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HelpTest Code FMVCO MVista Coccidioides Quantitative Antigen EIA
Reporting Name
MVista Coccidioides Ag, UPerforming Laboratory
MiraVista DiagnosticsSpecimen Type
UrineSpecimen Required
Specimen Type: Urine
Container/Tube: Plastic preservative-free urine container
Specimen Volume: 2 mL
Collection Instructions: Collect 2 mL random urine specimen. Ship specimen refrigerated in a plastic, preservative-free urine container.
Note: Sputolysin and Sodium Hydroxide are interfering substances.
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Urine | Refrigerated (preferred) | 14 days | |
| Ambient | 48 hours | ||
| Frozen | |||
Reference Values
Reference interval: None Detected
Results reported as ng/mL in 0.07 - 8.2 ng/mL range
Results above 8.2 ng/mL are reported as 'Positive, Above the Limit of Quantification’
Day(s) Performed
Monday through Friday
CPT Code Information
87449
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| FMVCO | MVista Coccidioides Ag, U | Not Provided |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| Z2258 | MVista Coccidioides Ag, U | 93227-7 |
| Z2561 | Interpretation | Not Provided |
Report Available
3 to 5 daysReject Due To
| Thawing: | Warm OK; Cold OK |
| Other: | Specimen that is too viscous to pipette. Tissue, biopsy, sputum, bronchial brush, tracheal 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
Quantitative Sandwich Enzyme Immunoassay (EIA)