1. Developing standards of care for HIV prevention research in developing countries โ a case study of 10 research centers in Eastern and Southern Africa.
- Author
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Ngongo, PrinceBahati, Priddy, Frances, Park, Harriet, Becker, Julie, Bender, Bonnie, Fast, Pat, Anzala, Omu, Mutua, Gaudensia, Ruzagira, Eugene, Kamali, Anatoli, Karita, Etienne, Mugo, Peter, Chomba, Elwyn, Bekker, Linda-Gail, Roux, Surita, Nanvubya, Annet, and Mebrahtu, Tsedal
- Subjects
HIV prevention ,MEDICAL care ,CIRCUMCISION ,CONDOMS ,CONTRACEPTION ,COUNSELING ,DEVELOPING countries ,INTERVIEWING ,RESEARCH methodology ,RESEARCH evaluation ,RESEARCH funding ,SEXUALLY transmitted diseases ,SURVEYS ,HIGHLY active antiretroviral therapy ,FAMILY planning ,DATA analysis software ,MEDICAL coding ,CD4 lymphocyte count - Abstract
Standards of care provided to volunteers in HIV prevention research in developing countries are evolving. Inconsistency in standards, particularly within a research network highlights the need to balance volunteers' health and wellness with the efficient conduct of research. Ten research centers (RC's) in East and Southern Africa affiliated with the International AIDS Vaccine Initiative (IAVI) were studied using a mixed methods approach to understand variations, similarities and gaps in services provided, recipients of services, referral systems, and barriers to referral uptake. These data were then used to develop expected standards across the 10 RCs. Findings indicated that RCs consistently provided HIV risk reduction and family planning (FP) counseling, male condoms, management of sexually transmitted infections, CD-4 counts, and general medical care to volunteers and non-research volunteers. Services that were less consistently provided on-site included: female condoms, adult male circumcision (AMC), antiretroviral therapy (ART) and post-exposure prophylaxis (PEP) in case of rape. The FP options provided on-site varied, with few providing implants, intrauterine devices, tubal ligation, and vasectomy. Most RCs had established referral systems for ART, AMC, PEP, and FP, but few had referral points for psychosocial services. Few RCs had comprehensive guidelines on referrals other than those related to adverse events. Findings indicate that the greatest challenges for referral uptake were transportation and health care costs, poor quality and inconsistency of services at some referral points. Few RCs covered the cost of referrals for non-study related adverse events. A collaborative process between IAVI and the RCs was undertaken to reach consensus on expected standards of care. A set of required and recommended services to be provided on-site or by referral was developed. In developing such standards, we tried to balance scientific priorities, equity, contextual realities, community expectations, and cost-effectiveness. [ABSTRACT FROM AUTHOR]
- Published
- 2012
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