Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty

BACKGROUND: The study aimed to report the outcomes of patients treated with cenegermin 0.002% for neurotrophic keratopathy (NK) following penetrating keratoplasty (PK). MATERIALS AND METHODS: This retrospective case series included patients evaluated at a tertiary care hospital who completed an 8-we...

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Main Authors: Alexandra R. Zaloga, Ashley Khalili, Brandon D. Ayres, Brenton D. Finklea, Beeran B. Meghpara, Christopher J. Rapuano, Zeba A. Syed
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2025-05-01
Series:Oman Journal of Ophthalmology
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Online Access:https://journals.lww.com/10.4103/ojo.ojo_311_24
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author Alexandra R. Zaloga
Ashley Khalili
Brandon D. Ayres
Brenton D. Finklea
Beeran B. Meghpara
Christopher J. Rapuano
Zeba A. Syed
author_facet Alexandra R. Zaloga
Ashley Khalili
Brandon D. Ayres
Brenton D. Finklea
Beeran B. Meghpara
Christopher J. Rapuano
Zeba A. Syed
author_sort Alexandra R. Zaloga
collection DOAJ
description BACKGROUND: The study aimed to report the outcomes of patients treated with cenegermin 0.002% for neurotrophic keratopathy (NK) following penetrating keratoplasty (PK). MATERIALS AND METHODS: This retrospective case series included patients evaluated at a tertiary care hospital who completed an 8-week course of cenegermin for NK within 12 months following PK. The primary outcome measure was NK stage, while secondary outcomes included complete epithelial healing, epithelial defect size, and best-corrected visual acuity (BCVA) at baseline and four time points during and following treatment. We also evaluated disease progression. RESULTS: Fourteen eyes of 14 patients were included and demonstrated significant improvement in NK stage at 4 weeks (1.1 ± 0.7; P = 0.006) and 8 weeks after treatment initiation (0.9 ± 0.7; P = 0.002) and 1 month (0.6 ± 0.5; P < 0.001) and 6 months after treatment completion (0.8 ± 0.9; P = 0.002) compared to baseline (1.6 ± 0.5). Complete epithelial healing was noted 1 month (42.9%; P = 0.016) and 6 months after treatment completion (38.5%; P = 0.016). Epithelial defect size improved to <5 mm2 at all points (P < 0.05) during and after treatment compared to baseline (37.24 mm2). Improvement in BCVA was not significant at any time point. Two (14.3%) patients experienced disease progression up to 6 months of follow-up. CONCLUSIONS: Following an 8-week course of cenegermin, patients with a history of PK demonstrated improvement in NK stage, epithelial healing, and reduced epithelial defect size lasting 6 months after treatment completion. Patients with prior PK and NK may be considered candidates for cenegermin treatment.
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spelling doaj-art-6ddb2991e73449228716fcff60654f962025-08-20T02:44:50ZengWolters Kluwer Medknow PublicationsOman Journal of Ophthalmology0974-620X0974-78422025-05-0118219820410.4103/ojo.ojo_311_24Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplastyAlexandra R. ZalogaAshley KhaliliBrandon D. AyresBrenton D. FinkleaBeeran B. MeghparaChristopher J. RapuanoZeba A. SyedBACKGROUND: The study aimed to report the outcomes of patients treated with cenegermin 0.002% for neurotrophic keratopathy (NK) following penetrating keratoplasty (PK). MATERIALS AND METHODS: This retrospective case series included patients evaluated at a tertiary care hospital who completed an 8-week course of cenegermin for NK within 12 months following PK. The primary outcome measure was NK stage, while secondary outcomes included complete epithelial healing, epithelial defect size, and best-corrected visual acuity (BCVA) at baseline and four time points during and following treatment. We also evaluated disease progression. RESULTS: Fourteen eyes of 14 patients were included and demonstrated significant improvement in NK stage at 4 weeks (1.1 ± 0.7; P = 0.006) and 8 weeks after treatment initiation (0.9 ± 0.7; P = 0.002) and 1 month (0.6 ± 0.5; P < 0.001) and 6 months after treatment completion (0.8 ± 0.9; P = 0.002) compared to baseline (1.6 ± 0.5). Complete epithelial healing was noted 1 month (42.9%; P = 0.016) and 6 months after treatment completion (38.5%; P = 0.016). Epithelial defect size improved to <5 mm2 at all points (P < 0.05) during and after treatment compared to baseline (37.24 mm2). Improvement in BCVA was not significant at any time point. Two (14.3%) patients experienced disease progression up to 6 months of follow-up. CONCLUSIONS: Following an 8-week course of cenegermin, patients with a history of PK demonstrated improvement in NK stage, epithelial healing, and reduced epithelial defect size lasting 6 months after treatment completion. Patients with prior PK and NK may be considered candidates for cenegermin treatment.https://journals.lww.com/10.4103/ojo.ojo_311_24cenegerminneurotrophic keratopathypenetrating keratoplasty
spellingShingle Alexandra R. Zaloga
Ashley Khalili
Brandon D. Ayres
Brenton D. Finklea
Beeran B. Meghpara
Christopher J. Rapuano
Zeba A. Syed
Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty
Oman Journal of Ophthalmology
cenegermin
neurotrophic keratopathy
penetrating keratoplasty
title Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty
title_full Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty
title_fullStr Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty
title_full_unstemmed Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty
title_short Utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty
title_sort utility of cenegermin for the management of neurotrophic keratopathy after penetrating keratoplasty
topic cenegermin
neurotrophic keratopathy
penetrating keratoplasty
url https://journals.lww.com/10.4103/ojo.ojo_311_24
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