Trial-based cost-effectiveness analysis of Descemet membrane endothelial keratoplasty (DMEK) versus ultrathin Descemet stripping automated endothelial keratoplasty (UT-DSAEK)
the DMEK versus DSAEK Study Group
(2023) Acta Ophthalmologica, volume 101, issue 3, pp. 319 - 329
(Article)
Abstract
Purpose: To evaluate the cost-effectiveness of Descemet Membrane Endothelial Keratoplasy (DMEK) versus Ultrathin Descemet Stripping Automated Endothelial Keratoplasty (UT-DSAEK). Methods: A cost-effectiveness analysis using data from a multicenter randomized clinical trial was performed. The time horizon was 12 months postoperatively. Patients with Fuchs' endothelial dystrophy were randomized to DMEK (n =
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29) or UT-DSAEK (n = 24). Relevant resources from healthcare and societal perspectives were included in the cost analysis. Quality-Adjusted Life Years (QALYs) were determined using the Health Utilities Index Mark 3 (HUI3) and the EuroQol EQ-5D-5L questionnaires. The main outcome was the incremental cost-effectiveness ratio (ICER; incremental societal costs per QALY). Results: Societal costs averaged €8851 (US$11 406) for DMEK and €8320 (US$10 722) for UT-DSAEK. Higher costs in the DMEK group were mainly caused by higher rebubbling and regraft rates (21% and 7%, vs. 4% and 0% in the UT-DSAEK group). HUI3 QALYs were 0.70 (DMEK) and 0.79 (UT-DSAEK). EQ-5D-5L QALYs were 0.83 (DMEK) and 0.86 (UT-DSAEK). The ICER indicated DMEK was dominated by UT-DSAEK in both analyses. The cost-effectiveness probability for DMEK ranged from 21% to 5% (HUI3 QALYs) and 27%–14% (EQ-5D-5L QALYs), assuming the maximum acceptable ICER ranged from €2500 to €80.000 (US$3222–US$103 093) per QALY. Conclusion: The base case cost-effectiveness analysis favoured UT-DSAEK over DMEK, as costs of DMEK were higher while QALYs were lower. Further studies are required to assess long-term rebubbling and regraft rates and graft survival.
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Keywords: corneal transplantation, cost-effectiveness, costs, DMEK, Fuchs' endothelial dystrophy, QALY, UT-DSAEK, Ophthalmology, Journal Article
ISSN: 1755-375X
Publisher: Wiley-Blackwell
Note: Funding Information: Presentations at meetings: European Society of Cataract and Refractive Surgeons (ESCRS) congress, Paris, France, September 2019. Funding Information: This work was supported by The Netherlands Organization for Health Research and Development, The Hague, The Netherlands; Algemene Nederlandse Vereniging Ter Voorkoming Van Blindheid, Doorn, The Netherlands; Oogfonds, Utrecht, The Netherlands; Dr. F.P. Fischer‐Stichting, Utrecht, The Netherlands; and Landelijke Stichting Blinden en Slechtzienden (LSBS), Ede, The Netherlands. The funding organizations had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. Mor M. Dickman is a consultant at Chiesi Farmaceuticals. Rudy M.M.A. Nuijts is a consultant at Alcon (Fort Worth, TX, USA) and ThéaPharma (Clermont‐Ferrand, France), receives financial support for research from Alcon and Ophtec (Groningen, the Netherlands), and receives lecture fees from Alcon. Robert P.L. Wisse receives financial support from Carl‐Zeiss (Breda, The Netherlands) and ThéaPharma, and is equity owner of Easee (Amsterdam, The Netherlands.). Pieter J. Kruit is employee of ETB‐BISLIFE (Leiden, Netherlands). All other authors report no financial disclosures. Publisher Copyright: © 2022 The Authors. Acta Ophthalmologica published by John Wiley & Sons Ltd on behalf of Acta Ophthalmologica Scandinavica Foundation.
(Peer reviewed)