Influenza Type A and B and RSV RNA, Qualitative, Real-Time RT-PCR
Main ContentTest code: 16086
CPT code(s): 87631
Methodology: Real-time polymerase chain reaction (rt-pcr)
Reference range(s): Not detected
Alternative name(s): Flu A/B,RSV, Influenza virus A/B RNA, QL Real Time PCR
Methodology: Real-time polymerase chain reaction (PCR) laboratory developed test (LDT) . This test was developed and its performance characteristics have been determined by Focus Diagnostics. Performance characteristics refer to the analytical performance of the test. This test is performed pursuant to a license agreement with Roche molecular systems, Inc.
Clinical significance: This test is used to determine the presence of Influenza A or B 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.
Additional Preferred Specimen: Nasal swab with VCM medium
Supply: OF06 - Sputum Collection Tube
Preferred specimen(s): 0.85 ml nasopharyngeal, bronchial, or tracheal lavage/wash or sputum respiratory samples in a sterile leak-proof container.
Instructions: Collect 0.85 mL in a sputum collection kit or a sterile, plastic container with a leak-proof cap.
Alternative specimen(s): 0.85 ml nasopharyngeal, bronchial, or tracheal lavage/wash or sputum respiratory samples in a sterile leak-proof container.
Transport container: Leak-proof container
Transport temperature: Refrigerated (cold packs)
- Room temperature: 48 hours
- Refrigerated: 7 days
- Frozen: 30 days
For additional supply or collection device information, please contact DLO's Customer Service at (800) 891-2917, option 2.
The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed.
CLIA