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Transscleral cyclophotocoagulation and its histological effects on the conjunctiva

Micropulse transscleral cyclophotocoagulation (MP-TCP) is increasingly being used as an initial procedure prior to conjunctival filtration surgeries. However, it is uncertain whether MP-TCP may cause inflammation and scarring of the bulbar conjunctiva. Thus, we aimed to study the histological effect...

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Autores principales: Tan, Nicholas Y. Q., Ang, Marcus, Chan, Anita S. Y., Barathi, Veluchamy A., Tham, Clement C., Barton, Keith, Sng, Chelvin C. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904490/
https://www.ncbi.nlm.nih.gov/pubmed/31822709
http://dx.doi.org/10.1038/s41598-019-55102-0
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author Tan, Nicholas Y. Q.
Ang, Marcus
Chan, Anita S. Y.
Barathi, Veluchamy A.
Tham, Clement C.
Barton, Keith
Sng, Chelvin C. A.
author_facet Tan, Nicholas Y. Q.
Ang, Marcus
Chan, Anita S. Y.
Barathi, Veluchamy A.
Tham, Clement C.
Barton, Keith
Sng, Chelvin C. A.
author_sort Tan, Nicholas Y. Q.
collection PubMed
description Micropulse transscleral cyclophotocoagulation (MP-TCP) is increasingly being used as an initial procedure prior to conjunctival filtration surgeries. However, it is uncertain whether MP-TCP may cause inflammation and scarring of the bulbar conjunctiva. Thus, we aimed to study the histological effects of MP-TCP (compared to controls and continuous wave [CW]-TCP) on the conjunctiva. Our study included 10 Dutch Belted Rabbits that underwent TCP in their right eyes (n = 5, MP-TCP; n = 5, CW-TCP), while their left eyes served as controls. The rabbits were euthanised at 4 weeks, and their dissected globes underwent histopathological and immunohistochemical examination. We observed greater conjunctival inflammation in MP-TCP or CW-TCP-treated eyes compared to controls, but not between each other. The majority of the lymphocytic infiltrates were CD4 T-cells. Increased conjunctival fibrosis was evident in MP-TCP or CW-TCP-treated eyes, to similar extents, compared to controls. However, the increased staining for myofibroblasts was not statistically significant in TCP-treated eyes. We concluded that MP-TCP causes significantly greater overall conjunctival inflammation and scarring compared to controls, similar to CW-TCP. As these are risk-factors for fibrosis and failure of the conjunctival bleb, further studies are required to explore the effect, if any, of post-TCP conjunctival changes on future bleb morphology and survival.
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spelling pubmed-69044902019-12-13 Transscleral cyclophotocoagulation and its histological effects on the conjunctiva Tan, Nicholas Y. Q. Ang, Marcus Chan, Anita S. Y. Barathi, Veluchamy A. Tham, Clement C. Barton, Keith Sng, Chelvin C. A. Sci Rep Article Micropulse transscleral cyclophotocoagulation (MP-TCP) is increasingly being used as an initial procedure prior to conjunctival filtration surgeries. However, it is uncertain whether MP-TCP may cause inflammation and scarring of the bulbar conjunctiva. Thus, we aimed to study the histological effects of MP-TCP (compared to controls and continuous wave [CW]-TCP) on the conjunctiva. Our study included 10 Dutch Belted Rabbits that underwent TCP in their right eyes (n = 5, MP-TCP; n = 5, CW-TCP), while their left eyes served as controls. The rabbits were euthanised at 4 weeks, and their dissected globes underwent histopathological and immunohistochemical examination. We observed greater conjunctival inflammation in MP-TCP or CW-TCP-treated eyes compared to controls, but not between each other. The majority of the lymphocytic infiltrates were CD4 T-cells. Increased conjunctival fibrosis was evident in MP-TCP or CW-TCP-treated eyes, to similar extents, compared to controls. However, the increased staining for myofibroblasts was not statistically significant in TCP-treated eyes. We concluded that MP-TCP causes significantly greater overall conjunctival inflammation and scarring compared to controls, similar to CW-TCP. As these are risk-factors for fibrosis and failure of the conjunctival bleb, further studies are required to explore the effect, if any, of post-TCP conjunctival changes on future bleb morphology and survival. Nature Publishing Group UK 2019-12-10 /pmc/articles/PMC6904490/ /pubmed/31822709 http://dx.doi.org/10.1038/s41598-019-55102-0 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tan, Nicholas Y. Q.
Ang, Marcus
Chan, Anita S. Y.
Barathi, Veluchamy A.
Tham, Clement C.
Barton, Keith
Sng, Chelvin C. A.
Transscleral cyclophotocoagulation and its histological effects on the conjunctiva
title Transscleral cyclophotocoagulation and its histological effects on the conjunctiva
title_full Transscleral cyclophotocoagulation and its histological effects on the conjunctiva
title_fullStr Transscleral cyclophotocoagulation and its histological effects on the conjunctiva
title_full_unstemmed Transscleral cyclophotocoagulation and its histological effects on the conjunctiva
title_short Transscleral cyclophotocoagulation and its histological effects on the conjunctiva
title_sort transscleral cyclophotocoagulation and its histological effects on the conjunctiva
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904490/
https://www.ncbi.nlm.nih.gov/pubmed/31822709
http://dx.doi.org/10.1038/s41598-019-55102-0
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