Gowda Vykuntaraju K, Kulhalli Preeti, Benakappa Naveen, Benakappa Asha
Department of Pediatric Neurology, Indira Gandhi Institute of Child Health, Bengaluru, Karnataka, India.
Department of Pediatrics, Indira Gandhi Institute of Child Health, Bengaluru, Karnataka, India.
J Pediatr Neurosci. 2019 Apr-Jun;14(2):82-85. doi: 10.4103/jpn.JPN_61_18.
Seizure is the most common neurological illness in pediatric population and its risk is highest in the first year of life. Studies regarding etiology of afebrile seizures worldwide and in India are limited; hence, the current study was undertaken.
The objective of this work was to study the etiology of afebrile seizures in infants aged 1 month to 1 year.
A retrospective study of afebrile infantile seizure was conducted at pediatric neurology outpatient department between January 2015 and September 2017. All children with first episode of afebrile seizures were included. Biochemical and hematological investigations, imaging, and electroencephalogram were performed whenever necessary. Simple descriptive statistics were used to analyze the data in the form of frequencies with percentages and median as applicable.
One hundred twenty-one children with a mean age of 8.1 months were analyzed. Of these children, 58% were males. Positive family history was found in 1.65% children, developmental delay in 70%, and dysmorphism in 8%. Presenting seizure type were generalized (74%), focal (21%), and unknown (6%) onset. Etiology was deducible in 92% cases. Structural etiology was the most common (66%), followed by metabolic (12%), infections (7%), and others (6%). In structural pathology, common causes were perinatal insult (38%) and cerebral malformations (18%). Imaging was done in 98 cases and yield was 83% (85 cases).
Etiology was deducible in 92% of children. Seizures due to structural etiology, secondary to perinatal insult followed by metabolic and infections, are important causes. Imaging aids are important in etiological diagnosis. Etiological evaluation should be considered in children following first episode of afebrile seizures, especially in developing countries like India.
癫痫发作是儿科人群中最常见的神经系统疾病,其风险在生命的第一年最高。全球和印度关于无热惊厥病因的研究有限;因此,开展了本研究。
本研究的目的是探讨1个月至1岁婴儿无热惊厥的病因。
2015年1月至2017年9月在儿科神经科门诊对无热婴儿惊厥进行了回顾性研究。纳入所有首次发作无热惊厥的儿童。必要时进行生化和血液学检查、影像学检查和脑电图检查。采用简单描述性统计方法,以频率、百分比和中位数(如适用)的形式分析数据。
分析了121例平均年龄为8.1个月的儿童。其中,58%为男性。1.65%的儿童有阳性家族史,70%有发育迟缓,8%有畸形。发作类型为全身性(74%)、局灶性(21%)和不明(6%)发作。92%的病例病因可推断。结构性病因最为常见(66%),其次是代谢性(12%)、感染性(7%)和其他(6%)。在结构性病变中,常见原因是围产期损伤(38%)和脑畸形(18%)。98例进行了影像学检查,阳性率为83%(85例)。
92%的儿童病因可推断。结构性病因导致的癫痫发作,继发于围产期损伤,其次是代谢性和感染性病因,是重要原因。影像学辅助检查在病因诊断中很重要。对于首次发作无热惊厥的儿童,尤其是在印度这样的发展中国家,应考虑进行病因评估。