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Early Outcomes of an Artificial Endothelial Replacement Membrane Implantation After Failed Repeat Endothelial Keratoplasty.

Authors :
Fontana L
di Geronimo N
Cennamo M
Mencucci R
Versura P
Moramarco A
Source :
Cornea [Cornea] 2024 Sep 01; Vol. 43 (9), pp. 1088-1094. Date of Electronic Publication: 2023 Nov 22.
Publication Year :
2024

Abstract

Purpose: The purpose of this study was to report the outcomes of a novel artificial endothelial replacement membrane implant for treating corneal edema after failed repeat endothelial keratoplasty (EK).<br />Design: This was a retrospective interventional case series.<br />Methods: Patients with chronic corneal edema underwent removal of the EK graft and implantation of an artificial endothelial replacement membrane (EndoArt, EyeYon Medical, Israel) several months after 2 or more Descemet stripping endothelial keratoplasty procedures. The implant was secured to the posterior corneal surface using an air-gas bubble. Outcome measures included corrected distance visual acuity (logMAR), central corneal thickness, device-related complications, and ocular discomfort.<br />Results: Five eyes of 5 patients underwent EndoArt implantation. Six months after surgery, the synthetic endothelial replacement membrane was well-centered and adherent to the posterior corneal surface, with improvement in central corneal transparency in all patients. Corrected distance visual acuity increased from mean 1.26 ± 0.25 (logMAR) preoperatively to 0.74 ± 0.44 (logMAR) postoperatively ( P = 0.06). Central corneal thickness significantly decreased from a mean of 805 ± 135 μm (excluding the EK graft) preoperatively to 588 ± 60 μm (excluding the EndoArt) postoperatively ( P = 0.015). No severe device-related complications developed after surgery, although most patients required more than 1 air-gas bubble injection to achieve complete implant adhesion. All patients experienced preoperative reduction in subjective ocular pain.<br />Conclusions: Synthetic endothelial replacement membrane implantation improves central corneal transparency and visual acuity in patients with failed EK and guarded prognosis for repeat keratoplasty. No significant implant-related adverse events occurred after surgery.<br />Competing Interests: The authors have no funding or conflicts of interest to disclose.<br /> (Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc.)

Details

Language :
English
ISSN :
1536-4798
Volume :
43
Issue :
9
Database :
MEDLINE
Journal :
Cornea
Publication Type :
Academic Journal
Accession number :
38015948
Full Text :
https://doi.org/10.1097/ICO.0000000000003433