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Lyme Antibody w/ Western Blot Confirmation

Test Summary

Lyme disease is caused by a bacterium borrelia burgdorferi and is transmitted by ticks. EIA is the screening test with high sensitivity for antibody detection. Western blot testing qualitatively examines with high specificity antibodies in a patient's specimen. Western blot testing is appropriate for confirming a detected EIA test result.

Aliases

  • B Burgdorferi
  • Borrelia B Earl
  • Borrelia Burgdorferi (serum)
  • Borrelia Burgdorferi Antibodies
  • Lyme (serum)
  • Lyme Disease
  • Lime Disease AB Screen (Total), EIA
  • Lyme Early
  • Lyme IgG &
  • IgM
  • &nbs

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum (minimum 0.5 mL) 

Minimum Volume

N/A

Instructions

SST or Red top: Avoid hemolysis. Invert a minimum of 5 times, then allow to clot in an upright position for 30 minutes. Centrifuge the tube for at least 10 minutes. Keep tightly stoppered.

Patient Preparation

N/A

Storage

SST (speckled top), Red top , Plastic Vial (transfer) tube

Transport Temperature

Refrigerated (preferred)

Specimen Stability

  • Room Temperature = n/a
  • Refrigerated = 7 days
  • Frozen = at least 7 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Rejected for gross hemolysis, and lipemia. Microbial contamination may interfere. Plasma will be rejected

Order Code

LYME

EPIC (Premier) Code

LAB4342

Includes

Western blot confirmation CPT code(s) 86617x2 performed when screen is positive at an additional charge.

CPT Code

  • 86618 (reflex 86617(2))

Billing Code

  • 300000

CPT Statement

Methodology

Enzyme Immunoassay (EIA)

FDA Status

Approved

Physician Attestation of Informed Consent

N/A

Testing Laboratory

CompuNet Clinical Laboratories, LLC
2308 Sandridge Drive
Moraine OH, 45439

Reference Range

SEX AGE Report Normals Units
N/M/F 133Y < OR = 0.90 Negative  
    0.91 - 1.09 Equivocal  
    > OR = 1.10 Positive  
Due to recommendations by the food and drug administration (FDA), all positive or equivocal Borrelia Burgdorferi Antibody EIA (screening) tests will be followed by the western blot.  The screening test for B. Burgdorferi has a low predictive value for a negative result when used to detect early infection and a low predictive value of a positive result when exposure history, symptoms, and clinical findings are not consistent with Lyme disease.  Positive or equivocal results should not be interpreted as true positives until a second-step testing of the specimen is done using a method that is more specific for antibodies to B. Burgdorferi (e.g. Western Blot). 

Setup Schedule / Expected Turnaround Time

Tuesday - Thursday; BS; Report available: 6 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum (minimum 0.5 mL) 

Minimum Volume

N/A

Instructions

SST or Red top: Avoid hemolysis. Invert a minimum of 5 times, then allow to clot in an upright position for 30 minutes. Centrifuge the tube for at least 10 minutes. Keep tightly stoppered.

Patient Preparation

N/A

Storage

SST (speckled top), Red top , Plastic Vial (transfer) tube

Transport Temperature

Refrigerated (preferred)

Specimen Stability

  • Room Temperature = n/a
  • Refrigerated = 7 days
  • Frozen = at least 7 days

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Rejected for gross hemolysis, and lipemia. Microbial contamination may interfere. Plasma will be rejected

Billing

CPT Code

  • 86618 (reflex 86617(2))

Billing Code

  • 300000

CPT Statement

Result Information

Methodology

Enzyme Immunoassay (EIA)

Testing Laboratory

N/A

Reference Range

SEX AGE Report Normals Units
N/M/F 133Y < OR = 0.90 Negative  
    0.91 - 1.09 Equivocal  
    > OR = 1.10 Positive  
Due to recommendations by the food and drug administration (FDA), all positive or equivocal Borrelia Burgdorferi Antibody EIA (screening) tests will be followed by the western blot.  The screening test for B. Burgdorferi has a low predictive value for a negative result when used to detect early infection and a low predictive value of a positive result when exposure history, symptoms, and clinical findings are not consistent with Lyme disease.  Positive or equivocal results should not be interpreted as true positives until a second-step testing of the specimen is done using a method that is more specific for antibodies to B. Burgdorferi (e.g. Western Blot). 

Setup Schedule / Expected Turnaround Time

Tuesday - Thursday; BS; Report available: 6 days