Evaluation of the point-of-care Becton Dickinson Veritor™ Rapid influenza diagnostic test in Kenya, 2013-2014

We evaluated the performance of the Becton Dickinson Veritor™ System Flu A + B rapid influenza diagnostic test (RIDT) to detect influenza viruses in respiratory specimens from patients enrolled at five surveillance sites in Kenya, a tropical country where influenza seasonality is variable. Nasal swa...

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Veröffentlicht in:BMC infectious diseases 2017-01, Vol.17 (1), p.60-60, Article 60
Hauptverfasser: Ndegwa, Linus K, Emukule, Gideon, Uyeki, Timothy M, Mailu, Eunice, Chaves, Sandra S, Widdowson, Marc-Alain, Lewa, Bandika V, Muiruri, Francis K, Omoth, Peter, Fields, Barry, Mott, Joshua A
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creator Ndegwa, Linus K
Emukule, Gideon
Uyeki, Timothy M
Mailu, Eunice
Chaves, Sandra S
Widdowson, Marc-Alain
Lewa, Bandika V
Muiruri, Francis K
Omoth, Peter
Fields, Barry
Mott, Joshua A
description We evaluated the performance of the Becton Dickinson Veritor™ System Flu A + B rapid influenza diagnostic test (RIDT) to detect influenza viruses in respiratory specimens from patients enrolled at five surveillance sites in Kenya, a tropical country where influenza seasonality is variable. Nasal swab (NS) and nasopharyngeal (NP)/oropharyngeal (OP) swabs were collected from patients with influenza like illness and/or severe acute respiratory infection. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the RIDT using NS specimens were evaluated against nasal swabs tested by real time reverse transcription polymerase chain reaction (rRT-PCR). The performance parameter results were expressed as 95% confidence intervals (CI) calculated using binomial exact methods, with P < 0.05 considered significant. Two-sample Z tests were used to test for differences in sample proportions. Analysis was performed using SAS software version 9.3. From July 2013 to July 2014, 3,569 patients were recruited, of which 78.7% were aged
doi_str_mv 10.1186/s12879-016-2131-9
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Nasal swab (NS) and nasopharyngeal (NP)/oropharyngeal (OP) swabs were collected from patients with influenza like illness and/or severe acute respiratory infection. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the RIDT using NS specimens were evaluated against nasal swabs tested by real time reverse transcription polymerase chain reaction (rRT-PCR). The performance parameter results were expressed as 95% confidence intervals (CI) calculated using binomial exact methods, with P &lt; 0.05 considered significant. Two-sample Z tests were used to test for differences in sample proportions. Analysis was performed using SAS software version 9.3. From July 2013 to July 2014, 3,569 patients were recruited, of which 78.7% were aged &lt;5 years. Overall, 14.4% of NS specimens were influenza-positive by RIDT. RIDT overall sensitivity was 77.1% (95% CI 72.8-81.0%) and specificity was 94.9% (95% CI 94.0-95.7%) compared to rRT-PCR using NS specimens. RIDT sensitivity for influenza A virus compared to rRT-PCR using NS specimens was 71.8% (95% CI 66.7-76.4%) and was significantly higher than for influenza B which was 43.8% (95% CI 33.8-54.2%). PPV ranged from 30%-80% depending on background prevalence of influenza. 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Nasal swab (NS) and nasopharyngeal (NP)/oropharyngeal (OP) swabs were collected from patients with influenza like illness and/or severe acute respiratory infection. