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
Transfer 1 mL CSF to an ARUP Standard Transport Tube. (Min: 0.2 mL)
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.
Treponema pallidum (VDRL), Cerebrospinal Fluid with Reflex to Titer (0050206) is the recommended test for CSF specimens. If suspicion of neurosyphilis remains after VDRL testing, testing of the CSF with FTA-ABS may be considered.
Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
|Component Test Code*||Component Chart Name||LOINC|
|0055273||Fluorescent Treponema Antibody CSF||9826-9|
- Fluorescent Treponemal Antibody
- T pallidum IgG CSF by IFA