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Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography

To determine the risk factors and unique characteristics of keratoconus (KC) progression after penetrating keratoplasty (PK), anterior segment optical coherence tomography parameters were statistically analyzed in comparison with eyes undergoing PK for other diseases as a control. Ninety-one eyes ma...

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Autores principales: Yoshida, Junko, Toyono, Tetsuya, Shirakawa, Rika, Miyai, Takashi, Usui, Tomohiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596038/
https://www.ncbi.nlm.nih.gov/pubmed/33122764
http://dx.doi.org/10.1038/s41598-020-75412-y
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author Yoshida, Junko
Toyono, Tetsuya
Shirakawa, Rika
Miyai, Takashi
Usui, Tomohiko
author_facet Yoshida, Junko
Toyono, Tetsuya
Shirakawa, Rika
Miyai, Takashi
Usui, Tomohiko
author_sort Yoshida, Junko
collection PubMed
description To determine the risk factors and unique characteristics of keratoconus (KC) progression after penetrating keratoplasty (PK), anterior segment optical coherence tomography parameters were statistically analyzed in comparison with eyes undergoing PK for other diseases as a control. Ninety-one eyes maintaining clear PK grafts for over 10 years were divided into 2 groups according to the primary indication for PK (KC vs Others groups). Corneal thinning indicators (inferior host thinnest corneal thickness/central corneal thickness [IHT/CCT], inferior graft thinnest corneal thickness/CCT [IGT/CCT]), were smaller whereas anterior chamber depth, and steepest corneal power (Ks), and maximum corneal power (K(max)) were larger in the KC group with statistical significance. Graft size, K(max) and Ks correlated with IHT/CCT and IGT/CCT in the KC group. These correlations were not detected in controls. Graft size and postoperative period were selected by multivariate regression analysis as factors for corneal ectatic changes in the KC group. In conclusion, KC eyes long after PK show inferior graft and host corneal thinning, and corneal protrusion. Corneal power parameters such as K(max) or Ks can be used to monitor KC progression after PK. A small graft might lead to KC progression after PK.
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spelling pubmed-75960382020-10-30 Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography Yoshida, Junko Toyono, Tetsuya Shirakawa, Rika Miyai, Takashi Usui, Tomohiko Sci Rep Article To determine the risk factors and unique characteristics of keratoconus (KC) progression after penetrating keratoplasty (PK), anterior segment optical coherence tomography parameters were statistically analyzed in comparison with eyes undergoing PK for other diseases as a control. Ninety-one eyes maintaining clear PK grafts for over 10 years were divided into 2 groups according to the primary indication for PK (KC vs Others groups). Corneal thinning indicators (inferior host thinnest corneal thickness/central corneal thickness [IHT/CCT], inferior graft thinnest corneal thickness/CCT [IGT/CCT]), were smaller whereas anterior chamber depth, and steepest corneal power (Ks), and maximum corneal power (K(max)) were larger in the KC group with statistical significance. Graft size, K(max) and Ks correlated with IHT/CCT and IGT/CCT in the KC group. These correlations were not detected in controls. Graft size and postoperative period were selected by multivariate regression analysis as factors for corneal ectatic changes in the KC group. In conclusion, KC eyes long after PK show inferior graft and host corneal thinning, and corneal protrusion. Corneal power parameters such as K(max) or Ks can be used to monitor KC progression after PK. A small graft might lead to KC progression after PK. Nature Publishing Group UK 2020-10-29 /pmc/articles/PMC7596038/ /pubmed/33122764 http://dx.doi.org/10.1038/s41598-020-75412-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yoshida, Junko
Toyono, Tetsuya
Shirakawa, Rika
Miyai, Takashi
Usui, Tomohiko
Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography
title Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography
title_full Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography
title_fullStr Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography
title_full_unstemmed Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography
title_short Risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography
title_sort risk factors and evaluation of keratoconus progression after penetrating keratoplasty with anterior segment optical coherence tomography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596038/
https://www.ncbi.nlm.nih.gov/pubmed/33122764
http://dx.doi.org/10.1038/s41598-020-75412-y
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