Management and outcomes among older adults with generalized epilepsy in routine clinical practice

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Epilepsia Open Pub Date : 2024-12-27 DOI:10.1002/epi4.13123
MarieElena Byrnes, Majed Alzahrany, Vineet Punia
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Abstract

Generalized epilepsy is classically thought of as a disease of the young and adolescent, with rarely reported cases among older adults. We aimed to analyze management and outcomes in a population sparsely described in the literature through a retrospective single-center cohort design. After excluding individuals without follow-up, we identified 151 people ≥50 years at the time of electrographically confirmed generalized epilepsy. Just over a quarter were late-onset (≥26 years), and 77% were diagnosed with genetic generalized epilepsy (GGE). Active seizures (in the last year of follow-up) were present in 57% of individuals, despite most of them having experienced prolonged seizure remission periods (median 7 years) in the past. Only five people were off antiseizure medication (ASM) at their last appointment, with most on an average of 2 ASMs. The odds of active epilepsy at the last follow-up were significantly higher among those with polyspikes (odds ratio [OR] = 2.42; 95% confidence interval [CI] = 1.01–6.01), myoclonic seizure history (OR = 2.88, 1.23–6.96), and developmental delay (OR = 4.75, 1.45–19.3). The odds were 60% lower in older adults with family history (OR = 0.4, 0.17–5.68). Our findings suggest that most older adults with generalized epilepsy achieve years of seizure remission, but the likelihood of epilepsy resolution is low.

Plain Language Summary

Generalized epilepsy is seldom seen in older adults. We looked at 151 patients diagnosed with generalized epilepsy over the age of 50 to see how they are managed and what influences their outcomes. We found that although these patients can control their seizures with medication, the chance that their epilepsy resolves is low. Patients with certain characteristics classically seen in an epilepsy called “Juvenile Myoclonic Epilepsy” (JME) may have a more intractable course.

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常规临床实践中老年全身性癫痫患者的管理和结局。
一般认为,全身性癫痫是年轻人和青少年的疾病,很少有老年人发病的报道。我们旨在通过回顾性单中心队列设计分析文献中描述较少的人群的管理和结果。在排除了没有随访的个体后,我们确定了151例年龄≥50岁的电图确诊的全身性癫痫患者。超过四分之一为迟发性(≥26岁),77%被诊断为遗传性全身性癫痫(GGE)。57%的个体存在活动性癫痫发作(在随访的最后一年),尽管他们中的大多数过去经历过较长的癫痫发作缓解期(中位数为7年)。只有5人在最后一次预约时停用抗癫痫药物(ASM),大多数人平均停用2次ASM。最后一次随访时,多峰性癫痫患者发生活动性癫痫的几率显著高于其他患者(优势比[OR] = 2.42;95%可信区间[CI] = 1.01-6.01)、肌阵挛发作史(OR = 2.88, 1.23-6.96)和发育迟缓(OR = 4.75, 1.45-19.3)。有家族史的老年人患病几率低60% (OR = 0.4, 0.17-5.68)。我们的研究结果表明,大多数患有广泛性癫痫的老年人癫痫发作数年缓解,但癫痫消退的可能性很低。摘要:全身性癫痫在老年人中很少见。我们研究了151名50岁以上被诊断为全身性癫痫的患者,以了解他们是如何治疗的,以及影响他们预后的因素。我们发现,虽然这些患者可以通过药物控制癫痫发作,但癫痫发作的几率很低。具有典型癫痫“幼年型肌阵挛性癫痫”(JME)特征的患者可能有更棘手的病程。
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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
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