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多模态夜间癫痫发作检测在癫痫儿童中的应用:一项前瞻性、多中心、长期、家庭内的试验。

Multimodal nocturnal seizure detection in children with epilepsy: A prospective, multicenter, long-term, in-home trial.

机构信息

Stichting Epilepsie Instellingen Nederland (SEIN), Heemstede and Zwolle, the Netherlands.

Department of Neurology and Clinical Neurophysiology, Leiden University Medical Center, Leiden, the Netherlands.

出版信息

Epilepsia. 2023 Aug;64(8):2137-2152. doi: 10.1111/epi.17654. Epub 2023 Jun 14.

Abstract

OBJECTIVE

There is a pressing need for reliable automated seizure detection in epilepsy care. Performance evidence on ambulatory non-electroencephalography-based seizure detection devices is low, and evidence on their effect on caregiver's stress, sleep, and quality of life (QoL) is still lacking. We aimed to determine the performance of NightWatch, a wearable nocturnal seizure detection device, in children with epilepsy in the family home setting and to assess its impact on caregiver burden.

METHODS

We conducted a phase 4, multicenter, prospective, video-controlled, in-home NightWatch implementation study (NCT03909984). We included children aged 4-16 years, with ≥1 weekly nocturnal major motor seizure, living at home. We compared a 2-month baseline period with a 2-month NightWatch intervention. The primary outcome was the detection performance of NightWatch for major motor seizures (focal to bilateral or generalized tonic-clonic [TC] seizures, focal to bilateral or generalized tonic seizures lasting >30 s, hyperkinetic seizures, and a remainder category of focal to bilateral or generalized clonic seizures and "TC-like" seizures). Secondary outcomes included caregivers' stress (Caregiver Strain Index [CSI]), sleep (Pittsburgh Quality of Sleep Index), and QoL (EuroQol five-dimension five-level scale).

RESULTS

We included 53 children (55% male, mean age = 9.7 ± 3.6 years, 68% learning disability) and analyzed 2310 nights (28 173 h), including 552 major motor seizures. Nineteen participants did not experience any episode of interest during the trial. The median detection sensitivity per participant was 100% (range = 46%-100%), and the median individual false alarm rate was .04 per hour (range = 0-.53). Caregiver's stress decreased significantly (mean total CSI score = 8.0 vs. 7.1, p = .032), whereas caregiver's sleep and QoL did not change significantly during the trial.

SIGNIFICANCE

The NightWatch system demonstrated high sensitivity for detecting nocturnal major motor seizures in children in a family home setting and reduced caregiver stress.

摘要

目的

在癫痫护理中,迫切需要可靠的自动癫痫发作检测。基于动态脑电图的癫痫发作检测设备的性能证据较低,而关于其对护理人员压力、睡眠和生活质量(QoL)影响的证据仍然缺乏。我们旨在确定在家庭环境中使用可穿戴夜间癫痫发作检测设备 NightWatch 在癫痫儿童中的性能,并评估其对护理人员负担的影响。

方法

我们进行了一项 4 期、多中心、前瞻性、视频对照、家庭内 NightWatch 实施研究(NCT03909984)。我们纳入了年龄在 4-16 岁之间、每周有≥1 次夜间主要运动性癫痫发作且居住在家中的儿童。我们将 2 个月的基线期与 2 个月的 NightWatch 干预期进行了比较。主要结局是 NightWatch 对主要运动性癫痫发作(局灶性到双侧或全面强直阵挛[TC]发作、局灶性到双侧或全面强直发作持续>30 秒、运动性发作和其余的局灶性到双侧或全面性阵挛性发作和“TC 样”发作)的检测性能。次要结局包括护理人员的压力(护理人员压力指数[CSI])、睡眠(匹兹堡睡眠质量指数)和 QoL(EuroQol 五维五分量表)。

结果

我们纳入了 53 名儿童(55%为男性,平均年龄为 9.7±3.6 岁,68%存在学习障碍),并分析了 2310 个夜晚(28173 小时),包括 552 次主要运动性癫痫发作。19 名参与者在试验期间均未经历任何感兴趣的发作。每名参与者的中位检测灵敏度为 100%(范围为 46%-100%),中位个体假警报率为每小时 0.04(范围为 0-.53)。护理人员的压力显著降低(总 CSI 评分的平均值为 8.0 与 7.1,p=0.032),而护理人员的睡眠和 QoL 在试验期间没有显著变化。

意义

NightWatch 系统在家庭环境中对儿童夜间主要运动性癫痫发作的检测具有高灵敏度,并降低了护理人员的压力。

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