首页> 外文期刊>BMJ Open >Cardiovascular and neuropsychiatric safety of varenicline and bupropion compared with nicotine replacement therapy for smoking cessation: study protocol of a retrospective cohort study using the QResearch general practice database
【24h】

Cardiovascular and neuropsychiatric safety of varenicline and bupropion compared with nicotine replacement therapy for smoking cessation: study protocol of a retrospective cohort study using the QResearch general practice database

机译:伐尼克兰和安非他酮与尼古丁替代疗法在戒烟方面的心血管和神经精神安全性:一项使用QResearch常规数据库的回顾性队列研究的研究方案

获取原文
       

摘要

Introduction Cigarette smoking continues to be the leading cause of preventable death and is the main risk factor of major diseases such as chronic obstructive pulmonary disease (COPD). The best treatment to help smokers quit is a combination of behavioural support with pharmacotherapy. Varenicline is the newest drug on the market and has been shown to be effective in the general smoking population and in smokers with COPD. The safety profile of varenicline was initially established using standard approaches to pharmacovigilance, but postmarketing reports have raised concerns about a possible association between the use of varenicline and cardiovascular and neuropsychiatric events. Although recent studies have not confirmed such an association, further research is needed given the large number of smokers who are being prescribed varenicline, including important subgroups such as smokers with COPD who may be particularly vulnerable to side effects of drugs. The aim of this study is to assess the cardiovascular and neuropsychiatric safety of varenicline using data from the QResearch general practice (GP) database. Methods and analysis We will conduct a retrospective cohort study in the QResearch GP database. Patients will be categorised into three exposure groups: prescription of (1) varenicline, (2) bupropion or (3) nicotine replacement therapy (NRT Rx; =reference group). We will separately consider major incident neuropsychiatric and cardiovascular outcomes that occur during 6?months of follow-up using Cox proportional hazards models, adjusted for confounders. Furthermore, propensity score analysis will be used as an analytical approach to account for potential confounding by indication. Ethics and dissemination This work involves analysis of anonymised, routinely collected data. The protocol has been independently peer-reviewed by the QResearch Scientific Board and meets the requirements of the Trent research ethics committee. We plan to disseminate the results from this study via articles in international peer-reviewed journals and presentations at relevant national and international health conferences.
机译:引言吸烟仍然是可预防死亡的主要原因,并且是诸如慢性阻塞性肺疾病(COPD)等主要疾病的主要危险因素。帮助吸烟者戒烟的最佳治疗方法是将行为支持与药物治疗相结合。瓦伦尼克林是市场上最新的药物,已被证明对普通吸烟人群和患有COPD的吸烟者有效。伐尼克兰的安全性最初是使用药物警戒的标准方法建立的,但是上市后的报告引起了人们对伐尼克兰的使用与心血管和神经精神疾病之间可能相关性的担忧。尽管最近的研究尚未证实这种关联,但鉴于正在开处方伐尼克兰的大量吸烟者,包括重要的亚组,例如患有COPD的吸烟者,可能特别容易受到药物副作用的影响,因此需要进一步的研究。这项研究的目的是使用QResearch通用(GP)数据库中的数据评估伐尼克兰的心血管和神经精神安全性。方法和分析我们将在QResearch GP数据库中进行回顾性队列研究。患者将被分为三个暴露组:(1)伐尼克兰,(2)安非他酮或(3)尼古丁替代疗法(NRT Rx; =参考组)。我们将使用针对混杂因素进行调整的Cox比例风险模型,分别考虑在6个月的随访期间发生的重大神经精神疾病和心血管事件。此外,倾向得分分析将用作一种分析方法,以解决适应症的潜在混淆。道德与传播这项工作涉及对匿名收集的常规数据的分析。该协议已由QResearch科学委员会进行了独立的同行评审,并且符合Trent研究道德委员会的要求。我们计划通过国际同行评审期刊上的文章以及在相关的国家和国际健康会议上的演讲来传播本研究的结果。

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