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使用尼古丁替代疗法“减量戒烟”:有效性的系统评价与经济分析

'Cut down to quit' with nicotine replacement therapies in smoking cessation: a systematic review of effectiveness and economic analysis.

作者信息

Wang D, Connock M, Barton P, Fry-Smith A, Aveyard P, Moore D

机构信息

Department of Public Health and Epidemiology, University of Birmingham, UK.

出版信息

Health Technol Assess. 2008 Feb;12(2):iii-iv, ix-xi, 1-135. doi: 10.3310/hta12020.

Abstract

OBJECTIVES

To examine the effectiveness and cost-effectiveness of nicotine replacement therapy (NRT) for 'cut down to quit' (CDTQ) smoking.

DATA SOURCES

Major electronic databases were searched up to July 2006.

REVIEW METHODS

Data from studies meeting the criteria were reviewed and analysed. A decision analytical model was constructed to estimate the cost-effectiveness of CDTQ from the NHS perspective.

RESULTS

No systematic reviews of the effectiveness of CDTQ and no randomised controlled trials (RCTs) specifically addressing CDTQ were identified. Seven randomised placebo-controlled trials satisfied the inclusion criteria; six of these were industry sponsored. However, sustained smoking cessation was only reported as a secondary outcome in these trials and required commencement of cessation within the first 6 weeks of treatment. Meta-analyses of the study level results demonstrated statistically significant superiority of NRT compared with placebo. Individual patient data from unpublished reports of five RCTs were used to calculate sustained abstinence of at least 6 months starting at any time during the treatment period (generally 12 months). From this the meta-analysis indicated statistically significant superiority of NRT versus placebo [relative risk 2.06, 95% confidence interval (CI) 1.34 to 3.15]. The proportions achieving this outcome across all five RCTs were 6.75% of participants in receipt of NRT and 3.29% of those receiving placebo. The number-needed-to-treat was 29. This measure of sustained abstinence was used for economic modelling. No existing economic analyses of CDTQ were identified. A de novo decision analytic model was constructed to estimate the cost-effectiveness of making CDTQ with NRT available for smokers unwilling or unable to attempt an abrupt quit. The outcome measure was expected quality-adjusted life-years (QALYs). The model results suggest that CDTQ with NRT delivers incremental cost-effectiveness ratios (ICERs) ranging from around 1500 pounds/QALY to 7700 pounds/QALY depending on the age at which smoking cessation was achieved and the modes of CDTQ delivery. Assuming applicability to a single population, CDTQ was not cost-effective compared with abrupt quitting. If CDTQ with NRT were to be offered on the NHS as a matter of policy, the base-case results suggest that it would only be effective and cost-effective if a substantial majority of the people attempting CDTQ with NRT were those who would otherwise make no attempt to quit. This result is robust to considerable variation in the forms of CDTQ with NRT offered, and to the assumptions about QALY gained per quit success.

CONCLUSIONS

Meta-analysis of RCT evidence of quit rates in NRT-supported smoking reduction studies indicates that NRT is an effective intervention in achieving sustained smoking abstinence for smokers who declare unwillingness or inability to attempt an abrupt quit. The 12-month sustained abstinence success rate in this population (approximately 5.3% with NRT versus approximately 2.6% with placebo) is considerably less than that documented for an abrupt quit NRT regime in smokers willing to attempt an abrupt quit with NRT (which according to other systematic reviews is around 16% with NRT versus 10% with placebo). Most of the evidence of effectiveness of CDTQ came from trials that required considerable patient-investigator contact. Therefore, for CDTQ with NRT to generate similar abstinence rates for this recalcitrant population in a real-world setting would probably require a similar mode of delivery. The modelling undertaken, which was based on reasonable assumptions about costs, benefits and success rates, suggests that CDTQ is highly cost-effective compared with no quit attempt. CDTQ remains cost-effective if dilution from abrupt quitting forms a small proportion of CDTQ attempts. In an alternative analysis in which smokers who switch from an abrupt quit to CDTQ retain the success rate of abrupt quitters, all forms of CDTQ appear cost-effective. Randomised trials in recalcitrant smokers allowing head-to-head comparison of CDTQ delivered with various modalities would be informative.

摘要

目的

探讨尼古丁替代疗法(NRT)用于“逐步减量戒烟”(CDTQ)的有效性和成本效益。

数据来源

检索主要电子数据库至2006年7月。

综述方法

对符合标准的研究数据进行综述和分析。构建决策分析模型,从英国国家医疗服务体系(NHS)的角度估计CDTQ的成本效益。

结果

未发现关于CDTQ有效性的系统综述,也未识别出专门针对CDTQ的随机对照试验(RCT)。七项随机安慰剂对照试验符合纳入标准;其中六项由行业资助。然而,在这些试验中,持续戒烟仅作为次要结果报告,且要求在治疗的前6周内开始戒烟。对研究水平结果的荟萃分析表明,与安慰剂相比,NRT具有统计学上的显著优势。使用来自五项RCT未发表报告的个体患者数据,计算从治疗期间的任何时间开始至少持续6个月(通常为12个月)的持续戒断率。由此进行的荟萃分析表明,NRT相对于安慰剂具有统计学上的显著优势[相对风险2.06,95%置信区间(CI)1.34至3.15]。在所有五项RCT中,达到这一结果的比例在接受NRT的参与者中为6.75%,在接受安慰剂的参与者中为3.29%。所需治疗人数为29。这种持续戒断的衡量标准用于经济建模。未发现现有的关于CDTQ的经济分析。构建了一个全新的决策分析模型,以估计为不愿或无法尝试突然戒烟的吸烟者提供NRT辅助的CDTQ的成本效益。结果指标为预期质量调整生命年(QALY)。模型结果表明,根据实现戒烟的年龄和CDTQ的实施方式,NRT辅助的CDTQ产生的增量成本效益比(ICER)范围约为1500英镑/QALY至7700英镑/QALY。假设适用于单一人群,与突然戒烟相比,CDTQ不具有成本效益。如果将NRT辅助的CDTQ作为一项政策在NHS中提供,基础案例结果表明,只有当绝大多数尝试NRT辅助的CDTQ的人是那些否则不会尝试戒烟的人时,它才会有效且具有成本效益。这一结果对于所提供的NRT辅助的CDTQ形式的相当大变化以及关于每次戒烟成功所获得的QALY的假设具有稳健性。

结论

对NRT支持的减少吸烟研究中戒烟率的RCT证据进行荟萃分析表明,对于宣称不愿或无法尝试突然戒烟的吸烟者,NRT是实现持续戒烟的有效干预措施。该人群中12个月的持续戒烟成功率(NRT约为5.3%,安慰剂约为2.6%)远低于愿意尝试NRT突然戒烟的吸烟者中NRT突然戒烟方案的记录成功率(根据其他系统综述,NRT约为16%,安慰剂约为10%)。CDTQ有效性的大多数证据来自需要大量患者与研究者接触的试验。因此,要使NRT辅助的CDTQ在现实环境中为这一顽固人群产生相似的戒断率,可能需要类似的实施方式。所进行的建模基于对成本、效益和成功率的合理假设,表明与不尝试戒烟相比,CDTQ具有很高的成本效益。如果突然戒烟的稀释在CDTQ尝试中占较小比例,CDTQ仍然具有成本效益。在另一项分析中,从突然戒烟转为CDTQ的吸烟者保持突然戒烟者的成功率,所有形式的CDTQ似乎都具有成本效益。对顽固吸烟者进行随机试验,允许对以各种方式实施的CDTQ进行直接比较,将提供有价值的信息。

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