Crowe Christopher L, Tao Cui
University of Virginia, Charlottesville, VA.
University of Texas School of Biomedical Informatics, Houston, TX.
AMIA Jt Summits Transl Sci Proc. 2015 Mar 25;2015:173-7. eCollection 2015.
The amount of time and money required to screen patients for clinical trial and guideline eligibility presents the need for an automated screening process to streamline clinical trial enrollment and guideline implementation. This paper introduces an ontology-based approach for defining a set of patterns that can be used to represent various types of time-relevant eligibility criteria that may appear in clinical protocols. With a focus only on temporal requirements, we examined the criteria of 600 protocols and extracted a set of 37 representative time-relevant eligibility criteria. 16 patterns were designed to represent these criteria. Using a test set of an additional 100 protocols, it was found that these 16 patterns could sufficiently represent 98.5% of the time-relevant criteria. After the time-relevant criteria are modeled by these patterns, it will allow the potential to (1) use natural language processing algorithms to automatically extract temporal constraints from criteria; and (2) develop computer rules and queries to automate the processing of the criteria.
筛选患者以确定其是否符合临床试验和指南要求所需的时间和金钱,表明需要一种自动化筛选流程来简化临床试验入组和指南实施。本文介绍了一种基于本体的方法,用于定义一组模式,这些模式可用于表示临床方案中可能出现的各种与时间相关的资格标准。仅关注时间要求,我们检查了600个方案的标准,并提取了一组37个具有代表性的与时间相关的资格标准。设计了16种模式来表示这些标准。使用另外100个方案的测试集发现,这16种模式可以充分表示98.5%的与时间相关的标准。在用这些模式对与时间相关的标准进行建模后,将有可能:(1)使用自然语言处理算法从标准中自动提取时间约束;(2)开发计算机规则和查询以实现标准处理的自动化。