For CSF specimens, Treponema pallidum (VDRL), Cerebrospinal Fluid with Reflex to Titer is preferred. May aid in the workup of neurosyphilis.
Semi-Quantitative Indirect Fluorescent Antibody
This test is New York DOH approved.
- Patient Preparation
- Specimen Preparation
- Transfer 1 mL CSF to an ARUP Standard Transport Tube. (Min: 0.2 mL)
- Storage/Transport Temperature
- Unacceptable Conditions
- Serum. Contaminated, heat-inactivated, or hemolyzed specimens.
- Ambient: 48 hours; Refrigerated: 5 days; Frozen: 1 year
The significance of a reactive result in the FTA-ABS CSF test is unknown. The CSF from persons treated in the secondary or latent stage of syphilis and without signs of neurosyphilis may be reactive. A nonreactive result in the FTA-ABS CSF test suggests the absence of neurosyphilis.
The FTA test is not recommended for cerebrospinal fluid specimens. For CSF specimens, Treponema pallidum (VDRL), Cerebrospinal Fluid with Reflex to Titer (0050206) test is recommended.
See Compliance Statement B: www.aruplab.com/CS
Inconclusive final reports indicate the initial specimen submitted has been tested twice and cannot be interpreted as either reactive or nonreactive. If it is the second specimen submitted on a patient and the report is again inconclusive, it is impossible to state definitively that the patient does or does not have syphilitic infection.
|Component Test Code*||Component Chart Name|
|0055273||Fluorescent Treponema Antibody CSF|
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, contact interface support at firstname.lastname@example.org.
- Fluorescent Treponemal Antibody (Treponema pallidum Antibody, IgG by IFA (CSF))