The Australian moratorium on genetics and life insurance: evaluating policy compared to Parliamentary recommendations regarding genetic discrimination.

IF 2.5 Q2 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Jane Tiller, Paul Lacaze, Margaret Otlowski
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引用次数: 1

Abstract

Objectives and importance of study: Genetic discrimination is a health policy issue of international concern to clinicians, patients, researchers, and policy makers, and threatens the success of genomic medicine. In Australia, genetic discrimination in life insurance is legal and leads to public health harms, including deterring at-risk individuals from clinically indicated testing. In 2018, a Parliamentary Joint Committee recommended an urgent ban on the use of predictive genetic test results in life insurance underwriting in Australia, to be implemented in a form similar to the UK Code on genetic testing and life insurance. In 2019, the insurance industry, through the Financial Services Council (FSC), introduced a self-regulated moratorium that applies until 2024, but only to life insurance policies up to certain financial limits. The FSC moratorium will be reviewed in late 2022, but has no government oversight.

Study type: Policy implementation evaluation Methods: We used policy evaluation methods to 1) summarise the key recommendations of the 2018 Parliamentary Committee that are directed towards practical aspects of policy development and content; and 2) assess the level of disparity between the implemented moratorium and the recommendations of the Committee.

Results: There is a substantial disparity between the Australian moratorium and the Parliamentary Committee recommendations across key areas, including addressing self-regulation, co-development of policy, protection of tests taken during its term, and similarity with the UK Code. The FSC moratorium offers less protection to consumers than the UK Code on a number of measures, including the level of financial coverage, the involvement of government, certainty provided to individuals who have genetic testing, and the treatment of research results.

Conclusions: The FSC moratorium is a step forward for Australia, but falls short of the Parliamentary recommendations. Further regulation by the Australian Government may be required to achieve the aims of the Parliamentary recommendations and ensure the intended level of consumer protection.

澳大利亚暂停遗传学和人寿保险:与议会关于遗传歧视的建议相比,评估政策。
研究目的和重要性:基因歧视是临床医生、患者、研究人员和决策者关注的国际卫生政策问题,威胁着基因组医学的成功。在澳大利亚,人寿保险中的基因歧视是合法的,会对公众健康造成危害,包括阻止有风险的个人进行临床指示的检测。2018年,议会联合委员会建议紧急禁止在澳大利亚人寿保险承保中使用预测性基因检测结果,并以类似于英国基因检测和人寿保险法典的形式实施。2019年,保险业通过金融服务委员会(FSC)推出了一项自我监管的暂停令,有效期至2024年,但仅适用于达到一定财务限制的人寿保险单。FSC的暂停将在2022年底进行审查,但没有政府监督。研究类型:政策实施评估方法:我们使用政策评估方法来1)总结2018年议会委员会针对政策制定和内容的实际方面的关键建议;及2)评估已实施的暂停兴建计划与委员会的建议之间的差异程度。结果:澳大利亚的暂停与议会委员会的建议在关键领域存在巨大差异,包括解决自我监管、共同制定政策、保护在其任期内进行的测试,以及与英国法典的相似性。与英国法典相比,FSC暂停对消费者提供的保护在一些措施上要少一些,包括财务覆盖水平、政府参与、为进行基因检测的个人提供的确定性,以及对研究结果的处理。结论:FSC的暂停是澳大利亚向前迈出的一步,但没有达到议会的建议。为了实现议会建议的目标和确保消费者保护的预期水平,可能需要澳大利亚政府进一步监管。
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来源期刊
Public Health Research & Practice
Public Health Research & Practice PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
6.70
自引率
0.00%
发文量
51
审稿时长
20 weeks
期刊介绍: Public Health Research & Practice is an open-access, quarterly, online journal with a strong focus on the connection between research, policy and practice. It publishes innovative, high-quality papers that inform public health policy and practice, paying particular attention to innovations, data and perspectives from policy and practice. The journal is published by the Sax Institute, a national leader in promoting the use of research evidence in health policy. Formerly known as The NSW Public Health Bulletin, the journal has a long history. It was published by the NSW Ministry of Health for nearly a quarter of a century. Responsibility for its publication transferred to the Sax Institute in 2014, and the journal receives guidance from an expert editorial board.
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