Gastrointestinal adverse effects of varenicline at maintenance dose: a meta-analysis.

Lawrence K Leung, Francis M Patafio, Walter W Rosser
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引用次数: 21

Abstract

Background: Tobacco smoking remains the leading modifiable health hazard and varenicline is amongst the most popular pharmacological options for smoking cessation. The purpose of this study is to critically evaluate the extent of gastrointestinal adverse effects of varenicline when used at maintenance dose (1 mg twice a day) for smoking cessation.

Methods: We conducted a meta-analysis of randomised controlled trials published in PUBMED and EMBASE according to the PRISMA guidelines. Selected studies satisfied the following criteria: (i) duration of at least 6 weeks, (ii) titrated dose of varenicline for 7 days then a maintenance dose of 1 mg twice-per-day, (iii) randomized placebo-controlled design, (iv) extractable data on adverse event - nausea, constipation or flatulence. Data was synthesized into pooled odd ratios (OR) basing on random effects model. Quality of studies was also rated as per Cochrane risk-of-bias assessment. Number need to harm (NNH) was calculated for each adverse effect.

Results: 98 potentially relevant studies were identified, 12 of which met the final inclusion criteria (n = 5114). All 12 studies reported adverse events on nausea, which led to an OR of 4.45 (95% CI = 3.79-5.23, p < 0.001; I(2) = 0.06%, CI = 0%-58.34%) and a NNH of 5. Eight studies (n = 3539) contain data on constipation pooled into an OR of 2.45 (95% CI = 1.61-3.72, p < 0.001; I(2) = 34.09%, CI = 0%-70.81%) with a NNH of 24. Finally, five studies (n = 2516) reported adverse events of flatulence, which pooled an OR of 1.74 (95% CI = 1.23-2.48, p = 0.002; I(2) = 0%, CI = 0%- 79.2%) with a NNH of 35.

Conclusions: Use of varenicline at maintenance dose of 1 mg twice a day for longer than 6 weeks is associated with adverse gastrointestinal effects. In realistic terms, for every 5 treated subjects, there will be an event of nausea, and for every 24 and 35 treated subjects, we will expect an event of constipation and flatulence respectively. Family physicians should counsel patients of such risks accordingly during their maintenance therapy with varenicline.

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维持剂量伐尼克兰的胃肠道不良反应:一项荟萃分析。
背景:吸烟仍然是主要的可改变的健康危害,伐尼克兰是戒烟最流行的药物选择之一。本研究的目的是严格评估伐尼克兰以维持剂量(1毫克,每天2次)戒烟时胃肠道不良反应的程度。方法:我们根据PRISMA指南对发表在PUBMED和EMBASE上的随机对照试验进行了荟萃分析。所选研究满足以下标准:(i)持续时间至少6周,(ii) varenicline滴定剂量为7天,然后维持剂量为1mg,每天两次,(iii)随机安慰剂对照设计,(iv)可提取的不良事件数据-恶心,便秘或胀气。基于随机效应模型,将数据合成为混合奇比(OR)。研究质量也根据Cochrane风险偏倚评估进行评分。计算每个不良反应的需要伤害数(NNH)。结果:确定了98项可能相关的研究,其中12项符合最终纳入标准(n = 5114)。所有12项研究都报告了恶心的不良事件,导致OR为4.45 (95% CI = 3.79-5.23, p < 0.001;I(2) = 0.06%, CI = 0% ~ 58.34%), NNH为5。8项研究(n = 3539)包含便秘的数据,合并OR为2.45 (95% CI = 1.61-3.72, p < 0.001;I(2) = 34.09%, CI = 0% ~ 70.81%), NNH为24。最后,5项研究(n = 2516)报告了肠胃胀气的不良事件,合并OR为1.74 (95% CI = 1.23-2.48, p = 0.002;I(2) = 0%, CI = 0%- 79.2%), NNH为35。结论:使用伐尼克兰维持剂量为1 mg,每日2次,持续6周以上会产生不良胃肠道反应。在现实中,每5个接受治疗的受试者中,将会出现恶心事件,每24个和35个接受治疗的受试者中,我们预计分别会出现便秘和胀气事件。家庭医生应在患者使用伐尼克兰维持治疗期间相应地告知这些风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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