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本文引用的文献

1
: Distributed Representations of Adverse Event Reporting System Data as a Means to Identify Drug/Side-Effect Associations.不良事件报告系统数据的分布式表示作为识别药物/副作用关联的一种手段
AMIA Annu Symp Proc. 2020 Mar 4;2019:717-726. eCollection 2019.
2
Retrofitting Concept Vector Representations of Medical Concepts to Improve Estimates of Semantic Similarity and Relatedness.改造医学概念的向量表示以改进语义相似性和相关性的估计。
Stud Health Technol Inform. 2017;245:657-661.
3
Indexed Pain Journals.索引疼痛期刊。
J Pain Palliat Care Pharmacother. 2008;22(1):45-46. doi: 10.1080/15360280801989377.
4
A time-indexed reference standard of adverse drug reactions.一份按时间索引的药品不良反应参考标准。
Sci Data. 2014 Nov 11;1:140043. doi: 10.1038/sdata.2014.43.
5
Zoo or savannah? Choice of training ground for evidence-based pharmacovigilance.动物园还是大草原?循证药物警戒的训练场选择
Drug Saf. 2014 Sep;37(9):655-9. doi: 10.1007/s40264-014-0198-z.
6
Defining a reference set to support methodological research in drug safety.定义参考集以支持药物安全性方法学研究。
Drug Saf. 2013 Oct;36 Suppl 1:S33-47. doi: 10.1007/s40264-013-0097-8.
7
A reference standard for evaluation of methods for drug safety signal detection using electronic healthcare record databases.用于评估使用电子医疗记录数据库进行药物安全信号检测方法的参考标准。
Drug Saf. 2013 Jan;36(1):13-23. doi: 10.1007/s40264-012-0002-x.
8
Pharmacovigilance in the 21st century: new systematic tools for an old problem.21世纪的药物警戒:解决老问题的新系统工具
Pharmacotherapy. 2004 Sep;24(9):1099-104. doi: 10.1592/phco.24.13.1099.38090.
9
The reporting odds ratio and its advantages over the proportional reporting ratio.报告比值比及其相对于比例报告比值比的优势。
Pharmacoepidemiol Drug Saf. 2004 Aug;13(8):519-23. doi: 10.1002/pds.1001.
10
The Unified Medical Language System (UMLS): integrating biomedical terminology.统一医学语言系统(UMLS):整合生物医学术语。
Nucleic Acids Res. 2004 Jan 1;32(Database issue):D267-70. doi: 10.1093/nar/gkh061.

将不良事件报告数据的向量表示形式改造为结构化知识以改进药物警戒信号检测。

Retrofitting Vector Representations of Adverse Event Reporting Data to Structured Knowledge to Improve Pharmacovigilance Signal Detection.

作者信息

Ding Xiruo, Cohen Trevor

机构信息

University of Washington, Seattle, WA, USA.

出版信息

AMIA Annu Symp Proc. 2021 Jan 25;2020:383-392. eCollection 2020.

PMID:33936411
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8075473/
Abstract

Adverse drug events (ADE) are prevalent and costly. Clinical trials are constrained in their ability to identify potential ADEs, motivating the development of spontaneous reporting systems for post-market surveillance. Statistical methods provide a convenient way to detect signals from these reports but have limitations in leveraging relationships between drugs and ADEs given their discrete count-based nature. A previously proposed method, aer2vec, generates distributed vector representations of ADE report entities that capture patterns of similarity but cannot utilize lexical knowledge. We address this limitation by retrofitting aer2vec drug embeddings to knowledge from RxNorm and developing a novel retrofitting variant using vector rescaling to preserve magnitude. When evaluated in the context of a pharmacovigilance signal detection task, aer2vec with retrofitting consistently outperforms disproportionality metrics when trained on minimally preprocessed data. Retrofitting with rescaling results in further improvements in the larger and more challenging of two pharmacovigilance reference sets used for evaluation.

摘要

药物不良事件(ADE)普遍存在且代价高昂。临床试验在识别潜在ADE方面能力有限,这推动了用于上市后监测的自发报告系统的发展。统计方法提供了一种从这些报告中检测信号的便捷方式,但鉴于其基于离散计数的性质,在利用药物与ADE之间的关系方面存在局限性。先前提出的方法aer2vec生成了ADE报告实体的分布式向量表示,可捕捉相似性模式,但无法利用词汇知识。我们通过将aer2vec药物嵌入与RxNorm中的知识进行适配,并开发一种使用向量重缩放来保留幅度的新型适配变体,来解决这一局限性。在药物警戒信号检测任务的背景下进行评估时,经过适配的aer2vec在对最少预处理数据进行训练时,始终优于不成比例性指标。在用于评估的两个药物警戒参考集中,规模更大且更具挑战性的参考集中,采用重缩放的适配会带来进一步的改进。