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[围产期发作继发先天性偏瘫患儿的癫痫]

[Epilepsy in children with congenital hemiparesis secondary to perinatal ictus].

作者信息

Revilla Orías M Daniela, Alonso Xenia, Campistol Jaume, Macaya Alfons, Escofet Conchita, Fons Carmen

机构信息

Servicio de Neuropediatría Hospital Sant Joan de Déu, Barcelona, España. E-mail:

Servicio de Neuropediatría Hospital Sant Joan de Déu, Barcelona, España.

出版信息

Medicina (B Aires). 2019;79 Suppl 3:6-9.

PMID:31603835
Abstract

The objective was to describe the frequency, mode of presentation and characteristics of epilepsy in children with congenital hemiparesis (CH). It is a etrospective, descriptive and multicenter study, based on the collection of data from the clinical records of patients from 0 to 19 years with CH secondary to perinatal infarction in different centers of the community of Catalonia. A total of 310 children were included (55% males and 45% females), from a total of 13 centers in Catalonia. Average age of onset of the crises was 2 ± 1 year. Epilepsy was present in 29.5% (n = 76), among which the most frequent vascular subtype was arterial presumed perinatal ischemic stroke (51.3%), followed by neonatal arterial ischemic stroke (18.4%), periventricular venous infarction (15.8%), neonatal hemorrhagic stroke (10.5%) and neonatal cerebral sinovenous thrombosis (3.9%). Semiology of the most frequent seizures was motor focal in 82%, followed by focal motor with secondary bilateralization in 23%, focal discognitive in 13.5%, generalized by 2% and spasms in 6.5%. The 67.3% were controlled with monotherapy and the drugs used were valproate, levetiracetam or carbamazepine. The antecedent of electrical status during sleep was identified in 3 patients, all associated with extensive lesions that included the thalamus. Of the total number of children with epilepsy, 35% began with neonatal seizu res in the first 3 days of life. The 30% of children with perinatal stroke and CH present a risk of epilepsy during childhood. Children with ischemic strock have the highest risk, so they will require a follow-up aimed at detecting prematurely the epilepsy and start a treatment.

摘要

目的是描述先天性偏瘫(CH)患儿癫痫的发生率、表现方式及特征。这是一项回顾性、描述性多中心研究,基于加泰罗尼亚社区不同中心0至19岁因围产期梗死继发CH的患者临床记录收集数据。共纳入310名儿童(55%为男性,45%为女性),来自加泰罗尼亚的13个中心。发作的平均起始年龄为2±1岁。癫痫的发生率为29.5%(n = 76),其中最常见的血管亚型是推测的围产期动脉缺血性卒中(51.3%),其次是新生儿动脉缺血性卒中(18.4%)、脑室周围静脉梗死(15.8%)、新生儿出血性卒中(10.5%)和新生儿脑静脉窦血栓形成(3.9%)。最常见发作的症状学表现为82%为局灶性运动发作,其次是23%的局灶性运动发作继发双侧化,13.5%为局灶性认知障碍发作,2%为全身性发作,6.5%为痉挛发作。67.3%的患者通过单一疗法得到控制,使用的药物为丙戊酸盐、左乙拉西坦或卡马西平。3例患者被确定有睡眠期电持续状态,均与包括丘脑在内的广泛病变相关。在所有癫痫患儿中,35%在出生后的头3天开始出现新生儿惊厥。30%的围产期卒中合并CH患儿在儿童期有癫痫发作风险。缺血性卒中患儿的风险最高,因此需要进行随访,以便早期发现癫痫并开始治疗。

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Medicina (B Aires). 2019;79 Suppl 3:6-9.
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