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Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report

INTRODUCTION: Status epilepticus (SE) has a mortality rate of 20 to 50%, with acute symptomatic SE having a higher risk compared to chronic SE. Electroconvulsive therapy (ECT) has been utilized for the treatment of refractory SE with a success rate estimate of 57.9%. There are no known reported case...

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Autores principales: Katzell, Lauren, Beydler, Emily M., Holbert, Richard, Rodriguez-Roman, Laura, Carr, Brent R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935692/
https://www.ncbi.nlm.nih.gov/pubmed/36816412
http://dx.doi.org/10.3389/fpsyt.2023.1126956
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author Katzell, Lauren
Beydler, Emily M.
Holbert, Richard
Rodriguez-Roman, Laura
Carr, Brent R.
author_facet Katzell, Lauren
Beydler, Emily M.
Holbert, Richard
Rodriguez-Roman, Laura
Carr, Brent R.
author_sort Katzell, Lauren
collection PubMed
description INTRODUCTION: Status epilepticus (SE) has a mortality rate of 20 to 50%, with acute symptomatic SE having a higher risk compared to chronic SE. Electroconvulsive therapy (ECT) has been utilized for the treatment of refractory SE with a success rate estimate of 57.9%. There are no known reported cases of concomitant use of vagus nerve stimulation (VNS) and ECT for the treatment of super refractory SE (SRSE) available in the literature. CASE DESCRIPTION: We present a 44-year-old female with a history of developmental delay, epilepsy, an implantable VNS for 6 years, and traumatic brain injury with subsequent hygroma who presented with progressive aphasia, declining mental status, and daily generalized seizures lasting up to 20 min. Seizures had increased from her baseline of one seizure per day controlled with topiramate 200 mg three times daily and lamotrigine 400 mg twice daily. She was diagnosed with SRSE after being intubated and placed on eight anti-epileptic drugs (AEDs) that failed to abort SE. ECT was attempted to terminate SE. Due to a prior right craniotomy with subsequent right hygroma, eight treatments of ECT were performed over three sessions using a right anterior, left temporal (RALT) and subsequently a bitemporal electrode placement. The VNS remained active throughout treatment. Various ECT dosing parameters were attempted, varying pulse width and frequency. Although ECT induced mild transient encephalographic (EEG) changes following ECT stimulations, it was unable to terminate SE. DISCUSSION: This case describes various treatment strategies, constraints, and device limitations when using ECT for the treatment of SE. With wide variability in efficacy rates of ECT in the treatment of SE in the literature, successful and unsuccessful cases offer information on optimizing ECT total charge dose and parameters that yielded success. This case demonstrates an instance of ECT inefficacy in the treatment of SRSE. Here, we discuss the rationale behind the various ECT settings that were selected, and constraints arising from the antiepileptic burden, VNS, and intrinsic limitations of the ECT device itself.
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spelling pubmed-99356922023-02-18 Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report Katzell, Lauren Beydler, Emily M. Holbert, Richard Rodriguez-Roman, Laura Carr, Brent R. Front Psychiatry Psychiatry INTRODUCTION: Status epilepticus (SE) has a mortality rate of 20 to 50%, with acute symptomatic SE having a higher risk compared to chronic SE. Electroconvulsive therapy (ECT) has been utilized for the treatment of refractory SE with a success rate estimate of 57.9%. There are no known reported cases of concomitant use of vagus nerve stimulation (VNS) and ECT for the treatment of super refractory SE (SRSE) available in the literature. CASE DESCRIPTION: We present a 44-year-old female with a history of developmental delay, epilepsy, an implantable VNS for 6 years, and traumatic brain injury with subsequent hygroma who presented with progressive aphasia, declining mental status, and daily generalized seizures lasting up to 20 min. Seizures had increased from her baseline of one seizure per day controlled with topiramate 200 mg three times daily and lamotrigine 400 mg twice daily. She was diagnosed with SRSE after being intubated and placed on eight anti-epileptic drugs (AEDs) that failed to abort SE. ECT was attempted to terminate SE. Due to a prior right craniotomy with subsequent right hygroma, eight treatments of ECT were performed over three sessions using a right anterior, left temporal (RALT) and subsequently a bitemporal electrode placement. The VNS remained active throughout treatment. Various ECT dosing parameters were attempted, varying pulse width and frequency. Although ECT induced mild transient encephalographic (EEG) changes following ECT stimulations, it was unable to terminate SE. DISCUSSION: This case describes various treatment strategies, constraints, and device limitations when using ECT for the treatment of SE. With wide variability in efficacy rates of ECT in the treatment of SE in the literature, successful and unsuccessful cases offer information on optimizing ECT total charge dose and parameters that yielded success. This case demonstrates an instance of ECT inefficacy in the treatment of SRSE. Here, we discuss the rationale behind the various ECT settings that were selected, and constraints arising from the antiepileptic burden, VNS, and intrinsic limitations of the ECT device itself. Frontiers Media S.A. 2023-02-03 /pmc/articles/PMC9935692/ /pubmed/36816412 http://dx.doi.org/10.3389/fpsyt.2023.1126956 Text en Copyright © 2023 Katzell, Beydler, Holbert, Rodriguez-Roman and Carr. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Katzell, Lauren
Beydler, Emily M.
Holbert, Richard
Rodriguez-Roman, Laura
Carr, Brent R.
Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report
title Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report
title_full Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report
title_fullStr Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report
title_full_unstemmed Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report
title_short Electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: A case report
title_sort electroconvulsive therapy use for refractory status epilepticus in an implantable vagus nerve stimulation patient: a case report
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9935692/
https://www.ncbi.nlm.nih.gov/pubmed/36816412
http://dx.doi.org/10.3389/fpsyt.2023.1126956
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