CPT code for the rapid flu test. Seventy-six patients, who were negative for all respiratory tract viruses, were included as the control group. Rapid Immunoassay for Direct Detection and . The codes are for multi-virus tests that can detect both COVID-19 and other viruses, like the flu. CPT codes, descriptions and other data only are copyright 2022 American Medical Association. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Please review and accept the agreements in order to view Medicare Coverage documents, which may include licensed information and codes. Applications are available at the American Dental Association web site. The LOINC codes are copyright 1994-2021, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. Next video. ID NOW Influenza A & B 2 Product Insert 4. Rapid influenza diagnostic tests (RIDTs) RIDTs, also called flu antigen tests, are the most common type of flu test. Title XVIII of the Social Security Act (SSA) 1833(e) prohibits Medicare payment for any claim lacking the necessary documentation to process the claim. Code 87804 (infectious agent antigen detection by immunoassay with direct optical observation; influenza) is appropriate for these tests, which are Clinical Laboratory Improvement Amendments (CLIA) waived (ie . that coverage is not influenced by Bill Type and the article should be assumed to While every effort has been made to provide accurate and However, please note that once a group is collapsed, the browser Find function will not find codes in that group. CPT code (s): 87804 (x2) Methodology: Optical Immunoassay. Current Dental Terminology © 2022 American Dental Association. 23-043-070. RIDTs can provide results within approximately 15 minutes. not endorsed by the AHA or any of its affiliates. The AMA disclaims responsibility for any consequences or liability attributable to or related to any use, non-use, or interpretation of information contained or not contained in this file/product. Room Temperature. Residents and fellows deciding on a practice setting should be armed with all the relevant details. You can collapse such groups by clicking on the group header to make navigation easier. As the only medical association that convenes 190+ state and specialty medical societies and other critical stakeholders, the AMA represents physicians with a unified voice to all key players in health care. Absence of a Bill Type does not guarantee that the article does not apply to that Bill Type. The scope of this license is determined by the AMA, the copyright holder. Influenza Viruses Detected Influenza A Virus Subtypes Differentiated Other Respiratory Viruses Differentiated Approved Specimens 3 Test Time 4; High, Moderate: BioFire Diagnostics, LLC (Commercially Available) BioFire Respiratory Panel 2.1 (RP2.1) Nucleic Acid Detection: FILMARRAY 2.0 and FILMARRAY TORCH systems: Influenza A, Influenza B: A . HOWEVER, WHAN ANOTHER ALREADY ESTABLISHED MODIFIER IS APPROPRIATE IT SHOULD BE USED RATHER THAN MODIFIER -59. In the United States, a number of RIDTs are commercially available. RT-PCR or other amplification methods to detect viral nucleic acids, Results available in < 24 hours (often in less than 2-4 hours), Detects from 1-2 to up to 20 respiratory pathogens from 1 specimen. Alternative name (s): Influenza A&B EIA; Rapid Flu; Rapid Influenza. The document is broken into multiple sections. According to the FDA, in individuals with symptoms, the home test correctly identified 99.3% of negative and 90.1% of positive Influenza A samples, 100% of negative and 88.3% of positive COVID-19 . In addition, we will perform experimental evolution in Escherichia coli and influenza to test hypotheses related to the change of fitness effects across environments, and to adaptation by means of highly epistatic mutations. According to the EUA, it correctly correctly identified 99.3% of negative and 90.1% of positive flu A samples; 99.9% of negative flu B samples; and 100% of negative and 88.3% of positive COVID-19 . Will the QuickVue Influenza A+B Test specify that a patient has avian influenza? Complete absence of all Revenue