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Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis
PURPOSE: To describe the long-term outcome of the use of a specialized scleral lens known as a prosthetic replacement of the ocular surface ecosystem (PROSE) device to support the ocular surface in patients with a Boston Keratoprosthesis (KPro) Type I. All patients in this series were unable to purs...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495601/ https://www.ncbi.nlm.nih.gov/pubmed/37705757 http://dx.doi.org/10.1016/j.ajoc.2023.101919 |
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author | Asghari, Bita Carrasquillo, Karen G. Kwok, Alan Sippel, Kimberly C. |
author_facet | Asghari, Bita Carrasquillo, Karen G. Kwok, Alan Sippel, Kimberly C. |
author_sort | Asghari, Bita |
collection | PubMed |
description | PURPOSE: To describe the long-term outcome of the use of a specialized scleral lens known as a prosthetic replacement of the ocular surface ecosystem (PROSE) device to support the ocular surface in patients with a Boston Keratoprosthesis (KPro) Type I. All patients in this series were unable to pursue continuous wear of a bandage soft contact lens (BSCL) – a critical aspect of post KPro implantation management intended to protect the corneal carrier tissue from desiccation and stromal melting. OBSERVATIONS: Four eyes of four patients with a Boston KPro Type I were included. All four had failed BSCL wear and were instead treated with PROSE device wear. All four patients had underlying diagnoses associated with a diseased ocular surface (Stevens-Johnson Syndrome [one patient], prior failed penetrating keratoplasty associated with herpes zoster-related neurotrophic keratopathy [one patient], and prior failed penetrating keratoplasty associated with severe dry eye disease [two patients]). Causes of failure of BSCL wear included poor retention, discomfort, and poor vision. PROSE device wear was initiated on average seven and a half (range four to 14) months post-KPro implantation. The wear schedule varied and ranged from waking-hour wear only to 24-h wear. The average duration of device wear was 59.3 (range 28–103) months. Two patients exhibited persistent corneal epithelial defect formation with waking-hour wear, which resolved within 10 days with 24-h device wear. All patients exhibited improvement in vision with PROSE compared to baseline, averaging six and a half (range six to eight) lines of improvement in Snellen acuity, and all patients reported increased comfort. There was no incidence of microbial keratitis, KPro device instability, or other complication throughout the duration of device wear. CONCLUSIONS AND IMPORTANCE: This report offers a novel alternate approach to long-term support of the ocular surface in patients with a Boston KPro who fail standard continuous BSCL wear. |
format | Online Article Text |
id | pubmed-10495601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-104956012023-09-13 Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis Asghari, Bita Carrasquillo, Karen G. Kwok, Alan Sippel, Kimberly C. Am J Ophthalmol Case Rep Case Report PURPOSE: To describe the long-term outcome of the use of a specialized scleral lens known as a prosthetic replacement of the ocular surface ecosystem (PROSE) device to support the ocular surface in patients with a Boston Keratoprosthesis (KPro) Type I. All patients in this series were unable to pursue continuous wear of a bandage soft contact lens (BSCL) – a critical aspect of post KPro implantation management intended to protect the corneal carrier tissue from desiccation and stromal melting. OBSERVATIONS: Four eyes of four patients with a Boston KPro Type I were included. All four had failed BSCL wear and were instead treated with PROSE device wear. All four patients had underlying diagnoses associated with a diseased ocular surface (Stevens-Johnson Syndrome [one patient], prior failed penetrating keratoplasty associated with herpes zoster-related neurotrophic keratopathy [one patient], and prior failed penetrating keratoplasty associated with severe dry eye disease [two patients]). Causes of failure of BSCL wear included poor retention, discomfort, and poor vision. PROSE device wear was initiated on average seven and a half (range four to 14) months post-KPro implantation. The wear schedule varied and ranged from waking-hour wear only to 24-h wear. The average duration of device wear was 59.3 (range 28–103) months. Two patients exhibited persistent corneal epithelial defect formation with waking-hour wear, which resolved within 10 days with 24-h device wear. All patients exhibited improvement in vision with PROSE compared to baseline, averaging six and a half (range six to eight) lines of improvement in Snellen acuity, and all patients reported increased comfort. There was no incidence of microbial keratitis, KPro device instability, or other complication throughout the duration of device wear. CONCLUSIONS AND IMPORTANCE: This report offers a novel alternate approach to long-term support of the ocular surface in patients with a Boston KPro who fail standard continuous BSCL wear. Elsevier 2023-09-01 /pmc/articles/PMC10495601/ /pubmed/37705757 http://dx.doi.org/10.1016/j.ajoc.2023.101919 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Asghari, Bita Carrasquillo, Karen G. Kwok, Alan Sippel, Kimberly C. Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis |
title | Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis |
title_full | Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis |
title_fullStr | Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis |
title_full_unstemmed | Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis |
title_short | Use of PROSE for long-term ocular surface support in patients with a permanent keratoprosthesis |
title_sort | use of prose for long-term ocular surface support in patients with a permanent keratoprosthesis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495601/ https://www.ncbi.nlm.nih.gov/pubmed/37705757 http://dx.doi.org/10.1016/j.ajoc.2023.101919 |
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