基利菲地区医院惊厥性癫痫持续状态患儿的长期生存率和转归。

Epilepsy research and treatment Pub Date : 2014-01-01 Epub Date: 2014-01-30 DOI:10.1155/2014/643747
Agnes Prins, Eddie Chengo, Victor Mung'ala Odera, Manish Sadarangani, Claire Seaton, Penny Holding, Greg Fegan, Charles R Newton
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引用次数: 11

摘要

目标。惊厥性癫痫持续状态(CSE)在非洲的发病率很高,但其长期预后尚不清楚。我们检查了在肯尼亚一家医院接受CSE治疗的儿童出院后3至4年的神经认知结果和生存率。方法。确定了这组儿童神经功能缺陷的频率和性质,并与对照组进行了比较。如果孩子们还活着,就用十题问卷对他们进行神经发育障碍的筛查,那些筛查呈阳性的孩子被邀请进行进一步的评估,以确定他们损伤的模式和程度。对死者进行了口头解剖,以确定死因。结果。在随访的119例病例中,出院后死亡9例(8%),其中大多数在致命疾病期间发生癫痫发作。110名幸存者(中位年龄5岁)在筛查时的神经损伤明显多于282名对照组(34/110(30.9%)对11/282 (3.9%),OR = 11.0, 95% CI 5.3-22.8)。15%的患者患有活动性癫痫。结论。这项研究表明,非洲儿童的CSE负担相当沉重。需要探索社区可以接受的管理全面性CSE儿童的战略,以改善长期结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Long-term survival and outcome in children admitted to kilifi district hospital with convulsive status epilepticus.

Long-term survival and outcome in children admitted to kilifi district hospital with convulsive status epilepticus.

Objectives. The incidence of convulsive status epilepticus (CSE) is high in Africa but the long-term outcome is unknown. We examined the neurocognitive outcome and survival of children treated for CSE in a Kenyan hospital 3 to 4 years after discharge. Methods. The frequency and nature of neurological deficits among this group of children were determined and compared to a control group. The children were screened with the Ten Questions Questionnaire for neurodevelopmental impairment if alive and those that screened positive were invited for further assessment to determine the pattern and extent of their impairment. A verbal autopsy was performed to determine the cause of death in those that died. Results. In the 119 cases followed-up, 9 (8%) died after discharge, with the majority having seizures during their fatal illness. The 110 survivors (median age 5 years) had significantly more neurological impairments on the screening compared to 282 controls (34/110 (30.9%) versus 11/282 (3.9%), OR = 11.0, 95% CI 5.3-22.8). Fifteen percent of the cases had active epilepsy. Conclusions. This study demonstrates the considerable burden of CSE in African children. Strategies to manage children with CSE that are acceptable to the community need to be explored to improve the longer-term outcome.

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