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Donor cross-linking for keratoplasty: a laboratory evaluation
PURPOSE: This laboratory-based investigation compares the topographic outcomes of conventional penetrating keratoplasty with that of a novel procedure in which donor corneas are cross-linked prior to keratoplasty. METHODS: Penetrating keratoplasty procedures with continuous running sutures were carr...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653237/ https://www.ncbi.nlm.nih.gov/pubmed/26345527 http://dx.doi.org/10.1007/s00417-015-3160-6 |
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author | Mukherjee, Achyut Hayes, Sally Aslanides, Ioannis Lanchares, Elena Meek, Keith M. |
author_facet | Mukherjee, Achyut Hayes, Sally Aslanides, Ioannis Lanchares, Elena Meek, Keith M. |
author_sort | Mukherjee, Achyut |
collection | PubMed |
description | PURPOSE: This laboratory-based investigation compares the topographic outcomes of conventional penetrating keratoplasty with that of a novel procedure in which donor corneas are cross-linked prior to keratoplasty. METHODS: Penetrating keratoplasty procedures with continuous running sutures were carried out in a porcine whole globe model. Sixty eyes were randomly paired as ‘donor’ and ‘host’ tissue before being assigned to one of two groups. In the cross-linked group, donor corneas underwent riboflavin/UVA cross-linking prior to being trephined and sutured to untreated hosts. In the conventional keratoplasty group, both host and donor corneas remained untreated prior to keratoplasty. Topographic and corneal wavefront measurements were performed following surgery, and technical aspects of the procedure evaluated. RESULTS: Mean keratometric astigmatism was significantly lower in the cross-linked donor group at 3.67D (SD 1.8 D), vs. 8.43 D (SD 2.4 D) in the conventional keratoplasty group (p < 0.005). Mean wavefront astigmatism was also significantly reduced in the cross-linked donor group 4.71 D (SD 2.1) vs. 8.29D (SD 3.6) in the conventional keratoplasty group (p < 0.005). Mean RMS higher order aberration was significantly lower in the cross-linked donor group at 1.79 um (SD 0.98), vs. 3.05 um (SD 1.9) in the conventional keratoplasty group (P = 0.02). Qualitative analysis revealed less tissue distortion at the graft-host junction in the cross-linked group. CONCLUSION: Cross-linking of donor corneas prior to keratoplasty reduces intraoperative induced astigmatism and aberrations in an animal model. Further studies are indicated to evaluate the implications of this potential modification of keratoplasty surgery. |
format | Online Article Text |
id | pubmed-4653237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-46532372015-11-27 Donor cross-linking for keratoplasty: a laboratory evaluation Mukherjee, Achyut Hayes, Sally Aslanides, Ioannis Lanchares, Elena Meek, Keith M. Graefes Arch Clin Exp Ophthalmol Cornea PURPOSE: This laboratory-based investigation compares the topographic outcomes of conventional penetrating keratoplasty with that of a novel procedure in which donor corneas are cross-linked prior to keratoplasty. METHODS: Penetrating keratoplasty procedures with continuous running sutures were carried out in a porcine whole globe model. Sixty eyes were randomly paired as ‘donor’ and ‘host’ tissue before being assigned to one of two groups. In the cross-linked group, donor corneas underwent riboflavin/UVA cross-linking prior to being trephined and sutured to untreated hosts. In the conventional keratoplasty group, both host and donor corneas remained untreated prior to keratoplasty. Topographic and corneal wavefront measurements were performed following surgery, and technical aspects of the procedure evaluated. RESULTS: Mean keratometric astigmatism was significantly lower in the cross-linked donor group at 3.67D (SD 1.8 D), vs. 8.43 D (SD 2.4 D) in the conventional keratoplasty group (p < 0.005). Mean wavefront astigmatism was also significantly reduced in the cross-linked donor group 4.71 D (SD 2.1) vs. 8.29D (SD 3.6) in the conventional keratoplasty group (p < 0.005). Mean RMS higher order aberration was significantly lower in the cross-linked donor group at 1.79 um (SD 0.98), vs. 3.05 um (SD 1.9) in the conventional keratoplasty group (P = 0.02). Qualitative analysis revealed less tissue distortion at the graft-host junction in the cross-linked group. CONCLUSION: Cross-linking of donor corneas prior to keratoplasty reduces intraoperative induced astigmatism and aberrations in an animal model. Further studies are indicated to evaluate the implications of this potential modification of keratoplasty surgery. Springer Berlin Heidelberg 2015-09-08 2015 /pmc/articles/PMC4653237/ /pubmed/26345527 http://dx.doi.org/10.1007/s00417-015-3160-6 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Cornea Mukherjee, Achyut Hayes, Sally Aslanides, Ioannis Lanchares, Elena Meek, Keith M. Donor cross-linking for keratoplasty: a laboratory evaluation |
title | Donor cross-linking for keratoplasty: a laboratory evaluation |
title_full | Donor cross-linking for keratoplasty: a laboratory evaluation |
title_fullStr | Donor cross-linking for keratoplasty: a laboratory evaluation |
title_full_unstemmed | Donor cross-linking for keratoplasty: a laboratory evaluation |
title_short | Donor cross-linking for keratoplasty: a laboratory evaluation |
title_sort | donor cross-linking for keratoplasty: a laboratory evaluation |
topic | Cornea |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4653237/ https://www.ncbi.nlm.nih.gov/pubmed/26345527 http://dx.doi.org/10.1007/s00417-015-3160-6 |
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