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find Keyword "抗癫痫" 64 results
  • An analysis on clinical characteristics of 36 epileptics with pregnancy

    ObjectiveTo investigate the clinical characteristics of epileptics with pregnancy and then provide reference for standardized management of epileptics with pregnancy. MethodsFrom June 2012 to June 2021, epileptics with pregnancy who delivered in Jinan Central Hospital were selected as the research subjects. The clinical data such as the application of Antiseizure medications (ASMs) during pregnancy, seizure frequency, pregnancy outcomes, delivery ways, offspring feeding ways and the incidence of complications were investigated and analyzed. ResultsAmong 36 epileptics with pregnancy, 20 cases (55.56%) were treated with ASMs alone, 5 cases (13.88%) were treated with combined medication, and 11 cases (30.56%) were treated without ASMs during pregnancy. 15 cases (41.67%) adhered to systematic application of ASMs, 17 cases (47.22%) did not adhere to systematic application of ASMs, and 4 cases (11.11%) had unknown medication history. The frequency of seizures increased in 5 cases, decreased in 7 cases and unchanged in 24 cases during pregnancy. Pregnancy outcomes: full-term delivery in 33 cases (91.67%), preterm delivery in 1 case (2.78%) and abortion in 2 cases (5.56%). Delivery mode: cesarean section in 31 cases (91.18%), vaginal delivery in 3 cases (8.82%). After delivery, 4 cases (11.76%) were fed with milk powder and 30 cases (88.24%) were breast-fed. Complications: There were 6 cases complicated with anemia (16.67%), 5 cases complicated with gestational hypertension (13.89%), 3 cases complicated with gestational diabetes (8.33%), 4 cases complicated with premature rupture of membranes (11.11%), 2 cases complicated with fetal growth restriction (5.56%), 2 cases complicated with oligohydramnios (5.56%), 3 cases complicated with fetal distress (8.33%) and 3 cases complicated with neonatal asphyxia (8.33%). ConclusionsThe proportion of epileptics with pregnancy who were systematically treated with ASMs was low and the seizures were poorly controlled. There is a lack of standardized management for such patients in clinical practice.

    Release date:2022-06-27 04:41 Export PDF Favorites Scan
  • 2023美国癫痫学会年会荟萃报道(一)

    美国癫痫学会(American Epilepsy Society,AES)年会是每年一度国际癫痫学界及工业界最受关注的会议。本年度的AES年会自2023年12月1日在奥兰多召开,为期5天,讨论了目前最受关注的癫痫学术领域及重点突破。本系列文章将分为五期,分别对大会每日的精彩内容进行荟萃报道:本文对大会第一日学术议程的内容进行了整理汇总,重点内容包括癫痫及癫痫持续状态药物治疗进展,癫痫认知相关共病,额叶癫痫,癫痫靶向治疗等。

    Release date:2024-03-07 01:49 Export PDF Favorites Scan
  • 芳香族抗癫痫药物所致严重皮肤不良反应的研究进展

    芳香族抗癫痫药物(AEDs)所致皮肤不良反应在临床治疗过程中较为常见,其中严重皮肤不良反应可对患者的生命造成致死性威胁。现主要对芳香族AEDs所致严重皮肤不良反应的临床表现、可能机制及治疗方法等方面的研究进行综述,从而进一步指导合理用药避免其不良反应的发生。

    Release date:2017-07-26 04:06 Export PDF Favorites Scan
  • 癫痫患者更换抗癫痫药物后的预后分析:一项配对的前瞻性研究

    一系列单队列研究已对癫痫患者更换抗癫痫药物(AEDs)预后进行了分析。研究以对照研究方式第一次探究了这个问题,针对服用所有类型的AEDs的控制不佳和癫痫无发作的癫痫患者,通过配对前瞻性研究方法对这些结果作进一步补充。研究回顾9个月内所有的门诊患者以确定单药治疗局灶性癫痫患者。并将更换AEDs的患者作为病例组,维持原来单药治疗方案作为对照组。分别针对发作现状(前6个月内是否有癫痫发作)、目前AEDs和控制不佳的AEDs数量对病例组和对照组进行配对,并在6个月后评估结果。病例组中癫痫无发作患者(n=12) 在6个月随访期间癫痫发作复发率为16.7%,对照组为2.8%(n=36,P=0.11)。病例组中控制不佳癫痫患者(n=27) 在6个月随访期癫痫发作缓解率为37%,对照组为55.6%(n=27,P=0.18)。控制不佳癫痫患者中治疗失败的药物在2种或2种以上的患者更不容易在6个月内达到病情缓解(P=0.057)。AEDs的药理机制和改变AEDs剂量均对癫痫预后无影响。研究进一步对癫痫无发作患者进行评估,更换药物的患者比维持原药物治疗患者癫痫发作的复发风险高14%。与维持原来药物方案相比,更换AEDs对控制不佳癫痫患者来说并不可能更易获得缓解,说明癫痫缓解是疾病的自发性改变,而非药物作用。

