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[甲基强的松龙治疗儿童睡眠期癫痫性电持续状态的疗效]

[Efficacy of methylprednisolone therapy for electrical status epilepticus during sleep in children].

作者信息

Chen Jing, Yang Zhixian, Liu Xiaoyan, Ji Taoyun, Fu Na, Wu Ye, Xiong Hui, Wang Shuang, Chang Xingzhi, Zhang Yuehua, Bao Xinhua, Jiang Yuwu, Qin Jiong

机构信息

The first author is now in Department of Neurology, Nanjing Children's Hospital Affiliated to Nanjing Medical University, Nanjing 210008, China.

The first author is now in Department of Neurology, Nanjing Children's Hospital Affiliated to Nanjing Medical University, Nanjing 210008, China. Email:

出版信息

Zhonghua Er Ke Za Zhi. 2014 Sep;52(9):678-82.

Abstract

OBJECTIVE

To evaluate the therapeutic effect of methylprednisolone for electrical status epilepticus during sleep (ESES) in children.

METHOD

The clinical and EEG data of 82 epilepsy patients with ESES, which included benign childhood epilepsy with centro temporal spikes (BECT) variants, epilepsy with continuous spikes and waves during slow sleep (CSWS) , Landau-Kleffner syndrome (LKS) collected from department of pediatrics, Peking University First Hospital were analyzed from July 2007 to September 2012. During ESES period, all patients received methylprednisolone treatment for three courses, which included methylprednisolone intravenous infusion for three days, followed by oral prednisone for four days every time. After three courses, prednisone [1-2 mg/(kg × d)] were taken by all patients for 6 months. The ESES phenomenon and seizures were observed before and after treatment. The efficacy of corticosteroid on ESES suppression, seizure control of three epilepsy syndrome were analyzed.

RESULT

Thirty-nine cases were male and 43 cases were female. The epilepsy syndromes included 49 patients diagnosed as benign childhood epilepsy with centrotemporal spike (BECT) variants, 27 patients diagnosed as epilepsy with continuous spikes and waves during slow sleep (CSWS), and 6 patients diagnosed as LKS. Age of onset ranged from 1 year and 4 months to 11 years. The age of ESES newly monitored was from 2 years to 10 years and 8 months. The total effective rate of corticosteroid was 83% (68/82) for ESES, BECT variants was 82% (40/49), CSWS was 81% (22/27), LKS was 100% (6/6). There was no statistically significant difference in effective rates between the front two (χ² = 0.09, P > 0.05). The seizures were improved in the first month after methylprednisolone treatment in 3 epilepsy syndromes. The recurrence rate of BECT variants was 47% (23/49) , CSWS was 59% (16/27) , LKS was 50% (3/6) after 1 year follow up. There was no association between disease parameters, including age at seizure onset, duration of ESES and the treatment effect of ESES examined by Kruskal-Wallis method (χ² = 3.585, 0.932, P > 0.05).

CONCLUSION

Methylprednisolone was effective for improving ESES and seizures in 3 epilepsy syndromes combined with ESES. There was no significant correlation between age at seizure onset, duration of ESES and treatment effect of ESES.

摘要

目的

评估甲泼尼龙治疗儿童睡眠中癫痫性电持续状态(ESES)的疗效。

方法

分析2007年7月至2012年9月北京大学第一医院儿科收集的82例患有ESES的癫痫患者的临床及脑电图数据,这些患者包括伴中央颞区棘波的儿童良性癫痫(BECT)变异型、慢波睡眠期持续棘慢波癫痫(CSWS)、Landau-Kleffner综合征(LKS)。在ESES发作期,所有患者接受甲泼尼龙治疗3个疗程,包括甲泼尼龙静脉输注3天,随后每次口服泼尼松4天。3个疗程后,所有患者服用泼尼松[1 - 2 mg/(kg×d)] 6个月。观察治疗前后的ESES现象及癫痫发作情况。分析皮质类固醇对ESES抑制、3种癫痫综合征癫痫控制的疗效。

结果

男性39例,女性43例。癫痫综合征包括49例诊断为伴中央颞区棘波的儿童良性癫痫(BECT)变异型,27例诊断为慢波睡眠期持续棘慢波癫痫(CSWS),6例诊断为Landau-Kleffner综合征(LKS)。发病年龄为1岁4个月至11岁。新监测到ESES的年龄为2岁至10岁8个月。皮质类固醇对ESES的总有效率为83%(68/82),对BECT变异型为82%(40/49),对CSWS为81%(22/27),对LKS为100%(6/6)。前两者有效率差异无统计学意义(χ² = 0.09,P > 0.05)。3种癫痫综合征在甲泼尼龙治疗后的第1个月癫痫发作均有改善。随访1年后,BECT变异型的复发率为47%(23/49),CSWS为59%(16/27),LKS为50%(3/6)。采用Kruskal-Wallis法检验,包括癫痫发作起始年龄、ESES持续时间等疾病参数与ESES的治疗效果之间无关联(χ² = 3.585,0.932,P > 0.05)。

结论

甲泼尼龙对改善合并ESES的3种癫痫综合征的ESES及癫痫发作有效。癫痫发作起始年龄、ESES持续时间与ESES的治疗效果之间无显著相关性。

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