Codes indicates Follow manufacturers instructions, including handling of respiratory specimens, as described in the device package insert. of the Medicare program. You agree to take all necessary steps to insure that your employees and agents abide by the terms of this agreement. You can use your browser's Print function (Ctrl-P on a PC or Command-P on a Mac) to view a print preview and then select PDF as the output. The client will not be telephoned to approve this charge. A positive result (on testing of an upper respiratory tract specimen) in a person who recently received intranasal administration of live attenuated influenza virus vaccine (LAIV) may indicate detection of vaccine virus. If you are acting on behalf of an organization, you represent that you are authorized to act on behalf of such organization and that your acceptance of the terms of this agreement creates a legally enforceable obligation of the organization. THE UNITED STATES Room temperature (15C to 30C/59F to 86F) Internal controls. Draft articles have document IDs that begin with "DA" (e.g., DA12345). 352 0 obj <>stream THIS MAY REPRESENT A DIFFERENT SESSION OR PATIENT ENCOUNTER, DIFFERENT PROCEDURE OR SURGERY, DIFFERNET SITE OR ORGAN SYSTEM, SEPARATE INCISION/EXCISION, SEPARATE LESION, OR SEPARATE INJURY (OR AREA OF INJURY IN EXTENSIVE INJURIES) NOT ORDINARILY ENCOUNTERED OR PERFORMED ON THE SAME DAY BY THE SAME PHYSICIAN. CPT codes, descriptions and other data only are copyright 2022 American Medical Association. An asterisk (*) indicates a In accordance with the above revision, the CPT Editorial Panel approved a new category I code, 87811, to report infectious agent antigen detection by immunoassay with direct visual observation. Please help me in coding this. "The new CPT code for antigen testing to detect the coronavirus is the latest in a series of CPT codes developed in rapid response to the pandemic," said AMA President Susan R. Bailey, M.D. By clicking below on the button labeled "I accept", you hereby acknowledge that you have read, understood and agreed to all terms and conditions set forth in this agreement. Complete absence of all Bill Types indicates The ability to use just one swab during a healthcare visit, rather than four separate tests, aims to decrease discomfort, lessen cost demands for doctors and lab workers . MACs are Medicare contractors that develop LCDs and Articles along with processing of Medicare claims. preparation of this material, or the analysis of information provided in the material. Re-evaluation of test . opportunity for Oseltamivir (Tamiflu) treatment for positive patients, Results available in approximately 2-4 hours, Article - Billing and Coding: Influenza Diagnostic Tests (A59055). These tests provide results in 10-15 minutes and differentiate between influenza A and B. Article document IDs begin with the letter "A" (e.g., A12345). It is typified by the Quidel's QuickVue Influenza test. Making copies or utilizing the content of the UB‐04 Manual, including the codes and/or descriptions, for internal purposes, Intended for the qualitative detection ofinfluenza type A and type B nucleoproteinantigens directly from nasal andnasopharyngeal swab specimens frompatients with signs and symptoms ofrespiratory infection. Consider sending respiratory specimens (from symptomatic patients) for RT-PCR to confirm results of RIDTs, especially in the following situations: When community influenza activity is low and the rapid diagnostic test result is positive. The laboratory has the capacity for a maximum of 8 rapid tests (FABRCV + NCVRPD) every hour. Submit one specimen per test requested. Response to Comment (RTC) articles list issues raised by external stakeholders during the Proposed LCD comment period. 