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find Keyword "难治性癫痫" 76 results
  • 抗 B 型 γ-氨基丁酸受体脑炎三例

    Release date:2017-11-24 10:58 Export PDF Favorites Scan
  • Analysis of 24 cases of intractable temporal lobe epilepsy surgery

    ObjectiveTo investigate the status and prognosis effect of surgical operation for Temporal lobe epilepsy.MethodsRetrospective analyses were performed on 24 patients with intractable temporal lobe epilepsy who were treated by surgery in Zibo Changguo Hospital and had complete clinical and follow-up data, during the period from April 2011 to June 2014. Among them, 14 were male and 10 were female, 16 to 44 years old, the average age was (24.40±6.26) years old, and the average course of disease was (12.50±8.42) years old. The clinical characteristics and prognosis of the patients were analyzed.ResultsAll 24 patients had hippocampal sclerosis and underwent "anterior temporal lobe and medial temporal structural resection". Patients were followed up for 5~7 years, the postoperative epileptic seizure of the patient reached grade Engel Ⅰ in 20 cases (83.3%), grade Engel Ⅱ in 2 cases (8.3%) and grade Engel Ⅳ in 2 cases (8.3%).ConclusionHippocampal sclerosis and cortical dysplasia were common in 24 patients, and the operation controlling intractable epilepsy was better. In order to improve the prognosis of patients, surgical treatment should be carried out as soon as possible.

    Release date:2021-02-27 02:57 Export PDF Favorites Scan
  • Clinical Diagnosis Value of Video-electroencephalography and MRI on Pharmacal Intractable Epilepsy

    【摘要】 目的 探讨用视频脑电图和MRI诊断药物难治性癫痫的临床价值。 方法 收集2006年12月-2010年5月间经手术和病理证实的药物难治性癫痫患者38例。其中,海马硬化25例,颞叶萎缩伴脑发育不良2例,脑灰质移位及巨脑回4例,血管畸形3例,胶质瘤2例,脑内囊肿1例,外伤性癫痫1例。用视频脑电图监测癫痫发作期及发作间期痫样放电的来源部位及脑电活动特点,用MRI扫描显示痫灶区的表现特征,并与手术、病理改变对照,进行回顾性分析。 结果 视频脑电图对癫痫发作期的致痫灶来源定位准确率为100%(38/38),发作间期定位准确率为53%(20/38)。MRI对发作间期的致痫灶及相关病变定位诊断准确率为89%(34/38),病变定性准确率为79%(30/38)。 结论 视频脑电图和MRI检查有机结合,对药物难治性癫痫,能更有效检出致痫灶的部位及性质,为药物难治性癫痫患者的手术治疗,提供重要信息。【Abstract】 Objective To study the clinical diagnosis value of video-electroencephalography (EEG) and MRI on pharmacal intractable epilepsy. Methods From December 2006 to May 2010, 38 cases of pharmacal intractable epilepsy were confirmed through operation and pathologic examination. Among them, there were 25 cases of hippocampal sclerosis, 2 cases of temporal lobe atrophy combined with brain dysplasia, 4 cases of heterotopic gray matter and macrogyria, 3 cases of vascular malformation, 2 cases of glioma, 1 case of cyst in brain, and 1 case of traumatic epilepsy. Video-EEG was applied to monitor the source of epileptoid discharge and the features of brain electrical activity during and between the occurrences of epilepsy. MRI was used to detect the manifestation characteristics of the epilepsy focus, and retrospective analysis was done to compare these findings with operational and pathological results. Results The accuracy rate of Video-EEG in locating the epilepsy focus was 100% (38/38) during the occurrence of epilepsy, and 53% (20/38) between the occurrences of epilepsy. The accuracy rate of MRI in diagnosing the epilepsy focus and relevant abnormalities during the occurrence of epilepsy was 89% (34/38), and 79% (30/38) in characterizing the abnormalities. Conclusion Video-EEG combined with MRI examination is effective in locating and characterizing the epilepsy focus, which can provide more useful information for the surgery in treating pharmacal intractable epilepsy.

