High-Resolution Imaging of the Human Retina In Vivo after Scatter Photocoagulation Treatment Using a Semiautomated Laser System

Purpose To image the ultrastructural morphology of retinal laser effects and their healing response in vivo using spectral domain optical coherence tomography (SD-OCT). Design Prospective, interventional study. Participants Ten patients undergoing panretinal photocoagulation for proliferative diabet...

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Veröffentlicht in:Ophthalmology (Rochester, Minn.) Minn.), 2010-03, Vol.117 (3), p.545-551
Hauptverfasser: Kriechbaum, Katharina, MD, Bolz, Matthias, MD, Deak, Gabor G., MD, Prager, Sonja, MD, Scholda, Christoph, MD, Schmidt-Erfurth, Ursula, MD
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container_end_page 551
container_issue 3
container_start_page 545
container_title Ophthalmology (Rochester, Minn.)
container_volume 117
creator Kriechbaum, Katharina, MD
Bolz, Matthias, MD
Deak, Gabor G., MD
Prager, Sonja, MD
Scholda, Christoph, MD
Schmidt-Erfurth, Ursula, MD
description Purpose To image the ultrastructural morphology of retinal laser effects and their healing response in vivo using spectral domain optical coherence tomography (SD-OCT). Design Prospective, interventional study. Participants Ten patients undergoing panretinal photocoagulation for proliferative diabetic retinopathy. Methods Panretinal photocoagulation (PRP) was performed using a semiautomated patterned scanning laser system providing a raster of effects with homogenous intensity. Retinal morphology and localization of effects owing to laser–tissue interaction were imaged at 1 day, 1 week, and at monthly intervals for 6 months. The characteristic, specific structural changes during the healing process were followed over time using an SD-OCT device (Spectralis OCT) allowing for high-resolution raster scanning of the entire lesion pattern with identification of identical retinal sites (tracking modality). Main Outcome Measures Retinal morphology and localization of effects of photocoagulation on SD-OCT images. Results At day 1 after PRP, the photocoagulation effects were sharply delineated from the surrounding unaffected retina and all spots seemed to be identical in size and location. The area of tissue destruction was confined to the outer retinal layers, extending from the outer nuclear layer (ONL) to the retinal pigment epithelium (RPE). At 1 week, images showed a progressive loss of the affected outer retinal layers, namely, the ONL and the outer plexiform layer. Concomitant distortion of the inner nuclear and plexiform layers generated a pattern of “archways” between adjacent laser spots. The photoreceptor layers (PRL) seemed to be eliminated in the photocoagulated area, particularly at the borders of each lesion. The lesion center contained a condensed RPE and PRL segment. The ONL recovered partially, but the PRL inner and outer segments remained absent. During the long-term follow-up, RPE cells migrated to the center of the lesion, forming a hyperplastic scar. Conclusions The characteristic morphology of retinal photocoagulation effects in vivo and over time was identified for the first time in human eyes using SD-OCT. The OCT imaging demonstrated a well-defined reproducible area of destruction confined to the outer retinal layers. Healing proceeded as the condensation of the RPE and PRL in the lesion center. Financial Disclosure(s) The authors have no proprietary or commercial interest in any of the materials discussed in this article.
