Allergens, Upper Respiratory Disease Profile, Region 9A
Also known as: R9A URD
Use
The Allergens, Upper Respiratory Disease Profile, Region 9A test is used to assess allergic reactions related to specific allergens prevalent in Upper Respiratory diseases. It quantitatively measures the concentration of allergen-specific IgE to help determine the likelihood of an IgE-mediated allergic reaction. The results assist healthcare professionals in evaluating potential allergies and planning appropriate management or treatment strategies based on a patient's clinical history and exposure to specific allergens.
Special Instructions
Not provided.
Limitations
The presence of allergen-specific IgE does not always correlate with the severity of clinical symptoms. Allergen results in the range of 0.10-0.34 kU/L are intended for specialist use as the clinical relevance is undetermined. Clinical correlation with patient history and in vivo reactivity is essential for accurate diagnosis. A negative result does not rule out allergies or anaphylaxis, and hemolyzed, icteric or lipemic specimens are unacceptable.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Fluorescent Enzyme Immunoassay)
Biomarkers
LOINC Codes
- 6020-2 - A alternata IgE Qn
- 7155-5 - Boxelder IgE Qn
- 6833-8 - Cat Dander IgE Qn
- 6090-5 - Cottonwood IgE Qn
- 6153-1 - Kent blue grass IgE Qn
- 7604-2 - Cmn pigweed IgE Qn
- 6234-9 - Saltwort IgE Qn
- 6075-6 - C herbarum IgE Qn
- 48767-8 - Annotation comment Imp
- 6109-3 - White Elm IgE Qn
- 6189-5 - White Oak IgE Qn
- 6025-1 - A fumgtus IgE Qn
- 6095-4 - D farinae IgE Qn
- 6085-5 - Common Ragweed IgE Qn
- 6078-0 - Roach IgE Qn
- 6098-8 - Dog Dander IgE Qn
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1.65 mL
Minimum Volume
0.80 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Collect via serum separator tube, separate serum from cells ASAP or within 2 hours, and transfer to ARUP tube.
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 |
Other tests from different labs that may be relevant