KCNQ2和KCNQ3新生儿癫痫的独特振幅积分脑电图发作模式和卡马西平靶向治疗:一系列病例。

IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY Neuropediatrics Pub Date : 2024-02-01 Epub Date: 2023-10-12 DOI:10.1055/a-2190-9521
Ana Vilan, Ana Grangeia, José Mendes Ribeiro, Maria Roberta Cilio, Linda S de Vries
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引用次数: 0

摘要

背景:卡马西平(CBZ)可有效治疗KCNQ2/3相关癫痫,该癫痫可能表现出独特的aEEG模式。目的:评估如何提高对与KCNQ2/3变异相关的独特aEEG发作模式的识别,从而使CBZ能够早期有效地进行靶向治疗。方法:对5名在三级新生儿重症监护室(NICU)住院的KCNQ2/3致病基因变异新生儿进行为期8年的回顾性描述性研究。结果:4名新生儿在首次临床电性发作后平均61.5小时(最短12小时,最长120小时)发现了独特的发作aEEG模式,并促使使用CBZ,这在所有情况下都是有效的。最近确诊的两名患者可以避免多种治疗,因为他们分别接受CBZ作为第一种和第二种抗癫痫药物(ASM)。持续正常电压(CNV)、睡眠-觉醒周期(SWC)和发作后抑制时间较短的五分之三的患者神经发育结果正常。关于其余两名婴儿,其中一名婴儿未接受CBZ试验,癫痫发作负担高,两名婴儿都表现出长期的发作后抑制,没有SWC,并有中度至重度发育迟缓。除了一名有产前诊断的婴儿外,所有婴儿在新生儿期后都有遗传结果。结论:在新生儿重症监护室识别出独特的发作性脑电模式后,早在遗传结果出来之前,CBZ就可以对四名新生儿进行早期有效的靶向治疗。此外,具有SWC和短暂发作后抑制的CNV背景模式与正常发育结果相关。
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Distinctive Amplitude-Integrated EEG Ictal Pattern and Targeted Therapy with Carbamazepine in KCNQ2 and KCNQ3 Neonatal Epilepsy: A Case Series.

Background: Carbamazepine (CBZ) is effective in treating KCNQ2/3-related seizures, which may present with a distinctive amplitude-integrated electroencephalography (aEEG) pattern.

Objective: To assess how improved recognition of the distinctive aEEG ictal pattern associated with KCNQ2/3 variants has enabled early and effective targeted therapy with CBZ.

Methods: Retrospective descriptive study of five neonates with KCNQ2/3 pathogenic gene variants admitted at a level 3 neonatal intensive care unit (NICU) over an 8-year period.

Results: The distinctive ictal aEEG pattern was recognized in four neonates after an average of 61.5 hours (minimum 12 hours, maximum 120 hours) from the first electroclinical seizure and prompted the use of CBZ that was effective in all. The two most recently diagnosed patients could avoid polytherapy as they received CBZ as the first and second antiseizure medication, respectively. Three out of five patients with continuous normal voltage (CNV), sleep-wake cycling (SWC), and shorter postictal suppression had normal neurodevelopmental outcome. Regarding the remaining two infants, one was not trialed with CBZ and had a high seizure burden, both presented with a prolonged postictal suppression, no SWC, and had moderate-to-severe developmental delay. Genetic results became available after the neonatal period in all but one of the infants, who had a prenatal diagnosis.

Conclusion: Recognition of the distinctive ictal aEEG pattern in the NICU allowed early and effective targeted therapy with CBZ in four neonates, well before genetic results became available. Furthermore, a CNV background pattern with SWC and short postictal suppression were associated with normal developmental outcomes.

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来源期刊
Neuropediatrics
Neuropediatrics 医学-临床神经学
CiteScore
2.80
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: For key insights into today''s practice of pediatric neurology, Neuropediatrics is the worldwide journal of choice. Original articles, case reports and panel discussions are the distinctive features of a journal that always keeps abreast of current developments and trends - the reason it has developed into an internationally recognized forum for specialists throughout the world. Pediatricians, neurologists, neurosurgeons, and neurobiologists will find it essential reading.
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