ADEpedia 2.0-Integration of Normalized Adverse Drug Events (ADEs)
ADEpedia 2.0-Integration of Normalized Adverse Drug Events (ADEs)
0: Integration of Normalized Adverse Drug Events (ADEs) Knowledge from the UMLS
Guoqian Jiang, MD, PhD Mayo Clinic
2013 AMIA Summit on Clinical Research Informatics March 22, 2013
Acknowledgements
Co-authors Hongfang Liu, PhD Harold R. Solbrig Christopher G. Chute, MD. Dr. PH This work was supported in part by the SHARP Area 4: Secondary Use of EHR Data (90TR000201)
Introduction
Adverse drug events (ADEs) are a well-recognized cause of patient morbidity and increased health care costs in the United States. Traditionally, spontaneous reporting is used as the main source for drug safety surveillance. Notably, the US Food and Drug Administration (FDA) uses an adverse event reporting system (AERS) to monitor for new adverse events and medication errors that might occur with all approved drug and therapeutic biologic products
2013 MFMER | slide-3
Introduction
To facilitate the ADE reporting and detection, there is emerging interest in secondary use of clinical data from the electronic medical records (EMRs). A fundamental challenge is that the community lacks a publicly-available, standardized ADE knowledge base that encodes known ADE information for drug surveillance.
Introduction
The known ADE information is very useful for avoiding over-alerting of ADE signals detected by data mining algorithms, and reducing pharmacovigilance study noise levels, so that only novel signals are considered for further exploration. ADEpedia: a standardized knowledge base of ADEs for drug safety surveillance FDA Structured Product Labeling (SPL), FDA Adverse Event Reporting System (AERS) and the Unified Medical Language System (UMLS) http://adepedia.org
Introduction
The Unified Medical Language System (UMLS), developed by the National Library of Medicine (NLM), intends to promote creation of more effective and interoperable biomedical information system and services [12]. A systematic review and organization of known ADE knowledge from the UMLS would be a good starting point to facilitate the integration of known ADE knowledge and ultimately form a comprehensive ADE knowledge base.
Co-occurrence
Co-occurrence is one of essential statistics that has been widely used in ADE text mining and knowledge acquisition from biomedical and clinical documents. Wright et al. used co-occurrence-based association rule mining technique to identify a large number of clinical accurate associations that may be useful for identifying probable gaps in the problem list. Liu Y, et al demonstrated an approach that statistically significant co-occurrence of drug-disease mentions in the clinical notes can be used to detect ADE signals .
Methods
Profiled the Drug-Disorder Pairs and Relationships in the UMLS Chemicals & Drugs Disorders Enriched the UMLS ADE data with the EMR cooccurrence statistics Evaluated the Utility of the UMLS ADE Data
70.4% 7.3% 7.3% 3.1% 2.1% 0.7% 0.7% 0.7% 0.6% 0.6% 0.6% 0.6% 0.6% 0.6% 0.6% 0.5% 0.4% 0.4% 0.3% 0.3% 10.0% 20.0% 30.0% 40.0% 50.0% 60.0% 70.0% 80.0%
0.0%
ADE knowledge extracted from the UMLS for the drug Digoxin|C0012265
Discussion
The profiling results of the UMLS clearly demonstrated that the drug-disorder associations in the UMLS are largely underspecified. Only 1.69% (14,256) concepts from the group Chemicals & Drugs and 3.53% (19,006) concepts from the group Disorders in the UMLS had drug-disorder associations asserted.
Discussion
From the perspective of ADE detection application, we classified the asserted relationships between the drug-disorder pairs into 4 categories. This kind of categorization would provide aggregation capability for the knowledge source and improve its utility for the purpose of drug surveillance.
Discussion
We enriched the knowledge base with the statistical co-occurrence information extracted from the EMRs. The co-occurrence information extracted from a 51-million-document EMR system will be useful for validating ADE detection algorithm across clinical institutions and across text corpora. In future, we will explore the characteristics of the UMLS term occurrences, focusing on the ADE detection use case.
2013 MFMER | slide-20
Summary
The UMLS is a useful source for providing standardized ADE knowledge relevant to indications, contraindications and adverse effects, and complementary to the ADE data from drug product labels. The statistics enrichment from EMRs would potentially enable the meaningful use of ADE data for drug safety surveillance. The EMR-enriched ADE dataset is available for download at the ADEpedia website (http://adepedia.org).
ADE Detection / Drug Surveillance Applications Semantic Web RESTful Services (JSON, XML, RDF, TTL, etc.)
Data Layer
ADE
Knowledge From UMLS
ADE
Knowledge From EMRs