Test ID RPB Respiratory Panel, PCR, Varies
Ordering Guidance
This assay is not predicted to detect severe acute respiratory syndrome (SARS)-associated coronavirus or Middle East respiratory syndrome (MERS)-coronavirus.
This test is appropriate for bronchoalveolar lavage or bronchial washings only. For nasopharyngeal swab specimens order RP / Respiratory Panel, PCR, Nasopharyngeal.
This test is not intended for otherwise healthy, immunocompetent patients who are likely to have a mild, self-limited respiratory infection. If testing is desired, these patients should be tested using the more targeted diagnostic assays based on their exposure history and clinical presentation. These tests are also not recommended to be concomitantly ordered when this test is ordered.
-HPFLU / Influenza Virus Type A and Type B, and Respiratory Syncytial Virus (RSV), Molecular Detection, PCR, Nasopharyngeal Swab
-LADV / Adenovirus, Molecular Detection, PCR, Varies
-LENT / Enterovirus, Molecular Detection, PCR, Varies
-BPRPV / Bordetella pertussis and Bordetella parapertussis, Molecular Detection, PCR, Varies
-MPRP / Mycoplasma pneumoniae, Molecular Detection, PCR, Varies
-COVID / Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) RNA Detection, PCR, Varies
Shipping Instructions
Specimens that cannot be shipped refrigerated to Mayo Clinic Laboratories within 3 days (72 hours) should be frozen prior to shipment. Specimens received older than 72 hours (refrigerated) or older than 30 days (frozen) will be canceled.
Specimen Required
Specimen Type: Respiratory fluid
Sources: Bronchoalveolar lavage (BAL) or bronchial washing
Collection Container/Tube: Sterile container
Specimen Volume: 1 mL
Useful For
Rapid detection of respiratory infections caused by the following:
-Adenovirus
-Coronavirus (serotypes HKU1, NL63, 229E, OC43)
-SARS-CoV-2
-Human metapneumovirus
-Human rhinovirus/enterovirus
-Influenza A (H1, H1-2009, H3)
-Influenza B
-Parainfluenza virus (serotypes 1-4)
-Respiratory syncytial virus (RSV)
-Bordetella pertussis
-Bordetella parapertussis
-Chlamydia pneumoniae
-Mycoplasma pneumoniae
This test is not recommended as a test of cure.
Highlights
This test is a multiplex polymerase chain reaction test capable of qualitatively detecting DNA or RNA of 22 pathogens (bacteria and viruses) in approximately 1 hour using bronchoalveolar lavage and bronchial washing specimens.
This test may diagnose infections caused by adenovirus, coronavirus (HKU1, NL63, 229E, OC43), SARS-CoV-2, human metapneumovirus, human rhinovirus/enterovirus, influenza A (H1, H1-2009, H3), influenza B, parainfluenza (1, 2, 3, 4), respiratory syncytial virus, Bordetella pertussis, Bordetella parapertussis, Chlamydia pneumoniae, and Mycoplasma pneumoniae.
Testing Algorithm
For information see Coronavirus Disease 2019 (COVID-19), Influenza, and Respiratory Syncytial Virus Testing Algorithm.
Special Instructions
Method Name
Multiplex Polymerase Chain Reaction (PCR)
Reporting Name
Respiratory Panel, PCR, VSpecimen Type
VariesSpecimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Varies | Refrigerated (preferred) | 72 hours | |
Frozen | 30 days | ||
Ambient | 4 hours |
Reference Values
Undetected (for all targets)
Day(s) Performed
Monday through Sunday
Report Available
1 to 2 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
0202U
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
RPB | Respiratory Panel, PCR, V | 92958-8 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
SSRPB | Specimen Source | 31208-2 |
610529 | Adenovirus | 92987-7 |
610530 | Coronavirus 229E | 94479-3 |
610531 | Coronavirus HKU1 | 94480-1 |
610532 | Coronavirus NL63 | 94481-9 |
610533 | Coronavirus OC43 | 94482-7 |
610534 | SARS Coronavirus-2 | 95608-6 |
610535 | Human Metapneumovirus | 92978-6 |
610536 | Human Rhinovirus/ Enterovirus | 92956-2 |
610537 | Influenza A | 92977-8 |
610538 | Influenza B | 92976-0 |
610539 | Parainfluenza Virus 1 | 94483-5 |
610540 | Parainfluenza Virus 2 | 94484-3 |
610541 | Parainfluenza Virus 3 | 94485-0 |
610542 | Parainfluenza Virus 4 | 94486-8 |
610543 | Respiratory Syncytial Virus | 92957-0 |
610544 | Bordetella pertussis | 94478-5 |
610545 | Bordetella parapertussis | In Process |
610546 | Chlamydia pneumoniae | 92986-9 |
610547 | Mycoplasma pneumoniae | 92964-6 |
610548 | Interpretation | 59464-8 |
NY State Approved
YesReflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
RPMPM | M. pneumoniae Macrolide Resist PCR | Yes | No |