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Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis

BACKGROUND: Adverse drug events (ADEs) detection and assessment is at the center of pharmacovigilance. Data mining of systems, such as FDA’s Adverse Event Reporting System (AERS) and more recently, Electronic Health Records (EHRs), can aid in the automatic detection and analysis of ADEs. Although di...

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Autores principales: Vilar, Santiago, Harpaz, Rave, Santana, Lourdes, Uriarte, Eugenio, Friedman, Carol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404072/
https://www.ncbi.nlm.nih.gov/pubmed/22911794
http://dx.doi.org/10.1371/journal.pone.0041471
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author Vilar, Santiago
Harpaz, Rave
Santana, Lourdes
Uriarte, Eugenio
Friedman, Carol
author_facet Vilar, Santiago
Harpaz, Rave
Santana, Lourdes
Uriarte, Eugenio
Friedman, Carol
author_sort Vilar, Santiago
collection PubMed
description BACKGROUND: Adverse drug events (ADEs) detection and assessment is at the center of pharmacovigilance. Data mining of systems, such as FDA’s Adverse Event Reporting System (AERS) and more recently, Electronic Health Records (EHRs), can aid in the automatic detection and analysis of ADEs. Although different data mining approaches have been shown to be valuable, it is still crucial to improve the quality of the generated signals. OBJECTIVE: To leverage structural similarity by developing molecular fingerprint-based models (MFBMs) to strengthen ADE signals generated from EHR data. METHODS: A reference standard of drugs known to be causally associated with the adverse event pancreatitis was used to create a MFBM. Electronic Health Records (EHRs) from the New York Presbyterian Hospital were mined to generate structured data. Disproportionality Analysis (DPA) was applied to the data, and 278 possible signals related to the ADE pancreatitis were detected. Candidate drugs associated with these signals were then assessed using the MFBM to find the most promising candidates based on structural similarity. RESULTS: The use of MFBM as a means to strengthen or prioritize signals generated from the EHR significantly improved the detection accuracy of ADEs related to pancreatitis. MFBM also highlights the etiology of the ADE by identifying structurally similar drugs, which could follow a similar mechanism of action. CONCLUSION: The method proposed in this paper provides evidence of being a promising adjunct to existing automated ADE detection and analysis approaches.
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spelling pubmed-34040722012-07-30 Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis Vilar, Santiago Harpaz, Rave Santana, Lourdes Uriarte, Eugenio Friedman, Carol PLoS One Research Article BACKGROUND: Adverse drug events (ADEs) detection and assessment is at the center of pharmacovigilance. Data mining of systems, such as FDA’s Adverse Event Reporting System (AERS) and more recently, Electronic Health Records (EHRs), can aid in the automatic detection and analysis of ADEs. Although different data mining approaches have been shown to be valuable, it is still crucial to improve the quality of the generated signals. OBJECTIVE: To leverage structural similarity by developing molecular fingerprint-based models (MFBMs) to strengthen ADE signals generated from EHR data. METHODS: A reference standard of drugs known to be causally associated with the adverse event pancreatitis was used to create a MFBM. Electronic Health Records (EHRs) from the New York Presbyterian Hospital were mined to generate structured data. Disproportionality Analysis (DPA) was applied to the data, and 278 possible signals related to the ADE pancreatitis were detected. Candidate drugs associated with these signals were then assessed using the MFBM to find the most promising candidates based on structural similarity. RESULTS: The use of MFBM as a means to strengthen or prioritize signals generated from the EHR significantly improved the detection accuracy of ADEs related to pancreatitis. MFBM also highlights the etiology of the ADE by identifying structurally similar drugs, which could follow a similar mechanism of action. CONCLUSION: The method proposed in this paper provides evidence of being a promising adjunct to existing automated ADE detection and analysis approaches. Public Library of Science 2012-07-24 /pmc/articles/PMC3404072/ /pubmed/22911794 http://dx.doi.org/10.1371/journal.pone.0041471 Text en Vilar et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Vilar, Santiago
Harpaz, Rave
Santana, Lourdes
Uriarte, Eugenio
Friedman, Carol
Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis
title Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis
title_full Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis
title_fullStr Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis
title_full_unstemmed Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis
title_short Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis
title_sort enhancing adverse drug event detection in electronic health records using molecular structure similarity: application to pancreatitis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404072/
https://www.ncbi.nlm.nih.gov/pubmed/22911794
http://dx.doi.org/10.1371/journal.pone.0041471
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