Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy

Purpose : To verify the efficacy and safety of lamotrigine (LTG) monotherapy in newly diagnosed children with epilepsy. Methods : We prospectively enrolled 148 children who had undergone LTG monotherapy at our institution between September 2002 and June 2009. Twenty-nine patients were excluded: 19 d...

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Main Authors: Ji Hye Han, Jung Eun Oh, Sun Jun Kim
Format: Article
Language:English
Published: Korean Pediatric Society 2010-04-01
Series:Korean Journal of Pediatrics
Online Access:http://www.kjp.or.kr/upload/2010530416-20100605184705.PDF
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spelling doaj-49c57f0f1e97431b921eff1ef0318e0d2020-11-24T22:40:42ZengKorean Pediatric SocietyKorean Journal of Pediatrics1738-10612092-72582010-04-0153456557010.3345/kjp.2010.53.4.565Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsyJi Hye HanJung Eun OhSun Jun KimPurpose : To verify the efficacy and safety of lamotrigine (LTG) monotherapy in newly diagnosed children with epilepsy. Methods : We prospectively enrolled 148 children who had undergone LTG monotherapy at our institution between September 2002 and June 2009. Twenty-nine patients were excluded: 19 due to incomplete data and 10 were lost to follow up. The data of the remaining 119 patients was analyzed. Results : We enrolled 119 pediatric epilepsy patients (aged 2.8-19.3 years&#59; 66 males and 53 females) in this study. Out of 119 patients, 29 (25.2%) had generalized epilepsy and 90 (74.8%) had partial epilepsy. The responses of seizure reduction were as follows: Seizure freedom (no seizure attack for at least 6 months) in 87/111 (78.4%, n=111) patients&#59; partial response (reduced seizure frequency compared to baseline) in 13 (11.7%) patients&#59; and persistent seizure in 11 (9.9%) patients. The seizure freedom rate was in 81.6% in patients with partial seizure (75.9% for complex partial seizure and 90.9% for benign rolandic epilepsy) and 44.8% in patients with generalized epilepsy (30.0% for absence seizure, 35.7% for juvenile myoclonic epilepsy patients, and 100.0% for idiopathic generalized epilepsy patients). Adverse reactions were reported in 17 (14.3%) patients, and 8 patients (6.7%) discontinued LTG because of rash and tic. No patient experienced severe adverse reaction such as Stevens-Johnson syndrome. Conclusion : LTG showed excellent therapeutic response and had few significant adverse effects. Our findings report may contribute in promoting the use of LTG monotherapy in epileptic children.http://www.kjp.or.kr/upload/2010530416-20100605184705.PDF
collection DOAJ
language English
format Article
sources DOAJ
author Ji Hye Han
Jung Eun Oh
Sun Jun Kim
spellingShingle Ji Hye Han
Jung Eun Oh
Sun Jun Kim
Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy
Korean Journal of Pediatrics
author_facet Ji Hye Han
Jung Eun Oh
Sun Jun Kim
author_sort Ji Hye Han
title Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy
title_short Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy
title_full Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy
title_fullStr Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy
title_full_unstemmed Clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy
title_sort clinical efficacy and safety of lamotrigine monotherapy in newly diagnosed pediatric patients with epilepsy
publisher Korean Pediatric Society
series Korean Journal of Pediatrics
issn 1738-1061
2092-7258
publishDate 2010-04-01
description Purpose : To verify the efficacy and safety of lamotrigine (LTG) monotherapy in newly diagnosed children with epilepsy. Methods : We prospectively enrolled 148 children who had undergone LTG monotherapy at our institution between September 2002 and June 2009. Twenty-nine patients were excluded: 19 due to incomplete data and 10 were lost to follow up. The data of the remaining 119 patients was analyzed. Results : We enrolled 119 pediatric epilepsy patients (aged 2.8-19.3 years&#59; 66 males and 53 females) in this study. Out of 119 patients, 29 (25.2%) had generalized epilepsy and 90 (74.8%) had partial epilepsy. The responses of seizure reduction were as follows: Seizure freedom (no seizure attack for at least 6 months) in 87/111 (78.4%, n=111) patients&#59; partial response (reduced seizure frequency compared to baseline) in 13 (11.7%) patients&#59; and persistent seizure in 11 (9.9%) patients. The seizure freedom rate was in 81.6% in patients with partial seizure (75.9% for complex partial seizure and 90.9% for benign rolandic epilepsy) and 44.8% in patients with generalized epilepsy (30.0% for absence seizure, 35.7% for juvenile myoclonic epilepsy patients, and 100.0% for idiopathic generalized epilepsy patients). Adverse reactions were reported in 17 (14.3%) patients, and 8 patients (6.7%) discontinued LTG because of rash and tic. No patient experienced severe adverse reaction such as Stevens-Johnson syndrome. Conclusion : LTG showed excellent therapeutic response and had few significant adverse effects. Our findings report may contribute in promoting the use of LTG monotherapy in epileptic children.
url http://www.kjp.or.kr/upload/2010530416-20100605184705.PDF
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