87426 Infectious agent antigen detection by immunoassay technique, (eg, enzyme immunoassay [EIA], enzyme-linked immunosorbent assay [ELISA], fluorescence immunoassay [FIA], immunochemiluminometric assay [IMCA]) qualitative or semiquantitative; severe acute respiratory syndrome coronavirus (eg, SARS-CoV, SARS-CoV-2 [COVID-19]). The Alinity m Resp-4-Plex assay was validated with nasopharyngeal swabs. Best answers. Sofia 2 with Advance Result Technology (ART) delivers accurate, objective and automated results in as few as three minutes. Qty Check Availability. In no event shall CMS be liable for direct, indirect, special, incidental, or consequential 3M Rapid Detection Flu A + B Test: A new diagnostic test for rapid detection of influenza A and influenza B. Mol Diagn Ther. Van Voris LP. The test is intended for use in the simultaneous rapid in vitro detection and differentiation of SARS-CoV-2, influenza A virus, and influenza B virus nucleocapsid protein antigen , but does not . AHA copyrighted materials including the UB‐04 codes and INFLUENZA A & B - CONTROL SWAB KIT 425-080 CPT CODE: 87502-QW . CMS has defined "not usually self-administered" according to how the Medicare population as a whole uses the drug, not how an individual patient or physician may choose to use a particular drug. What is the CMS suggested CPT code and National Limit for the Sofia Influenza A+B FIA? Includes: influenza A (non-novel), influenza B, influenza C. Vignette. Some older versions have been archived. Nov 4, 2009. You can use the Contents side panel to help navigate the various sections. hb```G@(p+PjHQTWO:-:Tp20Wi! Reproduced with permission. Administration of influenza virus vaccine (allowable same as CPT 90471) 90653: Influenza virus vaccine, inactivated, subunit, adjuvanted, for intramuscular use: 90662: Influenza virus vaccine, split virus, preservative free, enhanced immunogenicity via increased antigen content, for intramuscular use: 90672 Absence of a Bill Type does not guarantee that the Paulson J. Centers for Disease Control and Prevention (CDC) recommendations: Use rapid diagnostic tests with high sensitivity and specificity. For quick reference, the new category I CPT codes and long descriptors are: 87636 Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]) and influenza virus types A and B, multiplex amplified probe technique, 87637 Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]), influenza virus types A and B, and respiratory syncytial virus, multiplex amplified probe technique. You acknowledge that the ADA holds all copyright, trademark and other rights in CDT. Effective March 5, 2020. Your first thought is to code this as acute laryngitis, J04.0; however, this code falls in the J00-J06 range titled "Acute upper respiratory infections" and you see no evidence that this is an . The CDC says some rapid flu tests are only 50-70% accurate Doctors of the Baylor University Medical Center in Dallas aren't solely on tests but are also keeping an eye on patient symptoms. Article document IDs begin with the letter "A" (e.g., A12345). The views and/or positions If a rapid antigen test is performed and then confirmed using PCR, the second test may require the -59 modifier. Issue briefs summarize key health policy issues by providing concise and digestible content for both relevant stakeholders and those who may know little about the topic. Applications are available at the AMA Web site, http://www.ama-assn.org/go/cpt. "lV $10120^ &'@ A A Draft article will eventually be replaced by a Billing and Coding article once the Proposed LCD is released to a final LCD. Any use not authorized herein is prohibited, including by way of illustration and not by way of limitation, making copies of CDT for resale and/or license, transferring copies of CDT to any party not bound by this agreement, creating any modified or derivative work of CDT, or making any commercial use of CDT. Use modifier 59 when separate results are reported for different species or strains, same laboratory test on the same day to obtain subsequent test results. Similarly, tests (and CPT codes) for which there are no accompanying ICD-10 codes in the associated Billing and Coding Article will require registration with MolDX . and/or making any commercial use of UB‐04 Manual or any portion thereof, including the codes and/or descriptions, is only CMS has defined "not usually self-administered" according to how the Medicare population