印度一家公立医院小儿难治性癫痫的临床病因简介。

Journal of epilepsy research Pub Date : 2019-06-30 eCollection Date: 2019-06-01 DOI:10.14581/jer.19004
K C Sadik, Devendra Mishra, Monica Juneja, Urmila Jhamb
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引用次数: 8

摘要

背景和目的:难治性癫痫持续状态(RSE)很少在印度儿童中进行研究。这项研究是为了研究公立医院1个月至12岁痉挛性RSE儿童的临床病因特征和短期结果。方法:该研究于2016年4月1日至2017年2月28日在获得机构伦理委员会批准后进行。所有因痉挛性癫痫持续状态(SE)或在住院期间出现SE的儿童(1个月至12岁)均被纳入三级公立医院儿科。根据标准方案对所有患者进行调查和管理。根据格拉斯哥结果量表评估结果。将进展为RSE的儿童的详细信息与未发展为RSE儿童的详细情况进行比较。结果:50名患有CSE的儿童(28名男性)被纳入研究,其中20名(40%)进展为RSE。中枢神经系统(CNS)感染是最常见的病因(SE为53%,RSE为55%,p>0.05)。不遵守抗癫痫药物是第二常见的病因。总死亡率为38%,尽管RSE的死亡率(50%)高于SE的死亡率(30%),但这一差异在统计学上并不显著(p=0.15)。与SE儿童相比,RSE儿童不良结局的几率高出6倍(比值比6.0;95%置信区间1.6-22.3;p=0.005)。结论:在处理中枢神经系统感染时,儿科医生需要意识到患RSE的高风险。此外,在重症监护环境中,应考虑并及时管理RSE的可能性,以降低这种严重神经系统疾病的死亡率和发病率。
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Clinico-Etiological Profile of Pediatric Refractory Status Epilepticus at a Public Hospital in India.

Background and purpose: Refractory status epilepticus (RSE) has been infrequently studied in Indian children. This research was conducted to study the clinico-etiological profiles and short-term outcomes of children aged 1 month to 12 years with convulsive RSE, at a public hospital.

Methods: The study was conducted between 1st April 2016 and 28th February 2017 after receiving clearance from an Institutional Ethics Committee. All children (aged 1 month to 12 years) who presented to the pediatrics department of a tertiary-care public hospital with convulsive status epilepticus (SE), or who developed SE during their hospital stay, were enrolled. All patients were investigated and managed according to a standard protocol. Outcomes were assessed based on the Glasgow Outcome Scale. Details of children who progressed to RSE were compared to those without RSE.

Results: Fifty children (28 males) with CSE were enrolled, of which 20 (40%) progressed to RSE. Central nervous system (CNS) infection was the most common etiology (53% in SE and 55% in RSE, p > 0.05). Non-compliance with anti-epileptic drugs was the second most common etiology. The overall mortality rate was 38%, and although the odds of death in RSE (50%) were higher than in SE (30%), this difference was not statistically significant (p = 0.15). The odds of having a poor outcome was six times higher in children with RSE as compared to those with SE (odds ratio, 6.0; 95% confidence interval, 1.6-22.3; p = 0.005).

Conclusions: When managing CNS infections, pediatricians need to be aware of the high risk of developing RSE. In addition, the possibility of RSE should be considered and managed promptly in an intensive-care setting, to reduce the mortality and morbidity of this severe neurological condition.

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