Aspergillus Antigen, Bronchoalveolar Lavage

Message
Sendout, Mayo test code: ASPBA


Test Code
LAB1311


Alias/See Also
Aspergillosis
Invasive Aspergillosis
Platelia Aspergillus Ag
Galactomannan
ASPBA


CPT Codes
87305

Preferred Specimen
2 mL in a sterile, leak-proof container


Minimum Volume
1.5 mL


Transport Container
Sterile, leak-proof container
Note: Specimen trap collection containers (with suction catheters attached) will be rejected due to high-risk of leakage and contamination upon opening. Avoid use of these for bronchoalveolar lavage specimens.


Transport Temperature
Refrigerated


Specimen Stability
Refrigerated (preferred): 14 days
Frozen: 14 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Bronchial washing: Reject
Thick/viscous/mucoid specimens: Reject
Specimen in a non-leak proof container: Reject


Methodology
Enzyme Immunoassay (EIA)

FDA Status
Approved

Setup Schedule
Monday through Friday, Sunday


Report Available
1-2 days


Limitations
False-positive results are reported to occur at rates of 8% to 14% with this assay when performed on serum. Numerous foods (eg, pasta, rice, etc) contain galactomannan. It is thought that damage to the gut wall by cytotoxic therapy, irradiation, or graft-versus-host disease enables translocation of the galactomannan from the gut lumen into the blood and may be partially responsible for the high false-positive rate of this assay when serum is tested. Whether false-positive results in bronchoalveolar lavage (BAL) fluid are associated with the consumption of certain foods, as is observed in serum samples, remains to be determined.
 
Other genera of fungi such as Penicillium and Paecilomyces have shown reactivity with the rat EBA-2 monoclonal antibody used in the assay. These species are rarely implicated in invasive fungal disease. Specimens containing Histoplasma antigen may cross-react in the Aspergillus antigen assay. Cross-reactivity with Alternaria species has also been reported.
 
The specificity of the assay for Aspergillus species cannot exclude the involvement of other fungal pathogens with similar clinical presentations such as FusariumAlternaria, and Mucorales.
 
The performance of the assay has not been evaluated other specimen types such as urine or cerebrospinal fluid.
 
The assay may exhibit reduced detection of Aspergillus antigen in patients with chronic granulomatous disease or autosomal dominant hyper-IgE syndrome (formerly known as Job syndrome).
 
The concomitant use of antifungal therapy in some patients with invasive aspergillosis may result in reduced sensitivity of the assay.


Reference Range
Included with report


Clinical Significance
Aiding in the diagnosis of invasive aspergillosis using bronchoalveolar lavage specimens
 
Assessing response to therapy


Performing Laboratory
Mayo Clinic Laboratories, Rochester, Minnesota

Additional Information
Aspergillus Antigen, Bronchoalveolar Lavage


The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.