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奥氮平。对其治疗精神分裂症及相关精神病的药理特性和疗效的综述。

Olanzapine. A review of its pharmacological properties and therapeutic efficacy in the management of schizophrenia and related psychoses.

作者信息

Fulton B, Goa K L

机构信息

Adis International Limited, Auckland, New Zealand.

出版信息

Drugs. 1997 Feb;53(2):281-98. doi: 10.2165/00003495-199753020-00007.

Abstract

Olanzapine is a thienobenzodiazepine derivative which displays efficacy in patients with schizophrenia and related psychoses. It has structural and pharmacological properties resembling those of the atypical antipsychotic clozapine and an improved tolerability profile compared with the classical antipsychotic haloperidol. In several large, well controlled trials in patients with schizophrenia or related psychoses, olanzapine generally 5 to 20 mg/day was at least as effective as haloperidol (5 to 20mg) and more so than placebo, as assessed by overall rating scales for psychoses. Olanzapine improved negative symptoms to a greater extent than haloperidol in 2 of 3 comparative trials, including the largest trial. Efficacy of olanzapine has a rapid onset (within 1 to 2 weeks). Its clinical benefits appear to be maintained for treatment periods of up to 1 year, as shown by analysis of the extension phase of several trials demonstrating decreased probability of hospitalisation over this period compared with haloperidol. Preliminary data suggest the drug may also improve quality of life. Olanzapine was associated with significantly fewer adverse movement disorders (e.g. akathisia, dystonia, hypertonia, extrapyramidal symptoms) than haloperidol. There have been no reports of agranulocytosis (as occurs with clozapine) or any other haemotoxicity attributed to olanzapine, and the drug has shown minimal effect on prolactin levels. Transient increases in levels of hepatic transaminases seem to be clinically important. The only events recorded more frequently during olanzapine than during haloperidol therapy were weight gain, dry mouth and increased appetite. Although the antipsychotic activity of olanzapine has been well demonstrated. Its efficacy in refractory schizophrenia and its place relative to other atypical antipsychotics remain to be determined. Nevertheless, if the long term tolerability profile of olanzapine is confirmed, the drug should provide a valuable therapeutic alternative in the management of schizophrenia and related psychoses.

摘要

奥氮平是一种噻吩并苯二氮䓬衍生物,对精神分裂症及相关精神病患者显示出疗效。它具有与非典型抗精神病药物氯氮平相似的结构和药理特性,与经典抗精神病药物氟哌啶醇相比,耐受性有所改善。在几项针对精神分裂症或相关精神病患者的大型、严格对照试验中,奥氮平一般每日5至20毫克,根据精神病总体评定量表评估,其疗效至少与氟哌啶醇(5至20毫克)相当,且优于安慰剂。在三项比较试验中的两项(包括最大规模的试验)中,奥氮平改善阴性症状的程度比氟哌啶醇更大。奥氮平的疗效起效迅速(1至2周内)。几项试验的延长期分析表明,与氟哌啶醇相比,在此期间住院概率降低,这表明其临床益处似乎可维持长达1年的治疗期。初步数据表明该药物还可能改善生活质量。与氟哌啶醇相比,奥氮平引起的不良运动障碍(如静坐不能、肌张力障碍、张力亢进、锥体外系症状)明显更少。未报告有粒细胞缺乏症(如氯氮平所致)或任何其他归因于奥氮平的血液毒性,且该药物对催乳素水平的影响极小。肝转氨酶水平的短暂升高在临床上似乎具有重要意义。在奥氮平治疗期间比氟哌啶醇治疗期间更频繁记录到的唯一事件是体重增加、口干和食欲增加。尽管奥氮平的抗精神病活性已得到充分证实,但其在难治性精神分裂症中的疗效及其相对于其他非典型抗精神病药物的地位仍有待确定。然而,如果奥氮平的长期耐受性得到证实,该药物在精神分裂症及相关精神病的治疗中应能提供一种有价值的治疗选择。

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