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Test Code LENT Enterovirus, Molecular Detection, PCR, Varies


Advisory Information


This test will detect enterovirus, but will not differentiate viruses in this family or provide serotyping information.

Necessary Information


1. Specimen source is required.

2. Source information should include main anatomical site of collection.



Specimen Required


Submit a raw clinical sample (not a culture isolate) for enterovirus PCR.

 

Submit only 1 of the following specimens:

 

Specimen Type: Body fluid

Sources: Pericardial, peritoneal

Container/Tube: Sterile container

Specimen Volume: 0.5 mL

Collection Instructions: Do not centrifuge.

 

Specimen Type: Spinal fluid

Container/Tube: Sterile vial

Specimen Volume: 0.5 mL

Collection Instructions: Do not centrifuge.

 

Specimen Type: Swab

Supplies:

-Culturette (BBL Culture Swab) (T092)

-M4-RT (T605)

Sources: Dermal, eye, rectal, genital, urethral

Container/Tube: Multimicrobe media (M4-RT) or similar viral transport media (M4 or M5) and Eswab

Specimen Volume: Entire specimen

Collection Instructions:

1. Rectal swab must have no visible fecal matter

2. Place swab back into multimicrobe media (M4-RT, M4, or M5)


Forms

If not ordering electronically, complete, print, and send a Microbiology Test Request (T244) with the specimen.

Useful For

Aids in diagnosing enterovirus infections

 

This test should not be used to screen asymptomatic patients

Testing Algorithm

See Meningitis/Encephalitis Panel Algorithm in Special Instructions.

Method Name

Real-Time Polymerase Chain Reaction (PCR)/RNA Probe Hybridization

Reporting Name

Enterovirus PCR

Specimen Type

Varies

Specimen Minimum Volume

Body Fluid, Spinal Fluid: 0.3 mL

Specimen Stability Information

Specimen Type Temperature Time Special Container
Varies Refrigerated (preferred) 7 days
  Frozen  7 days

Reject Due To

Swab Calcium alginate-tipped swab, wood swab, or transport swab containing gel
 

Reference Values

Negative

Day(s) and Time(s) Performed

Monday through Sunday; Varies

Performing Laboratory

Mayo Clinic Laboratories in Rochester

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.

CPT Code Information

87498

LOINC Code Information

Test ID Test Order Name Order LOINC Value
LENT Enterovirus PCR 93856-3

 

Result ID Test Result Name Result LOINC Value
SRC68 Specimen Source 39111-0
80066 Enterovirus PCR 93856-3