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伐伦克林用于戒烟和减少严重精神疾病患者:系统评价和荟萃分析。

Varenicline for smoking cessation and reduction in people with severe mental illnesses: systematic review and meta-analysis.

机构信息

Mental Health and Addiction Research Group, Department of Health Sciences, University of York, Heslington, York, UK.

出版信息

Addiction. 2016 Sep;111(9):1554-67. doi: 10.1111/add.13415. Epub 2016 Jun 9.

DOI:10.1111/add.13415
PMID:27043328
Abstract

AIMS

To determine the effectiveness and safety of varenicline in treating tobacco dependence in patients with severe mental illness.

DESIGN

A systematic review and meta-analysis of randomised controlled trials that compared varenicline with a placebo or an alternative intervention for smoking cessation or reduction.

SETTING

Both in- and out-patient settings in any country.

PARTICIPANTS

Adult patients aged 18 years and over with any type of severe mental illness. The systematic review included eight studies comprising 398 participants.

MEASURES

Primary outcome measures were (1) smoking cessation, (2) smoking reduction measured by changes in the number of cigarettes smoked per day and (3) number of psychiatric adverse events, which were collected at the end of treatment.

FINDINGS

The random-effect pooled estimates from the five studies that reported smoking-related outcomes found that varenicline is statistically superior to placebo in smoking cessation [risk ratios 4.33; 95% confidence interval (CI) = 1.96-9.56], and smoking reduction was higher in varenicline groups (mean reduced daily cigarettes was 6.39; 95% CI = 2.22-10.56). There is no significant difference regarding neuropsychiatric and other adverse events.

CONCLUSIONS

Varenicline appears to be significantly more effective than placebo in assisting with smoking cessation and reduction in people with severe mental illness. There appears to be no clear evidence that varenicline was associated with an increased risk of neuropsychiatric or other adverse events compared with placebo.

摘要

目的

评估伐伦克林治疗伴有严重精神疾病患者烟草依赖的有效性和安全性。

设计

系统评价和随机对照试验的荟萃分析,比较了伐伦克林与安慰剂或其他戒烟或减少吸烟的干预措施的效果。

设置

任何国家的门诊和住院环境。

参与者

年龄在 18 岁及以上的任何类型严重精神疾病的成年患者。系统评价包括 8 项研究,共 398 名参与者。

测量

主要结局指标为(1)戒烟,(2)通过每日吸烟量的变化衡量的吸烟减少,(3)治疗结束时收集的精神科不良事件的数量。

发现

报告与吸烟相关的结局的五项研究中的随机效应汇总估计发现,伐伦克林在戒烟方面明显优于安慰剂[风险比 4.33;95%置信区间(CI)= 1.96-9.56],伐伦克林组的吸烟减少量更高(平均每日减少香烟 6.39 支;95%CI= 2.22-10.56)。在神经精神和其他不良事件方面没有显著差异。

结论

伐伦克林似乎比安慰剂更有效地帮助患有严重精神疾病的人戒烟和减少吸烟量。与安慰剂相比,伐伦克林似乎没有明显增加神经精神或其他不良事件的风险的证据。

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