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GENERAL COLLECTION INFORMATION
Collection Tubes
Proper Order of Draw
NEW TESTS
New Tests

Influenza A H1N1 (2009) Real-Time RT-PCR - (16807)

Influenza A H1N1 (2009) Real-Time RT-PCR

16807


CPT Code(s): 87798 (x2)
FDA authorized this test under an Emergency Use Authorization. Please refer to health care provider and patient fact sheets at www.QuestDiagnostics.com/2009H1N1Physician and www.QuestDiagnostics.com/2009H1N1Patient for more information.

This test is performed pursuant to a license agreement with Roche Molecular Systems, Inc.
Includes
Influenza A RNA and 2009 Influenza H1 Gene
Preferred Specimen(s)
Nasal swabs, nasopharyngeal swabs, throat swabs, or nasal aspirates in 3 mL viral transport media, V-C-M medium (green-cap) tube or equivalent (UTM), or multimicrobe media (M4)
Instructions
Use only sterile swabs: Dacron ®, nylon, or rayon with plastic shafts. DO NOT use calcium alginate swabs.
Transport Container
Viral transport media, V-C-M medium (green-cap) tube or equivalent (UTM) or multimicrobe media (M4)
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Room temperature: 48 hours
Refrigerated: 7 days
Frozen: 30 days
Reject Criteria
Sputum • Bronchial lavage
Methodology
Real-Time Reverse Transcriptase Polymerase Chain Reaction (RT-PCR)
Reference Range(s)
Not detected
Clinical Significance
Aid in the detection and differentiation of seasonal influenza A virus infection and infection by the 2009 H1N1 influenza virus.
Aliases
H1N1
(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 payer being billed.)