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1.
In this paper a novel method for the monitoring of disease maps over time in a surveillance setting is described. The approach relies upon the use of a spatial model that is fitted to current spatial data and is smoothed with historical spatial estimates. The method of smoothing is a vector exponentially weighted moving average procedure. A simulation study with a range of scenarios is presented and finally a case study of monitoring infectious disease spread is presented.  相似文献   

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2005年修订的《国际卫生条例》强调要加强基于指标监测以及基于事件监测,WHO先后于2008年和2014年针对基于事件监测体系出台了技术指南。为了实现早期预警的目的,全文系统总结了目前国内外基于事件监测体系的理论及发展情况,评估了上海市基于事件监测体系的建设情况,在此基础上提出未来适应市公共卫生安全保障的基于事件监测体系目标架构,即整合舆情监测、医疗卫生及相关机构监测和社区监测信息来源,通过信号侦测、核实、分析评估工作以满足上海市公共卫生安全需要。下一步要加强信息整合,推动“互联网+事件监测”,进一步完善突发公共卫生事件苗子监测,全面贯彻风险管理理念。  相似文献   

3.
In the context of Bayesian disease mapping, recent literature presents generalized linear mixed models that engender spatial smoothing. The methods assume spatially varying random effects as a route to partially pooling data and 'borrowing strength' in small-area estimation. When spatiotemporal disease rates are available for sequential risk mapping of several time periods, the 'smoothing' issue may be explored by considering spatial smoothing, temporal smoothing and spatiotemporal interaction. In this paper, these considerations are motivated and explored through development of a Bayesian semiparametric disease mapping model framework which facilitates temporal smoothing of rates and relative risks via regression B-splines with mixed-effect representation of coefficients. Specifically, we develop spatial priors such as multivariate Gaussian Markov random fields and non-spatial priors such as unstructured multivariate Gaussian distributions and illustrate how time trends in small-area relative risks may be explored by splines which vary in either a spatially structured or unstructured manner. In particular, we show that with suitable prior specifications for the random effects ensemble, small-area relative risk trends may be fit by 'spatially varying' or randomly varying B-splines. A recently developed Bayesian hierarchical model selection criterion, the deviance information criterion, is used to assess the trade-off between goodness-of-fit and smoothness and to select the number of knots. The methodological development aims to provide reliable information about the patterns (both over space and time) of disease risks and to quantify uncertainty. The study offers a disease and health outcome surveillance methodology for flexible and efficient exploration and assessment of emerging risk trends and clustering. The methods are motivated and illustrated through a Bayesian analysis of adverse medical events (also known as iatrogenic injuries) among hospitalized elderly patients in British Columbia, Canada.  相似文献   

4.
Disease mapping studies have been widely performed at univariate level, that is considering only one disease in the estimated models. Nonetheless, simultaneous modelling of different diseases can be a valuable tool both from the epidemiological and from the statistical point of view. In this paper we propose a model for multivariate disease mapping that generalizes the univariate conditional auto‐regressive distribution. The proposed model is proven to be an effective alternative to existing multivariate models, mainly because it overcome some restrictive hypotheses underlying models previously proposed in this context. Model performances are checked via a simulation study and via application to a case study. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

5.
We present Bayesian hierarchical spatial models for the analysis of the geographical distribution of a non-rare disease or event. The work is motivated by the need for ascertaining regional variations in health services outcomes and resource use and for assessing the potential sources of these variations. The models discussed herein readily accommodate random spatial effects and covariate effects. We discuss Bayesian inferential framework and implementation of a hybrid Markov chain Monte Carlo method for full Bayesian model inference. The methods are illustrated through an analysis of regional variation in chronic lung disease (CLD) rates among neonatal intensive care unit (NICU) patients across Canada. Specifically, we first present a random effects binomial model for spatially correlated CLD rates, with random spatial effects accounting for latent or covariate effects. These random spatial effects depict regional or spatial variation in chronic lung disease occurrence. We then extend this model to include covariates. With this extension, we assess residual spatial effects and the extent to which risk factors such as illness severity at NICU admission, low birth weight, and very low birth weight influence the CLD rate variation.  相似文献   

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