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Access to Care and Treatment in Microbicide Trials: Findings from the SOC Mapping Exercise. Sean Philpott, PhD, MSBioethics Science and Ethics Officer Consultation on Operationalizing Access to HIV Treatment and Care June 19th, 2008. Standard of Care.
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Access to Care and Treatmentin Microbicide Trials: Findings from the SOC Mapping Exercise Sean Philpott, PhD, MSBioethics Science and Ethics Officer Consultation on Operationalizing Access to HIV Treatment and Care June 19th, 2008
Standard of Care • The concept of standard of care is rooted in the physician’s obligation to provide patients with the best possible care. • Boundary between expected standards of practice and medical negligence. • Over the past 15 years, the concept of standard of care has migrated into the general discourse of research ethics.
Standard of Care (2) • Standard of care within a research context is an ambiguous and problematic concept. • Ambiguity. • Meaning (a): what is routinely done: “standard practice” • Meaning (b): what ought to be done: “a standard that should be attained”
Standard of Care (3) • ‘Standard practice’ has never been well-defined in medicine. • Standards of care can vary within and between developed and developing countries according to: • Provider knowledge, comfort, training and belief; • Local resources and context; and • Ability of the patient to pay.
Standard of Care (4) • What standard of care should be assured individuals who participate in HIV prevention trials? • What HIV prevention package should be provided to the control group? • What should be provided to participants who acquire the HIV during the trial? • What should be provided to participants who become ill with a disease other than that being studied?
SOC Mapping Exercise: Genesis • Despite lengthy debates, it was felt that information on how researchers and sites were addressing in different countries and contexts was limited. • It was also felt that empiric evidence from the field could inform discussion among all stakeholders on trial ethics, as well as generate ideas for future trial design.
SOC Mapping Exercise: Goals • Document progress made by researchers toward meeting ethical guidance and aspirations; • Compare context-specific challenges in provision of care and prevention; and • Describe different SOC strategies and how sites implemented them.
SOC Mapping Exercise: Methods • Development of survey guide with input from investigators and staff; • Desk review of 7 study protocols & international and site-level documents (SOPs, manuals); • In depth interviews with international investigators and sponsors; • Visits to a sample of 6 sites and community clinical facilities in 4 countries; • In-depth interviews with site trial staff; and • Consultation in Johannesburg, SA.
HIV risk reduction STI services Cervical screening Contraception Pregnancy Research-related harms SOC Mapping Exercise: Range of Issues Examined • Care for Seroconverters • Care of HIV+ Screen-outs • Continuity of care • Capacity building • Ancillary care
SOC Mapping Exercise: Variations in Services • What services were provided: • Study-related care only. • Provision of other non study-related care (primary health care). • Who services were for: • Participants only. • Partners and family members of participants; Screened out women. • Where services were provided: • On site. • Using different referral mechanisms.
SOC Mapping Exercise: Care for Seroconverters • All but one trial allowed women to continue in study and receive study related care. • At a minimum, all trials provided ‘assisted referrals’ to public HIV care services, but the level of assistance varied.
SOC Mapping Exercise: Care for Seroconverters (2) • Some trials also offered: • WHO clinical staging; and • Baseline lab evaluations (CD4, LFTs). • Only one study actually provided funds up front to pay for ART if and when needed in the future.
SOC Mapping Exercise: Care for Screen-Outs • All staff interviewed were increasingly concerned and responsive to need for services for women screened out • All trials offered extra post-test counseling and referral. • All trials provided STI screening and treatment to the woman. Most provided it to her partner.
SOC Mapping Exercise: Care for Screen-Outs (2) • Some trials also provided WHO staging and CD4 counts. • One trial provided an on-site positive-living support group. • One trial provided the same level care (including ART) to everyone. • Seoconverting participants; • Screen-outs; and • The broader community.
SOC Mapping Exercise: Examples of Different Strategies • CONRAD (Benin) • Complete HIV/AIDS care to all, including ART, regardless of study participation. • Post-trial ART for seroconverters funded before study began. • MIRA (Zimbabwe) • Referral to public clinics for HIV care and treatment, with system to track access. • Some ARTs provided during trial. • Implemented a SOC study to look at referral process and barriers to access.
SOC Mapping Exercise: Examples of Different Strategies (2) • Population Council (SA) • Referral to public clinics for HIV care and treatment. At some sites, this relationship was formalized. • Each site also given a discretionary $100K budget. • Gugulethu: Additional HIV care clinic. • Shoshanguve: Positive-living support group. • SOC study to look at access.
SOC Mapping Exercise: Examples of Different Strategies • MDP (SA) • Research clinics co-located with public services. • Also benefits from the research center having a separate PEPFAR-funded ARV program. • MDP (Tanzania) • Mobile clinics for high-risk women. • Women referred without assistance to local services (although monitoring of access and uptake now takes place).
Donor-Imposed Obligations and Restrictions • There are few donor policies that clearly establish the minimum level of prevention and care services that should be made available to all research participants. • Some donors place restrictions on the use of research funds for the provision of non-trial related services, prohibit the use of resources for ancillary care and post-trial care and treatment.
Donor-Imposed Obligations and Restrictions (2) National Institutes of Health (NIH) • “The NIH's authority to ‘encourage and support research’ does not extend to providing treatment following the completion of that research.” (42 USC 284). • Nevertheless, some funded applications must include plans for post-trial access to treatment. • E.g., NIH Guidance for Addressing the Provision of ART for Trial Participants Following Their Completion of NIH-funded HIV ART Trials in Developing Countries
Donor-Imposed Obligations and Restrictions (3) Medical Research Council (MRC) • Will only choose sites where infrastructure exists to complement study concerning ART and care. • Participants identified as HIV infected at enrolment or during study will be referred to local structures.
Donor-Imposed Obligations and Restrictions (4) Agence Nationale de Recherche sur le Sida (ANRS) • Commitment that trial participants will receive treatment and care (also for illnesses that may not be focus of trial). • National country programs will provide ART when required. • People becoming HIV infected during trials must be eligible for ART through national programs; if this is not assured, trial will not be funded by ANRS.
SOC Mapping Exercise:Key Observations • The sites most successful at providing long-term access to comprehensive HIV care: • Allocated resources for HIV care and treatment from the start; • Formed working partnerships with government; and • Co-located research clinics with existing public health facilities.
SOC Mapping Exercise:Site-Level Challenges to Providing Care • Weak referral mechanisms; • Fragile public health systems; • Stigma and/or transport issues; • Lack of established partnerships to provide care; and • Remote location of some trial sites. • Co-location with other facilities vs. Stand-alone or mobile clinics.
SOC Mapping Exercise:Broader Challenges to Providing Care Uncertainty about: • The ethical obligation of researchers; • The expectations and/or restrictions imposed by donors; • The meaning of “standard”; and • The feasibility of providing long-term access to standard care.
Acknowledgments • Lori Heise. • Kathy Shapiro. • Katie West. • Trial network and research site staff. • USAID.