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Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions

This study evaluates the long-term effects of selective retina therapy (SRT) on the retinal pigment epithelium (RPE) and neuroretina in patients with central serous chorioretinopathy. SRT was performed on 36 patients using a Nd:YLF-Laser at 527 nm (R:GEN(®), Lutronic, Goyang-Si, Republic of Korea)....

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Autores principales: Binter, Maximilian, Lindziute, Migle, Rosenstein, Christopher, Framme, Carsten, Tode, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146613/
https://www.ncbi.nlm.nih.gov/pubmed/37109415
http://dx.doi.org/10.3390/life13040886
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author Binter, Maximilian
Lindziute, Migle
Rosenstein, Christopher
Framme, Carsten
Tode, Jan
author_facet Binter, Maximilian
Lindziute, Migle
Rosenstein, Christopher
Framme, Carsten
Tode, Jan
author_sort Binter, Maximilian
collection PubMed
description This study evaluates the long-term effects of selective retina therapy (SRT) on the retinal pigment epithelium (RPE) and neuroretina in patients with central serous chorioretinopathy. SRT was performed on 36 patients using a Nd:YLF-Laser at 527 nm (R:GEN(®), Lutronic, Goyang-Si, Republic of Korea). A total of 994 titration spots were examined using up to three years’ multimodal imaging. Leakage in fluorescein angiography (FA) was observed after SRT in 523 lesions and resolved after one month. SRT lesions were not visible clinically, but appeared as brightly reflective areas in infrared and multicolor images. Normal morphology was observed in optical coherence tomography (OCT) immediately after SRT. After one month, thickening of the RPE and interdigitation zone changes were seen and disappeared after 539 ± 308 days. No RPE atrophies occurred during the observation period. Decreased fundus autofluorescence (FAF) was mostly observed directly after SRT followed by increased FAF at one month, which faded over time. A significant decrease in the number of visible lesions in the FA and FAF was observed within the three-year follow-up. OCT findings are consistent with animal studies showing SRT-related defect closure by hypertrophy and migration of neighboring cells without RPE atrophy or photoreceptor damage. This suggests that SRT is a safe treatment option for macular diseases and does not lead to retinal atrophy.
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spelling pubmed-101466132023-04-29 Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions Binter, Maximilian Lindziute, Migle Rosenstein, Christopher Framme, Carsten Tode, Jan Life (Basel) Article This study evaluates the long-term effects of selective retina therapy (SRT) on the retinal pigment epithelium (RPE) and neuroretina in patients with central serous chorioretinopathy. SRT was performed on 36 patients using a Nd:YLF-Laser at 527 nm (R:GEN(®), Lutronic, Goyang-Si, Republic of Korea). A total of 994 titration spots were examined using up to three years’ multimodal imaging. Leakage in fluorescein angiography (FA) was observed after SRT in 523 lesions and resolved after one month. SRT lesions were not visible clinically, but appeared as brightly reflective areas in infrared and multicolor images. Normal morphology was observed in optical coherence tomography (OCT) immediately after SRT. After one month, thickening of the RPE and interdigitation zone changes were seen and disappeared after 539 ± 308 days. No RPE atrophies occurred during the observation period. Decreased fundus autofluorescence (FAF) was mostly observed directly after SRT followed by increased FAF at one month, which faded over time. A significant decrease in the number of visible lesions in the FA and FAF was observed within the three-year follow-up. OCT findings are consistent with animal studies showing SRT-related defect closure by hypertrophy and migration of neighboring cells without RPE atrophy or photoreceptor damage. This suggests that SRT is a safe treatment option for macular diseases and does not lead to retinal atrophy. MDPI 2023-03-27 /pmc/articles/PMC10146613/ /pubmed/37109415 http://dx.doi.org/10.3390/life13040886 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Binter, Maximilian
Lindziute, Migle
Rosenstein, Christopher
Framme, Carsten
Tode, Jan
Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions
title Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions
title_full Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions
title_fullStr Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions
title_full_unstemmed Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions
title_short Long-Term Multimodal Imaging Analysis of Selective Retina Therapy Laser Lesions
title_sort long-term multimodal imaging analysis of selective retina therapy laser lesions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146613/
https://www.ncbi.nlm.nih.gov/pubmed/37109415
http://dx.doi.org/10.3390/life13040886
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