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Summary   Objective  Using the electronic medical record ( EMR ) to capture structured clinical data at the point of care would be a practical way to support quality improvement and practice‐based research in epilepsy.    Methods  We describe our stepwise process for building structured clinical documentation support tools in the  EMR  that define best practices in epilepsy, and we describe how we incorporated these toolkits into our clinical workflow.    Results  These tools write notes and capture hundreds of fields of data including several score tests: Generalized Anxiety Disorder‐7 items, Neurological Disorders Depression Inventory for Epilepsy, Epworth Sleepiness Scale, Quality of Life in Epilepsy–10 items, Montreal Cognitive Assessment/Short Test of Mental Status, and Medical Research Council Prognostic Index. The tools summarize brain imaging, blood laboratory, and electroencephalography results, and document neuromodulation treatments. The tools provide Best Practices Advisories and other clinical decision support when appropriate. The tools prompt enrollment in a  DNA  biobanking study. We have thus far enrolled 231 patients for initial visits and are starting our first annual follow‐up visits and provide a brief description of our cohort.    Significance  We are sharing these  EMR  tools and captured data with other epilepsy clinics as part of a Neurology Practice Based Research Network, and are using the tools to conduct pragmatic trials using subgroup‐based adaptive designs.

Structured clinical documentation in the electronic medical record to improve quality and to support practice‐based research in epilepsy