Influences on willingness to use vaginal or oral HIV PrEP during pregnancy and breastfeeding in Africa: the multisite MAMMA study

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Study Justification:
The study aimed to explore attitudes and perceptions regarding the use of vaginal rings or oral pills for pre-exposure prophylaxis (PrEP) among pregnant and breastfeeding women in sub-Saharan Africa. This population faces limited options for HIV prevention during these maternal stages. The study aimed to gather insights to inform future prevention trials and identify key influences on willingness to use these products.
Highlights:
– Participants recognized the high risk of HIV during pregnancy and breastfeeding, primarily due to their partner’s infidelities.
– New prevention options were welcomed, and participants valued having multiple options.
– Women reported that health decisions during pregnancy and breastfeeding are typically made jointly with their partners.
– Participants emphasized the importance of HIV protection for the mother-child dyad and the overall health of the family.
– Health care providers’ knowledge and approval of product use during pregnancy and breastfeeding were seen as crucial to address anticipated fears.
Recommendations for Lay Reader and Policy Maker:
1. Involve partners and health care providers in sensitization efforts for future trials: Participants recommended including partners and health care providers in raising awareness and educating the community about new prevention options. This can help address concerns and increase acceptance of these products.
2. Emphasize the importance of the mother-child dyad and family health: Highlight the significance of protecting the mother and child from HIV transmission during pregnancy and breastfeeding. Emphasize that the use of these prevention methods can contribute to the overall health and well-being of the family.
3. Provide multiple options and consider personal preferences: Ensure that a range of prevention options is available to pregnant and breastfeeding women. Recognize that personal preference plays a key role in product choice and acceptability.
Key Role Players:
1. Partners: Engage partners in the decision-making process and sensitization efforts to increase acceptance and support for the use of these prevention methods.
2. Health care providers: Involve health care providers, including doctors and nurses, in educating and counseling pregnant and breastfeeding women about the use of these products. Their knowledge and endorsement are crucial in addressing fears and concerns.
3. Community advisory boards: Collaborate with community advisory boards to disseminate information, raise awareness, and address community concerns regarding the use of these prevention methods.
4. Religious leaders: Engage religious leaders to promote understanding and acceptance of these prevention methods within the community.
Cost Items for Planning Recommendations:
1. Sensitization and education materials: Develop and distribute educational materials, including brochures, posters, and videos, to raise awareness and provide accurate information about the use of vaginal rings and oral pills for PrEP during pregnancy and breastfeeding.
2. Training and capacity building: Provide training to health care providers on the use and benefits of these prevention methods. This may include workshops, seminars, and ongoing support to ensure they are well-informed and able to address concerns.
3. Community engagement activities: Organize community meetings, workshops, and focus group discussions to engage partners, community members, and religious leaders in discussions about the importance and acceptability of these prevention methods.
4. Monitoring and evaluation: Allocate resources for monitoring and evaluating the implementation and impact of the sensitization efforts and the use of these prevention methods among pregnant and breastfeeding women.
Note: The actual cost of these items will depend on various factors, such as the scale of implementation, geographical location, and available resources.

The strength of evidence for this abstract is 8 out of 10.
The evidence in the abstract is strong because it is based on a multisite study conducted in four different countries. The study used focus group discussions and collected data through questionnaires, interviews, and observations. The findings are supported by quotes from participants and are analyzed using a socio-ecological framework. However, to improve the evidence, the abstract could provide more specific details about the sample size, recruitment methods, and data analysis techniques used in the study.

Introduction: Women in sub-Saharan Africa spend a substantial portion of their reproductive lives pregnant and/or breastfeeding (P/BF), yet they have limited options to prevent HIV during these maternal stages. In preparation for phase 3b prevention trials in P/BF women, we explored attitudes about using a vaginal ring or oral pills for pre-exposure prophylaxis (PrEP), perceptions of HIV risk during P/BF and key influences on future PrEP use. Methods: In 2018, we conducted 16 single-sex focus group discussions (FGDs) with community- and clinic-recruited HIV-uninfected women, currently or recently P/BF, aged 18 to 40, and men with (currently or recently) P/BF partners, aged 18+. Participants completed a behavioural questionnaire, viewed an educational video and handled prototype placebo products. FGDs were conducted in local languages and transcribed, coded and analysed, using a socio-ecological framework, for key influences on willingness to use products, HIV risk perceptions and opinions on product attributes. Results: Of the 128 participants (65 women, 63 men) 75% lived with their partner and 84% had a child. Women reported the most important influencers when P/BF were partners, and all stated that health decisions when P/BF are typically made jointly (e.g. medication use; ante/postnatal and baby care). There was consensus that P/BF women are at high risk for HIV, primarily because of their partner’s infidelities, and new prevention options were welcomed. Participants valued multiple options and stated that woman’s personal preference would be key to product choice. Anticipated concerns about products included risk of miscarriage, impact on infant development, complications during delivery and adequate production or taste of breastmilk. Specific perceived disadvantages emerged for the ring (e.g. vaginal discomfort, difficulty inserting/removing) and for pills (e.g. nausea/vomiting) that may be exacerbated during pregnancy. Health care providers’ (HCPs) knowledge and approval of product use during P/BF was needed to mitigate anticipated fears. Conclusions: Participants perceived pregnancy and breastfeeding as high HIV risk periods and valued new prevention options. HIV protection of the mother-child dyad, safety of the baby, and ultimately, health of the family were paramount. Endorsement by HCPs and support from partners were key to future product acceptance. Participants recommended involving partners and HCPs in sensitization efforts for future trials.

