Rapid Plasma Reagin Screen with Reflex, Serum
Use
Aiding in the diagnosis of recent or past Treponema pallidum infection. This test performs rapid plasma reagin screening when Treponema pallidum antibody screen is positive. It is particularly useful in identifying active syphilis infection, recent syphilis, or as a screening tool post-treatment to ensure the effectiveness of therapy.
Special Instructions
Not provided.
Limitations
Not useful as a screening or confirmatory test for blood donor specimens. Although treponemal tests may remain reactive for life even after adequate treatment, non-treponemal assays like RPR are needed to determine a patient's current disease state and prior treatment history. False negatives can occur in late or latent syphilis or in severely immunocompromised patients, where non-treponemal antibodies are not present.
FDA ApprovedNew York Approved
Methodology
Immunoassay (Multiplex Flow Immunoassay)
Biomarkers
Treponema pallidum
Microorganism
LOINC Codes
- 20507-0 - RPR Ser Ql
- 20507-0 - RPR Ser Ql
Result Turnaround Time
1-4 days
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
0.5 mL
Minimum Volume
0.4 mL
Container
Serum gel or Red top tube, submit in plastic vial
Collection Instructions
Centrifuge and aliquot serum into plastic vial.
Storage Instructions
Refrigerated (preferred) for up to 14 days or frozen for up to 14 days
Causes for Rejection
Gross hemolysis, gross lipemia, heat-inactivated specimen
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 14 days |
| Frozen | 14 days |