Bateman D N, Coxon A, Legg N J, Reid J L
J Neurol Neurosurg Psychiatry. 1978 Dec;41(12):1109-13. doi: 10.1136/jnnp.41.12.1109.
The addition of bromocriptine, given in divided doses up to 30 mg per day, to conventional anti-Parkinsonism therapy has been studied in a double-blind placebo controlled clinical trial in 11 patients with Parkinsonism with the "on-off" syndrome. Four patients withdrew because of side effects. Of the seven remaining, three had clinical benefit from bromocriptine with reduction in severity and frequency of fluctuations. There was, however, no statistically significant benefit of bromocriptine when the group as a whole was assessed in terms of severity or frequency of fluctuations measured by three different methods. The mean frequency of major fluctuations on placebo was 2.9/day and on bromocriptine 1.8/day (P less than 0.1 greater than 0.05). There appears to be a limited role for bromocriptine as additional therapy in the management of some patients with the on-off syndrome.
在一项针对11名患有“开-关”综合征的帕金森病患者的双盲安慰剂对照临床试验中,研究了在传统抗帕金森病治疗基础上加用溴隐亭(每日分剂量服用,最高达30毫克)的效果。4名患者因副作用退出。在剩下的7名患者中,3名从溴隐亭治疗中获得了临床益处,症状严重程度和波动频率有所降低。然而,当用三种不同方法评估整个组的波动严重程度或频率时,溴隐亭并没有统计学上的显著益处。安慰剂组主要波动的平均频率为每天2.9次,溴隐亭组为每天1.8次(P小于0.1大于0.05)。在一些“开-关”综合征患者的治疗中,溴隐亭作为辅助治疗的作用似乎有限。