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左心室辅助装置在现实世界中的临床结局与医疗支出——CLEAR-LVAD研究

Clinical outcomes and healthcare expenditures in the real world with left ventricular assist devices - The CLEAR-LVAD study.

作者信息

Pagani Francis D, Mehra Mandeep R, Cowger Jennifer A, Horstmanshof Douglas A, Silvestry Scott C, Atluri Pavan, Cleveland Joseph C, Lindenfeld JoAnn, Roberts Gregory J, Bharmi Rupinder, Dalal Nirav, Kormos Robert L, Rogers Joseph G

机构信息

Department of Cardiac Surgery, University of Michigan, Ann Arbor, Michigan.

Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School, Boston, Massachusetts.

出版信息

J Heart Lung Transplant. 2021 May;40(5):323-333. doi: 10.1016/j.healun.2021.02.010. Epub 2021 Feb 22.

Abstract

BACKGROUND

Several distinctly engineered left ventricular assist devices (LVADs) are in clinical use. However, contemporaneous real world comparisons have not been conducted, and clinical trials were not powered to evaluate differential survival outcomes across devices.

OBJECTIVES

Determine real world survival outcomes and healthcare expenditures for commercially available durable LVADs.

METHODS

Using a retrospective observational cohort design, Medicare claims files were linked to manufacturer device registration data to identify de-novo, durable LVAD implants performed between January 2014 and December 2018, with follow-up through December 2019. Survival outcomes were compared using a Cox proportional hazards model stratified by LVAD type and validated using propensity score matching. Healthcare resource utilization was analyzed across device types by using nonparametric bootstrap analysis methodology. Primary outcome was survival at 1-year and total Part A Medicare payments.

RESULTS

A total of 4,195 de-novo LVAD implants were identified in fee-for-service Medicare beneficiaries (821 HeartMate 3; 1,840 HeartMate II; and 1,534 Other-VADs). The adjusted hazard ratio for mortality at 1-year (confirmed in a propensity score matched analysis) for the HeartMate 3 vs HeartMate II was 0.64 (95% CI; 0.52-0.79, p< 0.001) and for the HeartMate 3 vs Other-VADs was 0.51 (95% CI; 0.42-0.63, p < 0.001). The HeartMate 3 cohort experienced fewer hospitalizations per patient-year vs Other-VADs (respectively, 2.8 vs 3.2 EPPY hospitalizations, p < 0.01) and 6.1 fewer hospital days on average (respectively, 25.2 vs 31.3 days, p < 0.01). The difference in Medicare expenditures, conditional on survival, for HeartMate 3 vs HeartMate II was -$10,722, p < 0.001 (17.4% reduction) and for HeartMate 3 vs Other-VADs was -$17,947, p < 0.001 (26.1% reduction).

CONCLUSIONS

In this analysis of a large, real world, United States. administrative dataset of durable LVADs, we observed that the HeartMate 3 had superior survival, reduced healthcare resource use, and lower healthcare expenditure compared to other contemporary commercially available LVADs.

摘要

背景

几种经过独特设计的左心室辅助装置(LVAD)已投入临床使用。然而,尚未进行同期的真实世界比较,且临床试验也未设定足够的样本量来评估不同装置之间的生存差异结果。

目的

确定市售耐用型LVAD的真实世界生存结果和医疗保健支出。

方法

采用回顾性观察队列设计,将医疗保险理赔档案与制造商的设备注册数据相链接,以识别2014年1月至2018年12月期间进行的初次、耐用型LVAD植入手术,并随访至2019年12月。使用Cox比例风险模型按LVAD类型进行分层比较生存结果,并通过倾向得分匹配进行验证。使用非参数自助分析方法对不同装置类型的医疗资源利用情况进行分析。主要结局为1年生存率和医疗保险A部分的总支付费用。

结果

在按服务收费的医疗保险受益人中,共识别出4195例初次LVAD植入手术(821例HeartMate 3;1840例HeartMate II;1534例其他VAD)。HeartMate 3与HeartMate II相比,1年死亡率的调整后风险比(在倾向得分匹配分析中得到确认)为0.64(95%CI:0.52 - 0.79,p < 0.001),HeartMate 3与其他VAD相比为0.51(95%CI:0.42 - 0.63,p < 0.001)。与其他VAD相比,HeartMate 3队列中每位患者每年的住院次数更少(分别为2.8次与3.2次每患者年住院次数,p < 0.01),平均住院天数少6.1天(分别为25.2天与31.3天,p < 0.01)。在生存条件下,HeartMate 3与HeartMate II相比,医疗保险支出差异为 - 10722美元,p < 0.001(降低17.4%),HeartMate 3与其他VAD相比为 - 17947美元,p < 0.001(降低26.1%)。

结论

在对美国一个大型真实世界的耐用型LVAD行政数据集的分析中,我们观察到与其他当代市售LVAD相比,HeartMate 3具有更好的生存率、更低的医疗资源使用和更低的医疗保健支出。

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