Aarli J A, Gilhus N E
Department of Neurology, University Hospital, University of Bergen, Norway.
Neurology. 1989 Nov;39(11 Suppl 2):82-5; discussion 95.
The efficacy of controlled-release Sinemet was evaluated in a 52-week open trial involving 20 patients (14 men, 6 women; mean age 66 years, range 56 to 82) with idiopathic Parkinson's disease of 8 years' mean duration. The mean daily dosage of levodopa was 662.5 mg (200 to 1600 mg) on entering the study and 800 mg (200 to 2400 mg) after 52 weeks. The mean number of daily doses was reduced from 5.0 (2 to 16) at entry to 3.3 (1 to 6) after 52 weeks. Rigidity, tremor, and bradykinesia were scored at 3 intervals during baseline and 8 intervals during the study on controlled-release levodopa. All parameters improved, with maximum improvement seen at week 12. Side effects were less frequent on the controlled-release preparation. After 5 months, 1 patient developed protracted dyskinesia with freezing episodes and end-of-dose deterioration on dose frequency reduction.
在一项为期52周的开放性试验中,对20例(14例男性,6例女性;平均年龄66岁,范围56至82岁)平均病程8年的特发性帕金森病患者,评估了控释息宁的疗效。进入研究时左旋多巴的平均日剂量为662.5毫克(200至1600毫克),52周后为800毫克(200至2400毫克)。每日平均给药次数从入组时的5.0次(2至16次)降至52周后的3.3次(1至6次)。在基线期对强直、震颤和运动迟缓进行了3次评分,在研究期间对控释左旋多巴进行了8次评分。所有参数均有改善,在第12周时改善最为明显。控释制剂的副作用较少。5个月后,1例患者出现持续性运动障碍,伴有冻结发作和在减少给药频率时出现剂末恶化。