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25247 Respiratory Panel by PCR

Respiratory Panel by PCR
Test Code: FARP
Synonyms/Keywords
​Respiratory Virus, Virus Culture, Flu, RSV, Adeno, Entero, Rhino Virus
Test Components
​Adenovirus, Coronavirus 229E, Coronavirus HKU1, Coronavirus NL63, Coronavirus OC43, Enterovirus/Rhinovirus, Human Metapneumovirus, Influenza A H1, Influenza A H1-2009, Influenza A H3, Influenza B, Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, Parainfluenza 4, Respiratory Syncytial Virus, Bordetella pertussis, Chlamydophilia pneumoniae,  and Mycoplasma pneumoniae.
Useful For
​RESTRICTED USE:
Test is available for ordering by Marshfield Medical Center, St. Clare's Hospital, Flambeau Hospital and MMC-Rice Lake.  Marshfield Center is the only performing site.  Not available to Outreach clients at this time.
Not for routine diagnosis of viral syndrome illness. To be used in serious lower respiratory illness in urgent care/emergency room/intensive care settings. The FilmArray® Respiratory Panel is used for the qualitative detection and identification of multiple respiratory viral and bacterial nucleic acids in nasopharyngeal (NP) swabs and bronchoalveolar lavage fluid or bronchial washings from individuals with suspected respiratory tract infections.  The panel detects the following upper respiratory viruses and bacteria: Adenovirus, Coronavirus 229E, Coronavirus HKU1,Cornavirus NL63, Coronavirus OC43, Human Metapneumovirus, Influenza A, Influenza A subtype H1, Influenza A subtype H3, Influenza A subtype H1-2009, Influenza B, Parainfluenza virus 1, Parainfluenza virus 2, Parainfluenza virus 3, Parainfluenza virus 4, Human Rhinovirus/Enterovirus, Respiratory Syncytial virus, Bordetella pertussis, Chlamydophila pneumoniae, and Mycoplasma pneumonia.
 
For more information on Specimen Collection Media/Swab,
Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)		 Pediatric Minimum Volume
(no repeat)
​No Nasopharyngeal swab​ Viral transport media​ ​ ​1 swab ​ ​
No​ ​Bronchial Lavage (BAL) or Wash ​Sterile leakproof container ​ ​1.0 mL ​0.5 mL ​0.5 mL
Specimen Stability Information
Specimen​ Temperature Time
NP Swab​ ​ ​ Room Temperature​ ​4 hours
​Refrigerate ​3 days
​Frozen ​30 days
​Bronchial Lavage or Wash ​ ​Room Temperature 4 hours
​Refrigerate ​3 days
Rejection Criteria

Specimens from sites other than nasopharyngeal and bronchial.

Specimens received passed specimen stability time limits.

Specimens that leak in transit.

Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Marshfield Labs Monday through Sunday​ ​1 day PCR/FilmArray®
Test Information
This test was developed and its performance characteristics determined by Marshfield Labs. This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) to perform high complexity testing.
 
This information applies only to bronchial specimens only.​
 
FilmArray® is a registered trademark of BioFire Diagnostics, LLC.
Reference Range Information
Not Detected
Outreach CPTs
CPT Modifier
(if needed)		 Quantity Description Comments
​87633 ​ ​ ​Respiratory agents, multiplex amplification ​
Classification
This test was developed and its performance characteristics determined by Marshfield Labs. This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) to perform high complexity testing.
​
Synonyms/Keywords
​Respiratory Virus, Virus Culture, Flu, RSV, Adeno, Entero, Rhino Virus
Test Components
​Adenovirus, Coronavirus 229E, Coronavirus HKU1, Coronavirus NL63, Coronavirus OC43, Enterovirus/Rhinovirus, Human Metapneumovirus, Influenza A H1, Influenza A H1-2009, Influenza A H3, Influenza B, Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, Parainfluenza 4, Respiratory Syncytial Virus, Bordetella pertussis, Chlamydophilia pneumoniae,  and Mycoplasma pneumoniae.
Ordering Applications
Ordering Application Description
​Cerner ​Respiratory Viral Panel by PCR
COM​​ ​Respiratory Viral Panel by PCR
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Fasting Required Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)		 Pediatric Minimum Volume
(no repeat)
​No Nasopharyngeal swab​ Viral transport media​ ​ ​1 swab ​ ​
No​ ​Bronchial Lavage (BAL) or Wash ​Sterile leakproof container ​ ​1.0 mL ​0.5 mL ​0.5 mL
Specimen Stability Information
Specimen​ Temperature Time
NP Swab​ ​ ​ Room Temperature​ ​4 hours
​Refrigerate ​3 days
​Frozen ​30 days
​Bronchial Lavage or Wash ​ ​Room Temperature 4 hours
​Refrigerate ​3 days
Rejection Criteria

Specimens from sites other than nasopharyngeal and bronchial.

Specimens received passed specimen stability time limits.

Specimens that leak in transit.

Useful For
​RESTRICTED USE:
Test is available for ordering by Marshfield Medical Center, St. Clare's Hospital, Flambeau Hospital and MMC-Rice Lake.  Marshfield Center is the only performing site.  Not available to Outreach clients at this time.
Not for routine diagnosis of viral syndrome illness. To be used in serious lower respiratory illness in urgent care/emergency room/intensive care settings. The FilmArray® Respiratory Panel is used for the qualitative detection and identification of multiple respiratory viral and bacterial nucleic acids in nasopharyngeal (NP) swabs and bronchoalveolar lavage fluid or bronchial washings from individuals with suspected respiratory tract infections.  The panel detects the following upper respiratory viruses and bacteria: Adenovirus, Coronavirus 229E, Coronavirus HKU1,Cornavirus NL63, Coronavirus OC43, Human Metapneumovirus, Influenza A, Influenza A subtype H1, Influenza A subtype H3, Influenza A subtype H1-2009, Influenza B, Parainfluenza virus 1, Parainfluenza virus 2, Parainfluenza virus 3, Parainfluenza virus 4, Human Rhinovirus/Enterovirus, Respiratory Syncytial virus, Bordetella pertussis, Chlamydophila pneumoniae, and Mycoplasma pneumonia.
 
For more information on Specimen Collection Media/Swab,
Test Components
​Adenovirus, Coronavirus 229E, Coronavirus HKU1, Coronavirus NL63, Coronavirus OC43, Enterovirus/Rhinovirus, Human Metapneumovirus, Influenza A H1, Influenza A H1-2009, Influenza A H3, Influenza B, Parainfluenza 1, Parainfluenza 2, Parainfluenza 3, Parainfluenza 4, Respiratory Syncytial Virus, Bordetella pertussis, Chlamydophilia pneumoniae,  and Mycoplasma pneumoniae.
Reference Range Information
Not Detected
For more information visit:
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Marshfield Labs Monday through Sunday​ ​1 day PCR/FilmArray®
For billing questions, see Contacts
Outreach CPTs
CPT Modifier
(if needed)		 Quantity Description Comments
​87633 ​ ​ ​Respiratory agents, multiplex amplification ​
Classification
This test was developed and its performance characteristics determined by Marshfield Labs. This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) to perform high complexity testing.
​
For most current information refer to the Marshfield Laboratory online reference manual.