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Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation
After liver transplantation, patients may develop seizures or epilepsy due to a variety of etiologies. The ideal antiepileptic drugs for these patients are those with fewer drug interactions and less hepatic toxicity. In this study, we present patients using levetiracetam to control seizures after l...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635739/ https://www.ncbi.nlm.nih.gov/pubmed/26402799 http://dx.doi.org/10.1097/MD.0000000000001350 |
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author | Lin, Chih-Hsiang Chen, Chao-Long Lin, Tsu-Kung Chen, Nai-Ching Tsai, Meng-Han Chuang, Yao-Chung |
author_facet | Lin, Chih-Hsiang Chen, Chao-Long Lin, Tsu-Kung Chen, Nai-Ching Tsai, Meng-Han Chuang, Yao-Chung |
author_sort | Lin, Chih-Hsiang |
collection | PubMed |
description | After liver transplantation, patients may develop seizures or epilepsy due to a variety of etiologies. The ideal antiepileptic drugs for these patients are those with fewer drug interactions and less hepatic toxicity. In this study, we present patients using levetiracetam to control seizures after liver transplantation. We retrospectively enrolled patients who received levetiracetam for seizure control after liver transplantation. We analyzed the etiology of liver failure that required liver transplantation, etiology of the seizures, outcomes of seizure control, and the condition of the patient after follow-up at the outpatient department. Hematological and biochemical data before and after the use of levetiracetam were also collected. Fifteen patients who received intravenous or oral levetiracetam monotherapy for seizure control after liver transplantation were enrolled into this study. All of the patients remained seizure-free during levetiracetam treatment. Two patients died during the follow-up, and the other 13 patients were alive at the end of the study period and all were seizure-free without neurological sequelae that interfered with their daily activities. No patients experienced liver failure or rejection of the donor liver due to ineffective immunosuppressant medications. The dosage of immunosuppressants did not change before and after levetiracetam treatment, and there were no changes in hematological and biochemical data before and after treatment. Levetiracetam may be a suitable antiepileptic drug for patients who undergo liver transplantation due to fewer drug interactions and a favorable safety profile. |
format | Online Article Text |
id | pubmed-4635739 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-46357392015-11-30 Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation Lin, Chih-Hsiang Chen, Chao-Long Lin, Tsu-Kung Chen, Nai-Ching Tsai, Meng-Han Chuang, Yao-Chung Medicine (Baltimore) 5300 After liver transplantation, patients may develop seizures or epilepsy due to a variety of etiologies. The ideal antiepileptic drugs for these patients are those with fewer drug interactions and less hepatic toxicity. In this study, we present patients using levetiracetam to control seizures after liver transplantation. We retrospectively enrolled patients who received levetiracetam for seizure control after liver transplantation. We analyzed the etiology of liver failure that required liver transplantation, etiology of the seizures, outcomes of seizure control, and the condition of the patient after follow-up at the outpatient department. Hematological and biochemical data before and after the use of levetiracetam were also collected. Fifteen patients who received intravenous or oral levetiracetam monotherapy for seizure control after liver transplantation were enrolled into this study. All of the patients remained seizure-free during levetiracetam treatment. Two patients died during the follow-up, and the other 13 patients were alive at the end of the study period and all were seizure-free without neurological sequelae that interfered with their daily activities. No patients experienced liver failure or rejection of the donor liver due to ineffective immunosuppressant medications. The dosage of immunosuppressants did not change before and after levetiracetam treatment, and there were no changes in hematological and biochemical data before and after treatment. Levetiracetam may be a suitable antiepileptic drug for patients who undergo liver transplantation due to fewer drug interactions and a favorable safety profile. Wolters Kluwer Health 2015-09-25 /pmc/articles/PMC4635739/ /pubmed/26402799 http://dx.doi.org/10.1097/MD.0000000000001350 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5300 Lin, Chih-Hsiang Chen, Chao-Long Lin, Tsu-Kung Chen, Nai-Ching Tsai, Meng-Han Chuang, Yao-Chung Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation |
title | Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation |
title_full | Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation |
title_fullStr | Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation |
title_full_unstemmed | Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation |
title_short | Levetiracetam in the Treatment of Epileptic Seizures After Liver Transplantation |
title_sort | levetiracetam in the treatment of epileptic seizures after liver transplantation |
topic | 5300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4635739/ https://www.ncbi.nlm.nih.gov/pubmed/26402799 http://dx.doi.org/10.1097/MD.0000000000001350 |
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