Visudtibhan Anannit, Limhirun Janjira, Chiemchanya Surang, Visudhiphan Pongsakdi
Division of Neurology, Department of Pediatrics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
J Med Assoc Thai. 2006 Jun;89(6):803-8.
Convulsive Status Epilepticus (SE) is an emergency neurological condition with high morbidity and mortality. The outcome of this condition in children depends on the etiology and the duration of convulsion. There is no report of this condition in Thai children.
To study the etiology, clinical course and outcome in children with convulsive SE in a referral hospital in Thailand.
The medical records of infants and children aged between one month and 15 years with the diagnosis of SE who were admitted to the Department of Pediatrics, Ramathibodi Hospital, Bangkok from January 1st, 1981 to December 31st, 2000 were retrospectively reviewed. The demographic data, types of seizure, duration of seizure, underlying diseases, precipitating factors, laboratory results, treatment, clinical course and outcomes were collected for descriptive analysis.
Thirty-two patients (15 boys, 17 girls) whose ages ranged from 2 months to 14.4 years (mean 6.5 years) were included Twenty-four patients had underlying epilepsy. Twelve patients had prior diagnosis of symptomatic and idiopathic/cryptogenic epilepsy. Seven patients had acute insults to the central nervous system leading to SE. One patient with acute lymphoblastic leukemia presented with SE without association to either the underlying disease or the treatment. Fever with or without specific infection was the most common precipitating factor observed in these patients. The mean duration of SE was 64.4 minutes. The mean duration from initiation of treatment to the cessation of seizure was 41.4 minutes. Twelve patients were lost to follow up. Of the two patients who died, one had severe infection and the other had renal failure. Twelve patients had severe neurological deficits and six had mild neurological deficits. Among the thirteen patients who had > or = 1 hour of convulsion, eleven had severe neurological deficits or died.
Infantile SE occurred more frequently in children with pre-existing epilepsy or neurological disorder Acute febrile illness and infection were the most common precipitating causes in the present study. Early recognition and treatment of fever and infection in conjunction with prompt and appropriate termination of seizure in epileptic children may prevent the occurrence of SE and its morbidity.
惊厥性癫痫持续状态(SE)是一种具有高发病率和死亡率的紧急神经系统疾病。儿童这种疾病的预后取决于病因和惊厥持续时间。泰国儿童中尚无关于这种疾病的报告。
研究泰国一家转诊医院中惊厥性SE患儿的病因、临床病程及预后。
回顾性分析1981年1月1日至2000年12月31日期间入住曼谷拉玛蒂博迪医院儿科、诊断为SE的1个月至15岁婴幼儿及儿童的病历。收集人口统计学数据、癫痫发作类型、发作持续时间、基础疾病、诱发因素、实验室检查结果、治疗方法、临床病程及预后,进行描述性分析。
纳入32例患者(15例男孩,17例女孩),年龄范围为2个月至14.4岁(平均6.5岁)。24例患者有基础癫痫。12例患者先前被诊断为症状性及特发性/隐源性癫痫。7例患者因中枢神经系统急性损伤导致SE。1例急性淋巴细胞白血病患者出现SE,与基础疾病及治疗均无关。有或无特定感染的发热是这些患者中最常见的诱发因素。SE的平均持续时间为64.4分钟。从开始治疗到惊厥停止的平均持续时间为41.4分钟。12例患者失访。在2例死亡患者中,1例有严重感染,另1例有肾衰竭。12例患者有严重神经功能缺损,6例有轻度神经功能缺损。在13例惊厥持续时间≥1小时的患者中,11例有严重神经功能缺损或死亡。
婴儿SE在已有癫痫或神经系统疾病的儿童中更常见。急性发热性疾病和感染是本研究中最常见的诱发原因。对癫痫患儿早期识别和治疗发热及感染,同时迅速、适当地终止惊厥,可能预防SE的发生及其发病率。