Alternaria tenuis, IgE, Serum
Use
This test is utilized to establish a diagnosis of allergy to Alternaria tenuis, define the allergen responsible for eliciting signs and symptoms, and identify allergens responsible for allergic response and/or anaphylactic episodes. It is also used to confirm sensitization prior to beginning immunotherapy and to investigate the specificity of allergic reactions to insect venom allergens, drugs, or chemical allergens. However, testing for IgE antibodies is not useful in patients previously treated with immunotherapy to determine if residual clinical sensitivity exists, or in patients whose medical management does not depend on identification of allergen specificity.
Special Instructions
Forms: If not ordering electronically, complete, print, and send an Allergen Test Request (T236) with the specimen.
Limitations
Some individuals with clinically insignificant sensitivity to allergens may have measurable levels of IgE antibodies in serum, and results must be interpreted in the clinical context. False-positive IgE antibodies may occur in patients with markedly elevated serum IgE (>2500 kU/L) due to nonspecific binding.
Methodology
Immunoassay (FEIA)
Biomarkers
LOINC Codes
- 6020-2
- 6020-2
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL for every 5 allergens requested
Minimum Volume
0.3 mL for 1 allergen
Container
Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |
