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一项随机、双盲、安慰剂对照研究,评估伐伦克林在精神分裂症或分裂情感障碍患者中的戒烟安全性和疗效。

A randomized, double-blind, placebo-controlled study evaluating the safety and efficacy of varenicline for smoking cessation in patients with schizophrenia or schizoaffective disorder.

机构信息

Division of Addiction Psychiatry, University of Medicine and Dentistry of New Jersey-Robert Wood Johnson Medical School, New Brunswick, NJ 08901, USA.

出版信息

J Clin Psychiatry. 2012 May;73(5):654-60. doi: 10.4088/JCP.11m07522.

Abstract

OBJECTIVE

Effective smoking cessation treatments are needed for patients with schizophrenia, who, compared with the general population, have high rates of cigarette smoking and more difficulty quitting. We evaluated the safety and efficacy of varenicline for smoking cessation in outpatients with stable schizophrenia or schizoaffective disorder.

METHOD

In this 12-week, randomized, double-blind, multicenter trial (May 8, 2008, to April 1, 2010), 127 smokers (≥ 15 cigarettes/d) with DSM-IV-confirmed schizophrenia or schizoaffective disorder received varenicline or placebo (2:1 ratio). The primary outcome was safety and tolerability of varenicline assessed by adverse events frequency and changes in ratings on the Positive and Negative Syndrome Scale and other psychiatric scales from baseline to 24 weeks. Abstinence was defined as no smoking 7 days prior to weeks 12 and 24, verified by carbon monoxide level.

RESULTS

Eighty-four participants received varenicline; 43, placebo. At 12 weeks (end of treatment), 16/84 varenicline-treated patients (19.0%) met smoking cessation criteria versus 2/43 (4.7%) for placebo (P = .046). At 24 weeks, 10/84 (11.9%) varenicline-treated and 1/43 (2.3%) placebo-treated patients, respectively, met abstinence criteria (P = .090). Total adverse event rates were similar between groups, with no significant changes in symptoms of schizophrenia or in mood and anxiety ratings. Rates of suicidal ideation adverse events were 6.0% (varenicline) and 7.0% (placebo) (P = 1.0). There was 1 suicide attempt by a varenicline patient with a lifetime history of similar attempts and no completed suicides.

CONCLUSIONS

Varenicline was well tolerated, with no evidence of exacerbation of symptoms, and was associated with significantly higher smoking cessation rates versus placebo at 12 weeks. Our findings suggest varenicline is a suitable smoking cessation therapy for patients with schizophrenia or schizoaffective disorder.

TRIAL REGISTRATION

ClinicalTrials.gov identifier: NCT00644969.

摘要

目的

需要为精神分裂症患者提供有效的戒烟治疗,与一般人群相比,精神分裂症患者的吸烟率更高,戒烟难度更大。我们评估了瓦伦尼克林(varenicline)用于治疗稳定期精神分裂症或分裂情感障碍患者的戒烟效果和安全性。

方法

在这项为期 12 周、随机、双盲、多中心试验(2008 年 5 月 8 日至 2010 年 4 月 1 日)中,127 名符合 DSM-IV 确诊标准的精神分裂症或分裂情感障碍吸烟者(≥15 支/天),接受了瓦伦尼克林或安慰剂(2:1 比例)治疗。主要结局是通过不良反应发生率以及从基线到 24 周期间阳性和阴性症状量表(Positive and Negative Syndrome Scale)和其他精神科量表评分的变化来评估瓦伦尼克林的安全性和耐受性。戒烟定义为在第 12 周和第 24 周前 7 天不吸烟,并通过一氧化碳水平验证。

结果

84 名参与者接受了瓦伦尼克林治疗,43 名接受了安慰剂治疗。在 12 周(治疗结束时),84 名瓦伦尼克林治疗组中有 16 名(19.0%)患者达到戒烟标准,而 43 名安慰剂组中只有 2 名(4.7%)达到标准(P =.046)。在 24 周时,84 名瓦伦尼克林治疗组中有 10 名(11.9%),43 名安慰剂治疗组中有 1 名(2.3%)患者分别达到了戒烟标准(P =.090)。两组总的不良反应发生率相似,精神分裂症症状或情绪和焦虑评分均无明显变化。自杀意念不良事件发生率分别为 6.0%(瓦伦尼克林)和 7.0%(安慰剂)(P = 1.0)。有 1 名瓦伦尼克林治疗的患者有自杀企图,且有类似自杀企图的既往病史,但没有完成自杀。

结论

瓦伦尼克林耐受性良好,没有证据表明症状加重,与安慰剂相比,在 12 周时,戒烟率显著更高。我们的研究结果表明,瓦伦尼克林是精神分裂症或分裂情感障碍患者的一种合适的戒烟治疗方法。

试验注册

ClinicalTrials.gov 标识符:NCT00644969。

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