Test Code RPRT3 Rapid Plasma Reagin (RPR) with Reflex to Treponema pallidum Particle Agglutination, Serum
Ordering Guidance
This assay should only be used following an initial reactive treponemal antibody assay result as part of the reverse syphilis testing algorithm.
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 0.3 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Useful For
Diagnosing syphilis
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
RPRT4 | RPR, Titer, S | No | No |
RTPPA | Syphilis Ab, TP-PA, S | Yes, (Order TPPA) | No |
Testing Algorithm
If this test is positive, then the rapid plasma reagin titer will be performed at an additional charge.
If this test is negative, then the Treponema pallidum particle agglutination test will be performed at an additional charge.
For more information see Syphilis Serology Algorithm.
Special Instructions
Method Name
RPRT3, RPRT4: Flocculation/Agglutination
RTPPA: Particle Agglutination
Reporting Name
RPR w/ Reflex to TP-PA, SSpecimen Type
SerumSpecimen Minimum Volume
See Specimen Required
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 |
Clinical Information
Syphilis is caused by infection with the spirochete Treponema pallidum subspecies pallidum. The infection is systemic, and the disease is characterized by periods of latency. These features, together with the fact that T pallidum cannot be isolated in culture, mean that serologic techniques play a major role in the diagnosis and follow-up of treatment for syphilis.
Historically, the serologic testing algorithm for syphilis included an initial nontreponemal screening test, such as the rapid plasma reagin (RPR) or the VDRL tests. Because these tests measure the host's immune response to nontreponemal antigens, they lack specificity. Therefore, a positive result by RPR or VDRL requires confirmation by a treponemal-specific test, such as the fluorescent treponemal antibody-absorption (FTA-ABS) or microhemagglutination (MHA-TP) assay. Although the FTA-ABS and MHA-TP assays are technically simple to perform, they are labor intensive and require subjective interpretation by testing personnel.
As an alternative to the traditional syphilis screening algorithm, many laboratories utilize the reverse syphilis screening algorithm. This algorithm starts with an automated treponemal assay to detect antibodies specific to T pallidum. If this screening assay is positive, the sample is reflexed for testing by RPR, which, if positive, is reported with a titer and is indicative of active or recent syphilis infection. If the RPR is negative, the sample is reflexed to a second treponemal assay, such as the T pallidum particle agglutination (TP-PA) assay. If the TP-PA is positive, this would indicate previously treated or late-stage syphilis infection. Alternatively, if the TP-PA is negative, the initial positive screen is interpreted as a false positive result.
Patients with primary or secondary syphilis are typically tested by RPR to their monitor response to treatment. Typically, RPR titers decrease following successful treatment, but this may occur over a period of months to years. Additionally, testing of maternal and neonate serum, collected concurrently, by RPR can be used as an aid to diagnose congenital syphilis.
Reference Values
Negative
Reference values apply to all ages.
Interpretation
Negative:
Non-treponemal antibodies not detected. Testing on a new specimen collected in 2 to 3 weeks is recommended if acute infection is suspected. Sample reflexed for detection of Treponema pallidum specific antibodies by the T pallidum particle agglutination assay.
Positive:
Specimen reflexed to determine rapid plasma reagin titer.
Cautions
Biological false-positive reactions with cardiolipin-type antigens have been reported in diseases such as infectious mononucleosis, leprosy, malaria, lupus erythematosus, vaccinia, and viral pneumonia.
Pregnancy, autoimmune diseases, and narcotic addictions may give false-positive results. Pinta, yaws, bejel, and other treponemal diseases may also produce false-positive results with this test.
Day(s) Performed
Monday through Saturday
Report Available
Same day/1 to 4 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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
86592
86593- (if appropriate)
86780- (if appropriate)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
RPRT3 | RPR w/ Reflex to TP-PA, S | 20507-0 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
616970 | RPR w/ Reflex to TP-PA, S | 20507-0 |
Forms
If not ordering electronically, complete, print, and send an Infectious Disease Serology Test Request (T916) with the specimen.