创伤后遗忘症和创伤性脑损伤早期恢复期间的睡眠障碍。

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY
Journal of neurotrauma Pub Date : 2024-08-01 Epub Date: 2024-05-06 DOI:10.1089/neu.2023.0656
Bianca Fedele, Gavin Williams, Dean McKenzie, Robert Giles, Adam McKay, John Olver
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引用次数: 0

摘要

中度至重度创伤性脑损伤(TBI)后,睡眠障碍通常会在混乱的创伤后遗忘(PTA)恢复阶段出现。然而,对 PTA 期间早期睡眠障碍、其恢复轨迹和影响因素的评估十分有限。本研究的目的是利用非卧床黄金标准多导睡眠图(PSG)和唾液内源性褪黑激素(一种影响睡眠-觉醒周期的激素)两个时间点评估 PTA 患者的睡眠结果。此外,还评估了 PSG 导出的睡眠-觉醒参数与 PTA 症状(即躁动和认知障碍)之间的关系。在一个患者子集中,在 PTA 缓解后重复 PSG,以评估睡眠障碍的轨迹。PTA 的参与者是从 Epworth HealthCare 的创伤性脑损伤康复住院部招募的。训练有素的护士在患者床边使用 Compumedics Somté 便携式 PSG 设备(Compumedics Ltd,澳大利亚)进行夜间 PSG。PTA 缓解两周后,再次进行 PSG 检查。在另外一个晚上,采集了两份唾液样本(24:00 和 06:00)用于褪黑激素测试。此外,还收集了医院的日常常规指标(即躁动行为量表和韦斯特米德 PTA 量表)。29 名患者接受了 PSG 监测(平均值:创伤后 41.6 天;标准差 [SD]:28.3)。患者的平均睡眠时间缩短(5.6 小时,标准差:1.2),且睡眠碎片化,频繁觉醒(平均:27.7,标准差:15.0)。深慢波恢复性睡眠减少或完全消失(37.9% 的患者)。PSG 的使用似乎并未加剧患者的躁动或认知障碍。两个时间点的平均褪黑激素水平普遍超出正常参考范围。PTA 解除后,患者(11 人)的平均睡眠时间明显延长(5.3 小时 [PTA 前];6.5 小时 [PTA 外],平均值之间的差异:1.2,P=.005)。然而,PTA 解除后,其他睡眠-觉醒参数(如觉醒次数、觉醒时间和睡眠潜伏期增加)的干扰仍然存在。这是第一项评估患者在创伤性脑损伤早期恢复阶段的睡眠障碍的研究。目前,PTA 并不属于医院常规评估的一部分,因此显然需要对 PTA 期间的睡眠障碍进行有针对性的评估,以提出新的治疗范例,促进患者康复并减少其长期影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sleep Disturbance During Post-Traumatic Amnesia and Early Recovery After Traumatic Brain Injury.

After moderate to severe traumatic brain injury (TBI), sleep disturbance commonly emerges during the confused post-traumatic amnesia (PTA) recovery stage. However, the evaluation of early sleep disturbance during PTA, its recovery trajectory, and influencing factors is limited. This study aimed to evaluate sleep outcomes in patients experiencing PTA using ambulatory gold-standard polysomnography (PSG) overnight and salivary endogenous melatonin (a hormone that influences the sleep-wake cycle) assessment at two time-points. The relationships between PSG-derived sleep-wake parameters and PTA symptoms (i.e., agitation and cognitive disturbance) were also evaluated. In a patient subset, PSG was repeated after PTA had resolved to assess the trajectory of sleep disturbance. Participants with PTA were recruited from Epworth HealthCare's inpatient TBI Rehabilitation Unit. Trained nurses administered overnight PSG at the patient bedside using the Compumedics Somté portable PSG device (Compumedics, Ltd., Australia). Two weeks after PTA had resolved, PSG was repeated. On a separate evening, two saliva specimens were collected (at 24:00 and 06:00) for melatonin testing. Results of routine daily hospital measures (i.e., Agitated Behavior Scale and Westmead PTA Scale) were also collected. Twenty-nine patients were monitored with PSG (mean: 41.6 days post-TBI; standard deviation [SD]: 28.3). Patients' mean sleep duration was reduced (5.6 h, SD: 1.2), and was fragmented with frequent awakenings (mean: 27.7, SD: 15.0). Deep, slow-wave restorative sleep was reduced, or completely absent (37.9% of patients). The use of PSG did not appear to exacerbate patient agitation or cognitive disturbance. Mean melatonin levels at both time-points were commonly outside of normal reference ranges. After PTA resolved, patients (n = 11) displayed significantly longer mean sleep time (5.3 h [PTA]; 6.5 h [out of PTA], difference between means: 1.2, p = 0.005). However, disturbances to other sleep-wake parameters (e.g., increased awakenings, wake time, and sleep latency) persisted after PTA resolved. This is the first study to evaluate sleep disturbance in a cohort of patients as they progressed through the early TBI recovery phases. There is a clear need for tailored assessment of sleep disturbance during PTA, which currently does not form part of routine hospital assessment, to suggest new treatment paradigms, enhance patient recovery, and reduce its long-term impacts.

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来源期刊
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
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