Syphilis Rapid Plasma Reagin (RPR)

Laboratory Fee Schedule

Procedure: MBY0264A

CPT: 86592

Synonym(s):STI, Treponema pallidum, qualitative, non-treponemal test
Requisition FormG-2A
Test DescriptionAgglutination test for the serological detection of reagin antibodies in human serum.
Pre-Approval NeededN/A
Supplemental Information RequiredN/A
Supplemental Form(s)N/A
Performed on Specimens from (sources)Human
Sample/Specimen Type for TestingSerum
Minimum Volume/Size Required200 µL
Storage/Preservation Prior to Shipping
  • Store at 2°C to 8°C for up to 5 days.
  • For long term storage, store frozen at -20°C or colder.
Transport MediumN/A
Specimen Labeling
  • At least two patient-specific identifiers required on specimen (e.g. patient full name, date of birth, medical record number).
  • Three unique patient identifiers are preferred. 
  • Patient identifiers on specimen label must exactly match identifiers on G-2A submission form. (e.g. abbreviated name on label and full name on form is not acceptable.)
  • Additional DSHS Laboratory specimen labeling guidelines available online here.
Shipping and Specimen Handling Requirements
  • Ship according to Dangerous Goods Regulations, IATA, and/or CFR 49.
  • Category B Biological Substance, UN3373 shipping requirements apply.
  • Submitters are responsible for packaging and shipping specimens according to regulatory requirements. 
  • Additional DSHS Laboratory specimen shipping guidelines online here.
  • Store and ship cold at 2°C–8°C if specimen will arrive at the Laboratory within 5 days of collection.
  • Store and ship frozen at -20°C or colder if specimen will arrive at Laboratory more than 5 days after collection.
MethodQualitative RPR agglutination test with reflex to RPR titer.
Turn-around Time3 working days
Interferences/Limitations
  • A specimen is too hemolyzed for testing when printed matter cannot be read through it.
  • Icteric, lipemic and grossly hemolyzed specimens should not be used because of the possibility of nonspecific reactions.
Common Causes for Rejection
  • insufficient specimen quantity
  • unacceptable specimen type or source
  • improper shipping conditions
  • expired media or collection container
  • discrepancies between specimen label and submission form
  • incomplete or missing submission form
Additional InformationSpecimens with reactive RPR Qualitative test results will automatically reflex to RPR titer.