Poor performance of the rapid test for human brucellosis in health facilities in Kenya
Human brucellosis is considered to be an important but typically under-diagnosed cause of febrile illness in many low and middle-income countries. In Kenya, and throughout East Africa, laboratory diagnosis for the disease is based primarily on the febrile antigen Brucella agglutination test (FBAT),...
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creator | de Glanville, William A Conde-Álvarez, Raquel Moriyón, Ignacio Njeru, John Díaz, Ramón Cook, Elizabeth A J Morin, Matilda Bronsvoort, Barend M de C Thomas, Lian F Kariuki, Samuel Fèvre, Eric M |
description | Human brucellosis is considered to be an important but typically under-diagnosed cause of febrile illness in many low and middle-income countries. In Kenya, and throughout East Africa, laboratory diagnosis for the disease is based primarily on the febrile antigen Brucella agglutination test (FBAT), yet few studies of the diagnostic accuracy of this test exist. Assessment of the performance of the FBAT is essential for its appropriate clinical use, as well as for evaluating surveillance data reported by public health systems. To assess FBAT performance, we collected sera from people with symptoms compatible with brucellosis attending two health facilities in Busia County, Kenya. Sera were tested using the FBAT and results compared with those from the Rose Bengal Test (RBT), an assay with well-known performance characteristics. Positives on either test were confirmed using the classical serum agglutination test (SAT)-Coombs test combination and a rapid IgM/IgG lateral flow immunochromatography assay (LFA). A questionnaire focussing on known risk factors for exposure to Brucella spp. was also conducted, and relationships with FBAT positivity examined using logistic regression. Out of 825 recruited individuals, 162 (19.6%) were classified as positive using the FBAT. In contrast, only eight (1.0%) were positive using the RBT. Of the 162 FBAT positives, one (0.62%) had an atypical agglutination in SAT and three (1.9%) showed low Coombs titres. Out of 148 FBAT positive individuals tested using the LFA, five (3.4%) were IgM positive and none were IgG positive. Poor or no correlation was observed between FBAT results and most established risk factors for Brucella infection. We observed substantial disagreement between the FBAT and a number of well-known serological tests, with the majority of reactive FBAT results appearing to be false positives. Poor FBAT specificity, combined with a lack of confirmatory testing, strongly suggests overdiagnosis of brucellosis is common in this low prevalence setting. This is expected to have important economic impacts on affected patients subjected to the long and likely unnecessary courses of multiple antibiotics required for treatment of the disease. |
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In Kenya, and throughout East Africa, laboratory diagnosis for the disease is based primarily on the febrile antigen Brucella agglutination test (FBAT), yet few studies of the diagnostic accuracy of this test exist. Assessment of the performance of the FBAT is essential for its appropriate clinical use, as well as for evaluating surveillance data reported by public health systems. To assess FBAT performance, we collected sera from people with symptoms compatible with brucellosis attending two health facilities in Busia County, Kenya. Sera were tested using the FBAT and results compared with those from the Rose Bengal Test (RBT), an assay with well-known performance characteristics. Positives on either test were confirmed using the classical serum agglutination test (SAT)-Coombs test combination and a rapid IgM/IgG lateral flow immunochromatography assay (LFA). A questionnaire focussing on known risk factors for exposure to Brucella spp. was also conducted, and relationships with FBAT positivity examined using logistic regression. Out of 825 recruited individuals, 162 (19.6%) were classified as positive using the FBAT. In contrast, only eight (1.0%) were positive using the RBT. Of the 162 FBAT positives, one (0.62%) had an atypical agglutination in SAT and three (1.9%) showed low Coombs titres. Out of 148 FBAT positive individuals tested using the LFA, five (3.4%) were IgM positive and none were IgG positive. Poor or no correlation was observed between FBAT results and most established risk factors for Brucella infection. We observed substantial disagreement between the FBAT and a number of well-known serological tests, with the majority of reactive FBAT results appearing to be false positives. Poor FBAT specificity, combined with a lack of confirmatory testing, strongly suggests overdiagnosis of brucellosis is common in this low prevalence setting. This is expected to have important economic impacts on affected patients subjected to the long and likely unnecessary courses of multiple antibiotics required for treatment of the disease.