McCoy Jacqui, Nielsen Suzanne, Bruno Raimondo
University of Tasmania, Hobart, Australia.
Monash University, Melbourne, Australia.
JMIR Res Protoc. 2020 Mar 13;9(3):e15540. doi: 10.2196/15540.
On February 1, 2018, Australia rescheduled codeine to a prescription-only medication. Many concerns were associated with this change, including increased financial costs, reduced service accessibility, the potential for poorer pain management, and a decline in physical and mental health if codeine could not be accessed. In the research literature, there is limited knowledge about the long-term consequences of rescheduling pharmaceutical opioids and, as Australia has followed many countries in implementing a restriction on codeine, further study of these consequences is critical.
The goal of this study was to examine the impact of rescheduling codeine from an over-the-counter (OTC) product to a prescription-only medicine on the primary measures of codeine use and dependence in a prospective cohort of people who are frequent consumers of OTC codeine. Secondary measures included pain and self-efficacy, health service use, and mental health.
The Codeine Cohort study aimed to recruit 300 participants in Australia who regularly (at least a few times per week for the past 6 months) used OTC codeine. Using an online survey, participants were followed up at three time points (February 2018, June 2018, and February 2019) after codeine was rescheduled.
All four waves of data collection are complete, with the final round of data collection finalized in August 2019. Data analyses are yet to be completed. Information on demographics, codeine use and dependence, physical and mental health, medication use, and health service use will be analyzed using mixed models.
Results of this study will provide insight into the effectiveness of regulatory restriction in curtailing nonmedical use of and harms associated with codeine. Additionally, results will explore positive and negative outcomes of codeine rescheduling for individual patients, which informs health professionals who support patients who use codeine and further community education.
INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/15540.
2018年2月1日,澳大利亚将可待因重新归类为仅凭处方使用的药物。这一变化引发了诸多担忧,包括经济成本增加、服务可及性降低、疼痛管理可能变差,以及如果无法获取可待因,身心健康会下降。在研究文献中,关于重新安排药用阿片类药物的长期后果的知识有限,而且由于澳大利亚效仿许多国家对可待因实施了限制,进一步研究这些后果至关重要。
本研究的目的是在一个经常使用非处方可待因的前瞻性队列中,考察将可待因从非处方(OTC)产品重新归类为仅凭处方使用的药物对可待因使用和依赖的主要指标的影响。次要指标包括疼痛和自我效能感、医疗服务利用情况以及心理健康状况。
可待因队列研究旨在招募300名澳大利亚参与者,这些参与者过去6个月经常(每周至少几次)使用非处方可待因。通过在线调查,在可待因重新归类后的三个时间点(2018年2月、2018年6月和2019年2月)对参与者进行随访。
四轮数据收集均已完成,最后一轮数据收集于2019年8月完成。数据分析尚未完成。将使用混合模型分析有关人口统计学、可待因使用和依赖情况、身心健康状况、药物使用情况以及医疗服务利用情况的信息。
本研究结果将有助于深入了解监管限制在减少可待因非医疗使用及相关危害方面的有效性。此外,研究结果还将探讨可待因重新归类对个体患者的积极和消极影响,为支持使用可待因的患者的医护人员以及进一步的社区教育提供参考。
国际注册报告识别码(IRRID):DERR1-10.2196/15540