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奥氮平治疗对典型和非典型抗精神病药物难治的精神分裂症:一项开放标签的前瞻性试验。

Olanzapine for schizophrenia refractory to typical and atypical antipsychotics: an open-label, prospective trial.

作者信息

Lindenmayer J P, Volavka J, Lieberman J, Sheitman B, Citrome L, Chakos M, Czobor P, Parker B, Iskander A

机构信息

Psychopharmacology Research Unit, Manhattan Psychiatric Unit, Manhattan Psychiatric Center, Wards Island, New York 10035, USA.

出版信息

J Clin Psychopharmacol. 2001 Aug;21(4):448-53. doi: 10.1097/00004714-200108000-00014.

Abstract

The role of olanzapine in treatment-resistant schizophrenia is still unresolved. This article presents an open-label, prospective, 14-week trial with olanzapine in patients with schizophrenia and schizoaffective disorder selected for unambiguous resistance to either clozapine or risperidone and to typical antipsychotics. Forty-three inpatients (mean age, 41.6 years; mean duration of illness, 21.7 years) were enrolled and treated after cross-titration from their previous antipsychotic treatment with olanzapine 10 to 40 mg daily without any concomitant antipsychotic medication. Patients were evaluated with the Positive and Negative Syndrome Scale (PANSS), the Clinical Global Impressions Scale, and the Extrapyramidal Symptom Rating Scale. The change with olanzapine treatment was associated with a PANSS total score improvement of 3.7 (SD = 15.6; not significant). There was a significant improvement for the PANSS cognitive and depression/anxiety factors, whereas the PANSS excitement factor worsened. The improvement rate was superior in patients receiving olanzapine doses higher than 20 mg. A total of 16.7% of patients reached response criteria set forth by a previous study. There was a significant decrease in extrapyramidal side effects (t = 2.04; p < 0.05) and statistically significant, yet modest, weight gain. These results indicate that olanzapine is only modestly effective in these severely treatment-resistant patients with schizophrenia. However, a trial with olanzapine can be recommended in these patients before moving to augmentation strategies, given the lack of proven alternatives and the observation that 16.7% of patients reached the response criteria.

摘要

奥氮平在难治性精神分裂症治疗中的作用仍未明确。本文介绍了一项开放标签、前瞻性、为期14周的试验,该试验使用奥氮平治疗对氯氮平或利培酮以及典型抗精神病药物明确耐药的精神分裂症和分裂情感性障碍患者。43名住院患者(平均年龄41.6岁;平均病程21.7年)入组,在从之前的抗精神病药物交叉滴定至每日10至40毫克奥氮平且不使用任何其他抗精神病药物的情况下接受治疗。使用阳性和阴性症状量表(PANSS)、临床总体印象量表和锥体外系症状评定量表对患者进行评估。奥氮平治疗带来的变化与PANSS总分改善3.7分相关(标准差=15.6;无显著性差异)。PANSS认知和抑郁/焦虑因子有显著改善,而PANSS兴奋因子恶化。接受高于20毫克奥氮平剂量的患者改善率更高。共有16.7%的患者达到了先前研究设定的反应标准。锥体外系副作用显著减少(t=2.04;p<0.05),体重增加虽有统计学意义但增幅不大。这些结果表明,奥氮平对这些严重难治性精神分裂症患者的疗效有限。然而,鉴于缺乏经证实的替代药物且观察到16.7%的患者达到反应标准,在采用强化治疗策略之前,可建议对这些患者进行奥氮平试验。

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