Mining drug-drug interactions for healthcare professionals

Lizzy Farrugia, C. Abela
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引用次数: 2

Abstract

The fourth leading cause of death in the US are Adverse Drug Reactions (ADRs)1 that can be brought about through Drug-Drug Interactions (DDIs). In this paper, we propose medicX, a system that can detect DDIs in biomedical texts by leveraging on different machine learning techniques. The main components within medicX are the Drug Named Entity Recognition (DNER) component and the DDI Identification component. The DNER component was evaluated using the CHEMDNER and the DDIExtraction 2013 (DDI2013) challenge corpora. On the other hand, the DDI Identification component was evaluated using the DDI2013 challenge corpus. The DNER component is implemented using an approach based on LSTM-CRF. This method achieves an F1-score of 84.89% when it is trained and evaluated on the DDI2013 corpus, which is 1.43% higher than the system that placed first in the DDI2013 challenge. On the other hand, the DDI Identification component is implemented using a two-stage rich feature-based linear-kernel SVM. This classifier achieves an F1-score of 66.18%, as compared to the SVM state-of-the-art DDI system that reported an F1-score of 71.79%.
为医疗保健专业人员挖掘药物-药物相互作用
在美国,第四大死亡原因是药物不良反应(adr),这是由药物-药物相互作用(ddi)引起的。在本文中,我们提出了medicX,一个可以通过利用不同的机器学习技术检测生物医学文本中的ddi的系统。medicX中的主要组件是药物命名实体识别(DNER)组件和DDI识别组件。使用CHEMDNER和DDIExtraction 2013 (DDI2013)挑战语料库对DNER成分进行评估。另一方面,使用DDI2013挑战语料库对DDI识别组件进行评估。DNER组件使用基于LSTM-CRF的方法实现。该方法在DDI2013语料库上进行训练和评估时获得了84.89%的f1分数,比在DDI2013挑战中排名第一的系统高出1.43%。另一方面,DDI识别组件使用两阶段的基于丰富特征的线性核支持向量机实现。该分类器的f1得分为66.18%,而支持向量机最先进的DDI系统的f1得分为71.79%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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