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The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review
OBJECTIVE: In 2015, the WHO released new guidelines to reduce mother‐to‐child transmission (MTCT) of HIV. The recommendations, known as Option B+, included initiation of lifelong highly active antiretroviral therapy regardless of CD4 count for all HIV‐positive pregnant and breastfeeding mothers. For...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328372/ https://www.ncbi.nlm.nih.gov/pubmed/35477948 http://dx.doi.org/10.1111/tmi.13756 |
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author | Maingi, Mildred Stark, Aliza Hannah Iron‐Segev, Sharon |
author_facet | Maingi, Mildred Stark, Aliza Hannah Iron‐Segev, Sharon |
author_sort | Maingi, Mildred |
collection | PubMed |
description | OBJECTIVE: In 2015, the WHO released new guidelines to reduce mother‐to‐child transmission (MTCT) of HIV. The recommendations, known as Option B+, included initiation of lifelong highly active antiretroviral therapy regardless of CD4 count for all HIV‐positive pregnant and breastfeeding mothers. For infants, exclusive breastfeeding for 6 months and antiviral therapy were sanctioned. Targets of <5% transmission in breastfeeding populations and <2% in non‐breastfeeding populations were set. This review evaluated the impact of Option B+ on MTCT in African countries. METHODS: Using the PRISMA guidelines, a systematic search of PubMed and Google Scholar databases was conducted to identify relevant studies published between 2015 and 2021. All studies meeting inclusion criteria were evaluated. RESULTS: Of the 687 references screened, 22 studies from 11 countries (Cameroon, Ethiopia, Lesotho, Malawi, Rwanda, South Africa, Swaziland, Tanzania, Uganda, Zambia and Zimbabwe) met inclusion criteria. Six studies reported MTCT rates of <2%, 16 studies reported rates of 2–5% and two studies (Uganda and Zambia) reported 6% or more. Rates varied within the same study at different time points postpartum and amongst studies from the same country. Overall, reported MTCT rates appear to be close to WHO targets. However, diverse study designs, selection bias, extensive loss to follow‐up and undocumented adherence rates to Option B+ protocols may significantly underestimate MTCT rates of HIV in Africa. CONCLUSIONS: Standardised protocols for impact evaluation must be established to provide evidenced‐based data on the efficacy of Option B+ in Africa. |
format | Online Article Text |
id | pubmed-9328372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93283722022-07-30 The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review Maingi, Mildred Stark, Aliza Hannah Iron‐Segev, Sharon Trop Med Int Health Systematic Review OBJECTIVE: In 2015, the WHO released new guidelines to reduce mother‐to‐child transmission (MTCT) of HIV. The recommendations, known as Option B+, included initiation of lifelong highly active antiretroviral therapy regardless of CD4 count for all HIV‐positive pregnant and breastfeeding mothers. For infants, exclusive breastfeeding for 6 months and antiviral therapy were sanctioned. Targets of <5% transmission in breastfeeding populations and <2% in non‐breastfeeding populations were set. This review evaluated the impact of Option B+ on MTCT in African countries. METHODS: Using the PRISMA guidelines, a systematic search of PubMed and Google Scholar databases was conducted to identify relevant studies published between 2015 and 2021. All studies meeting inclusion criteria were evaluated. RESULTS: Of the 687 references screened, 22 studies from 11 countries (Cameroon, Ethiopia, Lesotho, Malawi, Rwanda, South Africa, Swaziland, Tanzania, Uganda, Zambia and Zimbabwe) met inclusion criteria. Six studies reported MTCT rates of <2%, 16 studies reported rates of 2–5% and two studies (Uganda and Zambia) reported 6% or more. Rates varied within the same study at different time points postpartum and amongst studies from the same country. Overall, reported MTCT rates appear to be close to WHO targets. However, diverse study designs, selection bias, extensive loss to follow‐up and undocumented adherence rates to Option B+ protocols may significantly underestimate MTCT rates of HIV in Africa. CONCLUSIONS: Standardised protocols for impact evaluation must be established to provide evidenced‐based data on the efficacy of Option B+ in Africa. John Wiley and Sons Inc. 2022-05-29 2022-06 /pmc/articles/PMC9328372/ /pubmed/35477948 http://dx.doi.org/10.1111/tmi.13756 Text en © 2022 The Authors Tropical Medicine & International Health Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Systematic Review Maingi, Mildred Stark, Aliza Hannah Iron‐Segev, Sharon The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review |
title | The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review |
title_full | The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review |
title_fullStr | The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review |
title_full_unstemmed | The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review |
title_short | The impact of Option B+ on mother‐to‐child transmission of HIV in Africa: A systematic review |
title_sort | impact of option b+ on mother‐to‐child transmission of hiv in africa: a systematic review |
topic | Systematic Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328372/ https://www.ncbi.nlm.nih.gov/pubmed/35477948 http://dx.doi.org/10.1111/tmi.13756 |
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