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An ensemble of neural models for nested adverse drug events and medication extraction with subwords

OBJECTIVE: This article describes an ensembling system to automatically extract adverse drug events and drug related entities from clinical narratives, which was developed for the 2018 n2c2 Shared Task Track 2. MATERIALS AND METHODS: We designed a neural model to tackle both nested (entities embedde...

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Autores principales: Ju, Meizhi, Nguyen, Nhung T H, Miwa, Makoto, Ananiadou, Sophia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913208/
https://www.ncbi.nlm.nih.gov/pubmed/31197355
http://dx.doi.org/10.1093/jamia/ocz075
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author Ju, Meizhi
Nguyen, Nhung T H
Miwa, Makoto
Ananiadou, Sophia
author_facet Ju, Meizhi
Nguyen, Nhung T H
Miwa, Makoto
Ananiadou, Sophia
author_sort Ju, Meizhi
collection PubMed
description OBJECTIVE: This article describes an ensembling system to automatically extract adverse drug events and drug related entities from clinical narratives, which was developed for the 2018 n2c2 Shared Task Track 2. MATERIALS AND METHODS: We designed a neural model to tackle both nested (entities embedded in other entities) and polysemous entities (entities annotated with multiple semantic types) based on MIMIC III discharge summaries. To better represent rare and unknown words in entities, we further tokenized the MIMIC III data set by splitting the words into finer-grained subwords. We finally combined all the models to boost the performance. Additionally, we implemented a featured-based conditional random field model and created an ensemble to combine its predictions with those of the neural model. RESULTS: Our method achieved 92.78% lenient micro F1-score, with 95.99% lenient precision, and 89.79% lenient recall, respectively. Experimental results showed that combining the predictions of either multiple models, or of a single model with different settings can improve performance. DISCUSSION: Analysis of the development set showed that our neural models can detect more informative text regions than feature-based conditional random field models. Furthermore, most entity types significantly benefit from subword representation, which also allows us to extract sparse entities, especially nested entities. CONCLUSION: The overall results have demonstrated that the ensemble method can accurately recognize entities, including nested and polysemous entities. Additionally, our method can recognize sparse entities by reconsidering the clinical narratives at a finer-grained subword level, rather than at the word level.
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spelling pubmed-69132082019-12-19 An ensemble of neural models for nested adverse drug events and medication extraction with subwords Ju, Meizhi Nguyen, Nhung T H Miwa, Makoto Ananiadou, Sophia J Am Med Inform Assoc Research and Applications OBJECTIVE: This article describes an ensembling system to automatically extract adverse drug events and drug related entities from clinical narratives, which was developed for the 2018 n2c2 Shared Task Track 2. MATERIALS AND METHODS: We designed a neural model to tackle both nested (entities embedded in other entities) and polysemous entities (entities annotated with multiple semantic types) based on MIMIC III discharge summaries. To better represent rare and unknown words in entities, we further tokenized the MIMIC III data set by splitting the words into finer-grained subwords. We finally combined all the models to boost the performance. Additionally, we implemented a featured-based conditional random field model and created an ensemble to combine its predictions with those of the neural model. RESULTS: Our method achieved 92.78% lenient micro F1-score, with 95.99% lenient precision, and 89.79% lenient recall, respectively. Experimental results showed that combining the predictions of either multiple models, or of a single model with different settings can improve performance. DISCUSSION: Analysis of the development set showed that our neural models can detect more informative text regions than feature-based conditional random field models. Furthermore, most entity types significantly benefit from subword representation, which also allows us to extract sparse entities, especially nested entities. CONCLUSION: The overall results have demonstrated that the ensemble method can accurately recognize entities, including nested and polysemous entities. Additionally, our method can recognize sparse entities by reconsidering the clinical narratives at a finer-grained subword level, rather than at the word level. Oxford University Press 2019-06-14 /pmc/articles/PMC6913208/ /pubmed/31197355 http://dx.doi.org/10.1093/jamia/ocz075 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of the American Medical Informatics Association. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research and Applications
Ju, Meizhi
Nguyen, Nhung T H
Miwa, Makoto
Ananiadou, Sophia
An ensemble of neural models for nested adverse drug events and medication extraction with subwords
title An ensemble of neural models for nested adverse drug events and medication extraction with subwords
title_full An ensemble of neural models for nested adverse drug events and medication extraction with subwords
title_fullStr An ensemble of neural models for nested adverse drug events and medication extraction with subwords
title_full_unstemmed An ensemble of neural models for nested adverse drug events and medication extraction with subwords
title_short An ensemble of neural models for nested adverse drug events and medication extraction with subwords
title_sort ensemble of neural models for nested adverse drug events and medication extraction with subwords
topic Research and Applications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6913208/
https://www.ncbi.nlm.nih.gov/pubmed/31197355
http://dx.doi.org/10.1093/jamia/ocz075
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