Efficacy of Perampanel in Nocturnal Seizures in Adult Patients with Epilepsy

IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY
Samuel López-Maza, Ariadna Gifreu, Elena Fonseca, Manuel Quintana, Estevo Santamarina, Laura Abraira, Daniel Campos, Manuel Toledo
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Abstract

Objective. Nocturnal seizures are usually underestimated and represent a major problem in adult patients with epilepsy. Our aim was to study the effectiveness of perampanel for the treatment of nocturnal seizures in adult patients with epilepsy. Methods. Observational study of a prospectively acquired sample of adult patients with focal and generalized epilepsy in which perampanel was started from January to October 2021 in a specialized epilepsy unit in a tertiary hospital. Demographic and clinical characteristics were recorded. All patients completed a follow-up period of at least 3 months. Seizure frequency during the 6-month period before the patient started treatment was obtained from medical records. Retention and responder rates (considered as a nocturnal seizure frequency reduction of ≥50%) and improvement of subjective sleep disturbances were analyzed as outcome measures. Results. Forty-eight patients were included (mean age 39.8 ± 17.4; 60.4% men), and 38 of them had a 6-month follow-up. Focal epilepsy was the most common diagnosis (81.3%), and most patients had a structural etiology (56.3%). Thirty-four (70.8%) patients had drug-resistant epilepsy. The mean nocturnal seizure frequency per month at baseline was 13.2 ± 35.9. Fifteen (31.3%) patients had subjective sleep disturbances at baseline, of which insomnia was the most frequent complaint (16.7%). Perampanel was started at a median dose of 4 mg/day (range = 2-14). At 3-month follow-up, the retention rate was 74.6%; 64.6% were considered responders (54.2% were seizure-free). Monthly nocturnal seizures decreased significantly at 3 months (8.2 ± 26.7 vs. 13.2 ± 35.9 seizures/month; p = 0.044) and 6 months (5.3 ± 18.2 vs. 13.2 ± 35.9 seizures/month; p = 0.006). Subjective sleep disturbances improved at 3-month follow-up (10.4% vs. 31.3%; p = 0.002) and 6-month follow-up (10.5% vs. 31.3%; p = 0.022). Significance. Perampanel can be a suitable treatment option in adult patients with both focal and generalized epilepsy with nocturnal seizures and can reduce the presence of sleep complaints.

佩兰帕奈对成年癫痫患者夜间发作的疗效
目的。夜间癫痫发作通常被低估,是成年癫痫患者的一个主要问题。我们的目的是研究培南帕尼治疗成年癫痫患者夜间癫痫发作的有效性。研究方法对一家三甲医院的癫痫专科病房从2021年1月至10月开始使用培南帕尼的局灶性和全身性成年癫痫患者进行前瞻性样本观察研究。研究人员记录了患者的人口统计学特征和临床特征。所有患者均完成了至少 3 个月的随访。从医疗记录中获取了患者开始治疗前 6 个月内的发作频率。结果分析指标包括保留率和应答率(夜间发作频率减少≥50%)以及主观睡眠障碍的改善情况。结果。研究共纳入48名患者(平均年龄为39.8±17.4岁;60.4%为男性),其中38人接受了6个月的随访。病灶性癫痫是最常见的诊断(81.3%),大多数患者的病因是结构性的(56.3%)。34名患者(70.8%)患有耐药性癫痫。基线值为每月平均夜间发作频率(13.2±35.9)次。15名患者(31.3%)在基线时有主观睡眠障碍,其中失眠是最常见的主诉(16.7%)。开始服用培南帕奈时的中位剂量为每天4毫克(范围=2-14)。随访3个月时,保留率为74.6%;64.6%被认为是应答者(54.2%无癫痫发作)。每月夜间癫痫发作次数在 3 个月和 6 个月时显著减少(分别为 8.2±26.7 次/月和 13.2±35.9 次/月;P=0.044)和(5.3±18.2 次/月和 13.2±35.9 次/月;P=0.006)。主观睡眠障碍在随访3个月(10.4% vs. 31.3%;p=0.002)和6个月(10.5% vs. 31.3%;p=0.022)时有所改善。意义重大。对于伴有夜间发作的局灶性和全身性癫痫成年患者来说,培南帕尼是一种合适的治疗选择,可以减少睡眠投诉。
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来源期刊
Acta Neurologica Scandinavica
Acta Neurologica Scandinavica 医学-临床神经学
CiteScore
6.70
自引率
2.90%
发文量
161
审稿时长
4-8 weeks
期刊介绍: Acta Neurologica Scandinavica aims to publish manuscripts of a high scientific quality representing original clinical, diagnostic or experimental work in neuroscience. The journal''s scope is to act as an international forum for the dissemination of information advancing the science or practice of this subject area. Papers in English will be welcomed, especially those which bring new knowledge and observations from the application of therapies or techniques in the combating of a broad spectrum of neurological disease and neurodegenerative disorders. Relevant articles on the basic neurosciences will be published where they extend present understanding of such disorders. Priority will be given to review of topical subjects. Papers requiring rapid publication because of their significance and timeliness will be included as ''Clinical commentaries'' not exceeding two printed pages, as will ''Clinical commentaries'' of sufficient general interest. Debate within the speciality is encouraged in the form of ''Letters to the editor''. All submitted manuscripts falling within the overall scope of the journal will be assessed by suitably qualified referees.
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