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An automated tool for an analysis of compliance to evidence-based clinical guidelines.

机译:用于分析依据基于证据的临床指南的自动化工具。

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Evidence-based clinical guidelines have been developed in an attempt to decrease practice variation and improve patient outcomes. Although a number of studies and a few commercial products have attempted to measure guideline compliance, there still exists a strong need for an automated product that can take as input large amounts of data and create systematic and detailed profiles of compliance to evidence-based guidelines. The Guideline Compliance Assessment Tool is a product presently under development in our group that will accept as input medical and pharmacy claims data and create a guideline compliance profile that assesses provider practice patterns as compared to evidence-based standards. The system components include an episode of care grouper to standardize classifications of illnesses, an evidence-based guideline knowledge base that potentially contains information on several hundred distinct conditions, a guideline compliance scoring system that emphasizes systematic guideline variance rather than random variances, and an advanced data warehouse that would allow drilling into specific areas of interest. As provider profiling begins to shift away from a primary emphasis on cost to an emphasis on quality, automated methods for measuring guideline compliance will become important in measuring provider performance and increasing guideline usage, consequently improving the standard of care and the potential for better patient outcomes.
机译:循证临床指南已经开发了一种试图减少实践的变化和改善患者的预后。虽然一些研究和一些商业产品试图衡量准则合规性,仍然存在一种自动化的产品,可以作为输入大量数据,并创建以证据为基础的准则合规的系统和详细的个人资料的强烈需求。该指导规则遵从评估工具是一种产品目前正在我们的集团化发展,将接受输入的医疗和药品要求数据,并创建一个指导规则遵从轮廓相比,基于证据的标准评估供应商的实践模式。该系统组件包括照顾石斑鱼的一个小插曲,规范疾病的分类,以证据为基础的准则知识基础,有可能包含了几百个不同的条件的信息,强调系统的指引差异,而不是随机变化的指导原则合规评分系统,以及先进的数据仓库,将允许钻入感兴趣的具体领域。作为供应商分析开始从主要重点放在成本上移开,以质量为重点,用于测量指导规则遵从自动化方法将成为衡量供应商绩效和提高方针的使用,从而提高医疗水平和潜力,改善患者治疗效果的重要。

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