Oropouche Virus RNA, Qualitative Real-Time Reverse Transcriptase (RT) PCR

Oropouche Virus RNA, Qualitative Real-Time Reverse Transcriptase (RT) PCR

Test Code

14328
87798
CPT Code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering.
14328
87798
CPT Code is subject to a Medicare Limited Coverage Policy and may require a signed ABN when ordering.
In-home collection may be available in your area for purchase through Quest Mobile.

Clinical Significance

Oropouche Virus RNA, Qualitative Real-Time Reverse Transcriptase (RT) PCR - This test is intended for the detection of Oropouche virus (OROV) RNA in serum or CSF from patients with exposure, signs or symptoms consistent with OROV infection. It can be used to help in the diagnosis of Oropouche fever infection during the acute phase of the disease, which is typically within 7 days post-symptom onset. Serological testing can be considered for confirmatory diagnosis during the convalescent phase of this disease (greater than 7 days). This molecular test cannot distinguish between closely related reassortant OROVs within the Orthobunyavirus genus including Madre de Dios Virus, ...

Test Details

Methodology

Real-Time Reverse Transcriptase Polymerase Chain Reaction (RT-PCR)

Assay Category

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.

Reference Range(s)

Not Detected

Alternative Name(s)

Arbovirus,Madre de Dios Virus,Iquitos Virus,Oropouche Fever,Perdoes Virus,Orthobunyavirus,OROV

LOINC® Codes, Performing Laboratory

Methodology

Real-Time Reverse Transcriptase Polymerase Chain Reaction (RT-PCR)
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.

Reference Range(s)

Not Detected

Alternative Name(s)

Arbovirus,Madre de Dios Virus,Iquitos Virus,Oropouche Fever,Perdoes Virus,Orthobunyavirus,OROV

Preferred Specimen(s)

1.5 mL serum or
1.5 mL CSF collected in a plastic sterile leak-proof container

Minimum Volume

0.5 mL

Transport Container

Plastic sterile leak-proof container

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 7 days
    Refrigerated: 14 days
    Frozen: 30 days

Reject Criteria

Samples using heparin as anticoagulant

Setup Schedule

1.5 mL serum or
1.5 mL CSF collected in a plastic sterile leak-proof container
0.5 mL
Plastic sterile leak-proof container
Room temperature
Room temperature: 7 days
Refrigerated: 14 days
Frozen: 30 days
Samples using heparin as anticoagulant
In-home collection may be available in your area for purchase through Quest Mobile.
Test Details

Clinical Significance

Test Resources

Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.

The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.

This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.

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