Allergen, Fungi and Molds, Phoma betae
Also known as: PHOMA
Use
The Allergen, Fungi and Molds, Phoma betae test measures specific IgE antibodies to this particular mold, helping to evaluate potential allergic responses in patients. The test results can aid in the diagnosis of allergic reactions and are intended for use by specialists, as they provide insights into the likelihood of IgE-mediated clinical reactions. Despite increasing IgE concentrations being indicative of heightened allergen sensitivity, they might not directly correlate with clinical symptoms or reactions during allergen exposure or skin testing. Thus, correlating laboratory results with clinical history is crucial.
Special Instructions
Not provided.
Limitations
While increasing concentrations of allergen-specific IgE may suggest greater sensitivity, these levels do not necessarily correlate with the severity of a clinical reaction or skin test outcomes. Hence, a negative result does not rule out the possibility of a clinical allergy or anaphylaxis. For IgE levels of 0.10-0.34 kU/L, the clinical relevance remains undetermined, necessitating specialist interpretation.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Multiplex Protein Panel)
Biomarkers
Phoma betae
Protein
LOINC Codes
- 6216-6 - P betae IgE Qn
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.25 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Collect serum in a serum separator tube and separate from cells as soon as possible or within 2 hours.
Patient Preparation
Avoid multiple patient encounters.
Storage Instructions
Refrigerate during transport.
Causes for Rejection
Hemolyzed, icteric, or lipemic specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
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