帕金森病的医疗系统净成本:加拿大安大略省倾向得分匹配健康管理数据队列研究》(Propensity Score-Matched Health Administrative Data Cohort Study in Ontario, Canada)。

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200371
Laura C Maclagan, Abby Emdin, Longdi Fu, Jun Guan, Claire de Oliveira, Connie Marras, Susan E Bronskill
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引用次数: 0

摘要

背景和目标:关于帕金森病各阶段的长期医疗系统成本的估算很少。我们估算了病例确定前后帕金森病的 10 年期和分期医疗系统净成本:利用加拿大安大略省基于人口的关联行政数据库,我们采用经过验证的算法确定了 2009 年至 2018 年期间 43149 名年龄在 40 岁及以上的社区居民帕金森病患者。根据人口统计学和倾向得分,这些人与无帕金森病的对照组进行了 1:1 匹配。我们从省政府的角度计算了确定前(指数前 3 年)、初始(指数后 1 年)、早期持续(指数后 >1-6 年)、晚期持续(指数后 >6-10 年)和终末(死亡前 1 年,如适用)阶段基于阶段的医疗系统净成本(标准化为 2020 年加元,按年计算)。通过将生存概率应用于月度成本估算,我们还确定了按性别和年龄分层的 10 年医疗系统净成本:帕金森病的年平均净成本在确定前阶段最低(212 加元,95% CI [20-404]美元),在初始阶段居中(4,576 美元(95% CI [4,217-4,935]美元),在早期持续阶段较高(7,078 美元,95% CI [6,717-7,438]美元)。持续治疗后期(12,500 美元,95% CI [12,060-12,940 美元])和终末期(13,933 美元,95% CI [13,123-14,743 美元])的费用最高。帕金森病的 10 年净成本为 82,153 美元(95% CI [77,965-86,341 美元]),女性(89,773 美元,95% CI [83,306-96,240 美元])明显高于男性(76、469美元,95% CI [70,983-81,953美元])和老年人(92,197美元,95% CI [87,087-97,307美元])的费用明显高于年轻人(62,580美元,95% CI [55,346-69,814美元])。在这 10 年间,医院、疗养院和家庭护理是帕金森病成本的最大来源:讨论:帕金森病的医疗系统成本巨大,尤其是在晚期。采取干预措施,减少帕金森病患者可避免的医院和疗养院服务的使用,可提高生活质量,并从医疗系统的角度节约成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Net Health System Costs of Parkinson Disease: A Propensity Score-Matched Health Administrative Data Cohort Study in Ontario, Canada.

Background and objectives: Few estimates of the long-term health system costs of Parkinson disease by phase of disease are available. We estimated 10-year and phase-based net health system costs of Parkinson disease before and after case ascertainment.

Methods: Using population-based linked administrative databases from Ontario, Canada, we identified 43,149 community-dwelling persons with incident Parkinson disease aged 40 years and older between 2009 and 2018 using a validated algorithm. These individuals were matched 1:1 to controls without Parkinson disease based on demographics and a propensity score. We calculated phase-based, net health system costs from the provincial government perspective during the preascertainment (3 years before index), initial (1 year after index), early continuing (>1-6 years after index), later continuing (>6-10 years after index), and terminal (1 year before death, if applicable) phases (standardized to 2020 $CAD and calculated on an annual basis). By applying survival probabilities to monthly cost estimates, we also determined 10-year net health system costs, stratified by sex and age.

Results: Annual mean net costs of Parkinson disease were lowest in the preascertainment phase ($212 CAD, 95% CI [$20-$404]), intermediate in the initial phase ($4,576 (95% CI [$4,217-$4,935]), and higher in the early continuing phase ($7,078, 95% CI [$6,717-$7,438]). The later continuing phase ($12,500, 95% CI [$12,060-$12,940]) and the terminal phase ($13,933, 95% CI [$13,123-$14,743]) showed the highest costs. The 10-year net cost of Parkinson disease was $82,153 (95% CI [$77,965-$86,341]) and was significantly higher in women ($89,773, 95% CI [$83,306-$96,240]) than in men ($76,469, 95% CI [$70,983-$81,953]) and older individuals ($92,197, 95% CI [$87,087-$97,307]), compared with younger individuals ($62,580, 95% CI [$55,346-$69,814]). Over the 10-year period, hospital, nursing home, and home care were the largest contributors to costs of Parkinson disease.

Discussion: Health system costs of Parkinson disease are substantial, particularly in the later phases. Interventions to reduce avoidable use of hospital and nursing home services by persons living with Parkinson disease may provide better quality of life and be cost saving from the health system perspective.

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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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