Test Directory
| Test Code | |||
| PARPR | |||
| Test Name | |||
| Parvovirus B19 Qualitative PCR | |||
| CPT Codes | |||
| 87798 | |||
| Expected Turnaround Time | |||
| 1 - 5 days | |||
| Clinical Utility | |||
| Diagnosing parvovirus B19 infection in plasma specimens. | |||
| Specimen and Container Info | |||
|
Specimen Type: Plasma Collection Container: Lavender Top (EDTA) Desired Specimen Volume: 0.5 mL |
|||
| Collection Instructions | |||
|
|||
| Processing and Submission Instructions | |||
|
|||
| Transport Instructions | |||
|
Transport to the laboratory refrigerated. |
|||
| Stability Requirements | |||
|
|||
| Causes for Rejection | |||
|
|||
| Methodology | |||
| Real-Time Polymerase Chain Reaction (Pcr)/Dna Probe Hybridization | |||
| Reference Intervals | |||
|
See patient report. |
|||
| Limitations | |||
|
A negative result does not necessarily indicate the absence of parvovirus B19 infection. False-negative results may be due to the virus being present at levels below the limit of detection for this assay, or to inhibitory substances that may be present in the specimen. This assay has only been validated for the detection of genotype 1 parvovirus B19 and its ability to detect the less common genotypes 2 and 3 is unknown. |
|||
| Reference Lab | |||
| Mayo Clinic Laboratories | |||
| Testing Schedule | |||
| Routine Monday-Friday | |||
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
© 2026 HNL Lab Medicine. All rights reserved.