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Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial

BACKGROUND: Integration of a sensitive point-of-care (POC) HIV viral load (VL) test into screening algorithms may help detect acute HIV infection earlier, identify people with HIV (PWH) who are not virally suppressed, and facilitate earlier referral to antiretroviral therapy (ART), or evaluation for...

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Autores principales: Bayan, Mohammad Harris, Smalls, Travis, Boudreau, Alec, Mirza, Agha W., Pasco, Courtney, Demko, Zoe O, Rothman, Richard E., Hsieh, Yu-Hsiang, Eshleman, Susan H., Mostafa, Heba H., Gonzalez-Jimenez, Nathalie, Chavez, Pollyanna R., Emerson, Brian, Delaney, Kevin P., Daugherty, Debra, MacGowan, Robin J., Manabe, Yukari C., Hamill, Matthew M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474693/
https://www.ncbi.nlm.nih.gov/pubmed/37658305
http://dx.doi.org/10.1186/s12879-023-08459-7
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author Bayan, Mohammad Harris
Smalls, Travis
Boudreau, Alec
Mirza, Agha W.
Pasco, Courtney
Demko, Zoe O
Rothman, Richard E.
Hsieh, Yu-Hsiang
Eshleman, Susan H.
Mostafa, Heba H.
Gonzalez-Jimenez, Nathalie
Chavez, Pollyanna R.
Emerson, Brian
Delaney, Kevin P.
Daugherty, Debra
MacGowan, Robin J.
Manabe, Yukari C.
Hamill, Matthew M.
author_facet Bayan, Mohammad Harris
Smalls, Travis
Boudreau, Alec
Mirza, Agha W.
Pasco, Courtney
Demko, Zoe O
Rothman, Richard E.
Hsieh, Yu-Hsiang
Eshleman, Susan H.
Mostafa, Heba H.
Gonzalez-Jimenez, Nathalie
Chavez, Pollyanna R.
Emerson, Brian
Delaney, Kevin P.
Daugherty, Debra
MacGowan, Robin J.
Manabe, Yukari C.
Hamill, Matthew M.
author_sort Bayan, Mohammad Harris
collection PubMed
description BACKGROUND: Integration of a sensitive point-of-care (POC) HIV viral load (VL) test into screening algorithms may help detect acute HIV infection earlier, identify people with HIV (PWH) who are not virally suppressed, and facilitate earlier referral to antiretroviral therapy (ART), or evaluation for pre-exposure prophylaxis (PrEP). This report describes a randomized clinical trial sponsored by the Centers for Disease Control and Prevention (CDC): “Ending the HIV Epidemic Through Point-of-Care Technologies” (EHPOC). The study’s primary aim is to evaluate the use of a POC HIV VL test as part of a testing approach and assess the impact on time to linkage to ART or PrEP. The study will recruit people in Baltimore, Maryland, including patients attending a hospital emergency department, patients attending an infectious disease clinic, and people recruited via community outreach. The secondary aim is to evaluate the performance characteristics of two rapid HIV antibody tests approved by the United States Food and Drug Administration (FDA). METHODS: The study will recruit people 18 years or older who have risk factors for HIV acquisition and are not on PrEP, or PWH who are not taking ART. Participants will be randomly assigned to either the control arm or the intervention arm. Participants randomized to the control arm will only receive the standard-of-care (SOC) HIV screening tests. Intervention arm participants will receive a POC HIV VL test in addition to the SOC HIV diagnostic screening tests. Follow up will consist of an interim phone survey conducted at week-4 and an in-person week-12 visit. Demographic and behavioral information, and oral fluid and blood specimens will be collected at enrollment and at week-12. Survey data will be captured in a Research Electronic Data Capture (REDCap) database. Participants in both arms will be referred for either ART or PrEP based on their HIV test results. DISCUSSION: The EHPOC trial will explore a novel HIV diagnostic technology that can be performed at the POC and provide viral assessment. The study may help inform HIV testing algorithms and contribute to the evidence to support same day ART and PrEP recommendations. TRIAL REGISTRATION: NIH ClinicalTrials.gov NCT04793750. Date: 11 March 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08459-7.
