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Abstract Details

Use of Ceribell Rapid-Response EEG in 100 consecutive cases correlated with a reduction in anti-seizure medication usage
Epilepsy/Clinical Neurophysiology (EEG)
S24 - Epilepsy/Clinical Neurophysiology (EEG): Clinical Epilepsy (4:42 PM-4:54 PM)
007

Diagnosis of non-convulsive or subclinical seizures is greatly aided by electroencephalography (EEG), but access to conventional EEG is often delayed by hours. It has been suggested that when physicians suspect subclinical seizures, they empirically treat patients with anti-seizure medications (ASMs) before EEG arrives. A recent multi-center clinical trial suggests that the Ceribell Rapid Response EEG (Rapid-EEG) can acquire EEG within minutes and improve physicians’ diagnostic decisions. In this study, we assessed whether Rapid-EEG diagnoses would correlate with changes in ASM usage.

In this study, we tested the hypothesis that diagnoses from a Rapid Response EEG during the initial neurological evaluation of patients with suspected subclinical seizures correlate with changes in anti-seizure medication (ASM) usage.

We performed a retrospective chart-review of 100 consecutive patients at an academic medical center who underwent Rapid-EEG monitoring. Cases were excluded if clinical course information or EEG reports were not available in the electronic medical record. EEG interpretation by the on-call EEG fellow and attending was used as the gold standard. We categorized EEG diagnoses as seizures (SZ), highly epileptiform patterns (HEP), diffuse or focal slowing, or normal.

Nineteen patients were diagnosed with SZ (N=5) or HEP (N=14) based on Rapid-EEG, while in 81 patients, seizures and epileptiform discharges were ruled out. In total, 46% of patients had already been treated with ASMs prior to Rapid-EEG. Patients were less likely to be continued or started on ASMs if the Rapid-EEG diagnosis was normal or slow compared to SZ/HEP (51% vs. 84.2% ; χ2 (1, N = 100) = 7.086, p = .0078).

Rapid-EEG helped identify patients with ongoing non-convulsive/subclinical seizures or highly epileptiform patterns. Patients in these high seizure-risk groups were more likely to be treated with ASMs after Rapid-EEG. By contrast, rapidly ruling out seizures correlated with a significant reduction in ASM treatment.

Authors/Disclosures
Deepika Kurup (Stanford University School of Medicine)
PRESENTER
Ms. Kurup has nothing to disclose.
Zach Davey, DO (Walter Reed National Military Medical Center) Dr. Davey has nothing to disclose.
Phuong Thi Hoang, MD, PhD (UCSF Movement Disorders and Neuromodulation Center) Dr. Hoang has nothing to disclose.
Katherine M. Clifford, MD Dr. Clifford has nothing to disclose.
Katherine Werbaneth No disclosure on file
Varun B. Shah, MD (The Permanente Medical Group) Dr. Shah has nothing to disclose.
Prasanthi Govindarajan Prasanthi Govindarajan has nothing to disclose.
Kimford J. Meador, MD, FAAN (Stanford University School of Medicine) The institution of Dr. Meador has received research support from NIH. The institution of Dr. Meador has received research support from Eisai. The institution of Dr. Meador has received research support from Medtronics. The institution of Dr. Meador has received research support from The Epilepsy Consortium.