Department of Anesthesia and Pain Therapy, Fondazione Policlinico Universitario Agostino Gemelli, IRCCS, Rome, Italy.
Eur Rev Med Pharmacol Sci. 2021 Oct;25(20):6349-6355. doi: 10.26355/eurrev_202110_27008.
Pupillometry has been used to assess pain intensity and response to analgesic drugs in adults. The aim of this study was to verify the usefulness and effectiveness of the pupillometer to assess pain and depth of sedation in pediatric patients undergoing painful procedures and to optimize pain management by observing pupillary variations induced by opioids.
This is a prospective, monocentric study conducted in the sedation room of the Pediatric Intensive Care Unit of Fondazione Policlinico A. Gemelli in Rome. A population of 22 pediatric patients who underwent painful procedures was enrolled. Eleven children were sedated by opioid drugs. Heart rate, systolic blood pressure, diastolic blood pressure, bispectral index, maximum pupil size (Size), pupil change (CH), Neurological Pupil Index (NPi) were collected over four times: before starting the procedure; before the painful stimulus (when the patient was sedated); when the painful stimulus was applied; at the end of the procedure. A NeurOptics NPi-200 pupillometer was used for the study.
Statistical significance in the variation of haemodynamic parameters was less significant than the variation obtained by analyzing the pupillary parameters: a significant change in NPi and CH in the transition from wakefulness to sedation and from the application of the painful stimulus to awakening was found in both study populations, patients who have received opioids and patients who have not received opioids. Changes in the mean CH of the pupil diameter correlate with the depth of sedation, and the size values vary in relation to the administration of opioids.
Our findings highlight the potential role of pupillometry as a non-invasive method to objectively quantitate pain response in children to reach an efficient analgesic approach.
瞳孔测量已被用于评估成人的疼痛强度和对镇痛药物的反应。本研究旨在验证瞳孔计在评估行有创操作的儿科患者疼痛和镇静深度的有用性和有效性,并通过观察阿片类药物引起的瞳孔变化来优化疼痛管理。
这是一项在罗马 Gemelli 综合医院儿科重症监护室镇静室进行的前瞻性单中心研究。共纳入 22 名接受有创操作的儿科患者。11 名儿童接受阿片类药物镇静。在四个时间点收集心率、收缩压、舒张压、双频谱指数、最大瞳孔大小(Size)、瞳孔变化(CH)、神经瞳孔指数(NPi):开始操作前;在给予疼痛刺激前(患者镇静时);给予疼痛刺激时;操作结束时。研究使用了 NeurOptics NPi-200 瞳孔计。
与分析瞳孔参数获得的变化相比,血流动力学参数的变化不那么显著:在清醒到镇静和从应用疼痛刺激到苏醒的过渡中,无论是接受阿片类药物的患者还是未接受阿片类药物的患者,NPi 和 CH 均发生了显著变化。瞳孔直径的平均 CH 变化与镇静深度相关,而大小值与阿片类药物的使用有关。
我们的研究结果强调了瞳孔测量作为一种非侵入性方法客观定量评估儿童疼痛反应的潜在作用,以达到有效的镇痛方法。