Gómez J C, Sacristán J A, Hernández J, Breier A, Ruiz Carrasco P, Antón Saiz C, Fontova Carbonell E
Eli Lilly and Company, Madrid, Spain.
J Clin Psychiatry. 2000 May;61(5):335-43. doi: 10.4088/jcp.v61n0503.
Results of controlled clinical trials should be confirmed through safety and effectiveness studies in nonselected patient cohorts treated according to routine clinical practice.
Outpatients with schizophrenia (ICD-10 criteria) entered this prospective, naturalistic study when they received a new prescription for an antipsychotic drug. Treatment assignment was based on purely clinical criteria, as the study did not include any experimental intervention. Safety was evaluated through the collection of spontaneous adverse events and a specific questionnaire for extrapyramidal symptoms. Global clinical status was measured through the Clinical Global Impressions-Severity (CGI-S) and the Global Assessment of Functioning (GAF) scales.
From the 2967 patients included, 2128 patients were treated with olanzapine as monotherapy or combined with other drugs (olanzapine group), and 821 were treated with other antipsychotic drugs as monotherapy or combined with other drugs (control group). There were no statistical differences between treatment groups at baseline regarding age, gender, disease duration, or severity of symptoms. Olanzapine was well tolerated and effective in this study. Overall incidence of adverse events was significantly lower in the olanzapine group compared with the control group (p < .001). Somnolence and weight gain were significantly more frequent in the olanzapine group, and akathisia, dystonia, extrapyramidal syndrome, hypertonia, hypokinesia, and tremor were significantly higher in the control group. Clinical improvement at endpoint, measured through the mean change in the CGI-S and the GAF, was significantly higher in the olanzapine group compared with the control group (p = .004).
These results show that olanzapine is safe and effective in nonselected schizophrenic outpatients and are consistent with the efficacy and safety profile that olanzapine has shown in previous controlled clinical trials.
对照临床试验的结果应通过在按照常规临床实践治疗的非选择性患者队列中进行安全性和有效性研究来加以证实。
符合精神分裂症(ICD - 10标准)的门诊患者在接受抗精神病药物新处方时进入这项前瞻性、自然主义研究。治疗分配基于纯粹的临床标准,因为该研究不包括任何实验性干预。通过收集自发不良事件以及一份针对锥体外系症状的特定问卷来评估安全性。通过临床总体印象 - 严重程度(CGI - S)和功能总体评定量表(GAF)来衡量整体临床状况。
在纳入的2967例患者中,2128例患者接受奥氮平单药治疗或与其他药物联合治疗(奥氮平组),821例患者接受其他抗精神病药物单药治疗或与其他药物联合治疗(对照组)。治疗组在基线时的年龄、性别、病程或症状严重程度方面无统计学差异。在本研究中,奥氮平耐受性良好且有效。奥氮平组不良事件的总体发生率显著低于对照组(p <.001)。嗜睡和体重增加在奥氮平组中明显更常见,而静坐不能、肌张力障碍、锥体外系综合征、张力亢进、运动减退和震颤在对照组中明显更高。通过CGI - S和GAF的平均变化衡量的终点临床改善情况,奥氮平组明显高于对照组(p =.004)。
这些结果表明奥氮平在非选择性精神分裂症门诊患者中安全有效,并且与奥氮平在先前对照临床试验中所显示的疗效和安全性概况一致。