Lyme Disease Antibodies (IgG, IgM) Immunblot

Message
Sendout, Mayo test code: LYWB


Test Code
LAB5210316


Alias/See Also
Lyme Disease Antibody, Western Blot Assay, Serum
Western Blot, Lyme Disease
Western Blot Assay
Lyme Western Blot
Lyme Disease Antibody, ImmunoBlot Assay, Serum
Lyme ImmunoBlot
ImmunoBlot Assay, Lyme Disease
Borrelia burgdorferi
LYWB


CPT Codes
86617 x 2

Preferred Specimen
0.75 mL serum from a gold serum gel tube


Minimum Volume
0.5 mL


Other Acceptable Specimens
Red tube


Instructions
Centrifuge and aliquot serum into a plastic vial.


Transport Temperature
Refrigerated


Specimen Stability
Refrigerated (preferred): 14 days
Frozen: 30 days


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Gross hemolysis: Reject
Gross lipemia: Reject
Gross icterus: Reject
Heat-inactivated specimen: Reject


Methodology
Immunoblot

FDA Status
Approved

Setup Schedule
Monday, Wednesday, Friday


Report Available
1-4 days


Limitations
The immunoblot result may be negative in specimens that are weakly positive by enzyme immunoassay or in patients with early Lyme disease.
 
Test results should be used in conjunction with clinical evaluation and information related to tick exposure.
 
A negative test result does not necessarily rule out current or recent infection. The specimen may have been collected before demonstrable antibody developed. Patients with early disease often have serum antibody titers below the diagnostic threshold for several weeks following disease onset.
 
Test results from pregnant women or patients who are immunosuppressed may be difficult to interpret.
 
Positive test results may not be valid in persons who have received blood or blood product transfusions within the past several months.
 
Antibiotic therapy administered early following exposure or disease onset may suppress the antibody response to the point that diagnostic threshold levels are never attained.
 
Lyme disease serology should not be used for monitoring treatment response, as IgG can remain detectable for years post-resolution of infection.
 
False-positive reactions may occur with patients with other spirochetal diseases (syphilis, yaws, pinta, relapsing fever, or leptospirosis), recent Epstein-Barr virus infection (ie, infectious mononucleosis), influenza, autoimmune disorders (eg, present of extractable nuclear antigens), multiple sclerosis, or amyotrophic lateral sclerosis.


Reference Range
Included with report


Clinical Significance
Aiding in the diagnosis of systemic Lyme disease
 
This test should not be used as a screening assay.


Performing Laboratory
Mayo Clinic Laboratories, Rochester, Minnesota

Additional Information
Lyme Disease Antibody, Immunoblot, Serum


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.