Enterovirus, Real-time PCR, Amniotic Fluid

CPT: 87498
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Expected Turnaround Time

4 - 6 days


Specimen Requirements


Specimen

Amniotic fluid, uncentrifuged


Volume

1 mL


Minimum Volume

0.2 mL


Container

Sterile plastic conical tube


Collection

Amniotic fluid should not be centrifuged. To avoid delays in turnaround time when requesting multiple tests on frozen samples, please submit separate frozen specimens for each test requested.


Storage Instructions

Freeze (preferred) or refrigerate.


Stability Requirements

Temperature

Period

Room temperature

7 days

Refrigerated

7 days

Frozen

90 days


Causes for Rejection

Quantity not sufficient for analysis; gross specimen contamination; specimen too old; leaking or broken tube


Test Details


Use

Aid in the diagnosis of enteroviral infections


Limitations

Weak cross-reactivity was observed with some strains of rhinovirus that could be present in respiratory samples, and a false-positive result is possible if samples contain these viruses.

This test was developed, and its performance characteristics determined, by ViroMed. It has not been cleared or approved by the US Food and Drug Administration (FDA). The FDA has determined that such clearance or approval is not necessary. Test results should be interpreted in conjunction with clinical observations and other laboratory data and not used as the sole basis for diagnosis.


Methodology

Real-time polymerase chain reaction (PCR)


LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
139348 Enterovirus RT-PCR, Amniotic 139347 Enterovirus RT-PCR, Amniotic 29591-5

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