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), or serum separator tube (SST).
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

Preferred transport temp: Frozen.

Unacceptable Conditions

Heparinized specimens.

Remarks

Specimen source required .

Stability

Room temperature: 8 hours; Refrigerated: 2 days; Frozen: 3 months

Methodology

Qualitative Polymerase Chain Reaction (PCR)

Performed

Mon, Wed, Fri

Reported

1-5 days

Reference Interval

Interpretive Data



Compliance Category

Laboratory Developed Test (LDT)

Note

Hotline History

N/A

CPT Codes

87798

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 Detection PCR
  • Parechovirus molecular detection
Parechovirus by PCR