Department of Behavioural Science and Health, University College London, London, UK.
Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
Cochrane Database Syst Rev. 2022 Jan 6;1(1):CD013790. doi: 10.1002/14651858.CD013790.pub2.
Heated tobacco products (HTPs) are designed to heat tobacco to a high enough temperature to release aerosol, without burning it or producing smoke. They differ from e-cigarettes because they heat tobacco leaf/sheet rather than a liquid. Companies who make HTPs claim they produce fewer harmful chemicals than conventional cigarettes. Some people report stopping smoking cigarettes entirely by switching to using HTPs, so clinicians need to know whether they are effective for this purpose and relatively safe. Also, to regulate HTPs appropriately, policymakers should understand their impact on health and on cigarette smoking prevalence.
To evaluate the effectiveness and safety of HTPs for smoking cessation and the impact of HTPs on smoking prevalence. SEARCH METHODS: We searched the Cochrane Tobacco Addiction Group's Specialised Register, CENTRAL, MEDLINE, and six other databases for relevant records to January 2021, together with reference-checking and contact with study authors and relevant groups.
We included randomised controlled trials (RCTs) in which people who smoked cigarettes were randomised to switch to exclusive HTP use or a control condition. Eligible outcomes were smoking cessation, adverse events, and selected biomarkers. RCTs conducted in clinic or in an ambulatory setting were deemed eligible when assessing safety, including those randomising participants to exclusively use HTPs, smoke cigarettes, or attempt abstinence from all tobacco. Time-series studies were also eligible for inclusion if they examined the population-level impact of heated tobacco on smoking prevalence or cigarette sales as an indirect measure.
We followed standard Cochrane methods for screening and data extraction. Our primary outcome measures were abstinence from smoking at the longest follow-up point available, adverse events, serious adverse events, and changes in smoking prevalence or cigarette sales. Other outcomes included biomarkers of harm and exposure to toxicants/carcinogens (e.g. NNAL and carboxyhaemoglobin (COHb)). We used a random-effects Mantel-Haenszel model to calculate risk ratios (RR) with 95% confidence intervals (CIs) for dichotomous outcomes. For continuous outcomes, we calculated mean differences on the log-transformed scale (LMD) with 95% CIs. We pooled data across studies using meta-analysis where possible.
We included 13 completed studies, of which 11 were RCTs assessing safety (2666 participants) and two were time-series studies. We judged eight RCTs to be at unclear risk of bias and three at high risk. All RCTs were funded by tobacco companies. Median length of follow-up was 13 weeks. No studies reported smoking cessation outcomes. There was insufficient evidence for a difference in risk of adverse events between smokers randomised to switch to heated tobacco or continue smoking cigarettes, limited by imprecision and risk of bias (RR 1.03, 95% CI 0.92 to 1.15; I = 0%; 6 studies, 1713 participants). There was insufficient evidence to determine whether risk of serious adverse events differed between groups due to very serious imprecision and risk of bias (RR 0.79, 95% CI 0.33 to 1.94; I = 0%; 4 studies, 1472 participants). There was moderate-certainty evidence for lower NNAL and COHb at follow-up in heated tobacco than cigarette smoking groups, limited by risk of bias (NNAL: LMD -0.81, 95% CI -1.07 to -0.55; I = 92%; 10 studies, 1959 participants; COHb: LMD -0.74, 95% CI -0.92 to -0.52; I = 96%; 9 studies, 1807 participants). Evidence for additional biomarkers of exposure are reported in the main body of the review. There was insufficient evidence for a difference in risk of adverse events in smokers randomised to switch to heated tobacco or attempt abstinence from all tobacco, limited by risk of bias and imprecision (RR 1.12, 95% CI 0.86 to 1.46; I = 0%; 2 studies, 237 participants). Five studies reported that no serious adverse events occurred in either group (533 participants). There was moderate-certainty evidence, limited by risk of bias, that urine concentrations of NNAL at follow-up were higher in the heated tobacco use compared with abstinence group (LMD 0.50, 95% CI 0.34 to 0.66; I = 0%; 5 studies, 382 participants). In addition, there was very low-certainty evidence, limited by risk of bias, inconsistency, and imprecision, for higher COHb in the heated tobacco use compared with abstinence group for intention-to-treat analyses (LMD 0.69, 95% CI 0.07 to 1.31; 3 studies, 212 participants), but lower COHb in per-protocol analyses (LMD -0.32, 95% CI -1.04 to 0.39; 2 studies, 170 participants). Evidence concerning additional biomarkers is reported in the main body of the review. Data from two time-series studies showed that the rate of decline in cigarette sales accelerated following the introduction of heated tobacco to market in Japan. This evidence was of very low-certainty as there was risk of bias, including possible confounding, and cigarette sales are an indirect measure of smoking prevalence.
AUTHORS' CONCLUSIONS: No studies reported on cigarette smoking cessation, so the effectiveness of heated tobacco for this purpose remains uncertain. There was insufficient evidence for differences in risk of adverse or serious adverse events between people randomised to switch to heated tobacco, smoke cigarettes, or attempt tobacco abstinence in the short-term. There was moderate-certainty evidence that heated tobacco users have lower exposure to toxicants/carcinogens than cigarette smokers and very low- to moderate-certainty evidence of higher exposure than those attempting abstinence from all tobacco. Independently funded research on the effectiveness and safety of HTPs is needed. The rate of decline in cigarette sales accelerated after the introduction of heated tobacco to market in Japan but, as data were observational, it is possible other factors caused these changes. Moreover, falls in cigarette sales may not translate to declining smoking prevalence, and changes in Japan may not generalise elsewhere. To clarify the impact of rising heated tobacco use on smoking prevalence, there is a need for time-series studies that examine this association.