    Release date:2016-09-08 09:27 Export PDF Favorites Scan
  • Clinical summary and analysis of patients with refractory epilepsy in tuberous sclerosis complex with peripheral blood gene negative

    ObjectiveTuberous sclerosis complex (TSC) is a multisystem disease, which often manifests as refractory epilepsy in the nervous system and multifocality in Magnetic resonance imaging (MRI). We summarized patients with TSC whose peripheral blood gene test was negative,and analyzed their medical history, EEG, MRI and postoperative conditions. MethodsWe summarized and analyzed 205 patients with TSC diagnosed clinically and pathologically and underwent surgery from April 2008 to February 2024. 11 patients with TSC whose peripheral blood gene test was negative and underwent surgery were screened out.All patients underwent gene examination, MRI and long-range video EEG monitoring. All patients underwent detailed preoperative evaluation and direct resection surgery, intracranial electrode thermocoagulation surgery or laser surgery. ResultsOf the 11 patients with peripheral blood gene test negative, 11 (100%) patients achieved Engel Ⅰ within 1 year after surgery, and 10 (91%) patients achieved Engel Ⅰwithin 2 years. The median age of onset of 11 patients was 6 months, and 8 patients (73%) had onset less than 1 year old. All patients had multiple nodules in the brain. Except for the brain, the changes of the other organs were polycystic kidney and skin changes in 2 patients, skin changes in 8 patients, and normal in 1 patients. ConclusionTSC patients with peripheral blood gene negative who have young onset age, frequent seizures, and multiple nodules on MRI often present with refractory epilepsy. However, the postoperative effect is good, and the postoperative EEG of most patients is normal.

    Release date:2024-07-03 08:46 Export PDF Favorites Scan
  • The expression of EPO-R, JAK2 and STAT-5 in the human brain with refractory epilepsy

    Objective The purpose of this study was to explore the expressions of EPO-R, JAK2 and STAT-5 in the human brain with refractory epilepsy and the role in neural apotosis. Methods Collecting the brain tissue of 24 patients with intractable epilepsy (as experimental group) who were hospitalized and underwent surgery in the Epilepsy Center of the First Hospital Jilin University between March 2010 to July 2011 and 6 cases of accidental or unnatural death immediately following autopsy (as control group) as required by law during the same term. Immunohistochemical was performed to observe the expression of EPO-R, JAK2 and STAT-5 in brain tissue and statistical analysis was performed. Results ① EPO-R, JAK2 and STAT-5 were expressed in both experimental and control groups. In experimental group, the positive-cell number were 41.05±2.40, 50.21±2.50 and 60.18±2.84 under light microscope (400×). While in control group, the positive-cell number were 23.00±0.49, 27.00±0.88 and 25.93±0.33. There were significant differences between the 2 groups (P<0.001). ② There were the pathologic and ultrastructural changes in the human brain with refractory epilepsy. Under the optical microscope, we can observe that the distribution of neurons was uneven and immature neurons were visible. We can see that the nuclei were vacuolar, less cytoplasm, dark staining, hyalomitome acidophilic body, and the neurons became triangular due to degeneration. The proliferation and hyperemia appeared in small vascular and glial cells. Under the transmission electron microscope we observed degeneration and necrosis of the nerve cells, nuclear karyopyknosis, nucleolis dyssymmetry and karyolemma breakage and even dissolution. The mitochondria and astrocytes were swelling. We also saw that part of the mitochondrial cristae was abnormal. Conclusion ① We found neuronal apotosis in the human brain with refractory epilepsy. ② The expression of EPO-R, JAK2 and STAT-5 in intractable epilepsy was significantly increased in neurons and glial cells compared with the control group. The high expression of EPO-R, JAK2 and STAT-5 is unrelated with course and frequency of epileptic seizures. ③ The pathway of EPO-R/JAK2/STAT-5 may be involved in the pathophysiological processes of neural protective effect of endogenous EPO against brain injury induced by epileptic seizures.

    Release date:2018-11-21 02:23 Export PDF Favorites Scan
  • 经典生酮饮食和改良阿特金斯饮食治疗儿童难治性癫痫的效果比较

    研究旨在比较改良阿特金斯饮食(Modified Atkins diet,MAD)和经典生酮饮食(Ketogenic diet,KD)在治疗儿童难治性癫痫的疗效、安全性和耐受性。研究纳入 2011 年 3 月—2014 年 3 月就诊的 1~18 岁难治性癫痫患者,将其随机分配至一种饮食治疗组(ClinicalTrials.gov,编号 NCT2100501)。痫性发作记录被用于比较饮食治疗后 3、6 个月痫性发作频率与饮食治疗前基线发作频率。研究纳入 KD 组 51 例患者,MAD 组 53 例患者。KD 组平均基线痫性发作百分比在治疗后 3 个月(KD 组 38.6%,MAD 组 47.9%)和 6 个月(KD 组 33.8%,MAD 组 44.6%)均低于 MAD 组,但差异无统计学意义[3 个月,95%CI (24.1,50.8),P=0.291;6 个月,95%CI(17.8,46.1),P=0.255]。然而,在<2 岁患儿中,KD 组痫性发作控制效果优于 MAD 组。这些患者饮食治疗开始的 3 个月内,KD 组癫痫无发作率高于 MAD 组,差异有统计学意义(KD 组 53%,MAD 组 20%,P=0.047)。MAD 组耐受性更好并且副反应更少。MAD 可能是治疗儿童难治性癫痫的首要选择,但经典 KD 更适合<2 岁患者的一线饮食治疗方案。

