Rehman Zia Ur
Pediatric Neurology, The Children's Hospital and Institute of Child Health, Multan, PAK.
Cureus. 2022 Apr 5;14(4):e23854. doi: 10.7759/cureus.23854. eCollection 2022 Apr.
Background Epilepsy is described as an enduring disposition toward recurrent unprovoked seizures and by the neurobiological, cognitive, psychological, and social consequences of this condition. This study aimed to find the clinical characteristics and etiology of epilepsy in children aged below two years. Methodology This cross-sectional study was conducted at the department of pediatric neurology, the Children's Hospital and Institute of Child Health, Multan, Pakistan, from February 2021 to July 2021. During the study period, a total of 226 children of both genders, aged below two years, presenting with epilepsy and who underwent electroencephalography (EEG) were included. Socio-demographic and clinical data along with clinical features and radiological/imaging findings were noted. Results In a total of 226 children, 121 (53.5%) were male and 105 (46.5%) female. Overall, the mean age was calculated to be 14.6±5.2 months while 107 (47.3%) children were aged between 13 to 24 months. Residential status was found to be rural in 142 (62.8%) children. Generalized seizures (both primary and secondary) were reported in 205 (90.7%) children while the remaining 21 (9.3%) children had focal seizures. The most common etiology of epilepsy was noted to be structural/metabolic in 122 (54.0%) children. Abnormal EEG findings were observed among 150 (66.4%) children. Developmental delay (p=0.0016), hypotonia (p<0.0001), microcephaly or macrocephaly (p<0.0001), abnormal brain CT or MRI (p<0.0001), and abnormal EEG findings (p=0.0161) were found to have a significant association with etiology of epilepsy. Conclusion Generalized seizures like tonic-clonic and clonic types were the most common findings among children below two years of age with epilepsy. Structural abnormalities were the most common etiology in children with epilepsy. Age between one to two years was the commonest age of onset of seizures among young children.
癫痫被描述为一种对反复发作的无诱因癫痫发作的持久倾向,以及这种状况所带来的神经生物学、认知、心理和社会后果。本研究旨在找出2岁以下儿童癫痫的临床特征和病因。方法:这项横断面研究于2021年2月至2021年7月在巴基斯坦木尔坦儿童医院及儿童健康研究所的儿科神经科进行。在研究期间,共纳入了226名2岁以下患有癫痫且接受了脑电图(EEG)检查的男女儿童。记录了社会人口学和临床数据以及临床特征和放射学/影像学检查结果。结果:在总共226名儿童中,121名(53.5%)为男性,105名(46.5%)为女性。总体而言,平均年龄计算为14.6±5.2个月,其中107名(47.3%)儿童年龄在13至24个月之间。发现142名(62.8%)儿童的居住状况为农村。205名(90.7%)儿童报告有全身性发作(包括原发性和继发性),其余21名(9.3%)儿童有局灶性发作。癫痫最常见的病因是122名(54.0%)儿童存在结构/代谢异常。150名(66.4%)儿童观察到脑电图异常结果。发现发育迟缓(p = 0.0016)、肌张力低下(p < 0.0001)、小头畸形或大头畸形(p < 0.0001)、脑部CT或MRI异常(p < 0.0001)以及脑电图异常结果(p = 0.0161)与癫痫病因有显著关联。结论:强直阵挛和阵挛型等全身性发作是两岁以下癫痫儿童中最常见的表现。结构异常是癫痫儿童中最常见的病因。1至2岁是幼儿癫痫发作最常见的发病年龄。