Utility of the Determine Syphilis TP rapid test in commercial sex venues in Peru

Objectives: This study sought to evaluate the utility of the Determine Syphilis TP test performed in Peruvian commercial sex venues for the detection of active syphilis; and determine the feasibility of integrating rapid syphilis testing for female sex workers (FSW) into existing health outreach ser...

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Veröffentlicht in:Sexually transmitted infections 2006-12, Vol.82 (suppl 5), p.v22-v25
Hauptverfasser: Campos, P E, Buffardi, A L, Chiappe, M, Buendía, C, Garcia, P J, Carcamo, C P, Garnett, G, White, P, Holmes, K K
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container_end_page v25
container_issue suppl 5
container_start_page v22
container_title Sexually transmitted infections
container_volume 82
creator Campos, P E
Buffardi, A L
Chiappe, M
Buendía, C
Garcia, P J
Carcamo, C P
Garnett, G
White, P
Holmes, K K
description Objectives: This study sought to evaluate the utility of the Determine Syphilis TP test performed in Peruvian commercial sex venues for the detection of active syphilis; and determine the feasibility of integrating rapid syphilis testing for female sex workers (FSW) into existing health outreach services. Methods: We tested 3586 female sex workers for syphilis by Determine in the field using whole blood fingerstick, and by rapid plasma reagin (RPR) and Treponema pallidum haemagglutination assay (TPHA) in a central laboratory in Lima using sera. Results: 97.4% of the FSW offered rapid syphilis testing participated; and among those who tested positive, 87% visited the local health centre for treatment. More than twice as many specimens were RPR reactive using serum in Lima (5.7%) than tested positive by whole blood Determine in the field (2.8%), and although most were confirmed by TPHA, only a small proportion (0.7%) were RPR reactive at ⩾1:8 dilutions, and likely indicating active syphilis. Sensitivity, specificity and positive predictive value of the Determine Syphilis TP test in whole blood when compared to serum RPR reactivity at any dilution confirmed by TPHA as the gold standard were 39.3%, 99.2% and 71.4%, respectively. Sensitivity improved to 64.0% when using serum RPR ⩾1:8 confirmed by TPHA. Invalid tests were rare (0.3%). Conclusions: Rapid syphilis testing in sex work venues proved feasible, but Determine using whole blood obtained by fingerstick was substantially less sensitive than reported in previous laboratory-based studies using serum. Although easy to perform in outreach venues, the utility of this rapid syphilis test was relatively low in settings where a large proportion of the targeted population has been previously tested and treated.
doi_str_mv 10.1136/sti.2006.023325
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Methods: We tested 3586 female sex workers for syphilis by Determine in the field using whole blood fingerstick, and by rapid plasma reagin (RPR) and Treponema pallidum haemagglutination assay (TPHA) in a central laboratory in Lima using sera. Results: 97.4% of the FSW offered rapid syphilis testing participated; and among those who tested positive, 87% visited the local health centre for treatment. More than twice as many specimens were RPR reactive using serum in Lima (5.7%) than tested positive by whole blood Determine in the field (2.8%), and although most were confirmed by TPHA, only a small proportion (0.7%) were RPR reactive at ⩾1:8 dilutions, and likely indicating active syphilis. Sensitivity, specificity and positive predictive value of the Determine Syphilis TP test in whole blood when compared to serum RPR reactivity at any dilution confirmed by TPHA as the gold standard were 39.3%, 99.2% and 71.4%, respectively. Sensitivity improved to 64.0% when using serum RPR ⩾1:8 confirmed by TPHA. Invalid tests were rare (0.3%). Conclusions: Rapid syphilis testing in sex work venues proved feasible, but Determine using whole blood obtained by fingerstick was substantially less sensitive than reported in previous laboratory-based studies using serum. Although easy to perform in outreach venues, the utility of this rapid syphilis test was relatively low in settings where a large proportion of the targeted population has been previously tested and treated.