Lime, IgE, Serum
Use
Establishing the diagnosis of an allergy to lime, defining the allergen responsible for eliciting signs and symptoms, and confirming sensitization prior to beginning immunotherapy. This test is also beneficial in investigating specific allergic reactions to insect venom allergens, drugs, or chemical allergens. However, it is not useful in patients previously treated with immunotherapy to determine if residual clinical sensitivity exists, or in patients where medical management does not depend on allergen specificity.
Special Instructions
Not provided.
Limitations
IgE antibodies tests may show measurable levels in individuals with clinically insignificant sensitivity to allergens. High levels of serum IgE (>2500 kU/L) can result in false-positive results due to nonspecific binding. Test results must be interpreted in the clinical context to avoid diagnostic confusion.
New York Approved
Methodology
Immunoassay (Fluorescence Enzyme Immunoassay (FEIA))
Biomarkers
Lime IgE
Analyte
LOINC Codes
- 7464-1 - Lime IgE Qn
- 7464-1 - Lime IgE Qn
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL for every 5 allergens requested
Minimum Volume
0.3 mL
Container
Preferred: Serum gel; Acceptable: Red top; Submission: Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Causes for Rejection
Gross hemolysis: OK; Gross lipemia: OK
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |