Syphilis Serology
Alias: VDRL, TP, Treponema pallidum, T pallidum
Discipline: Virology
Test information: Syphilis is caused by infection with the bacterium Treponema pallidum which can be transmitted congenitally or by sexual contact. The disease can evolve into a latent phase in which syphilis is clinically inapparent. Serological tests (nontreponemal and treponemal specific), in addition to patients' clinical history, are currently the primary methods for the diagnosis and management of syphilis. Newly reactive samples are sent to reference laboratory for confirmatory testing.
Availability: Available locally Monday - Friday during routine hours: 08:45 - 17:15.
Turnaround Time: 3 Days
- Specimen Type(s)
-
- Clotted blood;
- Other Acceptable Specimen Type(s)
- N/A
- Specimen Container - Adult
-
- Gold Top SST BD;
- Specimen Container - Paediatric
-
- Plain Top Sarstedt;
- Analytes
-
- Rapid Plasma Reagin (RPR);
- Treponema pallidum antibodies;
- Part of a test profile?
- No
- Volume (min) of sample to be sent to laboratory
- 5 - 10mL
- Patient Preparation, Sample Handling and Transport
-
- Minimum-clotting time 30 minutes.
- Specimens should be transported to the laboratory as soon as possible.
- Outside of normal hours samples should be refrigerated (2 °C to 8 °C).
- Please indicate if patient is contact of a known positive.
- Please provide exposure details including date of contact.
- For antenatal screening samples, consent to test must be obtained.
- Do NOT send grossly haemolyzed specimens (>500 mg/dL haemoglobin).
- Do NOT send specimens with obvious microbial contamination.
- Maximum add on time
- N/A
- Units and Reference Ranges / Interpretation
-
Syphilis Results: Non-reactive / Reactive
A negative result does not preclude the possibility of exposure to infection with syphilis, additional information may be required for diagnosis. - UKAS number
- 8869
- UKAS accredited test?
- Yes
- Comments
-
False positive results can be expected with any test kit. The proportion of these falsely reactive specimens is dependent upon the specificity of the test kit, specimen integrity, and the
characteristics of the local population being screened.
If results are inconsistent with clinical evidence, additional testing is suggested to confirm the result.
If you have any queries about a test or results interpretation please contact us.
Last updated: 06-06-2023