Isocyanate TDI, IgE, Serum
Use
This test is useful for establishing a diagnosis of an allergy to isocyanate TDI and for defining the allergen responsible for eliciting signs and symptoms. It helps identify allergens responsible for allergic responses and/or anaphylactic episodes, confirm sensitization prior to immunotherapy, and investigate the specificity of allergic reactions to insect venom, drugs, or chemical allergens.
Special Instructions
Not provided.
Limitations
Testing for IgE antibodies is not useful in patients previously treated with immunotherapy to determine if residual clinical sensitivity exists or in patients where the medical management does not depend on identification of allergen specificity. False-positive results for IgE antibodies may occur in patients with markedly elevated serum IgE (>2500 kU/L) due to nonspecific binding to allergen solid phases.
FDA ApprovedNew York Approved
Methodology
Immunoassay (FEIA)
Biomarkers
IgE
Protein
LOINC Codes
- 7431-0 - Isocyanate TDI IgE Qn
- 7431-0 - Isocyanate TDI 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 for 1 allergen
Container
Plastic vial
Collection Instructions
Centrifuge and aliquot serum into a plastic vial.
Storage Instructions
Refrigerated (preferred) 14 days, Frozen 90 days.
Causes for Rejection
Gross hemolysis: OK, Gross lipemia: OK
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |