首页> 外文OA文献 >A Cluster-randomized Controlled Trial to Assess the Effectiveness of using 15 DEET Topical Repellent with Long-lasting Insecticidal Nets (LLINs) Compared to a Placebo Lotion on Malaria Transmission.
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A Cluster-randomized Controlled Trial to Assess the Effectiveness of using 15 DEET Topical Repellent with Long-lasting Insecticidal Nets (LLINs) Compared to a Placebo Lotion on Malaria Transmission.

机译:一项集群随机对照试验,以评估使用15%DEET局部驱虫剂和持久性杀虫剂网(LLIN)的效果与安慰剂乳液对疟疾传播的效果。

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摘要

Long-lasting insecticidal nets (LLINs) have limited effect on malaria transmitted outside of sleeping hours. Topical repellents have demonstrated reduction in the incidence of malaria transmitted in the early evening. This study assessed whether 15% DEET topical repellent used in combination with LLINs can prevent greater malaria transmission than placebo and LLINs, in rural Tanzania. A cluster-randomized, placebo-controlled trial was conducted between July 2009 and August 2010 in a rural Tanzanian village. Sample size calculation determined that 10 clusters of 47 households with five people/household were needed to observe a 24% treatment effect at the two-tailed 5% significance level, with 90% power, assuming a baseline malaria incidence of one case/person/year. Ten clusters each were randomly assigned to repellent and control groups by lottery. A total of 4,426 individuals older than six months were enrolled. All households in the village were provided with an LLIN per sleeping space. Repellent and placebo lotion was replaced monthly. The main outcome was rapid diagnostic test (RDT)-confirmed malaria measured by passive case detection (PCD). Incidence rate ratios were estimated from a Poisson model, with adjustment for potential confounders, determined a priori. According-to-protocol approach was used for all primary analyses. The placebo group comprised 1972.3 person-years with 68.29 (95% C.I 37.05-99.53) malaria cases/1,000 person-years. The repellent group comprised 1,952.8 person-years with 60.45 (95% C.I 48.30-72.60) cases /1,000 person-years, demonstrating a non-significant 11.44% reduction in malaria incidence rate in this group, (Wilcoxon rank sum z = 0.529, p = 0.596). Principal components analysis (PCA) of the socio-economic status (SES) of the two groups demonstrated that the control group had a higher SES (Pearson's chi square = 13.38, p = 0.004). Lack of an intervention effect was likely a result of lack of statistical power, poor capture of malaria events or bias caused by imbalance in the SES of the two groups. Low malaria transmission during the study period could have masked the intervention effect and a larger study size was needed to increase discriminatory power. Alternatively, topical repellents may have no impact on malaria transmission in this scenario. Design and implementation of repellent intervention studies is discussed.Trial registration: The trial was registered
机译:持久的杀虫网(LLIN)对在睡眠时间以外传播的疟疾影响有限。局部驱蚊剂已证明在傍晚传播的疟疾发病率降低。这项研究评估了在坦桑尼亚农村地区是否将15%的DEET局部驱虫剂与LLINs组合使用能够预防比安慰剂和LLINs更大的疟疾传播。在2009年7月至2010年8月之间,在坦桑尼亚的一个农村村庄进行了一项随机,安慰剂对照的试验。样本量计算确定,假设基线疟疾发病率为1例/人/人,则需要10集群的47户家庭(5人/户)在2尾5%显着性水平上以90%的功效观察24%的治疗效果。年。通过抽签将十个簇分别随机分配给驱避组和对照组。共有4426个年龄超过6个月的个人参加。每个睡眠空间为村庄的所有家庭提供了LLIN。每月更换驱虫剂和安慰剂乳液。主要结果是通过被动病例检测(PCD)测量的快速诊断测试(RDT)确认的疟疾。发病率比率是根据Poisson模型估算的,并根据先验确定了潜在混杂因素的调整。所有的主要分析均采用了按方案进行的方法。安慰剂组包括1972.3人年/ 1,000人年/68.29(95%C.I 37.05-99.53)疟疾病例。驱避剂组包括1,952.8人/年,其中60.45(95%CI 48.30-72.60)例/ 1,000人-年,表明该组疟疾发病率降低了11.44%,无明显下降,(Wilcoxon等级总和z = 0.529,p = 0.596)。两组的社会经济地位(SES)的主成分分析(PCA)表明,对照组的SES较高(Pearson卡方= 13.38,p = 0.004)。缺乏干预效果可能是由于缺乏统计能力,两组疟疾事件捕获不佳或两组SES失衡引起的偏见。在研究期间,低疟疾传播可能掩盖了干预效果,需要更大的研究规模以增加歧视能力。或者,在这种情况下,局部驱避剂可能对疟疾传播没有影响。讨论了驱避剂干预研究的设计和实施。试验注册:该试验已注册

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