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Real-time clinical note monitoring to detect conditions for rapid follow-up: A case study of clinical trial enrollment in drug-induced torsades de pointes and Stevens-Johnson syndrome
Author(s) -
Sarah Delozier,
Peter Speltz,
Jason Brito,
Leigh Anne Tang,
Janey Wang,
Joshua C. Smith,
Dario A. Giuse,
Elizabeth J. Phillips,
Kristina Williams,
Teresa Strickland,
Giovanni Davogustto,
Dan M. Roden,
Joshua C. Denny
Publication year - 2020
Publication title -
journal of the american medical informatics association
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.614
H-Index - 150
eISSN - 1527-974X
pISSN - 1067-5027
DOI - 10.1093/jamia/ocaa213
Subject(s) - torsades de pointes , medicine , clinical trial , drug , drug trial , intensive care medicine , qt interval , pharmacology
Identifying acute events as they occur is challenging in large hospital systems. Here, we describe an automated method to detect 2 rare adverse drug events (ADEs), drug-induced torsades de pointes and Stevens-Johnson syndrome and toxic epidermal necrolysis, in near real time for participant recruitment into prospective clinical studies. A text processing system searched clinical notes from the electronic health record (EHR) for relevant keywords and alerted study personnel via email of potential patients for chart review or in-person evaluation. Between 2016 and 2018, the automated recruitment system resulted in capture of 138 true cases of drug-induced rare events, improving recall from 43% to 93%. Our focused electronic alert system maintained 2-year enrollment, including across an EHR migration from a bespoke system to Epic. Real-time monitoring of EHR notes may accelerate research for certain conditions less amenable to conventional study recruitment paradigms.

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