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伐仑克林:作用机制、疗效、安全性以及针对临床人群的累积经验要点。

Varenicline: mode of action, efficacy, safety and accumulated experience salient for clinical populations.

机构信息

Department of Preventive Cardiology, Oslo University Hospital, Aker, Oslo, Norway.

Pfizer Inc, New York, NY, USA.

出版信息

Curr Med Res Opin. 2020 May;36(5):713-730. doi: 10.1080/03007995.2020.1729708. Epub 2020 Mar 14.

DOI:10.1080/03007995.2020.1729708
PMID:32050807
Abstract

Varenicline, a selective partial agonist of the α4β2 nicotinic acetylcholine receptor, is a smoking cessation pharmacotherapy that more than doubles the chance of quitting smoking at 6 months compared with placebo. This article reviews salient knowledge of the discovery, pharmacological characteristics, and the efficacy and safety of varenicline in general and in specific populations of smokers and provides recommendations to support use in clinical practice.: Literature searches for varenicline were conducted using PubMed, with date limitations of 2000-2018 inclusive, using search terms covering the discovery, mechanism of action, pharmacokinetics, efficacy and safety in different populations of smokers, alternative quit approaches and combination therapy. Selection of safety and efficacy data was limited to clinical trials, meta-analyses and observational studies. Standard administration of varenicline is efficacious in helping smokers to quit, including smokers with cardiovascular disease and chronic obstructive pulmonary disease. Furthermore, varenicline efficacy may be improved with pre-loading, a gradual quitting approach for smokers unwilling or unable to quit abruptly, and extended treatment in smokers who have recently quit to help maintain abstinence. Initial concerns regarding the association of varenicline with increased risk of neuropsychiatric and cardiovascular adverse events have been disproven after extensive clinical evaluations, and the benefit-risk profile of varenicline is considered favorable. Varenicline is efficacious and safe for all adult smokers with a range of clinical characteristics. Evidence suggests that approaches offering greater flexibility in timing and duration of treatment may further extend treatment efficacy and clinical reach.

摘要

伐伦克林是一种选择性部分激动剂α4β2 烟碱型乙酰胆碱受体,是一种戒烟药物治疗,与安慰剂相比,能将戒烟的几率提高一倍以上。本文综述了伐伦克林的发现、药理学特征以及在一般和特定吸烟人群中的疗效和安全性的相关知识,并提出了支持其在临床实践中应用的建议。:使用 PubMed 对伐伦克林进行了文献检索,时间限制为 2000 年至 2018 年,使用了涵盖发现、作用机制、药代动力学、不同吸烟人群的疗效和安全性、替代戒烟方法和联合治疗的搜索词。安全性和疗效数据的选择仅限于临床试验、荟萃分析和观察性研究。标准剂量的伐伦克林有助于吸烟者戒烟,包括心血管疾病和慢性阻塞性肺疾病患者。此外,对于不愿意或不能突然戒烟的吸烟者,采用逐渐戒烟的方法预加载伐伦克林可能会提高其疗效,并且对最近戒烟的吸烟者延长治疗有助于维持戒断。经过广泛的临床评估,已经证明最初对伐伦克林与神经精神和心血管不良事件风险增加相关的担忧是没有根据的,伐伦克林的获益风险状况被认为是有利的。伐伦克林对具有多种临床特征的所有成年吸烟者均有效且安全。有证据表明,在治疗时间和持续时间上提供更大灵活性的方法可能会进一步提高治疗效果和临床应用范围。

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