...
首页> 外文期刊>Depression and anxiety >Efficacy and safety of pharmacotherapies for smoking cessation in anxiety disorders: Subgroup analysis of the randomized, active- and placebo-controlled EAGLES trial
【24h】

Efficacy and safety of pharmacotherapies for smoking cessation in anxiety disorders: Subgroup analysis of the randomized, active- and placebo-controlled EAGLES trial

机译:焦虑症戒烟的药物治疗的疗效和安全性:随机,活跃和安慰剂控制的老鹰试验的亚组分析

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Background Smoking rates are high in adults with anxiety disorders (ADs), yet little is known about the safety and efficacy of smoking-cessation pharmacotherapies in this group. Methods Post hoc analyses in 712 smokers with AD (posttraumatic stress disorder [PTSD], n = 192; generalized anxiety disorder [GAD], n = 243; panic disorder [PD], n = 277) and in a nonpsychiatric cohort (NPC; n = 4,028). Participants were randomly assigned to varenicline, bupropion, nicotine-replacement therapy (NRT), or placebo plus weekly smoking-cessation counseling for 12 weeks, with 12 weeks follow-up. General linear models were used to test the effects of treatment group, cohort, and their interaction on neuropsychiatric adverse events (NPSAEs), and continuous abstinence weeks 9-12 (treatment) and 9-24 (follow-up). Results NPSAE incidence for PTSD (6.9%), GAD (5.4%), and PD (6.2%) was higher versus NPC (2.1%), regardless of treatment. Across all treatments, smokers with PTSD (odds ratio [OR] = 0.58), GAD (OR = 0.72), and PD (OR = 0.53) had lower continuous abstinence rates weeks 9-12 (CAR9-12) versus NPC. Varenicline demonstrated superior efficacy to placebo in smokers with GAD and PD, respectively (OR = 4.53; 95% confidence interval [CI] = 1.20-17.10; and OR = 8.49; 95% CI = 1.57-45.78); NRT was superior to placebo in smokers with PD (OR = 7.42; 95% CI = 1.37-40.35). While there was no statistically significant effect of any treatment on CAR9-12 for smokers with PTSD, varenicline improved 7-day point prevalence abstinence at end of treatment in this subcohort. Conclusion Individuals with ADs were more likely than those without psychiatric illness to experience moderate to severe NPSAEs during smoking-cessation attempts, regardless of treatment. While the study was not powered to evaluate abstinence outcomes with these subgroups of smokers with ADs, varenicline provided significant benefit for cessation in those with GAD and PD, while NRT provided significant benefit for those with PD.
机译:背景吸烟率在成年人中患有焦虑障碍(广告),但对于该组中吸烟药物检察会的安全性和有效性毫无熟悉。方法在712个吸烟者中分析HOOC分析(PTEROUMATIC胁迫障碍[PTSD],N = 192;广义焦虑症[GAD],N = 243;恐慌障碍[PD],N = 277)和非心理队列(NPC; n = 4,028)。参与者被随机分配给varenicline,Bupropion,尼古丁替代疗法(NRT),或安慰剂加上每周吸烟咨询12周,随访12周。通用线性模型用于测试治疗组,队列和它们对神经精神不良事件(NPSAES)的相互作用的影响,以及连续禁因周9-12(治疗)和9-24(随访)。结果NPSAE接触(6.9%),GAD(5.4%)和Pd(6.2%)对NPC(2.1%),无论治疗如何。在所有治疗中,具有PTSD的吸烟者(差距[或] = 0.58),GAD(或= 0.72)和Pd(或= 0.53)的连续禁欲率较低,与NPC为NPC。 varenicline分别对吸烟者分别表现出优异的疗效,分别在吸烟者中放置(或= 4.53; 95%置信区间[CI] = 1.20-17.10;和= 8.49; 95%CI = 1.57-45.78); NRT在具有PD的吸烟者中优于安慰剂(或= 7.42; 95%CI = 1.37-40.35)。虽然对具有PTSD的吸烟者对CAR9-12的任何治疗没有统计学显着的效果,但在该亚脉冲中治疗结束时,varenicline在varenicline提高了7天的患病症。结论患有广告的个体比没有精神疾病的人更有可能在吸烟的尝试中经历中度至严重的NPSA,而不管治疗如何。虽然该研究没有得到通过广告的吸烟者的禁止结果评估禁欲结果,但Varenicline在用GAD和PD的那些中提供了显着的益处,而NRT则为PD的人提供了显着的益处。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号