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

  • Suehyun Lee
  • , Jongsoo Han
  • , Rae Woong Park
  • , Grace Juyun Kim
  • , John Hoon Rim
  • , Jooyoung Cho
  • , Kye Hwa Lee
  • , Jisan Lee
  • , Sujeong Kim
  • , Ju Han Kim
  • Seoul National University
  • Konyang University
  • Ajou University
  • Yonsei University
  • Yonsei University Mirae Campus
  • Catholic University of Pusan

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

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 ® PTs); (2) two teaching hospitals’ codes for laboratory test results mapped to the Logical Observation Identifiers Names and Codes (LOINC) terms and MedDRA ® 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 ® PTs. Results: Of the standard 4514 MedDRA ® 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.

Original languageEnglish
Pages (from-to)657-670
Number of pages14
JournalDrug Safety
Volume42
Issue number5
DOIs
StatePublished - 1 May 2019

Bibliographical note

Publisher Copyright:
© 2019, Springer Nature Switzerland AG.

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