2014-2023年在公共资助医疗系统中使用资助基因和基因组测试的情况。

IF 3.7 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Chris Schilling, Florencia Sjaaf, Ilias Goranitis, Kim Dalziel, Melissa Martyn, Zornitza Stark, Clara Gaff
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引用次数: 0

摘要

澳大利亚政府通过一项联邦资助计划补贴医疗服务,包括一些基因和基因组测试。我们探讨的趋势和变化,利用公共资助的基因和基因组测试在过去十年。我们使用的是2014至2023财政年度列出的基因和基因组测试的行政数据。2023年,共有102项基因测试和9项基因组测试获得了公共补贴,涉及65种不同的临床测试适应症,而2014年这一数字为32项,涉及20种不同的测试。服务数量从250,881增加到376,140,增长了50%,支付的福利从4,200万澳元增加到7,680万澳元,增长了83%。这占2023年公共资助医疗服务总开支276亿澳元的0.3%。躯体癌、罕见病和生殖检查是最普遍的检查。育龄妇女比男性使用更多的服务,但在非育龄妇女,男性比女性使用更多的服务。目前在澳大利亚,公共资助的基因和基因组检测的使用相对适度,强调了整合常规临床实践的挑战。然而,最近补贴项目的迅速扩大表明,对基因组学研究的投资正开始产生为这些服务获得公共资金所需的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Utilisation of subsidised genetic and genomic testing in a publicly funded healthcare system 2014-2023.

The Australian government subsidises medical services, including several genetic and genomic tests, through a federal funding scheme. We explore trends and variation in the utilisation of the publicly funded genetic and genomic tests over the last decade. We make use of administrative data of the listed genetic and genomic tests from financial year 2014 to 2023. In 2023, 102 genetic and nine genomic tests were publicly subsidised across 65 distinct clinical test indications, up from 32 items across 20 distinct tests in 2014. Service volumes have increased by 50% from 250,881 to 376,140, and benefits paid have risen by 83% from AU$42.0 million to AU$76.8 million. This accounts for 0.3% of the total AU$27.6 billion expenditure on publicly subsidised medical services in 2023. Somatic cancer, rare disease, and reproductive tests are the most prevalent tests. Women of childbearing ages used more services than men, however in nonchildbearing ages, men used more services than women. The current usage of publicly funded genetic and genomic testing within Australia is relatively modest, underscoring challenges in integration to routine clinical practice. However, the recent rapid expansion of subsidised items indicates that investments into genomics research are beginning to yield the evidence necessary to secure public funding for these services.

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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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