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Test Code HISAGM MVista Histoplasma Ag Quantitative, Serum

Additional Codes

 

MAYO Test ID

FHIST

EPIC Test ID

LAB909

 

Reporting Name

MVista Histoplasma Ag, S

Performing Laboratory

MiraVista Diagnostics

Specimen Type

Serum


Specimen Required


Specimen Type: Serum

Container/Tube: Red or SST

Specimen Volume: 2 mL

Collection Instructions: Draw blood in a plain red-top tube(s). (Serum gel tube is acceptable.) Spin down and send 2 mL serum refrigerate in a plastic vial


Specimen Minimum Volume

1.2 mL

Specimen Stability Information

Specimen Type Temperature Time
Serum Refrigerated (preferred) 14 days
  Ambient  14 days
  Frozen 

Reference Values

Reference interval:         None Detected

 

Results reported as ng/mL in 0.4 – 19.0 ng/mL range

 

Results above the limit of detection, but below 0.4 ng/mL are reported as 'Positive, Below the Limit of Quantitation'.

 

Results above 19.0 ng/mL are reported as 'Positive, Above the Limit of Quantitation'.

 

Day(s) and Time(s) Performed

Monday through Friday

CPT Code Information

87385

LOINC Code Information

Test ID Test Order Name Order LOINC Value
FHIST MVista Histoplasma Ag, S In Process

 

Result ID Test Result Name Result LOINC Value
Z1711 Result: 51753-2
Z1035 Interpretation In Process

Analytic Time

1 day

Reject Due To

Hemolysis

NA

Thawing

Warm OK; Cold OK

Lipemia

NA

Icterus

NA

Other

Specimen that is too viscous to pipette.

Tissue, biopsy, sputum, bronchial aspirate, FNA, bone marrow aspirate, stool or samples in transport media, fixative or Isolator tubes.

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 not intended to be used as the sole means for clinical diagnosis or patient management decisions.

Method Name

Enzyme Immunoassay (EIA)