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Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula
PURPOSE: Retinal photocoagulation and nondamaging laser therapy are used for treatment of macular disorders, without understanding of the response mechanism and with no rationale for dosimetry. To establish a proper titration algorithm, we measured the range of tissue response and damage threshold....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995023/ https://www.ncbi.nlm.nih.gov/pubmed/27159441 http://dx.doi.org/10.1167/iovs.15-18981 |
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author | Lavinsky, Daniel Wang, Jenny Huie, Philip Dalal, Roopa Lee, Seung Jun Lee, Dae Yeong Palanker, Daniel |
author_facet | Lavinsky, Daniel Wang, Jenny Huie, Philip Dalal, Roopa Lee, Seung Jun Lee, Dae Yeong Palanker, Daniel |
author_sort | Lavinsky, Daniel |
collection | PubMed |
description | PURPOSE: Retinal photocoagulation and nondamaging laser therapy are used for treatment of macular disorders, without understanding of the response mechanism and with no rationale for dosimetry. To establish a proper titration algorithm, we measured the range of tissue response and damage threshold. We then evaluated safety and efficacy of nondamaging retinal therapy (NRT) based on this algorithm for chronic central serous chorioretinopathy (CSCR) and macular telangiectasia (MacTel). METHODS: Retinal response to laser treatment below damage threshold was assessed in pigmented rabbits by expression of the heat shock protein HSP70 and glial fibrillary acidic protein (GFAP). Energy was adjusted relative to visible titration using the Endpoint Management (EpM) algorithm. In clinical studies, 21 eyes with CSCR and 10 eyes with MacTel were treated at 30% EpM energy with high spot density (0.25-diameter spacing). Visual acuity, retinal and choroidal thickness, and subretinal fluid were monitored for 1 year. RESULTS: At 25% EpM energy and higher, HSP70 was expressed acutely in RPE, and GFAP upregulation in Müller cells was observed at 1 month. Damage appeared starting at 40% setting. Subretinal fluid resolved completely in 81% and partially in 19% of the CSCR patients, and visual acuity improved by 12 ± 3 letters. Lacunae in the majority of MacTel patients decreased while preserving the retinal thickness, and vision improved by 10 letters. CONCLUSIONS: Heat shock protein expression in response to hyperthermia helps define the therapeutic window for NRT. Lack of tissue damage enables high-density treatment to boost clinical efficacy, therapy in the fovea, and retreatments to manage chronic diseases. |
format | Online Article Text |
id | pubmed-5995023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-59950232018-06-12 Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula Lavinsky, Daniel Wang, Jenny Huie, Philip Dalal, Roopa Lee, Seung Jun Lee, Dae Yeong Palanker, Daniel Invest Ophthalmol Vis Sci Retina PURPOSE: Retinal photocoagulation and nondamaging laser therapy are used for treatment of macular disorders, without understanding of the response mechanism and with no rationale for dosimetry. To establish a proper titration algorithm, we measured the range of tissue response and damage threshold. We then evaluated safety and efficacy of nondamaging retinal therapy (NRT) based on this algorithm for chronic central serous chorioretinopathy (CSCR) and macular telangiectasia (MacTel). METHODS: Retinal response to laser treatment below damage threshold was assessed in pigmented rabbits by expression of the heat shock protein HSP70 and glial fibrillary acidic protein (GFAP). Energy was adjusted relative to visible titration using the Endpoint Management (EpM) algorithm. In clinical studies, 21 eyes with CSCR and 10 eyes with MacTel were treated at 30% EpM energy with high spot density (0.25-diameter spacing). Visual acuity, retinal and choroidal thickness, and subretinal fluid were monitored for 1 year. RESULTS: At 25% EpM energy and higher, HSP70 was expressed acutely in RPE, and GFAP upregulation in Müller cells was observed at 1 month. Damage appeared starting at 40% setting. Subretinal fluid resolved completely in 81% and partially in 19% of the CSCR patients, and visual acuity improved by 12 ± 3 letters. Lacunae in the majority of MacTel patients decreased while preserving the retinal thickness, and vision improved by 10 letters. CONCLUSIONS: Heat shock protein expression in response to hyperthermia helps define the therapeutic window for NRT. Lack of tissue damage enables high-density treatment to boost clinical efficacy, therapy in the fovea, and retreatments to manage chronic diseases. The Association for Research in Vision and Ophthalmology 2016-05 /pmc/articles/PMC5995023/ /pubmed/27159441 http://dx.doi.org/10.1167/iovs.15-18981 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Retina Lavinsky, Daniel Wang, Jenny Huie, Philip Dalal, Roopa Lee, Seung Jun Lee, Dae Yeong Palanker, Daniel Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula |
title | Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula |
title_full | Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula |
title_fullStr | Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula |
title_full_unstemmed | Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula |
title_short | Nondamaging Retinal Laser Therapy: Rationale and Applications to the Macula |
title_sort | nondamaging retinal laser therapy: rationale and applications to the macula |
topic | Retina |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995023/ https://www.ncbi.nlm.nih.gov/pubmed/27159441 http://dx.doi.org/10.1167/iovs.15-18981 |
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