Test Code HSVC Herpes Simplex Virus (HSV), Molecular Detection, PCR, Spinal Fluid
Useful For
Aiding in the rapid diagnosis of herpes simplex virus (HSV)-1 and HSV-2 infections of the central nervous system
Method Name
Real-Time Polymerase Chain Reaction (RT-PCR)
Reporting Name
Herpes Simplex Virus, PCR, CSFSpecimen Type
CSFSpecimen Required
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Container/Tube: Plastic vial
Specimen Volume: 0.2 mL
Collection Instructions:
1. Submit from second spinal fluid collection vial.
2. Transfer into aliquot vial using sterile technique.
3. Do not centrifuge or heat inactivate.
Additional Information:
1. The high sensitivity of amplification by polymerase chain reaction (PCR) requires the specimen to be processed in an environment in which contamination of the specimen by herpes simplex virus DNA is not likely.
2. Specimens that are received with less than the minimum volume required for all testing requested will be canceled.
Specimen Minimum Volume
0.1 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
CSF | Refrigerated (preferred) | 7 days | |
Frozen | 7 days |
Reference Values
Negative
Interpretation
A positive result suggests the presence of herpes simplex virus (HSV)-1 and/or HSV-2 DNA in the cerebrospinal fluid (CSF) sample.
A negative result suggests that HSV-1 and HSV-2 DNA are not present in the CSF sample.
An invalid result points to the inability to determine presence or absence of HSV-1 or HSV-2 DNA in the CSF sample.
Clinical Reference
1. Lawrence C. Herpes Simplex virus. In: Mandell GL, Bennet JE, Dolin R, eds. Principles and Practice of Infectious Diseases. 6th ed. Elsevier, Churchill and Livingstone; 2004:1762-1780
2. Szpara ML, Parsons L, Enquist LW. Sequence variability in clinical and laboratory isolates of herpes simplex virus 1 reveals new mutations. J Virol. 2010;84(10):5303-5313
3. Tunkel AR, Glaser CA, Bloch KC, et al. The management of encephalitis: clinical practice guidelines by the Infectious Diseases Society of America. Clin Infect Dis. 2008;47(3):303-327
4. Brown ZA, Wald A, Morrow RA, et al. Effect of serologic status and cesarean delivery on transmission rates of herpes simplex virus from mother to infant. JAMA. 2003;289(2):203-209
5. Clinical Management Guidelines for Obstetrician-Gynecologists. ACOG Practice Bulletin No. 57, 104 (5 pt 1). 2004;1111-1118
6. Binnicker MJ, Espy MJ, Irish CL. Rapid and direct detection of herpes simplex virus in cerebrospinal fluid using a commercial real-time PCR assay. J Clin Microbiol. 2014;52(12):4361-4362
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 to 2 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest 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
87529 x 2
87529 (if appropriate for government payers)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
HSVC | Herpes Simplex Virus, PCR, CSF | 92865-5 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
36858 | HSV 1 PCR, C | 16952-4 |
36859 | HSV 2 PCR, C | 16960-7 |
Testing Algorithm
For more information see Meningitis/Encephalitis Panel Algorithm.
Special Instructions
Forms
If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.