Department of Neurosurgery and Epilepsy, University Medical Center Utrecht, Utrecht, the Netherlands; Nesmos Department, Faculty of Medicine and Psychology, Sapienza University, Roma, Italy.
Department of Clinical Neurophysiology, Birmingham Women's and Children's Hospital NHS Foundation Trust, Birmingham, UK.
Epilepsy Res. 2020 Sep;165:106377. doi: 10.1016/j.eplepsyres.2020.106377. Epub 2020 Jun 1.
The assessment of the effect of photic stimulation is an integral component of an EEG exam and is especially important in patients referred for ascertained or suspected photosensitivity with or without a diagnosis of epilepsy. A positive test result relies on eliciting a specific abnormality defined as the "photoparoxysmal response". Reliability of this assessment is strongly influenced by technical and procedural variables, a critical one represented by the physical properties of the stimulators used. Established clinical norms are based on data acquired with the "gold-standard" Grass PS stimulators. These are no longer commercially available and have been replaced by stimulators using light emitting diode (LED) technology. To our knowledge no comparative study on their efficacy has been conducted. To address this gap, we recruited 39 patients aged 5-54 years, referred to two specialized centers with confirmed of suspected diagnosis of photosensitive epilepsy or generalized epilepsy with photosensitivity in a prospective randomized single-blind cross-over study to compare two commercially available LED-bases stimulation systems (FSA 10® and Lifeline® stimulators) against the Grass PS 33 xenon lamp device. Our findings indicate that the LED systems tested are equivalent to the Grass stimulator both in identifying the PPR in affected individuals.
光刺激评估是脑电图检查的一个组成部分,对于已确诊或疑似光敏感性的患者,无论是否患有癫痫,该评估尤其重要。阳性测试结果依赖于诱发出被定义为“光惊厥反应”的特定异常。这种评估的可靠性受到技术和程序变量的强烈影响,其中一个关键变量是所使用刺激器的物理特性。既定的临床规范是基于使用“金标准”Grass PS 刺激器获得的数据。这些刺激器已不再商业化,并且已被使用发光二极管 (LED) 技术的刺激器所取代。据我们所知,尚未对其疗效进行比较研究。为了解决这一差距,我们招募了 39 名年龄在 5 至 54 岁的患者,他们在一项前瞻性随机单盲交叉研究中被转诊到两个专门的中心,以确认或疑似光敏感性癫痫或伴有光敏感性的全身性癫痫,以比较两种市售的基于 LED 的刺激系统(FSA 10®和 Lifeline®刺激器)与 Grass PS 33 氙灯设备的疗效。我们的研究结果表明,在所测试的 LED 系统中,在识别受影响个体中的 PPR 方面,它们与 Grass 刺激器等效。