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Test Code BLSAGSO Blastomyces Quantitative Antigen, Serum (316)

Additional Codes

Miravista Diagnostics Test Code: 316

Useful For

Aid in diagnosis of blastomycosis


Monitor the response to therapy and to determine when treatment can be modified or stopped.

Monitor Blastomyces antigen levels to help determine relapse of disease.

Synonyms/Keywords

Blastomyces Dermatitidis QNT AG

Specimen Requirements

Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Minimum Volume
(allows for 1 repeat)
Serum

Red Top Tube (RTT)  

Serum Separator Tube (SST) 0.8 mL
Plasma EDTA Lavender Top Tube (LTT)

Sodium-heparin OR Lithium-heparin Green Top Tube (GTT)

OR

Sodium citrate tube (BTT)

0.8 mL

Collection/Processing Instructions

Serum:

  • Collect serum or plasma in serum separator (SST) or red top tube (RTT).   
  • Allow blood serum samples to clot for 30 minutes, then centrifuge.
  • Pipette serum into a plastic leak-proof container. 

 

Plasma:

  • Collect plasma specimens in an EDTA, Heparin or Sodium Citrate tube.
  • Centrifuge for 15 minutes and pipette plasma into a plastic screw cap vial.

 

Ship to arrive Monday through Friday using a next day delivery service. 

Samples may be shipped on dry ice, frozen ice packs, or ambient.

Specimen Stability Information

Specimen Type Temperature Time
Serum/Plasma Room temperature  14 days
Refrigerate (preferred)  14 days
Frozen 2 months

 

Rejection Criteria

  • Cold or room temperature > 14 days old.
  • Non-pipettable specimens, tissue, biopsy, sputum, bronchial brush, tracheal aspirate, FNA, bone marrow, aspirate or stool
  • Samples in transport media, fixative of Isolator tubes.

Test Information

The MVista® Blastomyces Antigen Quantitative EIA can detect and quantify the amount of Blastomyces antigen in patient samples.

During validation testing, the sensitivity was found to be 95.00% and specificity 100% with an assay cutoff of 0.31 ng/mL.

​Negative results do not exclude blastomycosis. Testing of both urine and serum offers the highest sensitivity. Failure of the antigen to rise does not exclude relapse.

​​Positive samples may require confirmation which could extend TAT.

Interpretations

None Detected: <0.31 ng/mL
Positive: 0.31 ng/mL 20.00 ng/mL
 

Positive Above the Limit of Quantifications
Results greater than 20.00 ng/mL fall outside the linear range of the assay. These results are positive, but not accurately quantifiable.


Results should be correlated with clinical presentation and history

Reference Range Information

Reference Interval:  None Detected

Reportable Range:  0.31 ng/mL 20.00 ng/mL


Results above 20.00 ng/mL are reported as 'Positive, Above the Limit of Quantification' 

When tested in cultures of 10⁵ – 10⁶ organisms/mL, cross-reactions occurred with Histoplasma spp., Coccidioides spp., Paracoccidioides brasiliensis, Talaromyces marneffei, Aspergillus nidulans, and Candida tropicalis.

Performing Laboratory Name

Miravista Diagnostics

Referral Laboratory Information

Address Telephone Website Link Marshfield Lab Account #

4444 Decatur Blvd, Suite 300

Indianapolis, IN 46241

866-647-2847 www.miravistalabs.com MARSH

Performing Information

Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
Miravista Diagnostics Monday through Friday 1 day

Quantitative sandwich enzyme immunoassay (EIA)

Serum is pre-treated to improve accuracy

CPT Codes

CPT Modifier
(if needed)
Quantity Description Comments
87449        

Outreach CPT Codes

CPT Modifier
(if needed)
Quantity Description Comments
87449        

Ordering Applications

Ordering Application Description
Cerner Blastomyces Quantitative Antigen, Serum (316)