Respiratory Syncytial Virus (RSV) RNA, Qualitative Real-Time PCR
Use
This test is used to determine the presence of respiratory syncytial virus (RSV) in a patient's specimen. Organisms may be detected by PCR prior to diagnosis by immunological methods. PCR provides more rapid results than other methods, including culture.
Special Instructions
Not provided.
Limitations
This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes. It has not been cleared or approved by the FDA. Specimens containing calcium alginate swabs; specimens containing heparin; samples in uncapped or broken container; leaking samples; specimens other than bronch lavage, bronch wash, nasopharyngeal or throat swabs, nasopharyngeal aspirate, sputum may cause the specimen to be rejected.
New York Approved
Methodology
PCR-based (qPCR)
Biomarkers
Respiratory Syncytial Virus
Microorganism
LOINC Codes
- 40988-8 - RSV RNA Spec Ql NAA+probe
- 31208-2 - Specimen source
- 40988-8 - RSV RNA Spec Ql NAA+probe
Result Turnaround Time
3-7 days
Related Documents
For more information, please review the documents below
Specimen
Bronchoalveolar Lavage
Volume
2 mL
Minimum Volume
0.6 mL
Container
Sterile container
Collection Instructions
Collect in a sterile leak-proof container (no media or preservative). Ship refrigerated.
Causes for Rejection
Specimens containing calcium alginate swabs; specimens containing heparin; Samples in uncapped or broken container; leaking samples; specimens other than bronch lavage, bronch wash, nasopharyngeal or throat swabs, nasopharyngeal aspirate, sputum
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 7 days |
| Refrigerated | 14 days |
| Frozen | 30 days |