Allergen Profile, Mini Profile
Also known as: Mini Allergen Profile
Use
Detect possible allergic responses to various substances in the environment (see Test Includes), and evaluate for hay fever, asthma, atopic eczema, and respiratory allergy. The quantitative allergen-specific IgE test is indicated (1) to determine whether an individual has elevated allergen-specific IgE antibodies; (2) if specific allergic sensitivity is needed to allow immunotherapy to be initiated; (3) when testing individuals for agents that may potentially cause anaphylaxis; (4) when evaluating individuals who are taking medication (eg, long-acting antihistamines) that may interfere with other testing modalities (eg, skin testing); (5) if immunotherapy or other therapeutic measures based on skin testing results have not led to a satisfactory remission of symptoms; (6) when an individual is unresponsive to medical management where identification of offending allergens may be beneficial.
Special Instructions
The test utilizes Thermo Fisher ImmunoCAP® methodology for accurate allergen-specific IgE detection. Ensure proper labeling to avoid rejection.
Limitations
This test may not detect all possible allergens. Results should be interpreted in conjunction with a detailed clinical history and other diagnostic tests. False negatives could occur if the allergen was not included in the test panel.
Methodology
Immunoassay (Multiplex Protein Panel)
Biomarkers
LOINC Codes
- 8251-1
- 6096-2
- 6095-4
- 6833-8
- 6098-8
- 6041-8
- 6153-1
- 6020-2
- 6189-5
- 6109-3
- 6085-5
- 6110-1
- 6181-2
Result Turnaround Time
3-5 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
2 mL
Minimum Volume
Not provided
Container
Red-top tube or gel-barrier tube
Storage Instructions
Room temperature
Causes for Rejection
Improper labeling; gross hemolysis
