Allergen, Fungi and Molds, Candida albicans
Also known as: CAN RAST
Use
This test is used to detect the presence of allergen-specific IgE antibodies in the blood serum for Candida albicans. It helps in the identification of patients with allergic reactivity to this specific allergen, and it is especially useful for diagnosing mold allergies caused by Candida albicans. The test quantitatively measures the concentration of IgE specific to this allergen using a fluorescent enzyme immunoassay method, which is sensitive for detecting low levels of allergen-specific IgE.
Special Instructions
Not provided.
Limitations
This test measures the concentration of Candida albicans-specific IgE, but the results do not always correlate with clinical symptoms. IgE levels in the 0.10-0.34 kU/L range need careful consideration by a specialist, as their clinical relevance is uncertain. Low IgE levels may not rule out the allergy or anaphylaxis, and high levels might not directly relate to the severity of clinical symptoms. The allergen test should be combined with patient history and in vivo testing for a precise diagnosis.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Fluorescent Enzyme Immunoassay)
Biomarkers
LOINC Codes
- 6059-0 - C albicans 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
ARUP Standard Transport Tube
Collection Instructions
Separate serum from cells ASAP or within 2 hours of collection. Use a serum separator tube to collect the specimen.
Patient Preparation
Avoid multiple patient encounters.
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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