    Release date:2017-09-26 05:09 Export PDF Favorites Scan
  • 儿童失神癫痫药物治疗预后的研究进展

    儿童失神癫痫(Childhood absence epilepsy,CAE)是由多种遗传病因引起的最常见的特发性全面性非惊厥性癫痫,与 CAE 预后相关的因素众多,但目前尚未有确切共识的指南供临床参考,本文对 CAE 患儿药物治疗、预后情况和预后影响因素作一综述,以期能为 CAE 患儿临床的诊疗实践提供一定的参考和意见。

    Release date:2021-12-30 06:08 Export PDF Favorites Scan
  • Efficacy and safety of new anti-epileptic drugs in the treatment of epilepsy: a meta-analysis

    ObjectiveTo systematically review the efficacy and safety of new anti-epileptic drugs in the treatment of epilepsy. MethodsPubMed, EMbase, The Cochrane Library, CNKI and WanFang Data databases were electronically searched to collect randomized controlled trials (RCTs) of new anti-epileptic drugs rufinamide, zonisamide, and perampanel in the treatment of epilepsy from January 2006 to May 2021. Two reviewers independently screened literature, extracted data and assessed the risk of bias of included studies; then, meta-analysis was performed by using RevMan 5.3 and Stata 16.0 software. ResultsA total of 16 RCTs involving 4 382 patients were included. The results of meta-analysis showed that the effective rate (RR=1.66, 95%CI 1.45 to 1.89, P<0.000 01) and seizure-free rate (RR=2.82, 95%CI 2.01 to 3.96, P<0.000 01) in new anti-epileptic drugs group were higher than those in the control group, while it did not increase the serious adverse events (RR=0.95, 95%CI 0.72 to 1.27, P=0.75). ConclusionCurrent evidence shows that new anti-epileptic drugs have trends of better effectiveness, and their safety is satisfactory. Due to limited quality and quantity of the included studies, more high-quality studies are needed to verify above conclusion.

    Release date:2022-12-22 09:08 Export PDF Favorites Scan
  • High anxiety level and the underlying reason of people with epilepsy during the outbreak of 2019 Novel Coronavirus Diseases

    ObjectiveTo investigate the anxious level of people with epilepsy (PWE) during the outbreak of 2019 Novel Coronavirus Diseases (COVID-19) and explore the reasons of anxiety.MethodsAn internet questionnaire survey were conducted on the anxiety state of PWE and health controls (HC) aged 18 to 45 years old between Feb 9, 2020 and Feb 17, 2020. The questionnaire included demographic information, general status and the State-Trait Anxiety Inventory (STAI).ResultsIn all, 148 PWE and 300 HC were included in this study. The total SAI score (46.72±9.98 vs. 41.77±10.20, P<0.001) and the total TAI score (44.18±8.88 vs. 31.27±17.44, P<0.001) were significantly higher in PWE than in HC. PWE concerned most (69.9%) about the difficulty of obtaining antiepileptic drugs (AEDs) while HC concerned most about the lack of face masks (73.3%).ConclusionHigh anxious level in PWE during the outbreak of COVID is probably due to the difficulty of obtaining AEDs. Thus, the society should strengthen the solution of the problem of purchasing AEDs and conduct timely psychological counseling.

    Release date:2020-05-19 01:07 Export PDF Favorites Scan
  • 癫痫患儿注意缺陷多动障碍筛查、诊断和管理的系统评价:国际抗癫痫联盟儿科委员会共病工作组共识

