Allergen Profile With Component Reflexes, Respiratory–Area 20
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 includes reflex components based on specific IgE levels. For example, if Dog IgE is ≥ 0.35 kU/L, further IgE tests for Can f 1 to Can f 6 will be performed. Similarly, if Cat IgE is ≥ 0.35 kU/L, additional IgE tests for Fel d components will be done.
Limitations
The quantitative allergen-specific IgE test may not capture all potential allergens an individual may react to. Results should be interpreted in conjunction with clinical history. This test may not replace skin testing in certain scenarios, and results could vary based on patient's medication, age, and specific medical condition.
Methodology
Immunoassay (Other)
Biomarkers
LOINC Codes
- 6098-8
- 6110-1
- 6113-5
- 6075-6
- 6173-9
- 6179-6
- 6182-0
- 6222-4
- 6212-5
- 7369-2
- 7604-2
- 6282-8
- 6286-9
- 6281-0
- 6181-2
- 8251-1
- 19113-0
- 6020-2
- 6025-1
- 6034-3
- 7124-1
- 6041-8
- 6833-8
- 6077-2
- 6078-0
- 6085-5
- 6096-2
- 6095-4
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
