Allergen, Occupational, Isocyanate MDI
Also known as: ISO MDI
Use
This test is used to measure the concentration of IgE antibodies specific to methylene diphenyl diisocyanate (MDI), an occupational allergen, in the patient's serum. It provides an indication of potential allergic reactions in individuals who are exposed to isocyanates, commonly used in manufacturing and construction industries. The presence and concentration of specific IgE antibodies are indicative of sensitization and help in assessing the risk of an allergic response upon exposure.
Special Instructions
Not provided.
Limitations
While this test measures the concentration of allergen-specific IgE antibodies, the correlation between quantitative results and clinical allergy symptoms is not absolute. The test results must be interpreted in conjunction with the patient's medical history and other diagnostic findings. A negative test result does not entirely exclude the possibility of clinical allergy or anaphylaxis. The clinical relevance of results in the range of 0.10-0.34 kU/L is undetermined and intended for specialist use.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Fluorescent Enzyme Immunoassay)
Biomarkers
Isocyanate MDI IgE
Analyte
LOINC Codes
- 7430-2 - Isocyanate MDI 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.
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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