Histoplasma and Blastomyces Antigen, Urine (Sendout)

General Information

Lab Name

Histoplasma and Blastomyces Antigen, Urine (Sendout)

Lab Code

RUHIBG

Epic Name

Histoplasma and Blastomyces Antigen, Urine (Sendout)

External Test Id

UHBAG

Description

Useful For:

  • Diagnosing Histoplasma capsulatum or Blastomyces dermatitidis infection without differentiation between the organisms

  • Monitor antigen levels following initiation of antifungal treatment

Test Highlights:

  • This test detects Histoplasma and Blastomyces antigen in urine, without differentiation between the 2 fungal pathogens.

  • This test 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

Synonyms

Blastomyces dermatitidis, Histoplasma Antigen, Histoplasma capsulatum, Histoplasma galactomannan Antigen, Histoplasma Polysaccharides, Histoplasma/Blastomyces antigen EIA, RHSTOU, UHBAG

Components

Code Name
RUHBAR Histoplasma and Blastomyces Antigen Result, Urine
RUHBAV Histoplasma and Blastomyces Antigen Value, Urine

Interpretation

Method

Enzyme Immunoassay (EIA)

Reference Range

See individual components

Ref. Range Notes

Reference Values:

Histoplasma/Blastomyces Antigen Result, Urine: Not Detected
Histoplasma/Blastomyces Antigen Value, Urine: 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, <1.3 ng/mL: Antigen from Histoplasma or Blastomyces (unable to differentiate) was detected, below the limit of quantification (<1.3 ng/mL). Result should be correlated with clinical presentation, exposure history, and other diagnostic procedures, including culture, serology, histopathology, and radiographic findings to aid in the differentiation between histoplasmosis or blastomycosis.

Detected, 1.3-20.0 ng/mL: Antigen from Histoplasma or Blastomyces (unable to differentiate) detected. Result should be correlated with clinical presentation, exposure history, and other diagnostic procedures, including culture, serology, histopathology, and radiographic findings, to aid in the differentiation between histoplasmosis and blastomycosis.

Detected, >20.0 ng/mL: Antigen from Histoplasma or Blastomyces (unable to differentiate) detected, above the limit of quantification (>20.0 ng/mL). Result should be correlated with clinical presentation, exposure history, and other diagnostic procedures, including 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

Urine

Collection

Collect random urine in a preservative-free urine collection container.

Handling Instructions

Outside Laboratories:

  • Transfer 3 mL urine (2.5 mL min) to a separate screw-cap vial. Do not centrifuge to remove particulates.
  • Refrigerate sample while awaiting shipment. Transport with a cold pack.

Stability: Refrigerated (preferred): 14 days; Frozen: 28 days; Ambient: 7 days.

Quantity

requested: 3 mL urine
minimum: 2.5 mL urine

Processing

Transfer 3 mL urine (2.5 mL min) to a separate screw-cap vial. Do not centrifuge to remove particulates. Refrigerate urine.

Sendouts:

  • Order Mayo Test: UHBAG
  • Interfaced: Yes [Interface: 601; Worksheet: MARF]

Stability: Refrigerated (preferred): 14 days; Frozen: 28 days; Ambient: 7 days.

Performance

LIS Dept Code

Sendouts Mayo Lab (RF) (MARF)

Performing Location(s)

Sendout Mayo Clinic Laboratories (Superior Drive)
800-533-1710

3050 Superior Drive NW
Rochester, MN 55901

Frequency

Performed: Monday through Sunday. Reported: 1-3 days from sample receipt at Mayo Clinic Laboratories.

Available STAT?

No

Billing & Coding

CPT codes

87449

LOINC

18725-2

Interfaced Order Code

UOW5363