Test Catalog

Test Id : FLUMS

Influenza Virus Type A and Type B, and Respiratory Syncytial Virus (RSV), Molecular Detection, PCR, Varies

Useful For
Suggests clinical disorders or settings where the test may be helpful

Rapid and accurate detection of influenza A, influenza B, and respiratory syncytial virus in a single test


This test should not be performed unless the patient meets clinical and epidemiologic criteria for testing.

Method Name
A short description of the method used to perform the test

Multiplex Real-Time Polymerase Chain Reaction (RT-PCR)

NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.


Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test

Influenza A/B and RSV, PCR, Misc

Lists additional common names for a test, as an aid in searching

Respiratory Syncytial Virus (RSV)



Specimen Type
Describes the specimen type validated for testing


Necessary Information

Specimen source is required.


Question ID Description Answers
SS020 Specimen Source

Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Submit only 1 of the following specimens:



Specimen Type: Nasal or nasopharyngeal aspirate

Container/Tube: Sterile container

Specimen Volume: 0.5 mL


Specimen Type: Throat, nasal, or nasal mid-turbinate swab

Supplies: Culturette (BBL Culture Swab) (T092)

Container/Tube: Sterile container with viral transport media

Collection Instructions:

1. Collect specimen by swabbing back and forth over mucosa surface to maximize recovery of cells.

2. Swab must be placed in viral transport media (for example, M4-RT, M4, or M5 media); BBL Culture Swab container includes a stabilizing media.



Specimen Type: Nasopharyngeal washing

Container/Tube: Sterile container

Specimen Volume: 0.5 mL


Specimen Type: Bronchial washing or bronchoalveolar lavage fluid

Container/Tube: Sterile container

Specimen Volume: 0.5 mL

Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory

0.3 mL

Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected

E-swab, calcium alginate-tipped swab, wood swab, dry swab, or transport swab containing gel Reject

Specimen Stability Information
Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included

Specimen Type Temperature Time Special Container
Varies Refrigerated (preferred) 7 days
Frozen 7 days

Useful For
Suggests clinical disorders or settings where the test may be helpful

Rapid and accurate detection of influenza A, influenza B, and respiratory syncytial virus in a single test


This test should not be performed unless the patient meets clinical and epidemiologic criteria for testing.

Clinical Information
Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

Influenza, otherwise known as the "flu," is an acute, contagious respiratory illness caused by influenza A, B, and C viruses. Of these, only influenza A and B are thought to cause significant disease, with infections due to influenza B usually being milder than infections with influenza A. Influenza A viruses are further categorized into subtypes based on the 2 major surface protein antigens: hemagglutinin (H) and neuraminidase (N).


Common symptoms of influenza infection include fever, chills, sore throat, muscle pains, severe headache, weakness, fatigue, and a nonproductive cough. Certain patients, including infants, older individuals, patients who are immunocompromised, and those with impaired lung function, are at risk for serious complications. In the United States, influenza results in approximately 36,000 deaths and more than 200,000 hospitalizations each year.(1)


In the northern hemisphere, annual epidemics of influenza typically occur during the fall or winter months. However, the peak of influenza activity can occur as late as April or May, and the timing and duration of flu seasons vary. In 2009 to 2010, a novel influenza virus (called 2009 H1N1, previously "swine" flu) appeared in Mexico and quickly spread worldwide, causing the first influenza pandemic in more than 40 years. The resultant influenza season had an atypical distribution, with illness occurring during normally low-incidence months. Following a pandemic, disease incidence usually returns to the typical seasonal distribution within 1 to 2 years.(1)


Influenza infection may be treated with supportive therapy, as well as antiviral drugs such as the neuraminidase inhibitors, oseltamivir (TAMIFLU) and zanamivir (RELENZA). These drugs are most effective when given within the first 48 hours of infection, so prompt diagnosis and treatment are essential for proper management.


Respiratory syncytial virus (RSV) is a respiratory virus that also infects the respiratory system and can cause an influenza-like illness. Most otherwise healthy people recover from RSV infection in 1 to 2 weeks. However, infection can be severe in infants, young children, and older adults. RSV is the most common cause of bronchiolitis (inflammation of the small airways in the lung) and pneumonia in children under 1 year of age in the United States, and is more frequently being recognized as an important cause of respiratory illness in older adults.(2)


RSV and influenza virus RNA can be detected by polymerase chain reaction (PCR) in respiratory secretions, including upper and lower respiratory specimens. Nasopharyngeal swabs or aspirates are the preferred specimen types for detection of RNA from influenza A, influenza B, and RSV. Nasal swabs have also been shown to provide equivalent yield to nasopharyngeal specimens for molecular detection of influenza A and B RNA, but not RSV RNA.(3,4) Tracheal aspirates are generally not acceptable for testing due to the viscous nature of these specimens.

Reference Values
Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.


Provides information to assist in interpretation of the test results

A positive test result indicates that the patient is presumptively infected with the indicated virus. The test does not indicate the stage of infection. Rarely, more than 1 virus may be detected from the same patient specimen. Laboratory test results should always be considered in the context of clinical observations and epidemiologic data in making a final diagnosis.


A negative test result suggests that the patient is not infected with influenza A, influenza B, or respiratory syncytial virus (RSV).

Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances

Given that influenza A and B and respiratory syncytial virus (RSV) are common and can cause an indistinguishable clinical disease, this test is offered only as a panel.


This test has been designed to minimize the likelihood of false-positive test results. However, should false-positive results occur, risks to patients could include a recommendation for quarantine of household or other close contacts, a recommendation for patient isolation that might limit contact with family or friends, the ability to work, or the ability to receive certain medical care, prescription of an antiviral drug or other therapy, or other unintended adverse effects.


The sensitivity of the assay is very dependent upon the quality of the specimen submitted. Nasopharyngeal swabs or aspirates are the preferred specimen types and are optimal for detection of RSV RNA. However, the test is validated for use with most upper and lower respiratory specimens, including nasal swabs, throat swabs, bronchoalveolar lavage specimens, and bronchial washings. Tracheal aspirates are not acceptable for testing due to the viscous nature of these specimens.


The test is specific for influenza A, influenza B, and RSV; therefore, the results do not exclude the possibility of infection with other respiratory viruses. Influenza C virus is not detected by this assay.


This assay detects influenza A virus RNA, but does not distinguish between the different subtypes of influenza A.


Negative results do not preclude infection with influenza A, influenza B, or RSV viruses and should not be used as the sole basis for treatment or other patient management decisions.


This assay detects both viable and nonviable virus. Test performance depends on viral load in the specimen and may not correlate with cell culture performed on the same specimen.


The assay has not been Food and Drug Administration approved for detection of Influenza A H7N9, though comparison of primer and probe sequences suggest that the assay will detect the H7N9 virus.

Supportive Data


To assess accuracy, clinical or spiked specimens were tested by the proposed Simplexa Flu A/B and respiratory syncytial virus (RSV) assay and the results compared to those of the current method (Gen-Probe/Hologic ProFlu assay).


Table 1. Comparison of the proposed Simplexa assay to the Gen-Probe/Hologic ProFlu assay using clinical and spiked samples (n=60).






Respiratory Non-Swab

Influenza A




Respiratory Non-Swab

Influenza B




Respiratory Non-Swab





Clinical Reference
Recommendations for in-depth reading of a clinical nature

1. Centers for Disease Control and Prevention. Influenza (Flu). Reviewed July 2, 2020. Accessed July 8, 2020. Available at www.cdc.gov/flu/

2. Lee N, Lui GC, Wong KT, et al: High morbidity and mortality of adults hospitalized for respiratory syncytial virus infections. Clin Infect Dis. 2013;57(8):1069-1077

3. Meerhoff TJ, Houben ML, Coenjaerts FE, et al: Detection of multiple respiratory pathogens during primary respiratory infection: nasal swab versus nasopharyngeal aspirate using real-time polymerase chain reaction. Eur J Clin Microbiol Infect Dis. 2010;29:365-371

4. Heikkinen T, Marttila J, Salmi AA, Ruuskanen O: Nasal swab versus nasopharyngeal aspirate for isolation of respiratory viruses. J Clin Microbiol. 2002;40(11):4337-4339

Method Description
Describes how the test is performed and provides a method-specific reference

The Simplexa Flu A/B and respiratory syncytial virus (RSV) direct assay system is a real-time reverse transcription polymerase chain reaction (RT-PCR) assay for the in vitro qualitative direct detection and differentiation of influenza A virus, influenza B virus, and RSV RNA directly from clinical samples. The system consists of the Simplexa Flu A/B and RSV direct assay, the 3M Integrated Cycler (with Integrated Cycler Studio Software), the Direct Amplification Disc and associated accessories.


The test is a real-time RT-PCR amplification and detection system that utilizes a bifunctional fluorescent probe-primer for the detection and differentiation of human influenza A virus RNA, human influenza B virus RNA and RSV RNA in nasopharyngeal swabs (NPS). The assay is composed of 2 principal steps: (1) extraction of RNA from patient specimens, (2) a bifunctional fluorescent probe-primer is used together with a reverse primer to amplify a specific target (for each analyte and the RNA internal control). The assay targets 3 viral gene segments, including conserved regions of influenza A virus (matrix gene), influenza B virus (matrix gene), and RSV (M gene). An RNA internal control is used to monitor the extraction process and to detect RT-PCR inhibition.(Package Insert: Simplexa Flu A/B and RSV Direct. DiaSorin; 09/2015)

PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information


Day(s) Performed
Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.

Monday through Sunday

Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

Same day/1 to 2 days

Specimen Retention Time
Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

14 days

Performing Laboratory Location
Indicates the location of the laboratory that performs the test


Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.

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  • Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
  • Prospective clients should contact their account representative. For assistance, contact Customer Service.

Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

This test has been modified from the manufacturer's instructions. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.

CPT codes are provided by the performing laboratory.


LOINC® Information
Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

Test Id Test Order Name Order LOINC Value
FLUMS Influenza A/B and RSV, PCR, Misc 92143-7
Result Id Test Result Name Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
SS020 Specimen Source 31208-2
35980 Influenza A, PCR In Process
35981 Influenza B, PCR In Process
35982 Respiratory Syncytial Virus, PCR In Process

Test Setup Resources

Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | PHP Pdf | CMS Pdf

Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports