首页> 美国卫生研究院文献>EFSA Journal >Annual assessment of Echinococcus multilocularis surveillance reports submitted in 2018 in the context of Commission Regulation (EU) No 1152/2011
【2h】

Annual assessment of Echinococcus multilocularis surveillance reports submitted in 2018 in the context of Commission Regulation (EU) No 1152/2011

机译:在欧盟法规(EU)第1152/2011号的背景下于2018年提交的多球棘球surveillance虫监视报告的年度评估

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

This report is part of the ` surveillance’ scientific reports which are presented annually by to the European Commission and are intended to assess the sampling strategy, data collection and detection methods used by Finland, Ireland, Malta, the United Kingdom ( ) and Norway in their respective surveillance programmes. The surveillance programmes of these five countries were evaluated by checking the information submitted by each of them and verifying that the technical requirements laid down in Regulation ( ) No 1152/2011 were complied. The information was divided in four different categories for assessment: the type and sensitivity of the detection method, the selection of the target population, the sampling strategy and the methodology. For each category, the main aspects that need to be considered in order to accomplish the technical requirements of the legislation were checked against compliance of several criteria. All of the countries participating in this surveillance (Finland, the , Norway, Malta and Ireland) succeeded in the fulfilment of the technical legal requirements foreseen in Regulation ( ) No 1152/2011 concerning these four different categories. Northern Ireland ( ) fulfils those requirements only when assuming a diagnostic test sensitivity value of 0.99, which is higher than the sensitivity value suggested by (conservative value of 0.78). None of the five countries recorded positive samples in the 12‐month reporting period.
机译:该报告是“监视”科学报告的一部分,该报告每年提交给欧洲委员会,旨在评估芬兰,爱尔兰,马耳他,英国()和挪威在2003年使用的采样策略,数据收集和检测方法。他们各自的监视程序。通过检查每个国家/地区提交的信息并验证是否符合第(1152/2011)号法规中的技术要求,对这五个国家/地区的监视计划进行了评估。信息分为四个不同类别进行评估:检测方法的类型和敏感性,目标人群的选择,抽样策略和方法。对于每个类别,要检查是否符合主要技术要求,以实现法规的技术要求,并对照若干标准进行检查。参与此监视的所有国家(芬兰,挪威,挪威,马耳他和爱尔兰)都成功实现了第(1152/2011)号法规中针对这四个不同类别的技术法规要求。北爱尔兰()仅在假设诊断测试灵敏度值为0.99时才满足这些要求,该灵敏度值高于所建议的灵敏度值(保守值0.78)。在12个月的报告期内,五个国家均未记录到阳性样本。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号