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Design and evaluation of an associative classification framework to identify disease cohorts in the electronic health record.

机译:设计和评估关联分类框架,以识别电子健康记录中的疾病队列。

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摘要

With the growing national dissemination of the electronic health record (EHR), there are expectations that the public will benefit from biomedical research and discovery enabled by electronic health data. Clinical data are needed for many diseases and conditions to meet the demands of rapidly advancing genomic and proteomic research. Many biomedical research advancements require rapid access to clinical data as well as broad population coverage. A fundamental issue in the secondary use of clinical data for scientific research is the identification of study cohorts of individuals with a disease or medical condition of interest. The problem addressed in this work is the need for generalized, efficient methods to identify cohorts in the EHR for use in biomedical research.;To approach this problem, an associative classification framework was designed with the goal of accurate and rapid identification of cases for biomedical research: (1) a set of exemplars for a given medical condition are presented to the framework, (2) a predictive rule set comprised of EHR attributes is generated by the framework, and (3) the rule set is applied to the EHR to identify additional patients that may have the specified condition. Based on this functionality, the approach was termed the 'cohort amplification' framework.;The development and evaluation of the cohort amplification framework are the subject of this dissertation. An overview of the framework design is presented. Improvements to some standard associative classification methods are described and validated. A qualitative evaluation of predictive rules to identify diabetes cases and a study of the accuracy of identification of asthma cases in the EHR using framework-generated prediction rules are reported. The framework demonstrated accurate and reliable rules to identify diabetes and asthma cases in the EHR and contributed to methods for identification of biomedical research cohorts.
机译:随着电子健康记录(EHR)在全国范围内的传播日益增长,人们期望公众将从电子健康数据支持的生物医学研究和发现中受益。为了满足快速发展的基因组和蛋白质组学研究的需要,许多疾病和病症都需要临床数据。许多生物医学研究的进步要求快速访问临床数据以及广泛的人口覆盖范围。临床数据在科学研究中的二次使用中的一个基本问题是确定患有特定疾病或医学状况的个体的研究队列。这项工作解决的问题是需要一种通用,有效的方法来识别EHR中用于生物医学研究的队列。为了解决此问题,设计了一个关联分类框架,其目的是准确,快速地识别生物医学病例。研究:(1)将给定医疗条件的一组示例介绍给框架;(2)由框架生成由EHR属性组成的预测规则集;(3)将规则集应用于EHR以确定可能患有指定疾病的其他患者。基于此功能,该方法被称为“同类群组扩增”框架。同类群组扩增框架的开发和评估是本文的主题。介绍了框架设计的概述。描述和验证了对某些标准关联分类方法的改进。报告了对预测规则进行定性评估以鉴定糖尿病病例的方法,并报道了使用框架生成的预测规则在EHR中鉴定哮喘病例的准确性。该框架展示了在EHR中识别糖尿病和哮喘病例的准确而可靠的规则,并为生物医学研究人群的识别方法做出了贡献。

著录项

  • 作者

    Welch, Susan Rea.;

  • 作者单位

    The University of Utah.;

  • 授予单位 The University of Utah.;
  • 学科 Biology Bioinformatics.;Computer Science.;Health Sciences Epidemiology.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 149 p.
  • 总页数 149
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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