Allergen, Grass, Bahia
Also known as: BAHIA
Use
The Allergen, Grass, Bahia test is designed to measure the concentration of specific Immunoglobulin E (IgE) antibodies to Bahia grass pollen in the serum. It helps in the diagnosis and management of allergic diseases such as allergic rhinitis and asthma associated with grass pollen. Detection of Bahia grass-specific IgE can assist in identifying potential allergen triggers, guide management strategies, and evaluate response to therapy.
Special Instructions
Not provided.
Limitations
The test is limited by its inability to correlate quantified levels of allergen-specific IgE with the severity of clinical allergies or predict reactions to skin testing accurately. A negative result does not entirely rule out an allergy to Bahia grass. Results in the range of 0.10-0.34 kU/L are inconclusive and meant for use by specialists, as their clinical relevance remains undefined. It is crucial to integrate test results with clinical history and in-vivo reactivity to obtain an accurate diagnosis.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay)
Biomarkers
Bahia Grass IgE
Analyte
LOINC Codes
- 6034-3 - Bahia 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
Minimum Volume
0.25 mL
Container
Serum separator tube
Collection Instructions
Separate serum 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
Causes for Rejection
Hemolyzed, icteric, or lipemic specimens.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 48 hours |
| Refrigerated | 2 weeks |
| Frozen | 1 year |
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