Lees A J, Haddad S, Shaw K M, Kohout L J, Stern G M
Arch Neurol. 1978 Aug;35(8):503-5. doi: 10.1001/archneur.1978.00500320023005.
Bromocriptine was given in a controlled trial to 86 parkinsonian patients. Eight of 30 previously untreated patients with early and mild disease showed sustained benefit for two years and did not develop "on-off" effects or dyskinesias. Only two of 23 patients unable to tolerate or failing to respond to levodopa benefited from bromocriptine. Thirty-three patients with residual disabilities despite maximum tolerated doses of levodopa were also given bromocriptine: although benefit accrued, treatment was abandoned because of unacceptable side effects, and there was no improvement in the 11 with severe "on-off" disabilities. Although it was found that benefit from 70 mg daily of bromocriptine was comparable to that from 750 mg of levodopa with carbidopa, bromocriptine seems to offer no advantage to the majority of patients who have received or are receiving levodopa and/or carbidopa.
在一项对照试验中,对86名帕金森病患者使用了溴隐亭。30名先前未接受治疗的早期轻症患者中,有8名显示出持续两年的疗效,且未出现“开-关”效应或运动障碍。在23名无法耐受左旋多巴或对其无反应的患者中,只有2名从溴隐亭治疗中获益。33名尽管服用了最大耐受剂量的左旋多巴仍有残余残疾的患者也接受了溴隐亭治疗:虽然有疗效,但因不可接受的副作用而停止治疗,11名有严重“开-关”残疾的患者病情没有改善。尽管发现每日70毫克溴隐亭的疗效与750毫克左旋多巴加卡比多巴的疗效相当,但对于大多数已经接受或正在接受左旋多巴和/或卡比多巴治疗的患者来说,溴隐亭似乎并无优势。