Cost-Effectiveness of a Government Policy to Incentivise Chronic Disease Management following Stroke: A Modelling Study.

IF 3.2 3区 医学 Q2 CLINICAL NEUROLOGY
Neuroepidemiology Pub Date : 2024-01-01 Epub Date: 2024-01-30 DOI:10.1159/000536224
Zhomart Orman, Dominique A Cadilhac, Nadine E Andrew, Monique F Kilkenny, Muideen T Olaiya, Amanda G Thrift, David Ung, Lachlan L Dalli, Leonid Churilov, Vijaya Sundararajan, Natasha A Lannin, Mark R Nelson, Velandai Srikanth, Joosup Kim
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Abstract

Introduction: Little is known about the cost-effectiveness of government policies that support primary care physicians to provide comprehensive chronic disease management (CDM). This paper aimed to estimate the potential cost-effectiveness of CDM policies over a lifetime for long-time survivors of stroke.

Methods: A Markov model, using three health states (stable, hospitalised, dead), was developed to simulate the costs and benefits of CDM policies over 30 years (with 1-year cycles). Transition probabilities and costs from a health system perspective were obtained from the linkage of data between the Australian Stroke Clinical Registry (cohort n = 12,368, 42% female, median age 70 years, 45% had CDM claims) and government-held hospital, Medicare, and pharmaceutical claims datasets. Quality-adjusted life years (QALYs) were obtained from a comparable cohort (n = 512, 34% female, median age 69.6 years, 52% had CDM claims) linked with Medicare claims and death data. A 3% discount rate was applied to costs in Australian dollars (AUD, 2016) and QALYs beyond 12 months. Probabilistic sensitivity analyses were used to understand uncertainty.

Results: Per-person average total lifetime costs were AUD 142,939 and 8.97 QALYs for those with a claim, and AUD 103,889 and 8.98 QALYs for those without a claim. This indicates that these CDM policies were costlier without improving QALYs. The probability of cost-effectiveness of CDM policies was 26.1%, at a willingness-to-pay threshold of AUD 50,000/QALY.

Conclusion: CDM policies, designed to encourage comprehensive care, are unlikely to be cost-effective for stroke compared to care without CDM. Further research to understand how to deliver such care cost-effectively is needed.

政府激励中风后慢性病管理政策的成本效益:一项模型研究。
背景:目的:估算 CDM 政策在中风长期幸存者一生中的潜在成本效益:方法:建立一个马尔可夫模型,使用三种健康状态(稳定、住院、死亡)来模拟 CDM 政策在 30 年内(周期为 1 年)的成本和效益。从卫生系统的角度来看,过渡概率和成本来自澳大利亚中风临床登记数据(队列人数=12368,42%为女性,中位年龄为70岁,45%有索赔)与政府持有的医院、医疗保险和药品索赔数据集之间的关联数据。质量调整生命年(QALYs)是从与医疗保险理赔和死亡数据相关联的可比队列(人数=512,34%为女性,中位年龄69.6岁,52%有理赔记录)中获得的。以澳元(AUD,2016 年)为单位的成本和 12 个月以上的 QALY 采用了 3% 的贴现率。采用概率敏感性分析来了解不确定性:有索赔者的人均终身总成本为 142,939 澳元和 8.97 QALY,无索赔者的人均终身总成本为 103,889 澳元和 8.98 QALY。这表明,这些 CDM 政策的成本较高,却没有改善 QALY。CDM 的成本效益概率为 26.1%,支付意愿阈值为 50,000 澳元/QALY:结论:与没有 CDM 的护理相比,旨在鼓励全面护理的 CDM 政策不太可能对中风具有成本效益。需要进一步研究如何以具有成本效益的方式提供此类护理。
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
Neuroepidemiology
Neuroepidemiology 医学-公共卫生、环境卫生与职业卫生
CiteScore
9.90
自引率
1.80%
发文量
49
审稿时长
6-12 weeks
期刊介绍: ''Neuroepidemiology'' is the only internationally recognised peer-reviewed periodical devoted to descriptive, analytical and experimental studies in the epidemiology of neurologic disease. The scope of the journal expands the boundaries of traditional clinical neurology by providing new insights regarding the etiology, determinants, distribution, management and prevention of diseases of the nervous system.
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