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Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus
BACKGROUND: Patients in refractory status epilepticus (RSE) may require treatment with continuous intravenous anesthetic drugs (cIVADs) for seizure control. The use of cIVADs, however, was recently associated with poor outcome in status epilepticus (SE), raising the question of whether cIVAD therapy...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249897/ https://www.ncbi.nlm.nih.gov/pubmed/30463604 http://dx.doi.org/10.1186/s13054-018-2235-2 |
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author | Madžar, Dominik Reindl, Caroline Giede-Jeppe, Antje Bobinger, Tobias Sprügel, Maximilian I. Knappe, Ruben U. Hamer, Hajo M. Huttner, Hagen B. |
author_facet | Madžar, Dominik Reindl, Caroline Giede-Jeppe, Antje Bobinger, Tobias Sprügel, Maximilian I. Knappe, Ruben U. Hamer, Hajo M. Huttner, Hagen B. |
author_sort | Madžar, Dominik |
collection | PubMed |
description | BACKGROUND: Patients in refractory status epilepticus (RSE) may require treatment with continuous intravenous anesthetic drugs (cIVADs) for seizure control. The use of cIVADs, however, was recently associated with poor outcome in status epilepticus (SE), raising the question of whether cIVAD therapy should be delayed for attempts to halt seizures with repeated non-anesthetic antiepileptic drugs. In this study, we aimed to determine the impact of differences in therapeutic approaches on RSE outcome using timing of cIVAD therapy as a surrogate for treatment aggressiveness. METHODS: This was a retrospective cohort study over 14 years (n = 77) comparing patients with RSE treated with cIVADs within and after 48 h after RSE onset, and functional status at last follow-up was the primary outcome (good = return to premorbid baseline or modified Rankin Scale score of less than 3). Secondary outcomes included discharge functional status, in-hospital mortality, RSE termination, induction of burst suppression, use of thiopental, duration of RSE after initiation of cIVADs, duration of mechanical ventilation, and occurrence of super-refractory SE. Analysis was performed on the total cohort and on subgroups defined by RSE severity according to the Status Epilepticus Severity Score (STESS) and by the variables contained therein. RESULTS: Fifty-three (68.8%) patients received cIVADs within the first 48 h. Early cIVAD treatment was independently associated with good outcome (adjusted risk ratio [aRR] 3.175, 95% confidence interval [CI] 1.273–7.918; P = 0.013) as well as lower chance of both induction of burst suppression (aRR 0.661, 95% CI 0.507–0.861; P = 0.002) and use of thiopental (aRR 0.446, 95% CI 0.205–0.874; P = 0.043). RSE duration after cIVAD initiation was shorter in the early cIVAD cohort (hazard ratio 1.796, 95% CI 1.047–3.081; P = 0.033). Timing of cIVAD use did not impact the remaining secondary outcomes. Subgroup analysis revealed early cIVAD impact on the primary outcome to be driven by patients with STESS of less than 3. CONCLUSIONS: Patients with RSE treated with cIVADs may benefit from early initiation of such therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2235-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6249897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62498972018-11-26 Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus Madžar, Dominik Reindl, Caroline Giede-Jeppe, Antje Bobinger, Tobias Sprügel, Maximilian I. Knappe, Ruben U. Hamer, Hajo M. Huttner, Hagen B. Crit Care Research BACKGROUND: Patients in refractory status epilepticus (RSE) may require treatment with continuous intravenous anesthetic drugs (cIVADs) for seizure control. The use of cIVADs, however, was recently associated with poor outcome in status epilepticus (SE), raising the question of whether cIVAD therapy should be delayed for attempts to halt seizures with repeated non-anesthetic antiepileptic drugs. In this study, we aimed to determine the impact of differences in therapeutic approaches on RSE outcome using timing of cIVAD therapy as a surrogate for treatment aggressiveness. METHODS: This was a retrospective cohort study over 14 years (n = 77) comparing patients with RSE treated with cIVADs within and after 48 h after RSE onset, and functional status at last follow-up was the primary outcome (good = return to premorbid baseline or modified Rankin Scale score of less than 3). Secondary outcomes included discharge functional status, in-hospital mortality, RSE termination, induction of burst suppression, use of thiopental, duration of RSE after initiation of cIVADs, duration of mechanical ventilation, and occurrence of super-refractory SE. Analysis was performed on the total cohort and on subgroups defined by RSE severity according to the Status Epilepticus Severity Score (STESS) and by the variables contained therein. RESULTS: Fifty-three (68.8%) patients received cIVADs within the first 48 h. Early cIVAD treatment was independently associated with good outcome (adjusted risk ratio [aRR] 3.175, 95% confidence interval [CI] 1.273–7.918; P = 0.013) as well as lower chance of both induction of burst suppression (aRR 0.661, 95% CI 0.507–0.861; P = 0.002) and use of thiopental (aRR 0.446, 95% CI 0.205–0.874; P = 0.043). RSE duration after cIVAD initiation was shorter in the early cIVAD cohort (hazard ratio 1.796, 95% CI 1.047–3.081; P = 0.033). Timing of cIVAD use did not impact the remaining secondary outcomes. Subgroup analysis revealed early cIVAD impact on the primary outcome to be driven by patients with STESS of less than 3. CONCLUSIONS: Patients with RSE treated with cIVADs may benefit from early initiation of such therapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2235-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-21 /pmc/articles/PMC6249897/ /pubmed/30463604 http://dx.doi.org/10.1186/s13054-018-2235-2 Text en © The Author(s). 2018 Open Access This 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 | Research Madžar, Dominik Reindl, Caroline Giede-Jeppe, Antje Bobinger, Tobias Sprügel, Maximilian I. Knappe, Ruben U. Hamer, Hajo M. Huttner, Hagen B. Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus |
title | Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus |
title_full | Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus |
title_fullStr | Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus |
title_full_unstemmed | Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus |
title_short | Impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus |
title_sort | impact of timing of continuous intravenous anesthetic drug treatment on outcome in refractory status epilepticus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249897/ https://www.ncbi.nlm.nih.gov/pubmed/30463604 http://dx.doi.org/10.1186/s13054-018-2235-2 |
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