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Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study
OBJECTIVE: To evaluate the clinical impact of ketogenic diet (KD) on children with pharmacoresistant epileptic encephalopathy. METHODS: In all, 52 children with pharmacoresistant epileptic encephalopathy that diagnosed in our hospital from July 2012 to June 2015 were selected, including West syndrom...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943818/ https://www.ncbi.nlm.nih.gov/pubmed/29761022 http://dx.doi.org/10.1002/brb3.973 |
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author | Wu, Qiong Wang, Hua Fan, Yu Ying Zhang, Jun Mei Liu, Xue Yan Fang, Xiu Ying Yang, Feng Hua Cao, Qing Jun Qi, Ying |
author_facet | Wu, Qiong Wang, Hua Fan, Yu Ying Zhang, Jun Mei Liu, Xue Yan Fang, Xiu Ying Yang, Feng Hua Cao, Qing Jun Qi, Ying |
author_sort | Wu, Qiong |
collection | PubMed |
description | OBJECTIVE: To evaluate the clinical impact of ketogenic diet (KD) on children with pharmacoresistant epileptic encephalopathy. METHODS: In all, 52 children with pharmacoresistant epileptic encephalopathy that diagnosed in our hospital from July 2012 to June 2015 were selected, including West syndrome 38 cases, Lennox–Gastaut Syndrome 7 cases, Doose Syndrome 1 case, and Dravet syndrome 6 cases, and the effect, compliance, adverse reactions, electroencephalogram (EEG), and cognitive function were analyzed. Modified Johns Hopkins protocol was used to initiate KD, and Engel scale was used to evaluate the effect, and evaluated the effect of KD on the cognition, language, and motor function. RESULTS: At 12 weeks of KD treatment, the patients achieved I, II, III, and IV grade effect were accounted for 26.9% (14/52 cases), 17.3% (9/52 cases), 11.5% (6/52 cases), and 44.2% (23/52 cases), respectively, according to Engel scale. KD has different effect on different epileptic syndromes, best effect on Doose syndromes of 100%, and better effect on West syndrome with the effect rate of 57.9%, and the total effect number was 22 cases. The reduction of epileptiform discharges in the awake state before KD treatment was correlated with the seizure time after 3 months of KD treatment (r = .330, p = .017). The cognitive function of 23 patients was improved, 12 patients had language improvement, and the motor function was improved in 10 patients. In all, 23 patients had adverse reactions, and all patients were tolerated and improved. CONCLUSION: KD has certain effect on children with pharmacoresistant epileptic encephalopathy, and it can reduce interictal epileptic discharge frequency, and improve the background rhythm of EEG. The reduction of epileptiform discharges in awake state is in favor of the reduction of seizures frequency, thus increasing the efficacy, and improve the cognitive function, language, and motor function to varying degrees, combined with less adverse reaction, which is worthy of clinical application. |
format | Online Article Text |
id | pubmed-5943818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59438182018-05-14 Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study Wu, Qiong Wang, Hua Fan, Yu Ying Zhang, Jun Mei Liu, Xue Yan Fang, Xiu Ying Yang, Feng Hua Cao, Qing Jun Qi, Ying Brain Behav Original Research OBJECTIVE: To evaluate the clinical impact of ketogenic diet (KD) on children with pharmacoresistant epileptic encephalopathy. METHODS: In all, 52 children with pharmacoresistant epileptic encephalopathy that diagnosed in our hospital from July 2012 to June 2015 were selected, including West syndrome 38 cases, Lennox–Gastaut Syndrome 7 cases, Doose Syndrome 1 case, and Dravet syndrome 6 cases, and the effect, compliance, adverse reactions, electroencephalogram (EEG), and cognitive function were analyzed. Modified Johns Hopkins protocol was used to initiate KD, and Engel scale was used to evaluate the effect, and evaluated the effect of KD on the cognition, language, and motor function. RESULTS: At 12 weeks of KD treatment, the patients achieved I, II, III, and IV grade effect were accounted for 26.9% (14/52 cases), 17.3% (9/52 cases), 11.5% (6/52 cases), and 44.2% (23/52 cases), respectively, according to Engel scale. KD has different effect on different epileptic syndromes, best effect on Doose syndromes of 100%, and better effect on West syndrome with the effect rate of 57.9%, and the total effect number was 22 cases. The reduction of epileptiform discharges in the awake state before KD treatment was correlated with the seizure time after 3 months of KD treatment (r = .330, p = .017). The cognitive function of 23 patients was improved, 12 patients had language improvement, and the motor function was improved in 10 patients. In all, 23 patients had adverse reactions, and all patients were tolerated and improved. CONCLUSION: KD has certain effect on children with pharmacoresistant epileptic encephalopathy, and it can reduce interictal epileptic discharge frequency, and improve the background rhythm of EEG. The reduction of epileptiform discharges in awake state is in favor of the reduction of seizures frequency, thus increasing the efficacy, and improve the cognitive function, language, and motor function to varying degrees, combined with less adverse reaction, which is worthy of clinical application. John Wiley and Sons Inc. 2018-04-18 /pmc/articles/PMC5943818/ /pubmed/29761022 http://dx.doi.org/10.1002/brb3.973 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Wu, Qiong Wang, Hua Fan, Yu Ying Zhang, Jun Mei Liu, Xue Yan Fang, Xiu Ying Yang, Feng Hua Cao, Qing Jun Qi, Ying Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study |
title | Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study |
title_full | Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study |
title_fullStr | Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study |
title_full_unstemmed | Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study |
title_short | Ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: A clinical prospective study |
title_sort | ketogenic diet effects on 52 children with pharmacoresistant epileptic encephalopathy: a clinical prospective study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5943818/ https://www.ncbi.nlm.nih.gov/pubmed/29761022 http://dx.doi.org/10.1002/brb3.973 |
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