</description><identifier>ISSN: 1368-4973</identifier><identifier>EISSN: 1472-3263</identifier><identifier>DOI: 10.1136/sti.2006.023325</identifier><identifier>PMID: 17116642</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd</publisher><subject>chlamydial infection ; Determine Syphilis TP ; Feasibility Studies ; Female ; female sex workers ; FSW ; gonorrhoea ; Hemagglutination Inhibition Tests - methods ; Hemagglutination Inhibition Tests - standards ; Humans ; Infections ; Laboratories ; PCR ; Peru ; Peruvian Ministry of Health HIV/STI Control Program ; Point-of-Care Systems - standards ; polymerase chain reaction ; positive predictive values ; PPV ; PROCETSS ; Rapid Diagnostics ; rapid plasma reagin ; rapid testing ; RPR ; Sensitivity and Specificity ; Sex industry ; Sex Work ; Sexually transmitted diseases ; sexually transmitted infections ; STD ; STI ; Syphilis ; Syphilis - diagnosis ; Syphilis Serodiagnosis - methods ; Syphilis Serodiagnosis - standards ; Teams ; TPHA ; TPPA ; Treponema pallidum ; Treponema pallidum - isolation &amp; purification ; Treponema pallidum haemagglutination assay ; Treponema pallidum particle agglutination assay ; trichomoniasis ; Vagina ; Workers ; Young adults</subject><ispartof>Sexually transmitted infections, 2006-12, Vol.82 (suppl 5), p.v22-v25</ispartof><rights>Copyright 2006 Sexually Transmitted Infections</rights><rights>Copyright: 2006 Copyright 2006 Sexually Transmitted Infections</rights><rights>Copyright ©2006 BMJ Publishing Group.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b523t-9b22ef346a52856cb6c902cf65300f6e63f5c47ccb131b5e86883273cd82cab13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://sti.bmj.com/content/82/suppl_5/v22.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://sti.bmj.com/content/82/suppl_5/v22.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,230,314,724,777,781,882,3183,23552,27905,27906,53772,53774,77349,77380</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17116642$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Campos, P E</creatorcontrib><creatorcontrib>Buffardi, A L</creatorcontrib><creatorcontrib>Chiappe, M</creatorcontrib><creatorcontrib>Buendía, C</creatorcontrib><creatorcontrib>Garcia, P J</creatorcontrib><creatorcontrib>Carcamo, C P</creatorcontrib><creatorcontrib>Garnett, G</creatorcontrib><creatorcontrib>White, P</creatorcontrib><creatorcontrib>Holmes, K K</creatorcontrib><title>Utility of the Determine Syphilis TP rapid test in commercial sex venues in Peru</title><title>Sexually transmitted infections</title><addtitle>Sex Transm Infect</addtitle><description>Objectives: This study sought to evaluate the utility of the Determine Syphilis TP test performed in Peruvian commercial sex venues for the detection of active syphilis; and determine the feasibility of integrating rapid syphilis testing for female sex workers (FSW) into existing health outreach services. Methods: We tested 3586 female sex workers for syphilis by Determine in the field using whole blood fingerstick, and by rapid plasma reagin (RPR) and Treponema pallidum haemagglutination assay (TPHA) in a central laboratory in Lima using sera. Results: 97.4% of the FSW offered rapid syphilis testing participated; and among those who tested positive, 87% visited the local health centre for treatment. More than twice as many specimens were RPR reactive using serum in Lima (5.7%) than tested positive by whole blood Determine in the field (2.8%), and although most were confirmed by TPHA, only a small proportion (0.7%) were RPR reactive at ⩾1:8 dilutions, and likely indicating active syphilis. Sensitivity, specificity and positive predictive value of the Determine Syphilis TP test in whole blood when compared to serum RPR reactivity at any dilution confirmed by TPHA as the gold standard were 39.3%, 99.2% and 71.4%, respectively. Sensitivity improved to 64.0% when using serum RPR ⩾1:8 confirmed by TPHA. Invalid tests were rare (0.3%). Conclusions: Rapid syphilis testing in sex work venues proved feasible, but Determine using whole blood obtained by fingerstick was substantially less sensitive than reported in previous laboratory-based studies using serum. Although easy to perform in outreach venues, the utility of this rapid syphilis test was relatively low in settings where a large proportion of the targeted population has been previously tested and treated.