Division of Psychiatry, Haukeland University Hospital, Sandviken, Norway.
BMC Psychiatry. 2011 Aug 31;11:145. doi: 10.1186/1471-244X-11-145.
Efficacy studies indicate anti-depressive effects of at least some second generation antipsychotics (SGAs). The Bergen Psychosis Project (BPP) is a 24-month, pragmatic, industry-independent, randomized, head-to-head comparison of olanzapine, quetiapine, risperidone and ziprasidone in patients acutely admitted with psychosis. The aim of the study is to investigate whether differential anti-depressive effectiveness exists among SGAs in a clinically relevant sample of patients acutely admitted with psychosis.
Adult patients acutely admitted to an emergency ward for psychosis were randomized to olanzapine, quetiapine, risperidone or ziprasidone and followed for up to 2 years. Participants were assessed repeatedly using the Positive and Negative Syndrome Scale-Depression factor (PANSS-D) and the Calgary Depression Scale for Schizophrenia (CDSS).
A total of 226 patients were included. A significant time-effect showing a steady decline in depressive symptoms in all medication groups was demonstrated. There were no substantial differences among the SGAs in reducing the PANSS-D score or the CDSS sum score. Separate analyses of groups with CDSS sum scores > 6 or ≤6, respectively, reflecting degree of depressive morbidity, revealed essentially identical results to the primary analyses. There was a high correlation between the PANSS-D and the CDSS sum score (r = 0.77; p < 0.01).
There was no substantial difference in anti-depressive effectiveness among olanzapine, quetiapine, risperidone or ziprasidone in this clinically relevant sample of patients acutely admitted to hospital for symptoms of psychosis. Based on our findings we can make no recommendations concerning choice of any particular SGA for targeting symptoms of depression in a patient acutely admitted with psychosis.
ClinicalTrials.gov ID; URL: http://www.clinicaltrials.gov/: NCT00932529.
疗效研究表明,至少某些第二代抗精神病药物(SGAs)具有抗抑郁作用。卑尔根精神病学项目(BPP)是一项为期 24 个月的、实用的、独立于行业的、随机的、头对头比较奥氮平、喹硫平、利培酮和齐拉西酮治疗急性精神病入院患者的研究。该研究的目的是调查在急性精神病入院患者的临床相关样本中,SGAs 是否存在不同的抗抑郁效果。
急性入住精神病急诊病房的成年患者被随机分配至奥氮平、喹硫平、利培酮或齐拉西酮组,并随访 2 年。使用阳性和阴性综合征量表-抑郁因子(PANSS-D)和 Calgary 精神分裂症抑郁量表(CDSS)对参与者进行反复评估。
共纳入 226 例患者。所有药物组均显示出抑郁症状持续下降的显著时间效应。在降低 PANSS-D 评分或 CDSS 总分方面,SGAs 之间没有实质性差异。分别对 CDSS 总分>6 或≤6 的组进行单独分析,分别反映抑郁发病率的程度,得到的结果与主要分析基本一致。PANSS-D 与 CDSS 总分之间存在高度相关性(r=0.77;p<0.01)。
在本项针对急性精神病入院患者的临床相关样本中,奥氮平、喹硫平、利培酮或齐拉西酮在抗抑郁疗效方面没有实质性差异。根据我们的研究结果,我们不能针对急性精神病入院患者的抑郁症状选择任何特定 SGA 提出建议。
ClinicalTrials.gov ID;网址:http://www.clinicaltrials.gov/:NCT00932529。