Allergen Profile With Component Reflexes, Respiratory–Area 13
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 multiple allergens common to a specific geographic area (Southern California). Reflex component testing will be triggered by specific IgE levels for dog or cat IgE, allowing for enhanced specificity in allergen assessment.
Limitations
This test may not capture all potential allergens specific to individual sensitivities outside of the common allergens tested. False negatives or positives may occur due to cross-reactivity among allergenic components or interference from medications. IgE levels should be interpreted in the context of clinical history since the presence of IgE does not always correlate with clinical allergies.
Methodology
Immunoassay
Biomarkers
LOINC Codes
- 8251-1
- 19113-0
- 6096-2
- 6095-4
- 6833-8
- 6098-8
- 6041-8
- 6265-3
- 6152-3
- 6078-0
- 6212-5
- 6075-6
- 6025-1
- 6020-2
- 15284-3
- 6178-8
- 6189-5
- 6109-3
- 6192-9
- 33982-0
- 6090-5
- 6281-0
- 6085-5
- 6183-8
- 6234-9
- 7604-2
- 6181-2
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
