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find Keyword "部分性癫痫" 8 results
  • 反应性神经刺激治疗成人局灶性药物难治性癫痫的中心试验结果

    为了验证在癫痫灶进行反应性神经刺激作为减少成人癫痫起源于一个或两个致痫灶的药物难治性部分性癫痫发作频率的辅助治疗方法的安全性及有效性。反应性局灶皮层刺激(Responsive focal cortical stimulation, RNS)的多中心随机对照双盲试验。对起源于一个或两个致痫灶的药物难治性部分性癫痫受试者进行皮下植入, 植入后1个月按1∶1随机分为真刺激及假刺激组。植入后第5个月过后, 所有受试者在一个开放标签期(Open label period, OLP)接受反应性神经刺激开放标签来完成2年的植入后随访。所有191例受试者进行了随机化。盲法期结束时真刺激组癫痫发作改变的百分比为37.9%, 假刺激组为17.3%(P=0.012, 广义估计方程)。开放标签期癫痫发作减少百分比中位数第1年为44%, 第2年为53%, 代表随着时间呈进行性且显著的改善(P<0.000 1)。严重不良事件发生率在真刺激及假刺激组间无差异。不良事件与植入医疗设备、癫痫发作及其它癫痫治疗方法的已知风险是一致的。未出现神经心理功能或情绪方面的不良效应。反应性神经刺激治疗局灶性癫痫快速减少了部分性癫痫发作的频率, 显示了随时间癫痫发作减少率的改善, 耐受性良好, 安全性可接受。RNS系统为药物难治性部分性癫痫发作患者提供了一种新的治疗选择

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  • Molecular characteristics of SCN1A mutation causing partial epilepsy with febrile seizures plus

    ObjectiveTo explore the molecular characteristics of partial epilepsy with febrile seizures plus(PEFS+). MethodsWe systematically reviewed all SCN1A mutation-related publications that published between Jan.2000 and Dec.2014 on Pubmed and established a database of SCN1A mutations (http://www.gzneurosci.com/SCN1Adatabase/). The characteristics of mutations that cause PEFS+ were analyzed and compared with that of severe myoclonic epilepsy in infancy (SMEI). ResultsThe database included 1, 257 SCN1A mutations, which identified from 1, 727 unrelated cases. In which there were 30 mutations, from 32 unrelated cases, were associated with PEFS+. 76.7% (23/30) mutations were missense, of which 47.8% (11/23) were located on pore region. Significant difference in the percentage of truncation mutation was observed between PEFS+ and SMEI (P < 0.05). There was no significant difference in the percentage of missense mutation that located on the pore region between PEFS+ and SMEI; but the differ significantly in D-value of the missense mutations, which quantified the alteration of amino acid(P=0.042, rank sum test). ConclusionsPEFS+, which distinguishes from GEFS+ and SMEI in clinical and molecular characteristics, is a special phenotype of epilepsy that is associated with SCN1A mutations.

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  • The analysis of the etiology, clinical features, treatment and prognosis of 17 partial statas epileptic cases

    ObjectiveTo investigate the etiology, clinical features, treatment, and prognosis of Partial status epilepticus (PSE). MethodsSeventeen PSE patients were hospitalized in the Department of Neurology at the First Hospital of Jilin University from April 2013 to June 2015. Clinical data were retrospectively analyzed. ResultsA total of 17 patients, 8 male and 9 female, 18~91years old, at mean age (48.90±21.17) years were included. About 12 cases (70.59%) had acute symptomatic status epilepticus, the etiologies including central nervous system inflammation (5 cases), cortical infarction (3 cases), metabolic disorder (1 case), hypoxic-ischemic encephalopathy (1 case), space-occupying lesions(1 case) and degeneration (1 case); four cases (23.53%) were diagnosed with epilepsy, one case (5.88%) had no definite pathogenesis. The seizure types included complex partial status epilepticus (8 cases, 47.06%), complex part of the secondary comprehensive status epilepticus (3 cases, 17.65%), supplementary motor area (SMA) status epilepticus (4 cases, 23.53%), epilepsia partialis continua (EPC) (1case, 5.88%)and complex partial status epilepticus & aura continua (1case, 5.88%). Nine cases (52.94%) were effective after one hour treament, eight cases (47.06%) were negative. 17 cases are followed-up and 4 cases lost, the average follow-up time is (10.89±8.64) months. 8 cases are completely seizure free, and 3 cases have experience less seizures or the symptom is relived; the other 2 cases die from Creutzfeldt-Jacob desease(case No.10) and Respiratory failure(case No.12). ConclusionsThe inpatients of partial status epilepticus are mostly "situation related". Patients with clinical suspect should be administrated with long term video-Electroencephalogram(EEG) monitoring timely. Early diagnosis, treatment and the aggressive treatment can help to improve the prognosis. Patients of encephalitis usually progress into refractory status epilepticus, the anesthetic drugs should be used as soon as possible.

