Jackson Melinda L, Kennedy Gerard A, Clarke Catherine, Gullo Melissa, Swann Philip, Downey Luke A, Hayley Amie C, Pierce Rob J, Howard Mark E
Institute for Breathing and Sleep, Department of Respiratory and Sleep Medicine, Austin Health, Australia; RMIT University, School of Health Sciences and Health Innovations Research Institute, Bundoora, Australia.
Institute for Breathing and Sleep, Department of Respiratory and Sleep Medicine, Austin Health, Australia; Cairnmillar Institute, Melbourne, Australia.
Accid Anal Prev. 2016 Feb;87:127-33. doi: 10.1016/j.aap.2015.11.033. Epub 2015 Dec 10.
Slowed eyelid closure coupled with increased duration and frequency of closure is associated with drowsiness. This study assessed the utility of two devices for automated measurement of slow eyelid closure in a standard poor performance condition (alcohol) and following 12-h sleep deprivation. Twenty-two healthy participants (mean age=20.8 (SD 1.9) years) with no history of sleep disorders participated in the study. Participants underwent one baseline and one counterbalanced session each over two weeks; one 24-hour period of sleep deprivation, and one daytime session during which alcohol was consumed after a normal night of sleep. Participants completed a test battery consisting of a 30-min simulated driving task, a 10-min Psychomotor Vigilance Task (PVT) and the Karolinska Sleepiness Scale (KSS) each in two baseline sessions, and in two randomised, counterbalanced experimental sessions; following sleep deprivation and following alcohol consumption. Eyelid closure was measured during both tasks using two automated devices (Copilot and Optalert™). There was an increase in the proportion of time with eyelids closed and the Johns Drowsiness Score (incorporating relative velocity of eyelid movements) following sleep deprivation using Optalert (p<0.05 for both). These measures correlated significantly with crashes, PVT lapses and subjective sleepiness (r-values 0.46-0.69, p<0.05). No difference between the two sessions for PERCLOS recorded during the PVT or the driving task as measured by the Copilot. The duration of eyelid closure predicted frequent lapses following sleep deprivation (which were equivalent to the average lapses at a blood alcohol concentration of 0.05% - area under curve for ROC curve 0.87, p<0.01). The duration of time with slow eyelid closure, assessed by the automated devices, increased following sleep deprivation and was associated with deterioration in psychomotor performance and subjective sleepiness. Comprehensive algorithms inclusive of ocular parameters may be a better indicator of performance impairment following sleep loss.
眼睑闭合减慢,同时闭合持续时间和频率增加,与嗜睡有关。本研究评估了两种设备在标准不良表现条件(酒精)下以及12小时睡眠剥夺后自动测量缓慢眼睑闭合的效用。22名无睡眠障碍病史的健康参与者(平均年龄=20.8(标准差1.9)岁)参与了该研究。参与者在两周内分别进行一次基线和一次平衡实验;一次24小时睡眠剥夺,一次白天实验,在正常睡眠一晚后饮用酒精。参与者在两个基线实验、两个随机、平衡的实验中分别完成一组测试,包括30分钟模拟驾驶任务、10分钟心理运动警觉任务(PVT)和卡罗林斯卡嗜睡量表(KSS);分别在睡眠剥夺后和饮酒后进行。在两项任务中使用两种自动设备(副驾驶和Optalert™)测量眼睑闭合情况。使用Optalert在睡眠剥夺后,眼睑闭合时间比例和约翰斯嗜睡评分(包括眼睑运动的相对速度)增加(两者p<0.05)。这些测量结果与撞车、PVT失误和主观嗜睡显著相关(r值0.46 - 0.69,p<0.05)。由副驾驶测量的PVT或驾驶任务期间记录的PERCLOS在两次实验之间没有差异。眼睑闭合持续时间可预测睡眠剥夺后的频繁失误(相当于血液酒精浓度为0.05%时的平均失误 - ROC曲线下面积为0.87,p<0.01)。通过自动设备评估的缓慢眼睑闭合持续时间在睡眠剥夺后增加,并且与心理运动表现和主观嗜睡的恶化有关。包含眼部参数的综合算法可能是睡眠不足后表现受损的更好指标。