Lapierre Y D, Nair N P, Chouinard G, Awad A G, Saxena B, Jones B, McClure D J, Bakish D, Max P, Manchanda R
Royal Ottawa Hospital, Ottawa, Ontario, Canada.
Acta Psychiatr Scand Suppl. 1990;358:72-7. doi: 10.1111/j.1600-0447.1990.tb05293.x.
The efficacy and side-effect profile for three dose ranges of remoxipride were compared with haloperidol in 242 schizophrenic inpatients in 13 centres. All patients were in a productive phase of schizophrenia according to DSM-III criteria. Relative efficacy of low dose (30-90 mg daily) vs middle dose (120-240 mg daily) vs high dose (300-600 mg daily) was compared with the standard dose of haloperidol (15-45 mg daily), as were the side effects. It was concluded that the therapeutic efficacy of remoxipride was comparable to that of haloperidol for acute episodes of schizophrenia; that the low dose range was significantly less effective than the higher ranges; that there was a clear advantage of remoxipride over haloperidol with respect to incidence and severity of extrapyramidal symptoms. The general safety profile of remoxipride as assessed from clinical chemistry, haematology, and cardiovascular variables suggests that remoxipride in the dose ranges studied can be used safely for the treatment of schizophrenic patients.
在13个中心的242例精神分裂症住院患者中,比较了3个剂量范围的瑞莫必利与氟哌啶醇的疗效和副作用。根据《精神疾病诊断与统计手册》第三版标准,所有患者均处于精神分裂症的发病期。将低剂量(每日30 - 90毫克)、中剂量(每日120 - 240毫克)和高剂量(每日300 - 600毫克)瑞莫必利的相对疗效与氟哌啶醇标准剂量(每日15 - 45毫克)进行比较,同时也比较了副作用。得出的结论是:瑞莫必利对精神分裂症急性发作的治疗效果与氟哌啶醇相当;低剂量范围明显不如高剂量范围有效;在锥体外系症状的发生率和严重程度方面,瑞莫必利明显优于氟哌啶醇。从临床化学、血液学和心血管变量评估的瑞莫必利总体安全性表明,在所研究的剂量范围内,瑞莫必利可安全用于治疗精神分裂症患者。