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Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus

BACKGROUND: Nonconvulsive status epilepticus (NCSE) is a diagnosis that is often challenging and one that may progress to refractory NCSE. Ketamine is a noncompetitive N-methyl-d-aspartate antagonist that increasingly has been used to treat refractory status epilepticus. Current Neurocritical Care S...

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Autores principales: Pizzi, Michael A., Kamireddi, Prasuna, Tatum, William O., Shih, Jerry J., Jackson, Daniel A., Freeman, William D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549373/
https://www.ncbi.nlm.nih.gov/pubmed/28808577
http://dx.doi.org/10.1186/s40560-017-0248-6
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author Pizzi, Michael A.
Kamireddi, Prasuna
Tatum, William O.
Shih, Jerry J.
Jackson, Daniel A.
Freeman, William D.
author_facet Pizzi, Michael A.
Kamireddi, Prasuna
Tatum, William O.
Shih, Jerry J.
Jackson, Daniel A.
Freeman, William D.
author_sort Pizzi, Michael A.
collection PubMed
description BACKGROUND: Nonconvulsive status epilepticus (NCSE) is a diagnosis that is often challenging and one that may progress to refractory NCSE. Ketamine is a noncompetitive N-methyl-d-aspartate antagonist that increasingly has been used to treat refractory status epilepticus. Current Neurocritical Care Society guidelines recommend intravenous (IV) ketamine infusion as an alternative treatment for refractory status epilepticus in adults. On the other hand, enteral ketamine use in NCSE has been reported in only 6 cases (1 adult and 5 pediatric) in the literature to date. CASE PRESENTATION: A 33-year-old woman with a history of poorly controlled epilepsy presented with generalized tonic-clonic seizures, followed by recurrent focal seizures that evolved into NCSE. This immediately recurred within 24 h of a prior episode of NCSE that was treated with IV ketamine. Considering her previous response, she was started again on an IV ketamine infusion, which successfully terminated NCSE. This time, enteral ketamine was gradually introduced while weaning off the IV formulation. Treatment with enteral ketamine was continued for 6 months and then tapered off. There was no recurrence of NCSE or seizures and no adverse events noted during the course of treatment. CONCLUSION: This case supports the use of enteral ketamine as a potential adjunct to IV ketamine in the treatment of NCSE, especially in cases without coma. Introduction of enteral ketamine may reduce seizure recurrence, duration of stay in ICU, and morbidity associated with intubation.
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spelling pubmed-55493732017-08-14 Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus Pizzi, Michael A. Kamireddi, Prasuna Tatum, William O. Shih, Jerry J. Jackson, Daniel A. Freeman, William D. J Intensive Care Case Report BACKGROUND: Nonconvulsive status epilepticus (NCSE) is a diagnosis that is often challenging and one that may progress to refractory NCSE. Ketamine is a noncompetitive N-methyl-d-aspartate antagonist that increasingly has been used to treat refractory status epilepticus. Current Neurocritical Care Society guidelines recommend intravenous (IV) ketamine infusion as an alternative treatment for refractory status epilepticus in adults. On the other hand, enteral ketamine use in NCSE has been reported in only 6 cases (1 adult and 5 pediatric) in the literature to date. CASE PRESENTATION: A 33-year-old woman with a history of poorly controlled epilepsy presented with generalized tonic-clonic seizures, followed by recurrent focal seizures that evolved into NCSE. This immediately recurred within 24 h of a prior episode of NCSE that was treated with IV ketamine. Considering her previous response, she was started again on an IV ketamine infusion, which successfully terminated NCSE. This time, enteral ketamine was gradually introduced while weaning off the IV formulation. Treatment with enteral ketamine was continued for 6 months and then tapered off. There was no recurrence of NCSE or seizures and no adverse events noted during the course of treatment. CONCLUSION: This case supports the use of enteral ketamine as a potential adjunct to IV ketamine in the treatment of NCSE, especially in cases without coma. Introduction of enteral ketamine may reduce seizure recurrence, duration of stay in ICU, and morbidity associated with intubation. BioMed Central 2017-08-08 /pmc/articles/PMC5549373/ /pubmed/28808577 http://dx.doi.org/10.1186/s40560-017-0248-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Pizzi, Michael A.
Kamireddi, Prasuna
Tatum, William O.
Shih, Jerry J.
Jackson, Daniel A.
Freeman, William D.
Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus
title Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus
title_full Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus
title_fullStr Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus
title_full_unstemmed Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus
title_short Transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus
title_sort transition from intravenous to enteral ketamine for treatment of nonconvulsive status epilepticus
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5549373/
https://www.ncbi.nlm.nih.gov/pubmed/28808577
http://dx.doi.org/10.1186/s40560-017-0248-6
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