Assessment of Seizure Action Plans in Pediatric Convulsive Status Epilepticus: Focus on Benzodiazepine-Responsive and Resistant Cases.

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-06-01 Epub Date: 2025-04-01 DOI:10.1212/CPJ.0000000000200449
Coral M Stredny, Sahar Rostamian, Theodore Alexander Sheehan, Marina Gaínza-Lein, Shannon Carey, Samuel Lewis, Justice Clark, Bethany Bucciarelli, Madeline Chiujdea, Annalee Antonetty, Bo Zhang, Luisa Fernanda Atunes Ortega, Lillian Voke, Tobias Loddenkemper
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引用次数: 0

Abstract

Background and objectives: Optimal acute treatment is crucial in pediatric convulsive status epilepticus (CSE). However, data on the benefits of seizure action plans (SAPs) and treatment algorithm implementation in relation to process and outcome measures in CSE are scarce. Our study examines treatment algorithm adherence in benzodiazepine (BZD)-responsive and BZD-resistant groups and specifically focuses on the relationship with personalized SAPs.

Methods: We performed a prospective observational cohort study evaluating patient care processes and outcomes in young patients with CSE lasting ≥5 minutes, requiring admission and an antiseizure medication(s) (ASM) for seizure termination from February 2016 to July 2018. Patients with infantile spasms, invasive EEG monitoring, unclear seizure duration, unclear ASM administration time, or seizure cluster were excluded. We used univariate statistics to analyze the data.

Results: We enrolled 60 patients (median age 3.7 [1.9-7.0] years, 48% female), including 34 BZD-responsive and 26 BZD-resistant patients. Patients who had access to a personalized SAP, even if it was not adhered to, experienced a median (p25-p75) time to first ASM of 6 minutes (5-18; n = 34). By contrast, patients without access to a personalized SAP had a longer median (p25-p75) time to the first ASM of 15 minutes (8-27; n = 24; p < 0.05). The median (p25-p75) time to administer the first ASM was 6 (5-15; n = 33) minutes in BZD-responsive patients vs 15 (6-32; n = 25; p < 0.05) minutes in BZD-resistant patients. Treatment protocol implementation rates were lower in BZD-resistant vs BZD-responsive patients. The median (p25-p75) time to administer the first ASM was 5 minutes (4-5; n = 14) in patients who implemented a personalized SAP compared with 16 minutes (6-31; n = 20; p < 0.001) in patients without SAP implementation. The median (p25-p75) seizure duration in personalized SAP implementation and nonimplementation groups was 9 (6-16; n = 14) and 22 (11-64; n = 20; p < 0.01) minutes, respectively. The intubation rate was 14% for those who implemented the personalized SAP and 53% for those who did not (p < 0.05).

Discussion: Seizure duration was shorter in patients with personalized SAP, and the time to administer ASM was faster. In addition, BZD-resistant patients were less likely to follow treatment protocols, and the time to first-line therapy was slower. SAP and algorithm implementation was associated with a lower intubation rate, indicating potential benefits, including improved process and patient outcome measures.

评估癫痫持续状态儿童癫痫发作行动计划:关注苯二氮卓类药物反应和抵抗病例。
背景和目的:小儿癫痫持续状态(CSE)的最佳急性治疗是至关重要的。然而,关于癫痫发作行动计划(sap)和治疗算法实施与CSE的过程和结果测量相关的益处的数据很少。我们的研究检查了苯二氮卓类药物(BZD)反应组和BZD耐药组的治疗算法依从性,并特别关注与个性化sap的关系。方法:我们进行了一项前瞻性观察队列研究,评估了2016年2月至2018年7月期间持续≥5分钟的年轻CSE患者的患者护理过程和结果,这些患者需要入院并服用抗癫痫药物(ASM)以终止癫痫发作。排除有婴儿痉挛、有创脑电图监测、癫痫发作持续时间不明确、ASM给药时间不明确或癫痫发作聚集的患者。我们使用单变量统计来分析数据。结果:我们纳入了60例患者(中位年龄3.7[1.9-7.0]岁,48%为女性),其中34例bzd应答,26例bzd耐药。有机会使用个性化SAP的患者,即使没有坚持使用,到首次ASM的中位时间(p25-p75)为6分钟(5-18;N = 34)。相比之下,没有获得个性化SAP的患者到第一次ASM的中位时间(p25-p75)更长,为15分钟(8-27;N = 24;P < 0.05)。给予第一次ASM的中位时间(p25-p75)为6 (5-15;bzd应答患者n = 33分钟vs 15分钟(6-32;N = 25;p < 0.05) min。bzd耐药患者与bzd应答患者的治疗方案执行率较低。给予第一次ASM的中位时间(p25-p75)为5分钟(4-5;n = 14),与16分钟(6-31;N = 20;p < 0.001)。个性化SAP实施组和非实施组的癫痫发作持续时间中位数(p25-p75)为9 (6-16;N = 14)和22 (11-64;N = 20;P < 0.01) min。实施个性化SAP的患者插管率为14%,未实施个性化SAP的患者插管率为53% (p < 0.05)。讨论:个体化SAP患者的癫痫发作时间更短,给药时间更快。此外,bzd耐药患者不太可能遵循治疗方案,一线治疗的时间也较慢。SAP和算法的实施与较低的插管率相关,表明潜在的益处,包括改进的流程和患者结果测量。
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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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