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Unihemispheric Burst Suppression

Burst suppression (BS) consists of bursts of high-voltage slow and sharp wave activity alternating with periods of background suppression in the electroencephalogram (EEG). When induced by deep anesthesia or encephalopathy, BS is bihemispheric and is often viewed as a non-epileptic phenomenon. In co...

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Autores principales: Mader, Edward C., Villemarette-Pittman, Nicole R., Rogers, Cornel T., Torres-Delgado, Frank, Olejniczak, Piotr W., England, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192435/
https://www.ncbi.nlm.nih.gov/pubmed/25309713
http://dx.doi.org/10.4081/ni.2014.5487
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author Mader, Edward C.
Villemarette-Pittman, Nicole R.
Rogers, Cornel T.
Torres-Delgado, Frank
Olejniczak, Piotr W.
England, John D.
author_facet Mader, Edward C.
Villemarette-Pittman, Nicole R.
Rogers, Cornel T.
Torres-Delgado, Frank
Olejniczak, Piotr W.
England, John D.
author_sort Mader, Edward C.
collection PubMed
description Burst suppression (BS) consists of bursts of high-voltage slow and sharp wave activity alternating with periods of background suppression in the electroencephalogram (EEG). When induced by deep anesthesia or encephalopathy, BS is bihemispheric and is often viewed as a non-epileptic phenomenon. In contrast, unihemispheric BS is rare and its clinical significance is poorly understood. We describe here two cases of unihemispheric BS. The first patient is a 56-year-old woman with a left temporoparietal tumor who presented in convulsive status epilepticus. EEG showed left hemispheric BS after clinical seizure termination with lorazepam and propofol. The second patient is a 39-year-old woman with multiple medical problems and a vague history of seizures. After abdominal surgery, she experienced a convulsive seizure prompting treatment with propofol. Her EEG also showed left hemispheric BS. In both cases, increasing the propofol infusion rate resulted in disappearance of unihemispheric BS and clinical improvement. The prevailing view that typical bihemispheric BS is non-epileptic should not be extrapolated automatically to unihemispheric BS. The fact that unihemispheric BS was associated with clinical seizure and resolved with propofol suggests that, in both cases, an epileptic mechanism was responsible for unihemispheric BS.
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spelling pubmed-41924352014-10-10 Unihemispheric Burst Suppression Mader, Edward C. Villemarette-Pittman, Nicole R. Rogers, Cornel T. Torres-Delgado, Frank Olejniczak, Piotr W. England, John D. Neurol Int Case Report Burst suppression (BS) consists of bursts of high-voltage slow and sharp wave activity alternating with periods of background suppression in the electroencephalogram (EEG). When induced by deep anesthesia or encephalopathy, BS is bihemispheric and is often viewed as a non-epileptic phenomenon. In contrast, unihemispheric BS is rare and its clinical significance is poorly understood. We describe here two cases of unihemispheric BS. The first patient is a 56-year-old woman with a left temporoparietal tumor who presented in convulsive status epilepticus. EEG showed left hemispheric BS after clinical seizure termination with lorazepam and propofol. The second patient is a 39-year-old woman with multiple medical problems and a vague history of seizures. After abdominal surgery, she experienced a convulsive seizure prompting treatment with propofol. Her EEG also showed left hemispheric BS. In both cases, increasing the propofol infusion rate resulted in disappearance of unihemispheric BS and clinical improvement. The prevailing view that typical bihemispheric BS is non-epileptic should not be extrapolated automatically to unihemispheric BS. The fact that unihemispheric BS was associated with clinical seizure and resolved with propofol suggests that, in both cases, an epileptic mechanism was responsible for unihemispheric BS. PAGEPress Publications, Pavia, Italy 2014-08-13 /pmc/articles/PMC4192435/ /pubmed/25309713 http://dx.doi.org/10.4081/ni.2014.5487 Text en ©Copyright E.C. Mader Jr. et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mader, Edward C.
Villemarette-Pittman, Nicole R.
Rogers, Cornel T.
Torres-Delgado, Frank
Olejniczak, Piotr W.
England, John D.
Unihemispheric Burst Suppression
title Unihemispheric Burst Suppression
title_full Unihemispheric Burst Suppression
title_fullStr Unihemispheric Burst Suppression
title_full_unstemmed Unihemispheric Burst Suppression
title_short Unihemispheric Burst Suppression
title_sort unihemispheric burst suppression
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192435/
https://www.ncbi.nlm.nih.gov/pubmed/25309713
http://dx.doi.org/10.4081/ni.2014.5487
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