Suppr超能文献

一项关于安非他酮预防注意缺陷/多动障碍儿童及青少年吸烟的随机、安慰剂对照临床试验。

A randomized, placebo-controlled clinical trial of bupropion for the prevention of smoking in children and adolescents with attention-deficit/hyperactivity disorder.

作者信息

Monuteaux Michael C, Spencer Thomas J, Faraone Stephen V, Wilson Angela M, Biederman Joseph

机构信息

Pediatric Psychopharmacology Program, Massachusetts General Hospital, USA.

出版信息

J Clin Psychiatry. 2007 Jul;68(7):1094-101. doi: 10.4088/jcp.v68n0718.

Abstract

OBJECTIVE

Since attention-deficit/hyperactivity disorder (ADHD) is a well-documented risk factor for smoking and bupropion has been shown to be effective for smoking cessation, we tested the efficacy of bupropion as a prophylactic agent for the prevention of smoking in children and adolescents with ADHD.

METHOD

We conducted a longitudinal, randomized, double-blind, placebo-controlled, parallel-group study of bupropion at a large, urban, outpatient medical center. Recruitment began in April 1999, and the last subject was followed until September 2004. Patients were nonsmoking youth, of both sexes, between 9 and 18 years of age, with DSM-IV ADHD. After random assignment to either bupropion or placebo, subjects were assessed weekly for 8 weeks, biweekly for 4 weeks, and monthly thereafter for up to 6.5 years (mean 12 months). Also, patients received treatment with psychostimulants for ADHD symptoms as needed. To assess smoking, we used an assay of cotinine in urine.

RESULTS

Fifty-seven subjects (28 receiving bupropion and 29 receiving placebo) were randomly assigned and included in the analysis. No differences were found between the bupropion and placebo groups on demographic factors. About half of each group was treated with stimulants for ADHD. Statistical separation between bupropion and placebo in the rate of smoking initiation or continued smoking was not demonstrated. However, secondary post hoc analyses revealed that concurrent stimulant treatment was significantly associated with a lower rate of smoking onset (hazard ratio [HR] = 0.2, 95% CI = 0.08 to 0.89; z = -2.2, p = .03) and a lower rate of continued smoking (HR = 0.3, 95% CI = 0.11 to 0.85; z = -2.3, p = .02).

CONCLUSION

While bupropion was not associated with a lower rate of smoking in youth with ADHD, post hoc analyses suggest that stimulant treatment was. Future controlled studies should investigate the role of stimulants in the prevention of smoking in children and adolescents with ADHD.

摘要

目的

鉴于注意力缺陷多动障碍(ADHD)是一个有充分文献记载的吸烟风险因素,且安非他酮已被证明对戒烟有效,我们测试了安非他酮作为预防ADHD儿童和青少年吸烟的预防剂的疗效。

方法

我们在一个大型城市门诊医疗中心进行了一项关于安非他酮的纵向、随机、双盲、安慰剂对照、平行组研究。招募工作于1999年4月开始,最后一名受试者随访至2004年9月。患者为9至18岁、患有DSM-IV ADHD的不吸烟青少年,男女不限。随机分配至安非他酮组或安慰剂组后,受试者在8周内每周评估一次,接下来4周每两周评估一次,此后每月评估一次,最长6.5年(平均12个月)。此外,患者根据需要接受用于治疗ADHD症状的精神兴奋剂治疗。为评估吸烟情况,我们检测了尿液中的可替宁。

结果

57名受试者(28名接受安非他酮治疗,29名接受安慰剂治疗)被随机分配并纳入分析。安非他酮组和安慰剂组在人口统计学因素上未发现差异。每组约一半的受试者接受了用于治疗ADHD的兴奋剂治疗。未证明安非他酮组和安慰剂组在开始吸烟率或持续吸烟率上存在统计学差异。然而,事后的二次分析显示,同时使用兴奋剂治疗与较低的吸烟起始率(风险比[HR]=0.2,95%可信区间=0.08至0.89;z=-2.2;p=0.03)和较低的持续吸烟率(HR=0.3,95%可信区间=0.11至0.85;z=-2.3;p=0.02)显著相关。

结论

虽然安非他酮与ADHD青少年较低的吸烟率无关,但事后分析表明兴奋剂治疗与较低吸烟率有关。未来的对照研究应调查兴奋剂在预防ADHD儿童和青少年吸烟中的作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验