as a whole uses the drug, not how an individual patient or physician may choose to use a particular drug. Billing and Coding articles provide guidance for the related Local Coverage Determination (LCD) and assist providers in submitting correct claims for payment. New aspects of influenza viruses. Kidney disease can be prevented, and even reversed in its early stages. Applicable Federal Acquisition Regulation Clauses (FARS)/Department of Defense Federal Acquisition Regulation supplement (DFARS) Restrictions Apply to Government Use. $634.00 / Pack of 25. Read the House of Delegates (HOD) speakers' updates for the 2023 Annual HOD Annual Meeting. and/or making any commercial use of UB‐04 Manual or any portion thereof, including the codes and/or descriptions, is only Please enable "JavaScript" and revisit this page or proceed with browsing CMS.gov with ONLY IF NO MORE DESCRIPTIVE MODIFIER IS AVAILABLE, AND THE USE OF MODIFIER -59 BEST EXPLAINS THE CIRCUMSTANCES, SHOULD MODIFIER -59 BE USED. License to use CDT for any use not authorized herein must be obtained through the American Dental Association, 211 East Chicago Avenue, Chicago, IL 60611. If a CLIA-waived test is performed, the -QW modifier should be reported for the waived test. The document is broken into multiple sections. recommending their use. You agree to take all necessary steps to ensure that your employees and agents abide by the terms of this agreement. No. CPT codes, descriptions and other data only are copyright 2022 American Medical Association. The product we use is "Quick Vue Influenza". The Panbio COVID-19/Flu A&B Rapid Panel test kit was used in the assays. CDT is a trademark of the ADA. An official website of the United States government. of every MCD page. 2016;54(11):2763-2766. Another option is to use the Download button at the top right of the document view pages (for certain document types). Any questions pertaining to the license or use of the CPT should be addressed to the AMA. Please visit the. An official website of the United States government. MACs are Medicare contractors that develop LCDs and Articles along with processing of Medicare claims. A patient has had recent close exposure (this does NOT include eating cooked meat) to pigs or birds (including poultry) or other animals, and there is concern for infection with a novel influenza A virus. LOINC Code 95942-9 Influenza virus A and B and SARS-CoV+SARS-CoV-2 (COVID-19) Ag panel - Upper respiratory specimen by Rapid immunoassay. 8,384. Test Includes. of the Medicare program. That's why we've developed Alinity TM m Resp-4-Plex, a new assay running on our advanced Alinity m system that tests for COVID-19, flu A, flu B, and RSV using only one swab. Applicable FARS/HHSARS apply. GOVERNMENT AND ITS EMPLOYEES ARE NOT LIABLE FOR ANY ERRORS, OMISSIONS, OR OTHER INACCURACIES IN THE INFORMATION, PRODUCT, OR PROCESSES All rights reserved. required field. CPT coding for microbiology and virology procedures often cannot be determined before the culture is performed. Streamlines laboratory operations. Complete absence of all Revenue Codes indicates The Xpert Xpress SARS-CoV-2/Flu/RSV PLUS test is a rapid, multiplexed real-time RT-PCR test intended for the detection and differentiation of SARS-CoV-2, influenza A, influenza B, and respiratory syncytial virus (RSV) viral RNA in specimens collected from individuals suspected of respiratory viral infection consistent with COVID-19. In: Belshe RB, ed. The views and/or positions presented in the material do not necessarily represent the views of the AHA. Learn more with the AMA. I verify that Im in the U.S. and agree to receive communication from the AMA or third parties on behalf of AMA. Yes, agreed. To submit a comment or question to CMS, please use the Feedback/Ask a Question link available at the bottom ONLY IF NO MORE DESCRIPTIVE MODIFIER IS AVAILABLE, AND THE USE OF MODIFIER -59 BEST EXPLAINS THE CIRCUMSTANCES, SHOULD MODIFIER -59 BE USED. Applicable Federal Acquisition Regulation Clauses (FARS)/Department of Defense Federal Acquisition Regulation supplement (DFARS) Restrictions