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SARS-CoV-2 RNA (COVID-19) and Influenza A and B, Qualitative NAAT : 31688
Test CodeQCVFLU or 31688
Alias/See Also
COVID19, Novel Coronavirus, nCOV, Wuhan, Coronavirus
CPT Codes
87636
Instructions
Each COVID-19 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 (NP) swab collected in VCM (UTM) medium tube, UTM-RT or equivalent Viral Transport Media (VTM); phosphate buffered saline (PBS) or 0.9% physiological saline
OR
One (1) nasal swab (Anterior Nares) collected in VCM (UTM) medium tube or equivalent Viral Transport Media (VTM); 0.9% physiological saline; phosphate buffered saline (PBS)
Minimum Volume
1 swab or 1 mL
One (1) nasopharyngeal (NP) swab collected in VCM (UTM) medium tube, UTM-RT or equivalent Viral Transport Media (VTM); phosphate buffered saline (PBS) or 0.9% physiological saline
OR
One (1) nasal swab (Anterior Nares) collected in VCM (UTM) medium tube or equivalent Viral Transport Media (VTM); 0.9% physiological saline; phosphate buffered saline (PBS)
Minimum Volume
1 swab or 1 mL
Transport Temperature
Refrigerated.
Specimen Stability
Room temperature: 7 days
Refrigerated: 14 days
Frozen:
Nasopharyngeal swab or Nasal (Anterior Nares) swab collected in VCM (UTM) medium tube, UTM-RT or equivalent Viral Transport media (VTM): 30 days
Nasal (Anterior Nares) swab collected in 0.9% physiological saline: 7 days
Nasopharyngeal swab or Nasal (Anterior Nares) swab collected in phosphate buffered saline (PBS): Unacceptable
Refrigerated: 14 days
Frozen:
Nasopharyngeal swab or Nasal (Anterior Nares) swab collected in VCM (UTM) medium tube, UTM-RT or equivalent Viral Transport media (VTM): 30 days
Nasal (Anterior Nares) swab collected in 0.9% physiological saline: 7 days
Nasopharyngeal swab or Nasal (Anterior Nares) swab collected in phosphate buffered saline (PBS): Unacceptable
Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Calcium alginate swabs; Cotton swabs with wooden shaft; Amies liquid or gel transport used for bacterial cultures
Methodology
Nucleic Acid Amplification Test (NAAT) includes RT-PCR or TMA
Setup Schedule
Monday - Saturday
Report Available
1-3 days (From receipt at performing laboratory)
Limitations
This test has been authorized by the FDA under an Emergency Use Authorization (EUA) for use by authorized laboratories.
Reference Range
FLU A Not detected
FLU B Not detected
SARS CoV 2 RNA Not detected
FLU B Not detected
SARS CoV 2 RNA Not detected
Clinical Significance
SARS-CoV-2 RNA (COVID-19) and Influenza A and B, Qualitative NAAT is a qualitative multi-target molecular diagnostics test that aids in simultaneous detection of COVID-19, influenza A and influenza B. This test is intended to be performed on respiratory specimens collected by a healthcare provider from individuals suspected of respiratory viral infection consistent with COVID-19 or influenza.
Performing Laboratory
Quest Diagnostics