Medicinal Cannabis and Consumer Vulnerability in Australia: A Nexus of Policy and Market Factors

IF 3.2 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2025-02-10 DOI:10.1111/hex.70176
Katrina Gething, Daniel Erku, Paul Scuffham
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Abstract

Introduction

Following the 2016 legalization of medicinal cannabis (MC) in Australia, significant barriers have led patients to seek unregulated cannabis for therapeutic use. This study examines consumer (patient, carer and family) submissions to a senate inquiry on these barriers to understand how future policy might better reflect patient needs and facilitate access to regulated MC.

Methods

Sixty submissions from patients (n = 44), their caregivers or family members (n = 16) were coded using NVivo 12 software and thematically analysed. The findings were presented narratively using a consumer vulnerability framework.

Results

The analysis identified three primary barriers to accessing regulated MC: (1) Health practitioners' reluctance to prescribe MC, hindering prescription access, (2) High costs associated with MC and its access process, disproportionately affecting low-income consumers and (3) Dependence on imported MC products, leading to shortages and necessitating product substitutions that incur additional costs and bureaucratic hurdles. Despite these barriers, consumers demonstrated resilience by educating themselves about MC, planning for prescription needs and forming support networks. Patients also turned to illicit MC markets.

Conclusion

The study reveals significant barriers to regulated MC access in Australia, highlighting the complex challenges consumers face. The reliance on unregulated sources of MC not only poses legal and health risks but also underscores the urgent need for policy reforms. By addressing the identified barriers, such as alleviating the costs associated with MC and improving approval processes and ensuring product availability, policymakers can better meet consumer needs and facilitate safer access to regulated MC.

Patient or Public Contribution

The materials of this document analysis were patient and public submissions to a government enquiry into barriers to a health technology. By providing submissions, both patients and the public were actively engaging in the development of health policy.

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药用大麻和消费者脆弱性在澳大利亚:政策和市场因素的关系
自2016年澳大利亚医用大麻(MC)合法化以来,重大障碍导致患者寻求不受管制的大麻用于治疗用途。本研究调查了消费者(患者、护理人员和家庭)向参议院提交的关于这些障碍的调查,以了解未来的政策如何更好地反映患者的需求,并促进获得受监管的MC。方法使用NVivo 12软件对来自患者(n = 44)、其护理人员或家庭成员(n = 16)的60份意见书进行编码,并进行主题分析。研究结果使用消费者脆弱性框架进行叙述。结果分析确定了获得受监管的MC的三个主要障碍:(1)卫生从业者不愿开MC,阻碍了处方的获取;(2)与MC相关的高成本及其获取过程,不成比例地影响低收入消费者;(3)依赖进口MC产品,导致短缺并需要产品替代,从而产生额外的成本和官僚障碍。尽管存在这些障碍,但消费者通过自我教育、规划处方需求和形成支持网络,表现出了适应力。患者还转向非法MC市场。该研究揭示了澳大利亚监管MC接入的重大障碍,突出了消费者面临的复杂挑战。依赖不受管制的MC来源不仅会带来法律和健康风险,而且还强调了迫切需要进行政策改革。通过解决已确定的障碍,例如减轻与MC相关的成本,改进审批程序和确保产品可用性,决策者可以更好地满足消费者的需求,并促进更安全地获得受监管的MC。患者或公众贡献本文件分析的材料是患者和公众向政府调查卫生技术障碍的意见。通过提交意见书,病人和公众都积极参与卫生政策的制定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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