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首页> 外文期刊>PLoS Medicine >Estimating the real-world effects of expanding antiretroviral treatment eligibility: Evidence from a regression discontinuity analysis in Zambia
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Estimating the real-world effects of expanding antiretroviral treatment eligibility: Evidence from a regression discontinuity analysis in Zambia

机译:评估扩大抗逆转录病毒治疗资格的现实效果:来自赞比亚的回归间断分析的证据

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Background Although randomized trials have established the clinical efficacy of treating all persons living with HIV (PLWHs), expanding treatment eligibility in the real world may have additional behavioral effects (e.g., changes in retention) or lead to unintended consequences (e.g., crowding out sicker patients owing to increased patient volume). Using a regression discontinuity design, we sought to assess the effects of a previous change to Zambia’s HIV treatment guidelines increasing the threshold for treatment eligibility from 350 to 500 cells/μL to anticipate effects of current global efforts to treat all PLWHs. Methods and findings We analyzed antiretroviral therapy (ART)-na?ve adults who newly enrolled in HIV care in a network of 64 clinics operated by the Zambian Ministry of Health and supported by the Centre for Infectious Disease Research in Zambia (CIDRZ). Patients were restricted to those enrolling in a narrow window around the April 1, 2014 change to Zambian HIV treatment guidelines that raised the CD4 threshold for treatment from 350 to 500 cells/μL (i.e., August 1, 2013, to November 1, 2014). Clinical and sociodemographic data were obtained from an electronic medical record system used in routine care. We used a regression discontinuity design to estimate the effects of this change in treatment eligibility on ART initiation within 3 months of enrollment, retention in care at 6 months (defined as clinic attendance between 3 and 9 months after enrollment), and a composite of both ART initiation by 3 months and retention in care at 6 months in all new enrollees. We also performed an instrumental variable (IV) analysis to quantify the effect of actually initiating ART because of this guideline change on retention. Overall, 34,857 ART-na?ve patients (39.1% male, median age 34 years [IQR 28–41], median CD4 268 cells/μL [IQR 134–430]) newly enrolled in HIV care during this period; 23,036 were analyzed after excluding patients around the threshold to allow for clinic-to-clinic variations in actual guideline uptake. In all newly enrolling patients, expanding the CD4 threshold for treatment from 350 to 500 cells/μL was associated with a 13.6% absolute increase in ART initiation within 3 months of enrollment (95% CI, 11.1%–16.2%), a 4.1% absolute increase in retention at 6 months (95% CI, 1.6%–6.7%), and a 10.8% absolute increase in the percentage of patients who initiated ART by 3 months and were retained at six months (95% CI, 8.1%–13.5%). These effects were greatest in patients who would have become newly eligible for ART with the change in guidelines: a 43.7% increase in ART initiation by 3 months (95% CI, 37.5%–49.9%), 13.6% increase in retention at six months (95% CI, 7.3%–20.0%), and a 35.5% increase in the percentage of patients on ART at 3 months and still in care at 6 months [95% CI, 29.2%–41.9%). We did not observe decreases in ART initiation or retention in patients not directly targeted by the guideline change. An IV analysis found that initiating ART in response to the guideline change led to a 37.9% (95% CI, 28.8%–46.9%) absolute increase in retention in care. Limitations of this study include uncertain generalizability under newer models of care, lack of laboratory data (e.g., viral load), inability to account for earlier stages in the HIV care cascade (e.g., HIV testing and linkage), and potential for misclassification of eligibility status or outcome. Conclusions In this study, guidelines raising the CD4 threshold for treatment from 350 to 500 cells/μL were associated with a rapid rise in ART initiation as well as enhanced retention among newly treatment-eligible patients, without negatively impacting patients with lower CD4 levels. These data suggest that health systems in Zambia and other high-prevalence settings could substantially enhance engagement even among those with high CD4 levels (i.e., above 500 cells/μL) by expanding treatment without undermining existing care standards.
机译:背景技术尽管随机试验已确立了治疗所有HIV感染者(PLWHs)的临床疗效,但扩大现实世界中的治疗资格可能会产生其他行为影响(例如,保留率的变化)或导致意想不到的后果(例如,将病者挤出人群)因患者数量增加而导致患者死亡)。我们使用回归间断设计,试图评估先前对赞比亚的HIV治疗指南所做的更改所产生的影响,从而将治疗资格的阈值从350个细胞/微升提高至500个细胞/微升,以预测当前全球治疗所有PLWH的努力所产生的影响。方法和结果我们分析了由赞比亚卫生部运营,并得到赞比亚传染病研究中心(CIDRZ)支持的由64个诊所组成的网络中新加入HIV护理的初次接受抗逆转录病毒治疗的成年人。患者仅限于2014年4月1日左右更改为赞比亚HIV治疗指南的狭窄窗口中登记的患者,该指南将CD4的治疗阈值从350个细胞/微升提高至500个细胞/微升(即,2013年8月1日至2014年11月1日) 。临床和社会人口统计学数据是从常规医疗中使用的电子病历系统获得的。我们使用回归不连续性设计来评估这种治疗资格变化对入组3个月内开始抗病毒治疗,6个月保留护理(定义为入组3到9个月之间的临床出诊率)以及两者的综合影响所有新入组者均需在3个月后开始抗逆转录病毒治疗,并在6个月时保留护理。我们还进行了一项工具变量(IV)分析,以量化实际启动抗逆转录病毒治疗的效果,因为该指南对保留率的改变。总体而言,在此期间新招募了34,857例首次接受过抗病毒治疗的患者(男性39.1%,中位年龄34岁[IQR 28-41],中位CD4 268细胞/μL[IQR 134-430]);在排除阈值附近的患者后,对23,036例患者进行了分析,以允许实际的临床指导摄入量因临床而异。在所有新入组患者中,将治疗的CD4阈值从350个细胞/μL扩展到500个细胞/μL,与入组3个月内ART起始绝对增加13.6%有关(95%CI,11.1%–16.2%),4.1%六个月时保留的绝对增加(95%CI,1.6%–6.7%),开始三个月并保留六个月的患者的绝对百分比增加了10.8%(95%CI,8.1%– 13.5%)。这些变化在指南改变后将重新获得抗病毒治疗的患者中最为明显:3个月抗病毒治疗起始增加43.7%(95%CI,37.5%–49.9%),六个月保留率增加13.6% (95%CI,7.3%–20.0%),并且在3个月时接受ART治疗并在6个月仍在接受护理的患者百分比增加了35.5%[95%CI,29.2%–41.9%)。我们未观察到未由指南更改直接靶向的患者的ART起始或保留率下降。一项IV分析发现,根据指南更改发起抗逆转录病毒治疗可以使护理保留绝对增加37.9%(95%CI,28.8%–46.9%)。这项研究的局限性包括在较新的护理模式下的普遍性不确定,缺乏实验室数据(例如病毒载量),无法解释艾滋病毒护理工作的早期阶段(例如艾滋病毒检测和关联)以及资格分类错误的可能性状态或结果。结论在这项研究中,将治疗的CD4阈值从350细胞/μL提高到500细胞/μL的指南与ART起始的迅速增加以及新治疗患者的保留率提高有关,而不会对CD4水平较低的患者产生负面影响。这些数据表明,即使在CD4水平高(即高于500个细胞/μL)的CD4水平高的患者中,赞比亚和其他高流行环境的卫生系统也可以通过扩大治疗而不会破坏现有的护理标准,从而大大提高参与度。

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