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Test ID FHSAG MVista Histoplasma Ag Quantitative, Spinal Fluid

Method Name

Enzyme Immunoassay (EIA)

Reporting Name

MVista Histoplasma Ag, CSF

Specimen Type


Specimen Required

Specimen Type: Spinal Fluid

Sources: CSF

Container/Tube: Sterile container

Specimen Volume: 2 mL

Collection Instructions:  Collect 2 mL of spinal fluid (CSF). Ship refrigerated. 2 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

Reference Values

Reference interval:        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 Quantification”.

Day(s) Performed

Monday through Saturday



Performing Laboratory

MiraVista Diagnostics

CPT Code Information


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

Test 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 intended to be used as the sole means for clinical diagnosis or patient management decisions.

Report Available

1 to 8 days

NY State Approved