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Preparatory work for the future development of scientific opinions on animal health

机译:为动物健康科学观点的未来发展做准备

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This final report summarizes the results of two reviews and a scoping study related to Canine leishmaniosis (CanL). Three objectives were addressed in this project. Objective 1 was to summarize relative sensitivity and specificity estimates of assays used to detect infection in dogs with Leishmania infantum in studies of na?ve dogs in areas where Leishmania infantum infection is endemic. Objective 2 was to summarize data available to estimate the prevalence of parasitological cure (failure to detect organism) after a 12-month follow-up period in animals treated with meglumine antimoniate, miltefosine, and allopurinol or combinations of these drugs for canine leishmaniosis. Objective 3 was to assess diagnostic test characteristics of PCR assays and serological assays (ELISA or IFAT) from studies that use experimental models of Canine leishmaniosis. The same comprehensive search was used for all objectives. The searches yielded 7,405 records. After duplicates were removed, 3,865 records remained. Of these, 243 were broadly identified as diagnostic test evaluation studies and at the 2nd level of screening 18 were considered longitudinal studies. The 18 references were then assessed based on the full text and 7 were considered relevant to the review. The assays assessed by these studies were PCR on skin, buffy coat, bone marrow, blood and conjunctiva, and IFAT and ELISA. For objective 2, 40 potentially relevant records were identified as treatment comparison studies. After full-text screening, 13 studies were included in the review. The treatments varied greatly, and few comparative efficacy estimates were provided. No treatment was associated with 100% cure after 180 days follow-up. For objective 3, 513 citations were identified and the full texts of 169 articles were obtained. Sixty-two articles described at least one of the assays requested (PCR, ELISA or IFAT) and 18 articles described the use of a PCR and either ELISA and/or IFAT.
机译:这份最终报告总结了两项与犬利什曼病(CanL)相关的评论和一项范围界定研究。该项目解决了三个目标。目的1是总结在婴儿利什曼原虫感染流行地区的幼犬研究中用于检测婴儿利什曼原虫狗感染的检测方法的相对灵敏度和特异性估计。目标2是总结可用数据评估在接受葡甲胺锑酸盐,米替福辛和别嘌呤醇或这些药物组合治疗犬利什曼病后12个月的随访期内的寄生虫病治愈率(未能检测到生物)。目的3是从使用犬利什曼病的实验模型进行的研究中评估PCR检测和血清检测(ELISA或IFAT)的诊断测试特征。相同的全面搜索用于所有目标。搜索产生了7,405条记录。删除重复项后,剩余3,865条记录。其中,243项被广泛鉴定为诊断测试评估研究,而在筛查的第二级中,有18项被认为是纵向研究。然后根据全文评估了18篇参考文献,并认为其中7篇与本综述相关。这些研究评估的检测方法是:在皮肤,血沉棕黄层,骨髓,血液和结膜上的PCR以及IFAT和ELISA。对于目标2,确定了40项可能相关的记录作为治疗比较研究。经过全文筛选后,本评价纳入了13项研究。治疗方法差异很大,很少提供比较的疗效评估。 180天的随访后,没有任何治疗与100%治愈相关。对于目标3,确定了513条引用,获得了169条的全文。 62篇文章描述了至少一种要求的检测(PCR,ELISA或IFAT),而18篇文章描述了PCR和ELISA和/或IFAT的使用。

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