2014
DOI: 10.1136/amiajnl-2013-001612
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Mining clinical text for signals of adverse drug-drug interactions

Abstract: It is feasible to identify DDI signals and estimate the rate of adverse events among patients on drug combinations, directly from clinical text; this could have utility in prioritizing drug interaction surveillance as well as in clinical decision support.

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Cited by 141 publications
(130 citation statements)
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“…In other cases, NLP is implemented using basic text search of a list of 'key words' identified by the authors and subsequent analysis of the set of terms extracted with Boolean logic [150,151], disproportionality analysis [152], contingency tables, [153] logistic regression [154], and classification methods [155]. Fields of applications include EHR-data driven phenotyping, ADR signaling, and the assessment of effects of mood instability on clinical outcomes.…”
Section: F Extraction Of Information From Unstructured Clinical Datamentioning
confidence: 99%
“…In other cases, NLP is implemented using basic text search of a list of 'key words' identified by the authors and subsequent analysis of the set of terms extracted with Boolean logic [150,151], disproportionality analysis [152], contingency tables, [153] logistic regression [154], and classification methods [155]. Fields of applications include EHR-data driven phenotyping, ADR signaling, and the assessment of effects of mood instability on clinical outcomes.…”
Section: F Extraction Of Information From Unstructured Clinical Datamentioning
confidence: 99%
“…Thus, it is difficult to detect adverse drug reactions SDRs in a timely manner and some adverse drug reactions may even not be captured by those reporting system. Alternative sources of data have already been used to detect drug-adverse event associations including claims data [1], electronic medical records (EMRs) [2][3][4] and consumer search logs [5][6]. In addition, approaches have also been developed to combine SDRs from data sources such as EMRs, claims, internet search logs with SDRs from FDA Adverse Event Reporting System (FAERS) [5,[7][8].…”
Section: Introductionmentioning
confidence: 99%
“…For pharmacovigilance, analysis of large data sets (4,5 ) has uncovered novel adverse events (6 -8 ), off-label usage patterns (9 ), and interactions between drugs (10 ).…”
mentioning
confidence: 99%