首页> 外文期刊>Clinical trials: journal of the Society for Clinical Trials >Establishing a continuum of care between HIV prevention trials and public healthcare systems: the MIRA Standard of Care program.
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Establishing a continuum of care between HIV prevention trials and public healthcare systems: the MIRA Standard of Care program.

机译:在HIV预防试验和公共医疗体系之间建立连续的护理体系:MIRA护理标准计划。

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BACKGROUND: The ability of researchers to provide sustainable care to individuals who acquire HIV during participation in HIV prevention trials has rapidly expanded along with national treatment options. The METHODS: for Improving Reproductive Health in Africa (MIRA) trial (2003-2006), a phase III multi-site randomized controlled trial, measured the effectiveness of the diaphragm used with Replens lubricant gel in preventing heterosexual acquisition of HIV among women in Zimbabwe and South Africa. The MIRA Standard of Care program, which started towards the end of the trial period and continued for 5 months after trial closeout, enabled women who acquired HIV during the trial to receive additional counseling and clinical care and facilitated links to long-term HIV-related care and treatment from public health facilities. PURPOSE: To describe eligible participants' uptake of these optional services and evaluate the program's strengths and limitations. Methods All women who acquired HIV during their MIRA participation were re-contacted and invited to return to the study clinics for additional care and referrals. Sites reported monthly statistics of uptake of services. RESULTS: From start to end, 185 of 323 (57%) HIV-positive participants accepted additional care; 81 (25%) could not be relocated. 142 (44%) women received referrals to government healthcare facilities and 90 (28%) enrolled in wellness/ treatment programs. Fifty-seven (18%) declined further care, but reasons for doing so were not recorded systematically. LIMITATIONS: The program began after most participants had exited from the MIRA trial and required re-contacting women, resulting in difficulty in locating some participants. CONCLUSIONS: In the future, care for participants who seroconvert should be offered at the trial onset and fully integrated into clinical trials to avoid losing these participants for further care. More research is needed to identify and understand perceived barriers to establishing a continuum of care between clinical trials and public sector health facilities. Clinical Trials 2010; 7: 256-264. http:// ctj.sagepub.com.
机译:背景:研究人员向参加艾滋病毒预防试验期间感染艾滋病毒的人提供可持续护理的能力与国民治疗选择一起迅速发展。方法:用于改善非洲生殖健康(MIRA)的试验(2003年至2006年)是一项III期多站点随机对照试验,测量了Replens润滑脂膜用于预防津巴布韦妇女异性感染HIV的有效性。和南非。 MIRA护理标准计划始于试验期结束,并在试验结束后持续了5个月,使在试验期间感染HIV的妇女能够获得更多的咨询和临床护理,并促进与长期与HIV相关的联系公共卫生机构的护理和治疗。目的:描述符合条件的参与者对这些可选服务的接受程度,并评估该计划的优势和局限性。方法与所有参加MIRA期间感染HIV的妇女进行重新联系,并邀请他们返回研究诊所接受进一步护理和转诊。网站报告了服务使用情况的每月统计数据。结果:从头到尾,在323名HIV阳性参与者中,有185名(57%)接受了额外的护理。 81(25%)无法迁移。 142名(44%)妇女接受了政府医疗机构的转诊,90名(28%)妇女参加了健康/治疗计划。 57(18%)拒绝进一步护理,但未系统记录其原因。局限性:该计划是在大多数参与者退出MIRA试验并要求重新联系女性后开始的,这导致难以找到一些参与者。结论:将来,应在试验开始时为血清转化患者提供护理,并将其完全整合到临床试验中,以避免失去这些患者以进行进一步护理。需要开展更多研究,以识别和理解在临床试验与公共部门卫生机构之间建立连续医疗保健的障碍。 2010年临床试验; 7:256-264。 http://ctj.sagepub.com。

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