Detect parechovirus in CSF, plasma, or serum specimens.
Qualitative Polymerase Chain Reaction
Mon, Wed, Fri
New York DOH Approval Status
Lavender (EDTA), pink (K2EDTA), serum separator tube or CSF.
Separate serum or plasma from cells. Transfer 1 mL plasma, serum or CSF to a sterile container. (Min: 0.5 mL)
Specimen source required.
Ambient: 8 hours; Refrigerated: 48 hours; Frozen: 3 months
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.
Laboratory Developed Test (LDT)
|Component Test Code*||Component Chart Name||LOINC|
|2005733||Parechovirus by PCR||60525-3|
- Parechovirus Detection PCR
- Parechovirus molecular detection