NHMRC Centre of Research Excellence on Achieving the Tobacco Endgame, School of Public Health, The University of Queensland, Queensland, Australia.
NHMRC Centre of Research Excellence on Achieving the Tobacco Endgame, School of Public Health, The University of Queensland, Queensland, Australia.
Int J Drug Policy. 2024 Mar;125:104353. doi: 10.1016/j.drugpo.2024.104353. Epub 2024 Feb 16.
Deciding how to regulate nicotine vaping products (NVPs) is a challenge for many countries. Balanced regulation should consider the potential harms to young people from uptake of NVPs alongside the possible benefits of NVPs as a smoking cessation aid. One option is to make NVPs only available via medical prescription to adults who smoke. From October 2021, Australia adopted a unique model that allows prescription access to NVPs that meet a product standard without requiring the NVPs to be approved as therapeutic goods. This research explored the impact of this regulatory model on the smoking cessation practices of health professionals, and their views on the model.
Semi-structured interviews were conducted with 39 Australian health professionals recruited from professional networks and social media. Health professionals were eligible if they provided smoking cessation advice as part of their role, and included medical practitioners (n = 9), pharmacists (n = 9), and other health professionals that provided smoking cessation counselling (n = 21). Interviews were mostly completed by phone and online teleconferencing software. Questions focused on smoking cessation practices, advice and information provided to patients about NVPs, views about the effectiveness of the model for supporting use of NVPs for smoking cessation and preventing youth uptake, and barriers and facilitators to prescribing and dispensing NVPs. Coding and analysis used a combination of inductive and deductive approaches.
Findings indicated a lack of consensus amongst the participants about NVPs as a cessation or harm reduction tool. Participants broadly agreed that the model has not been effective in improving quality control of NVPs, or in reducing youth access. Many participants eligible to prescribe or dispense NVPs felt that the current regulatory model placed an undue time and responsibility burden on clinicians.
Our research identified several limitations associated with the current Australian prescription-only regulatory model. These were perceived by healthcare professionals to limit the potential for the regulations to reduce youth use and to increase access to safer NVP products for people who smoke to use for smoking cessation.
许多国家在如何监管尼古丁电子烟产品(NVPs)方面面临挑战。平衡监管应考虑到年轻人使用 NVPs 的潜在危害,以及 NVPs 作为戒烟辅助手段的可能益处。一种选择是仅向有吸烟习惯的成年人提供通过医疗处方获得 NVPs。自 2021 年 10 月起,澳大利亚采用了一种独特的模式,允许处方获得符合产品标准的 NVPs,而无需将 NVPs 批准为治疗性商品。这项研究探讨了这种监管模式对卫生专业人员戒烟实践的影响,以及他们对该模式的看法。
通过专业网络和社交媒体招募了 39 名澳大利亚卫生专业人员进行半结构化访谈。如果卫生专业人员在其工作中提供戒烟建议,则有资格参加访谈,包括医生(n=9)、药剂师(n=9)和其他提供戒烟咨询的卫生专业人员(n=21)。访谈主要通过电话和在线电话会议软件完成。问题集中在戒烟实践、向患者提供的关于 NVPs 的建议和信息、对该模式支持使用 NVPs 戒烟和防止年轻人使用的有效性的看法、以及处方和配药 NVPs 的障碍和促进因素。编码和分析采用了归纳和演绎相结合的方法。
研究结果表明,参与者对 NVPs 作为戒烟或减少危害工具的看法存在分歧。参与者普遍认为,该模式在提高 NVPs 的质量控制或减少年轻人获取方面并未取得成效。许多有资格开具或配药 NVPs 的参与者认为,当前的监管模式给临床医生带来了不必要的时间和责任负担。
我们的研究发现,与澳大利亚目前的处方监管模式相关的一些局限性。卫生保健专业人员认为,这些局限性限制了这些法规减少年轻人使用和增加吸烟人群获得更安全的 NVP 产品用于戒烟的潜力。