Yu Sheng, Liao Katherine P, Shaw Stanley Y, Gainer Vivian S, Churchill Susanne E, Szolovits Peter, Murphy Shawn N, Kohane Isaac S, Cai Tianxi
Partners HealthCare Personalized Medicine, Boston, MA, USA Brigham and Women's Hospital, Boston, MA, USA Harvard Medical School, Boston, MA, USA
Brigham and Women's Hospital, Boston, MA, USA Harvard Medical School, Boston, MA, USA.
J Am Med Inform Assoc. 2015 Sep;22(5):993-1000. doi: 10.1093/jamia/ocv034. Epub 2015 Apr 29.
Analysis of narrative (text) data from electronic health records (EHRs) can improve population-scale phenotyping for clinical and genetic research. Currently, selection of text features for phenotyping algorithms is slow and laborious, requiring extensive and iterative involvement by domain experts. This paper introduces a method to develop phenotyping algorithms in an unbiased manner by automatically extracting and selecting informative features, which can be comparable to expert-curated ones in classification accuracy.
Comprehensive medical concepts were collected from publicly available knowledge sources in an automated, unbiased fashion. Natural language processing (NLP) revealed the occurrence patterns of these concepts in EHR narrative notes, which enabled selection of informative features for phenotype classification. When combined with additional codified features, a penalized logistic regression model was trained to classify the target phenotype.
The authors applied our method to develop algorithms to identify patients with rheumatoid arthritis and coronary artery disease cases among those with rheumatoid arthritis from a large multi-institutional EHR. The area under the receiver operating characteristic curves (AUC) for classifying RA and CAD using models trained with automated features were 0.951 and 0.929, respectively, compared to the AUCs of 0.938 and 0.929 by models trained with expert-curated features.
Models trained with NLP text features selected through an unbiased, automated procedure achieved comparable or slightly higher accuracy than those trained with expert-curated features. The majority of the selected model features were interpretable.
The proposed automated feature extraction method, generating highly accurate phenotyping algorithms with improved efficiency, is a significant step toward high-throughput phenotyping.
分析电子健康记录(EHR)中的叙述性(文本)数据可改善临床和基因研究的群体规模表型分析。目前,为表型分析算法选择文本特征既缓慢又费力,需要领域专家广泛且反复地参与。本文介绍了一种以无偏方式开发表型分析算法的方法,即自动提取和选择信息性特征,其在分类准确性方面可与专家策划的特征相媲美。
以自动化、无偏的方式从公开可用的知识源中收集综合医学概念。自然语言处理(NLP)揭示了这些概念在EHR叙述性记录中的出现模式,从而能够选择用于表型分类的信息性特征。当与其他编码特征相结合时,训练一个惩罚逻辑回归模型来对目标表型进行分类。
作者应用我们的方法开发算法,以从大型多机构EHR中识别类风湿性关节炎患者以及类风湿性关节炎患者中的冠状动脉疾病病例。使用自动特征训练的模型对类风湿性关节炎和冠心病进行分类的受试者工作特征曲线下面积(AUC)分别为0.951和0.929,而使用专家策划特征训练的模型的AUC分别为0.938和0.929。
通过无偏、自动化程序选择的NLP文本特征训练的模型,其准确性与使用专家策划特征训练的模型相当或略高。所选模型特征中的大多数是可解释的。
所提出的自动特征提取方法,生成了具有更高效率的高精度表型分析算法,是朝着高通量表型分析迈出的重要一步。