Allergen Profile With Total IgE, Respiratory–Area 19
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
Test includes analysis for a range of environmental allergens specific to Area 19, namely Puerto Rico, including allergens like Alternaria alternata, Aspergillus fumigatus, and various grass and tree pollens. The test uses Thermo Fisher's ImmunoCAP technology for IgE quantification.
Limitations
The test is limited to the detection of IgE antibodies specific to the allergens included in the Area 19 profile. It may not detect all possible allergens or anaphylactic triggers. Cross-reactivity among allergens and variations in individual immune response can affect results. The presence of total IgE does not confirm that IgE antibodies are responsible for specific allergic symptoms.
Methodology
Immunoassay (Thermo Fisher ImmunoCAP®)
Biomarkers
LOINC Codes
- 6020-2
- 6029-3
- 6189-5
- 6109-3
- 6113-5
- 6282-8
- 7604-2
- 6244-8
- 6200-0
- 6181-2
- 8251-1
- 19113-0
- 6096-2
- 6095-4
- 10921-5
- 6833-8
- 6098-8
- 6041-8
- 6228-1
- 6152-3
- 6078-0
- 6212-5
- 6075-6
- 6025-1
Result Turnaround Time
3-5 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
3.5 mL
Minimum Volume
Not provided
Container
Red-top tube or gel-barrier tube
Storage Instructions
Room temperature
Causes for Rejection
Inadequate labeling; gross hemolysis
