Weiner W J., Factor S A., Jankovic J, Hauser R A., Tetrud J W., Waters C H., Shulman L M., Glassman P M., Beck B, Paume D, Doyle C
Department of Neurology, University of Miami School of Medicine, 1501 N.W. 9 Avenue, 33136, Miami, FL, USA
Parkinsonism Relat Disord. 2001 Apr;7(2):115-120. doi: 10.1016/s1353-8020(00)00031-6.
Objective: To assess the long-term safety and efficacy of pramipexole in advanced Parkinson's disease over a four year time period.Methods: This study is an open-label extension trial of pramipexole for Parkinson's disease open to patients completing a double-blind placebo controlled safety and efficacy trial of this drug. Three hundred and six patients entered the trial. These patients had moderate to severe PD (stage II-IV Hoehn and Yahr during off time) and were experiencing motor fluctuations. Patients were titrated over a six week period and then entered a maintenance phase which lasted up to 50 months. Patients were evaluated every 3 months using the Unified Parkinson's Disease Rating Scale (UPDRS II, III and IV) and modified Schwab and England scale (S/E).Results: Sixty-four percent (197) of the 306 patients who entered this study completed it. Patients showed steady improvement over the 6 week ascending dose interval when pramipexole was reintroduced into the trial as the open-label study medication. Over the duration of the trial patients slowly returned to their baseline levels. This was true for all measures evaluated except for the UPDRS part IV. On UPDRS part IV patients remained below their baseline score which indicated an improvement for the duration of the study. Patterns similar to the overall scores were seen when the individual components of the UPDRS scale part II for "on" and "off" periods and part III were evaluated. However tremor during "on" periods showed improvement over baseline for the duration of the trial. The most common adverse events secondary to pramipexole occurring in greater than 10% of patients included dyskinesias, asymptomatic orthostatic hypotension, dizziness, insomnia, and hallucinations.Conclusion: Pramipexole was well tolerated for up to 4 years. Pramipexole treatment appeared to show continued efficacy in the treatment of Parkinson's disease for 3 years in this open-label descriptive study. After 3 years there was a gradual return to baseline motor states perhaps suggesting progression of Parkinson's disease.
评估普拉克索在四年时间内对晚期帕金森病的长期安全性和有效性。方法:本研究是一项普拉克索治疗帕金森病的开放标签扩展试验,面向完成该药物双盲安慰剂对照安全性和有效性试验的患者。306名患者进入试验。这些患者患有中度至重度帕金森病(非服药期Hoehn和Yahr分级为II - IV期)且存在运动波动。患者在六周内进行滴定,然后进入长达50个月的维持期。每3个月使用统一帕金森病评定量表(UPDRS II、III和IV)以及改良的施瓦布和英格兰量表(S/E)对患者进行评估。结果:进入本研究的306名患者中有64%(197名)完成了研究。当普拉克索作为开放标签研究药物重新引入试验时,患者在6周的递增剂量间隔内显示出稳步改善。在试验期间,患者逐渐恢复到基线水平。除UPDRS第四部分外,所有评估指标均如此。在UPDRS第四部分,患者得分仍低于基线水平,这表明在研究期间有所改善。对UPDRS量表第二部分“服药期”和“非服药期”以及第三部分的各个组成部分进行评估时,观察到与总体得分相似的模式。然而,服药期的震颤在试验期间较基线有所改善。普拉克索引发的、发生率超过10%的最常见不良事件包括运动障碍、无症状性体位性低血压、头晕、失眠和幻觉。结论:在长达4年的时间里,普拉克索耐受性良好。在这项开放标签描述性研究中,普拉克索治疗似乎在治疗帕金森病方面持续有效3年。3年后,运动状态逐渐恢复到基线水平,这可能提示帕金森病有所进展。