Respiratory Pathogen Panel PCR
Use
The detection and identification of specific pathogen nucleic acids from individuals exhibiting signs and symptoms of respiratory infection aids in proper diagnosis. This assay facilitates differentiation between multiple viral and bacterial pathogens to guide clinical decision-making.
Special Instructions
Not provided.
Limitations
This assay will not detect SARS‑CoV‑2 (COVID‑19). Results should be used in conjunction with other clinical and laboratory findings.
Methodology
Other
Biomarkers
LOINC Codes
- 76070‑2
- 88604‑4
- 88618‑4
- 88610‑1
- 88626‑7
- 77024‑8
- 76078‑5
- 77026‑3
- 77027‑1
- 76080‑1
- 76084‑3
- 76085‑0
- 76086‑8
- 76087‑6
- 40991‑2
- 77022‑2
- 77023‑0
- 91804‑5
- 92577‑6
- 88613‑5
- 8251‑1
Result Turnaround Time
1 day
Related Documents
For more information, please review the documents below
Specimen
Nasal Swab
Volume
Not provided
Minimum Volume
One swab in transport
Container
V‑C‑M medium (green or purple cap) or equivalent (M4 or M4RT)
Collection Instructions
Swab must be sterile Dacron, nylon or rayon with plastic shafts. Place swab in sterile viral transport media containing protein stabilizer, antibiotics and buffer.
Causes for Rejection
Received room temperature; sources other than nasopharyngeal
Stability Requirements
| Temperature | Period |
|---|---|
| Refrigerated | 7 days |