Test Code RESPCOVID Respiratory Panel with SARS-CoV-2 PCR
Additional Codes
ALAB: RESPCOVID
PowerChart: Respiratory Pathogen Panel PCR with COVID-19
MA Cerner: Respiratory Panel with SARS-CoV-2 PCR
Specimen Requirement
Nasopharyngeal specimen is required using the flexible mini-tipped swab and Universal Transport Media (UTM) tube (Diagnostics Hybrids #403CP).
Additional Specimen Collection Information
Flexible flocked nasopharyngeal swab in universal transport media. The flocked swab and UTM kit is available from the laboratory by calling the Client Liaison (563-690-4129) or Microbiology Dept (563-589-9991). The specimen must be transported to the lab at refrigerated temperature using cold packs, wet ice or other refrigerant coolants.
Collect the nasopharyngeal swab:
- Open the sterile, flexible mini-tipped swab package and remove the swab.
- Tilt the patient’s head back (head should be inclined from vertical).
- Gently insert the sterile swab along the nasal septum just above the floor of the passage to the nasopharynx until resistance is met.
- Rotate the swab gently against the nasopharyngeal mucosa for 10-15 seconds and then gently remove the swab.
- Insert the swab into the UTM tube pushing it all the way to the bottom of the tube.
- Holding the swab shaft close to the rim of the tube and point the tube away, break the swab shaft along the pre-scored breakpoint indentation.
- Label the specimen appropriately with two identifiers, patient name and another identifier, (patient ID number, DOB, etc.) include specimen source, date and time of collection.
- Transport the specimen to the laboratory immediately after collection. When transporting specimens, use cold pack, wet ice or other refrigerant coolants. If specimen testing will be delayed the specimen in UTM may be held at room temperatue (18-30 C) for up to 4 hours, at refrigerator temperature (2-8 C) for up to 3 days, or at freezer temperature (<-15 C) for up to 30 days.
Useful For
Evaluating patients suspected of having a respiratory viral or bacterial infection.
Fact sheets for this Emergency Use Authorization (EUA) assay can be found at the following links:
For Healthcare Providers:
https://docs.biofiredx.com/wp-content/uploads/BFR0000-9067-RP2.1-EUA-Provider-Fact-Sheet-3.pdf
For Patients: https://docs.biofiredx.com/wp-content/uploads/BFR0000-9066-RP2.1-EUA-Patient-Fact-Sheet-1.pdf
Performance
Test performed Monday through Sunday.
Typically completed within 24 hours after the specimen arrives at the testing site.
CPT Code Information
0202U
LOINC Code Information
94565-9 (SARS-CoV-2-specific)
Test Method
Nested Multiplex PCR (nmPCR) and High Resolution Melting Analysis; FilmArray
Reference Values
Respiratory Syncytial Virus: Not detected
Adenovirus: Not detected
Coronavirus HKU1: Not detected
Coronavirus NL63: Not detected
Coronavirus 229E: Not detected
Coronavirus OC43: Not detected
Human Rhinovirus/Enterovirus: Not detected
Human Metapneumovirus: Not detected
Influenza A/H1: Not detected
Influenza A/H1-2009: Not detected
Influenza A/H3: Not detected
Influenza B: Not detected
Parainfluenza 1: Not detected
Parainfluenza 2: Not detected
Parainfluenza 3: Not detected
Parainfluenza 4: Not detected
Bordetella pertussis: Not detected
Bordetella parapertussis: Not detected
Chlamydophila pneumoniae: Not detected
Mycoplasma pneumoniae: Not detected
Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2):
Not Detected
SARS-CoV-2 Critical Value: Detected