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尼古丁雾化产品在国内合法销售对国家卫生和成本的潜在影响。

Potential Country-level Health and Cost Impacts of Legalizing Domestic Sale of Vaporized Nicotine Products.

机构信息

From the Burden of Disease Epidemiology, Equity, and Cost-Effectiveness (BODE), Department of Public Health, University of Otago, Wellington, New Zealand.

Centre for Applied Health Economics (CAHE), School of Medicine, Griffith University, Nathan, Queensland, Australia.

出版信息

Epidemiology. 2019 May;30(3):396-404. doi: 10.1097/EDE.0000000000000975.

Abstract

BACKGROUND

The net impact on population health and health system costs of vaporized nicotine products is uncertain. We modeled, with uncertainty, the health and cost impacts of liberalizing the vaporized nicotine market for a high-income country, New Zealand (NZ).

METHODS

We used a multistate life-table model of 16 tobacco-related diseases to simulate lifetime quality-adjusted life-years (QALYs) and health system costs at a 0% discount rate. We incorporated transitions from never, former, and current smoker states to, and from, regularly using vaporized nicotine and literature estimates for relative risk of disease incidence for vaping compared with smoking.

RESULTS

Compared with continuation of baseline trends in smoking uptake and cessation rates and negligible vaporized nicotine use, we projected liberalizing the market for these products to gain 236,000 QALYs (95% uncertainty interval [UI] = 27,000 to 457,000) and save NZ$3.4 billion (2011 NZ$) (95% UI = NZ$370 million to NZ$7.1 billion) or US$2.5 billion (2017 NZ$). However, estimates of net health gains for 0- to 14-year olds and 65+ year olds had 95% UIs including the null. Uncertainty around QALYs gained was mainly driven by uncertainty around the impact of vaporized nicotine products on population-wide cessation rates and the relative health risk of vaping compared with smoking.

CONCLUSIONS

This modeling suggested that a fairly permissive regulatory environment around vaporized nicotine products achieves net health gain and cost savings, albeit with wide uncertainty. Our results suggest that optimal strategies will also be influenced by targeted smoking cessation advice, regulations around chemical constituents of these products, and marketing and age limits to prevent youth uptake of vaping.

摘要

背景

蒸发尼古丁产品对人群健康和卫生系统成本的净影响尚不确定。我们对高收入国家新西兰(NZ)的蒸发尼古丁市场自由化对健康和成本的影响进行了建模,同时考虑了不确定性。

方法

我们使用 16 种与烟草相关疾病的多状态生命表模型,以 0%贴现率模拟终生质量调整生命年(QALY)和卫生系统成本。我们纳入了从不吸烟、前吸烟者和当前吸烟者状态向经常使用蒸发尼古丁状态的转变,以及从经常使用蒸发尼古丁状态向从不吸烟状态的转变,同时还纳入了与吸烟相比,使用蒸发尼古丁与疾病发病风险的相对风险的文献估计值。

结果

与继续保持目前的吸烟率上升和戒烟率以及蒸发尼古丁使用率微不足道的趋势相比,我们预计放宽这些产品的市场准入将获得 236,000 个 QALY(95%置信区间[UI]为 27,000 至 457,000)和节省 34 亿新西兰元(2011 年新西兰元)(95% UI 为 3.7 亿至 71 亿新西兰元)或 25 亿美元(2017 年新西兰元)。然而,0 至 14 岁和 65 岁以上人群的净健康收益估计值的 95%UI 包含零值。QALY 收益的不确定性主要是由蒸发尼古丁产品对人群戒烟率的影响以及与吸烟相比使用蒸发尼古丁的相对健康风险的不确定性所驱动的。

结论

这项建模研究表明,对蒸发尼古丁产品采取相当宽松的监管环境可以实现净健康收益和成本节约,尽管存在很大的不确定性。我们的研究结果表明,最佳策略还将受到有针对性的戒烟建议、这些产品化学成分的监管以及营销和年龄限制的影响,以防止青少年使用蒸发尼古丁。

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