延长癫痫发作和癫痫持续状态的预测因素:一项单中心研究

M. Ayanoğlu, E. Ongun
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引用次数: 1

摘要

目的:分析儿童重症监护病房(PICU)住院患者长时间癫痫发作和癫痫持续状态的临床特征,并对超难治性癫痫持续状态(SRSE)进行风险分析。方法:分析2015 - 2019年重症监护病房住院患者的人口学特征、潜在病因、治疗方式、脑电图和神经影像学结果。结果:71名儿童入组。引起长时间癫痫发作的常见病因为发热(45.1%)(其中中枢神经系统感染占16.9%,中枢神经系统以外感染占28.2%)、停药(40.9%)、中毒(12.7%)和动静脉畸形所致颅内出血(1例,1.4%)。初步诊断为23.9%的低血糖,18.3%的低钙血症,15.5%的低钠血症,35.2%的酸中毒,25.4%的乳酸升高。根据发热和新发癫痫进行分组。大约45.1%的人口在发病时发热,其中包括年龄较小的儿童(p=0.023)。既往癫痫患儿兄弟姐妹死亡的发生率较高,而新发癫痫患儿乳酸水平明显升高、酸中毒、需要机械通气的发生率较高(p=0.002, p=0.008, p=0.017)。12例(16.9%)患者发生SRSE。低血清钠、钙水平与发生SRSE相关(OR: 10.800, 95%CI: 2.518-46.318;Or: 4.554, 95%ci: 1.159-17.892);然而,PRISM-3评分已被确定为儿童进入SRSE的单一独立危险因素(OR: 1.174, 95% CI: 1.039-1.327)。3名(4.2%)儿童死于继发性并发症。2例(16.7%)SRSE患者因神经系统无法维持气道通畅而行气管造口插管。结论:PRISM-3评分是SRSE的独立危险因素。电解质异常(低钠血症和低钙血症)与SRSE的发生有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The predictive factors for prolonged seizures and status epilepticus: a single center study
Objectives: To analyze the clinical features of prolonged seizures and status epilepticus and perform risk analysis on super refractory status epilepticus (SRSE) in pediatric intensive care unit (PICU) admissions. Method: Demographic features, underlying etiologies, treatment modalities, electroencephalographic and neuroimaging outcome of intensive care unit admissions between 2015 and 2019 were analyzed. Results: Seventy-one children were enrolled. The common etiology for prolonged seizure was fever in 45.1% of the children (central nervous system infection: 16.9%, infection other than central nervous system: 28.2%), withdrawal of the antiepileptic medication in 40.9%, intoxications in 12.7% of the children and intracranial hemorrhage due to arteriovenous malformation in one (1.4%) patient. Initial diagnostics exhibited 23.9% of hypoglycemia, 18.3% of hypocalcemia, 15.5% of hyponatremia, 35.2% of acidosis, and 25.4% of elevated lactate. Group categorizations were based on fever and new onset of seizure. Approximately 45.1% of the population acquired fever at the onset and consisted of younger children compared to their counterparts (p=0.023). Children with pre-existing epilepsy had frequent history of sibling death, while patients with new-onset of seizure possessed significant lactate elevations, acidosis, and required mechanical ventilation more often (p=0.002, p=0.008, p=0.017). Twelve (16.9%) patients developed SRSE. Low serum sodium and calcium levels were associated with developing SRSE (OR: 10.800, 95%CI: 2.518-46.318; OR: 4.554, 95%CI: 1.159-17.892); however PRISM-3 score has been identified the single independent risk factor in children proceeding to SRSE (OR: 1.174, 95% CI: 1.039-1.327). Three (4.2%) children died of secondary complications. Tracheostomy cannulation was performed in two (16.7%) SRSE patients due to neurological incapability to maintain a patent airway. Conclusion: PRISM-3 score is the independent risk factor of SRSE. Electrolyte abnormalities (hyponatremia and hypocalcemia) are associated with developing SRSE.
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