Ikeda A, Shibasaki H, Tashiro K, Mizuno Y, Kimura J
Department of Brain Pathophysiology, Kyoto University School of Medicine, Japan.
Mov Disord. 1996 Nov;11(6):691-700. doi: 10.1002/mds.870110615.
Sixty patients with disabling myoclonus excluding mainly spinal myoclonus were treated by piracetam as an open-labeled study, and myoclonus score, neurological symptoms, functional disability, and intensity of myoclonus were scored before and after treatment, including a blinded video inspection. Electrophysiological correlation also was investigated before and after treatment. Piracetam was effective in myoclonus, especially that of cortical origin, in both monotherapy and polytherapy. Piracetam also had positive benefits on gait ataxia and convulsions but not on dysarthria, and feeding and hand writing improved much more significantly. Psychologically significant improvement was seen in decreased motivation, sleep disturbance, attention deficit, and depression, all of which might be possibly secondary benefits associated with improvement of myoclonus. There was no positive correlation between clinical and electrophysiological improvement. Tolerance was good, and side effects were transient. However, hematological abnormalities observed in at least two patients in the present study should be kept in mind when relatively large doses of piracetam are administered, especially in combination with other antimyoclonic drugs.
60例主要排除脊髓性肌阵挛的致残性肌阵挛患者接受了吡拉西坦的开放标签研究治疗,在治疗前后对肌阵挛评分、神经症状、功能残疾和肌阵挛强度进行评分,包括盲法视频检查。还在治疗前后研究了电生理相关性。吡拉西坦在单药治疗和联合治疗中对肌阵挛均有效,尤其是皮质起源的肌阵挛。吡拉西坦对步态共济失调和惊厥也有积极作用,但对构音障碍无效,进食和书写改善更为显著。在动机减退、睡眠障碍、注意力缺陷和抑郁方面有心理上的显著改善,所有这些可能是与肌阵挛改善相关的继发益处。临床改善与电生理改善之间无正相关。耐受性良好,副作用是短暂的。然而,在本研究中至少有两名患者观察到血液学异常,当给予相对大剂量的吡拉西坦时,尤其是与其他抗肌阵挛药物联合使用时,应牢记这一点。