The impact of Option B+ on mother-to-child transmission of HIV in Africa: A systematic review.

Trop Med Int Health

The Hebrew University of Jerusalem, Robert H. Smith Faculty of Agriculture, Food and Environment, Rehovot, Israel.

Published: June 2022

AI Article Synopsis

  • The WHO's Option B+ guidelines, introduced in 2015, aim to reduce HIV transmission from mothers to children by promoting lifelong antiretroviral therapy for pregnant and breastfeeding women, and specifying exclusive breastfeeding for infants for the first six months.
  • A systematic review of studies from 2015 to 2021 identified 22 relevant studies across 11 African countries, revealing mixed MTCT rates: 6 studies reported rates below 2%, while others ranged between 2-6% or more, indicating variability over time and across locations.
  • The review highlights the need for standard evaluation protocols to accurately assess the effectiveness of Option B+, as current methodologies may underestimate MTCT rates due to factors like selection bias

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328372PMC
http://dx.doi.org/10.1111/tmi.13756DOI Listing

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