Electroclinical characteristics and therapies of tonic spasms.

IF 1.2 Q4 CLINICAL NEUROLOGY
Xi Peng, Yangmei Chen, Zezhi Wang, Xinbo Zhang, Bi Wang, Lang Jin, Xiaoli Wang, Na Yuan, Xiaojing Hu, Xiaomu Wang, Yonghong Liu
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Abstract

Backgroud: Epileptic spasms followed by a tonic component have been frequently observed in patients with late-onset spasms (LOS). However, there is a lack of comprehensive analysis and summary of clinical data related to tonic spasms (TS), including seizures, video-electroencephalogram (V-EEG), synchronous electromyography (EMG) and follow-up data.

Methods: To investigate the characteristics of TS, we prospectively collected the clinical data, including 24-h V-EEG and synchronous EMG data of 32 enrolled patients who suffered from epileptic spasms followed by a TS onset at least once during the 24-h V-EEG in the epilepsy center of Xijing Hospital between June 2015 and July 2020. The patients were prescribed anti-seizure medications (ASMs) and followed up for 2-7 years.

Results: The average age of epilepsy onset was 48.06 ± 16.07 months (range: 25 to 88 months). Among the enrolled patients, 22 patients presented with mild intellectual deficits. During the 24-h video-EEG monitoring, an average of 6.94 TS events (range: 3 to 21) were recorded, and these TS seizures often occurred in clusters. In addition to TS, 26 patients experienced generalized tonic-clonic seizures (GTCS), atypical absence seizures, myoclonic seizure, and epileptic spasms. None of the 32 patients with TS displayed hypsarrhythmia during the 24-h video-EEG recording. A total of 28 patients showed normal EEG backgrounds. Interictal epileptic discharges, including slow waves (SW), spike/sharp slow waves (SSW), and spikes, often displayed multifocally. Notably, two patients achieved seizure freedom for more than 2 years through monotherapy with oxcarbazepine (OXC), which was associated with normalization of the EEG.

Conclusions: It is difficult to classify the patients with TS as any existing epileptic syndromes, which were distinct from West syndrome or Lennox-Gastaut syndrome. TS might be an underreported seizure type and further studies are needed to gain a more comprehensive understanding of the electro-clinical features and appropriate choice of ASMs for treating tonic spasms.

强直性痉挛的电临床特征及治疗。
背景:在迟发性痉挛(LOS)患者中经常观察到癫痫性痉挛伴强直性成分。然而,缺乏对强直性痉挛(TS)相关临床数据的全面分析和总结,包括癫痫发作、视频脑电图(V-EEG)、同步肌电图(EMG)和随访数据。方法:为探讨TS的特征,前瞻性收集2015年6月至2020年7月在西京医院癫痫中心就诊的32例24 h V-EEG期间至少发生一次TS发作的癫痫性痉挛患者的临床资料,包括24 h V-EEG和同步肌电图数据。给予抗癫痫药物治疗,随访2 ~ 7年。结果:癫痫发作的平均年龄为48.06±16.07个月(25 ~ 88个月)。在纳入的患者中,22例患者表现为轻度智力缺陷。在24 h视频脑电图监测期间,平均记录到6.94次TS事件(范围:3 ~ 21次),且这些TS发作多聚集性发生。除TS外,26例患者出现全身性强直-阵挛性发作(GTCS)、非典型失神发作、肌阵挛性发作和癫痫性痉挛。在24小时的视频脑电图记录中,32例TS患者均未出现心律失常。28例患者脑电图背景正常。癫痫发作间期放电,包括慢波(SW)、尖峰慢波(SSW)和尖峰,通常表现为多灶性。值得注意的是,两名患者通过奥卡西平(OXC)单药治疗获得了超过2年的癫痫发作自由,这与脑电图正常化有关。结论:很难将TS患者归类为现有的任何癫痫综合征,与West综合征或Lennox-Gastaut综合征不同。TS可能是一种被低估的癫痫类型,需要进一步的研究来获得更全面的了解电临床特征和治疗强直性痉挛的合适选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Epileptologica
Acta Epileptologica Medicine-Neurology (clinical)
CiteScore
2.00
自引率
0.00%
发文量
38
审稿时长
20 weeks
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