Test ID: VDSF VDRL, Spinal Fluid
Reporting Name
VDRL, CSFUseful For
Aiding in the diagnosis of neurosyphilis
Clinical Information
VDRL is a nontreponemal serologic test for syphilis that uses a cardiolipin-cholesterol-lecithin antigen to detect reaginic antibodies. The VDRL test performed on cerebrospinal fluid can be used to diagnose neurosyphilis in patients with a prior history of syphilis infection.
The presence of neurosyphilis in untreated patients can be detected by the presence of pleocytosis, elevated protein, and a positive VDRL.
Interpretation
A positive VDRL result on spinal fluid is highly specific for neurosyphilis.
A single negative VDRL result should not be used to exclude neurosyphilis and repeat testing on a new specimen may be necessary.
Positive results will be titered.
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
VDSFQ | VDRL Titer, CSF | No | No |
Testing Algorithm
If this test is positive, a VDRL titer will be performed at an additional charge.
For more information, see Meningitis/Encephalitis Panel Algorithm.
Report Available
1 to 4 daysDay(s) Performed
Monday through Friday
Clinical Reference
1. Miller JN: Value and limitations of nontreponemal and treponemal tests in the laboratory diagnosis of syphilis. Clin Obstet Gynecol. 1975 Mar;18(1):191-203
2. Radolf JD, Tramont EC, Salazar JC: Syphilis (Treponema pallidum). In: Bennett JE, Dolin R, Blaser MJ, eds. Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases. 9th ed. Elsevier; 2020:2865-2892
Method Name
Flocculation/Agglutination
Specimen Type
CSFSpecimen Required
Collection Container/Tube: Sterile vial
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL
Collection Instructions: Submit specimen collected in vial 2, if possible. If not, note which vial from which the aliquot was obtained.
Specimen Minimum Volume
0.2 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
CSF | Frozen (preferred) | 14 days | |
Refrigerated | 14 days |
Special Instructions
Reference Values
Negative
Reference values apply to all ages.
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86592
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
VDSF | VDRL, CSF | 5290-2 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
9028 | VDRL, CSF | 5290-2 |
mml-Behavioral, mml-CNS-Infections, mml-Neuromuscular, mml-Pediatric, mml-Spinal-Cord