable to differentiate) detected. Result should be correlated with clinical presentation, exposure history, and other diagnostic procedures, such as culture, serology, histopathology, and radiographic findings, to aid in the differentiation between histoplasmosis and blastomycosis.
Detected, >25.0 ng/mL: Antigen from Histoplasma or Blastomyces (unable to differentiate) detected, above the limit of quantification (>25.0 ng/mL). Result should be correlated with clinical presentation, exposure history, and other diagnostic procedures, such as culture, serology, histopathology, and radiographic findings, to aid in the differentiation between histoplasmosis or blastomycosis.
- Interferences and Limitations
Cautions:
Due to significant cross-reactivity between galactomannan antigens from Blastomyces and Histoplasma, this assay does not differentiate between these 2 dimorphic fungal agents. To differentiate, consider fungal culture, molecular testing, or serology testing.
Positive results should be correlated with other clinical and laboratory findings (e.g., culture, serology).
Low-level positive antigen levels may persist following resolution of infection and completion of appropriate treatment regimen.
Sensitivity of this assay to detect antigen from species other than Blastomyces dermatitidis or Histoplasma capsulatum is unknown.
False positive results may occur less frequently with other dimorphic agents (e.g., Coccidioides).
- Guidelines
Ordering & Collection
- Specimen Type
- Blood
- Collection
-
5 mL in GOLD SST or RED TOP tube
- Handling Instructions
Outside Laboratories: Centrifuge sample and transfer serum to a separate plastic vial. Refrigerate serum while awaiting shipment. Transport with a cold pack.
Stability: Refrigerated (preferred): 28 days; Frozen: 28 days; Ambient: 72 hours.
Reject Due To: Gross hemolysis, gross lipemia, gross icterus, or heat-inactivated specimen.
- Quantity
-
requested: 1.5 mL serum
minimum: 1.2 mL serum
Processing
- Processing
Centrifuge sample and transfer serum to a separate plastic vial. Refrigerate serum.
Sendouts:
- Order Mayo Test: HIBAG
- Interfaced: Yes [Interface: 601; Worksheet: MARF]
Stability: Refrigerated (preferred): 28 days; Frozen: 28 days; Ambient: 72 hours.
Reject Due To: Gross hemolysis, gross lipemia, gross icterus, or heat-inactivated specimen.
Performance
- LIS Dept Code
- Sendouts Mayo Lab (RF) (MARF)
- Performing Location(s)
-
Sendout Mayo Clinic Laboratories (Superior Drive)
800-533-17103050 Superior Drive NW
Rochester, MN 55901 - Frequency
- Performed: Monday through Saturday. Reported: 1-3 days from sample receipt at Mayo Clinic Labs.
- Available STAT?
- No
Billing & Coding
- CPT codes
- 87449
- LOINC
- 19145-2