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住院吸烟者的烟草依赖治疗:使用伐尼克兰的随机对照初步试验。

Tobacco dependence treatment for hospitalized smokers: a randomized, controlled, pilot trial using varenicline.

机构信息

Division of General Internal Medicine, University of Medicine and Dentistry of New Jersey--Robert Wood Johnson Medical School, 125 Paterson Street, Suite 2304, New Brunswick, NJ 08903, USA.

出版信息

Addict Behav. 2011 Dec;36(12):1127-32. doi: 10.1016/j.addbeh.2011.07.002. Epub 2011 Jul 23.

Abstract

OBJECTIVE

The hospital can be an important opportunity for smoking cessation interventions. This is the first randomized, double-blinded, placebo-controlled pilot trial utilizing varenicline and post-discharge, in-person behavioral treatment for hospitalized smokers.

METHOD

Seventy-nine smokers admitted to a university-based hospital with various diagnoses were enrolled from 2007 to 2009. The primary outcome was biochemically confirmed abstinence at 24 weeks following discharge. Secondary outcomes included withdrawal symptoms, motivation, utilization of treatment, and medical events.

RESULTS

Overall abstinence at 24 weeks was 27% with no difference between varenicline and placebo treatment groups (23% vs. 31%). There were no significant differences in motivation to stop smoking or withdrawal symptoms. Over 40% of all subjects utilized post-discharge behavioral treatment with significantly higher abstinence rates compared with those who did not (53.1% vs. 8.5%, p<0.01). Overall adverse events were similar in both treatment groups with the only significant difference being more nausea in the varenicline group (25% vs. 5%; p<0.01). Twenty-three subjects were re-hospitalized with no significant differences between treatment groups (13 varenicline vs. 10 placebo).

CONCLUSION

This pilot trial of varenicline in hospitalized smokers demonstrated feasibility of implementation, produced some hypothesis-generating findings, and suggested the potential benefit of face-to-face treatment following discharge.

摘要

目的

医院可以成为戒烟干预的重要机会。这是首次利用伐尼克兰(varenicline)并在出院后进行面对面的行为治疗,对住院吸烟者进行随机、双盲、安慰剂对照的初步试验。

方法

2007 年至 2009 年,从一所大学附属医院收治的各种诊断的吸烟者中招募了 79 名吸烟者。主要结局是出院后 24 周时通过生物化学方法确认的戒烟。次要结局包括戒断症状、动机、治疗利用情况和医疗事件。

结果

24 周时的总体戒烟率为 27%,伐尼克兰和安慰剂治疗组之间无差异(23%比 31%)。戒烟动机或戒断症状无显著差异。超过 40%的所有受试者都利用了出院后的行为治疗,与未接受治疗的相比,其戒烟率显著更高(53.1%比 8.5%,p<0.01)。两组的总体不良事件相似,唯一的显著差异是伐尼克兰组的恶心症状更多(25%比 5%;p<0.01)。23 名受试者再次住院,两组之间无显著差异(13 名伐尼克兰组与 10 名安慰剂组)。

结论

这项住院吸烟者使用伐尼克兰的初步试验证明了实施的可行性,产生了一些产生假设的发现,并表明出院后面对面治疗的潜在益处。

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