Hely M A, Morris J G, Reid W G, O'Sullivan D J, Williamson P M, Rail D, Broe G A, Margrie S
Neurology Department, Westmead Hospital, Sydney, Australia.
J Neurol Neurosurg Psychiatry. 1994 Aug;57(8):903-10. doi: 10.1136/jnnp.57.8.903.
149 previously untreated patients with Parkinson's disease were recruited over a three year period and randomly allocated to either low dose levodopa-carbidopa (< or = 600/150 mg/day) or low dose bromocriptine (< or = 30 mg/day). A five year follow up is reported on the 126 patients who completed the dose titration and who have not developed features of atypical Parkinsonism. Levodopa-carbidopa in low dosage adequately controlled symptoms in most patients and delayed the appearance of dyskinesia and end of dose failure for about two years longer than conventional doses. Only a few patients could be managed for more than one year on low dose bromocriptine alone; these patients had mild disease and asymmetric signs. Patients randomised to bromocriptine did not develop dyskinesia or troublesome end of dose failure until levodopa-carbidopa was added. The prevalence of dyskinesia in this group was lower than in patients given levodopa-carbidopa alone. The prevalence of end of dose failure was similar in the two randomisation groups once levodopa was introduced.
在三年时间里招募了149名未经治疗的帕金森病患者,并将他们随机分为低剂量左旋多巴 - 卡比多巴组(≤600/150毫克/天)或低剂量溴隐亭组(≤30毫克/天)。本文报告了对126名完成剂量滴定且未出现非典型帕金森综合征特征的患者进行的五年随访结果。低剂量的左旋多巴 - 卡比多巴在大多数患者中能充分控制症状,与常规剂量相比,可将运动障碍和剂末失效的出现推迟约两年。仅少数患者仅用低剂量溴隐亭就能治疗一年以上;这些患者病情较轻且症状不对称。随机分配到溴隐亭组的患者在添加左旋多巴 - 卡比多巴之前未出现运动障碍或严重的剂末失效。该组运动障碍的发生率低于单独使用左旋多巴 - 卡比多巴的患者。引入左旋多巴后,两个随机分组中剂末失效的发生率相似。