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Abstract Details

Examining the Impact of Comorbid Depression on Healthcare Utilization, Cost, and Outcomes in Patients with Newly Diagnosed Epilepsy in the US
Epilepsy/Clinical Neurophysiology (EEG)
S41 - Epilepsy: Public Health and Epidemiology (1:12 PM-1:24 PM)
002

Describe all-cause healthcare resource utilization (HCRU), costs, and time-to-event outcomes among newly diagnosed epilepsy patients with and without comorbid depression.

Depression is linked to increased HCRU and costs in epilepsy, but few studies have examined changes across subsequent lines of therapy (LOTs) or their relation to time-to-event outcomes.

This retrospective study utilized 100% Medicare Fee-for-Service claims and Inovalon’s MORE2 database (01/01/2016–12/31/2023) to identify incident epilepsy patients (01/01/2017–12/31/2019), defined by ≥2 outpatient or ≥1 inpatient claims. Patients were stratified by the presence or absence of depression during pre-index period. The index date was initiation of the first LOT lasting ≥30 days. Continuous enrollment of ≥12 months pre-index and ≥24 months post-index was required. LOTs ended with treatment discontinuation (≥60-day gap), switch, augmentation, or partial drop. Four LOTs were captured. All-cause HCRU and costs were reported per patient per month (PPPM) for each LOT. Total costs included all medical and pharmacy spending, adjusted to 2023 U.S. dollars.

Among 90,738 patients, 21,388 (24%) had comorbid depression. Patients with depression had significantly higher HCRU vs. those without depression, including more office visits (1.14 vs. 0.97 visits PPPM), emergency department (ED) visits (0.49 vs. 0.27 visits PPPM), and longer mean length of stay (11.2 vs. 8.4 days; all p<.0001). Total healthcare costs were significantly higher at index ($6,209 vs. $4,239 PPPM, p<.0001) and remained elevated across subsequent LOTs. Median time to first hospitalization was 3.5 vs. 5.6 months; median time to first ED visit was 2.4 versus 3.9 months, respectively.

Patients with comorbid depression demonstrated significantly higher HCRU and costs compared to those without depression, persisting across subsequent LOTs. Earlier median times to hospitalization and ED visits were observed in the depression cohort. Findings underscore the clinical and economic burden of depression and the need for comprehensive management strategies addressing psychiatric comorbidities.

Authors/Disclosures
Samuel W. Terman, MD (University of Michigan, Neurology Dept)
PRESENTER
Dr. Terman has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Xenon Pharmaceuticals. Dr. Terman has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Jazz Pharmaceuticals. Dr. Terman has received research support from American Epilepsy Society. Dr. Terman has received research support from Epilepsy Study Consortium. Dr. Terman has received research support from New York University. The institution of Dr. Terman has received research support from NIH/NIA. Dr. Terman has received personal compensation in the range of $100,000-$499,999 for serving as a clinician scientist trainee for Susan S Spencer award with 好色先生.
Alvin Ong, PharmD Dr. Ong has received personal compensation for serving as an employee of Xenon Pharmaceuticals. Dr. Ong has stock in Xenon Pharmaceuticals.
Keenan W. Davis, PhD Dr. Davis has nothing to disclose.
Anthony Yu Mr. Yu has received personal compensation for serving as an employee of Inovalon.
Yecheng Huang Mr. Huang has received personal compensation for serving as an employee of Inovalon.
Jung Park An immediate family member of Dr. Park has received personal compensation for serving as an employee of Regeneron. An immediate family member of Dr. Park has stock in Regeneron.
Dan Thornton, MBA Mr. Thornton has received personal compensation for serving as an employee of Xenon Pharmaceuticals. Mr. Thornton has stock in Xenon Pharmaceuticals.