加热烟草制品(HTPs)旨在将烟草加热到足够高的温度以释放气溶胶,而不会燃烧或产生烟雾。它们与电子烟不同,因为它们加热的是烟叶/片,而不是液体。生产 HTPs 的公司声称,它们产生的有害化学物质比传统香烟少。一些人报告说,通过改用 HTPs 完全戒烟,因此临床医生需要了解它们在这方面的效果和相对安全性。此外,为了适当监管 HTPs,政策制定者应该了解它们对健康和吸烟流行率的影响。
评估 HTPs 戒烟的效果和安全性,以及 HTPs 对吸烟流行率的影响。
我们检索了 Cochrane 烟草成瘾组的专论注册库、CENTRAL、MEDLINE 和其他六个数据库,以获取截至 2021 年 1 月的相关记录,并通过参考文献检查和与研究作者和相关团体的联系进行补充。
我们纳入了将吸烟者随机分配到仅使用 HTP 组、对照组或尝试完全戒烟组的随机对照试验(RCTs)。合格的结局是戒烟、不良事件和选定的生物标志物。当评估安全性时,包括将参与者随机分配到仅使用 HTPs、吸烟或尝试完全戒烟的诊所或非卧床环境中的 RCTs 也符合条件。如果它们研究了加热烟草对吸烟流行率或香烟销售的人口水平影响作为间接衡量标准,那么时间序列研究也有资格纳入。
我们遵循了 Cochrane 标准方法进行筛查和数据提取。我们的主要结局指标是最长随访时间点的吸烟戒断率、不良事件、严重不良事件以及吸烟流行率或香烟销售的变化。其他结局指标包括危害和有毒物质/致癌物暴露的生物标志物(如 NNAL 和碳氧血红蛋白(COHb))。我们使用随机效应曼-惠特尼 H 检验模型计算风险比(RR)和 95%置信区间(CI)用于二分类结局。对于连续结局,我们计算了对数转换标度(LMD)上的均值差异(LMD)和 95%CI。我们尽可能使用荟萃分析汇总研究数据。
我们纳入了 13 项已完成的研究,其中 11 项是评估安全性的 RCTs(2666 名参与者),2 项是时间序列研究。我们判断 8 项 RCT 为不确定偏倚风险,3 项为高偏倚风险。所有 RCT 均由烟草公司资助。中位随访时间为 13 周。没有研究报告吸烟戒断结局。由于精确度有限且存在偏倚,吸烟者随机分配到改用加热烟草或继续吸烟的不良事件风险差异无统计学意义(RR 1.03,95%CI 0.92 至 1.15;I = 0%;6 项研究,1713 名参与者)。由于严重偏倚和精确度有限,严重不良事件风险差异无统计学意义(RR 0.79,95%CI 0.33 至 1.94;I = 0%;4 项研究,1472 名参与者)。与吸烟组相比,加热烟草组在随访时 NNAL 和 COHb 的证据具有中等确定性,这受到偏倚的限制(NNAL:LMD -0.81,95%CI -1.07 至 -0.55;I = 92%;10 项研究,1959 名参与者;COHb:LMD -0.74,95%CI -0.92 至 -0.52;I = 96%;9 项研究,1807 名参与者)。在综述的正文部分报告了其他暴露生物标志物的证据。由于偏倚和精确度有限,吸烟者随机分配到改用加热烟草或尝试完全戒烟的不良事件风险差异无统计学意义(RR 1.12,95%CI 0.86 至 1.46;I = 0%;2 项研究,237 名参与者)。5 项研究报告两组均无严重不良事件(533 名参与者)。由于偏倚的限制,与完全戒烟组相比,加热烟草组在随访时尿液 NNAL 浓度较高的证据具有中等确定性(LMD 0.50,95%CI 0.34 至 0.66;I = 0%;5 项研究,382 名参与者)。此外,由于偏倚、不一致和精确度有限,与完全戒烟组相比,加热烟草组的 COHb 在意向治疗分析中具有非常低的确定性(LMD 0.69,95%CI 0.07 至 1.31;3 项研究,212 名参与者),但在方案分析中较低(LMD -0.32,95%CI -1.04 至 0.39;2 项研究,170 名参与者)。关于其他生物标志物的证据在综述的正文部分报告。两项时间序列研究的数据表明,在日本加热烟草上市后,香烟销售的下降速度加快。由于存在偏倚,包括可能的混杂因素,并且香烟销售是吸烟流行率的间接衡量标准,因此这一证据的确定性较低。
没有研究报告加热烟草制品在这方面的效果,因此其用于此目的的效果仍不确定。在短期随访中,与随机分配到改用加热烟草、吸烟或尝试完全戒烟的人相比,在不良事件或严重不良事件风险方面没有差异。有中等确定性证据表明,加热烟草使用者的有毒物质/致癌物暴露低于吸烟者,而与试图完全戒烟者相比,暴露水平更高。需要独立资助的关于 HTPs 的有效性和安全性的研究。日本加热烟草上市后,香烟销售的下降速度加快,但由于数据为观察性的,因此其他因素也可能导致了这些变化。此外,香烟销量的下降不一定会转化为吸烟率的下降,日本的变化可能不会推广到其他地区。为了阐明加热烟草使用的增加对吸烟流行率的影响,需要进行时间序列研究,以检验这种关联。