Test Overview
Test Methodology

Polymerase Chain Reaction (PCR)

Test Usage

Rapid detection of Varicella zoster virus DNA in clinical specimens.

Reference Range *

Not detected.

* Reference ranges may change over time. Please refer to the original patient report when evaluating results.

Test Limitations

A negative test result does not rule out the presence of Varicella zoster virus. Results should be used in conjunction with other laboratory test results and the patient's clinical profile.

Test Details
Days Set Up
Daily
Analytic Time

3 hours

Soft Order Code
PCRVZ
MiChart Code
Varicella Zoster Virus DNA by PCR
Synonyms
  • VZV DNA detection by PCR
  • Herpes zoster virus detection, PCR
  • Chicken Pox detection, PCR
Laboratory
Microbiology
Section
Microbiology
Specimen Requirements
Collection

For blister, lesion, or vesicle, unroof and scrape the base of the lesion with a Dacron or rayon swab to collect fluid and cells. Place the swab into 1 Viral Transport Media (VTM).
Ideally specimens should be collected within 3-4 days of the onset of symptoms but no greater than 7 days. Specimens collected from lesions in the acute or vesicular stage will yield a higher number of viruses. Avoid contamination with creams, ointments, lotions, alcohol, Betadine solution or blood due to the potential for PCR inhibition. Transport to the laboratory as soon as possible. Calcium alginate swabs are not acceptable.

Normal Volume

1 Viral Transport Media (VTM)

Minimum Volume

1 Viral Transport Media (VTM)

Storage Temperature
Room temperature (15-25°C) ≤4 days
Refrigerate (15-25°C) ≤14 days
Freeze (-15 to -25°C) ≤90 days
Rejection Criteria
Specimens not received in Viral transport media (VTM).
Additional Information

The Varicella zoster virus PCR is a real-time polymerase chain reaction (PCR) amplification and detection system that utilizes a bi-functional fluorescent probe-primer for the detection of Varicella zoster virus in lesion/vesicle swabs. The assay has been validated as a direct protocol using unprocessed specimens. A DNA internal control is used to monitor the process for reagent integrity and to detect PCR inhibition. Results should be used in conjunction with other laboratory test results and the patient's clinical profile

Billing
CPT Code
87798
Fee Code
LA005
LOINC
11483-5
NY State Approved
No