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  • Meta analysis on the effectiveness of levetiracetam adjunctive treatment in children refractory partial epilepsy

    ObjectiveTo evaluate the effectiveness of levetiracetam (LEV) added on to usual care, in treating children refractory partial seizure epilepsy.MethodsWe searched the Cochrane library, EMBASE and PubMed between January 1998-January 2017, We systematically searched CNKI database and Wanfang data, Chinese biology medline and the manual retrieval related magazines.RevMan 5.3 statistical software for Meta analysis.ResultsAccording to the enrollment criteria, fourtrials were included involving 498 participants according to the intent-to-treat, 268 for LEV, and 230 for placebo groups.We assessed the following outcomes: 50% or greater seizure reduction, seizure freedom, adverse effects, proportion of dropouts and quality of life. There was no evidence of statistical heterogeneity between trials.We assessed outcomes by using a meta-analysis to calculate odds ratio (OR) with 95% confidence intervals (95% CI). For the 50% or greater reduction in focal seizure frequency outcome, the OR was significantly in favour of LEV [OR=2.94, 95% CI(1.99, 4.34)].Participants were significantly more likely in LEV groups than placebo groups to get seizure free[OR=5.31, 95% CI(2.49, 11.32)]. There was no significance between LEV groups and placebo groupsin the rate of Treatment withdrawal[OR=0.76, 95% CI(1.32, 1.82)]. Somnolence[OR=2.57, 95% CI(1.36, 4.86)]and changes in behaviour [OR=2.54, 95% CI(1.56, 4.14)] were significantly associated with LEV. Other adverse effects were not significantly associated with LEV in children.ConclusionThe existing evidence suggests that LEV add in treatment of children refractory epilepsy have definite curative effect, LEV long-term treatment effect is stable, good security, retention rate is higher, can be used in clinical further promotion.

    Release date:2017-04-01 08:51 Export PDF Favorites Scan
  • Efficacy of low to moderate doses of levetiracetam as initial monotherapy in adult patients with partial epilepsy

    Objective To explore the efficacy of low to moderate doses of levetiracetam in adult patients with newly diagnosed partial epilepsy and possible predictors for poor treatment response. Methods We retrospectively analyzed the clinical data of patients treated in West China Hospital from March 2011 to December 2015 whose clinical data were input into the Epilepsy database. Patients with newly diagnosed partial epilepsy and whose initial anti-epileptic drug was levetiracetam were screened out for this study. Their clinical data, especially responses to the treatment of levetiracetam were reviewed. Results Ninety-six patients were included in this study. Seventy-one of them achieved seizure-free for a complete year after initial treatment of levetiracetam. Forty-eight patients (50.0%) achieved seizure-free with levetiracetam monotherapy; 23 patients (24.0%) achieved seizure-free for one year with levetiracetam combination therapy. Sixty-nine (97.2%) of the 71 patients achieved seizure-free with low to moderate doses of levetiracetam (500 to 1 500 mg/day), with or without combination of other antiepileptic drugs. High baseline seizure frequency before initial therapy was an independent predictor of poor levetiracetam response in this multivariate logistic regression mode (P=0.019). Conclusions Low to moderate levetiracetam is both effective and well tolerated in newly diagnosed partial epilepsy patients. High baseline seizure frequency before initial therapy is an independent predictor of poor levetiracetam response.

    Release date:2017-05-18 01:09 Export PDF Favorites Scan
  • 拉考沙胺—部分性癫痫发作的新选择

    癫痫是神经科最常见的疾病之一,目前其治疗主要依赖于药物。传统抗癫痫药物(AEDs)通常不良反应较多,多和其他药物之间存在相互作用。拉考沙胺(LCM)作为第三代新型 AEDs,于 2008 年在美国上市,是目前唯一已知选择性作用于慢失活钠通道 AEDs,现欧美已获得≥4 岁部分性癫痫患者添加及单药治疗的适应证。在中日临床试验中作为≥16 岁难治性部分性发作癫痫患者的添加治疗,16 周 50% 有效率高达 49.2%。此外,真实世界研究也证明了 LCM 早期添加治疗 6 个月癫痫无发作率可达 45.5%。安全性方面,长达 8 年的开放标签研究显示长期用药耐受性好,不良反应多为轻中度,主要包括头晕、头痛、恶心、复视等。

