Evidence map›Paper›PMID 34111555›Full record

ArticleJournal of biomedical informatics2021

Augmenting aer2vec: Enriching distributed representations of adverse event report data with orthographic and lexical information.

Xiruo Ding, Justin Mower, Devika Subramanian, Trevor Cohen

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Xiruo DingDepartment of Biomedical Informatics & Medical Education, University of Washington, Seattle, WA, USA. Electronic address: xiruod@uw.edu.
Justin MowerDepartment of Computer Science, Rice University, Houston, TX, USA. Electronic address: jmm21@rice.edu.
Devika SubramanianDepartment of Computer Science, Rice University, Houston, TX, USA. Electronic address: devika@rice.edu.
Trevor CohenDepartment of Biomedical Informatics & Medical Education, University of Washington, Seattle, WA, USA. Electronic address: cohenta@uw.edu.

Funding

Using Biomedical Knowledge to Identify Plausible Signals for PharmacovigilanceR01LM011563 · NLM · UNIVERSITY OF WASHINGTON · PI COHEN, TREVOR · 2013 to 2020
$3.0M
NLM NIH HHS R01 LM011563
6 · The paper itself

Abstract

Adverse Drug Events (ADEs) are prevalent, costly, and sometimes preventable. Post-marketing drug surveillance aims to monitor ADEs that occur after a drug is released to market. Reports of such ADEs are aggregated by reporting systems, such as the Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS). In this paper, we consider the topic of how best to represent data derived from reports in FAERS for the purpose of detecting post-marketing surveillance signals, in order to inform regulatory decision making. In our previous work, we developed aer2vec, a method for deriving distributed representations (concept embeddings) of drugs and side effects from ADE reports, establishing the utility of distributional information for pharmacovigilance signal detection. In this paper, we advance this line of research further by evaluating the utility of encoding orthographic and lexical information. We do so by adapting two Natural Language Processing methods, subword embedding and vector retrofitting, which were developed to encode such information into word embeddings. Models were compared for their ability to distinguish between positive and negative examples in a set of manually curated drug/ADE relationships, with both aer2vec enhancements offering advantages in performances over baseline models, and best performance obtained when retrofitting and subword embeddings were applied in concert. In addition, this work demonstrates that models leveraging distributed representations do not require extensive manual preprocessing to perform well on this pharmacovigilance signal detection task, and may even benefit from information that would otherwise be lost during the normalization and standardization process.

Indexed as

Drug-Related Side Effects and Adverse ReactionsPharmacovigilanceAdverse Drug Reaction Reporting SystemsHumansNatural Language ProcessingUnited StatesUnited States Food and Drug AdministrationNatural language processingPharmacovigilancePost-marketing surveillanceRetrofittingSubword embeddingsWord embeddings

Identifiers

PMID34111555
PMCPMC8260467

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.