Blastomyces Antibody, Enzyme Immunoassay, Serum
Use
This test is useful for aiding in the diagnosis of blastomycosis, which is caused by Blastomyces dermatitidis and Blastomyces gilchristii. These are dimorphic fungi found in various regions of the United States and Canada. The test detects IgG and IgM antibodies to Blastomyces, offering high specificity. However, it may give false-negative results in acutely infected patients and those who are immunosuppressed.
Special Instructions
Not provided.
Limitations
The detection of antibodies to Blastomyces does not rule out the presence of other cross-reactive fungal infections. The test does not replace culture or molecular testing, which provide the gold standard for diagnosis but have longer turnaround times. Sensitivity may be affected in acute or localized disease.
FDA ApprovedNew York Approved
Methodology
Immunoassay (EIA)
Biomarkers
IgG and IgM antibodies to Blastomyces
Protein
LOINC Codes
- 7816-2 - B dermat Ab Ser Ql
- 7816-2 - B dermat Ab Ser Ql
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.8 mL
Container
Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Causes for Rejection
Gross hemolysis, gross lipemia, heat inactivated specimen
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 14 days |