Zancanaro Gabriele
EFSA J. 2021 Jan 29;19(1):e06382. doi: 10.2903/j.efsa.2021.6382. eCollection 2021 Jan.
This report is part of the surveillance scientific reports which are presented annually by EFSA to the European Commission and are intended to assess the sampling strategy, data collection and detection methods used by Finland, Ireland, the UK and Norway in their respective surveillance programmes. The surveillance programmes of these four countries were evaluated by checking the information submitted by each of them and verifying that the technical requirements were fulfilled as laid down in Commission Delegated Regulation (EU) 2018/772 of 21 November 2017 supplementing Regulation (EU) No 576/2013 of the European Parliament and of the Council with regard to preventive health measures for the control of infection in dogs, and repealing Delegated Regulation (EU) No 1152/2011. Due to the UK exiting the European Union and under the Withdrawal Act, the data submitted by the UK after the 31 January 2020 are excluded from this assessment. 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 the countries participating in this surveillance (Finland, the UK, Ireland and Norway) succeeded in the fulfilment of the technical legal requirements foreseen in Commission Delegated Regulation (EU) 2018/772 concerning these four different categories. Within the UK, Northern Ireland fulfils those requirements only when assuming a diagnostic test sensitivity value of 0.99, provided by the national reference laboratory, which is higher than the sensitivity value suggested by EFSA (conservative value of 0.78) and not supported by adequate scientific evidence. None of the four countries recorded positive samples in the 12-month reporting period.
本报告是欧洲食品安全局(EFSA)每年向欧盟委员会提交的监测科学报告的一部分,旨在评估芬兰、爱尔兰、英国和挪威在各自监测计划中使用的抽样策略、数据收集和检测方法。通过检查这四个国家各自提交的信息,并核实其是否符合2017年11月21日欧盟委员会授权法规(EU)2018/772的规定,对这四个国家的监测计划进行了评估。该法规补充了欧洲议会和理事会关于控制犬类感染的预防性健康措施的(EU)No 576/2013号法规,并废止了(EU)No 1152/2011号授权法规。由于英国脱欧,根据《脱欧法案》,2020年1月31日之后英国提交的数据被排除在本次评估之外。信息被分为四个不同类别进行评估:检测方法的类型和灵敏度、目标人群的选择、抽样策略和方法。对于每个类别,对照若干标准的合规情况,检查了为满足法规技术要求需要考虑的主要方面。参与此次监测的所有国家(芬兰、英国、爱尔兰和挪威)均成功满足了欧盟委员会授权法规(EU)2018/772中关于这四个不同类别的技术法律要求。在英国境内,北爱尔兰仅在假设国家参考实验室提供的诊断测试灵敏度值为0.99时才满足这些要求,该值高于欧洲食品安全局建议的灵敏度值(保守值为0.78),且没有充分的科学证据支持。在12个月的报告期内,这四个国家均未记录到阳性样本。