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赞比亚和南非教养机构的普遍检测与治疗:多地点前瞻性队列研究。

Universal test-and-treat in Zambian and South African correctional facilities: a multisite prospective cohort study.

机构信息

Centre for Infectious Disease Research in Zambia (CIDRZ), Lusaka, Zambia; Institute for Global Health and Infectious Diseases, School of Medicine, University of North Carolina, Chapel Hill, NC, USA.

School of Medicine, Johns Hopkins University, Baltimore, MD, USA; The Aurum Institute, Johannesburg, South Africa.

出版信息

Lancet HIV. 2020 Dec;7(12):e807-e816. doi: 10.1016/S2352-3018(20)30188-0. Epub 2020 Aug 4.

Abstract

BACKGROUND

Despite the global scale-up of antiretroviral therapy (ART), incarcerated people have not benefited equally from test-and-treat recommendations for HIV. To improve access to ART for incarcerated people with HIV, we introduced a universal test-and-treat (UTT) intervention in correctional facilities in South Africa and Zambia, and aimed to assess UTT feasibility and clinical outcomes.

METHODS

Treatment as Prevention (TasP) was a multisite, mixed methods, implementation research study done at three correctional complexes in South Africa (Johnannesburg and Breede River) and Zambia (Lusaka). Here, we report the clinical outcomes for a prospective cohort of incarcerated individuals who were offered the TasP UTT intervention. Incarcerated individuals were eligible for inclusion if they were aged 18 years or older, with new or previously diagnosed HIV, not yet on ART, and were expected to remain incarcerated for 30 days or longer. To enable the implementation of UTT at the included correctional facilities, we first strengthened on-site HIV service delivery. All participants were offered same-day ART initiation, and had two study-specific follow-up visits scheduled to coincide with routine clinic visits at 6 and 12 months. The main outcomes were ART uptake, time from cohort enrolment to ART initiation, and retention in care and viral suppression at 6 and 12 months. We estimated the association between baseline demographic characteristics and time to ART initiation using Cox proportional hazard models, and, in a post-hoc analysis, we used logistic regression models to assess the association between demographic and clinical variables, including time to ART initiation, and the proportion of participants with a composite poor outcome (defined as viral load >50 copies per mL, or for participants with a missing viral load, lack of retention in care in the on-site ART programme) at 6 months. This study is registered at ClinicalTrials.gov, NCT02946762.

FINDINGS

Between June 23, 2016, and Dec 31, 2017, we identified 1562 incarcerated people with HIV, of whom 1389 (89%) were screened, 1021 (74%) met eligibility criteria, and 975 (95%) were enrolled and followed up to March 31, 2018. At the end of follow-up, 835 (86%) of 975 participants had started ART. Median time from enrolment to ART initiation was 0 days (IQR 0-8). Of 346 participants who remained incarcerated at 6 months, 327 (95%) were retained in care and 269 (78%) had a documented viral load, of whom 262 (97%) achieved viral suppression (<1000 copies per mL). The mortality rate among the 835 participants who had initiated ART was 1·9 per 100 person-years (95% CI 0·9-3·9). No statistically significant associations were identified between any baseline characteristics and time to ART initiation or composite poor outcome.

INTERPRETATION

UTT implementation is feasible in correctional settings, and can achieve levels of same-day ART uptake, retention in care, and viral suppression among incarcerated people with HIV that are comparable to those observed in community settings.

FUNDING

UK Department for International Development, Swedish International Development Cooperation Agency, Norwegian Agency for Development Cooperation.

摘要

背景

尽管抗逆转录病毒疗法(ART)在全球范围内得到了扩展,但被监禁者并未平等受益于艾滋病毒的检测和治疗建议。为了改善被监禁的艾滋病毒感染者获得抗逆转录病毒治疗的机会,我们在南非和赞比亚的三个惩教所引入了普遍检测和治疗(UTT)干预措施,并旨在评估 UTT 的可行性和临床结果。

方法

治疗即预防(TasP)是在南非的三个惩教综合体(约翰内斯堡和布里德河)和赞比亚(卢萨卡)进行的一项多地点、混合方法、实施研究。在这里,我们报告了接受 TasP UTT 干预的被监禁个体的前瞻性队列的临床结果。如果被监禁者年龄在 18 岁或以上,新诊断或以前诊断出 HIV,尚未接受 ART,预计将被监禁 30 天或更长时间,则有资格被纳入。为了使 UTT 在纳入的惩教所实施,我们首先加强了现场的 HIV 服务提供。所有参与者都被提供当天开始 ART 的机会,并计划安排两次专门的研究随访,与 6 个月和 12 个月的常规诊所就诊同时进行。主要结果是 ART 使用率、从队列登记到开始 ART 的时间以及 6 个月和 12 个月时的护理保留和病毒抑制情况。我们使用 Cox 比例风险模型估计了基线人口统计学特征与开始 ART 时间之间的关联,并在事后分析中,使用逻辑回归模型评估了人口统计学和临床变量(包括开始 ART 的时间和在 6 个月时有复合不良结局的参与者比例)与时间之间的关联ART 开始和在现场 ART 方案中缺乏护理保留)。本研究在 ClinicalTrials.gov 上注册,编号为 NCT02946762。

发现

在 2016 年 6 月 23 日至 2017 年 12 月 31 日期间,我们确定了 1562 名感染艾滋病毒的被监禁者,其中 1389 人(89%)接受了筛查,1021 人(74%)符合入选标准,975 人(95%)入组并随访至 2018 年 3 月 31 日。随访结束时,975 名参与者中有 835 名(86%)开始接受 ART。从登记到开始 ART 的中位数时间为 0 天(IQR 0-8)。在 6 个月时仍被监禁的 346 名参与者中,327 名(95%)被保留在护理中,269 名(78%)有记录的病毒载量,其中 262 名(97%)实现了病毒抑制(<1000 拷贝/毫升)。开始 ART 的 835 名参与者中的死亡率为每 100 人年 1.9 人(95%CI 0.9-3.9)。在开始 ART 时间或复合不良结局方面,未发现任何基线特征与时间之间存在统计学显著关联。

解释

UTT 的实施在惩教环境中是可行的,并且可以在感染艾滋病毒的被监禁者中实现与社区环境中相当的当天开始 ART 的接受率、护理保留率和病毒抑制率。

资金

英国国际发展部、瑞典国际发展合作署、挪威发展合作署。

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