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spelling pubmed-104746932023-09-03 Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial Bayan, Mohammad Harris Smalls, Travis Boudreau, Alec Mirza, Agha W. Pasco, Courtney Demko, Zoe O Rothman, Richard E. Hsieh, Yu-Hsiang Eshleman, Susan H. Mostafa, Heba H. Gonzalez-Jimenez, Nathalie Chavez, Pollyanna R. Emerson, Brian Delaney, Kevin P. Daugherty, Debra MacGowan, Robin J. Manabe, Yukari C. Hamill, Matthew M. BMC Infect Dis Study Protocol BACKGROUND: Integration of a sensitive point-of-care (POC) HIV viral load (VL) test into screening algorithms may help detect acute HIV infection earlier, identify people with HIV (PWH) who are not virally suppressed, and facilitate earlier referral to antiretroviral therapy (ART), or evaluation for pre-exposure prophylaxis (PrEP). This report describes a randomized clinical trial sponsored by the Centers for Disease Control and Prevention (CDC): “Ending the HIV Epidemic Through Point-of-Care Technologies” (EHPOC). The study’s primary aim is to evaluate the use of a POC HIV VL test as part of a testing approach and assess the impact on time to linkage to ART or PrEP. The study will recruit people in Baltimore, Maryland, including patients attending a hospital emergency department, patients attending an infectious disease clinic, and people recruited via community outreach. The secondary aim is to evaluate the performance characteristics of two rapid HIV antibody tests approved by the United States Food and Drug Administration (FDA). METHODS: The study will recruit people 18 years or older who have risk factors for HIV acquisition and are not on PrEP, or PWH who are not taking ART. Participants will be randomly assigned to either the control arm or the intervention arm. Participants randomized to the control arm will only receive the standard-of-care (SOC) HIV screening tests. Intervention arm participants will receive a POC HIV VL test in addition to the SOC HIV diagnostic screening tests. Follow up will consist of an interim phone survey conducted at week-4 and an in-person week-12 visit. Demographic and behavioral information, and oral fluid and blood specimens will be collected at enrollment and at week-12. Survey data will be captured in a Research Electronic Data Capture (REDCap) database. Participants in both arms will be referred for either ART or PrEP based on their HIV test results. DISCUSSION: The EHPOC trial will explore a novel HIV diagnostic technology that can be performed at the POC and provide viral assessment. The study may help inform HIV testing algorithms and contribute to the evidence to support same day ART and PrEP recommendations. TRIAL REGISTRATION: NIH ClinicalTrials.gov NCT04793750. Date: 11 March 2021. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08459-7. BioMed Central 2023-09-01 /pmc/articles/PMC10474693/ /pubmed/37658305 http://dx.doi.org/10.1186/s12879-023-08459-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Bayan, Mohammad Harris
Smalls, Travis
Boudreau, Alec
Mirza, Agha W.
Pasco, Courtney
Demko, Zoe O
Rothman, Richard E.
Hsieh, Yu-Hsiang
Eshleman, Susan H.
Mostafa, Heba H.
Gonzalez-Jimenez, Nathalie
Chavez, Pollyanna R.
Emerson, Brian
Delaney, Kevin P.
Daugherty, Debra
MacGowan, Robin J.
Manabe, Yukari C.
Hamill, Matthew M.
Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial
title Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial
title_full Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial
title_fullStr Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial
title_full_unstemmed Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial
title_short Evaluating the impact of point-of-care HIV viral load assessment on linkage to care in Baltimore, MD: a randomized controlled trial
title_sort evaluating the impact of point-of-care hiv viral load assessment on linkage to care in baltimore, md: a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10474693/
https://www.ncbi.nlm.nih.gov/pubmed/37658305
http://dx.doi.org/10.1186/s12879-023-08459-7
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