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Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda

INTRODUCTION: The World Health Organization recommends that countries conduct two phase evaluations of HIV rapid tests (RTs) in order to come up with the best algorithms. In this report, we present the first ever such evaluation in Uganda, involving both blood and oral based RTs. The role of weak po...

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Autores principales: Kaleebu, Pontiano, Kitandwe, Paul Kato, Lutalo, Tom, Kigozi, Aminah, Watera, Christine, Nanteza, Mary Bridget, Hughes, Peter, Musinguzi, Joshua, Opio, Alex, Downing, Robert, Mbidde, Edward Katongole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389083/
https://www.ncbi.nlm.nih.gov/pubmed/29482500
http://dx.doi.org/10.1186/s12879-018-3001-4
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author Kaleebu, Pontiano
Kitandwe, Paul Kato
Lutalo, Tom
Kigozi, Aminah
Watera, Christine
Nanteza, Mary Bridget
Hughes, Peter
Musinguzi, Joshua
Opio, Alex
Downing, Robert
Mbidde, Edward Katongole
author_facet Kaleebu, Pontiano
Kitandwe, Paul Kato
Lutalo, Tom
Kigozi, Aminah
Watera, Christine
Nanteza, Mary Bridget
Hughes, Peter
Musinguzi, Joshua
Opio, Alex
Downing, Robert
Mbidde, Edward Katongole
author_sort Kaleebu, Pontiano
collection PubMed
description INTRODUCTION: The World Health Organization recommends that countries conduct two phase evaluations of HIV rapid tests (RTs) in order to come up with the best algorithms. In this report, we present the first ever such evaluation in Uganda, involving both blood and oral based RTs. The role of weak positive (WP) bands on the accuracy of the individual RT and on the algorithms was also investigated. METHODS: In total 11 blood based and 3 oral transudate kits were evaluated. All together 2746 participants from seven sites, covering the four different regions of Uganda participated. Two enzyme immunoassays (EIAs) run in parallel were used as the gold standard. The performance and cost of the different algorithms was calculated, with a pre-determined price cut-off of either cheaper or within 20% price of the current algorithm of Determine + Statpak + Unigold. In the second phase, the three best algorithms selected in phase I were used at the point of care for purposes of quality control using finger stick whole blood. RESULTS: We identified three algorithms; Determine + SD Bioline + Statpak; Determine + Statpak + SD Bioline, both with the same sensitivity and specificity of 99.2% and 99.1% respectively and Determine + Statpak + Insti, with sensitivity and specificity of 99.1% and 99% respectively as having performed better and met the cost requirements. There were 15 other algorithms that performed better than the current one but rated more than the 20% price. None of the 3 oral mucosal transudate kits were suitable for inclusion in an algorithm because of their low sensitivities. Band intensity affected the performance of individual RTs but not the final algorithms. CONCLUSION: We have come up with three algorithms we recommend for public or Government procurement based on accuracy and cost. In case one algorithm is preferred, we recommend to replace Unigold, the current tie breaker with SD Bioline. We further recommend that all the 18 algorithms that have shown better performance than the current one are made available to the private sector where cost may not be a limiting factor.
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spelling pubmed-63890832019-03-19 Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda Kaleebu, Pontiano Kitandwe, Paul Kato Lutalo, Tom Kigozi, Aminah Watera, Christine Nanteza, Mary Bridget Hughes, Peter Musinguzi, Joshua Opio, Alex Downing, Robert Mbidde, Edward Katongole BMC Infect Dis Research Article INTRODUCTION: The World Health Organization recommends that countries conduct two phase evaluations of HIV rapid tests (RTs) in order to come up with the best algorithms. In this report, we present the first ever such evaluation in Uganda, involving both blood and oral based RTs. The role of weak positive (WP) bands on the accuracy of the individual RT and on the algorithms was also investigated. METHODS: In total 11 blood based and 3 oral transudate kits were evaluated. All together 2746 participants from seven sites, covering the four different regions of Uganda participated. Two enzyme immunoassays (EIAs) run in parallel were used as the gold standard. The performance and cost of the different algorithms was calculated, with a pre-determined price cut-off of either cheaper or within 20% price of the current algorithm of Determine + Statpak + Unigold. In the second phase, the three best algorithms selected in phase I were used at the point of care for purposes of quality control using finger stick whole blood. RESULTS: We identified three algorithms; Determine + SD Bioline + Statpak; Determine + Statpak + SD Bioline, both with the same sensitivity and specificity of 99.2% and 99.1% respectively and Determine + Statpak + Insti, with sensitivity and specificity of 99.1% and 99% respectively as having performed better and met the cost requirements. There were 15 other algorithms that performed better than the current one but rated more than the 20% price. None of the 3 oral mucosal transudate kits were suitable for inclusion in an algorithm because of their low sensitivities. Band intensity affected the performance of individual RTs but not the final algorithms. CONCLUSION: We have come up with three algorithms we recommend for public or Government procurement based on accuracy and cost. In case one algorithm is preferred, we recommend to replace Unigold, the current tie breaker with SD Bioline. We further recommend that all the 18 algorithms that have shown better performance than the current one are made available to the private sector where cost may not be a limiting factor. BioMed Central 2018-02-27 /pmc/articles/PMC6389083/ /pubmed/29482500 http://dx.doi.org/10.1186/s12879-018-3001-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kaleebu, Pontiano
Kitandwe, Paul Kato
Lutalo, Tom
Kigozi, Aminah
Watera, Christine
Nanteza, Mary Bridget
Hughes, Peter
Musinguzi, Joshua
Opio, Alex
Downing, Robert
Mbidde, Edward Katongole
Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda
title Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda
title_full Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda
title_fullStr Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda
title_full_unstemmed Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda
title_short Evaluation of HIV-1 rapid tests and identification of alternative testing algorithms for use in Uganda
title_sort evaluation of hiv-1 rapid tests and identification of alternative testing algorithms for use in uganda
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6389083/
https://www.ncbi.nlm.nih.gov/pubmed/29482500
http://dx.doi.org/10.1186/s12879-018-3001-4
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