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Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation
PURPOSE: Photobiomodulation (PBM) refers to therapeutic irradiation of tissue with low-energy, 630- to 1000-nm wavelength light. An increasing body of evidence supports a beneficial effect of PBM in retinal disorders. To date, most studies have utilized light-emitting diode irradiation sources. Slit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Association for Research in Vision and Ophthalmology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396177/ https://www.ncbi.nlm.nih.gov/pubmed/32818109 http://dx.doi.org/10.1167/tvst.9.4.22 |
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author | Ao, Jack Chidlow, Glyn Wood, John P. M. Casson, Robert J. |
author_facet | Ao, Jack Chidlow, Glyn Wood, John P. M. Casson, Robert J. |
author_sort | Ao, Jack |
collection | PubMed |
description | PURPOSE: Photobiomodulation (PBM) refers to therapeutic irradiation of tissue with low-energy, 630- to 1000-nm wavelength light. An increasing body of evidence supports a beneficial effect of PBM in retinal disorders. To date, most studies have utilized light-emitting diode irradiation sources. Slit-lamp-mounted retinal lasers produce a coherent beam that can be delivered with precisely defined dosages and predetermined target area; however, the use of retinal lasers raises safety concerns that warrant investigation prior to clinical application. In this study, we determined safe dosages of laser-delivered PBM to the retina. METHODS: A custom-designed, slit-lamp-delivered, 670-nm, red/near-infrared laser was used to administer a range of irradiances to healthy pigmented and non-pigmented rat retinas. The effects of PBM on various functional and structural parameters of the retina were evaluated utilizing a combination of electroretinography, Spectral Domain Optical Coherence (SD-OCT), fluorescein angiography, histology and immunohistochemistry. RESULTS: In non-pigmented rats, no adverse events were identified at any irradiances up to 500 mW/cm(2). In pigmented rats, no adverse events were identified at irradiances of 25 or 100 mW/cm(2); however, approximately one-third of rats that received 500 mW/cm(2) displayed very localized photoreceptor damage in the peripapillary region, typically adjacent to the optic nerve head. CONCLUSIONS: A safety threshold exists for laser-delivered PBM in pigmented retinas and was identified as 500 mW/cm(2) irradiance; therefore, caution should be exercised in the dosage of laser-delivered PBM administered to pigmented retinas. TRANSLATIONAL RELEVANCE: This study provides important data necessary for clinical translation of laser-delivered PBM for retinal diseases. |
format | Online Article Text |
id | pubmed-7396177 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73961772020-08-17 Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation Ao, Jack Chidlow, Glyn Wood, John P. M. Casson, Robert J. Transl Vis Sci Technol Article PURPOSE: Photobiomodulation (PBM) refers to therapeutic irradiation of tissue with low-energy, 630- to 1000-nm wavelength light. An increasing body of evidence supports a beneficial effect of PBM in retinal disorders. To date, most studies have utilized light-emitting diode irradiation sources. Slit-lamp-mounted retinal lasers produce a coherent beam that can be delivered with precisely defined dosages and predetermined target area; however, the use of retinal lasers raises safety concerns that warrant investigation prior to clinical application. In this study, we determined safe dosages of laser-delivered PBM to the retina. METHODS: A custom-designed, slit-lamp-delivered, 670-nm, red/near-infrared laser was used to administer a range of irradiances to healthy pigmented and non-pigmented rat retinas. The effects of PBM on various functional and structural parameters of the retina were evaluated utilizing a combination of electroretinography, Spectral Domain Optical Coherence (SD-OCT), fluorescein angiography, histology and immunohistochemistry. RESULTS: In non-pigmented rats, no adverse events were identified at any irradiances up to 500 mW/cm(2). In pigmented rats, no adverse events were identified at irradiances of 25 or 100 mW/cm(2); however, approximately one-third of rats that received 500 mW/cm(2) displayed very localized photoreceptor damage in the peripapillary region, typically adjacent to the optic nerve head. CONCLUSIONS: A safety threshold exists for laser-delivered PBM in pigmented retinas and was identified as 500 mW/cm(2) irradiance; therefore, caution should be exercised in the dosage of laser-delivered PBM administered to pigmented retinas. TRANSLATIONAL RELEVANCE: This study provides important data necessary for clinical translation of laser-delivered PBM for retinal diseases. The Association for Research in Vision and Ophthalmology 2020-03-23 /pmc/articles/PMC7396177/ /pubmed/32818109 http://dx.doi.org/10.1167/tvst.9.4.22 Text en Copyright 2020 The Authors 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 | Article Ao, Jack Chidlow, Glyn Wood, John P. M. Casson, Robert J. Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation |
title | Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation |
title_full | Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation |
title_fullStr | Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation |
title_full_unstemmed | Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation |
title_short | Safety Profile of Slit-Lamp-Delivered Retinal Laser Photobiomodulation |
title_sort | safety profile of slit-lamp-delivered retinal laser photobiomodulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7396177/ https://www.ncbi.nlm.nih.gov/pubmed/32818109 http://dx.doi.org/10.1167/tvst.9.4.22 |
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