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Diagnostic accuracy and acceptability of rapid HIV oral testing among adults attending an urban public health facility in Kampala, Uganda

Diagnostic accuracy and acceptability of rapid HIV oral testing among adults attending an urban public health facility in Kampala, Uganda

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dc.contributor.author Nangendo, Joanita
dc.contributor.author Obuku, Ekwaro A.
dc.contributor.author Kawooya, Ismael
dc.contributor.author Mukisa, John
dc.contributor.author Nalutaaya, Annet
dc.contributor.author Musewa, Angella
dc.contributor.author Semitala, Fred C.
dc.contributor.author Karamagi, Charles A.
dc.contributor.author Kalyango, Joan N.
dc.date.accessioned 2021-01-01T21:58:03Z
dc.date.available 2021-01-01T21:58:03Z
dc.date.issued 2017
dc.identifier.issn 1932-6203
dc.identifier.uri http://combine.alvar.ug/handle/1/48140
dc.description.abstract Background The prevalence of HIV in Uganda is 7.3%, and yet nearly 40% of people living with HIV are unaware of their status. The current HIV testing policy which is strictly blood-based poses several challenges including: a need for high level laboratory skills, stringent waste disposal needs, and painful sample collection. It is envisaged that introduction of a rapid, painless HIV oral fluid test as a potential alternative is likely to increase the number of people testing. The aim of this study was to determine the diagnostic accuracy and acceptability of rapid HIV oral testing among adults attending Kisenyi Health Centre IV in Kampala. Methods and findings We conducted a cross-sectional study among 440 adults recruited consecutively at Kisenyi Health Centre IV from January to March 2016. The diagnostic accuracy of the HIV oral test was assessed by comparing to the national HIV serial testing algorithm. We also assessed for acceptability among patients and health care workers (HCWs) by triangulating responses from a structured questionnaire, three focus group discussions and seven key informant interviews. Acceptability was defined as willingness to take the test at the time of the study and intention for future use of the test if it was availed. The prevalence of HIV infection among study participants was 14.8%. The HIV oral fluid test was highly accurate with sensitivity of 100% (95% CI; 94.5-100.0), specificity of 100% (95% CI; 99.0-100.0), positive predictive value (PPV) of 100% (95% CI; 94.5-100.0) and negative predictive value (NPV) of 100% (95% CI; 99.0-100.0). Acceptability of HIV oral testing was also high at 87.0% (95% CI; 83.6-89.9). Participants preferred HIV oral testing because it was: pain free (91%, n = 399) and did not require blood draw (82%, n = 360). Conclusion The HIV oral fluid test has high diagnostic accuracy and acceptability. HIV oral testing is a suitable addition to the national HIV testing strategies with the potential of increasing access to HIV testing services in Uganda.
dc.description.sponsorship Fogarty International Center of the National Institutes of HealthUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH Fogarty International Center (FIC) [D43 TW010037]
dc.description.sponsorship FOGARTY INTERNATIONAL CENTERUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH Fogarty International Center (FIC) [D43TW010037, D43TW010037, D43TW010037, D43TW010037, D43TW010037, D43TW010037] Funding Source: NIH RePORTER
dc.language English
dc.publisher PUBLIC LIBRARY SCIENCE
dc.relation.ispartof PLOS One
dc.title Diagnostic accuracy and acceptability of rapid HIV oral testing among adults attending an urban public health facility in Kampala, Uganda
dc.type Article
dc.identifier.isi 000408355800010
dc.identifier.doi 10.1371/journal.pone.0182050
dc.identifier.pmid 28832588
dc.publisher.city SAN FRANCISCO
dc.publisher.address 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
dc.identifier.volume 12
dc.identifier.issue 8
dc.subject.wc Multidisciplinary Sciences
dc.subject.sc Science & Technology - Other Topics
dc.description.oa DOAJ Gold
dc.description.oa Green Published
dc.description.pages 13
dc.subject.kwp Performance
dc.identifier.articleno e0182050
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Sch Med, Clin Epidemiol Unit, Kampala, Uganda
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Africa Ctr Systemat Reviews & Knowledge Translat, Kampala, Uganda
dc.description.affiliation London Sch Hyg & Trop Med, Fac Epidemiol & Populat Hlth, London, England
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Dept Internal Med, Kampala, Uganda
dc.description.affiliation Makerere Univ, Joint AIDS Program MJAP, Kampala, Uganda
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Dept Pediat & Child Hlth, Kampala, Uganda
dc.description.affiliation Makerere Univ, Coll Hlth Sci, Dept Pharm, Kampala, Uganda
dc.description.email joannangendo@gmail.com
dc.description.email nakayaga2001@yahoo.com
dc.description.corr Nangendo, J (corresponding author), Makerere Univ, Coll Hlth Sci, Sch Med, Clin Epidemiol Unit, Kampala, Uganda.
dc.description.orcid Kawooya, Ismael/0000-0002-7159-7153
dc.description.orcid Kawooya, Ismael/0000-0002-7159-7153
dc.description.orcid mukisa, john/0000-0002-9208-0313


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