Enhancing adverse drug event detection in electronic health records using molecular structure similarity: application to pancreatitis
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PLOS
Abstract
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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Bibliographic citation
Vilar S, Harpaz R, Santana L, Uriarte E, Friedman C (2012) Enhancing Adverse Drug Event Detection in Electronic Health Records Using Molecular Structure Similarity: Application to Pancreatitis. PLoS ONE 7(7): e41471. https://doi.org/10.1371/journal.pone.0041471
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https://doi.org/10.1371/journal.pone.0041471Sponsors
This work was supported by grants R01 LM010016 (Dr. Friedman), R01 LM010016-0S1 (Dr. Friedman), R01 LM010016-0S2 (Dr. Friedman), R01 LM008635(Dr. Friedman), and T15 LM007079 (Dr. Harpaz) from the National Library of Medicine, “Plan Galego de Investigación, Innovación e Crecemento 2011–2015 (I2C)”, European Social Fund (ESF) and Angeles Alvariño program from Xunta de Galicia (Spain)
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© 2012 Vilar et al. 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 credited








