超难治性癫痫持续状态的诊断、管理和预后:一项国际调查研究。

IF 3.2 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-10-01 Epub Date: 2025-09-04 DOI:10.1212/CPJ.0000000000200520
Matthew Ryan Woodward, Jessica P Brown, Steven J Kittner, Neeraj Badjatia, Emily J Gilmore, Emily L Johnson, Nicholas A Morris
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引用次数: 0

摘要

背景和目的:目前缺乏超难治性癫痫持续状态(SRSE)的评估、管理和预后指南。对实践模式的描述可以确定未来调查的趋势和潜在领域。我们调查了管理SRSE的临床医生,以更好地了解SRSE评估、管理和预测的实践方法。方法:从2023年8月3日至2024年1月25日,我们对管理SRSE的临床医生进行了一项国际性的、包含66个问题的网络调查。我们收集了有关SRSE诊断和管理的数据。我们根据2个临床小插曲检查了预后方法。我们使用描述性统计和开发逻辑回归模型来确定与预测相关的关键因素。结果:245名受试者中,36名因无SRSE临床表现而被排除,209名被纳入;41名(20%)、66名(32%)和84名(40%)参与者分别是神经科医生、神经强化医生和普通强化医生,其中83%在美国执业。静脉麻醉治疗以咪达唑仑(n = 47, 38%)和异丙酚(n = 42, 34%)为一线,氯胺酮为二线(n = 34, 26%)和三线(n = 52, 41%)。关于静脉治疗的脑电图目标,爆发抑制(n = 96, 47%)或癫痫抑制(n = 70, 34%)最常见。这一目标在断奶前的中位数维持了49.5小时(四分位数范围为29.8-74小时)。关于预后,147名应答者中,75名(51%)报告了预测良好预后的能力,这与神经病学(OR: 4.4, 95% CI 1.5-13.5)或普通重症医师(OR: 4.6, 95% CI 1.6-14)实践与神经危重症护理(参考,少于5年的经验(OR: 3.9, 95% CI 1.6-10)有关;较高的年度SRSE病例负荷(OR: 2.9, 95% CI 1.7-7.3);使用临床严重程度评分(OR: 4.7, 95% CI 2-11.4)。确定无效的时间和建议停止生命维持治疗(WLST)遵循双峰分布,早期(0-4周)和延迟(26周)模式。预后乐观与延迟确定无效和推荐WLST相关(OR: 6.2, 95% CI 2.2-19.3)。讨论:在SRSE的评估和管理方面存在显著的可变性,包括治疗偏好、目标和治疗持续时间。预后与多种临床相关因素有关。预测的时间是高度可变的,并且与临床医生的乐观态度有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Super-Refractory Status Epilepticus Diagnosis, Management, and Prognostication: An International Survey Study.

Background and objectives: Guidelines for super-refractory status epilepticus (SRSE) evaluation, management, and prognostication are lacking. Characterization of practice patterns could identify trends and potential areas for future inquiry. We surveyed clinicians who manage SRSE to better understand practice approaches to SRSE evaluation, management, and prognostication.

Methods: We conducted an international cross-sectional 66-question, web-based survey of clinicians who manage SRSE, distributed through 4 scientific societies from August 3, 2023, through January 25, 2024. We collected data regarding SRSE diagnostics and management. We examined prognostic approaches based on 2 clinical vignettes. We characterized responses using descriptive statistics and developed logistic regression models to identify key factors associated with prognostication.

Results: Of 245 participants, 36 were excluded because of no clinical involvement with SRSE and 209 were included; 41 (20%), 66 (32%), and 84 (40%) participants were neurologists, neurointensivists, and general intensivists, respectively, 83% of whom practiced in the United States. For IV anesthetic treatment, midazolam (n = 47, 38%) and propofol (n = 42, 34%) were most often selected as first line while ketamine was most often 2nd (n = 34, 26%) or 3rd (n = 52, 41%) line. Regarding electroencephalography targets for IV treatment, burst suppression (n = 96, 47%) or seizure suppression (n = 70, 34%) was most popular. This goal was maintained for a median of 49.5 hours (interquartile range 29.8-74 hours) before weaning. Regarding prognostication, of 147 respondents, 75 (51%) reported an ability to predict favorable prognosis, which was associated with neurology (OR: 4.4, 95% CI 1.5-13.5) or general intensivist (OR: 4.6, 95% CI 1.6-14) practice vs neurocritical care (reference, fewer than 5 years of experience (OR: 3.9, 95% CI 1.6-10); higher annual SRSE case load (OR: 2.9, 95% CI 1.7-7.3); and use of clinical severity scores (OR: 4.7, 95% CI 2-11.4). Time to determine futility and recommendations for withdrawal of life-sustaining therapy (WLST) followed bimodal distributions, with early (0-4 weeks) and delayed (26 weeks) modes. Prognostic optimism was associated with delayed determination of futility and recommendation for WLST (OR: 6.2, 95% CI 2.2-19.3).

Discussion: There is significant variability in the evaluation and management of SRSE, including treatment preferences, targets, and duration of therapy. Prognostication is associated with multiple clinician-related factors. The timing of prognostication is highly variable and is associated with clinician optimism.

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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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