Test Code SYPH1 Syphilis IgG with Reflex, Enzyme Immunoassay, Serum
Specimen Required
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container/Tube: Plastic vial
Specimen Volume: 1.5 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Useful For
Aid for the diagnosis of infection with Treponema pallidum using an algorithmic approach
Routine prenatal screening
This test is not offered as a screening or confirmatory test for blood donor specimens.
This test is not useful for diagnosis of congenital syphilis.
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
RRPRS | RPR Screen w/ Reflex to Titer, S | No | No |
RTPPA | Syphilis Ab, TP-PA, S | Yes, (Order TPPA) | No |
RRPRQ | RPR Titer, S | No | No |
Testing Algorithm
If the syphilis IgG result is reactive or equivocal, then the rapid plasma reagin (RPR) screen will be performed at an additional charge.
If the RPR screen is positive, then the RPR titer will be performed at an additional charge.
If the RPR screen is negative, then syphilis antibody Treponema pallidum particle agglutination testing will be performed at an additional charge.
For more information see:
Special Instructions
Method Name
SYPH1: Enzyme Immunoassay (EIA)
RRPRS, RRPRQ: Flocculation/Agglutination
RTPPA: Particle Agglutination
Reporting Name
Syphilis IgG w/ Reflex, EIA, SSpecimen Type
SerumSpecimen Minimum Volume
1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum | Frozen | 14 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | Reject |
Heat-inactivated specimen | Reject |
Reference Values
SYPHILIS IgG SCREEN
Nonreactive
RAPID PLASMA REAGIN SCREEN
Negative
RAPID PLASMA REAGIN TITER
Negative
SYPHILIS ANTIBODY, Treponema pallidum-PARTICLE AGGLUTINATION
Negative
Reference values apply to all ages
Interpretation
Nonreactive:
No serologic evidence of infection to Treponema pallidum (syphilis). Repeat testing may be considered in patients with suspected acute or primary syphilis in 2 to 4 weeks.
Equivocal:
Rapid plasma reagin (RPR) has been ordered to help distinguish between infection with T pallidum (syphilis) versus a falsely reactive treponemal antibody result.
Reactive:
RPR has been ordered to help distinguish between infection with T pallidum (syphilis) versus a falsely reactive treponemal antibody result.
Day(s) Performed
Monday through Friday, Sunday
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
86780-Syphilis IgG Screen
86592-Syphilis Rapid Plasma Reagin Screen (if appropriate)
86593-Rapid Plasma Reagin Titer (if appropriate)
86780-Syphilis Antibody by TP-PA (if appropriate)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
SYPH1 | Syphilis IgG w/ Reflex, EIA, S | 47238-1 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
SYPH1 | Syphilis IgG w/ Reflex, EIA, S | 47238-1 |