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Optimal Population-Level Infection Detection Strategies for Malaria Control and Elimination in a Spatial Model of Malaria Transmission

机译:疟疾传播空间模型中控制和消除疟疾的最佳人群水平感染检测策略

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摘要

Mass campaigns with antimalarial drugs are potentially a powerful tool for local elimination of malaria, yet current diagnostic technologies are insufficiently sensitive to identify all individuals who harbor infections. At the same time, overtreatment of uninfected individuals increases the risk of accelerating emergence of drug resistance and losing community acceptance. Local heterogeneity in transmission intensity may allow campaign strategies that respond to index cases to successfully target subpatent infections while simultaneously limiting overtreatment. While selective targeting of hotspots of transmission has been proposed as a strategy for malaria control, such targeting has not been tested in the context of malaria elimination. Using household locations, demographics, and prevalence data from a survey of four health facility catchment areas in southern Zambia and an agent-based model of malaria transmission and immunity acquisition, a transmission intensity was fit to each household based on neighborhood age-dependent malaria prevalence. A set of individual infection trajectories was constructed for every household in each catchment area, accounting for heterogeneous exposure and immunity. Various campaign strategies—mass drug administration, mass screen and treat, focal mass drug administration, snowball reactive case detection, pooled sampling, and a hypothetical serological diagnostic—were simulated and evaluated for performance at finding infections, minimizing overtreatment, reducing clinical case counts, and interrupting transmission. For malaria control, presumptive treatment leads to substantial overtreatment without additional morbidity reduction under all but the highest transmission conditions. Compared with untargeted approaches, selective targeting of hotspots with drug campaigns is an ineffective tool for elimination due to limited sensitivity of available field diagnostics. Serological diagnosis is potentially an effective tool for malaria elimination but requires higher coverage to achieve similar results to mass distribution of presumptive treatment.
机译:开展抗疟疾药物的大规模运动可能是当地消除疟疾的有力工具,但是目前的诊断技术对识别所有感染者的敏感性不够。同时,对未感染个体的过度治疗增加了加速出现耐药性和丧失社区接受度的风险。传播强度的局部异质性可以使对索引病例有反应的竞选策略成功地靶向亚专利感染,同时限制过度治疗。尽管已经提出了选择性靶向传播热点作为控制疟疾的策略,但尚未在消除疟疾的背景下测试过这种靶向性。使用来自赞比亚南部四个卫生设施集水区的调查的住户位置,人口统计学和流行率数据,以及基于媒介的疟疾传播和免疫力获取模型,根据邻里年龄相关的疟疾患病率,每个家庭都适合传播强度。为每个集水区的每个家庭构建了一套个体感染轨迹,说明了不同的接触和免疫力。模拟并评估了各种运动策略,例如大规模药物管理,大规模筛查和治疗,局部大规模药物管理,滚雪球反应性病例检测,合并采样以及假设的血清学诊断,以评估发现感染,最大程度地减少过度治疗,减少临床病例数,并中断传输。为了控制疟疾,推定性治疗会导致严重的过度治疗,而除了最高传播条件外,其他所有疾病的发病率均未降低。与非针对性方法相比,由于现有现场诊断方法的敏感性有限,通过毒品运动选择性地针对热点是一种无效的消除手段。血清学诊断可能是消除疟疾的有效工具,但需要更高的覆盖率才能实现与推定治疗的质量分布相似的结果。

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