Detect parechovirus in CSF, plasma, or serum specimens.
Qualitative Polymerase Chain Reaction
Mon, Wed, Fri
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
Compliance Statement B: For laboratory developed tests not using a RUO kit, and for FDA approved, cleared or 510(k) exempt assays with alterations. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
|Component Test Code*||Component Chart Name||LOINC|
|2005733||Parechovirus by PCR||60525-3|
- Parechovirus Detection PCR
- Parechovirus molecular detection