Ordering Recommendation

Detect enterovirus and parechovirus.

Mnemonic
EVPEHV
Methodology

Qualitative Polymerase Chain Reaction

Performed

Sun-Sat

Reported

1-2 days

New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect

(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

Reference Interval
Interpretive Data



Compliance Statement A: For laboratory developed tests using a manufacturer labeled ASR as the reagent providing the specificity of the assay. Analyte Specific Reagent. 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, the FDA has determined that such clearance or approval is not necessary.

Note
Hotline History
N/A
CPT Codes

87498; 87798

Components
Component Test Code* Component Chart Name LOINC
0050249 Enterovirus by PCR 29591-5
2005733 Parechovirus by PCR 60525-3
2005824 Enterovirus and Parechovirus Source 31208-2
* 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
  • EV and Parechovirus RNA detection
Enterovirus and Parechovirus by PCR