Test Code FHSAG MVista Histoplasma Ag Quantitative, Spinal Fluid
Reporting Name
MVista Histoplasma Ag, CSFPerforming Laboratory
MiraVista DiagnosticsSpecimen Type
CSFSpecimen Required
Specimen Type: Spinal Fluid
Sources: CSF
Container/Tube: Sterile container
Specimen Volume: 0.8 mL
Collection Instructions:Â Collect 0.8 mL of spinal fluid (CSF). Ship refrigerated, 0.8 mL of spinal fluid. Send specimen in a plastic, screw-capped vial refrigerated.
Specimen Minimum Volume
0.8 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
CSF | Refrigerated (preferred) | 14 days | |
Ambient | 14 days | ||
Frozen |
Reference Values
Reference interval:Â Â Â Â Â Â Â None Detected
Reportable Range: Positive Results reported in ng/mL from 0.20 ng/mL to 20.00 ng/mL.
Positive Results above 20.00 ng/mL are reported as “Above the Limit of Quantificationâ€.
Day(s) Performed
Monday through Friday
CPT Code Information
87385
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
FHSAG | MVista Histoplasma Ag, CSF | 51754-0 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
Z1722 | Result: | 51754-0 |
Z1034 | Interpretation | Not Provided |
Report Available
3 to 5 daysTest Classification
This test was developed and its performance characteristics determined by MiraVista Diagnostics. It has not been cleared or approved by the FDA; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.Method Name
Quantitative Sandwich Enzyme Immunoassay (EIA)