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Development of a Controlled Vocabulary-Based Adverse Drug Reaction Signal Dictionary for Multicenter Electronic Health Record-Based Pharmacovigilance

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dc.contributor.authorLee, S-
dc.contributor.authorHan, J-
dc.contributor.authorPark, RW-
dc.contributor.authorKim, GJ-
dc.contributor.authorRim, JH-
dc.contributor.authorCho, J-
dc.contributor.authorLee, KH-
dc.contributor.authorLee, J-
dc.contributor.authorKim, S-
dc.contributor.authorKim, JH-
dc.date.accessioned2020-11-17T05:25:12Z-
dc.date.available2020-11-17T05:25:12Z-
dc.date.issued2019-
dc.identifier.issn0114-5916-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/19029-
dc.description.abstractINTRODUCTION: Integration of controlled vocabulary-based electronic health record (EHR) observational data is essential for real-time large-scale pharmacovigilance studies.
OBJECTIVE: To provide a semantically enriched adverse drug reaction (ADR) dictionary for post-market drug safety research and enable multicenter EHR-based extensive ADR signal detection and evaluation, we developed a comprehensive controlled vocabulary-based ADR signal dictionary (CVAD) for pharmacovigilance.
METHODS: A CVAD consists of (1) administrative disease classifications of the International Classification of Diseases (ICD) codes mapped to the Medical Dictionary for Regulatory Activities Preferred Terms (MedDRA((R)) PTs): (2) two teaching hospitals' codes for laboratory test results mapped to the Logical Observation Identifiers Names and Codes (LOINC) terms and MedDRA((R)) PTs: and (3) clinical narratives and ADRs encoded by standard nursing statements (encoded by the International Classification for Nursing Practice [ICNP]) mapped to the World Health Organization-Adverse Reaction Terminology (WHO-ART) terms and MedDRA((R)) PTs.
RESULTS: Of the standard 4514 MedDRA((R)) PTs from Side Effect Resources (SIDER) 4.1, 1130 (25.03%), 942 (20.86%), and 83 (1.83%) terms were systematically mapped to clinical narratives, laboratory test results, and disease classifications, respectively. For the evaluation, we loaded multi-source EHR data. We first performed a clinical expert review of the CVAD clinical relevance and a three-drug ADR case analyses consisting of linezolid-induced thrombocytopenia, warfarin-induced bleeding tendency, and vancomycin-induced acute kidney injury.
CONCLUSION: CVAD had a high coverage of ADRs and integrated standard controlled vocabularies to the EHR data sources, and researchers can take advantage of these features for EHR observational data-based extensive pharmacovigilance studies to improve sensitivity and specificity.
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dc.language.isoen-
dc.subject.MESHAdverse Drug Reaction Reporting Systems-
dc.subject.MESHElectronic Health Records-
dc.subject.MESHHumans-
dc.subject.MESHPharmacovigilance-
dc.subject.MESHVocabulary, Controlled-
dc.titleDevelopment of a Controlled Vocabulary-Based Adverse Drug Reaction Signal Dictionary for Multicenter Electronic Health Record-Based Pharmacovigilance-
dc.typeArticle-
dc.identifier.pmid30649749-
dc.contributor.affiliatedAuthor박, 래웅-
dc.type.localJournal Papers-
dc.identifier.doi10.1007/s40264-018-0767-7-
dc.citation.titleDrug safety-
dc.citation.volume42-
dc.citation.number5-
dc.citation.date2019-
dc.citation.startPage657-
dc.citation.endPage670-
dc.identifier.bibliographicCitationDrug safety, 42(5). : 657-670, 2019-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.identifier.eissn1179-1942-
dc.relation.journalidJ001145916-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Biomedical Informatics
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