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Evaluation of positive and negative predictors of seizure outcomes among patients with immune-mediated epilepsy: a meta-analysis

机译:免疫介导的癫痫患者癫痫发作结果的阳性和阴性预测指标的评估:一项荟萃分析

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The objective of this study was to analyze published literature on autoimmune epilepsy and assess predictors of seizure outcome. From PubMed and EMBASE databases, two reviewers independently identified publications reporting clinical presentations, management and outcomes of patients with autoimmune epilepsy. A meta-analysis of 46 selected studies was performed. Demographic/clinical variables (sex, age, clinical presentation, epilepsy focus, magnetic resonance imaging [MRI] characteristics, time to diagnosis and initiation of immunomodulatory therapy, and type of immunomodulatory therapy) were compared between two outcome groups (responders and nonresponders). Clinical response was defined as >50% reduction in seizure frequency. Unstandardized effect sizes were collected for the studies for responder and nonresponder groups. Sample size was used as the weight in the meta-analysis. The random effects model was used to account for heterogeneity in the studies. The 46 reports included 186 and 96 patients in responder and nonresponder groups respectively. Mean age of the responders and nonresponders was 43 and 31 years (p 0.01). Responders were more likely to have cell-surface antibodies (68% versus 39%, p 0.05), particularly voltage-gated potassium channel complex antibodies (p 0.01). Mean duration from symptom onset to diagnosis, and symptom onset to initiation of immunomodulation was significantly lower among the responders (75 versus 431 days, p 0.05, and 80 versus 554, p 0.01, respectively). There was no outcome difference based on gender, MRI characteristics, seizure type, type of acute immunomodulatory therapy, or use of chronic immunomodulation. Among published cases to date, older age, presence of cell-surface antibodies, early diagnosis and immunomodulatory treatment are associated with better seizure outcomes among patients with autoimmune epilepsy.
机译:这项研究的目的是分析关于自身免疫性癫痫的已发表文献并评估癫痫发作结果的预测因子。两位审查者从PubMed和EMBASE数据库中独立确定了报告自身免疫性癫痫患者的临床表现,治疗和结果的出版物。对46项选定研究进行荟萃分析。比较了两个结局组(应答者和非应答者)的人口统计学/临床变量(性别,年龄,临床表现,癫痫病灶,磁共振成像[MRI]特征,诊断和开始免疫调节疗法的时间以及免疫调节疗法的类型)。临床反应定义为癫痫发作频率降低> 50%。收集了非标准化效应量用于研究反应者和非反应者组。样本量用作荟萃分析中的权重。随机效应模型用于解释研究中的异质性。 46份报告分别包括有反应者和无反应者组的186和96位患者。有反应者和无反应者的平均年龄分别为43岁和31岁(P = 0.01)。反应者更可能具有细胞表面抗体(68%比39%,p 0.05),特别是电压门控钾通道复合物抗体(p 0.01)。在应答者中,从症状发作到诊断的平均持续时间以及从症状发作到开始免疫调节的平均持续时间显着降低(分别为75天和431天,分别为p 0.05和80 vs 554,分别为p 0.01)。根据性别,MRI特征,癫痫发作类型,急性免疫调节疗法的类型或慢性免疫调节的使用,结果无差异。在迄今已发表的病例中,年龄较大,细胞表面抗体的存在,早期诊断和免疫调节治疗与自身免疫性癫痫患者的癫痫发作预后较好相关。

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