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    Stud Health Technol Inform. 2010;160(Pt 1):518-22.

    Documentation in pharmacovigilance: using an ontology to extend and normalize Pubmed queries.

    Source

    INSERM U936, Université Rennes 1, IFR 140, Rennes, France. Denis.Delamarre@chu-rennes.fr

    Abstract

    OBJECTIVES:

    To assess and understand adverse drug reactions (ADRs), a systematic review of reference databases like Pubmed is a necessary and mandatory step in Pharmacovigilance. In order to assist pharmacovigilance team with a computerized tool, we performed a comparative study of 4 different approaches to query Pubmed through ADR-drug terms. The aim of this study is to assess how an ontology of adverse effects, used to normalize and extend queries, could improve this search.

    MATERIAL AND METHOD:

    The ontological resource OntoEIM contains 58,000 classes and integrates MedDRA terminology. The entry point is a ADR-Drug term and the four methods are (i) a direct search on Pubmed (ii) a search with a normalized query enhanced with domain-specific Mesh Heading criteria, (iii) a search with the same elaborated query extended to the MeSH sub-hierarchy of the adverse effect entry and (iv) a search with a set of MedDRA terms grouped by subsomption in the OntoEIM ontology. For each of the 16 queries performed and analysed, relevant publications are selected "manually" by two pharmacovigilant experts.

    RESULTS:

    The recall is respectively of 63%, 50%, 67% and 74%, the precision of 13%, 26%, 29% and 4%. The best recall is provided by the ontology-based method, for 4 cases out of 16 this method returns relevant publications when the others return no results.

    CONCLUSION:

    Results show that an ontology-based search tool improves the recall performance, but other tools and methods are needed to raise the precision.

    PMID:
    20841741
    [PubMed - indexed for MEDLINE]

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