Dallos V, Heathfield K, Stone P, Allen F
Postgrad Med J. 1972 Jun;48(560):354-8.
Sixty-nine patients with Parkinson's disease were randomly allocated in a trial to compare the therapeutic effects of levodopa and amantadine. The patients were assessed clinically and scored by occupational therapy tasks and degrees of disability. Both drugs were used for 2 months; in the first 4 weeks the doses were gradually increased to 400 mg of amantadine or 4 g of levodopa respectively, and in the second 4 weeks' period the maximum tolerated dose was maintained throughout. Fourteen patients withdrew and these were excluded from the series. Of the fifty-five patients who completed the trial, thirty-four were taking levodopa and twenty-one amantadine. The results showed an average 33% improvement on levodopa and 23% on amantadine as regards tremor, rigidity and akinesia and their total scores improved 26% and 18% respectively. More cases showed substantial improvement on levodopa. There was little difference in response between 200 and 400 mg amantadine daily, but side-effects with 400 mg amantadine daily were more frequent and severe. Side-effects with levodopa were similar to those reported in previous trials but we also noted brown body fluids in three patients. The average effective dose of levodopa was lower than in previous reports, and the largest number of patients received benefit from 1·5 g daily. The superior effect of levodopa was shown.
69名帕金森病患者被随机分配到一项试验中,以比较左旋多巴和金刚烷胺的治疗效果。对患者进行临床评估,并通过职业治疗任务和残疾程度进行评分。两种药物均使用2个月;在前4周,剂量分别逐渐增加至400毫克金刚烷胺或4克左旋多巴,在第二个4周期间,始终维持最大耐受剂量。14名患者退出,这些患者被排除在该系列之外。在完成试验的55名患者中,34名服用左旋多巴,21名服用金刚烷胺。结果显示,在震颤、强直和运动不能方面,左旋多巴平均改善33%,金刚烷胺平均改善23%,它们的总分分别提高26%和18%。更多病例在服用左旋多巴后有显著改善。每日服用200毫克和400毫克金刚烷胺的反应差异不大,但每日服用400毫克金刚烷胺的副作用更频繁、更严重。左旋多巴的副作用与以往试验报告的相似,但我们也注意到3名患者出现了棕色体液。左旋多巴的平均有效剂量低于以往报告,最大数量的患者每日服用1.5克受益。结果显示左旋多巴效果更佳。