Enterovirus by PCR
Ordering Recommendation
Detect enterovirus in blood, CSF, or nasopharyngeal specimens.
New York DOH Approval Status
Specimen Required
Lavender (EDTA), pink (K2EDTA) or serum separator tube. Also acceptable: CSF or nasopharyngeal swab.
Separate serum or plasma from cells. Transfer 1 mL serum, plasma or CSF to a sterile container. (Min: 0.5 mL) Swab: Place in viral transport media (ARUP Supply #12884). Available online through eSupply using ARUP Connect™ or contact ARUP Client Services at (800)522-2787.
Frozen.
Heparinized specimens.
Specimen source required.
Ambient: 8 hours; Refrigerated: 48 hours; Frozen: 3 months
Methodology
Qualitative Polymerase Chain Reaction
Performed
Sun-Sat
Reported
1-2 days
Reference Interval
Interpretive Data
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)
Note
Hotline History
CPT Codes
87498
Components
Component Test Code* | Component Chart Name | LOINC |
---|---|---|
0050104 | EV Source | 31208-2 |
0050249 | Enterovirus by PCR | 29591-5 |
Aliases
- Coxsackie Virus
- Echovirus
- EV Detection
- EV PCR
- EV RNA detection
- Poliovirus