Losito Emma, Eisermann Monika, Vignolo Patricia, Hovhannisyan Shushanik, Magny Jean François, Kaminska Anna
*Department of Clinical Neurophysiology, APHP, Necker-Enfants Malades Hospital, Paris, France; †INSERM U1129, Paris, France; ‡Paris Descartes University, Paris, France; §CEA, Gif sur Yvette, France; and ‖Department of Neonatology, APHP, Necker Enfants Malades Hospital, Paris, France.
J Clin Neurophysiol. 2017 Nov;34(6):484-491. doi: 10.1097/WNP.0000000000000412.
Benign neonatal sleep myoclonus is a common nonepileptic condition occurring in neurologically normal full-term newborns. During jerks, EEG has always been described as normal. The aim of this study was to describe EEG changes associated with the myoclonic jerks.
Polygraphic video-EEG recordings of four full-term neonates presenting benign neonatal sleep myoclonus were studied. Myoclonic jerks were analyzed regarding their topography, frequency, propagation pattern, and reflex component. EEG averaging time-locked to myoclonic jerks and to somatosensory stimuli (realized by tapping on palms and feet) was performed to study eventual EEG correlates of myoclonus and to asses somatosensory evoked responses-for the latter, two control newborns were added.
Visual analysis of the EEG disclosed theta band slow waves on central and vertex electrodes concomitant to myoclonic jerks and jerk-locked back-averaging disclosed a sequence of deflections, not preceding, but following the myoclonus. This response predominated on the vertex electrode (CZ) and consisted of five components (N1, P1, N2, P2, and N3), with only the three later components being constantly present (at 110, 200, and 350-500 ms, respectively). Back-averaging locked to the tactile stimuli in four subjects and two control newborns showed similar components and were comparable to those described in the literature as late somatosensory evoked responses in full-term newborns.
Myoclonic jerks in benign neonatal sleep myoclonus can evoke visually identifiable EEG potentials on vertex electrodes corresponding to somatosensory responses. This EEG aspect may be misleading and could give rise to an anti-seizure treatment that mostly worsens the condition.
良性新生儿睡眠肌阵挛是一种常见的非癫痫性病症,发生于神经功能正常的足月儿。在肌阵挛发作期间,脑电图一直被描述为正常。本研究的目的是描述与肌阵挛发作相关的脑电图变化。
对4例表现为良性新生儿睡眠肌阵挛的足月儿进行多导视频脑电图记录研究。分析肌阵挛发作的部位、频率、传播模式和反射成分。对与肌阵挛发作以及体感刺激(通过轻拍手掌和足部实现)时间锁定的脑电图进行平均,以研究肌阵挛可能的脑电图相关性,并评估体感诱发电位——为此增加了2例对照新生儿。
脑电图的视觉分析显示,在中央和头顶电极上,肌阵挛发作时伴有θ波段慢波,并且发作锁定反向平均显示出一系列偏转,不是在肌阵挛发作之前,而是在其后。这种反应在头顶电极(CZ)上占主导,由五个成分(N1、P1、N2、P2和N3)组成,只有后三个成分持续存在(分别在110、200和350 - 500毫秒)。对4例受试者和2例对照新生儿的触觉刺激进行反向平均显示出相似的成分,并且与文献中描述的足月儿晚期体感诱发电位相当。
良性新生儿睡眠肌阵挛的肌阵挛发作可在头顶电极上诱发与体感反应相对应的、视觉上可识别的脑电电位。这种脑电图表现可能会产生误导,并可能导致抗癫痫治疗,而这大多会使病情恶化。