PANDABox-EEG在Angelman综合征中的远程EEG采集。

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Kimberly Gálvez-Ortega, Roslyn Harold, Wei Siong Neo, Orlando S Hoilett, Amanda M Borosh, Alexa Friesen-Haarer, Stephanie Gombas, Dan Foti, Bridgette Kelleher
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引用次数: 0

摘要

目的:我们描述了PANDABox-EEG的开发和验证,这是一种针对Angelman综合征(AS)量身定制的无需现场技术人员的远程脑电图评估新方案。我们认为,该方案是可靠的,有效的,并广泛接受用于家庭受天使综合征的影响。背景:AS是一种罕见的神经遗传疾病,其特征是发育迟缓、睡眠问题、癫痫发作和快乐的举止。AS患者经常通过脑电图监测以告知临床护理,脑电图测量的delta活动已被提出作为监测治疗效果的可靠生物标志物。由于需要前往医疗中心完成评估,传统的脑电图评估给家庭带来了后勤和经济负担。然而,远程医疗方法提供了一条前进的道路。方法:PANDABox-EEG是由心理学家、心理生理学家、工程师和特殊教育学者等多学科合作开发的,采用照顾者反馈和以用户为中心的设计原则。它将用于罕见疾病生物行为评估的远程医疗平台PANDABox与干电极脑电图系统配对。28名参与者(7名自闭症患者,7名兄弟姐妹,14名看护人)在一周内完成了3次5分钟的EEG会话。护理人员被要求对设计的可接受性提供反馈,脑电图数据被量化并评估其信度和效度。结果:PANDABox-EEG具有较高的可行性和可接受性,91%的护理人员满意度评价舒适。脑电图数据质量令人满意,具有较高的内部一致性(AS儿童的二分信度范围:r = 0.96 - 0.98)和delta幂的重测信度(AS儿童的重测信度范围:ρ = 0.88 - 0.96)。最后,我们成功地检测到AS的特征增加的δ功率(AS和非AS兄弟姐妹之间的效应量:d = 1.56-2.85)及其与年龄的关联(非AS兄弟姐妹和照顾者之间的效应量:d = 2.19-2.72)。结论:PANDABox-EEG为AS患者提供了一种可行、经济、可靠的远程脑电评估方法。它的高照顾者满意度和捕获相关神经生理标记的能力表明它有更广泛的应用潜力。经过进一步验证,PANDABox-EEG可以提高可及性和包容性,通过消除旅行的需要,有利于AS和其他需要频繁EEG监测的临床人群的临床管理和研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Remote EEG acquisition in Angelman syndrome using PANDABox-EEG.

Objective: We describe the development and validation of PANDABox-EEG, a novel protocol for remote EEG assessment with no on-site technician, tailored for Angelman syndrome (AS). We argue that this protocol is reliable, valid, and widely acceptable for use in families affected by Angelman syndrome.

Background: AS is a rare neurogenetic condition characterized by developmental delays, sleep problems, seizures, and a happy demeanor. People with AS are frequently monitored via EEG to inform clinical care, and EEG-measured delta activity has been proposed as a reliable biomarker to monitor treatment effectiveness. Traditional EEG assessments pose logistical and financial burdens for families due to the need to travel to a medical center to complete assessments. Telehealth methods, however, offer a pathway forward.

Methods: PANDABox-EEG was developed through multidisciplinary collaboration with psychologists, psychophysiologists, engineers, and special-education scholars, incorporating caregiver feedback and user-centered design principles. It pairs PANDABox, a telehealth platform for biobehavioral assessment in rare disorders, with a dry electrode EEG system. Twenty-eight participants (7 AS, 7 siblings, 14 caregivers) completed three 5-min EEG sessions each over the course of a week. Caregivers were asked to provide feedback on acceptability of the design, and EEG data was quantified and assessed for metrics of reliability and validity.

Results: PANDABox-EEG demonstrated high feasibility and acceptability, with 91% of caregivers reporting strong satisfaction assessment comfort. EEG data quality was promising, with high internal consistency (split-half reliability range for children with AS: r = .96-.98) and test-retest reliability for delta power among (test-retest reliability range for children with AS: ρ = .88-.96). Finally, we successfully detected the characteristic increased delta power in AS (effect size between AS and non-AS siblings: d = 1.56-2.85) and its association with age (effect size between non-AS siblings and caregivers: d = 2.19-2.72).

Conclusion: PANDABox-EEG provides a feasible, cost-effective, and reliable method for remote EEG assessment in AS. Its high caregiver satisfaction and ability to capture relevant neurophysiological markers suggest potential for broader application. With further validation, PANDABox-EEG can enhance accessibility and inclusivity, benefiting clinical management and research in AS and other clinical populations in need of frequent EEG monitoring by eliminating the need to travel.

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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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