Patil Sandeep B, Roy Arun Grace, Vinayan Kollencheri Puthenveettil
Division of Pediatric Neurology, Department of Neurology, Amrita Institute of Medical Sciences, Kochi, Kerala, India.
Ann Indian Acad Neurol. 2016 Apr-Jun;19(2):188-94. doi: 10.4103/0972-2327.173305.
To describe the clinical features and outcome of febrile infection-related epilepsy syndrome (FIRES), a catastrophic epileptic encephalopathy, in a cohort of South Indian children.
We performed a retrospective chart review of a cohort of children with previously normal development who presented with status epilepticus or encephalopathy with recurrent seizures following a nonspecific febrile illness during the period between January 2007 and January 2012. They were divided into two groups super refractory status epilepticus (SRSE) and refractory status epilepticus (RSE) depending on the duration and severity of the seizures.
Fifteen children who met the inclusion criteria were included for the final analysis. The age of the children at presentation ranged 3-15 years (median 6.3 years). All the children presented with prolonged or recurrent seizures occurring 1-12 days (median 4 days) after the onset of fever. Eight children had SRSE while seven children had refractory seizures with encephalopathy. Cerebrospinal fluid (CSF) analysis was done in all the children in the acute phase, and the cell count ranged 0-12 cells/μL (median 2 cells/μL) with normal sugar and protein levels. Initial neuroimaging done in all children (MRI in 10 and CT in 5), and it was normal in 13 children. Treatment modalities included multiple antiepileptic drugs (AEDs) (4-9 drugs) (median 5 drugs). Midazolam (MDZ) infusion was administered in seven patients. Eight patients required barbiturate coma to suppress the seizure activity. The duration of the barbiturate coma ranged 2-90 days (median 3 days). Steroids were used in 14 children and intravenous immunoglobulin (2 g/kg) in 7 children. Three children died in the acute phase. All children were maintained on multiple AEDs till the last follow-up, the number of AEDs ranged 1-6 (median 5 AEDs). The patients with super refractory status in the acute phase were found to be more severely disabled at the follow-up; the median score of these patients on the Glasgow Outcome Scale (GOS) was 2 compared to 5 in the RSE group.
This study reports one of the largest single center cohorts from India, with an adverse long-term developmental and seizure outcome. The duration and severity of seizures in the acute period correlated directly with the short-term and long-term clinical outcomes. There is an urgent need for developing new effective therapeutic strategies to treat this acute catastrophic epileptic syndrome.
描述热性感染相关癫痫综合征(FIRES)这一灾难性癫痫性脑病在一组南印度儿童中的临床特征及预后。
我们对2007年1月至2012年1月期间一群先前发育正常、在非特异性发热性疾病后出现癫痫持续状态或伴有反复癫痫发作的脑病儿童进行了回顾性病历审查。根据癫痫发作的持续时间和严重程度,将他们分为两组:超级难治性癫痫持续状态(SRSE)和难治性癫痫持续状态(RSE)。
15名符合纳入标准的儿童纳入最终分析。患儿就诊时年龄为3至15岁(中位数6.3岁)。所有儿童在发热开始后1至12天(中位数4天)出现持续性或反复性癫痫发作。8名儿童患有SRSE,7名儿童患有伴有脑病的难治性癫痫发作。急性期对所有儿童进行了脑脊液(CSF)分析,细胞计数范围为0至12个/μL(中位数2个/μL),糖和蛋白水平正常。对所有儿童均进行了初始神经影像学检查(10例行MRI,5例行CT),13名儿童结果正常。治疗方式包括多种抗癫痫药物(AEDs)(4至9种药物)(中位数5种药物)。7例患者给予咪达唑仑(MDZ)静脉输注。8例患者需要巴比妥类药物昏迷以抑制癫痫活动。巴比妥类药物昏迷持续时间为2至90天(中位数3天)。14名儿童使用了类固醇,7名儿童使用了静脉注射免疫球蛋白(2 g/kg)。3名儿童在急性期死亡。所有儿童在最后一次随访前均维持使用多种AEDs,AEDs数量为1至6种(中位数5种AEDs)。急性期处于超级难治状态的患者在随访时残疾程度更严重;这些患者在格拉斯哥预后量表(GOS)上的中位数评分为2分,而RSE组为5分。
本研究报告了来自印度的最大单中心队列之一,具有不良的长期发育和癫痫预后。急性期癫痫发作的持续时间和严重程度与短期和长期临床结果直接相关。迫切需要开发新的有效治疗策略来治疗这种急性灾难性癫痫综合征。