年轻成人癫痫的临床特点、病因和治疗:一项24年的回顾性研究。

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Epilepsia Open Pub Date : 2024-12-30 DOI:10.1002/epi4.13126
Xu Zhang, Feng Xiang, Ziyu Wang, Yang Li, Chenjing Shao, Xiaoyang Lan, Senyang Lang, Xiangqing Wang
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引用次数: 0

摘要

目的:分析青壮年癫痫的临床特点、病因、药物治疗及相关因素。方法:选取年龄在18 ~ 44岁的癫痫患者为研究对象,分析24年间(1999年2月~ 2023年3月)年轻人癫痫的临床特点及对抗癫痫药物(ASM)的反应。结果:共有4227例患者在18至44岁之间发生癫痫发作。发病年龄中位数为26岁(四分位数间距[IQR]: 21-33),从首次发作到开始治疗的中位数持续时间为3个月(IQR: 1.0-6.0)。结构病因是最常见的癫痫病因,占43.2%(1827/4227),其中头部外伤和开颅史占64.9%(1186/1827)。然而,这两个原因并不一定导致及时用药或癫痫控制不良。共病性认知衰退比头痛和焦虑/抑郁更为普遍。多因素回归分析显示,与癫痫发作控制不良相关的因素包括癫痫发作持续时间较长(优势比[OR] 1.85;95%置信区间[CI] 1.58-2.16;p意义:青壮年癫痫多由颅脑外伤或开颅手术引起。共病性认知衰退比头痛和焦虑/抑郁更为普遍。从首次发作到随访治疗的中位时间为3个月(IQR: 1.0-6.0)。在两次癫痫发作后开始治疗并不一定表明药物效果差。摘要:在本文中,我们观察到青壮年癫痫主要由头部外伤和开颅所致;共病性认知衰退更为常见。从首次癫痫发作到开始治疗的中位持续时间为3个月,超过三分之一的患者在治疗前经历了两次以上的癫痫发作,但这一因素对药物有效性没有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Clinical characteristics, etiology, and treatment of young adult-onset epilepsy: A 24-year retrospective study

Objective

To analyze the clinical characteristics, etiology, drug treatment, and related factors of patients with young adult-onset epilepsy.

Methods

The study included patients with epilepsy aged between 18 and 44 years and aimed to analyze the clinical characteristics of epilepsy in young people and their response to antiseizure medication (ASM) over a 24-year period (February 1999 and March 2023).

Results

A total of 4227 patients experienced epilepsy onset between 18 and 44 years of age. The median age of onset was 26 years (interquartile range [IQR]: 21–33), and the median duration from the first seizure to starting treatment was 3 months (IQR: 1.0–6.0). Structural etiology was the most common cause of epilepsy, accounting for 43.2% (1827/4227) of cases, of which head trauma and a history of craniotomy accounted for 64.9% (1186/1827). However, these two causes did not necessarily result in prompt medication or poor epilepsy control. Co-morbid cognitive decline was more prevalent than headache and anxiety/depression. Multifactorial regression analysis showed that the factors associated with poor seizure control included longer seizure duration (odds ratio [OR] 1.85; 95% confidence interval [CI] 1.58-2.16; p < 0.001), electroencephalography (EEG) epileptic discharge (OR 1.37; 95% CI 1.17–1.67; p < 0.001), focal seizure (OR 1.69; 95% CI 1.38–2.07; p < 0.001), and seizure clusters (OR 3.35; 95% CI 2.70–4.15; p < 0.001). Initiating treatment after two seizures (OR, 1.18; 95% CI 0.98–1.15; p = .08) or 6 months after the first seizure (OR 0.84; 95% CI 0.67–1.03; p = .09) did not worsen effectiveness.

Significance

Young adult-onset epilepsy was frequently caused by head trauma or craniotomies. Co-morbid cognitive decline was more prevalent than headache and anxiety/depression. The median time from the first seizure to follow-up treatment was 3 months (IQR: 1.0–6.0). Initiating treatment after two seizures did not necessarily indicate poor drug effectiveness.

Plain Language Summary

In this article, we observed that young adult-onset epilepsy was mainly caused by head trauma and craniotomy; co-morbid cognitive decline was more common. The median duration from first seizure to initiation of treatment for young-onset epilepsy was 3 months, and more than one-third of patients experienced more than two seizures prior to treatment, but this factor had no effect on the drug effectiveness.

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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
期刊最新文献
Efficacy and tolerability of low versus standard daily doses of antiseizure medications in newly diagnosed focal epilepsy. A multicenter, randomized, single-blind, non-inferiority trial (STANDLOW). Three cases of atypical Rasmussen's encephalitis with delayed-onset seizures. GATAD2B-related developmental and epileptic encephalopathy (DEE): Extending the epilepsy phenotype and a literature appraisal. Intrinsic brain network stability during kainic acid-induced epileptogenesis. Diagnostic yield of utilizing 24-72-hour video electroencephalographic monitoring in the diagnosis of seizures presenting as paroxysmal events in resource-limited settings.
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