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Automatic data source identification for clinical trial eligibility criteria resolution

机译:自动数据源识别用于临床试验资格标准解析

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摘要

Clinical trial coordinators refer to both structured and unstructured sources of data when evaluating a subject for eligibility. While some eligibility criteria can be resolved using structured data, some require manual review of clinical notes. An important step in automating the trial screening process is to be able to identify the right data source for resolving each criterion. In this work, we discuss the creation of an eligibility criteria dataset for clinical trials for patients with two disparate diseases, annotated with the preferred data source for each criterion (i.e., structured or unstructured) by annotators with medical training. The dataset includes 50 heart-failure trials with a total of 766 eligibility criteria and 50 trials for chronic lymphocytic leukemia (CLL) with 677 criteria. Further, we developed machine learning models to predict the preferred data source: kernel methods outperform simpler learning models when used with a combination of lexical, syntactic, semantic, and surface features. Evaluation of these models indicates that the performance is consistent across data from both diagnoses, indicating generalizability of our method. Our findings are an important step towards ongoing efforts for automation of clinical trial screening.
机译:在评估受试者的资格时,临床试验协调员会同时参考结构化和非结构化数据源。虽然某些合格标准可以使用结构化数据来解决,但某些标准需要人工检查临床记录。自动化试验筛选过程的重要一步是能够确定用于解决每个标准的正确数据源。在这项工作中,我们讨论了为两种不同疾病的患者进行临床试验的资格标准数据集的创建,并通过医学培训的注释者为每种标准(即结构化或非结构化)的首选数据源进行了注释。该数据集包括50项心脏衰竭试验,总共有766项入选标准,以及50项慢性慢性淋巴细胞白血病(CLL)的有677项标准。此外,我们开发了机器学习模型来预测首选的数据源:与词汇,句法,语义和表面特征结合使用时,内核方法的性能优于简单的学习模型。对这些模型的评估表明,两次诊断的数据之间的性能是一致的,这表明我们方法的普遍性。我们的发现是朝着不断进行的临床试验筛选自动化迈出的重要一步。

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