</description><identifier>ISSN: 1935-2735</identifier><identifier>ISSN: 1935-2727</identifier><identifier>EISSN: 1935-2735</identifier><identifier>DOI: 10.1371/journal.pntd.0005508</identifier><identifier>PMID: 28388625</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Agglutination ; Agglutination tests ; Animal health ; Antibiotics ; Biochemistry ; Biodiversity ; Biology and Life Sciences ; Biotechnology ; Brucellosis ; Brucellosis - diagnosis ; Child ; Child, Preschool ; Children ; Data processing ; Diagnosis ; Economic impact ; Electromagnetic fields ; Epidemiology ; Evolution ; False Positive Reactions ; Female ; Fever ; Health Facilities ; Health risks ; Humans ; Immunoglobulin G ; Immunoglobulin M ; Infections ; Infectious diseases ; Kenya ; Leptospirosis ; Livestock ; Low frequency ; Malaria ; Male ; Management ; Medical tests ; Medicine and Health Sciences ; Middle Aged ; People and Places ; Public health ; Risk assessment ; Risk factors ; Serologic Tests - methods ; Serological tests ; Surveys and Questionnaires ; Testing ; Time Factors ; Tropical diseases ; Workers ; Young Adult ; Zoonoses</subject><ispartof>PLoS neglected tropical diseases, 2017-04, Vol.11 (4), p.e0005508-e0005508</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: de Glanville WA, Conde-Álvarez R, Moriyón I, Njeru J, Díaz R, Cook EAJ, et al. (2017) Poor performance of the rapid test for human brucellosis in health facilities in Kenya. PLoS Negl Trop Dis 11(4): e0005508. https://doi.org/10.1371/journal.pntd.0005508</rights><rights>2017 de Glanville et al 2017 de Glanville et al</rights><rights>2017 Public Library of Science. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: de Glanville WA, Conde-Álvarez R, Moriyón I, Njeru J, Díaz R, Cook EAJ, et al. (2017) Poor performance of the rapid test for human brucellosis in health facilities in Kenya. PLoS Negl Trop Dis 11(4): e0005508. https://doi.org/10.1371/journal.pntd.0005508</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c661t-511dfba66b3db39b0f1e9217aa74b02a6f34a2b46cae37f6c8340e4bf106b6263</citedby><cites>FETCH-LOGICAL-c661t-511dfba66b3db39b0f1e9217aa74b02a6f34a2b46cae37f6c8340e4bf106b6263</cites><orcidid>0000-0003-2474-0356</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413359/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413359/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,551,724,777,781,861,882,2096,2915,23847,27905,27906,53772,53774,79349,79350</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28388625$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-359805$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><contributor>Zinsstag, Jakob</contributor><creatorcontrib>de Glanville, William A</creatorcontrib><creatorcontrib>Conde-Álvarez, Raquel</creatorcontrib><creatorcontrib>Moriyón, Ignacio</creatorcontrib><creatorcontrib>Njeru, John</creatorcontrib><creatorcontrib>Díaz, Ramón</creatorcontrib><creatorcontrib>Cook, Elizabeth A J</creatorcontrib><creatorcontrib>Morin, Matilda</creatorcontrib><creatorcontrib>Bronsvoort, Barend M de C</creatorcontrib><creatorcontrib>Thomas, Lian F</creatorcontrib><creatorcontrib>Kariuki, Samuel</creatorcontrib><creatorcontrib>Fèvre, Eric M</creatorcontrib><title>Poor performance of the rapid test for human brucellosis in health facilities in Kenya</title><title>PLoS neglected tropical diseases</title><addtitle>PLoS Negl Trop Dis</addtitle><description>Human brucellosis is considered to be an important but typically under-diagnosed cause of febrile illness in many low and middle-income countries. In Kenya, and throughout East Africa, laboratory diagnosis for the disease is based primarily on the febrile antigen Brucella agglutination test (FBAT), yet few studies of the diagnostic accuracy of this test exist. Assessment of the performance of the FBAT is essential for its appropriate clinical use, as well as for evaluating surveillance data reported by public health systems. To assess FBAT performance, we collected sera from people with symptoms compatible with brucellosis attending two health facilities in Busia County, Kenya. Sera were tested using the FBAT and results compared with those from the Rose Bengal Test (RBT), an assay with well-known performance characteristics. Positives on either test were confirmed using the classical serum agglutination test (SAT)-Coombs test combination and a rapid IgM/IgG lateral flow immunochromatography assay (LFA). A questionnaire focussing on known risk factors for exposure to Brucella spp. was also conducted, and