Allergen, Region 17 Respiratory Panel IgE, Pacific Northwest (NW CA, W. OR, WA)
Also known as: REG17PANEL
Use
The Allergen, Region 17 Respiratory Panel IgE test is designed to evaluate patients for allergic responses specific to common allergens found in the Pacific Northwest, including northwest California, western Oregon, and Washington. This panel helps in identifying specific allergen sensitizations, aiding clinicians in diagnosing and managing allergic conditions such as allergic rhinitis, asthma, and other IgE-mediated allergic disorders. The test results provide quantitative measurements of allergen-specific IgE levels that assist in forming a comprehensive allergy treatment plan.
Special Instructions
Please ensure proper specimen collection and handling to maintain the integrity of the sample. Multiple patient encounters and specimen tubes should be avoided to reduce the risk of sample contamination or insufficient volume for analysis.
Limitations
Allergen-specific IgE levels may not directly correlate with the severity of allergic reactions experienced by patients. Results should be interpreted alongside clinical history and physical examination to assess in vivo reactivity to specific allergens. A negative result does not definitively rule out the possibility of an allergy or anaphylaxis. Testing is limited by cross-reactivity in some allergens, and low-level results (0.10-0.34 kU/L) should be considered indeterminate and interpreted with caution by specialists.
Methodology
Immunoassay (Other)
Biomarkers
Expression
LOINC Codes
- 19113-0
- 6020-2
- 7155-5
- 6833-8
- 6178-8
- 6090-5
- 7604-2
- 6265-3
- 6075-6
- 6109-3
- 6189-5
- 15283-5
- 6025-1
- 6096-2
- 6095-4
- 6278-6
- 6212-5
- 6085-5
- 6078-0
- 33982-0
- 6179-6
- 6182-0
- 15284-3
- 6098-8
- 6186-1
- 6244-8
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
4 mL
Minimum Volume
1.3 mL
Container
Serum Separator Tube (SST)
Collection Instructions
Separate from cells ASAP or within 2 hours of collection. Transfer serum to an ARUP Standard Transport Tube.
Patient Preparation
Multiple patient encounters should be avoided.
Storage Instructions
Refrigerated transport is required.
Causes for Rejection
Hemolyzed, icteric, or lipemic specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