    注意缺陷多动障碍(Attention-deficit/hyperactivity disorder,ADHD)是癫痫患儿一种常见且富有挑战的共患病。国际抗癫痫联盟(ILAE)儿科委员会共病工作组发现,关键问题在于识别和管理癫痫患儿中的 ADHD。对支持这些问题的方法的证据进行了系统评价,并根据美国神经病学学会实践参数的标准进行了整理和分级。遵循系统评价和 Meta 分析优先报告的条目(Preferred Reporting Items for Systematic Reviews and Meta-Analyses,PRISMA)要求,使用 PROSPERO 注册 (CRD42018094617)。与女性癫痫患儿相比,男性患儿无更高的共患 ADHD 风险(Level A)。孕期使用丙戊酸钠与子代注意力不集中和多动相关(1 项 I 级研究),且有智力和发育障碍的患儿合并 ADHD 的风险更高(A 级)。起病年龄对是否合并 ADHD 的影响尚不明确(U 级),但是发作控制欠佳的患儿合并 ADHD 的风险更高(B 级)。ADHD 的筛查应该从 6 岁或者明确诊断时开始,并且每年筛查一次(U 级),在抗癫痫药物调整后也应该重新评估(U 级)。ADHD 的诊断应该由受过 ADHD 专业培训的医务工作者参与(U 级)。支持使用优势和困难问卷筛查工具(B 级)。强烈建议有学习障碍的癫痫患儿进行正式的认知测试(U 级)。多药治疗的患儿出现行为问题的比例较单药治疗者更高(C 级)。丙戊酸钠可以加剧失神发作患儿的注意力集中障碍(A 级)。哌甲酯在癫痫患儿中耐受性及疗效均良好(B 级)。支持阿托莫西汀耐受性好的证据尚有限(C 级)。多学科参与过渡期和成人 ADHD 的诊治至关重要(U 级)。总之,虽然可以对一些研究问题提出建议,但这项系统评价强调了开展更全面、更有针对性的大样本前瞻性研究的必要性。

    Release date:2019-11-14 10:46 Export PDF Favorites Scan
  • 育龄期女性癫痫患者丙戊酸的选择策略

    鉴于丙戊酸(Valproate, VPA)宫内暴露的致畸风险及其对胎儿生长发育的影响, 2014年10月隶属于欧洲药品管理局(European Medicines Agency, EMA)的相互认证和分布处理协调小组(Coordination Group for Mutual Recognition and Decentralised Procedures-Human, CMDh)建议加强对女性使用VPA的限制, 随后国际抗癫痫联盟欧洲事务委员会(Commission on European Affairs of the International League Against Epilepsy, CEA-ILAE)及欧洲神经病学学会(European Academy of Neurology, EAN)组成的工作小组在《Epilepsia》上撰文, 旨在对育龄期女性使用VPA做出指导。撰文时, 工作小组充分考虑了使用VPA与其它替代药物的致畸风险、控制癫痫发作的重要性、癫痫发作对患者及胎儿的危害、VPA及其它抗癫痫药物对癫痫控制效力等因素。最终的建议包括以下7点:①育龄期女性应尽量避免使用VPA; ②应在医生及患者(必要时患者代理人)共同商议后决定治疗方案, 依据癫痫类型及发作形式选择合理的治疗方案时, 应仔细进行风险-获益评估; ③对于最适合VPA治疗的发作类型及综合征, 应该充分向患者及家属解释VPA及其它替代药物的获益和潜在风险; ④VPA不应作为局灶性癫痫的一线治疗药物; ⑤VPA或许可以作为治疗某些癫痫综合征的一线用药, 如特发性(遗传性)全面性癫痫伴有强直阵挛发作; ⑥VPA或许可作为生育可能性极小的女性癫痫患者的一线用药, 如合并严重的智力或身体残疾; ⑦应持续随访服用VPA的育龄期女性患者, 以确定最佳治疗方案

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  • Research progress of clinical application of perampanel

    Epilepsy is a common chronic disease of the nervous system, which has certain adverse effects on the cognitive, psychological and social functions of the patients. To date, anti-seizure medications (ASMs) remain the first-line treatment option for epilepsy, but many patients with epilepsy still do not have effective seizure control when multiple ASMs are used in combination. Therefore, there is an urgent need for a new target and mechanism ASMs to bring about new treatment options and hope for patients with intractable epilepsy. Perampanel, a new third-generation ASMs, whereas second-generation ASMs tend to exert anti-seizure effects mainly by regulating ion channels or enhancing related mechanisms such as gamma-aminobutyric acid (GABA) effects, perampanel exerts its effects mainly by targeting the excitatory neurotransmitter glutamate. Perampanel is the first selective α-amino-3-hydroxy-5-methyl-4-isoxazole-propionate (AMPA) receptor antagonist and the first selective inhibitory ASMs for excitatory postsynaptic function. Because of its unique target and mechanism, it has been approved by many countries in the world for adjuvant additive therapy and monotherapy for patients with focal and general epilepsy. In addition, with the discovery of the neuroprotective, antioxidant, neurotransmitter regulation effects of perampanel, it also provides a new potential choice for the treatment of other diseases. This article mainly reviews the mechanism of action, pharmacokinetics, clinical trials and treatment of other diseases other than epilepsy of perampanel.

    Release date:2023-05-04 04:20 Export PDF Favorites Scan
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