Influenza A (H5) Virus RNA, Qualitative Real-Time PCR, Respiratory

Influenza A (H5) Virus RNA, Qualitative Real-Time PCR, Respiratory

Test Code

13998
87502
13998
87502
Ordering Restrictions may apply. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection is not available in your area through Quest Mobile.

Clinical Significance

Influenza A (H5) Virus RNA, Qualitative Real-Time PCR, Respiratory - The Influenza A (H5) Virus RNA, Qualitative Real-Time PCR is a qualitative multi-target molecular diagnostic test that aids in the detection of the Influenza A H5 virus, including H5N1, commonly known as Avian Influenza. This test does not detect Influenza B or other respiratory viruses. This test is intended to be performed on respiratory specimens collected from individuals suspected of infection with Influenza A H5, or who meet the Centers for Disease Control and Prevention (CDC) clinical and/or epidemiological criteria for Influenza A H5N1 testing. For details visit:

Test Resources

Test FAQ

Influenza A (H5) Virus RNA, Qualitative Real-Time PCR, Respiratory and Conjunctiva

Test Details

Includes

  • Influenza A and Influenza H5

Methodology

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

Assay Category

This test is an Immediate Response test and can only be ordered by a licensed healthcare professional (for prescription use only). This test has not been reviewed or authorized by FDA. It was developed and its performance characteristics determined by Quest Diagnostics pursuant to CLIA regulations for clinical purposes.

This test is not available for New York patient testing.

Reference Range(s)

Influenza ANot detected
Influenza H5Not detected

Alternative Name(s)

H5N1,Avian Influenza A H5N1,H5,Avian Flu,Flu A

LOINC® Codes, Performing Laboratory

Service Area must be determined
Influenza A and Influenza H5

Methodology

Real-Time Reverse Transcriptase Polymerase Chain Reaction (RT-PCR)
This test is an Immediate Response test and can only be ordered by a licensed healthcare professional (for prescription use only). This test has not been reviewed or authorized by FDA. It was developed and its performance characteristics determined by Quest Diagnostics pursuant to CLIA regulations for clinical purposes.

This test is not available for New York patient testing.

Reference Range(s)

Influenza ANot detected
Influenza H5Not detected

Alternative Name(s)

H5N1,Avian Influenza A H5N1,H5,Avian Flu,Flu A
Service Area must be determined

Preferred Specimen(s)

1 swab nasopharyngeal, anterior nares, or oropharyngeal swab submitted in a VCM (green-cap), or equivalent (UTM) tube or
1 mL bronchial alveolar lavage (BAL)/wash collected in a sterile leak-proof container

Minimum Volume

1 swab • 1 mL

Collection Instructions

Each Influenza A H5 specimen should be accompanied by its own separate requisition and transported in its own sealed bag. If swabbing multiple upper respiratory sites, it is acceptable to place multiple swabs into one vial of VCM or equivalent. This test is not approved for observed-self collection at Quest Patient Service Centers.

Transport Container

VCM, UTM equivalent or Plastic leak-proof container

Transport Temperature

Refrigerated (cold packs)

Specimen Stability

  • Room temperature: 48 hours
    Refrigerated: 14 days
    Frozen: 30 days

Reject Criteria

Tubes containing guanidinium isothiocyanate (GITC) • Calcium alginate swabs • Cotton swabs with wooden shaft • Amies liquid or gel transport used for bacterial cultures • Tubes with clot activator • Glass tubes • Snap-cap tubes • 3D printed swabs

Setup Schedule

Service Area must be determined
1 swab nasopharyngeal, anterior nares, or oropharyngeal swab submitted in a VCM (green-cap), or equivalent (UTM) tube or
1 mL bronchial alveolar lavage (BAL)/wash collected in a sterile leak-proof container
1 swab • 1 mL
Each Influenza A H5 specimen should be accompanied by its own separate requisition and transported in its own sealed bag. If swabbing multiple upper respiratory sites, it is acceptable to place multiple swabs into one vial of VCM or equivalent. This test is not approved for observed-self collection at Quest Patient Service Centers.
VCM, UTM equivalent or Plastic leak-proof container
Refrigerated (cold packs)
Room temperature: 48 hours
Refrigerated: 14 days
Frozen: 30 days
Tubes containing guanidinium isothiocyanate (GITC) • Calcium alginate swabs • Cotton swabs with wooden shaft • Amies liquid or gel transport used for bacterial cultures • Tubes with clot activator • Glass tubes • Snap-cap tubes • 3D printed swabs
Service Area must be determined
Ordering Restrictions may apply. Please provide SERVICE AREA INFORMATION to find available tests you can order.
In-home collection is not available in your area 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.

The tests listed by specialty and category are a select group of tests offered. For a complete list of Quest Diagnostics tests, please adjust the filter options chosen, or refer to our Directory of Services.

Customize the test information for your Service Area