MTN‐041/MAMMA (Microbicide/PrEP Acceptability among Mothers and Male Partners in Africa), a multisite study in Blantyre, Malawi; Johannesburg, South Africa; Kampala, Uganda; and Chitungwiza, Zimbabwe, was conducted between May and November 2018. Sixteen single‐sex focus group discussions (FGDs) were conducted across all sites, with individuals independently recruited into the following groups: (a) self‐reported HIV‐uninfected women aged 18 to 40 who were currently or recently (in the past two years) P/BF; or (b) men aged 18+ with female partners who were currently or recently (in the past two years) P/BF. Participants were recruited from various community settings (e.g. street outreach, community advisory board members, word of mouth, construction sites (men only)), antenatal and postnatal clinics (women only)); 129 were screened and eligible and 128 joined the study. Placebo pills for daily oral PrEP (identical in appearance to Truvada, Gilead Sciences, Foster City, CA, USA) and a silicone elastomer placebo ring (identical in appearance to dapivirine vaginal ring, International Partnership for Microbicides, Silver Spring, MD, USA) were presented for handling during FGDs. Demographic and behavioural information were collected through interviewer‐administered questionnaires translated into local languages (Chichewa in Malawi, Zulu or English in South Africa, Luganda in Uganda and Shona in Zimbabwe). The decision‐making dominance subscale was adapted from Pulerwitz et al. [22]. The food insecurity item was based on the Household Food Insecurity Access Scale [23]. FGDs were conducted in these languages using semi‐structured guides by gender‐matched trained local social scientists. All site staff were fluent in the local language of their country, and FGD participants were required to speak and understand the language in order to participate. Topics discussed included HIV risk perceptions, health‐related decision making, key influencers, and interest in HIV prevention methods while P/BF. Just prior to discussing new HIV prevention options, participants viewed a brief educational video and handled prototype placebo products (Figure 1). FGDs were audio recorded, transcribed and translated into English. Interviewers completed a summary report after each FGD for rapid thematic analysis. Screenshots from educational video and demonstration placebo study products. The four‐minute educational video (https://vimeo.com/262813431/dd19ece7dc) was presented at midpoint into the FGD, just prior to moving to the section of the discussion on new prevention products. It described briefly the HIV prevention landscape and the two study products (daily oral pills and monthly vaginal ring), including mechanism of action and how each is to be used. Placebo products (as pictured) that were identical looking to the active dosage forms were passed along during the FGDs so participants could touch and feel both. FGDs, focus group discussions. Demographic and behavioural data on decision making, HIV prevention methods awareness/use and key influencers are presented descriptively in Tables 1 and ​and3.3. Differences by geographical site for women’s responses were calculated using Fisher’s exact tests (Table 3). Characteristics of sample by sex, country (alphabetically ordered) and overall P/BF, Pregnant and/or breastfeeding; PrEP, pre‐exposure prophylaxis. Women’s reported key influencers during pregnancy and breastfeeding, overall and by country Fisher’s Exact p‐value Fisher’s Exact p‐value At church they say that the head of the family is the man, so a woman may want [to use] but if the man doesn’t it cannot be possible. So, the first one to have the decision is the man. [Obama, 35, man, Blantyre] All sites research staff attended several analysis workshops and participated in a rapid preliminary analysis of the data they had collected [24]. The findings generated during the workshops directly informed the iterative development of the codebook, which in turn was used to systematically analyse all qualitative data. Transcripts were coded by four coders (Dedoose software, v7.0.23) using the codebook that followed a socio‐ecological framework (Figure 2). An acceptable level of intercoder reliability was set and maintained at approximately 80% agreement for 10 key codes representative of the main topics of interest. The analysis team met weekly to discuss coding questions, issues and emerging themes. Coded data reports were further summarized thematically into analytical memos that were reviewed by site teams. Pseudonyms are used in presenting quotes to protect the identity of participants. Socio‐ecological spheres of influences on future use of HIV prevention products during p/BF periods. Sphere of influence on future product use included the mother and baby dyad, the spouse (or male partner or father of the baby) at the closest interpersonal level, followed by family members (mostly grandmother of the baby, siblings and other family members). Institutionally, important stakeholder included health care providers (doctors, nurses, etc.) and religious leaders. At the socio‐structural level, salient influences included pregnant or breastfeeding‐related permissible or forbidden practices, community rumours that fuelled HIV stigma (influencing all levels from socio‐structural to their partner’s opinion of the products), fear of health innovations, such as PrEP, as a manifestation of general medical mistrust, and patriarchal gender norms favouring the sexual double standard. Salient health outcomes aligned with dyadic protection for efficacy, and with safety, for those exposed to PrEP and VR (the woman and the baby), as well as with the maternal stages of pregnancy and lactation.  = perceived facilitators;  = perceived barriers;  = other topics of influence acting either as perceived facilitators or barriers. Pregnant and/or breastfeeding. All participants provided written informed consent prior to participation. The study protocol was approved by the Western Institutional Review Board and by local IRBs at each of the study sites and was overseen by the regulatory infrastructure of the U.S. National Institutes of Health and the Microbicide Trials Network.