</description><subject>chlamydial infection</subject><subject>Determine Syphilis TP</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>female sex workers</subject><subject>FSW</subject><subject>gonorrhoea</subject><subject>Hemagglutination Inhibition Tests - methods</subject><subject>Hemagglutination Inhibition Tests - standards</subject><subject>Humans</subject><subject>Infections</subject><subject>Laboratories</subject><subject>PCR</subject><subject>Peru</subject><subject>Peruvian Ministry of Health HIV/STI Control Program</subject><subject>Point-of-Care Systems - standards</subject><subject>polymerase chain reaction</subject><subject>positive predictive values</subject><subject>PPV</subject><subject>PROCETSS</subject><subject>Rapid Diagnostics</subject><subject>rapid plasma reagin</subject><subject>rapid testing</subject><subject>RPR</subject><subject>Sensitivity and Specificity</subject><subject>Sex industry</subject><subject>Sex Work</subject><subject>Sexually transmitted diseases</subject><subject>sexually transmitted infections</subject><subject>STD</subject><subject>STI</subject><subject>Syphilis</subject><subject>Syphilis - diagnosis</subject><subject>Syphilis Serodiagnosis - methods</subject><subject>Syphilis Serodiagnosis - standards</subject><subject>Teams</subject><subject>TPHA</subject><subject>TPPA</subject><subject>Treponema pallidum</subject><subject>Treponema pallidum - isolation &amp; purification</subject><subject>Treponema pallidum haemagglutination assay</subject><subject>Treponema pallidum particle agglutination assay</subject><subject>trichomoniasis</subject><subject>Vagina</subject><subject>Workers</subject><subject>Young adults</subject><issn>1368-4973</issn><issn>1472-3263</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</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>GNUQQ</sourceid><recordid>eNqFkc1rFDEYxgdRbK2evUlA6EGY7SSZvMlcBF0_oa0LtiJeQib7jpt1PrZJpnT_e7PM0lovPSXk-eV5P54se0mLGaUcTkJ0M1YUMCsY50w8yg5pKVnOGfDH6c5B5WUl-UH2LIR1kUApqqfZAZWUApTsMFtcRte6uCVDQ-IKyQeM6DvXI_m-3aySFMjFgnizcUsSMUTiemKHrkNvnWlJwBtyjf2IYScs0I_PsyeNaQO-2J9H2eWnjxfzL_npt89f5-9O81owHvOqZgwbXoIRTAmwNdiqYLYBwYuiAQTeCFtKa2vKaS1QgVKcSW6XilmTHo-yt5PvZqw7XFrsozet3njXGb_Vg3H6vtK7lf49XGsmgFdUJoPjvYEfrtIAUXcuWGxb0-MwBg2KVaIE9SBIEyal3LX0-j9wPYy-T1vQVCoKkqaVJ-pkoqwfQvDY3PZMC70LVadQ9S5UPYWafrz6d9Q7fp9iAvIJcCHiza1u_B8Nkkuhz3_M9c9f5_IM3p9pnvg3E1936wer_wXbGLlN</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>Campos, P E</creator><creator>Buffardi, A L</creator><creator>Chiappe, M</creator><creator>Buendía, C</creator><creator>Garcia, P J</creator><creator>Carcamo, C P</creator><creator>Garnett, G</creator><creator>White, P</creator><creator>Holmes, K K</creator><general>BMJ Publishing Group Ltd</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7QL</scope><scope>C1K</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20061201</creationdate><title>Utility of the Determine Syphilis TP rapid test in commercial sex venues in Peru</title><author>Campos, P E ; Buffardi, A L ; Chiappe, M ; Buendía, C ; Garcia, P J ; Carcamo, C P ; Garnett, G ; White, P ; Holmes, K K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b523t-9b22ef346a52856cb6c902cf65300f6e63f5c47ccb131b5e86883273cd82cab13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>chlamydial infection</topic><topic>Determine Syphilis TP</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>female sex workers</topic><topic>FSW</topic><topic>gonorrhoea</topic><topic>Hemagglutination Inhibition Tests - methods</topic><topic>Hemagglutination Inhibition Tests - standards</topic><topic>Humans</topic><topic>Infections</topic><topic>Laboratories</topic><topic>PCR</topic><topic>Peru</topic><topic>Peruvian Ministry of Health HIV/STI Control Program</topic><topic>Point-of-Care Systems - standards</topic><topic>polymerase chain reaction</topic><topic>positive predictive values</topic><topic>PPV</topic><topic>PROCETSS</topic><topic>Rapid Diagnostics</topic><topic>rapid plasma reagin</topic><topic>rapid testing</topic><topic>RPR</topic><topic>Sensitivity and Specificity</topic><topic>Sex industry</topic><topic>Sex Work</topic><topic>Sexually transmitted diseases</topic><topic>sexually transmitted infections</topic><topic>STD</topic><topic>STI</topic><topic>Syphilis</topic><topic>Syphilis - diagnosis</topic><topic>Syphilis Serodiagnosis - methods</topic><topic>Syphilis Serodiagnosis - standards</topic><topic>Teams</topic><topic>TPHA</topic><topic>TPPA</topic><topic>Treponema pallidum</topic><topic>Treponema pallidum - isolation &amp; purification</topic><topic>Treponema pallidum haemagglutination assay</topic><topic>Treponema