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Enterovirus/Parechovirus RNA, Qualitative Real-Time PCR
Test Code70189
CPT Codes
87498, 87798 <br><strong>This test is not available for New York patient testing.</strong>
Preferred Specimen
0.7 mL CSF in a sterile leak-proof container, Plasma collected in an EDTA (lavender-top) or ACD (yellow-top) tube or Serum • 1 g stool in a sterile leak-proof container • Throat swab or rectal swab in VCM medium (green-cap) tube or equivalent (UTM)
Minimum Volume
0.3 mL serum, CSF, plasma • 0.5 gram stool
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: 1-2 days
Clinical Significance
Detection of Enterovirus and Parechovirus Genomic RNA is useful in the diagnosis of Aseptic Menignitis and Neonatal Sepsis.