Pyrethrum IgE
Use
The Pyrethrum IgE test is intended for the quantitative measurement of IgE antibodies specific to pyrethrum in the serum. It helps in diagnosing allergic reactions to pyrethrum, a common allergen found in certain plants and insecticides. This test can assist clinicians in identifying patients who have developed sensitization to pyrethrum, aiding in the management and treatment of allergic conditions associated with exposure to this substance.
Special Instructions
This test was developed and its performance characteristics were determined by Eurofins Viracor. It is available for New York State clients. Specimens must be appropriately prepared and handled according to the instructions provided to ensure the validity of test results.
Limitations
This test has not been cleared or approved by the U.S. Food and Drug Administration. False positives or negatives may occur, and results should be interpreted in the context of other clinical findings. The test's performance may be affected by improper specimen handling, lipemia, or the presence of interfering substances in the sample.
New York Approved
Methodology
Immunoassay (EIA)
Biomarkers
LOINC Codes
- 7639-8
- 7639-8
- 102549-3
Result Turnaround Time
4-7 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.5 mL
Container
Red or SST
Collection Instructions
Draw blood in a plain red-top tube(s), serum gel tube is acceptable. Spin down and send 0.5 mL of serum refrigerated in a plastic vial.
Causes for Rejection
Lipemia: Reject
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 28 days |
| Refrigerated | 28 days |
| Frozen | 365 days |