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首发精神分裂症患者的抑郁治疗:EUFEST 的研究结果。

Treatment of depression in first episode of schizophrenia: results from EUFEST.

机构信息

Department of Adult Psychiatry, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

Eur Neuropsychopharmacol. 2012 Dec;22(12):875-82. doi: 10.1016/j.euroneuro.2012.04.001. Epub 2012 May 23.

DOI:10.1016/j.euroneuro.2012.04.001
PMID:22627166
Abstract

Depressive symptomatology is an important target of treatment in first episode schizophrenia. This reanalysis of the European First Episode Schizophrenia Trial (EUFEST) describes the depressive symptomatology and the effect of antipsychotic treatment in patients suffering from first episode schizophrenia and schizophreniform disorder randomized to treatment with low dose haloperidol (n=103), amisulpride (n=104), olanzapine (n=105), quetiapine (n=104) or ziprasidone (n=82) for one year. At baseline, the mean score on the Calgary Depression Scale for Schizophrenia (CDSS) was 5.1 (±4.9) with 38.3% of patients having a CDSS score≥6, i.e. clinically relevant depressive symptom severity. During treatment depression scores decreased, the mean CDSS score being 1.1 (±2.1) and 3.0% of patients having a CDSS≥6 at 52 weeks. The proportion of patients using antidepressants during the complete trial was 18.5% in the haloperidol group, 28.6% in the olanzapine group compared to 5.8% in the quetiapine group, 12.5% in the amisulpride group, and 9.8% in the ziprasidone group. There were no differences over time in the probability of being depressed (CDSS≥6) between the 5 treatment groups after adjustment for antidepressant use, nor in a sub analysis of patients who did not take any antidepressant. Depression scores at baseline or during the trial had no effect on treatment discontinuation or on the reduction of positive symptoms. In summary, the results of EUFEST did not demonstrate a differential effect of the antipsychotics studied on depressive symptomatology in patients with first episode schizophrenia.

摘要

抑郁症状是首发精神分裂症治疗的重要目标。本研究重新分析了欧洲首发精神分裂症试验(EUFEST)的数据,描述了首发精神分裂症和分裂样障碍患者的抑郁症状,并评估了抗精神病药物治疗对其的影响。该研究将 394 例患者随机分为低剂量氟哌啶醇(n=103)、氨磺必利(n=104)、奥氮平(n=105)、喹硫平(n=104)或齐拉西酮(n=82)组,接受为期 1 年的治疗。基线时, Calgary 抑郁量表(CDSS)的平均得分为 5.1(±4.9),38.3%的患者 CDSS 评分≥6,即存在临床相关的抑郁严重程度。治疗期间,抑郁评分下降,CDSS 平均得分为 1.1(±2.1),52 周时 3.0%的患者 CDSS 评分≥6。在整个试验期间使用抗抑郁药的患者比例分别为:氟哌啶醇组 18.5%,奥氮平组 28.6%,喹硫平组 5.8%,氨磺必利组 12.5%,齐拉西酮组 9.8%。调整抗抑郁药使用后,5 种治疗组之间在抑郁(CDSS≥6)的可能性方面,以及在未使用任何抗抑郁药的患者亚组分析中,均无随时间变化的差异。基线时或试验期间的抑郁评分对停药或阳性症状的改善均无影响。总之,EUFEST 的结果并未显示研究中的抗精神病药物对首发精神分裂症患者的抑郁症状有差异作用。

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