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奥氮平治疗病理性赌博:一项阴性随机安慰剂对照试验。

Olanzapine in the treatment of pathological gambling: a negative randomized placebo-controlled trial.

作者信息

McElroy Susan L, Nelson Erik B, Welge Jeffrey A, Kaehler Laura, Keck Paul E

机构信息

Psychopharmacology Research Program, Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0559, USA.

出版信息

J Clin Psychiatry. 2008 Mar;69(3):433-40. doi: 10.4088/jcp.v69n0314.

Abstract

OBJECTIVE

Pathological gambling is associated with bipolar disorder and dopamine dysfunction. Olanzapine is a second-generation antipsychotic with mood-stabilizing properties and antagonistic activity at several dopamine receptors. The purpose of this study was to evaluate olanzapine in the treatment of pathological gambling.

METHOD

In this 12-week, single-center, randomized, double-blind, placebo-controlled, flexible-dose (2.5-15 mg/day) trial, 42 outpatients with pathological gambling by DSM-IV-TR criteria received olanzapine (N = 21) or placebo (N = 21). The primary outcome measure was the Pathological Gambling Adaptation of the Yale-Brown Obsessive Compulsive Scale (PG-YBOCS). The primary analysis of efficacy was a longitudinal analysis of the intent-to-treat sample, with treatment-by-time interaction as the effect measure. Subjects were enrolled from June 2, 2000, through November 28, 2005.

RESULTS

Compared with placebo, olanzapine was associated with a similar rate of reduction in total scores on the PG-YBOCS scale, as well as in gambling episodes/week, hours gambled/week, and Clinical Global Impressions-Severity of Illness scale scores. The mean (SD) olanzapine daily dose at endpoint evaluation was 8.9 (5.2) mg/day. Eleven subjects (52%) receiving olanzapine and 6 (29%) receiving placebo discontinued prematurely; 3 subjects receiving olanzapine and 2 receiving placebo discontinued because of adverse events. Events causing olanzapine discontinuation were pneumonia, sedation, and hypomania.

CONCLUSION

Olanzapine was not superior to placebo in the short-term treatment of pathological gambling. It was also associated with a high discontinuation rate.

TRIAL REGISTRATION

ClinicalTrials.gov identifier NCT00438776 (http://www.clinicaltrials.gov).

摘要

目的

病理性赌博与双相情感障碍及多巴胺功能障碍相关。奥氮平是一种第二代抗精神病药物,具有心境稳定特性,对多种多巴胺受体具有拮抗活性。本研究旨在评估奥氮平治疗病理性赌博的效果。

方法

在这项为期12周的单中心、随机、双盲、安慰剂对照、灵活剂量(2.5 - 15毫克/天)试验中,42名符合《精神疾病诊断与统计手册》第四版修订版(DSM-IV-TR)标准的病理性赌博门诊患者接受了奥氮平治疗(N = 21)或安慰剂治疗(N = 21)。主要结局指标是耶鲁-布朗强迫症状量表病理性赌博适应版(PG-YBOCS)。疗效的主要分析是对意向性治疗样本的纵向分析,以治疗时间交互作用作为效应量。研究对象从2000年6月2日至2005年11月28日入组。

结果

与安慰剂相比,奥氮平治疗后PG-YBOCS量表总分、每周赌博发作次数、每周赌博时长及临床总体印象-疾病严重程度量表评分的降低率相似。终点评估时奥氮平的平均(标准差)日剂量为8.9(5.2)毫克/天。11名接受奥氮平治疗的受试者(52%)和6名接受安慰剂治疗的受试者(29%)提前停药;3名接受奥氮平治疗的受试者和2名接受安慰剂治疗的受试者因不良事件停药。导致奥氮平停药的事件包括肺炎、镇静和轻躁狂。

结论

奥氮平在病理性赌博的短期治疗中并不优于安慰剂,且停药率较高。

试验注册

ClinicalTrials.gov标识符NCT00438776(http://www.clinicaltrials.gov)

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