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Enterovirus/Parechovirus RNA, Qualitative Real-Time PCR
Test Code70189
CPT Codes
87498, 87798
Preferred Specimen
0.7 mL serum or
0.7 mL CSF collected in a sterile, plastic leak-proof container or
0.7 mL plasma collected in an EDTA (lavender-top) tube or ACD (yellow-top) tube
0.7 mL CSF collected in a sterile, plastic leak-proof container or
0.7 mL plasma collected in an EDTA (lavender-top) tube or ACD (yellow-top) tube
Minimum Volume
0.3 mL serum, CSF, plasma • 0.5 gram stool
Other Acceptable Specimens
1 gram stool • Throat or rectal swab collected in an M4 or VCM medium (green-cap or equivalent (UTM))
Transport Temperature
Serum, CSF, plasma: Refrigerated (cold packs)
Stool: Frozen
Stool: Frozen
Specimen Stability
Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days
Refrigerated: 7 days
Frozen: 30 days
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Specimens containing heparin • Calcium alginate swabs
Methodology
Real-Time Polymerase Chain Reaction
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Mon-Sat; Report available: 2-3 days
Reference Range
Enterovirus RNA, QL PCR | Not detected |
Parechovirus RNA, QL PCR | Not detected |
Clinical Significance
Detection of Enterovirus and Parechovirus Genomic RNA is useful in the diagnosis of Aseptic Menignitis and Neonatal Sepsis.