    Release date:2019-11-14 10:46 Export PDF Favorites Scan
  • 儿童持续性部分性癫痫的诊断算法

    总结一组持续性部分性癫痫(Epilepsia partialis continua,EPC)患儿的特点,并提出一种整合关键鉴别诊断的诊断算法。对 2002 年—2019 年在三级儿科神经病学中心就诊的 EPC 患儿进行分析。54 例患儿符合 EPC 诊断标准。中位发病年龄为 7 岁(0.6~15 岁),中位随访时间为 4.3 年(0.2~16 年)。其中,诊断为 Rasmussen 脑炎(Rasmussen encephalitis,RE)30 例(56%),线粒体疾病 12 例(22.2%),磁共振成像(MRI)阳性病灶相关局灶性癫痫 6 例(11.1%),诊断不明 5 例(9%)。线粒体疾病患儿更早出现 EPC,EPC 发病年龄每增加一年,诊断线粒体疾病的几率降低 26%(P = 0.02)。EPC 发作前存在发育问题(OR=22,P<0.001),EPC 发作前无癫痫发作(OR=22,P<0.001), EEG 提示双侧半球慢波(OR 26,P<0.001),以及脑脊液(CSF)蛋白水平升高(OR=16)均预示着线粒体疾病。30 例 RE 患儿中有 18 例(60%)出现 EPC 发作时,MRI 提示明显不对称或一侧半球萎缩,其余患儿出现的中位时间则在 EPC 发作后 6 个月(3~15 个月)。首选诊断检查为头部 MRI。一侧半球萎缩结合临床表现及脑电图改变的偏侧性,提示诊断为 RE。对于初次扫描时不能诊断为 RE,但临床和影像学表现提示 RE 的儿童,建议每 6 个月重复影像学检查以排查进行性一侧半球皮质萎缩,并应考虑脑活检,鞘内炎症的证据(寡克隆带和新蝶呤升高)可为佐证。对于存在双侧半球源性 EPC 的患儿,建议进行快速 DNA 聚合酶 γ(POLG)基因检测,如为阴性,则应提取外周血 DNA 进行 mtDNA 测序及全外显子组测序。线粒体病所致 EPC 患儿表现出与 RE 和结构性癫痫不同的临床特征。这一针对 EPC 患儿的诊断算法有助于进行针对性检查并及时诊断。

    Release date:2021-06-24 01:24 Export PDF Favorites Scan
  • Clinical features, treatment and prognosis of Rasmussen encephalitis in 21 children

    ObjectiveTo summarize the clinical phenotype, electrophysiological characteristics, imaging characteristics, surgical treatment and prognosis of Rasmussen encephalitis (RE), so as to deepen the understanding of the disease. MethodsThe clinical data of patients with RE who underwent surgical therapy from October 2014 to October 2019 at Children's Epilepsy Center in Peking University First Hospital were retrospectively reviewed. Demographic characteristics, seizure forms, electroencephalogram (EEG), cranial nuclear magnetic resonance (MRI), operative methods as well as surgical outcomes evaluated by Engel classification during follow-up of the subjects were collected and analyzed. ResultsTotally 21 pediatric patients were enrolled, including 8 males and 13 females. The age at onset was (5.0±2.0) years old, the age at the time of surgery was (6.9±2.7) years old, and the disease duration at the time of surgery was (1.7±1.3) years. Twenty (20/21, 95.2%) patients had focal motor seizures, and 10 (10/21, 47.6%) patients had 2 or 3 forms of focal motor seizures. Fifteen patients (15/21, 71.4%) had epilepsia partialis continua (EPC), which occurred (0.7±0.6) years after the onset. All patients had hemiplegia, which appeared at (0.9±0.6) years after the onset. All patients showed a slow rhythm at their affected hemispheres during the EEG monitoring and 4 of them also showed slow rhythm at the contralateral hemispheres as the disease progressed. All patients had epileptiform discharges at the involved hemisphere, and 6 patients also had independent epileptiform discharges on the contralateral side. All 21 patients underwent hemispheric disconnection. The duration of follow-up was 2 to 7 years, and all patients achieved Engel class I after the surgery. The neurological dysfunction recovered to varying degrees during the postoperative period. ConclusionRE mostly occurs around the school age. Focal motor seizures are the main manifestations and the most common onset symptoms. With the progress of the disease, the condition of patients worsened gradually. The EEG of patients was mainly characterized by broad slow wave and spike wave in the affected hemisphere. Some patients can also have bilateral involvement, which was obviously asymmetrical. Through surgical treatment, the patients all achieved good results in terms of seizures and development.

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