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Issues with monitoring the safety of psychoactive products under a legal regulated market for new psychoactive substances (‘legal highs’) in New Zealand

机译:在新西兰新精神活性物质的合法监管市场(“合法高点”)下监测精神活性产品安全性的问题

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Abstract Introduction . New Zealand's Psychoactive Substances Act (2013) established the world's first regulated market for ‘low risk’ psychoactive products (‘legal highs’). Under an interim PSA regime, 47 existing products were permitted to be continued to be sold. Aim. To explore issues with the implementation of regulatory systems to monitor the safety of products on the legal market under the interim Psychoactive Substances Act regime. Methods. Semi‐structured interviews with 30 key stakeholders, including industry, government agency, health and drug service professionals were conducted, transcribed and analysed thematically. Results. In retrospect stakeholders questioned the decision to approve strong synthetic cannabinoid smoking products, noting their health risks because of product formulation, inconsistent manufacturing practices and smoking as the means of administration. Industry actors claimed the decision to approve synthetic cannabinoid smokeable products prevented potentially safer products from gaining market share. The system for withdrawing approved products which were subsequently found to be harmful was criticised for the poor quality of data available, limited engagement with health professionals and the slowness of product withdrawal. Many of the problems with the regime were attributed to the urgency under which the legal market under the interim Psychoactive Substances Act was established and implemented. Conclusions. The selection of ‘safer’ products, implementation of the product monitoring system, and engagement with health professionals may have benefited from more time and resources. An incremental approach to establishing the new market may have made the regulatory management of the new regime more workable. Rychert M, Wilkins C, Witten K. Issues with monitoring the safety of psychoactive products under a legal regulated market for new psychoactive substances (‘legal highs’) in New Zealand. Drug Alcohol Rev 2017;00:000‐000
机译:摘要介绍。新西兰的《精神活性物质法》(2013年)建立了世界上第一个受监管的“低风险”精神活性产品市场。在临时PSA制度下,允许继续销售47种现有产品。目的。探讨在临时《精神活性物质法》制度下实施监管制度以监测合法市场上产品安全性的问题。方法。对30个主要利益相关者进行了半结构化访谈,包括行业、政府机构、卫生和药物服务专业人员,并进行了主题分析。结果。回想起来,利益攸关方质疑批准强效合成大麻素吸烟产品的决定,并指出由于产品配方、不一致的制造实践和吸烟作为管理手段,它们存在健康风险。行业人士声称,批准合成大麻素可吸烟产品的决定阻止了潜在更安全的产品获得市场份额。撤回后来被发现有害的批准产品的系统因可用数据质量差、与卫生专业人员的接触有限以及产品撤回缓慢而受到批评。该制度的许多问题都归咎于根据《精神活性物质法》建立和实施合法市场的紧迫性。结论。选择“更安全”的产品、实施产品监测系统以及与卫生专业人员的接触可能受益于更多的时间和资源。建立新市场的渐进方法可能使新制度的监管管理更加可行。[Rychert M, Wilkins C, Witten K. 在新西兰新精神活性物质的合法监管市场(“合法高点”)下监测精神活性产品安全性的问题。药物酒精修订版 2017;00:000‐000]

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