Cost-Effectiveness of Transcatheter Versus Surgical Aortic Valve Replacement in Patients With Severe Aortic Stenosis at Intermediate Risk

Author:

Baron Suzanne J.1,Wang Kaijun1,House John A.2,Magnuson Elizabeth A.1,Reynolds Matthew R.3,Makkar Raj4,Herrmann Howard C.5,Kodali Susheel6,Thourani Vinod H.7,Kapadia Samir8,Svensson Lars8,Mack Michael J.9,Brown David L.9,Russo Mark J.10,Smith Craig R.6,Webb John11,Miller Craig12,Leon Martin B.,Cohen David J.1,

Affiliation:

1. Saint Luke’s Mid America Heart Institute, University of Missouri-Kansas City (S.J.B., K.W., E.A.M., D.J.C.).

2. Premier Research Services Inc, Charlotte, NC (J.A.H.).

3. Lahey Hospital and Medical Center, Burlington, MA (M.R.R.).

4. Cedars-Sinai Medical Center, Los Angeles, CA (R.M.).

5. Hospital of University of Pennsylvania, Philadelphia (H.C.H.).

6. Columbia University Medical Center, New York (S. Kodali, C.R.S.).

7. MedStar Heart and Vascular Institute/Georgetown University, Washington, DC (V.H.T.).

8. Cleveland Clinic, OH (S. Kapadia, L.S.).

9. Baylor Scott and White Healthcare, Plano, TX (M.J.M., D.L.B.).

10. RWJ Barnabas Health, West Orange, NJ (M.J.R.).

11. St. Paul’s Hospital, Vancouver, British Columbia, Canada (J.W.).

12. Stanford Medical Center, Palo Alto, CA (C.M.).

Abstract

Background: In patients with severe aortic stenosis (AS) at intermediate surgical risk, treatment with transcatheter aortic valve replacement (TAVR) or surgical aortic valve replacement (SAVR) results in similar rates of death or stroke at 2 years. Whether TAVR is cost-effective compared with SAVR for intermediate-risk patients remains uncertain. Methods: Between 2011 and 2014, 3110 intermediate-risk AS patients were treated with TAVR or SAVR in the PARTNER 2 trial (Placement of Aortic Transcatheter Valves 2). A total of 2032 patients were randomized to receive TAVR using the SAPIEN XT valve (XT-TAVR) or SAVR in the PARTNER 2A trial, whereas the PARTNER S3i registry included an additional 1078 patients treated with TAVR using the SAPIEN 3 valve (S3-TAVR), which offers a lower delivery profile and sealing skirt designed to reduce paravalvular regurgitation compared with XT-TAVR. Procedural costs were estimated using measured resource utilization. Other in-trial costs were assessed by linkage of trial data with Medicare claims (n=2333) or by linear regression models for unlinked patients (n=682). Health utilities were estimated using the EQ-5D at baseline and 1, 12, and 24 months. Using a Markov model informed by in-trial costs, utilities, and survival data, lifetime cost-effectiveness from the perspective of the US healthcare system was estimated in terms of cost per quality-adjusted life-year gained. Results: Although procedural costs were ≈$20 000 higher with TAVR than SAVR, total cost differences for the index hospitalization were only $2888 higher with XT-TAVR ( P =0.014) and were $4155 lower with S3-TAVR ( P <0.001) owing to reductions in length of stay with TAVR. Follow-up costs were significantly lower with XT-TAVR (Δ=−$9304; P <0.001) and S3-TAVR (Δ=−$11 377; P <0.001) than with SAVR. Over a lifetime horizon, TAVR was projected to lower total costs by $8000 to $10 000 and to increase quality-adjusted survival by 0.15 to 0.27 years. XT-TAVR and S3-TAVR were found to be economically dominant compared with SAVR in 84% and 97% of bootstrap replicates, respectively. Conclusions: Among intermediate-risk AS patients, TAVR is projected to be economically dominant from the perspective of the US healthcare system by providing both greater quality-adjusted life expectancy and lower long-term costs than SAVR. If long-term data demonstrate comparable late mortality with TAVR and SAVR, these findings suggest that TAVR might be the preferred treatment strategy for intermediate-risk AS patients based on both clinical and economic considerations. Clinical Trial Registration: URL: https://www.clinicaltrials.gov . Unique identifier: NCT01314313.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Cited by 143 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.7亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2025 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3