relationships with FBAT positivity examined using logistic regression. Out of 825 recruited individuals, 162 (19.6%) were classified as positive using the FBAT. In contrast, only eight (1.0%) were positive using the RBT. Of the 162 FBAT positives, one (0.62%) had an atypical agglutination in SAT and three (1.9%) showed low Coombs titres. Out of 148 FBAT positive individuals tested using the LFA, five (3.4%) were IgM positive and none were IgG positive. Poor or no correlation was observed between FBAT results and most established risk factors for Brucella infection. We observed substantial disagreement between the FBAT and a number of well-known serological tests, with the majority of reactive FBAT results appearing to be false positives. Poor FBAT specificity, combined with a lack of confirmatory testing, strongly suggests overdiagnosis of brucellosis is common in this low prevalence setting. This is expected to have important economic impacts on affected patients subjected to the long and likely unnecessary courses of multiple antibiotics required for treatment of the disease.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Agglutination</subject><subject>Agglutination tests</subject><subject>Animal health</subject><subject>Antibiotics</subject><subject>Biochemistry</subject><subject>Biodiversity</subject><subject>Biology and Life Sciences</subject><subject>Biotechnology</subject><subject>Brucellosis</subject><subject>Brucellosis - diagnosis</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Data processing</subject><subject>Diagnosis</subject><subject>Economic impact</subject><subject>Electromagnetic fields</subject><subject>Epidemiology</subject><subject>Evolution</subject><subject>False Positive Reactions</subject><subject>Female</subject><subject>Fever</subject><subject>Health Facilities</subject><subject>Health risks</subject><subject>Humans</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulin M</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Kenya</subject><subject>Leptospirosis</subject><subject>Livestock</subject><subject>Low frequency</subject><subject>Malaria</subject><subject>Male</subject><subject>Management</subject><subject>Medical tests</subject><subject>Medicine and Health Sciences</subject><subject>Middle Aged</subject><subject>People and Places</subject><subject>Public health</subject><subject>Risk assessment</subject><subject>Risk factors</subject><subject>Serologic Tests - methods</subject><subject>Serological tests</subject><subject>Surveys and Questionnaires</subject><subject>Testing</subject><subject>Time Factors</subject><subject>Tropical diseases</subject><subject>Workers</subject><subject>Young Adult</subject><subject>Zoonoses</subject><issn>1935-2735</issn><issn>1935-2727</issn><issn>1935-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>D8T</sourceid><sourceid>DOA</sourceid><recordid>eNptkktv1DAUhSMEoqXwDxBYQkIsmMGOH7E3SKPyqqgEC-jWsh17xlXGTu0E1H-PM5NWM6jJItH1d46vr09VvURwiXCDPlzHMQXVLfswtEsIIaWQP6pOkcB0UTeYPj74P6me5XxdGEE5elqd1Bxzzmp6Wl39jDGB3iYX01YFY0F0YNhYkFTvWzDYPICyBDZjWQU6jcZ2Xcw-Ax_Axqpu2ACnjO_84O2u-N2GW_W8euJUl-2L-XtW_f7y-df5t8Xlj68X56vLhWEMDQuKUOu0YkzjVmOhoUNW1KhRqiEa1oo5TFStCTPK4sYxwzGBlmiHINOsZviser337UtTch5JlogLgcvTwEJc7Ik2qmvZJ79V6VZG5eWuENNaqjR401lpkEW6LkKHa1JTJwxqGGwZVooT45ri9X7vlf_aftRHbp_81WrnNo4SU8EhLfjHublRb21rbBiS6o5UxyvBb-Q6_pGUIFw8isG72SDFm7Fchdz6PF2ACjaO0zE5FYRSzgv65j_04WHM1FqV8_rgYtnXTKZyRQQuSUFi2nb5AFXe1m69icE6X-pHgrcHgn0qcuzGwceQj0GyB02KOSfr7oeBoJxSfde1nFIt51QX2avDQd6L7mKM_wGL4vOe</recordid><startdate>20170407</startdate><enddate>20170407</enddate><creator>de Glanville, William A</creator><creator>Conde-Álvarez, Raquel</creator><creator>Moriyón, Ignacio</creator><creator>Njeru, John</creator><creator>Díaz, Ramón</creator><creator>Cook, Elizabeth A J</creator><creator>Morin, Matilda</creator><creator>Bronsvoort, Barend M de C</creator><creator>Thomas, Lian F</creator><creator>Kariuki, Samuel</creator><creator>Fèvre, Eric M</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>3V.</scope><scope>7QL</scope><scope>7SS</scope><scope>7T2</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FD</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>F1W</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>K9.