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Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response

BACKGROUND AND PURPOSE: Intravenous valproate (VPA) is an established treatment of status epilepticus (SE), but optimal loading dose was not fully assessed. We aimed at analyzing the correlation between VPA loading dose and subsequent plasma levels with clinical response in SE. METHODS: This was a r...

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Autores principales: Vijiala, Sergiu, André, Pascal, Buclin, Thierry, Decosterd, Laurent A., Rossetti, Andrea O., Novy, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545207/
https://www.ncbi.nlm.nih.gov/pubmed/35686387
http://dx.doi.org/10.1111/ene.15441
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author Vijiala, Sergiu
André, Pascal
Buclin, Thierry
Decosterd, Laurent A.
Rossetti, Andrea O.
Novy, Jan
author_facet Vijiala, Sergiu
André, Pascal
Buclin, Thierry
Decosterd, Laurent A.
Rossetti, Andrea O.
Novy, Jan
author_sort Vijiala, Sergiu
collection PubMed
description BACKGROUND AND PURPOSE: Intravenous valproate (VPA) is an established treatment of status epilepticus (SE), but optimal loading dose was not fully assessed. We aimed at analyzing the correlation between VPA loading dose and subsequent plasma levels with clinical response in SE. METHODS: This was a retrospective study in one referral center of all consecutive VPA‐naïve SE episodes treated with VPA between January 2013 and June 2019, in which total VPA trough plasma levels after intravenous loading dose were available. Response to VPA, defined as last antiseizure medication introduced before SE resolution (without the need for additional treatment), was correlated with VPA loading dose and trough level. Correlations were adjusted for other SE characteristics. RESULTS: Among 128 SE episodes, 53 (41%) responded to VPA. Median VPA loading dose was 25.2 mg/kg (range, 7–58 mg/kg). Loading doses and total plasma levels were not associated with the probability of response or mortality. Correcting for other possible confounders (number of previously tried treatment, demographics, SE severity) did not alter these findings. Only 3.8% of SE episodes that responded to VPA received >30 mg/kg. CONCLUSIONS: A high loading dose (>30 mg/kg) is not associated with a greater response rate in patients with SE. Therefore, it seems to bring little benefit. If confirmed in further studies, a dosage of 25–30 mg/kg appears adequate in SE.
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spelling pubmed-95452072022-10-14 Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response Vijiala, Sergiu André, Pascal Buclin, Thierry Decosterd, Laurent A. Rossetti, Andrea O. Novy, Jan Eur J Neurol Epilepsy BACKGROUND AND PURPOSE: Intravenous valproate (VPA) is an established treatment of status epilepticus (SE), but optimal loading dose was not fully assessed. We aimed at analyzing the correlation between VPA loading dose and subsequent plasma levels with clinical response in SE. METHODS: This was a retrospective study in one referral center of all consecutive VPA‐naïve SE episodes treated with VPA between January 2013 and June 2019, in which total VPA trough plasma levels after intravenous loading dose were available. Response to VPA, defined as last antiseizure medication introduced before SE resolution (without the need for additional treatment), was correlated with VPA loading dose and trough level. Correlations were adjusted for other SE characteristics. RESULTS: Among 128 SE episodes, 53 (41%) responded to VPA. Median VPA loading dose was 25.2 mg/kg (range, 7–58 mg/kg). Loading doses and total plasma levels were not associated with the probability of response or mortality. Correcting for other possible confounders (number of previously tried treatment, demographics, SE severity) did not alter these findings. Only 3.8% of SE episodes that responded to VPA received >30 mg/kg. CONCLUSIONS: A high loading dose (>30 mg/kg) is not associated with a greater response rate in patients with SE. Therefore, it seems to bring little benefit. If confirmed in further studies, a dosage of 25–30 mg/kg appears adequate in SE. John Wiley and Sons Inc. 2022-06-21 2022-09 /pmc/articles/PMC9545207/ /pubmed/35686387 http://dx.doi.org/10.1111/ene.15441 Text en © 2022 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Epilepsy
Vijiala, Sergiu
André, Pascal
Buclin, Thierry
Decosterd, Laurent A.
Rossetti, Andrea O.
Novy, Jan
Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response
title Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response
title_full Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response
title_fullStr Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response
title_full_unstemmed Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response
title_short Valproate in status epilepticus: Correlation between loading dose, serum levels, and clinical response
title_sort valproate in status epilepticus: correlation between loading dose, serum levels, and clinical response
topic Epilepsy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545207/
https://www.ncbi.nlm.nih.gov/pubmed/35686387
http://dx.doi.org/10.1111/ene.15441
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