Apply to Government Use. The Cepheid Xpert Xpress SARS-CoV-2/Flu/RSV assay is a rapid, real-time RT-PCR test intended for the simultaneous qualitative detection and differentiation of SARS-CoV-2, influenza A, influenza B, and respiratory syncytial virus (RSV) viral DNA in either nasopharyngeal swab, nasal swab or nasal wash/aspirate specimens collected from individuals suspected of respiratory viral infection . J Clin Microbiol. accuracy of any information contained in this material, nor was the AHA or any of its affiliates, involved in the Medicaid and the State Children's Health Insurance Programs, contracts with certain organizations to assist in the administration testing to when the result is released to the ordering provider. An asterisk (*) indicates a Copyright © 2022, the American Hospital Association, Chicago, Illinois. In individuals with symptoms, the Lucira COVID-19 & Flu Home Test correctly identified 99.3% of negative and 90.1% of positive Influenza A samples, 100% of negative and 88.3% of positive COVID-19 . October 07, 2020 - In response to the COVID-19 pandemic, the American Medical Association (AMA) is adding two new codes to the Current Procedural Terminology (CPT) code set. For purpose of this exclusion, "the term 'usually' means more than 50 percent of the time for all Medicare beneficiaries who use the drug. The AMA promotes the art and science of medicine and the betterment of public health. These materials contain Current Dental Terminology (CDTTM), copyright© 2022 American Dental Association (ADA). The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. Changes to the CPT code set are considered through an open editorial process managed by the CPT Editorial Panel that collects broad input from the health care community and beyond to ensure CPT content reflects the coding demands of digital health, precision medicine, augmented intelligence, and other aspects of a modern health care system. Some tests are waived from requirements under the Clinical Laboratory Improvement Amendments of 1988 (CLIA) and cleared for point-of-care use. All SARS-CoV-2 samples were expected to be Omicron sublineage according to the current epidemiological situation in Belgium. 87637 Infectious agent detection by nucleic acid (DNA or RNA); severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (Coronavirus disease [COVID-19]), influenza virus types A and B, and respiratory syncytial virus, multiplex amplified probe technique. The American Hospital Association ("the AHA") has not reviewed, and is not responsible for, the completeness or accuracy of any information contained in this material, nor was the AHA or any of its affiliates, involved in the preparation of this material, or the analysis of information provided in the material. In addition to SARS-CoV-2 and RSV, the Labcorp Seasonal Respiratory Virus RT-PCR DTC Test can detect influenza . All Rights Reserved (or such other date of publication of CPT). In no event shall CMS be liable for direct, indirect, special, incidental, or consequential damages arising out of the use of such information or material. A patient has had recent close exposure (this does NOT include eating cooked meat) to pigs or birds (including poultry) or other animals, and there is concern for infection with a novel influenza A virus. "The new CPT code for antigen testing to detect the coronavirus is the latest in a series of CPT codes developed in rapid response to the pandemic," said AMA . When community influenza activity is high and the rapid diagnostic test result is negative. Molnlycke Exufiber absorption comparison. The CPT Editorial Panel also revised CPT codes ranging from 87301 to 87430 by removing the undefined term multi step method from code descriptors. Copyright 1995 - 2023 American Medical Association. MODIFIER CODE 09959 MAY BE USED AS AN ALTERNATE TO MODIFIER -59. Add to cart. Self-Administered Drug (SAD) Exclusion List articles list the CPT/HCPCS codes that are excluded from coverage under this category. The following summary provides a list of the main available types of diagnostics tests: Contact your local or state health department for information about influenza activity. CHICAGO The American Medical Association (AMA) today published an update to the Current Procedural Terminology (CPT) code set that includes new code additions and editorial revisions for reporting medical services sparked by the public health response to the COVID-19 pandemic. 