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Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures
PURPOSE: This study compared the efficacy and tolerability of intravenous (i.v.) phenobarbital (PHB) and i.v. levetiracetam (LEV) in children with status epilepticus (SE) or acute repetitive seizure (ARS). METHODS: The medical records of children (age range, 1 month to 15 years) treated with i.v. PH...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Pediatric Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753198/ https://www.ncbi.nlm.nih.gov/pubmed/26893602 http://dx.doi.org/10.3345/kjp.2016.59.1.35 |
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author | Lee, Yun-Jeong Yum, Mi-Sun Kim, Eun-Hee Ko, Tae-Sung |
author_facet | Lee, Yun-Jeong Yum, Mi-Sun Kim, Eun-Hee Ko, Tae-Sung |
author_sort | Lee, Yun-Jeong |
collection | PubMed |
description | PURPOSE: This study compared the efficacy and tolerability of intravenous (i.v.) phenobarbital (PHB) and i.v. levetiracetam (LEV) in children with status epilepticus (SE) or acute repetitive seizure (ARS). METHODS: The medical records of children (age range, 1 month to 15 years) treated with i.v. PHB or LEV for SE or ARS at our single tertiary center were retrospectively reviewed. Seizure termination was defined as seizure cessation within 30 minutes of infusion completion and no recurrence within 24 hours. Information on the demographic variables, electroencephalography and magnetic resonance imaging findings, previous antiepileptic medications, and adverse events after drug infusion was obtained. RESULTS: The records of 88 patients with SE or ARS (median age, 18 months; 50 treated with PHB and 38 with LEV) were reviewed. The median initial dose of i.v. PHB was 20 mg/kg (range, 10–20 mg/kg) and that of i.v. LEV was 30 mg/kg (range, 20–30 mg/kg). Seizure termination occurred in 57.9% of patients treated with i.v. LEV (22 of 38) and 74.0% treated with i.v. PHB (37 of 50) (P=0.111). The factor associated with seizure termination was the type of event (SE vs. ARS) in each group. Adverse effects were reported in 13.2% of patients treated with i.v. LEV (5 of 38; n=4, aggressive behavior and n=1, vomiting), and 28.0% of patients treated with i.v. PHB (14 of 50). CONCLUSION: Intravenous LEV was efficacious and safe in children with ARS or SE. Further evaluation is needed to determine the most effective and best-tolerated loading dose of i.v. LEV. |
format | Online Article Text |
id | pubmed-4753198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Pediatric Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-47531982016-02-18 Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures Lee, Yun-Jeong Yum, Mi-Sun Kim, Eun-Hee Ko, Tae-Sung Korean J Pediatr Original Article PURPOSE: This study compared the efficacy and tolerability of intravenous (i.v.) phenobarbital (PHB) and i.v. levetiracetam (LEV) in children with status epilepticus (SE) or acute repetitive seizure (ARS). METHODS: The medical records of children (age range, 1 month to 15 years) treated with i.v. PHB or LEV for SE or ARS at our single tertiary center were retrospectively reviewed. Seizure termination was defined as seizure cessation within 30 minutes of infusion completion and no recurrence within 24 hours. Information on the demographic variables, electroencephalography and magnetic resonance imaging findings, previous antiepileptic medications, and adverse events after drug infusion was obtained. RESULTS: The records of 88 patients with SE or ARS (median age, 18 months; 50 treated with PHB and 38 with LEV) were reviewed. The median initial dose of i.v. PHB was 20 mg/kg (range, 10–20 mg/kg) and that of i.v. LEV was 30 mg/kg (range, 20–30 mg/kg). Seizure termination occurred in 57.9% of patients treated with i.v. LEV (22 of 38) and 74.0% treated with i.v. PHB (37 of 50) (P=0.111). The factor associated with seizure termination was the type of event (SE vs. ARS) in each group. Adverse effects were reported in 13.2% of patients treated with i.v. LEV (5 of 38; n=4, aggressive behavior and n=1, vomiting), and 28.0% of patients treated with i.v. PHB (14 of 50). CONCLUSION: Intravenous LEV was efficacious and safe in children with ARS or SE. Further evaluation is needed to determine the most effective and best-tolerated loading dose of i.v. LEV. The Korean Pediatric Society 2016-01 2016-01-22 /pmc/articles/PMC4753198/ /pubmed/26893602 http://dx.doi.org/10.3345/kjp.2016.59.1.35 Text en Copyright © 2016 by The Korean Pediatric Society http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Yun-Jeong Yum, Mi-Sun Kim, Eun-Hee Ko, Tae-Sung Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures |
title | Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures |
title_full | Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures |
title_fullStr | Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures |
title_full_unstemmed | Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures |
title_short | Intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures |
title_sort | intravenous levetiracetam versus phenobarbital in children with status epilepticus or acute repetitive seizures |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753198/ https://www.ncbi.nlm.nih.gov/pubmed/26893602 http://dx.doi.org/10.3345/kjp.2016.59.1.35 |
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