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Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial

BACKGROUND: Although the World Health Organization recommends HIV-exposed infants receive a 6-week diagnostic test, few receive results by 12 weeks. Point-of-care (POC) early infant diagnosis (EID) may improve timely diagnosis and treatment. This study assesses the impact of routine POC versus labor...

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Autores principales: Sacks, Emma, Cohn, Jennifer, Ochuka, Bernard, Mafaune, Haurovi, Chadambuka, Addmore, Odhiambo, Collins, Masaba, Rose, Githuka, George, Mahomva, Agnes, Mushavi, Angela, Lemaire, Jean-Francois, Bianchi, Flavia, Machekano, Rhoderick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JAIDS Journal of Acquired Immune Deficiency Syndromes 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302335/
https://www.ncbi.nlm.nih.gov/pubmed/32520909
http://dx.doi.org/10.1097/QAI.0000000000002383
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author Sacks, Emma
Cohn, Jennifer
Ochuka, Bernard
Mafaune, Haurovi
Chadambuka, Addmore
Odhiambo, Collins
Masaba, Rose
Githuka, George
Mahomva, Agnes
Mushavi, Angela
Lemaire, Jean-Francois
Bianchi, Flavia
Machekano, Rhoderick
author_facet Sacks, Emma
Cohn, Jennifer
Ochuka, Bernard
Mafaune, Haurovi
Chadambuka, Addmore
Odhiambo, Collins
Masaba, Rose
Githuka, George
Mahomva, Agnes
Mushavi, Angela
Lemaire, Jean-Francois
Bianchi, Flavia
Machekano, Rhoderick
author_sort Sacks, Emma
collection PubMed
description BACKGROUND: Although the World Health Organization recommends HIV-exposed infants receive a 6-week diagnostic test, few receive results by 12 weeks. Point-of-care (POC) early infant diagnosis (EID) may improve timely diagnosis and treatment. This study assesses the impact of routine POC versus laboratory-based EID on return of results by 12 weeks of age. METHODS: This was a cluster-randomized stepped-wedge trial in Kenya and Zimbabwe. In each country, 18 health facilities were randomly selected for inclusion and randomized to timing of POC implementation. FINDINGS: Nine thousand five hundred thirty-nine infants received tests: 5115 laboratory-based and 4424 POC. In Kenya and Zimbabwe, respectively, caregivers were 1.29 times [95% confidence interval (CI): 1.27 to 1.30, P < 0.001] and 4.56 times (95% CI: 4.50 to 4.60, P < 0.001) more likely to receive EID results by 12 weeks of age with POC versus laboratory-based EID. POC significantly reduced the time between sample collection and return of results to caregiver by an average of 23.03 days (95% CI: 4.85 to 21.21, P < 0.001) in Kenya and 62.37 days (95% CI: 58.94 to 65.80, P < 0.001) in Zimbabwe. For HIV-infected infants, POC significantly increased the percentage initiated on treatment, from 43.2% to 79.6% in Zimbabwe, and resulted in a nonsignificant increase in Kenya from 91.7% to 100%. The introduction of POC EID also significantly reduced the time to antiretroviral therapy initiation by an average of 17.01 days (95% CI: 9.38 to 24.64, P < 0.001) in Kenya and 56.00 days (95% CI: 25.13 to 153.76, P < 0.001) in Zimbabwe. CONCLUSIONS: POC confers significant advantage on the proportion of caregivers receiving timely EID results, and improves time to results receipt and treatment initiation for infected infants. Where laboratory-based EID systems are unable to deliver results to caregivers rapidly, POC should be implemented as part of an integrated testing system.
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spelling pubmed-73023352020-06-29 Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial Sacks, Emma Cohn, Jennifer Ochuka, Bernard Mafaune, Haurovi Chadambuka, Addmore Odhiambo, Collins Masaba, Rose Githuka, George Mahomva, Agnes Mushavi, Angela Lemaire, Jean-Francois Bianchi, Flavia Machekano, Rhoderick J Acquir Immune Defic Syndr Supplement Article BACKGROUND: Although the World Health Organization recommends HIV-exposed infants receive a 6-week diagnostic test, few receive results by 12 weeks. Point-of-care (POC) early infant diagnosis (EID) may improve timely diagnosis and treatment. This study assesses the impact of routine POC versus laboratory-based EID on return of results by 12 weeks of age. METHODS: This was a cluster-randomized stepped-wedge trial in Kenya and Zimbabwe. In each country, 18 health facilities were randomly selected for inclusion and randomized to timing of POC implementation. FINDINGS: Nine thousand five hundred thirty-nine infants received tests: 5115 laboratory-based and 4424 POC. In Kenya and Zimbabwe, respectively, caregivers were 1.29 times [95% confidence interval (CI): 1.27 to 1.30, P < 0.001] and 4.56 times (95% CI: 4.50 to 4.60, P < 0.001) more likely to receive EID results by 12 weeks of age with POC versus laboratory-based EID. POC significantly reduced the time between sample collection and return of results to caregiver by an average of 23.03 days (95% CI: 4.85 to 21.21, P < 0.001) in Kenya and 62.37 days (95% CI: 58.94 to 65.80, P < 0.001) in Zimbabwe. For HIV-infected infants, POC significantly increased the percentage initiated on treatment, from 43.2% to 79.6% in Zimbabwe, and resulted in a nonsignificant increase in Kenya from 91.7% to 100%. The introduction of POC EID also significantly reduced the time to antiretroviral therapy initiation by an average of 17.01 days (95% CI: 9.38 to 24.64, P < 0.001) in Kenya and 56.00 days (95% CI: 25.13 to 153.76, P < 0.001) in Zimbabwe. CONCLUSIONS: POC confers significant advantage on the proportion of caregivers receiving timely EID results, and improves time to results receipt and treatment initiation for infected infants. Where laboratory-based EID systems are unable to deliver results to caregivers rapidly, POC should be implemented as part of an integrated testing system. JAIDS Journal of Acquired Immune Deficiency Syndromes 2020-07-01 2020-06-15 /pmc/articles/PMC7302335/ /pubmed/32520909 http://dx.doi.org/10.1097/QAI.0000000000002383 Text en Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Supplement Article
Sacks, Emma
Cohn, Jennifer
Ochuka, Bernard
Mafaune, Haurovi
Chadambuka, Addmore
Odhiambo, Collins
Masaba, Rose
Githuka, George
Mahomva, Agnes
Mushavi, Angela
Lemaire, Jean-Francois
Bianchi, Flavia
Machekano, Rhoderick
Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial
title Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial
title_full Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial
title_fullStr Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial
title_full_unstemmed Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial
title_short Impact of Routine Point-of-Care Versus Laboratory Testing for Early Infant Diagnosis of HIV: Results From a Multicountry Stepped-Wedge Cluster-Randomized Controlled Trial
title_sort impact of routine point-of-care versus laboratory testing for early infant diagnosis of hiv: results from a multicountry stepped-wedge cluster-randomized controlled trial
topic Supplement Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302335/
https://www.ncbi.nlm.nih.gov/pubmed/32520909
http://dx.doi.org/10.1097/QAI.0000000000002383
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