Růzicka E, Streitová H, Jech R, Kanovský P, Roth J, Rektorová I, Mecír P, Hortová H, Bares M, Hejduková B, Rektor I
Movement Disorder Center, Department of Neurology, 1st Medical Faculty, Charles' University and General Teaching Hospital, Prague, Czech Republic.
J Neural Transm (Vienna). 2000;107(11):1297-306. doi: 10.1007/s007020070019.
Efficiency and safety of amantadine sulfate (AMS) infusions were investigated in late stage complications of Parkinson's disease (PD). In an open-label study, 21 PD patients suffering from motor fluctuations and/or dyskinesias were administered AMS infusions (PK-Merz, 400 mg per day) during seven days. Oral AMS treatment followed. Significant improvement of UPDRS motor scores was observed between day 0 and day 7, remaining improved until day 21. Based on patients' diary notes, both severity and occurrence of hypokinetic "off" state significantly decreased (from 6.6 to 3.1 hours, p < 0.001, average "off" time per day) as well as dopaminergic-induced dyskinesias (from 2.5 to 1.3 hours, p < 0.05, average duration of dyskinesias per day). AMS infusions followed by oral administration appeared as a safe method for improvement of both motor fluctuations and dyskinesias in advanced PD. In advantage to simple oral therapy, AMS infusions allowed fast introduction of a profound and durable treatment effect.
在帕金森病(PD)晚期并发症中研究了硫酸金刚烷胺(AMS)输注的有效性和安全性。在一项开放标签研究中,21名患有运动波动和/或异动症的PD患者接受了为期7天的AMS输注(PK-Merz,每天400毫克)。随后进行口服AMS治疗。在第0天至第7天观察到统一帕金森病评定量表(UPDRS)运动评分有显著改善,直至第21天仍保持改善。根据患者的日记记录,运动不能性“关”期的严重程度和发生次数均显著降低(从6.6小时降至3.1小时,p<0.001,每天平均“关”期时间),多巴胺能诱导的异动症也显著降低(从2.5小时降至1.3小时,p<0.05,每天异动症平均持续时间)。AMS输注后口服给药似乎是改善晚期PD运动波动和异动症的一种安全方法。与单纯口服治疗相比,AMS输注能够快速产生显著且持久的治疗效果。