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Validation of Artificial Intelligence to Support the Automatic Coding of Patient Adverse Drug Reaction Reports, Using Nationwide Pharmacovigilance Data
by
Micallef, Joëlle
, Pariente, Antoine
, Benkebil, Mehdi
, Salvo, Francesco
, Miremont, Ghada
, Létinier, Louis
, Martin, Guillaume L.
, Jouganous, Julien
, Bellec, Axel
, Savidan, Romain
, Goehrs, Clément
in
Artificial intelligence
/ Coding
/ Coronaviruses
/ COVID-19
/ COVID-19 vaccines
/ Data processing
/ Datasets
/ Disease transmission
/ Drug Safety and Pharmacovigilance
/ Language
/ Learning algorithms
/ Life Sciences
/ Machine learning
/ Mass media
/ Medicine
/ Medicine & Public Health
/ Natural language processing
/ Original
/ Original Research Article
/ Patients
/ Performance evaluation
/ Pharmacology
/ Pharmacology/Toxicology
/ Pharmacovigilance
/ Portable document format
/ Professionals
/ Santé publique et épidémiologie
/ Side effects
/ Transformers
/ Vaccines
/ Web portals
2022
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Validation of Artificial Intelligence to Support the Automatic Coding of Patient Adverse Drug Reaction Reports, Using Nationwide Pharmacovigilance Data
by
Micallef, Joëlle
, Pariente, Antoine
, Benkebil, Mehdi
, Salvo, Francesco
, Miremont, Ghada
, Létinier, Louis
, Martin, Guillaume L.
, Jouganous, Julien
, Bellec, Axel
, Savidan, Romain
, Goehrs, Clément
in
Artificial intelligence
/ Coding
/ Coronaviruses
/ COVID-19
/ COVID-19 vaccines
/ Data processing
/ Datasets
/ Disease transmission
/ Drug Safety and Pharmacovigilance
/ Language
/ Learning algorithms
/ Life Sciences
/ Machine learning
/ Mass media
/ Medicine
/ Medicine & Public Health
/ Natural language processing
/ Original
/ Original Research Article
/ Patients
/ Performance evaluation
/ Pharmacology
/ Pharmacology/Toxicology
/ Pharmacovigilance
/ Portable document format
/ Professionals
/ Santé publique et épidémiologie
/ Side effects
/ Transformers
/ Vaccines
/ Web portals
2022
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Validation of Artificial Intelligence to Support the Automatic Coding of Patient Adverse Drug Reaction Reports, Using Nationwide Pharmacovigilance Data
by
Micallef, Joëlle
, Pariente, Antoine
, Benkebil, Mehdi
, Salvo, Francesco
, Miremont, Ghada
, Létinier, Louis
, Martin, Guillaume L.
, Jouganous, Julien
, Bellec, Axel
, Savidan, Romain
, Goehrs, Clément
in
Artificial intelligence
/ Coding
/ Coronaviruses
/ COVID-19
/ COVID-19 vaccines
/ Data processing
/ Datasets
/ Disease transmission
/ Drug Safety and Pharmacovigilance
/ Language
/ Learning algorithms
/ Life Sciences
/ Machine learning
/ Mass media
/ Medicine
/ Medicine & Public Health
/ Natural language processing
/ Original
/ Original Research Article
/ Patients
/ Performance evaluation
/ Pharmacology
/ Pharmacology/Toxicology
/ Pharmacovigilance
/ Portable document format
/ Professionals
/ Santé publique et épidémiologie
/ Side effects
/ Transformers
/ Vaccines
/ Web portals
2022
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Validation of Artificial Intelligence to Support the Automatic Coding of Patient Adverse Drug Reaction Reports, Using Nationwide Pharmacovigilance Data
Journal Article
Validation of Artificial Intelligence to Support the Automatic Coding of Patient Adverse Drug Reaction Reports, Using Nationwide Pharmacovigilance Data
2022
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Overview
Introduction
Adverse drug reaction reports are usually manually assessed by pharmacovigilance experts to detect safety signals associated with drugs. With the recent extension of reporting to patients and the emergence of mass media-related sanitary crises, adverse drug reaction reports currently frequently overwhelm pharmacovigilance networks. Artificial intelligence could help support the work of pharmacovigilance experts during such crises, by automatically coding reports, allowing them to prioritise or accelerate their manual assessment. After a previous study showing first results, we developed and compared state-of-the-art machine learning models using a larger nationwide dataset, aiming to automatically pre-code patients’ adverse drug reaction reports.
Objectives
We aimed to determine the best artificial intelligence model identifying adverse drug reactions and assessing seriousness in patients reports from the French national pharmacovigilance web portal.
Methods
Reports coded by 27 Pharmacovigilance Centres between March 2017 and December 2020 were selected (
n
= 11,633). For each report, the Portable Document Format form containing free-text information filled by the patient, and the corresponding encodings of adverse event symptoms (in
Medical Dictionary for Regulatory Activities
Preferred Terms) and seriousness were obtained. This encoding by experts was used as the reference to train and evaluate models, which contained input data processing and machine-learning natural language processing to learn and predict encodings. We developed and compared different approaches for data processing and classifiers. Performance was evaluated using receiver operating characteristic area under the curve (AUC), F-measure, sensitivity, specificity and positive predictive value. We used data from 26 Pharmacovigilance Centres for training and internal validation. External validation was performed using data from the remaining Pharmacovigilance Centres during the same period.
Results
Internal validation: for adverse drug reaction identification, Term Frequency-Inverse Document Frequency (TF-IDF) + Light Gradient Boosted Machine (LGBM) achieved an AUC of 0.97 and an F-measure of 0.80. The Cross-lingual Language Model (XLM) [transformer] obtained an AUC of 0.97 and an F-measure of 0.78. For seriousness assessment, FastText + LGBM achieved an AUC of 0.85 and an F-measure of 0.63. CamemBERT (transformer) + Light Gradient Boosted Machine obtained an AUC of 0.84 and an F-measure of 0.63. External validation for both adverse drug reaction identification and seriousness assessment tasks yielded consistent and robust results.
Conclusions
Our artificial intelligence models showed promising performance to automatically code patient adverse drug reaction reports, with very similar results across approaches. Our system has been deployed by national health authorities in France since January 2021 to facilitate pharmacovigilance of COVID-19 vaccines. Further studies will be needed to validate the performance of the tool in real-life settings.
Publisher
Springer International Publishing,Springer Nature B.V,Springer Verlag
Subject
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