Neurotrophic keratopathy: Clinical presentation and effects of cenegermin

Purpose: To report on 4 patients (3 adults, 1 child) with neurotrophic keratopathy (NK) treated with cenegermin 20 μg/ml (Oxervate®), a recombinant human nerve growth factor (rhNGF), which was authorized by the European Medicines Agency for the treatment of neurotrophic keratopathy stage 2 and stage...

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Main Authors: Julia Bing Bu, Adrian Gericke, Norbert Pfeiffer, Joanna Wasielica-Poslednik
Format: Article
Language:English
Published: Elsevier 2022-06-01
Series:American Journal of Ophthalmology Case Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2451993622002341
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author Julia Bing Bu
Adrian Gericke
Norbert Pfeiffer
Joanna Wasielica-Poslednik
author_facet Julia Bing Bu
Adrian Gericke
Norbert Pfeiffer
Joanna Wasielica-Poslednik
author_sort Julia Bing Bu
collection DOAJ
description Purpose: To report on 4 patients (3 adults, 1 child) with neurotrophic keratopathy (NK) treated with cenegermin 20 μg/ml (Oxervate®), a recombinant human nerve growth factor (rhNGF), which was authorized by the European Medicines Agency for the treatment of neurotrophic keratopathy stage 2 and stage 3 of Mackie Classification in patients over 18 years of age. Observations: Three patients with neurotrophic keratopathy stage 2 and 1 patient with neurotrophic keratopathy stage 3, who were treated with cenegermin eye drops 6 times daily for 8 weeks, were observed. Two patients suffered from herpetic keratitis and 2 patients from neurotrophic keratopathy secondary to orbital radiation. In addition to closure of epithelial defects, an increase of corneal sensitivity and improvement of visual acuity has been shown in all treated patients at the end of therapy. One patient reported on neuralgic pain as a side effect. The corneal epithelium remained closed during the follow-up period of 11 weeks, 31 and 32 months after cessation of therapy in 3 patients, respectively. In one patient, corneal erosion recurred 4 weeks after completion of treatment due to recurrent HSV keratitis, which resolved after therapy adjustment and the corneal epithelium remained closed for 35 weeks. Conclusion: The cases presented suggest that treatment with cenegermin 20 μg/ml not only promotes corneal epithelial wound healing, but also significantly improves corneal sensitivity and visual acuity with minor side effects in adults and children.
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spelling doaj.art-4dd883646f334d03a09cc1bc075bf8a02022-12-22T00:36:01ZengElsevierAmerican Journal of Ophthalmology Case Reports2451-99362022-06-0126101488Neurotrophic keratopathy: Clinical presentation and effects of cenegerminJulia Bing Bu0Adrian Gericke1Norbert Pfeiffer2Joanna Wasielica-Poslednik3Corresponding author. University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstr. 1, 55131, Mainz, Germany.; Department of Ophthalmology, University Medical Center of the Johannes Gutenberg University Mainz, GermanyDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg University Mainz, GermanyDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg University Mainz, GermanyDepartment of Ophthalmology, University Medical Center of the Johannes Gutenberg University Mainz, GermanyPurpose: To report on 4 patients (3 adults, 1 child) with neurotrophic keratopathy (NK) treated with cenegermin 20 μg/ml (Oxervate®), a recombinant human nerve growth factor (rhNGF), which was authorized by the European Medicines Agency for the treatment of neurotrophic keratopathy stage 2 and stage 3 of Mackie Classification in patients over 18 years of age. Observations: Three patients with neurotrophic keratopathy stage 2 and 1 patient with neurotrophic keratopathy stage 3, who were treated with cenegermin eye drops 6 times daily for 8 weeks, were observed. Two patients suffered from herpetic keratitis and 2 patients from neurotrophic keratopathy secondary to orbital radiation. In addition to closure of epithelial defects, an increase of corneal sensitivity and improvement of visual acuity has been shown in all treated patients at the end of therapy. One patient reported on neuralgic pain as a side effect. The corneal epithelium remained closed during the follow-up period of 11 weeks, 31 and 32 months after cessation of therapy in 3 patients, respectively. In one patient, corneal erosion recurred 4 weeks after completion of treatment due to recurrent HSV keratitis, which resolved after therapy adjustment and the corneal epithelium remained closed for 35 weeks. Conclusion: The cases presented suggest that treatment with cenegermin 20 μg/ml not only promotes corneal epithelial wound healing, but also significantly improves corneal sensitivity and visual acuity with minor side effects in adults and children.http://www.sciencedirect.com/science/article/pii/S2451993622002341Neurotrophic keratopathyNerve growth factorCenegermin
spellingShingle Julia Bing Bu
Adrian Gericke
Norbert Pfeiffer
Joanna Wasielica-Poslednik
Neurotrophic keratopathy: Clinical presentation and effects of cenegermin
American Journal of Ophthalmology Case Reports
Neurotrophic keratopathy
Nerve growth factor
Cenegermin
title Neurotrophic keratopathy: Clinical presentation and effects of cenegermin
title_full Neurotrophic keratopathy: Clinical presentation and effects of cenegermin
title_fullStr Neurotrophic keratopathy: Clinical presentation and effects of cenegermin
title_full_unstemmed Neurotrophic keratopathy: Clinical presentation and effects of cenegermin
title_short Neurotrophic keratopathy: Clinical presentation and effects of cenegermin
title_sort neurotrophic keratopathy clinical presentation and effects of cenegermin
topic Neurotrophic keratopathy
Nerve growth factor
Cenegermin
url http://www.sciencedirect.com/science/article/pii/S2451993622002341
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AT norbertpfeiffer neurotrophickeratopathyclinicalpresentationandeffectsofcenegermin
AT joannawasielicaposlednik neurotrophickeratopathyclinicalpresentationandeffectsofcenegermin