出生后第一年的强直和强直阵挛发作:从电图特征中得到的启示。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-11-01 DOI:10.1016/j.yebeh.2024.110120
Marta Conti , Mattia Mercier , Domenico Serino , Ludovica M. Piscitello , Marta E. Santarone , Federico Vigevano , Nicola Specchio , Lucia Fusco
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引用次数: 0

摘要

目的:我们研究了出生后第一年内出现的伴有双侧收缩的强直性发作(TS)和无局灶征象的强直阵挛发作(TCS)的电图特征,以评估其是否与预后相关:我们回顾性分析了 2011 年至 2021 年期间在本院癫痫监护室至少有一次 TS 或 TCS 视频脑电图记录的 1 至 12 个月大的患者。我们分析了以下电图特征:发作持续时间、局灶性发作性脑电图起始的存在和持续时间以及发作后全身脑电图抑制(PGES)。在临床变量中,我们收集了癫痫发病年龄、TS和TCS记录年龄、对抗癫痫药物的反应、遗传和神经影像学检查结果、癫痫综合征分类:我们共记录了 1769 名患者的 2577 次癫痫发作。在 41 名患者(2%)中,有 128 次发作(5%)被临床标记为 TS 或 TCS。在 41 名患者中,17 人(41%)表现为 TS,24 人(59%)表现为 TCS。13名患者(32%)患有自限性癫痫,28名患者(68%)患有发育性癫痫脑病(DEE)。72%的基因检测患者有致病基因变异。没有人患有结构性癫痫。癫痫发病时的平均年龄为 4.48 个月(3 天-12 个月不等)。TS患者比TCS患者(2.31个月比6.01个月;P = 0.001)、DEE患者比自限性癫痫患者(3.23个月比7.16个月;P = 0.001)的癫痫发作年龄更早。TS仅出现在DEEs中(p = 0.001),而TCS在DEEs和自限性癫痫中均有记录。在 92% 的 TCS 中,局灶性发作性脑电图起病明显,而在 TS 中则没有。100 % 的 TS 和 8 % 的 TCS 记录有全身发作性脑电图发作。在自限性癫痫患者中,局灶性发作性脑电图起始的发生率更高(100% 对 32%;P = 0.000),且时间明显更长(30.61 秒对 16.22 秒;P = 0.020)。在 41 例中有 18 例(44%)观察到 PGES,自限性癫痫患者的 PGES 发生率更高(p = 0.026):这项研究有助于了解婴儿 TS 和 TCS 的临床电学特征,从而有助于在癫痫发病后不久将自限性癫痫与 DEE 区分开来。
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Tonic and tonic-clonic seizures in the first year of life: Insights from electrographic features

Objective

We studied the electrographic features of tonic seizures (TS) with bilateral contraction and tonic-clonic seizures (TCS) without focal signs occurring during the first year of life to evaluate if there is a correlation with outcome.

Methods

We retrospectively reviewed patients aged 1 to 12 months with at least one TS or TCS recorded with video-EEG between 2011 and 2021 in our Epilepsy Monitoring Unit. We analyzed the following electrographic features: seizure duration, presence and duration of focal ictal EEG onset, and post-ictal generalized EEG suppression (PGES). Among clinical variables, we collected age at epilepsy onset, age at TS and TCS recording, response to anti-seizure medications, genetic and neuroimaging findings, epileptic syndrome classification.

Results

Overall, we recorded 2577 seizures in 1769 patients. One-hundred-twenty-eight seizures (5%) were clinically labeled either as TS or TCS in 41 patients (2%). Out of 41 patients, 17 (41%) presented with TS, and 24 (59%) with TCS. Thirteen patients (32%) had a Self-limited Epilepsy, and 28 (68%) a Developmental and Epileptic Encephalopathy (DEE). Seventy-two percent of genetically tested patients had pathogenic gene variants. None had structural epilepsy.
Mean age at epilepsy onset was 4.48 months (range 3 days-12 months). Age at seizure onset was earlier in patients presenting with TS versus patients presenting with TCS (2.31 months vs. 6.01 months; p = 0.001) and in DEEs versus Self-limited Epilepsies (3.23 months vs. 7.16 months; p = 0.001). TS were exclusively present in DEEs (p = 0.001), and TCS were recorded in both DEEs and Self-limited Epilepsies. Focal ictal EEG onset was evident in 92 % of TCS, and in none of TS. Generalized ictal EEG onset was documented in 100 % of TS, and in 8 % of TCS. Focal ictal EEG onset occurred more frequently (100 % vs. 32 %; p = 0.000) and was significantly longer (30.61 s vs. 16.22 s; p = 0.020) in Self-limited Epilepsies versus DEEs. PGES was observed in 18 out of 41 (44 %) and was more frequent in Self-limited Epilepsies (p = 0.026).

Significance

This study provides insights into the electroclinical features of TS and TCS in infants that may help distinguish Self-limited Epilepsies from DEEs soon after epilepsy onset.
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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