Aid in diagnosing allergic bronchopulmonary aspergillosis (ABPA). Not appropriate for diagnosing invasive aspergillosis.
Quantitative ImmunoCAP Fluorescent Enzyme Immunoassay
Serum Separator Tube (SST).
Separate from cells ASAP or within 2 hours of collection. Transfer 0.5 mL serum to an ARUP Standard Transport Tube. (Min: 0.2 mL)
Hemolyzed, icteric, or lipemic specimens.
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year
|0.00-90.00 mcg/mL||Negative - No significant level of A. fumigatus IgG antibody detected.|
|90.01-99.99 mcg/mL||Equivocal - Questionable presence of A. fumigatus IgG antibody.|
|100.00 mcg/mL or greater||Positive - A. fumigatus IgG antibody detected. A positive result satisfies a single criterion in the determination of allergic bronchopulmonary aspergillosis (ABPA).|
Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
|Component Test Code*||Component Chart Name||LOINC|
|3000877||Aspergillus fumigatus Ab IgG||26954-8|
- A fumigatus
- Allergic bronchopulmonary aspergillosis
- Aspergillus fumigatus
- Aspergillus Fumigatus IgG
- IgG Antibodies
- IgG Serum