Sweet Vernal Grass, IgE, Serum
Use
This test is useful for establishing a diagnosis of an allergy to sweet vernal grass and for defining the allergen responsible for eliciting signs and symptoms. It helps in identifying allergens responsible for allergic response and/or anaphylactic episodes, confirming sensitization prior to beginning immunotherapy, and investigating the specificity of allergic reactions to insect venom allergens, 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. Test results must be interpreted in the clinical context, especially since false-positive results might occur in patients with markedly elevated serum IgE (>2500 kU/L) due to nonspecific binding to allergen solid phases. IgE testing may not be useful if the medical management does not depend on the identification of allergen specificity.
FDA ApprovedNew York Approved
Methodology
Immunoassay (ELISA)
Biomarkers
Sweet Vernal Grass IgE
Protein
LOINC Codes
- 6261-2 - Sw Vernal grass IgE Qn
- 6261-2 - Sw Vernal grass 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
For 1 allergen: 0.3 mL; For more than 1 allergen: (0.05 mL x number of allergens) + 0.25 mL deadspace
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 and gross lipemia are acceptable.
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 90 days |