Overview
EPIC Code:
- LAB400
Soft Test Code:
Send Out Test Code:
- 310
Alternate Names
- Histoplasma Quantitative EIA Test
Clinical Significance
The MVista® histoplasma quantitative antigen test aids the diagnosis of histoplasmosis. Monitoring the histoplasmosis helps determine when treatment can be stopped and to diagnose relapse.
The result is not intended to be used as the sole means for the clinical diagnosis or patient management decisions.
- Cross-reactions are seen with blastomycosis, paracoccidioidomycosis, penicilliosis, less frequently in coccidioidomycosis, rarely in aspergillosis and possibly sporotrichosis.
- Sputolysin, sodium hydroxide and potassium hydroxide treatment degrade the analyte detected in the assay.
Limitations
The result is not intended to be used as the sole means for the clinical diagnosis or patient management decisions.
- Cross-reactions are seen with blastomycosis, paracoccidioidomycosis, penicilliosis, less frequently in coccidioidomycosis, rarely in aspergillosis and possibly sporotrichosis.
- Sputolysin, sodium hydroxide and potassium hydroxide treatment degrade the analyte detected in the assay.
Specimen Collection & Preparation
Specimen Requirements:
-OR-
2.0 mL Urine in a Sterile Plastic Container
Minimum Volume:
0.5 mL Urine** This volume does not allow for repeat testing
Specimen Information:
Processing Instructions:
Identify specimen as urine on container
Rejection Criteria:
If specimen is too viscous to pipette
Stored in Transport Media, Fixative or Isolator Tubes
Tissue, Sputum, Bronchial Brushings, Stool, FNA, Biopsy, Tracheal or Bone Marrow Aspirate
Transport and Storage:
-
Ambient (18-24°C):
2 Weeks
-
Refrigerated (2-8°C):
2 Weeks
-
Frozen (-20° C or colder):
Indefinitely
Clinical Interpretation
Reference Range:
None Detected
Test Comments:
Positive: 0.20-20.00 ng/mL
Positive Above the Limit of Quantification: Results greater than 20.00 ng/mL fall outside the linear range of the assay. These results are positive, but not accurately quantifiable.
Methodology:
- Quantitative Sandwich Enzyme Immunoassay (EIA)
- Serum and CSF are pre-treated to improve sensativity
Clinical Significance
The MVista® histoplasma quantitative antigen test aids the diagnosis of histoplasmosis. Monitoring the histoplasmosis helps determine when treatment can be stopped and to diagnose relapse.
The result is not intended to be used as the sole means for the clinical diagnosis or patient management decisions.
- Cross-reactions are seen with blastomycosis, paracoccidioidomycosis, penicilliosis, less frequently in coccidioidomycosis, rarely in aspergillosis and possibly sporotrichosis.
- Sputolysin, sodium hydroxide and potassium hydroxide treatment degrade the analyte detected in the assay.
Limitations
The result is not intended to be used as the sole means for the clinical diagnosis or patient management decisions.
- Cross-reactions are seen with blastomycosis, paracoccidioidomycosis, penicilliosis, less frequently in coccidioidomycosis, rarely in aspergillosis and possibly sporotrichosis.
- Sputolysin, sodium hydroxide and potassium hydroxide treatment degrade the analyte detected in the assay.
Documentation
*New positives may require confirmation
Production Schedule
Sites Performed
- MiraVista
Days Performed
Monday
Tuesday
Wednesday
Thursday
Friday
Departments
- Sendouts - Clinical
Turn Around Time
1 to 3 days
Coding & Compliance
CDM
00917110
CPT Coding
87385