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the RIDT using NS specimens were evaluated against nasal swabs tested by real time reverse transcription polymerase chain reaction (rRT-PCR). The performance parameter results were expressed as 95% confidence intervals (CI) calculated using binomial exact methods, with P &lt; 0.05 considered significant. Two-sample Z tests were used to test for differences in sample proportions. Analysis was performed using SAS software version 9.3. From July 2013 to July 2014, 3,569 patients were recruited, of which 78.7% were aged &lt;5 years. Overall, 14.4% of NS specimens were influenza-positive by RIDT. RIDT overall sensitivity was 77.1% (95% CI 72.8-81.0%) and specificity was 94.9% (95% CI 94.0-95.7%) compared to rRT-PCR using NS specimens. RIDT sensitivity for influenza A virus compared to rRT-PCR using NS specimens was 71.8% (95% CI 66.7-76.4%) and was significantly higher than for influenza B which was 43.8% (95% CI 33.8-54.2%). PPV ranged from 30%-80% depending on background prevalence of influenza. Although the variable seasonality of influenza in tropical Africa presents unique challenges, RIDTs may have a role in making influenza surveillance sustainable in more remote areas of Africa, where laboratory capacity is limited.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens</subject><subject>Antigens, Viral - analysis</subject><subject>Betainfluenzavirus - genetics</subject><subject>Care and treatment</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chromatography</subject><subject>Diagnosis</subject><subject>Diagnostic tests</subject><subject>Evaluation</subject><subject>Female</subject><subject>Health surveillance</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Immunoassay</subject><subject>Infant</subject><subject>Infections</subject><subject>Influenza</subject><subject>Influenza A virus - genetics</subject><subject>Influenza, Human - diagnosis</subject><subject>Influenza, Human - virology</subject><subject>Informed consent</subject><subject>Kenya</subject><subject>Laboratories</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nasal Mucosa - virology</subject><subject>Nasopharynx - virology</subject><subject>Oropharynx - virology</subject><subject>Pneumonia</subject><subject>Point-of-Care Testing</subject><subject>Polymerase chain reaction</subject><subject>Predictive Value of Tests</subject><subject>Reagents</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Sensitivity and Specificity</subject><subject>Sentinel surveillance</subject><subject>Technology application</subject><subject>Viruses</subject><subject>Young Adult</subject><issn>1471-2334</issn><issn>1471-2334</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkt9OFTEQxjdGIog-gDemiTeSWOyf3W17QwKISCQhQeW26Xanh-Ke9rjtEvHaJ_HRfBJ7chA5xgvTpJ10fvM1M_2q6hklu5TK9nWiTAqFCW0xo5xi9aDaorWgmHFeP7wXb1aPU7oihArJ1KNqk0kiBFF8q4pH12aYTPYxoOhQvgS0iD5kHB22ZgR0ADaX3BtvP_uQSnQBo89x_Pn9Bzo3C98jH9wwQfhmUO_NLMSUvUUZUi4Z9B7CjXmFGKEcl61-Um04MyR4entuV5_eHn08fIdPz45PDvdPsW1aljHvhVLQ9C10fde2qnPQCNMRy9rOSait6yhrrLFWAK0Z46ZzTClZ1w3nUlm-Xe2tdBdTN4feQsijGfRi9HMz3uhovF7PBH-pZ_FaN4w1TVsXgZe3AmP8MpVu9NwnC8NgAsQpaSobSYkiUhb0xV_oVZzGUNorVMsFoaRWf6iZGUCXocXyrl2K6v1aiPKBTPFC7f6DKquHubcxgPPlfq1gZ62gMBm-5pmZUtInH87_nz27WGfpirVjTGkEdzc7SvTSfXrlPl3cp5fu08sWn98f-l3Fb7vxX-uo0vc</recordid><startdate>20170111</startdate><enddate>20170111</enddate><creator>Ndegwa, Linus K</creator><creator>Emukule, Gideon</creator><creator>Uyeki, Timothy M</creator><creator>Mailu, Eunice</creator><creator>Chaves, Sandra S</creator><creator>Widdowson, Marc-Alain</creator><creator>Lewa, Bandika V</creator><creator>Muiruri, Francis K</creator><creator>Omoth, Peter</creator><creator>Fields, Barry</creator><creator>Mott, Joshua A</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QL</scope><scope>7T2</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20170111</creationdate><title>Evaluation of the point-of-care Becton Dickinson Veritor™ Rapid influenza diagnostic test in Kenya, 2013-2014</title><author>Ndegwa, Linus K ; Emukule, Gideon ; Uyeki, Timothy M ; Mailu, Eunice ; Chaves, Sandra S ; Widdowson, Marc-Alain ; Lewa, Bandika V ; Muiruri, Francis K ; Omoth, Peter ; Fields, Barry ; Mott, Joshua A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c562t-3d799e5d6ebdb669bfe57ab0c26bf8e4cfb125cacc7e14223abf29984453389c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens</topic><topic>Antigens, Viral - analysis</topic><topic>Betainfluenzavirus - genetics</topic><topic>Care and treatment</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chromatography</topic><topic>Diagnosis</topic><topic>Diagnostic