Wearable sensors in paediatric neurology.

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Camila González Barral, Laurent Servais
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引用次数: 0

Abstract

Wearable sensors have the potential to transform diagnosis, monitoring, and management of children who have neurological conditions. Traditional methods for assessing neurological disorders rely on clinical scales and subjective measures. The snapshot of the disease progression at a particular time point, lack of cooperation by the children during assessments, and susceptibility to bias limit the utility of these measures. Wearable sensors, which capture data continuously in natural settings, offer a non-invasive and objective alternative to traditional methods. This review examines the role of wearable sensors in various paediatric neurological conditions, including cerebral palsy, epilepsy, autism spectrum disorder, attention-deficit/hyperactivity disorder, as well as Rett syndrome, Down syndrome, Angelman syndrome, Prader-Willi syndrome, neuromuscular disorders such as Duchenne muscular dystrophy and spinal muscular atrophy, ataxia, Gaucher disease, headaches, and sleep disorders. The review highlights their application in tracking motor function, seizure activity, and daily movement patterns to gain insights into disease progression and therapeutic response. Although challenges related to population size, compliance, ethics, and regulatory approval remain, wearable technology promises to improve clinical trials and outcomes for patients in paediatric neurology.

儿童神经病学中的可穿戴传感器。
可穿戴传感器有可能改变患有神经系统疾病的儿童的诊断、监测和管理。评估神经系统疾病的传统方法依赖于临床量表和主观测量。在特定时间点对疾病进展的快速了解,儿童在评估过程中缺乏合作,以及易受偏见的影响,限制了这些措施的效用。可穿戴传感器可以在自然环境中连续捕获数据,为传统方法提供了一种非侵入性和客观的替代方案。这篇综述探讨了可穿戴传感器在各种儿科神经系统疾病中的作用,包括脑瘫、癫痫、自闭症谱系障碍、注意力缺陷/多动障碍,以及Rett综合征、唐氏综合征、Angelman综合征、Prader-Willi综合征、神经肌肉疾病,如杜氏肌营养不良症和脊髓性肌萎缩症、共济失调、戈谢病、头痛和睡眠障碍。该综述强调了它们在跟踪运动功能、癫痫发作活动和日常运动模式方面的应用,以深入了解疾病进展和治疗反应。尽管在人群规模、合规性、伦理和监管批准等方面仍存在挑战,但可穿戴技术有望改善儿科神经病学患者的临床试验和结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
13.20%
发文量
338
审稿时长
3-6 weeks
期刊介绍: Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA). For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.
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