EEG changes as an indication of central nervous system involvement following cyclopentolate 1% eye drops; a randomized placebo-controlled pilot study in a pediatric population.

IF 0.8 Q4 OPHTHALMOLOGY
Strabismus Pub Date : 2023-06-01 Epub Date: 2023-06-06 DOI:10.1080/09273972.2023.2218455
Helena Maria van Minderhout, Maurits Victor Joosse, Erica Surya Klaassen, Nicoline Elisabeth Schalij-Delfos
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引用次数: 0

Abstract

To compare EEG-patterns after instillation of cyclopentolate versus placebo eye drops. Prospective, randomized, placebo-controlled, and observational pilot study is presented. Ophthalmology outpatient clinic Dutch metropolitan hospital. Healthy 6- to 15-year-old volunteers with normal or low BMI requiring a cycloplegic refraction/retinoscopy. Randomized; 1 visit 2 drops cyclopentolate-1% and 1 visit 2 drops placebo (saline-0.9%). Single-blind: conducting researcher. Double blind: subjects, parents, clinical-neurophysiology staff, neurologist, and statistician. A 10-min baseline EEG-recording, drop-application, and follow-up to at least 45 min. Primary outcome: Detection of CNS changes, i.e. EEG-pattern changes, following two drops of cyclopentolate-1%. Secondary outcome: Determination of the extent of these pattern changes. Thirty-six cyclopentolate-1% saline-0.9% EEG registrations were made in 33 subjects;  18 males and 15 females. Three subjects were tested twice (interval 7 months). Nine out of fourteen (64%) of the 11- to 15-year-old children reported impaired memory, attention, alertness, as well as mind wandering following cyclopentolate. Drowsiness and sleep were seen in EEG-recordings of 11 subjects (33%) following cyclopentolate. We observed no drowsiness nor sleep during placebo recordings. The mean time to drowsiness was 23 min. Nine subjects arrived in stage-3 sleep but none arrived in REM-sleep. In subjects without sleep (N=24), significant changes compared to placebo-EEG were present for many leads and parameters. The main findings during awake eye-open recording were as follows: 1) a significant increase of temporal Beta-1,2 and 3-power, and 2) a significant decrease in: a) the parietal and occipital Alpha-2-power, b) the frontal Delta-1-power, c) the frontal total power, and d) the occipital and parietal activation synchrony index. The former finding reflects cyclopentolate uptake in the CNS, and the latter findings provide evidence for CNS suppression. Cyclopentolate-1% eye drops can affect the CNS and may cause altered consciousness, drowsiness, and sleep with concomitant EEG results in both young children and children in puberty. There is evidence that cyclopentolate has the potency to act as a short acting CNS depressant. Nevertheless, however, cyclopentolate-1% can safely be used in children and young adolescents.

1%环戊烯酸滴眼液后脑电图变化作为中枢神经系统受累的指示;一项在儿科人群中进行的随机安慰剂对照试验研究。
比较环戊酯滴眼液与安慰剂滴眼液滴眼后的脑电图模式。介绍了前瞻性、随机、安慰剂对照和观察性的试点研究。荷兰大都会医院眼科门诊。健康的6-15岁志愿者,BMI正常或低,需要进行睫状肌麻痹屈光/视网膜镜检查。随机化;1次访视2滴环戊酯-1%,1次访问2滴安慰剂(盐-0.9%)。单盲:进行研究。双盲:受试者、父母、临床神经生理学人员、神经学家和统计学家。10分钟的基线脑电图记录、滴注和至少45分钟的随访。主要结果:两次滴注1%环戊酯后检测中枢神经系统变化,即脑电图模式变化。次要结果:确定这些模式变化的程度。33名受试者进行了36次环戊烯酸-1%盐-0.9%脑电图登记; 18名男性和15名女性。三名受试者接受了两次测试(间隔7个月)。在11至15岁的儿童中,十四分之九(64%)的儿童报告称环戊烯酸后记忆力、注意力、警觉性受损,以及走神。11名受试者(33%)在环戊烯酸后的脑电图记录中发现嗜睡和睡眠。在安慰剂记录期间,我们没有观察到嗜睡或睡眠。嗜睡的平均时间为23分钟。9名受试者进入第三阶段睡眠,但没有一人进入快速眼动睡眠。在没有睡眠的受试者(N=24)中,与安慰剂相比,许多导联和参数的脑电图发生了显著变化。清醒睁眼记录过程中的主要发现如下:1)颞叶Beta-1,2和3-功率显著增加,2):a)顶叶和枕叶Alpha-2-功率显著降低,b)额叶Delta-1-功率显著降低、c)额叶总功率显著降低以及d)枕叶和顶叶激活同步指数显著降低。前一项发现反映了环戊烯酸在中枢神经系统中的摄取,后一项发现为中枢神经系统抑制提供了证据。环戊酯-1%滴眼液会影响中枢神经系统,可能导致幼儿和青春期儿童意识、嗜睡和睡眠改变,并伴有脑电图。有证据表明环戊烯酸具有作为短效中枢神经系统抑制剂的效力。然而,环戊烯酸-1%可以安全地用于儿童和青少年。
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
Strabismus
Strabismus OPHTHALMOLOGY-
CiteScore
1.60
自引率
11.10%
发文量
30
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