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早期帕金森病中添加罗匹尼罗缓释或额外左旋多巴引起的运动障碍发作。

Onset of dyskinesia with adjunct ropinirole prolonged-release or additional levodopa in early Parkinson's disease.

机构信息

Department of Neurology, University of Alabama at Birmingham, Birmingham, Alabama 35294-0017, USA.

出版信息

Mov Disord. 2010 May 15;25(7):858-66. doi: 10.1002/mds.22890.

Abstract

Levodopa-induced dyskinesia can result in significant functional disability and reduced quality of life in patients with Parkinson's disease (PD). The goal of this study was to determine if the addition of once-daily ropinirole 24-hour prolonged-release (n = 104) in PD patients not optimally controlled with levodopa after up to 3 years of therapy with less than 600 mg/d delays the onset of dyskinesia compared with increasing doses of levodopa (n = 104). During the study, 3% of the ropinirole prolonged-release group (mean dose 10 mg/d) and 17% of the levodopa group (mean additional dose 284 mg/d) developed dyskinesia (P < 0.001). There were no significant differences in change in Unified Parkinson's Disease Rating Scale activities of daily living or motor scores, suggesting comparable efficacy between the two treatments. Adverse events were comparable in the two groups with nausea, dizziness, insomnia, back pain, arthralgia, somnolence, fatigue, and pain most commonly reported. Ropinirole prolonged-release delayed the onset of dyskinesia with comparable efficacy to increased doses of levodopa in early PD patients not optimally controlled with levodopa.

摘要

左旋多巴诱导的运动障碍可导致帕金森病(PD)患者出现显著的功能障碍和生活质量下降。本研究的目的是确定在接受左旋多巴治疗长达 3 年且剂量低于 600mg/d 的情况下,未能得到最佳控制的 PD 患者中,每日一次罗匹尼罗 24 小时延长释放(n = 104)的添加是否能延迟运动障碍的发生,与增加左旋多巴剂量(n = 104)相比。在研究过程中,罗匹尼罗延长释放组有 3%(平均剂量 10mg/d)和左旋多巴组有 17%(平均额外剂量 284mg/d)出现运动障碍(P < 0.001)。两组之间日常生活活动或运动评分的统一帕金森病评定量表变化无显著差异,提示两种治疗方法具有相当的疗效。两组的不良反应相似,最常见的不良反应有恶心、头晕、失眠、背痛、关节痛、嗜睡、疲劳和疼痛。在左旋多巴未能得到最佳控制的早期 PD 患者中,罗匹尼罗延长释放可延迟运动障碍的发生,与增加左旋多巴剂量的疗效相当。

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