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Parvovirus B19 DNA, Qualitative Real-Time PCR

Test Summary

Parvovirus B19 is the cause of an infection known as "Fifth Disease". This infection affects children primarily and causes a rash on the face, trunk, and limbs. Joint pain and swelling is more common in adults. Although a portion of those affected have only mild disease, patients with sickle cell anemia, or similar types of chronic anemia, can suffer from severe acute anemia. Infection during pregnancy can lead to severe complications for the fetus. Infections in immunocompromised patients may lead to serious complications including nephropathy, myocarditis, and persistent anemia. Although serologic detection of circulating antibodies (Parvovirus B-19 IgM & IgG) is useful to determine recent exposure to the virus, DNA testing provides the most reliable evidence of a persistent infection. Quantitative results of Parvovirus B19 viral load may be useful in determining the response to therapy (usually IVIG) and may be beneficial in assessing the risk for nosocomial transmission.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL plasma collected in EDTA (lavender-top), ACD (yellow-top) or PPT potassium EDTA (white-top) tube or
1 mL whole blood collected in EDTA (lavender-top) or ACD (yellow-top) tube or
1 mL amniotic fluid or amniotic fluid supernatant collected in a sterile, leak-proof container or
1 mL serum or
> 3 cubic mm tissue collected in a sterile, plastic leak-proof container

Minimum Volume

>3 cubic mm fresh tissue
0.3 mL all other specimens

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Whole blood: Refrigerated (cold packs)
All other samples: Frozen

Specimen Stability

  • Whole blood and bone marrow
  • Room temperature: 48 hours
  • Refrigerated: 7 days
  • Frozen: Unacceptable
  • All other specimens
  • Room temperature: 48 hours
  • Refrigerated: 7 days
  • Frozen:

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Hemolyzed whole blood • Heparin plasma or whole blood

Order Code

PB19QL

EPIC (Premier) Code

LAB3783

Includes

N/A

CPT Code

  • 87798

Billing Code

  • 670410

CPT Statement

Methodology

Real-Time Polymerase Chain Reaction (RT-PCR)

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly VA, 20153

Department

Reference Testing

Reference Range

Not detected

Setup Schedule / Expected Turnaround Time

Daily

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL plasma collected in EDTA (lavender-top), ACD (yellow-top) or PPT potassium EDTA (white-top) tube or
1 mL whole blood collected in EDTA (lavender-top) or ACD (yellow-top) tube or
1 mL amniotic fluid or amniotic fluid supernatant collected in a sterile, leak-proof container or
1 mL serum or
> 3 cubic mm tissue collected in a sterile, plastic leak-proof container

Minimum Volume

>3 cubic mm fresh tissue
0.3 mL all other specimens

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Whole blood: Refrigerated (cold packs)
All other samples: Frozen

Specimen Stability

  • Whole blood and bone marrow
  • Room temperature: 48 hours
  • Refrigerated: 7 days
  • Frozen: Unacceptable
  • All other specimens
  • Room temperature: 48 hours
  • Refrigerated: 7 days
  • Frozen:

Limitations

N/A

Other Acceptable Specimens

N/A

Unacceptable Specimens

Hemolyzed whole blood • Heparin plasma or whole blood

Billing

CPT Code

  • 87798

Billing Code

  • 670410

CPT Statement

Result Information

Methodology

Real-Time Polymerase Chain Reaction (RT-PCR)

Testing Laboratory

N/A

Reference Range

Not detected

Setup Schedule / Expected Turnaround Time

Daily