2037665 Officials and members gather to elect officers and address policy at the 2023 AMA Annual Meeting being held in Chicago, June 9-14, 2023. In some cases, additional time should be of every MCD page. The QuickVue Influenza A+B est has been shown to detect cultured avian influenza; as with other rapid tests for T influenza, the ability of the QuickVue Influenza A+B est to detect influenza Type A in patients infected with H5N1 T has not been established. Access reports from the Council on Medical Education presented during the AMA Annual and Interim Meetings. Shell vials or equivalent multiwell plate cell culture; identification (additional CPT codes/charges will apply) if culture results warrant. You must log in or register to reply here. 2009;13(1):15-18. Reference: Centers for Disease Control and Prevention. All rights reserved. This revision affects the newly developed descriptor for CPT code 87426. CPT is provided "as is" without warranty of any kind, either expressed or implied, including but not limited to, the implied warranties of merchantability and fitness for a particular purpose. NPA* (versus an FDA-cleared influenza A and B molecular assay) A: 97.8%, B: 99.1%. Previous video. You are leaving the CMS MCD and are being redirected to the CMS MCD Archive that contains outdated (No Longer In Effect) Local Coverage Determinations and Articles, You are leaving the CMS MCD and are being redirected to, Billing and Coding: Influenza Diagnostic Tests, AMA CPT / ADA CDT / AHA NUBC Copyright Statement, Less sensitive (50%-70%) and specific (90%-95%) compared to other methods and may require confirmation by. accuracy of any information contained in this material, nor was the AHA or any of its affiliates, involved in the complete information, CMS does not guarantee that there are no errors in the information displayed on this web site. Data for the 2017 to 2018 influenza season indicates that 84.1 percent of positive samples were influenza A, while 15.9 percent were influenza B. This revision is due to the 2022 Annual CPT/HCPCS Code Update and is effective on 1/1/2022. Organizations who contract with CMS acknowledge that they may have a commercial CDT license with the ADA, and that use of CDT codes as permitted herein for the administration of CMS programs does not extend to any other programs or services the organization may administer and royalties dues for the use of the CDT codes are governed by their commercial license. CMS WILL NOT BE LIABLE FOR ANY CLAIMS ATTRIBUTABLE TO ANY ERRORS, OMISSIONS, OR OTHER INACCURACIES IN THE INFORMATION OR MATERIAL CONTAINED ON THIS PAGE. Reference: Centers for Disease Control and Prevention. You are leaving the CMS MCD and are being redirected to the CMS MCD Archive that contains outdated (No Longer In Effect) Local Coverage Determinations and Articles, You are leaving the CMS MCD and are being redirected to, Billing and Coding: Influenza Diagnostic Tests, AMA CPT / ADA CDT / AHA NUBC Copyright Statement, Less sensitive (50%-70%) and specific (90%-95%) compared to other methods and may require confirmation by. Positive and negative included. CMS and its products and services are October 16, 2020. R5. The Medicare National Limit amount* is $16.36. Local Coverage Articles are a type of educational document published by the Medicare Administrative Contractors (MACs). Editor's note: While this department attempts to provide accurate information and useful advice, third-party . * For positive Flu only or RSV only. This page displays your requested Article. A positive result (on testing of an upper respiratory tract specimen) in a person who recently received intranasal administration of live attenuated influenza virus vaccine (LAIV) may