Teychenne P F, Leigh P N, Reid J L, Calne D B, Greenacre J K, Petrie A, Bamji A N
Lancet. 1975 Sep 13;2(7933):473-6. doi: 10.1016/s0140-6736(75)90546-2.
The efficacy and toxicity of bromocriptine, a drug which simulates dopamine, have been studied in twenty-eight patients with idiopathic parkinsonism. A double-blind, within-patient comparison between maximum tolerated doses of bromocriptine (mean 46-9 mg daily) and placebo revealed a substantial and statistically significant therapeutic response to the active drug. Adverse reactions were dose dependent, reversible, and similar to those encountered with levodopa. While taking bromocriptine fourteen patients were able to stop levodopa (with or without carbidopa); in five patients the dose of levodopa was reduced by 54% (mean). Eight patients could not tolerate bromocriptine; one patient failed to comply with prescribed adjustments of dosage.
对28例特发性帕金森病患者研究了一种模拟多巴胺的药物——溴隐亭的疗效和毒性。在患者自身内进行的双盲试验中,比较了溴隐亭最大耐受剂量(平均每日46.9毫克)与安慰剂,结果显示活性药物有显著且具有统计学意义的治疗反应。不良反应呈剂量依赖性、可逆性,且与左旋多巴引起的不良反应相似。服用溴隐亭期间,14例患者能够停用左旋多巴(加或不加卡比多巴);5例患者的左旋多巴剂量平均减少了54%。8例患者不能耐受溴隐亭;1例患者未遵医嘱调整剂量。