    Release date:2018-01-20 10:51 Export PDF Favorites Scan
  • Efficacy and predictive factors analysis of vagus nerve stimulation in patients with refractory MRI-negative epilepsy

    ObjectiveTo investigate the efficacy of vagus nerve stimulation (VNS) in patients with refractory magnetic resonance imaging (MRI)-negative epilepsy and to evaluate potential clinical predictors. MethodsA retrospective collection of efficacy data was conducted on 24 patients with intractable MRI-negative epilepsy treated with VNS, who were followed up for more than six months, at Beijing Tiantan Hospital and Beijing Fengtai Hospital from January 2016 to September 2023. Patients were divided into two subgroups based on their response to VNS: responders (≥50% reduction in seizure frequency) and non-responders (<50% reduction in seizure frequency). The relationship between preoperative clinical data and VNS efficacy was further analyzed to identify potential predictors of VNS efficacy. ResultsA total of 24 patients were included, with an average age of (14.26±8.39) years old. Seizure frequency was reduced by more than 50% in 37.5% of patients, and 8.3% of patients achieved seizure-free after VNS treatment. Preoperative seizure frequency and interictal epileptiform discharge type were significantly associated with VNS efficacy (P<0.05). Multivariate regression analysis showed that a monthly seizure frequency of less than 100 and focal interictal epileptiform discharges were independent predictors of VNS efficacy (P<0.05). ConclusionVNS is an effective treatment for patients with refractory MRI-negative epilepsy. Lower monthly seizure frequency and focal interictal epileptiform discharges are potential predictors of VNS efficacy. These findings provide important references for clinicians in selecting and evaluating patients for VNS treatment.

    Release date:2024-08-23 04:11 Export PDF Favorites Scan
  • 精准医疗在难治性癫痫中的现状

    癫痫是常见的神经系统疾病,其中高达 30% 的患者为药物难治性癫痫,不仅给患者造成身心的危害,也增加了社会、家庭的负担。而单纯依据临床特征和现行癫痫用药指南的给药方案,难以获得满意的治疗效果。随着基因测序技术的发展,越来越多的癫痫致病基因得以发现,可以精确地帮助医生明确癫痫发生的机制,辅助临床选择适合的个体化治疗方案,把握治疗时机。

    Release date:2019-05-21 08:51 Export PDF Favorites Scan
  • 芬氟拉明治疗难治性癫痫的研究进展

    癫痫是神经科常见病,60%在儿童期起病,最终有20%~30%发展为药物难治性癫痫。难治性癫痫是指在使用正确选择且能耐受的两种抗癫痫发作药物的情况下仍不能终止其发作的癫痫,儿童以Lennox-Gastaut综合征(Lennox-Gastaut syndrome,LGS)、Dravet综合征(Dravet syndrome,DS)等为代表,成人以颞叶癫痫为代表。难治性癫痫具有“低治愈率、高致残率、高致死率”的特点,给患者及家属造成巨大的生理和心理上的痛苦。目前,离子类抗癫痫发作药物已难在机制上实现重大突破,而非离子类抗癫痫发作药物的研究则具有广阔的前景,其机制可能涉及癫痫发生的根本机制,而近年来获批上市的芬氟拉明(Fenfluramine,FFA)就属于此类抗癫痫发作药物。多个Ⅲ期随机对照试验研究提示FFA对DS、LGS具有卓越的有效性,为难治性癫痫患者及家属带来了新希望。本文从FFA治疗难治性癫痫的作用机制、药动学、临床疗效、安全性及耐受性等方面进行综述。

    Release date:2023-01-04 02:32 Export PDF Favorites Scan
  • 外科手术与药物治疗对于难治性癫痫患者发作控制外的结局指标的比较

    约有1/3的癫痫患者发展为耐药性癫痫, 控制达无发作的可能性随着添加药物而降低。经适当筛选的患者, 癫痫手术增加了其达到无发作并彻底停药的可能性。癫痫手术和药物治疗一样, 并非没有副作用。为了给病人提供明智、全面的建议, 医疗人员需要了解这两种治疗的优势和劣势。随机对照试验结果显示对于颞叶癫痫, 手术比持续药物治疗效果更好。虽然所有治疗的最终目标都是无发作, 但它只代表了各种影响患者生活质量的其中一个预后指标。了解影响预后指标的变量以及预后指标间如何相互影响是有必要的。关于比较手术治疗与药物治疗难治性癫痫的研究数据有限, 对治疗结局相关指标的数据进行了回顾。这些结局指标除无发作以外, 还包括生活质量、认知、社会心理功能、死亡率及经济成本等

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