SARS-CoV-2 RNA, Influenza A/B, and RSV RNA, Qualitative NAAT : 39816

Test Code
CVFRSV or 39816


Alias/See Also
Novel Coronavirus, nCOV, COVID-19, COVID 19, Flu A/B, Wuhan, Coronavirus


CPT Codes
0241U

Includes
Includes: Influenza A RNA, Influenza B RNA,  RSV RNA, SARS CoV2 RNA 


Instructions
Cold packs/pouches should be used if placing specimens in a lockbox for courier pick-up. Each COVID-19/Flu AB/RSV specimen transport vial that is submitted should be accompanied by its own separate requisition and transported in its own sealed bag.


Transport Container
Preferred  Specimen:
One (1) nasopharyngeal or nasal swab collected in VCM, UTM, Saline, or equivalent media.

Alternate Specimen:
Nasal wash aspirate collected into VCM, UTM, Saline or equivalent media.

Minimum Volume:
1 swab in transport media; 1 swab in transport nasopharyngeal or nasal swab; 0.6 mL nasal wash aspirate in 3 mL viral transport.


Transport Temperature
Refrigerated.


Specimen Stability
Room temperature: 24 hours; Refrigerated: 7 days; Frozen: 30 days (-70 degrees Celsius)


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Calcium alginate swabs, Cotton swabs in wooden shaft, Amies liquid or gel transport for bacterial cultures, Tubes with clot activator, Glass tubes, Snap-cap tubes, 3D printed swabs, Media with guanidine isothiocyanate (GITC) due to safety concerns, Specimen at room temperature for >24 hours, Throat and lower respiratory samples, Transport tube with the swab inverted


Methodology
Real Time – Polymerase Chain Reaction (RT-PCR)

Setup Schedule
Sunday - Saturday


Report Available
1 day


Limitations
This test has been authorized by the FDA under an Emergency Use Authorization (EUA) for use by authorized laboratories.


Reference Range
Influenza A RNA Not detected 
Influenza B RNA Not detected 
RSV RNA Not detected 
SARS CoV2 RNA Not detected 


Clinical Significance
SARS-CoV-2 RNA, Influenza A/B, and RSV RNA, Qualitative NAAT - SARS-CoV-2 RNA, Influenza A/B, and RSV RNA, Qualitative NAAT is a multitarget molecular test that aids in simultaneous qualitative detection and differentiation of SARS-CoV-2 (COVID-19), influenza A, influenza B, and respiratory syncytial virus (RSV) viral RNA. This test is intended to be performed on respiratory specimens collected from individuals suspected of respiratory viral infection consistent with COVID-19 or influenza or RSV by their healthcare provider. Clinical signs and symptoms of respiratory viral infection due to SARS-CoV-2, influenza, and RSV can be similar.


Performing Laboratory
med fusion



The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.