Cited 0 times in
Development of a Controlled Vocabulary-Based Adverse Drug Reaction Signal Dictionary for Multicenter Electronic Health Record-Based Pharmacovigilance
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, S | - |
dc.contributor.author | Han, J | - |
dc.contributor.author | Park, RW | - |
dc.contributor.author | Kim, GJ | - |
dc.contributor.author | Rim, JH | - |
dc.contributor.author | Cho, J | - |
dc.contributor.author | Lee, KH | - |
dc.contributor.author | Lee, J | - |
dc.contributor.author | Kim, S | - |
dc.contributor.author | Kim, JH | - |
dc.date.accessioned | 2020-11-17T05:25:12Z | - |
dc.date.available | 2020-11-17T05:25:12Z | - |
dc.date.issued | 2019 | - |
dc.identifier.issn | 0114-5916 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/19029 | - |
dc.description.abstract | INTRODUCTION: 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. | - |
dc.language.iso | en | - |
dc.subject.MESH | Adverse Drug Reaction Reporting Systems | - |
dc.subject.MESH | Electronic Health Records | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Pharmacovigilance | - |
dc.subject.MESH | Vocabulary, Controlled | - |
dc.title | Development of a Controlled Vocabulary-Based Adverse Drug Reaction Signal Dictionary for Multicenter Electronic Health Record-Based Pharmacovigilance | - |
dc.type | Article | - |
dc.identifier.pmid | 30649749 | - |
dc.contributor.affiliatedAuthor | 박, 래웅 | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1007/s40264-018-0767-7 | - |
dc.citation.title | Drug safety | - |
dc.citation.volume | 42 | - |
dc.citation.number | 5 | - |
dc.citation.date | 2019 | - |
dc.citation.startPage | 657 | - |
dc.citation.endPage | 670 | - |
dc.identifier.bibliographicCitation | Drug safety, 42(5). : 657-670, 2019 | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.identifier.eissn | 1179-1942 | - |
dc.relation.journalid | J001145916 | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.