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Abstract Details

Anxiety and Depression Symptoms in the Epilepsy Clinic: Examining Psychiatric Treatment Characteristics in a Learning Health System Model
Epilepsy/Clinical Neurophysiology (EEG)
P1 - Poster Session 1 (5:30 PM-6:30 PM)
6-007

To assess psychiatric treatment history among adults presenting with active anxiety and/or depression symptoms at a tertiary care epilepsy clinic via a learning health system model.

Ample studies show that persons with epilepsy (PWE) have high rates of mood and anxiety disorders. Neuropsychiatric symptomatology is associated with worse response to pharmacologic and surgical treatment of epilepsy. Screening tools such as the Neurological Disorders Depression Inventory for Epilepsy (NDDI-E) and Generalized Anxiety Disorder-7 (GAD-7) have been validated in epilepsy. Anxiety and depression screening at every clinic visit is now a new epilepsy quality measure.

Touchscreen administration of NDDI-E and GAD-7 to epilepsy clinic patients upon arrival for a routine visit over a five-month period.  Positive screens (GAD-7≥10 or NDDI-E>15) triggered additional questions regarding current and prior mental health care.

Among 106 individuals with active anxiety or depression symptoms (mean age 41.8 years, 56.6% women), 41 (36.7%) were not receiving medication or mental health treatment. Prior psychiatric hospitalization was reported by 30 (28.3%), and only 50% of those were still under mental health care. Of the study population, 48.1% had active symptoms in spite of current treatment with an SSRI, SNRI, or buspirone. Mean NDDI-E and GAD-7 scores of patients receiving medication treatment (17.2&13.6) were similar to those who were not (16.5&12.3), suggesting undertreatment. Of 28 patients positive for anxiety alone, only 14.3% were under mental health care (compared to 34% for the entire study population).  Notably, 67.9% of anxiety-only patients were women; thus, low treatment rates may reflect or contribute to gender health disparity.

This epilepsy clinic population has a startlingly high level of psychiatric acuity.  This reinforces the importance of addressing and monitoring the psychiatric needs of epilepsy patients, in particular among those on psychotropic medications, many of whom appear to be undertreated.

Authors/Disclosures
Victor M. Jones
PRESENTER
No disclosure on file
No disclosure on file
No disclosure on file
Kelly R. Conner, PhD (Wake Forest University School of Medicine) Dr. Conner has received personal compensation in the range of $0-$499 for serving as a Consultant for Xenon Pharmaceuticals. Dr. Conner has received personal compensation in the range of $5,000-$9,999 for serving on a Speakers Bureau for SK Life Science, Inc. The institution of Dr. Conner has received research support from AAPA.
Pamela W. Duncan, PhD, FAHA, FAPTA (Duke University) Dr. Duncan has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for BrainQ Technologies. Dr. Duncan has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for University of Pittsburg Pepper Center. Dr. Duncan has stock in CareDirections. The institution of Dr. Duncan has received research support from PCORI. The institution of Dr. Duncan has received research support from NIA and NINDS. The institution of Dr. Duncan has received research support from AHRQ. Dr. Duncan has received intellectual property interests from a discovery or technology relating to health care.
No disclosure on file
Matthew H. Wong, MD (Matthew Wong) No disclosure on file
Cormac A. O'Donovan, MD (Wake Forest University) Dr. O'Donovan has nothing to disclose.
No disclosure on file
Beverly Snively The institution of Beverly Snively has received research support from National Institutes of Health. The institution of Beverly Snively has received research support from Duke Endowment. The institution of Beverly Snively has received research support from Department of Defense. The institution of Beverly Snively has received research support from PCORI.
Heidi Munger Clary, MD, MPH (Wake Forest University School of Medicine) Dr. Munger Clary has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Xenon. Dr. Munger Clary has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Prova 好色先生. Dr. Munger Clary has received personal compensation in the range of $0-$499 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Epilepsia Open. Dr. Munger Clary has stock in HCA Healthcare. Dr. Munger Clary has stock in Eli Lilly. Dr. Munger Clary has stock in Procter and Gamble. Dr. Munger Clary has stock in CVS. Dr. Munger Clary has stock in Johnson and Johnson. Dr. Munger Clary has stock in Novartis. Dr. Munger Clary has stock in Danahauer. The institution of Dr. Munger Clary has received research support from National Institute of Health. The institution of Dr. Munger Clary has received research support from Suzanne Marcus Collins Foundation. The institution of Dr. Munger Clary has received research support from Eysz, Inc. The institution of Dr. Munger Clary has received research support from Department of Defense. The institution of Dr. Munger Clary has received research support from Duke Endowment. Dr. Munger Clary has received personal compensation in the range of $500-$4,999 for serving as a speaker, Psychiatry Commission member with International League Against Epilepsy. Dr. Munger Clary has received personal compensation in the range of $0-$499 for serving as a Faculty with J. Kiffin Penry Epilepsy 好色先生 Programs. Dr. Munger Clary has a non-compensated relationship as a advisor, potential site PI with Liva Nova that is relevant to AAN interests or activities.