首页> 外文会议>Meeting of the Society for Veterinary Epidemiology and Preventive Medicine >DEMONSTRATING FREEDOM OF DISEASE AFTER AN EMERGENCY VACCINATION CAMPAIGN WITH AN E2 SUB-UNIT MARKER VACCINE AGAINST CLASSICAL SWINE FEVER: A SIMULATION
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DEMONSTRATING FREEDOM OF DISEASE AFTER AN EMERGENCY VACCINATION CAMPAIGN WITH AN E2 SUB-UNIT MARKER VACCINE AGAINST CLASSICAL SWINE FEVER: A SIMULATION

机译:用E2子单位标记疫苗展示紧急疫苗接种活动后展示疾病自由疫苗,针对古典猪瘟:模拟

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The aim of this study was to simulate end screening after an emergency vaccination campaign with a marker vaccine against Classical Swine Fever (CSF). In each run of the model, it is assumed that 500 herds are vaccinated. The number of infected herdsand the number of infected animals within an infected herd are modelled as binomial distributions. The animal-level sensitivity and specificity are modelled as beta distributions. At each iteration the number of animals to be sampled in a herd is calculated in order to detect a minimal within herd prevalence (e.g. 1%) with a given level of confidence (e.g. 99%). The model indicates for each herd whether it is categorized as infected or not, based upon a given threshold of positive samples (e.g. 5%). Bycomparing these results to the simulated proportion of infected herds, it becomes possible to determine the herd sensitivity and specificity. If a herd prevalence of 5% and a within-herd prevalence of 2% are assumed, the highest combined herd sensitivity(HSe) (77.54%) and specificity (HSp) (74.45%) is obtained at the threshold level of 2%. If a threshold level of 5% is used the HSe decreases to 36.95%, whereas the HSp increases to 98.93%. Varying other parameters (e.g. expected within-herd prevalence,sample size) never results in a situation where an acceptably high HSe and HSp are combined. Therefore, further efforts are needed to improve herd level diagnostics. Also these results should be used to review available simulation models as the choice may influence the conclusions dramatically.
机译:本研究的目的是在用标记疫苗与古典猪瘟(CSF)进行应急疫苗接种活动后模拟结束筛查。在每个模型的每次运行中,假设500种牛群接种疫苗。感染群的感染动物的数量被视为二项分子分布。动物水平敏感性和特异性被建模为β发行版。在每次迭代时,计算在牛群中进行采样的动物的数量,以便在给定的置信度(例如,例如99%)内检测群患病率(例如1%)的最小值。基于给定阈值的阳性样品(例如5%),该模型表示是否被归类为感染的群体。通过将这些结果进行了分配给被感染群的模拟比例,可以确定群体敏感性和特异性。假设牛群患有5%和牛群患病率为2%的血液患病率,在阈值水平为2%的阈值水平获得最高组合的血液敏感度(HSE)(HSE)(HSE)(77.54%)(74.45%)。如果使用5%的阈值水平,HSE降低至36.95%,而HSP增加到98.93%。改变其他参数(例如,剩下的内部流行率,样本大小)永远不会导致组合可接受的高HSE和HSP的情况。因此,需要进一步的努力来改善畜群诊断。此外,这些结果应用于审查可用的仿真模型,因为该选择可能会显着影响得出结论。

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