Allergen Profile With Component Reflexes, Respiratory–Area 8
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 quantitative allergen-specific IgE test is beneficial when testing individuals for agents that may cause anaphylaxis, or when skin testing results do not provide satisfactory symptom remission.
Limitations
The test results should be interpreted in the context of the patient's clinical history, especially when elevated allergen-specific IgE antibodies are detected, as cross-reactivity between allergens may occur. The reflex testing for specific components of dog and cat allergens is only triggered when certain IgE threshold levels are met.
Methodology
Immunoassay (Multiplex Protein Panel)
Biomarkers
LOINC Codes
- 8251-1
- 19113-0
- 6096-2
- 6095-4
- 6833-8
- 6098-8
- 6181-2
- 6041-8
- 6265-3
- 6078-0
- 6212-5
- 6075-6
- 6025-1
- 6020-2
- 7155-5
- 6178-8
- 6189-5
- 6109-3
- 15285-0
- 6090-5
- 6278-6
- 33982-0
- 6209-1
- 6281-0
- 6085-5
- 6234-9
- 7604-2
- 6232-3
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
