Allergens, Inhalant Multiallergen IgE, Qualitative
Also known as: INHALALL
Use
The Allergens, Inhalant Multiallergen IgE, Qualitative test is used to determine the presence of IgE antibodies to various inhalant allergens, which can indicate allergic sensitization. This qualitative test produces a positive or negative result that helps in the diagnosis of inhalant allergies, potentially caused by allergens such as dust mites, pet dander, grass pollen, or mold spores. It aids healthcare providers in identifying allergen triggers for allergic diseases like asthma and allergic rhinitis, facilitating better clinical management and patient care.
Special Instructions
Not provided.
Limitations
This test provides a qualitative result only, indicating the presence or absence of specific IgE antibodies. It does not measure specific IgE concentrations to individual allergens such as Dermatophagoides farinae, Cat epithelium and dander, Dog dander, Bermuda grass, Kentucky bluegrass, Alternaria alternata, Oak tree, Elm tree, Common ragweed, and Russian thistle. Results may be affected by hemolyzed, icteric, or lipemic specimens.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Fluorescent Enzyme Immunoassay)
Biomarkers
LOINC Codes
- 37989-1 - Inhalant Allerg Mix 8 IgE Ql
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.25 mL serum plus 0.1 mL for each additional allergen ordered
Minimum Volume
0.25 mL plus 0.04 mL for each allergen ordered
Container
ARUP Standard Transport Tube
Collection Instructions
Separate serum from cells ASAP or within 2 hours of collection.
Patient Preparation
Multiple patient encounters should be avoided.
Storage Instructions
Refrigerated.
Causes for Rejection
Hemolyzed, icteric, or lipemic specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
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