首页> 美国卫生研究院文献>The Journal of Neurology and Psychopathology >A randomised controlled study comparing bromocriptine to which levodopa was later added with levodopa alone in previously untreated patients with Parkinsons disease: a five year follow up.
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A randomised controlled study comparing bromocriptine to which levodopa was later added with levodopa alone in previously untreated patients with Parkinsons disease: a five year follow up.

机译:一项随机对照研究比较了后来接受左旋多巴的溴隐亭和以前未经治疗的帕金森氏病患者单独使用左旋多巴的情况:五年随访。

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摘要

This pilot study was performed to compare the occurrence of long term motor complications in Parkinson's disease when the introduction of levodopa was delayed by an initial treatment with high doses of bromocriptine alone. The trial was a prospective randomised controlled study comparing 31 previously untreated patients with Parkinson's disease initially given bromocriptine alone to which levodopa was later added (group B/D) and 29 other previously untreated patients with Parkinson's disease immediately given levodopa alone (group D). The end point was the occurrence of the first motor complications (wearing off or dyskinesia). Group B/D patients received bromocriptine (52 (SEM 5) mg/day) for 2.7 years, to which levodopa was later added (471 (SEM 46) mg/day). Group D patients received a comparable dose of levodopa alone (569 (SEM 47) mg/day). Both had similar disability scores at the end of the study. Motor complications were fewer and appeared later in group B/D than in group D (56% after 4.9 (SEM 0.5) years of treatment v 90% after 2.7 (SEM 0.5) years, p < 0.01). Wearing off appeared later (p < 0.01) in group B/D (4.5 (SEM 0.6) years) than in group D (2.9 (SEM 0.6) years). Peak dose dyskinesia occurred less often in group B/D patients (three v 14 cases, p < 0.01). This study showed that a three year initial monotherapy with high doses of bromocriptine followed by addition of levodopa delayed the occurrence of long term motor complications usually found in patients with Parkinson's disease treated with levodopa alone from the beginning.
机译:这项初步研究的目的是比较左旋多巴的引入由于单独使用高剂量溴隐亭的初始治疗而延迟引入帕金森氏病时长期运动并发症的发生。该试验是一项前瞻性随机对照研究,比较了31名先前未经治疗的帕金森氏病患者,最初单独接受溴隐亭治疗,后来又添加了左旋多巴(B / D组)和29名其他先前未经治疗的帕金森氏病患者,仅接受了左旋多巴(D组)。终点是首次运动并发症(疲倦或运动障碍)的发生。 B / D组患者接受溴隐亭(52(SEM 5)mg /天)治疗2.7年,之后再添加左旋多巴(471(SEM 46)mg /天)。 D组患者仅接受相当剂量的左旋多巴(569(SEM 47)毫克/天)。在研究结束时,两者的残疾评分相似。与D组相比,B / D组的运动并发症更少,出现较晚(在4.9(SEM 0.5)年的治疗后为56%,在2.7(SEM 0.5)年的治疗后为90%,p <0.01)。 B / D组(4.5(SEM 0.6)年)较D组(2.9(SEM 0.6)年)出现磨损(p <0.01)。峰值剂量运动障碍在B / D组患者中较少发生(3 v 14例,p <0.01)。这项研究表明,三年期高剂量溴隐亭单药治疗后再加上左旋多巴,从一开始就延缓了帕金森病患者单纯左旋多巴治疗后长期运动并发症的发生。

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