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Based on the information provided, here are some potential innovations that could improve access to maternal health:

1. Development of safe and effective HIV pre-exposure prophylaxis (PrEP) options specifically designed for pregnant and breastfeeding women.
2. Creation of educational materials and videos that provide accurate information about the benefits and risks of using PrEP during pregnancy and breastfeeding.
3. Involvement of partners and healthcare providers in sensitization efforts to increase awareness and acceptance of new prevention options.
4. Addressing concerns about potential risks, such as miscarriage, infant development, and complications during delivery, associated with using PrEP during pregnancy and breastfeeding.
5. Designing PrEP products with improved attributes, such as ease of use, minimal side effects, and compatibility with breastfeeding.
6. Ensuring that healthcare providers have the necessary knowledge and approval to support and guide pregnant and breastfeeding women in using PrEP.
7. Conducting phase 3b prevention trials in sub-Saharan Africa to gather more evidence on the safety and efficacy of PrEP for pregnant and breastfeeding women.
8. Collaborating with community organizations and leaders to reduce HIV stigma and promote acceptance of new prevention options.
9. Integrating PrEP services into existing maternal health programs and clinics to improve access and convenience for women.
10. Providing comprehensive support and counseling services to pregnant and breastfeeding women using PrEP, addressing their specific needs and concerns.

These innovations aim to address the challenges and barriers identified in the study, such as limited prevention options, partner and healthcare provider influence, concerns about safety and side effects, and the need for education and support.
AI Innovations Description
The recommendation from the study is to involve partners and healthcare providers (HCPs) in sensitization efforts for future trials to improve access to maternal health. The study found that partners and HCPs play a crucial role in decision-making regarding health interventions during pregnancy and breastfeeding. Participants emphasized the importance of partner involvement and HCP endorsement in accepting new prevention options. By involving partners and HCPs in sensitization efforts, pregnant and breastfeeding women can receive the necessary support and information to make informed decisions about maternal health interventions. This recommendation aims to address the barriers and concerns identified in the study, such as fears about product safety and potential side effects.
AI Innovations Methodology
Based on the provided information, here are some potential recommendations to improve access to maternal health:

1. Increase awareness and education: Develop comprehensive educational programs that provide accurate information about maternal health, including HIV prevention options during pregnancy and breastfeeding. These programs should target both women and their partners, as well as healthcare providers.

2. Involve partners and healthcare providers: Recognize the importance of partners and healthcare providers in decision-making regarding maternal health. Encourage their involvement in sensitization efforts and provide them with the necessary knowledge and support to endorse and approve the use of HIV prevention products during pregnancy and breastfeeding.

3. Provide multiple prevention options: Recognize the value of offering multiple prevention options to pregnant and breastfeeding women. This can include vaginal rings or oral pills for pre-exposure prophylaxis (PrEP). Taking into account women’s personal preferences can help increase product acceptance and adherence.

4. Address concerns and misconceptions: Address concerns related to the use of HIV prevention products during pregnancy and breastfeeding. This includes addressing fears of miscarriage, impact on infant development, complications during delivery, and the taste or production of breastmilk. Providing accurate information and addressing these concerns can help alleviate fears and increase acceptance.

To simulate the impact of these recommendations on improving access to maternal health, a methodology could include the following steps:

1. Baseline data collection: Collect data on the current access to maternal health services, including HIV prevention options, in the target population. This can involve surveys, interviews, and focus group discussions with pregnant and breastfeeding women, their partners, and healthcare providers.

2. Intervention implementation: Implement the recommended interventions, such as educational programs, involving partners and healthcare providers, and providing multiple prevention options. Ensure that these interventions are tailored to the specific needs and cultural context of the target population.

3. Monitoring and evaluation: Continuously monitor the implementation of the interventions and collect data on key indicators related to access to maternal health. This can include the number of women and partners reached through educational programs, changes in knowledge and attitudes, and the uptake of HIV prevention products during pregnancy and breastfeeding.

4. Impact assessment: Analyze the collected data to assess the impact of the interventions on improving access to maternal health. This can involve comparing the baseline data with the post-intervention data to identify changes in knowledge, attitudes, and behaviors related to maternal health. Additionally, assess the uptake of HIV prevention products and any changes in health outcomes, such as reduced HIV transmission rates.

5. Adjustments and improvements: Based on the findings from the impact assessment, make any necessary adjustments or improvements to the interventions. This can involve refining educational programs, addressing specific concerns or barriers identified during the evaluation, and further engaging partners and healthcare providers in the process.

By following this methodology, it is possible to simulate the impact of the recommended interventions on improving access to maternal health and assess their effectiveness in addressing the specific challenges faced by pregnant and breastfeeding women in sub-Saharan Africa.

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