Department of Epidemiology & Preventive Medicine, School of Public Health & Preventive Medicine, Alfred Hospital, Monash University, Melbourne, Victoria, 3004, Australia.
Cardiovasc Drugs Ther. 2010 Aug;24(4):359-67. doi: 10.1007/s10557-010-6246-8.
Smoking continues to be a major contributor to the burden of disease across the world although there has been a decrease in some developed countries such as USA and Australia. In countries of South-East Asia with a high prevalence of smoking, the incidence of tobacco-related diseases will continue to increase.
We reviewed the literature in relation to the pharmacology of nicotine, the measures used to determine the efficacy of anti-smoking therapies, and the randomised controlled trials and systematic reviews of pharmacotherapies published between 2004 and 2010. We focused primarily on the three first line therapies that are currently available: nicotine replacement therapy (NRT), bupropion and varenicline.
Randomised controlled trials and meta-analyses have demonstrated that single therapy with either NRT, bupropion or varenicline are all more effective than placebo for smoking cessation. Abstinence rates for monotherapies varies from 13.3% to 19% for NRT compared to 7.5% to 14% for placebo, 19% to 19.7% for bupropion versus 10.9% to 11% for placebo and 25.5% to 25.6% for varenicline versus 11.2% to 14.8% for placebo. Of current therapies varenicline appears to be more effective at achieving abstinence. Some combination therapies with one or two formulations of NRT or NRT plus bupropion have demonstrated superior results to monotherapy. To date there are no randomised controlled trials of varenicline in combination with NRT or bupropion.
Further studies are required to address the uncertainty that exists on the most appropriate duration of therapy as well as the effectiveness and safety of combination pharmacotherapy. Post-marketing surveillance continues to play an important role in monitoring the adverse effects events associated with these therapies.
尽管美国和澳大利亚等一些发达国家的吸烟率有所下降,但吸烟仍是全球疾病负担的主要因素之一。在东南亚一些吸烟率较高的国家,与烟草相关的疾病发病率将继续上升。
我们回顾了 2004 年至 2010 年间发表的关于尼古丁药理学、用于确定戒烟治疗效果的措施以及药物治疗随机对照试验和系统评价的文献。我们主要关注目前可用的三种一线治疗方法:尼古丁替代疗法(NRT)、安非他酮和伐尼克兰。
随机对照试验和荟萃分析表明,NRT、安非他酮或伐尼克兰单一疗法在戒烟方面均优于安慰剂。单一疗法的戒烟率从 NRT 的 13.3%到 19%不等,而安慰剂为 7.5%到 14%,安非他酮为 19%到 19.7%,而安慰剂为 10.9%到 11%,伐尼克兰为 25.5%到 25.6%,而安慰剂为 11.2%到 14.8%。目前的治疗方法中,伐尼克兰似乎在实现戒烟方面更有效。一些联合治疗方案,如一种或两种 NRT 制剂或 NRT 加安非他酮,已证明比单一疗法效果更好。迄今为止,还没有关于伐尼克兰与 NRT 或安非他酮联合使用的随机对照试验。
需要进一步研究以解决关于最佳治疗持续时间以及联合药物治疗的有效性和安全性的不确定性。上市后监测继续在监测与这些疗法相关的不良反应事件方面发挥重要作用。