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Test Code Billings Clinic: 6828 Mayo: TPPA Syphilis Antibody, Treponema pallidum Particle Agglutination, Serum

Reporting Name

Syphilis Ab by TP-PA, S

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Useful For

An aid to resolve discrepant results between screening treponemal and non-treponemal assays

 

This test is not recommended for general screening purposes for syphilis.

 

This test should not be used to evaluate response to therapy.

 

This test is not intended for medical-legal use.

Method Name

Particle Agglutination


Ordering Guidance


This assay is recommended by the Centers for Disease Control and Prevention for sera testing positive by a screening treponemal assay and negative by rapid plasma reagin (RPR). The results of this assay assist in determining whether the results of a screening treponemal test are truly or falsely positive.



Specimen Required


Collection Container/Tube:

Preferred: Serum gel

Acceptable: Red top

Submission Container/Tube: Plastic vial

Specimen Volume: 0.5 mL

Collection Instructions: Centrifuge and aliquot serum into a plastic vial.


Specimen Type

Serum

Specimen Minimum Volume

0.3 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 14 days
  Frozen  14 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject

Reference Values

Negative

Interpretation

Syphilis screening at Mayo Clinic is performed by using the reverse algorithm, which first tests sera for Treponema pallidum specific IgG antibodies using an automated immunoassay. Antibodies to syphilis can remain elevated despite appropriate antimicrobial treatment and a reactive result does not distinguish between recent or past infection. To further evaluate disease and treatment status, samples that are reactive by the syphilis screening test are reflexed to the rapid plasma reagin (RPR) assay, which detects antibodies to cardiolipin, a lipoidal antigen released from host cells damaged by T pallidum. Unlike treponemal-specific antibodies, RPR titers decrease and usually become undetectable following appropriate treatment and can be used to monitor response to therapy.

 

In some patients, the results of the treponemal screening test and RPR may be discordant (eg, syphilis IgG positive and RPR negative). To discriminate between a falsely reactive screening result and past syphilis, a second treponemal-specific antibody test is recommended using a method that is different from the initial screening test (eg, T pallidum particle agglutination: TP-PA).

 

In the setting of a positive syphilis IgG screening result and a negative RPR, a positive TP-PA result is consistent with one of the following:

1. Past, successfully treated syphilis

2. Early syphilis with undetectable RPR titers

3. Late/latent syphilis in patients who do not have a history of treatment for syphilis

Further historical evaluation is necessary to distinguish between these scenarios (Table).

 

In the setting of a positive syphilis IgG screening result and a negative RPR, a negative TP-PA result is most consistent with a falsely reactive syphilis IgG screen (Table). If syphilis remains clinically suspected, a second specimen should be submitted, order SYPH1 / Syphilis IgG with Reflex, Enzyme Immunoassay, Serum.

 

Table. Interpretation and follow-up of reverse screening results

Patient history

Test and result

Interpretation

Follow-up

EIA/CIA/MFI

RPR

TP-PA

Unknown history of syphilis

Nonreactive

N/A

N/A

No serologic evidence of syphilis

None, unless clinically indicated (eg, early/acute/ primary syphilis)

Unknown history of syphilis

Reactive

Reactive

N/A

Untreated or recently treated syphilis

See Centers for Disease Control and Prevention treatment guidelines  

Unknown history of syphilis

Reactive

Nonreactive

Nonreactive

Probable false-positive screening test

No follow-up testing, unless clinically indicated (eg, acute/primary syphilis)

Unknown history of syphilis

Reactive

Nonreactive

Reactive

Possible syphilis (eg, early or latent) or previously treated syphilis

Historical and clinical evaluation required

Known history of syphilis

Reactive

Nonreactive

Reactive or N/A

Past, successfully treated syphilis

None

CIA, chemiluminescence immunoassay; EIA, enzyme immunoassay; N/A, not applicable; RPR, rapid plasma reagin; TP-PA, Treponema pallidum particle agglutination.

Day(s) Performed

Monday through Friday

Report Available

Same day/1 to 4 days

Test Classification

This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

86780

LOINC Code Information

Test ID Test Order Name Order LOINC Value
TPPA Syphilis Ab by TP-PA, S 24312-1

 

Result ID Test Result Name Result LOINC Value
61480 Syphilis Ab by TP-PA, S 24312-1

Forms

If not ordering electronically, complete, print, and send Infectious Disease Serology Test Request (T916) with the specimen.

Testing Algorithm

For more information see Syphilis Serology Algorithm.

Special Instructions