LYME VISE Total Antibody IgG/IgM Screen LYME

Synonyms

Allscripts (AEHR) Order Name

Borrelia burgdorferi IgG/IgM Antibodies

Sunrise Clinical Manager (SCM) Order Name

Borrelia burgdorferi IgG/IgM Antibodies

Clinical Info

For more information on the interpretation of Lyme disease serology, please visit:
https://www.youtube.com/watch?v=Dei-8na9wZU
https://www.youtube.com/watch?v=LhF7vX5RynA
https://www.aphl.org/aboutAPHL/publications/Documents/ID-2021-Lyme-Disease-Serologic-Testing-Reporting.pdf

Specimen Type

Blood

Container

Gold Top Tube

Collection Instructions

Container/Tube: Gold-top tube(s)
Specimen: 1 mL of serum (0.5 mL min)
Transport Temperature: Refrigerate

Transport Instructions

Refrigerate

Specimen Stability

7 Days Refrigerated
30 Days Frozen

Methodology

Chemiluminescence Immunoassay (CLIA)
Test will reflex to Lyme IgG and Lyme IgM at an additional cost.
Measures antibody to Borrelia burgdorferi, Borrelia garnii and Borrelia afzelii.

Days Performed

Monday through Sunday, continuously

Performing Laboratory

Northwell Health Laboratories

CPT

86618

PDM

5700530

Result Interpretation

 0.01 - 0.89  Index Negative
   
 0.90 - 1.09  Index Equivocal
   
≥1.10  Index Positive

 

Suggested Interpretation of Lyme Disease Serologic Test Results using the Modified Two-Tiered Testing Algorithm

Test Sequence

Interpretation for Laboratories

Interpretation for Providers

Comments / Further Actions

Tier 1

Tier 2a

Tier 2b

Lyme VlsE IgM/IgG Total Immunoassay

Lyme IgM Immunoassay

Lyme IgG Immunoassay

Negative

Testing Not

Indicated

Testing Not

Indicated

 

Negative for antibodies to B. burgdorferi (Lyme disease).

 

No laboratory evidence of infection with B. burgdorferi (Lyme disease).

 

Negative results may occur in patients recently infected (≤14 days) with B. burgdorferi. If recent infection is suspected, repeat testing on a new sample collected in 7–14 days is recommended.

Positive/ Equivocal

Negative

Negative

Antibodies to B. burgdorferi (Lyme disease) not confirmed.

No laboratory evidence of infection with B. burgdorferi (Lyme disease).

Negative results may occur in patients recently infected (≤14 days) with B. burgdorferi. If recent infection is suspected, repeat testing on a new sample collected in 7–14 days is recommended.

Positive/ Equivocal

Positive/ Equivocal

Negative

  

 

 

IgM-class antibodies to B. burgdorferi (Lyme disease) detected.

 

 

Results are consistent with acute or recent infection with B. burgdorferi (Lyme disease).

IgM immunoassay results should only be considered as indicative of recent infections in patients presenting within 30 days of symptom onset. Consideration of IgM immunoblot results in patients with symptoms lasting >30 days is discouraged due to the risk of false positive IgM immunoblot results or prolonged IgM seropositivity following disease resolution.

 

Testing of a new specimen collected in 7–14 days to demonstrate IgG seroconversion may be considered to confirm infection. If both tests are equivocal consider repeat testing in 7-14 days if clinically warranted.

Positive/ Equivocal

Negative

Positive/ Equivocal

 

IgG-class antibodies to B. burgdorferi (Lyme disease) detected.

Results are consistent with B. burgdorferi (Lyme disease) infection in the recent or remote past. IgG-class antibodies may remain detectable for months to years following resolution of

infection.

Results should not be used to monitor or establish adequate response to therapy. Response to therapy is confirmed through resolution of clinical symptoms; additional laboratory testing should not be performed. If both tests are equivocal consider repeat testing in 7–14 days if clinically warranted.

Positive/ Equivocal

Positive/ Equivocal

Positive/ Equivocal

 IgM and IgG-class antibodies to B. burgdorferi (Lyme disease) detected.

Results are consistent with B. burgdorferi infection (Lyme disease) in the recent or remote past. Antibodies may remain detectable for months to years following resolution of infection.

Results should not be used to monitor or establish adequate response to therapy. Response to therapy is confirmed through resolution of clinical symptoms; additional laboratory testing should not be performed. If both tests are equivocal consider repeat testing in 7–14 days if clinically warranted.

NOTE: Testing for IgM antibodies to B. burgdorferi is not indicated in patients presenting >30 days post-symptom onset.

Adapted from APHL Suggested Reporting Language, Interpretation and Guidance Regarding Lyme Disease Serologic Test Results

 
 

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