pallidum particle agglutination assay</topic><topic>trichomoniasis</topic><topic>Vagina</topic><topic>Workers</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Campos, P E</creatorcontrib><creatorcontrib>Buffardi, A L</creatorcontrib><creatorcontrib>Chiappe, M</creatorcontrib><creatorcontrib>Buendía, C</creatorcontrib><creatorcontrib>Garcia, P J</creatorcontrib><creatorcontrib>Carcamo, C P</creatorcontrib><creatorcontrib>Garnett, G</creatorcontrib><creatorcontrib>White, P</creatorcontrib><creatorcontrib>Holmes, K K</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; 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Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Sexually transmitted infections</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Campos, P E</au><au>Buffardi, A L</au><au>Chiappe, M</au><au>Buendía, C</au><au>Garcia, P J</au><au>Carcamo, C P</au><au>Garnett, G</au><au>White, P</au><au>Holmes, K K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Utility of the Determine Syphilis TP rapid test in commercial sex venues in Peru</atitle><jtitle>Sexually transmitted infections</jtitle><addtitle>Sex Transm Infect</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>82</volume><issue>suppl 5</issue><spage>v22</spage><epage>v25</epage><pages>v22-v25</pages><issn>1368-4973</issn><eissn>1472-3263</eissn><abstract>Objectives: This study sought to evaluate the utility of the Determine Syphilis TP test performed in Peruvian commercial sex venues for the detection of active syphilis; and determine the feasibility of integrating rapid syphilis testing for female sex workers (FSW) into existing health outreach services. Methods: We tested 3586 female sex workers for syphilis by Determine in the field using whole blood fingerstick, and by rapid plasma reagin (RPR) and Treponema pallidum haemagglutination assay (TPHA) in a central laboratory in Lima using sera. Results: 97.4% of the FSW offered rapid syphilis testing participated; and among those who tested positive, 87% visited the local health centre for treatment. More than twice as many specimens were RPR reactive using serum in Lima (5.7%) than tested positive by whole blood Determine in the field (2.8%), and although most were confirmed by TPHA, only a small proportion (0.7%) were RPR reactive at ⩾1:8 dilutions, and likely indicating active syphilis. Sensitivity, specificity and positive predictive value of the Determine Syphilis TP test in whole blood when compared to serum RPR reactivity at any dilution confirmed by TPHA as the gold standard were 39.3%, 99.2% and 71.4%, respectively. Sensitivity improved to 64.0% when using serum RPR ⩾1:8 confirmed by TPHA. Invalid tests were rare (0.3%). Conclusions: Rapid syphilis testing in sex work venues proved feasible, but Determine using whole blood obtained by fingerstick was substantially less sensitive than reported in previous laboratory-based studies using serum. Although easy to perform in outreach venues, the utility of this rapid syphilis test was relatively low in settings where a large proportion of the targeted population has been previously tested and treated.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd</pub><pmid>17116642</pmid><doi>10.1136/sti.2006.023325</doi><oa>free_for_read</oa></addata></record>
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source MEDLINE; BMJ Journals - NESLi2; PubMed Central; Alma/SFX Local Collection
subjects chlamydial infection
Determine Syphilis TP
Feasibility Studies
Female
female sex workers
FSW
gonorrhoea
Hemagglutination Inhibition Tests - methods
Hemagglutination Inhibition Tests - standards
Humans
Infections
Laboratories
PCR
Peru
Peruvian Ministry of Health HIV/STI Control Program
Point-of-Care Systems - standards
polymerase chain reaction
positive predictive values
PPV
PROCETSS
Rapid Diagnostics
rapid plasma reagin
rapid testing
RPR
Sensitivity and Specificity
Sex industry
Sex Work
Sexually transmitted diseases
sexually transmitted infections
STD
STI
Syphilis
Syphilis - diagnosis
Syphilis Serodiagnosis - methods
Syphilis Serodiagnosis - standards
Teams
TPHA
TPPA
Treponema pallidum
Treponema pallidum - isolation & purification
Treponema pallidum haemagglutination assay
Treponema pallidum particle agglutination assay
trichomoniasis
Vagina
Workers
Young adults
title Utility of the Determine Syphilis TP rapid test in commercial sex venues in Peru
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