Conley R R, Tamminga C A, Bartko J J, Richardson C, Peszke M, Lingle J, Hegerty J, Love R, Gounaris C, Zaremba S
Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore 21228, USA.
Am J Psychiatry. 1998 Jul;155(7):914-20. doi: 10.1176/ajp.155.7.914.
The purpose of this study was to compare the efficacy of olanzapine with that of chlorpromazine plus benztropine in patients with treatment-resistant schizophrenia.
One hundred three previously treatment-resistant patients with schizophrenia diagnosed according to the DSM-III-R criteria were given a prospective 6-week trial of 10-40 mg/day of haloperidol. Eighty-four of them failed to respond to that trial and agreed to be randomly assigned to an 8-week fixed-dose trial of either 25 mg/day of olanzapine alone or 1200 mg/day of chlorpromazine plus 4 mg/day of benztropine mesylate.
Fifty-nine (70%) of the 84 subjects completed the trial. The primary outcome measures were Brief Psychiatric Rating Scale total score and positive symptom score, Scale for the Assessment of Negative Symptoms global score, and Clinical Global Impression score. An analysis of variance for the subjects who completed the study showed no difference in efficacy between the two drugs. Seven percent of the olanzapine-treated patients responded according to a priori criteria; no chlorpromazine-treated patients responded. The olanzapine-treated patients had fewer motor and cardiovascular side effects than the chlorpromazine-treated patients. Extrapyramidal symptoms and akathisia were similar in the two groups, although no antiparkinsonian drugs were used in the olanzapine group.
Olanzapine and chlorpromazine showed similar efficacy, and the total amount of improvement with either drug was modest. Olanzapine-treated patients had fewer side effects than chlorpromazine-treated patients.
本研究旨在比较奥氮平与氯丙嗪加苯海索治疗难治性精神分裂症患者的疗效。
103例先前难治性精神分裂症患者,根据DSM-III-R标准诊断,接受为期6周的前瞻性试验,给予每日10 - 40毫克的氟哌啶醇。其中84例对该试验无反应,并同意被随机分配到一个为期8周的固定剂量试验,即单独使用每日25毫克奥氮平或每日1200毫克氯丙嗪加4毫克甲磺酸苯海索。
84名受试者中有59名(70%)完成了试验。主要结局指标为简明精神病评定量表总分和阳性症状评分、阴性症状评定量表总体评分以及临床总体印象评分。对完成研究的受试者进行方差分析显示,两种药物在疗效上无差异。根据预先设定的标准,7%接受奥氮平治疗的患者有反应;接受氯丙嗪治疗的患者无反应。接受奥氮平治疗的患者比接受氯丙嗪治疗的患者有更少的运动和心血管副作用。两组的锥体外系症状和静坐不能相似,尽管奥氮平组未使用抗帕金森药物。
奥氮平和氯丙嗪显示出相似的疗效,且两种药物的总体改善程度均有限。接受奥氮平治疗的患者比接受氯丙嗪治疗的患者副作用更少。