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Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda
BACKGROUND: According to the user instructions from the manufacturer of OraQuick HIV self-test (HIVST) kits, individuals whose kits show one red band should be considered to be HIV-negative, no matter how weak the band is. However, recent reports show potential for a second false weak band after sto...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739989/ https://www.ncbi.nlm.nih.gov/pubmed/31514745 http://dx.doi.org/10.1186/s12981-019-0243-1 |
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author | Kisa, Rose Matovu, Joseph K. B. Buregyeya, Esther Musoke, William Vrana-Diaz, Caroline J. Korte, Jeffrey E. Wanyenze, Rhoda K. |
author_facet | Kisa, Rose Matovu, Joseph K. B. Buregyeya, Esther Musoke, William Vrana-Diaz, Caroline J. Korte, Jeffrey E. Wanyenze, Rhoda K. |
author_sort | Kisa, Rose |
collection | PubMed |
description | BACKGROUND: According to the user instructions from the manufacturer of OraQuick HIV self-test (HIVST) kits, individuals whose kits show one red band should be considered to be HIV-negative, no matter how weak the band is. However, recent reports show potential for a second false weak band after storage, thereby creating confusion in the interpretation of results. In this study, we re-tested individuals whose results were initially non-reactive but changed to weak reactive results to determine their true HIV status. METHODS: This study was nested within a large, cluster-randomized HIVST trial implemented among pregnant women attending antenatal care and their male partners in central Uganda between July 2016 and February 2017. Ninety-five initially HIV-negative respondents were enrolled into this study, including 52 whose kits developed a second weak band while in storage and 43 whose kits were interpreted as HIV-positive by interviewers at the next follow-up interview. Respondents were invited to return for repeat HIVST which was performed under the observation of a trained nurse counsellor. After HIVST, respondents underwent blood-based rapid HIV testing as per the national HIV testing algorithm (Determine (Abbot Laboratories), STAT-PAK (Chembio Diagnostic Systems Inc.) and Unigold (Trinity Biotech plc.) and dry blood spots were obtained for DNA/PCR testing. DNA/PCR was considered as the gold-standard HIV testing method. RESULTS: After repeat HIVST, 90 (94.7%) tested HIV-negative; 2 (2.1%) tested HIV-positive; and 3 (3.2%) had missing HIV test results. When respondents were subjected to blood-based rapid HIV testing, 97.9% (93/95) tested HIV-negative while 2.1% (2/95) tested HIV-positive. Finally, when the respondents were subjected to DNA/PCR, 99% (94/95) tested HIV-negative while 1.1% (1/95) tested HIV-positive. CONCLUSIONS: Nearly all initially HIV-negative individuals whose HIVST kits developed a second weak band while in storage or were interpreted as HIV-positive by interviewers were found to be HIV-negative after confirmatory DNA/PCR HIV testing. These findings suggest a need for HIV-negative individuals whose HIVST results change to false positive while under storage or under other sub-optimal conditions to be provided with an option for repeat testing to determine their true HIV status. |
format | Online Article Text |
id | pubmed-6739989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-67399892019-09-16 Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda Kisa, Rose Matovu, Joseph K. B. Buregyeya, Esther Musoke, William Vrana-Diaz, Caroline J. Korte, Jeffrey E. Wanyenze, Rhoda K. AIDS Res Ther Short Report BACKGROUND: According to the user instructions from the manufacturer of OraQuick HIV self-test (HIVST) kits, individuals whose kits show one red band should be considered to be HIV-negative, no matter how weak the band is. However, recent reports show potential for a second false weak band after storage, thereby creating confusion in the interpretation of results. In this study, we re-tested individuals whose results were initially non-reactive but changed to weak reactive results to determine their true HIV status. METHODS: This study was nested within a large, cluster-randomized HIVST trial implemented among pregnant women attending antenatal care and their male partners in central Uganda between July 2016 and February 2017. Ninety-five initially HIV-negative respondents were enrolled into this study, including 52 whose kits developed a second weak band while in storage and 43 whose kits were interpreted as HIV-positive by interviewers at the next follow-up interview. Respondents were invited to return for repeat HIVST which was performed under the observation of a trained nurse counsellor. After HIVST, respondents underwent blood-based rapid HIV testing as per the national HIV testing algorithm (Determine (Abbot Laboratories), STAT-PAK (Chembio Diagnostic Systems Inc.) and Unigold (Trinity Biotech plc.) and dry blood spots were obtained for DNA/PCR testing. DNA/PCR was considered as the gold-standard HIV testing method. RESULTS: After repeat HIVST, 90 (94.7%) tested HIV-negative; 2 (2.1%) tested HIV-positive; and 3 (3.2%) had missing HIV test results. When respondents were subjected to blood-based rapid HIV testing, 97.9% (93/95) tested HIV-negative while 2.1% (2/95) tested HIV-positive. Finally, when the respondents were subjected to DNA/PCR, 99% (94/95) tested HIV-negative while 1.1% (1/95) tested HIV-positive. CONCLUSIONS: Nearly all initially HIV-negative individuals whose HIVST kits developed a second weak band while in storage or were interpreted as HIV-positive by interviewers were found to be HIV-negative after confirmatory DNA/PCR HIV testing. These findings suggest a need for HIV-negative individuals whose HIVST results change to false positive while under storage or under other sub-optimal conditions to be provided with an option for repeat testing to determine their true HIV status. BioMed Central 2019-09-12 /pmc/articles/PMC6739989/ /pubmed/31514745 http://dx.doi.org/10.1186/s12981-019-0243-1 Text en © The Author(s) 2019 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 | Short Report Kisa, Rose Matovu, Joseph K. B. Buregyeya, Esther Musoke, William Vrana-Diaz, Caroline J. Korte, Jeffrey E. Wanyenze, Rhoda K. Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda |
title | Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda |
title_full | Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda |
title_fullStr | Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda |
title_full_unstemmed | Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda |
title_short | Repeat HIV testing of individuals with discrepant HIV self-test results in Central Uganda |
title_sort | repeat hiv testing of individuals with discrepant hiv self-test results in central uganda |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739989/ https://www.ncbi.nlm.nih.gov/pubmed/31514745 http://dx.doi.org/10.1186/s12981-019-0243-1 |
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