Purpose: To report the outcomes of Descemet membrane endothelial keratoplasty (DMEK) with intensive antiviral therapy for corneal edema secondary to herpes simplex virus type 1 (HSV-1)-mediated endotheliitis. Methods: All eyes with polymerase chain reaction positive for HSV-1 undergoing DMEK for endothelial decompensation between January 2014 and January 2018 were followed up prospectively at our tertiary referral center. All eyes had been free of active inflammation for a minimum of 9 months and were treated prophylactically with high-dose systemic and topical antivirals, which were continued for a prolonged period of time. Primary outcomes were the occurrence of immunological rejection and/or recurrence of endotheliitis, eventually resulting in graft failure. Secondary outcomes were best spectacle-corrected visual acuity and endothelial cell loss. Results: Four consecutive eyes of 4 patients were included with a mean (+/- SD) patient age of 68.5 +/- 15.1 years. The postoperative follow-up averaged 22 months. No eyes exhibited any signs of immunologic rejection, recurrence of endotheliitis, or graft failure. Mean (+/- SD) decimal best spectacle-corrected visual acuity improved from 0.2 +/- 0.1 to 0.7 +/- 0.2 (P = 0.007), whereas mean (+/- SD) endothelial cell loss was 56% +/- 10.2% at the final postoperative follow-up. Conclusions: DMEK is an effective option to treat corneal edema secondary to HSV-1-related endotheliitis. Intensive antiviral prophylaxis may reduce the risk of recurrence and subsequent graft failure.

Successful Descemet Membrane Endothelial Keratoplasty in Proven Herpetic Endothelial Decompensation Requires Intensive Antiviral Therapy

Giannaccare, Giuseppe;
2020-01-01

Abstract

Purpose: To report the outcomes of Descemet membrane endothelial keratoplasty (DMEK) with intensive antiviral therapy for corneal edema secondary to herpes simplex virus type 1 (HSV-1)-mediated endotheliitis. Methods: All eyes with polymerase chain reaction positive for HSV-1 undergoing DMEK for endothelial decompensation between January 2014 and January 2018 were followed up prospectively at our tertiary referral center. All eyes had been free of active inflammation for a minimum of 9 months and were treated prophylactically with high-dose systemic and topical antivirals, which were continued for a prolonged period of time. Primary outcomes were the occurrence of immunological rejection and/or recurrence of endotheliitis, eventually resulting in graft failure. Secondary outcomes were best spectacle-corrected visual acuity and endothelial cell loss. Results: Four consecutive eyes of 4 patients were included with a mean (+/- SD) patient age of 68.5 +/- 15.1 years. The postoperative follow-up averaged 22 months. No eyes exhibited any signs of immunologic rejection, recurrence of endotheliitis, or graft failure. Mean (+/- SD) decimal best spectacle-corrected visual acuity improved from 0.2 +/- 0.1 to 0.7 +/- 0.2 (P = 0.007), whereas mean (+/- SD) endothelial cell loss was 56% +/- 10.2% at the final postoperative follow-up. Conclusions: DMEK is an effective option to treat corneal edema secondary to HSV-1-related endotheliitis. Intensive antiviral prophylaxis may reduce the risk of recurrence and subsequent graft failure.
2020
herpetic corneal decompensation
DMEK
corneal edema
endotheliitis
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11584/426420
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