2005731
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Parechovirus by PCR

PEHV PCR
Example Reports
Detected
Not Detected

Ordering Recommendation

Detect parechovirus in CSF, plasma, or serum specimens.

New York DOH Approval Status

This test is New York state approved.

Specimen Required

Patient Preparation
Collect

Lavender (EDTA), pink (K2EDTA), serum separator tube or CSF.

Specimen Preparation

Separate serum or plasma from cells. Transfer 1 mL plasma, serum or CSF to a sterile container. (Min: 0.5 mL)

Storage/Transport Temperature

Frozen.

Unacceptable Conditions

Heparinized specimens.

Remarks

Specimen source required.

Stability

Ambient: 8 hours; Refrigerated: 48 hours; Frozen: 3 months

Methodology

Qualitative Polymerase Chain Reaction

Performed

Mon, Wed, Fri

Reported

1-5 days

Reference Interval

Interpretive Data

This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.

Compliance Category

Laboratory Developed Test (LDT)

Note

Hotline History

N/A

CPT Codes

87798

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Components

Component Test Code* Component Chart Name LOINC
2005732 Parechovirus Source 31208-2
2005733 Parechovirus by PCR 60525-3
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.

Aliases

  • Parechovirus molecular detection
  • Parechovirus Detection PCR
Parechovirus by PCR