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金刚烷胺静脉输注治疗帕金森病的运动波动和异动症

Amantadine infusion in treatment of motor fluctuations and dyskinesias in Parkinson's disease.

作者信息

Růzicka E, Streitová H, Jech R, Kanovský P, Roth J, Rektorová I, Mecír P, Hortová H, Bares M, Hejduková B, Rektor I

机构信息

Movement Disorder Center, Department of Neurology, 1st Medical Faculty, Charles' University and General Teaching Hospital, Prague, Czech Republic.

出版信息

J Neural Transm (Vienna). 2000;107(11):1297-306. doi: 10.1007/s007020070019.

Abstract

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.

摘要

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。

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