Ahlfors U G, Rimön R, Appelberg B, Hagert U, Harma P, Katila H, Mahlanen A, Mehtonen O P, Naukkarinen H, Outakoski J
Hesperia Hospital, Helsinki, Finland.
Acta Psychiatr Scand Suppl. 1990;358:99-103. doi: 10.1111/j.1600-0447.1990.tb05298.x.
Ninety-two patients with schizophrenia were included in a double-blind multicentre parallel-group trial comparing remoxipride and haloperidol. The mean daily dose during the last week of treatment was 316 mg (range, 150-600 mg) in the remoxipride group and 8.7 mg (range, 5-20 mg) in the haloperidol group. The study period was six weeks with at least one day of washout. Both Clinical Global Impression (CGI) rating, and Brief Psychiatric Rating Scale (BPRS) total scores declined at the end of the trial compared with pretreatment values in both groups. No significant differences were found between the remoxipride and haloperidol groups with regard to the treatment outcome. Treatment-emergent extrapyramidal symptoms were statistically more frequent and more severe during haloperidol than during remoxipride treatment. Haloperidol-treated patients reported also significantly more concentration difficulties. Severe extrapyramidal side effects in the haloperidol group and clinical ineffectiveness in the remoxipride group were the most frequent reasons for premature discontinuation of treatment.
92例精神分裂症患者被纳入一项比较瑞莫必利和氟哌啶醇的双盲多中心平行组试验。治疗最后一周的平均日剂量在瑞莫必利组为316mg(范围150 - 600mg),在氟哌啶醇组为8.7mg(范围5 - 20mg)。研究期为六周,至少有一天的洗脱期。试验结束时,两组的临床总体印象(CGI)评分和简明精神病评定量表(BPRS)总分均较治疗前值下降。瑞莫必利组和氟哌啶醇组在治疗结果方面未发现显著差异。与瑞莫必利治疗相比,氟哌啶醇治疗期间出现的治疗中出现的锥体外系症状在统计学上更频繁、更严重。接受氟哌啶醇治疗的患者还报告注意力不集中的情况明显更多。氟哌啶醇组严重的锥体外系副作用和瑞莫必利组的临床无效是治疗提前终止的最常见原因。