</scope><scope>L.G</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-2474-0356</orcidid></search><sort><creationdate>20170407</creationdate><title>Poor performance of the rapid test for human brucellosis in health facilities in Kenya</title><author>de Glanville, William A ; Conde-Álvarez, Raquel ; Moriyón, Ignacio ; Njeru, John ; Díaz, Ramón ; Cook, Elizabeth A J ; Morin, Matilda ; Bronsvoort, Barend M de C ; Thomas, Lian F ; Kariuki, Samuel ; Fèvre, Eric M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c661t-511dfba66b3db39b0f1e9217aa74b02a6f34a2b46cae37f6c8340e4bf106b6263</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>Agglutination</topic><topic>Agglutination tests</topic><topic>Animal health</topic><topic>Antibiotics</topic><topic>Biochemistry</topic><topic>Biodiversity</topic><topic>Biology and Life Sciences</topic><topic>Biotechnology</topic><topic>Brucellosis</topic><topic>Brucellosis - 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In Kenya, and throughout East Africa, laboratory diagnosis for the disease is based primarily on the febrile antigen Brucella agglutination test (FBAT), yet few studies of the diagnostic accuracy of this test exist. Assessment of the performance of the FBAT is essential for its appropriate clinical use, as well as for evaluating surveillance data reported by public health systems. To assess FBAT performance, we collected sera from people with symptoms compatible with brucellosis attending two health facilities in Busia County, Kenya. Sera were tested using the FBAT and results compared with those from the Rose Bengal Test (RBT), an assay with well-known performance characteristics. Positives on either test were confirmed using the classical serum agglutination test (SAT)-Coombs test combination and a rapid IgM/IgG lateral flow immunochromatography assay (LFA). A questionnaire focussing on known risk factors for exposure to Brucella spp. was also conducted, and relationships with FBAT positivity examined using logistic regression. Out of 825 recruited individuals, 162 (19.6%) were classified as positive using the FBAT. In contrast, only eight (1.0%) were positive using the RBT. Of the 162 FBAT positives, one (0.62%) had an atypical agglutination in SAT and three (1.9%) showed low Coombs titres. Out of 148 FBAT positive individuals tested using the LFA, five (3.4%) were IgM positive and none were IgG positive. Poor or no correlation was observed between FBAT results and most established risk factors for Brucella infection. We observed substantial disagreement between the FBAT and a number of well-known serological tests, with the majority of reactive FBAT results appearing to be false positives. Poor FBAT specificity, combined with a lack of confirmatory testing, strongly suggests overdiagnosis of brucellosis is common in this low prevalence setting. This is expected to have important economic impacts on affected patients subjected to the long and likely unnecessary courses of multiple antibiotics required for treatment of the disease.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28388625</pmid><doi>10.1371/journal.pntd.0005508</doi><orcidid>https://orcid.org/0000-0003-2474-0356</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1935-2735 |
ispartof | PLoS neglected tropical diseases, 2017-04, Vol.11 (4), p.e0005508-e0005508 |
issn | 1935-2735 1935-2727 1935-2735 |
language | eng |
recordid | cdi_plos_journals_1899333370 |
source | MEDLINE; DOAJ Directory of Open Access Journals; SWEPUB Freely available online; PubMed Central Open Access; Public Library of Science (PLoS); EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Adolescent Adult Aged Aged, 80 and over Agglutination Agglutination tests Animal health Antibiotics Biochemistry Biodiversity Biology and Life Sciences Biotechnology Brucellosis Brucellosis - diagnosis Child Child, Preschool Children Data processing Diagnosis Economic impact Electromagnetic fields Epidemiology Evolution False Positive Reactions Female Fever Health Facilities Health risks Humans Immunoglobulin G Immunoglobulin M Infections Infectious diseases Kenya Leptospirosis Livestock Low frequency Malaria Male Management Medical tests Medicine and Health Sciences Middle Aged People and Places Public health Risk assessment Risk factors Serologic Tests - methods Serological tests Surveys and Questionnaires Testing Time Factors Tropical diseases Workers Young Adult Zoonoses |
title | Poor performance of the rapid test for human brucellosis in health facilities in Kenya |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T15%3A03%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Poor%20performance%20of%20the%20rapid%20test%20for%20human%20brucellosis%20in%20health%20facilities%20in%20Kenya&rft.jtitle=PLoS%20neglected%20tropical%20diseases&rft.au=de%20Glanville,%20William%20A&rft.date=2017-04-07&rft.volume=11&rft.issue=4&rft.spage=e0005508&rft.epage=e0005508&rft.pages=e0005508-e0005508&rft.issn=1935-2735&rft.eissn=1935-2735&rft_id=info:doi/10.1371/journal.pntd.0005508&rft_dat=%3Cgale_plos_%3EA493735199%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1899333370&rft_id=info:pmid/28388625&rft_galeid=A493735199&rft_doaj_id=oai_doaj_org_article_c1e1b2933f32425f9c1760d63aa84cf7&rfr_iscdi=true |