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Abstract Details

Long-Term Anti-Seizure Medication Continuation after Acute Strokes
Epilepsy/Clinical Neurophysiology (EEG)
Epilepsy/Clinical Neurophysiology (EEG) Posters (7:00 AM-5:00 PM)
075

The primary aim of our study is to investigate the predictors of long-term anti-seizure medication (ASM) use in patients with acute stroke.

ASMs are commonly used for managing acute symptomatic seizures (ASyS) and epileptic abnormalities (EAs) after stroke. Many are discharged on ASMs. In absence of clear guidelines, patients may be continued on ASMs for a long period of time. Predictors of long-term ASM continuation in acute stroke patients remain unknown.

We performed a single-center, retrospective cohort study of patients fulfilling the following criteria from 2013 - 2018: adults (≥18 years), acute stroke [ischemic stroke (IS), intracerebral hemorrhage (ICH), or subarachnoid hemorrhage (SAH)], concern for ASyS [i.e. underwent continuous electroencephalogram (cEEG) monitoring], and attended out-patient clinic follow-up after hospitalization. The primary outcome was long-term ASM continuation, i.e. beyond the first post-hospitalization clinic visit. We performed a univariate, followed by multivariable logistic regression analysis.

A total of 504 patients were included and 290 (58%) were started on ASMs. The latter were included in the final analysis. Among them, 188 (37.3%) were discharged on ASMs. Primary outcome was met by 156 (30.9%) patients, accounting for 54% of those started on ASMs during admission. The multivariable model found that the odds of long-term ASM continuation were less if patients suffered SAH compared to IS [Odds ratio (OR) 0.38 [95% CI 0.15-0.97]) and were admitted to the neurological ICU (NICU) during admission (OR 0.37 [95% CI 0.15-0.92]). In contrast, history of an ASyS (clinical or electrographic) significantly increased the odds of ASM continuation (OR 19.73 [95% CI 9.16-47.16]) along with the presence of EAs on cEEG (OR 2.29 [95% CI 1.15-4.66]).

Close to one-third of acute stroke patients with ASyS concerns are continued on ASMs for a long-term after hospital discharge. This lack of deprescribing is primarily driven by ASyS and cEEG findings.

Authors/Disclosures
Pradeep Chandan, DO (Cleveland Clinic)
PRESENTER
Dr. Chandan has nothing to disclose.
No disclosure on file
Lisa Ellison (Cleveland Clinic) No disclosure on file
Nicholas Thompson The institution of Nicholas Thompson has received research support from EMD Serono.
Irene L. Katzan, MD (Cleveland Clinic, Neurology) Dr. Katzan has received personal compensation in the range of $5,000-$9,999 for serving on a Scientific Advisory or Data Safety Monitoring board for CSL Behring . The institution of Dr. Katzan has received research support from TEVA Pharmaceuticals.
Pravin George, DO (Cleveland Clinic) Dr. George has nothing to disclose.
Christopher R. Newey, DO (Sanford Health) Dr. Newey has nothing to disclose.
Stephen Hantus, MD (Cleveland Clinic) Dr. Hantus has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Eisai. Dr. Hantus has received personal compensation in the range of $0-$499 for serving as a Consultant for UCB.
Vineet Punia, MD (Cleveland Clinic) Dr. Punia has nothing to disclose.