indicate detection of vaccine virus. Among the 4 false positive cases for Influenza B, all were positive for Influenza A with RT-qPCR (Ct = 18.00, 19.12, 23.31 and 31.74) (Table 1). You agree to take all necessary steps to insure that your employees and agents abide by the terms of this agreement. The physician makes the determination to run both influenza A and B tests and a rapid . COVID-19/Flu A&B Diagnostic Test. This Agreement will terminate upon notice if you violate its terms. Objective: To present our experience regarding the use of a rapid diagnostic test for seasonal influenza A and B. Centers for Disease Control and Prevention (CDC) recommendations: Use rapid diagnostic tests with high sensitivity and specificity. You can collapse such groups by clicking on the group header to make navigation easier. They can identify the presence of influenza A and B, and they work by detecting the parts of the flu virus called antigens that trigger an immune response. damages arising out of the use of such information, product, or process. . Negative . Collect respiratory tract specimens as early in the illness as possible (within 3-4 days of illness onset). required field. Rapid Flu A & B, RSV, SARS-CoV-2 PCR Lab Code FABRCV Epic Ordering . Also, you can decide how often you want to get updates. announces CPT code for antigen tests in the CPT code approved for SARS-CoV-2 antigen testing. The AMA does not directly or indirectly practice medicine or dispense medical services. Use is limited to use in Medicare, Medicaid or other programs administered by the Centers for Medicare and Medicaid Services (CMS). AMA members get discounts on prep courses and practice questions. Organizations who contract with CMS acknowledge that they may have a commercial CDT license with the ADA, and that use of CDT codes as permitted herein for the administration of CMS programs does not extend to any other programs or services the organization may administer and royalties dues for the use of the CDT codes are governed by their commercial license. The revision clarifies the proper reporting for antigen tests that are read by a machine, as compared to those which can be visually interpreted without a machine. ICD-10-CM Codes that Support Medical Necessity, ICD-10-CM Codes that DO NOT Support Medical Necessity, Information for Clinicians on Rapid Diagnostic Testing for Influenza, VIRUS ISOLATION; TISSUE CULTURE INOCULATION, OBSERVATION, AND PRESUMPTIVE IDENTIFICATION BY CYTOPATHIC EFFECT, VIRUS ISOLATION; TISSUE CULTURE, ADDITIONAL STUDIES OR DEFINITIVE IDENTIFICATION (EG, HEMABSORPTION, NEUTRALIZATION, IMMUNOFLUORESCENCE STAIN), EACH ISOLATE, VIRUS ISOLATION; CENTRIFUGE ENHANCED (SHELL VIAL) TECHNIQUE, INCLUDES IDENTIFICATION WITH IMMUNOFLUORESCENCE STAIN, EACH VIRUS, INFECTIOUS AGENT ANTIGEN DETECTION BY IMMUNOFLUORESCENT TECHNIQUE; INFLUENZA B VIRUS, INFECTIOUS AGENT ANTIGEN DETECTION BY IMMUNOFLUORESCENT TECHNIQUE; INFLUENZA A VIRUS, INFECTIOUS AGENT ANTIGEN DETECTION BY IMMUNOASSAY TECHNIQUE (EG, ENZYME IMMUNOASSAY [EIA], ENZYME-LINKED IMMUNOSORBENT ASSAY [ELISA], FLUORESCENCE IMMUNOASSAY [FIA], IMMUNOCHEMILUMINOMETRIC ASSAY [IMCA]), QUALITATIVE OR SEMIQUANTITATIVE; INFLUENZA, A OR B, EACH, INFECTIOUS AGENT DETECTION BY NUCLEIC ACID (DNA OR RNA); INFLUENZA VIRUS, INCLUDES REVERSE TRANSCRIPTION, WHEN PERFORMED, AND AMPLIFIED PROBE TECHNIQUE, EACH TYPE OR SUBTYPE, INFECTIOUS AGENT DETECTION BY NUCLEIC ACID (DNA OR RNA); INFLUENZA VIRUS, FOR MULTIPLE TYPES OR SUB-TYPES, INCLUDES MULTIPLEX REVERSE TRANSCRIPTION, WHEN PERFORMED, AND MULTIPLEX AMPLIFIED PROBE TECHNIQUE, FIRST 2 TYPES OR SUB-TYPES, INFECTIOUS AGENT DETECTION BY NUCLEIC ACID (DNA OR RNA); INFLUENZA VIRUS, FOR MULTIPLE TYPES OR SUB-TYPES, INCLUDES MULTIPLEX REVERSE TRANSCRIPTION, WHEN PERFORMED, AND MULTIPLEX AMPLIFIED PROBE TECHNIQUE, EACH ADDITIONAL INFLUENZA VIRUS TYPE OR SUB-TYPE BEYOND 2 (LIST SEPARATELY IN ADDITION TO CODE FOR PRIMARY PROCEDURE), INFECTIOUS AGENT ANTIGEN DETECTION BY IMMUNOASSAY WITH DIRECT OPTICAL (IE, VISUAL) OBSERVATION; INFLUENZA.
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