首页> 外文OA文献 >The AvecNet Trial to assess whether addition of pyriproxyfen, an insect juvenile hormone mimic, to long-lasting insecticidal mosquito nets provides additional protection against clinical malaria over current best practice in an area with pyrethroid-resistant vectors in rural Burkina Faso: study protocol for a randomised controlled trial
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The AvecNet Trial to assess whether addition of pyriproxyfen, an insect juvenile hormone mimic, to long-lasting insecticidal mosquito nets provides additional protection against clinical malaria over current best practice in an area with pyrethroid-resistant vectors in rural Burkina Faso: study protocol for a randomised controlled trial

机译:AvecNet试验评估了在长效杀虫蚊帐中是否添加除虫幼激素模拟物吡虫洛芬是否比目前最佳实践为在布基纳法索农村地区具有拟除虫菊酯抗性的地区提供了针对临床疟疾的额外保护:研究方案随机对照试验

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摘要

Background\ud\udRecent reductions in malaria in sub-Saharan Africa have been associated with increased coverage with long-lasting insecticidal nets (LLINs). Pyrethroids are currently the only insecticide class used for treating nets, and the rapid increase in resistance to pyrethroids in vector mosquitoes may jeopardise future vector control. Nets containing a novel combination of permethrin, a pyrethroid, and pyriproxyfen, an insect juvenile hormone mimic, (PPF-LLIN) may enhance malaria control, as well as reducing the spread of pyrethroid-resistant mosquitoes. This trial will determine whether PPF-LLINs provide incremental protection against malaria over current best practice of LLINs and prompt treatment in an area with pyrethroid-resistant vectors.\ud\udMethods\ud\udA 2 armed cluster-randomised controlled trial will be conducted in Burkina Faso to assess whether PPF-LLIN (containing 2% permethrin and 1% pyriproxyfen w/w) provide better protection against clinical malaria in children than 2% permethrin-treated LLINs. Study subjects will be recruited and provided with LLINs at the start of the study. The LLINs will be exchanged for PPF-LLIN by cluster in a step-wedge fashion so 3 months before the end of the 2 year trial all participants will have a PPF-LLIN. The primary endpoint will be clinical malaria incidence measured by passive case detection in a cohort of children, aged 6 months to 5 years. Anaemia and parasite prevalence will also be measured in children during cross-sectional surveys. Exposure to malaria parasites will be assessed using light traps followed by identification of common vector species and their sporozoite infection rates. Safety evaluation will include recording of adverse events and pregnancy outcomes. The main endpoint analysis will include adjusting for distance between village clusters with different types of nets, as the impact of PPF-LLIN is likely to increase as larger areas are dominated by PPF-LLIN, reducing the spill over of mosquitoes from villages with LLINs.\ud\udDiscussion\ud\udThe step-wedge design is to measure the impact of an incrementally delivered environmental intervention where we expect the degree of control to be improved as more people use PPF-LLIN over a larger area. Trial findings will help inform policy makers on the effectiveness of PPF-LLIN nets for malaria control in areas of pyrethroid resistance.\ud\udTrial registration\ud\udISRCTN21853394 webcite – AvecNet, registered on 3 April 2013.
机译:背景\ ud \ ud撒哈拉以南非洲地区最近疟疾的减少与持久杀虫网(LLIN)的覆盖率增加有关。拟除虫菊酯是目前唯一用于处理蚊帐的杀虫剂,媒介蚊子对拟除虫菊酯的抗性迅速增加可能会危害未来的媒介控制。含有苄氯菊酯,拟除虫菊酯和吡虫杀酚(一种昆虫幼年激素模拟物)(PPF-LLIN)的新型组合的蚊帐可增强疟疾控制能力,并减少对拟除虫菊酯的抗性蚊子的传播。该试验将确定PPF-LLIN是否比目前的LLIN最佳实践提供更多的抗疟疾保护,并在具有拟除虫菊酯抗性载体的地区迅速进行治疗。布基纳法索评估PPF-LLIN(含2%苄氯菊酯和1%吡咯氧芬w / w)是否比2%苄氯菊酯治疗的LLINs对儿童的临床疟疾提供更好的保护。在研究开始时,将招募研究对象并为其提供LLIN。 LLIN将以逐步楔形的方式通过集群交换为PPF-LLIN,因此在2年试用期结束前3个月,所有参与者都将拥有PPF-LLIN。主要终点将是通过被动病例检测对6个月至5岁年龄段儿童进行的临床疟疾发病率测量。在横断面调查中还将对儿童的贫血和寄生虫患病率进行测量。将使用光阱评估疟疾寄生虫的暴露,然后鉴定常见的媒介物种及其子孢子感染率。安全性评估将包括不良事件和妊娠结局的记录。主要终点分析将包括调整具有不同类型蚊帐的村庄集群之间的距离,因为PPF-LLIN的影响可能会随着PPF-LLIN占较大面积而增加,从而减少蚊子从带有LLIN的村庄溢出。 \ ud \ ud讨论\ ud \ ud阶梯式设计旨在衡量增量交付的环境干预措施的影响,我们预计随着更多人在更大的面积上使用PPF-LLIN,控制程度将得到改善。试验结果将帮助决策者了解PPF-LLIN网络在拟除虫菊酯抗药性领域控制疟疾的有效性。\ ud \ ud试验注册\ ud \ udISRCTN21853394网站– AvecNet,于2013年4月3日注册。

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