Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0045168
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dc.titleAccuracy and User-Acceptability of HIV Self-Testing Using an Oral Fluid-Based HIV Rapid Test
dc.contributor.authorNg, O.T.
dc.contributor.authorChow, A.L.
dc.contributor.authorLee, V.J.
dc.contributor.authorChen, M.I.C.
dc.contributor.authorWin, M.K.
dc.contributor.authorTan, H.H.
dc.contributor.authorChua, A.
dc.contributor.authorLeo, Y.S.
dc.date.accessioned2014-11-26T05:02:13Z
dc.date.available2014-11-26T05:02:13Z
dc.date.issued2012-09-17
dc.identifier.citationNg, O.T., Chow, A.L., Lee, V.J., Chen, M.I.C., Win, M.K., Tan, H.H., Chua, A., Leo, Y.S. (2012-09-17). Accuracy and User-Acceptability of HIV Self-Testing Using an Oral Fluid-Based HIV Rapid Test. PLoS ONE 7 (9) : -. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0045168
dc.identifier.issn19326203
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/108859
dc.description.abstractBackground: The United States FDA approved an over-the-counter HIV self-test, to facilitate increased HIV testing and earlier linkage to care. We assessed the accuracy of self-testing by untrained participants compared to healthcare worker (HCW) testing, participants' ability to interpret sample results and user-acceptability of self-tests in Singapore. Methodology/Principal Findings: A cross-sectional study, involving 200 known HIV-positive patients and 794 unknown HIV status at-risk participants was conducted. Participants (all without prior self-test experience) performed self-testing guided solely by visual instructions, followed by HCW testing, both using the OraQuick ADVANCE Rapid HIV 1/2 Antibody Test, with both results interpreted by the HCW. To assess ability to interpret results, participants were provided 3 sample results (positive, negative, and invalid) to interpret. Of 192 participants who tested positive on HCW testing, self-testing was positive in 186 (96.9%), negative in 5 (2.6%), and invalid in 1 (0.5%). Of 794 participants who tested negative on HCW testing, self-testing was negative in 791 (99.6%), positive in 1 (0.1%), and invalid in 2 (0.3%). Excluding invalid tests, self-testing had sensitivity of 97.4% (95% CI 95.1% to 99.7%) and specificity of 99.9% (95% CI: 99.6% to 100%). When interpreting results, 96%, 93.1% and 95.2% correctly read the positive, negative and invalid respectively. There were no significant demographic predictors for false negative self-testing or wrongly interpreting positive or invalid sample results as negative. Eighty-seven percent would purchase the kit over-the-counter; 89% preferred to take HIV tests in private. 72.5% and 74.9% felt the need for pre- and post-test counseling respectively. Only 28% would pay at least USD15 for the test. Conclusions/Significance: Self-testing was associated with high specificity, and a small but significant number of false negatives. Incorrectly identifying model results as invalid was a major reason for incorrect result interpretation. Survey responses were supportive of making self-testing available. © 2012 Ng et al.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1371/journal.pone.0045168
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.contributor.departmentDUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE
dc.description.doi10.1371/journal.pone.0045168
dc.description.sourcetitlePLoS ONE
dc.description.volume7
dc.description.issue9
dc.description.page-
dc.identifier.isiut000309742800039
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