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Test ID NBLD0202 VDRL, Spinal Fluid

Reporting Name

VDRL, CSF

Useful For

Aiding in the diagnosis of neurosyphilis

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Specimen Type

CSF
Sanford Laboratories - Bismarck Note:

Per Mayo Medical Laboratories, this test can be performed using CSF supernatant.


Specimen 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

Reference Values

Negative

Reference values apply to all ages.

Day(s) Performed

Monday through Friday

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

Report Available

1 to 4 days

Reject Due To

Gross hemolysis Reject
Gross lipemia Reject

Method Name

Flocculation/Agglutination

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.