药物不良事件(ADE)和药物实体提取的迁移学习评价

S. Narayanan, Kaivalya Mannam, S. Rajan, P. Rangan
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引用次数: 8

摘要

我们使用2018年ADE和药物提取(Track 2) n2c2数据集评估了几种生物医学上下文嵌入(基于BERT、ELMo和Flair),用于检测电子健康记录(EHR)中的药物和不良药物事件(ADE)等药物实体。我们确定了迁移学习的最佳实践,如语言模型微调和标量混合。我们的迁移学习模型在整体任务(F1=92.91%)和ADE识别(F1=53.08%)方面表现优异。基于风格的嵌入在识别上下文相关实体(如ADE)方面表现更好。基于bert的嵌入在识别临床术语(如药物和表单实体)方面表现出色。基于elmo的嵌入在所有实体中提供具有竞争力的性能。我们开发了一种增强ADE识别的句子增强方法,使基于bert和基于elmo的模型的F1增益高达3.13%。最后,我们证明了这些模型的简单集成在ADE提取中超过了大多数当前方法(F1=55.77%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Transfer Learning for Adverse Drug Event (ADE) and Medication Entity Extraction
We evaluate several biomedical contextual embeddings (based on BERT, ELMo, and Flair) for the detection of medication entities such as Drugs and Adverse Drug Events (ADE) from Electronic Health Records (EHR) using the 2018 ADE and Medication Extraction (Track 2) n2c2 data-set. We identify best practices for transfer learning, such as language-model fine-tuning and scalar mix. Our transfer learning models achieve strong performance in the overall task (F1=92.91%) as well as in ADE identification (F1=53.08%). Flair-based embeddings out-perform in the identification of context-dependent entities such as ADE. BERT-based embeddings out-perform in recognizing clinical terminology such as Drug and Form entities. ELMo-based embeddings deliver competitive performance in all entities. We develop a sentence-augmentation method for enhanced ADE identification benefiting BERT-based and ELMo-based models by up to 3.13% in F1 gains. Finally, we show that a simple ensemble of these models out-paces most current methods in ADE extraction (F1=55.77%).
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