doi_str_mv 10.1016/j.ophtha.2009.07.031
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Design Prospective, interventional study. Participants Ten patients undergoing panretinal photocoagulation for proliferative diabetic retinopathy. Methods Panretinal photocoagulation (PRP) was performed using a semiautomated patterned scanning laser system providing a raster of effects with homogenous intensity. Retinal morphology and localization of effects owing to laser–tissue interaction were imaged at 1 day, 1 week, and at monthly intervals for 6 months. The characteristic, specific structural changes during the healing process were followed over time using an SD-OCT device (Spectralis OCT) allowing for high-resolution raster scanning of the entire lesion pattern with identification of identical retinal sites (tracking modality). Main Outcome Measures Retinal morphology and localization of effects of photocoagulation on SD-OCT images. Results At day 1 after PRP, the photocoagulation effects were sharply delineated from the surrounding unaffected retina and all spots seemed to be identical in size and location. The area of tissue destruction was confined to the outer retinal layers, extending from the outer nuclear layer (ONL) to the retinal pigment epithelium (RPE). At 1 week, images showed a progressive loss of the affected outer retinal layers, namely, the ONL and the outer plexiform layer. Concomitant distortion of the inner nuclear and plexiform layers generated a pattern of “archways” between adjacent laser spots. The photoreceptor layers (PRL) seemed to be eliminated in the photocoagulated area, particularly at the borders of each lesion. The lesion center contained a condensed RPE and PRL segment. The ONL recovered partially, but the PRL inner and outer segments remained absent. During the long-term follow-up, RPE cells migrated to the center of the lesion, forming a hyperplastic scar. Conclusions The characteristic morphology of retinal photocoagulation effects in vivo and over time was identified for the first time in human eyes using SD-OCT. The OCT imaging demonstrated a well-defined reproducible area of destruction confined to the outer retinal layers. Healing proceeded as the condensation of the RPE and PRL in the lesion center. 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Design Prospective, interventional study. Participants Ten patients undergoing panretinal photocoagulation for proliferative diabetic retinopathy. Methods Panretinal photocoagulation (PRP) was performed using a semiautomated patterned scanning laser system providing a raster of effects with homogenous intensity. Retinal morphology and localization of effects owing to laser–tissue interaction were imaged at 1 day, 1 week, and at monthly intervals for 6 months. The characteristic, specific structural changes during the healing process were followed over time using an SD-OCT device (Spectralis OCT) allowing for high-resolution raster scanning of the entire lesion pattern with identification of identical retinal sites (tracking modality). Main Outcome Measures Retinal morphology and localization of effects of photocoagulation on SD-OCT images. 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Design Prospective, interventional study. Participants Ten patients undergoing panretinal photocoagulation for proliferative diabetic retinopathy. Methods Panretinal photocoagulation (PRP) was performed using a semiautomated patterned scanning laser system providing a raster of effects with homogenous intensity. Retinal morphology and localization of effects owing to laser–tissue interaction were imaged at 1 day, 1 week, and at monthly intervals for 6 months. The characteristic, specific structural changes during the healing process were followed over time using an SD-OCT device (Spectralis OCT) allowing for high-resolution raster scanning of the entire lesion pattern with identification of identical retinal sites (tracking modality). Main Outcome Measures Retinal morphology and localization of effects of photocoagulation on SD-OCT images. Results At day 1 after PRP, the photocoagulation effects were sharply delineated from the surrounding unaffected retina and all spots seemed to be identical in size and location. The area of tissue destruction was confined to the outer retinal layers, extending from the outer nuclear layer (ONL) to the retinal pigment epithelium (RPE). At 1 week, images showed a progressive loss of the affected outer retinal layers, namely, the ONL and the outer plexiform layer. Concomitant distortion of the inner nuclear and plexiform layers generated a pattern of “archways” between adjacent laser spots. The photoreceptor layers (PRL) seemed to be eliminated in the photocoagulated area, particularly at the borders of each lesion. The lesion center contained a condensed RPE and PRL segment. The ONL recovered partially, but the PRL inner and outer segments remained absent. During the long-term follow-up, RPE cells migrated to the center of the lesion, forming a hyperplastic scar. Conclusions The characteristic morphology of retinal photocoagulation effects in vivo and over time was identified for the first time in human eyes using SD-OCT. The OCT imaging demonstrated a well-defined reproducible area of destruction confined to the outer retinal layers. Healing proceeded as the condensation of the RPE and PRL in the lesion center. Financial Disclosure(s) The authors have no proprietary or commercial interest in any of the materials discussed in this article.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20031226</pmid><doi>10.1016/j.ophtha.2009.07.031</doi><tpages>7</tpages></addata></record>
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subjects Biological and medical sciences
Diabetic Retinopathy - diagnosis
Diabetic Retinopathy - surgery
Female
Fluorescein Angiography
Humans
Laser Coagulation
Male
Medical sciences
Miscellaneous
Ophthalmology
Prospective Studies
Retina - pathology
Tomography, Optical Coherence
Visual Acuity - physiology
Wound Healing
title High-Resolution Imaging of the Human Retina In Vivo after Scatter Photocoagulation Treatment Using a Semiautomated Laser System
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