Kotz Daniel, Simpson Colin, Viechtbauer Wolfgang, van Schayck Onno C P, West Robert, Sheikh Aziz
Department of Family Medicine, CAPHRI School for Public Health and Primary Care, Maastricht University Medical Centre, Maastricht, The Netherlands Cancer Research UK Health Behaviour Research Centre, University College London, London, UK Allergy and Respiratory Research Group, Centre for Population Health Sciences, The University of Edinburgh, Edinburgh, UK.
Allergy and Respiratory Research Group, Centre for Population Health Sciences, The University of Edinburgh, Edinburgh, UK.
BMJ Open. 2014 Aug 28;4(8):e005281. doi: 10.1136/bmjopen-2014-005281.
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.
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.
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.
吸烟仍然是可预防死亡的主要原因,并且是慢性阻塞性肺疾病(COPD)等重大疾病的主要风险因素。帮助吸烟者戒烟的最佳治疗方法是行为支持与药物治疗相结合。伐尼克兰是市场上最新的药物,已被证明对一般吸烟人群和患有COPD的吸烟者有效。伐尼克兰的安全性最初是通过标准的药物警戒方法确定的,但上市后报告引发了对使用伐尼克兰与心血管和神经精神事件之间可能存在关联的担忧。尽管最近的研究尚未证实这种关联,但鉴于大量吸烟者正在服用伐尼克兰,包括可能特别容易受到药物副作用影响的重要亚组,如患有COPD的吸烟者,仍需要进一步研究。本研究的目的是使用QResearch全科医疗(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。
我们将在QResearch GP数据库中进行一项回顾性队列研究。患者将被分为三个暴露组:(1)伐尼克兰处方组、(2)安非他酮组或(3)尼古丁替代疗法(NRT Rx;=参照组)。我们将使用Cox比例风险模型分别考虑随访6个月期间发生的主要神经精神和心血管事件,并对混杂因素进行调整。此外,倾向评分分析将用作一种分析方法,以考虑适应症可能造成的混杂。
这项工作涉及对匿名的、常规收集的数据进行分析。该方案已由QResearch科学委员会进行独立同行评审,并符合特伦特研究伦理委员会的要求。我们计划通过在国际同行评审期刊上发表文章以及在相关的国家和国际健康会议上进行报告来传播本研究的结果。