Respiratory Virus Mini Panel by PCR
Also known as: RESPMINI
Use
The Respiratory Virus Mini Panel by PCR is used to confirm the presence of respiratory syncytial virus (RSV) or influenza viruses (Influenza A and B) in general inpatients and RSV in adults. This test is particularly important for the rapid and accurate diagnosis of respiratory infections, which can inform treatment decisions and infection control measures.
Special Instructions
Specimen source is required for testing. Specimens must be placed in viral transport media and refrigerated immediately. Ensure each specimen is in an individually sealed bag to prevent contamination or damage during transit.
Limitations
A negative result does not exclude the possibility of PCR inhibitors in the patient's specimen or that the nucleic acid is present below the limit of detection of the assay. It is also dependent on the quality of the specimen received, which must meet specific storage and transportation conditions to avoid degradation.
New York Approved
Methodology
PCR-based (RT-PCR)
Biomarkers
LOINC Codes
- 31208-2
- 34487-9
- 40982-1
- 40988-8
- 34487-9
- 40982-1
- 40988-8
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Bronchoalveolar Lavage
Volume
1 mL
Minimum Volume
0.5 mL
Container
Sterile container or viral transport media
Collection Instructions
Transfer 1 mL respiratory specimen to a sterile container. Available viral transport media can be obtained from ARUP Supply using ARUP Connect™ or by contacting ARUP Client Services.
Storage Instructions
Store and transport specimens refrigerated.
Causes for Rejection
Specimen not refrigerated immediately, improper container, damaged or leaking specimen bags.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | Unacceptable |
| Refrigerated | 4 days |
| Frozen | 1 month |
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