Lund Karl Erik, Vedøy Tord Finne
Norwegian Institute of Public Health, Oslo, Norway.
Nordisk Alkohol Nark. 2021 Dec;38(6):586-604. doi: 10.1177/14550725211021248. Epub 2021 Jun 24.
The tobacco industry plans to base their future earnings on the production of non-combustible nicotine products. These might replace or come in addition to the more harmful cigarettes that historically have dominated the nicotine market in the Nordic countries. The authorities in each country must decide whether the products should have market access and, in that case, how strictly they should be regulated. Our aim is to present a framework that can assist the health authorities to make a regulation where benefits will outweigh the harms.
In a public health perspective, health gains from substitution must be weighed against the health loss from additional use. The main elements of the weighing will be based on the information about the absolute risk of the products, their relative risk compared to conventional cigarettes and how the users are composed according to smoking status. We apply the framework on snus as used in Norway - a product with an established usage pattern and epidemiologically assessed health risks.
The framework consists of (i) a comprehensive set of specific user patterns that may result in health deterioration and user patterns that may result in health benefits, (ii) an estimation of the number of people with health-augmenting and health-impairing user patterns, respectively, and (iii) an estimation of the degree of health deterioration or health benefit that will affect the persons with the different user patterns.
The net effect on public health will appear as an overall result of the number of people with positive and negative user patterns, respectively, in combination with the magnitude of the change in health status these people will experience. The use of an explicit framework highlights how a political decision may affect nicotine use and health-related outcomes. The framework breaks open a large and complex question into smaller pieces and requires the authorities to expose and explain the kind of evidence and reasoning behind regulations of novel nicotine products.
烟草行业计划将其未来收益基于非可燃尼古丁产品的生产。这些产品可能会取代或补充历史上在北欧国家尼古丁市场占主导地位的危害更大的香烟。每个国家的当局必须决定这些产品是否应进入市场,以及在这种情况下应如何严格监管。我们的目的是提出一个框架,以协助卫生当局制定一项使益处大于危害的监管措施。
从公共卫生角度来看,替代带来的健康益处必须与额外使用造成的健康损失相权衡。权衡的主要因素将基于有关产品绝对风险的信息、与传统香烟相比的相对风险以及根据吸烟状况对用户构成的分析。我们将该框架应用于挪威使用的口含烟——一种具有既定使用模式且经流行病学评估健康风险的产品。
该框架包括:(i)一组全面的可能导致健康恶化的特定用户模式和可能带来健康益处的用户模式;(ii)分别对具有健康增强和健康损害用户模式的人数进行估计;(iii)对将影响不同用户模式人群的健康恶化或健康益处程度进行估计。
对公众健康的净影响将表现为分别具有积极和消极用户模式的人数的总体结果,以及这些人将经历的健康状况变化幅度。使用明确的框架突出了政治决策可能如何影响尼古丁使用和与健康相关的结果。该框架将一个庞大而复杂的问题分解为较小的部分,并要求当局公开并解释新型尼古丁产品监管背后的证据和推理类型。