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Recommendations when to order or not order the test. May include related or preferred tests.
Use to detect Treponema pallidum, Herpes simplex virus 1, and Herpes simplex virus 2 in genital and anorectal lesions/ulcers.
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
This test is New York state approved.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
Genital, anal, or rectal swabs with APTIMA Unisex Swab Specimen Collection kit (ARUP supply #28907) OR in Viral Transport Media (ARUP supply #12884) available online through eSupply using ARUP Connect, or contact ARUP Client Services at 800-522-2787.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
APTIMA Swab: Place blue swab in swab specimen transport tube, break shaft off at score line, then recap tube. Swab in Viral Transport Media (VTM): Transfer swab to viral transport media.
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Frozen
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
Serum, plasma
RemarksAdditional specimen collection, transport, or test submission information.
Specimen source required
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Expected turnaround time for a result, beginning when ARUP has received the specimen.
1-5 days
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
A negative result does not rule out the presence of PCR inhibitors in the patient specimen or test-specific nucleic acid in concentrations below the level of detection by this assay.
Compliance Category
Laboratory Developed Test (LDT)
Note
Additional information related to the test.
This test detects and differentiates Treponema pallidum, Herpes simplex virus 1, and Herpes simplex virus 2.
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
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