The Clinical Profile and Outcome of Children with Dengue Encephalitis at the Philippine Children’s Medical Center: A Retrospective Study From January 2011-June 2017

Kristine Alvarado-Dela Cruz, M. Pascual, Maria Eva Luna- Dizon
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Abstract

Background: Dengue, a mosquito-borne flavivirus, is hyperendemic in the Philippines. One of its rare complication is dengue encephalitis, characterized by altered sensorium, elevated liver enzymes, and high dengue-specific antibody titers. Previously known as non-neurotropic, dengue presents with an increasing incidence of neurologic manifestations. Objective: To describe the clinico-demographic profile and outcome of laboratory-confirmed dengue encephalitis patients. Methods: This is a retrospective study that used purposive sampling to describe laboratory-confirmed dengue encephalitis cases aged 0-18 years. The clinico-demographic profiles and outcomes were collected using chart review, and variables were analyzed using descriptive statistics. Results: 14 laboratory-confirmed cases were reviewed. Most (57%) were males aged 3 days-15 years. Fever lasted 3-11 days. Following nonspecific signs and symptoms, neurological manifestations developed within 1-5 days, the most common being seizures (71%). Majority (57%) had anemia. All, except one, exhibited leukopenia and thrombocytopenia. Elevated liver enzymes, bleeding parameter derangements, electrolyte, and glucose imbalances were noted. All were seropositive for dengue IgM, and 5 dengue IgM in the CSF. Most common EEG findings showed generalized slowing. Neuroimaging reports were normal in some or showed cerebral edema in the others. Half of the patients recovered fully, 3 showing partial recovery from neurologic changes, and 3 others had neurologic sequelae. One infant expired. Conclusions and Recommendations: Dengue encephalitis should be considered in patients living in an endemic country, presenting with fever with neurologic changes or elevated liver enzymes, with a risk for developing neurologic sequelae or death.
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菲律宾儿童医疗中心患登革脑炎儿童的临床概况和预后:2011年1月至2017年6月的回顾性研究
背景:登革热是一种蚊媒黄病毒,是菲律宾的高地方病。其罕见的并发症之一是登革脑炎,其特征是感觉改变,肝酶升高和高登革热特异性抗体滴度。登革热以前被称为非嗜神经性疾病,现在呈现出越来越多的神经系统表现。目的:描述实验室确诊的登革脑炎患者的临床人口学特征和转归。方法:这是一项回顾性研究,采用有目的的抽样来描述0-18岁实验室确诊的登革热脑炎病例。采用图表回顾法收集临床人口学概况和结果,并采用描述性统计分析变量。结果:共审查实验室确诊病例14例。大多数(57%)是3天至15岁的男性。发热持续3 ~ 11天。在非特异性体征和症状之后,1-5天内出现神经系统症状,最常见的是癫痫发作(71%)。大多数(57%)患有贫血。除一人外,其余均表现为白细胞减少和血小板减少。肝酶升高,出血参数紊乱,电解质和葡萄糖失衡。所有患者血清IgM阳性,脑脊液中有5例IgM阳性。最常见的脑电图表现为全身性迟缓。一些患者的神经影像学报告正常,另一些显示脑水肿。半数患者完全康复,3例神经系统病变部分恢复,3例有神经系统后遗症。一名婴儿死亡。结论和建议:生活在登革热流行国家的患者应考虑登革热脑炎,表现为发热、神经系统改变或肝酶升高,有发生神经系统后遗症或死亡的风险。
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