基于个体的动态模型,用于评估减轻阿片类药物过量风险的干预措施。

IF 4 2区 社会学 Q1 SUBSTANCE ABUSE
Kirsten Gallant, Ryan Lukeman
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引用次数: 0

摘要

背景:非法阿片类药物过量在北美持续上升,是导致死亡的主要原因之一。数学建模是研究这一公共卫生问题流行病学的重要工具,因为它可以描述人群结果的关键特征,并量化结构性和干预性变化对用药过量死亡率的广泛影响。本研究的目的是量化和预测在多伦多不受管制地使用阿片类药物的人群中,不同规模的主要减低伤害策略对致命和非致命性用药过量的影响:方法:建立了一个基于个体的阿片类药物过量模型,该模型具有人口统计学和行为学特征。在该模型中,模拟人群中的每个成员都具有一系列不同的特征,这些特征制约着人口统计学、干预措施的使用以及过量使用的发生率。该模型以 2019 年多伦多报告的致命和非致命用药过量事件为参数。考虑的干预措施包括阿片类激动剂疗法(OAT)、监督消费场所(SCS)、带回家的纳洛酮(THN)、毒品检查和减少毒品供应中的芬太尼。在基线模型的基础上探讨了减少危害的方案,以研究每种干预措施从 0% 使用到 100% 使用对用药过量事件的影响:结果:模型模拟结果显示,非致命过量吸毒人数为 3690.6 人,致命过量吸毒人数为 295.4 人,与多伦多 2019 年的数据相吻合。从这一基线出发,在全面推广时,通过 THN 可避免 290 例死亡,通过消除毒品供应中的芬太尼可避免 248 例死亡,通过使用 SCS 可避免 124 例死亡,通过 OAT 可避免 173 例死亡,通过毒品检查服务可避免 100 例死亡。毒品检查和减少毒品供应中的芬太尼是唯一能减少非致命性用药过量数量的减低危害策略:结论:在一种多方面的减低伤害方法中,扩大可带回家的纳洛酮的使用范围和减少毒品供应中的芬太尼可使多伦多阿片类药物过量致死的人数减少最多。详细的模型模拟研究为评估减少危害的公共卫生政策并为其提供信息提供了额外的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An individual-based dynamic model to assess interventions to mitigate opioid overdose risk.

Background: Illicit opioid overdose continues to rise in North America and is a leading cause of death. Mathematical modeling is a valuable tool to investigate the epidemiology of this public health issue, as it can characterize key features of population outcomes and quantify the broader effect of structural and interventional changes on overdose mortality. The aim of this study is to quantify and predict the impact of key harm reduction strategies at differing levels of scale-up on fatal and nonfatal overdose among a population of people engaging in unregulated opioid use in Toronto.

Methods: An individual-based model for opioid overdose was built featuring demographic and behavioural variation among members of the population. Key individual attributes known to scale the risk of fatal and nonfatal overdose were identified and incorporated into a dynamic modeling framework, wherein every member of the simulated population encompasses a set of distinct characteristics that govern demographics, intervention usage, and overdose incidence. The model was parametrized to fatal and nonfatal overdose events reported in Toronto in 2019. The interventions considered were opioid agonist therapy (OAT), supervised consumption sites (SCS), take-home naloxone (THN), drug-checking, and reducing fentanyl in the drug supply. Harm reduction scenarios were explored relative to a baseline model to examine the impact of each intervention being scaled from 0% use to 100% use on overdose events.

Results: Model simulations resulted in 3690.6 nonfatal and 295.4 fatal overdoses, coinciding with 2019 data from Toronto. From this baseline, at full scale-up, 290 deaths were averted by THN, 248 from eliminating fentanyl from the drug supply, 124 from SCS use, 173 from OAT, and 100 by drug-checking services. Drug-checking and reducing fentanyl in the drug supply were the only harm reduction strategies that reduced the number of nonfatal overdoses.

Conclusions: Within a multi-faceted harm reduction approach, scaling up take-home naloxone, and reducing fentanyl in the drug supply led to the largest reduction in opioid overdose fatality in Toronto. Detailed model simulation studies provide an additional tool to assess and inform public health policy on harm reduction.

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来源期刊
Harm Reduction Journal
Harm Reduction Journal Medicine-Public Health, Environmental and Occupational Health
CiteScore
5.90
自引率
9.10%
发文量
126
审稿时长
26 weeks
期刊介绍: Harm Reduction Journal is an Open Access, peer-reviewed, online journal whose focus is on the prevalent patterns of psychoactive drug use, the public policies meant to control them, and the search for effective methods of reducing the adverse medical, public health, and social consequences associated with both drugs and drug policies. We define "harm reduction" as "policies and programs which aim to reduce the health, social, and economic costs of legal and illegal psychoactive drug use without necessarily reducing drug consumption". We are especially interested in studies of the evolving patterns of drug use around the world, their implications for the spread of HIV/AIDS and other blood-borne pathogens.
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