tests</topic><topic>Evaluation</topic><topic>Female</topic><topic>Health surveillance</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Immunoassay</topic><topic>Infant</topic><topic>Infections</topic><topic>Influenza</topic><topic>Influenza A virus - genetics</topic><topic>Influenza, Human - diagnosis</topic><topic>Influenza, Human - virology</topic><topic>Informed consent</topic><topic>Kenya</topic><topic>Laboratories</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Nasal Mucosa - virology</topic><topic>Nasopharynx - virology</topic><topic>Oropharynx - virology</topic><topic>Pneumonia</topic><topic>Point-of-Care Testing</topic><topic>Polymerase chain reaction</topic><topic>Predictive Value of Tests</topic><topic>Reagents</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Sensitivity and Specificity</topic><topic>Sentinel surveillance</topic><topic>Technology application</topic><topic>Viruses</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ndegwa, Linus K</creatorcontrib><creatorcontrib>Emukule, Gideon</creatorcontrib><creatorcontrib>Uyeki, Timothy M</creatorcontrib><creatorcontrib>Mailu, Eunice</creatorcontrib><creatorcontrib>Chaves, Sandra S</creatorcontrib><creatorcontrib>Widdowson, Marc-Alain</creatorcontrib><creatorcontrib>Lewa, Bandika V</creatorcontrib><creatorcontrib>Muiruri, Francis K</creatorcontrib><creatorcontrib>Omoth, Peter</creatorcontrib><creatorcontrib>Fields, Barry</creatorcontrib><creatorcontrib>Mott, Joshua A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; 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Nasal swab (NS) and nasopharyngeal (NP)/oropharyngeal (OP) swabs were collected from patients with influenza like illness and/or severe acute respiratory infection. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of the RIDT using NS specimens were evaluated against nasal swabs tested by real time reverse transcription polymerase chain reaction (rRT-PCR). The performance parameter results were expressed as 95% confidence intervals (CI) calculated using binomial exact methods, with P &lt; 0.05 considered significant. Two-sample Z tests were used to test for differences in sample proportions. Analysis was performed using SAS software version 9.3. From July 2013 to July 2014, 3,569 patients were recruited, of which 78.7% were aged &lt;5 years. Overall, 14.4% of NS specimens were influenza-positive by RIDT. RIDT overall sensitivity was 77.1% (95% CI 72.8-81.0%) and specificity was 94.9% (95% CI 94.0-95.7%) compared to rRT-PCR using NS specimens. RIDT sensitivity for influenza A virus compared to rRT-PCR using NS specimens was 71.8% (95% CI 66.7-76.4%) and was significantly higher than for influenza B which was 43.8% (95% CI 33.8-54.2%). PPV ranged from 30%-80% depending on background prevalence of influenza. Although the variable seasonality of influenza in tropical Africa presents unique challenges, RIDTs may have a role in making influenza surveillance sustainable in more remote areas of Africa, where laboratory capacity is limited.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>28077093</pmid><doi>10.1186/s12879-016-2131-9</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Aged
Aged, 80 and over
Antigens
Antigens, Viral - analysis
Betainfluenzavirus - genetics
Care and treatment
Child
Child, Preschool
Chromatography
Diagnosis
Diagnostic tests
Evaluation
Female
Health surveillance
Hospitals
Humans
Immunoassay
Infant
Infections
Influenza
Influenza A virus - genetics
Influenza, Human - diagnosis
Influenza, Human - virology
Informed consent
Kenya
Laboratories
Male
Middle Aged
Nasal Mucosa - virology
Nasopharynx - virology
Oropharynx - virology
Pneumonia
Point-of-Care Testing
Polymerase chain reaction
Predictive Value of Tests
Reagents
Real-Time Polymerase Chain Reaction
Reverse Transcriptase Polymerase Chain Reaction
Sensitivity and Specificity
Sentinel surveillance
Technology application
Viruses
Young Adult
title Evaluation of the point-of-care Becton Dickinson Veritor™ Rapid influenza diagnostic test in Kenya, 2013-2014
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