Mao Yurong, Wu Zunyou, McGoogan Jennifer M, Liu David, Gu Diane, Erinoff Lynda, Ling Walter, VanVeldhuisen Paul, Detels Roger, Hasson Albert L, Lindblad Robert, Montaner Julio S G, Tang Zhenzhu, Zhao Yan
The National Centre for AIDS/STD Prevention and Control, Chinese Center for Disease Control and Prevention, 155 Changbai Road, Changping District, Beijing, 102206, China.
National Institute on Drug Abuse, US National Institutes of Health, Bethesda, USA.
BMC Health Serv Res. 2017 Jun 12;17(1):397. doi: 10.1186/s12913-017-2323-z.
The high rate of attrition along the care cascade of infection with human immunodeficiency virus (HIV) results in lost opportunities to provide timely antiretroviral therapy (ART) and to prevent unnecessarily high mortality. This study aims to assess the effectiveness of a structural intervention, the one-stop ("One4All") strategy that streamlines China's HIV care cascade with the intent to improve testing completeness, ART initiation, viral suppression, and mortality.
A two-arm, cluster-randomized controlled trial was implemented in twelve county hospitals in Guangxi China to test the effectiveness of the One4All strategy (intervention arm) compared to the current standard of care (SOC; control arm). The twelve study hospitals were selected for homogeneity and allocated one-to-one to the intervention and control arms. All patients screening HIV positive in study hospitals were enrolled. Target study enrollment was 180 participants per arm, 30 participants per hospital. Basic demographic information was collected as well as HIV risk behavior and route of infection. In intervention hospitals, patients then went on to receive point-of-care CD4 testing and in-parallel viral load (VL) testing whereas patients in control hospitals progressed through the usual SOC cascade. The primary outcome measure was testing completeness within 30 days of positive initial HIV screening result. Testing completeness was defined as receipt of all tests, test results, and post-test counseling. The secondary outcome measure was ART initiation (receipt of first ART prescriptions) within 90 days of positive initial HIV screening result. Tertiary outcome measures were viral suppression (≤200 copies/mL) and all-cause mortality at 12 months.
We expect that this first-ever, cluster-randomized controlled trial of a bundle of interventions intended to streamline the HIV care cascade in China (the One4All strategy) will provide strong evidence for the benefit of accelerating diagnosis, thorough clinical assessment, and ART initiation via an optimized HIV care cascade. We furthermore anticipate that this evidence will be valuable to policymakers looking to elevate China's overall HIV/AIDS response to meet the UNAIDS 90-90-90 targets and the broader, global goal of eradication of the HIV/AIDS epidemic.
ClinicalTrials.gov # NCT02084316 . (Registered on March 7, 2014).
在人类免疫缺陷病毒(HIV)感染的治疗流程中,较高的患者流失率导致失去了提供及时抗逆转录病毒疗法(ART)以及预防不必要的高死亡率的机会。本研究旨在评估一项结构性干预措施——一站式(“One4All”)策略的有效性,该策略简化了中国的HIV治疗流程,旨在提高检测完整性、ART启动率、病毒抑制率以及降低死亡率。
在中国广西的12家县级医院开展了一项双臂、整群随机对照试验,以测试One4All策略(干预组)相对于当前标准治疗(SOC;对照组)的有效性。选择这12家研究医院是因其同质性,并将它们一对一地分配到干预组和对照组。所有在研究医院筛查出HIV呈阳性的患者均被纳入研究。目标研究入组人数为每组180名参与者,每家医院30名参与者。收集了基本人口统计学信息以及HIV风险行为和感染途径。在干预医院,患者随后接受即时CD4检测和同时进行的病毒载量(VL)检测,而对照组医院的患者则按照常规的SOC流程进行。主要结局指标为初次HIV筛查结果呈阳性后的30天内的检测完整性。检测完整性定义为接受所有检测、检测结果以及检测后咨询。次要结局指标为初次HIV筛查结果呈阳性后的90天内的ART启动率(接受首张ART处方)。三级结局指标为12个月时的病毒抑制(≤200拷贝/毫升)和全因死亡率。
我们预计,这项首次针对旨在简化中国HIV治疗流程的一系列干预措施(One4All策略)的整群随机对照试验,将为通过优化HIV治疗流程加速诊断、全面临床评估以及ART启动的益处提供有力证据。我们还预计,这一证据对于希望提升中国总体HIV/AIDS应对水平以实现联合国艾滋病规划署90-90-90目标以及更广泛的全球消除HIV/AIDS流行目标的政策制定者而言将具有价值。
ClinicalTrials.gov # NCT02084316。(于2014年3月7日注册)