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Treponema pallidum (Syphilis)

Clinical Specimen Submission Guidance

Submit all specimens to 50 Orms St, Providence RI 02904. Open Monday to Friday 8:30 AM to 4:30 PM

Lab

STI & Arbovirus Laboratory 401-222-5591

Analyte Name

Treponema pallidum

Disease

Syphilis

Test Description

Syphilis testing is performed using U.S. Food and Drug Administration cleared assays, namely the ALINITY Syphilis TP Assay (Abbott Diagnostics) for screening, and both the RPR (ASI), and Serodia TP-PA (Fujirebio Diagnostics) for confirmation testing. The performance characteristics of these assays were verified by the Rhode Island State Health Laboratories.

The Centers for Disease Control's syphilis reverse algorithm should be followed to interpret the combined laboratory results and should be used in conjunction with the patient's clinical symptoms, medical history, and other clinical/laboratory findings to determine an overall clinical diagnosis.

Note that reactive test results could represent a new syphilis infection but could also represent previously treated disease. Please call the RI State Health Laboratory for further clarification, if needed.

Specimen

Collect 3 -8 mL blood or plasma in red top tube or 2 mL serum

Refrigerate at 2° - 8° C.

CLIA regulations require two patient identifiers on the specimen container and the test requisition.

Form Required

Rhode Island State Health Laboratories (RISHL) test requisition form

https://health.ri.gov/forms/LabRequisitionForm.pdf

Test Request

Syphilis

Transport

Transport within 24 to 48 hours of collection.

Specimens must be packaged & transported in accordance with current federal shipping regulations.

Containers specifically labeled for transport of specimens to RISHL STI & Arbovirus Laboratory are available in all Serology Laboratories and Laboratory Sendout Departments.

Integrity

Stable at 2° - 8° C for 5 days

Normal Value

Nonreactive

Reporting Requirement

Providers must report patient information on Syphilis (primary, secondary, early latent, late latent, congenital) within 4 days using the RIDOH reportable disease form.

Turnaround Time

Screen: 3 business days

Confirmation: 5 business days