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Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis
PURPOSE: To investigate spectral domain optical coherence tomography (SD-OCT) findings and compare them with time domain (TD)-OCT imaging of macula and retinochoroiditis lesions of patients with toxoplasmosis. DESIGN: Prospective cross-sectional study. METHODS: Ten eyes of 10 patients with active to...
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3104792/ https://www.ncbi.nlm.nih.gov/pubmed/21629569 http://dx.doi.org/10.2147/OPTH.S20033 |
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author | Diniz, Bruno Regatieri, Caio Andrade, Rafael Maia, Andre |
author_facet | Diniz, Bruno Regatieri, Caio Andrade, Rafael Maia, Andre |
author_sort | Diniz, Bruno |
collection | PubMed |
description | PURPOSE: To investigate spectral domain optical coherence tomography (SD-OCT) findings and compare them with time domain (TD)-OCT imaging of macula and retinochoroiditis lesions of patients with toxoplasmosis. DESIGN: Prospective cross-sectional study. METHODS: Ten eyes of 10 patients with active toxoplasmic retinochoroiditis were included. Morphologic features from the macula and retinochoroiditis lesions were obtained at baseline and at 6-week follow up. Scan acquisition protocols for TD-OCT included raster and radial lines through the retinochoroiditis lesion, fast macular, and a linear scan from the lesion to the fovea, whereas the acquisition protocols for SD-OCT also included horizontal volume scans at the lesion site and at the macula. Thickness measurements obtained by SD-OCT were analyzed. RESULTS: At baseline, macular serous retinal detachment was observed in five patients; two of them only seen by SD-OCT. Retinochoroidal lesions were 4260 μm distant from the fovea on average (R = 681–7130) and this distance had an indirect correlation to the presence of macular detachment. Epiretinal membrane and vitreo-macular traction were also observed. The posterior hyaloid was not identified in four patients by TD-OCT and only in one by SD-OCT at baseline. Perilesional subretinal fluid was observed in two patients. The median retinal thickness significantly decreased at the retinochoroiditis lesion (P = 0.0004), and all the patients remained with disorganized retinal layers reflectivity at follow up. CONCLUSION: SD-OCT is a useful tool in the diagnosis of macular changes related with toxoplasmic retinochoroiditis. SD-OCT is superior in evaluating retinal changes associated with ocular toxoplasmosis. |
format | Text |
id | pubmed-3104792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31047922011-05-31 Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis Diniz, Bruno Regatieri, Caio Andrade, Rafael Maia, Andre Clin Ophthalmol Original Research PURPOSE: To investigate spectral domain optical coherence tomography (SD-OCT) findings and compare them with time domain (TD)-OCT imaging of macula and retinochoroiditis lesions of patients with toxoplasmosis. DESIGN: Prospective cross-sectional study. METHODS: Ten eyes of 10 patients with active toxoplasmic retinochoroiditis were included. Morphologic features from the macula and retinochoroiditis lesions were obtained at baseline and at 6-week follow up. Scan acquisition protocols for TD-OCT included raster and radial lines through the retinochoroiditis lesion, fast macular, and a linear scan from the lesion to the fovea, whereas the acquisition protocols for SD-OCT also included horizontal volume scans at the lesion site and at the macula. Thickness measurements obtained by SD-OCT were analyzed. RESULTS: At baseline, macular serous retinal detachment was observed in five patients; two of them only seen by SD-OCT. Retinochoroidal lesions were 4260 μm distant from the fovea on average (R = 681–7130) and this distance had an indirect correlation to the presence of macular detachment. Epiretinal membrane and vitreo-macular traction were also observed. The posterior hyaloid was not identified in four patients by TD-OCT and only in one by SD-OCT at baseline. Perilesional subretinal fluid was observed in two patients. The median retinal thickness significantly decreased at the retinochoroiditis lesion (P = 0.0004), and all the patients remained with disorganized retinal layers reflectivity at follow up. CONCLUSION: SD-OCT is a useful tool in the diagnosis of macular changes related with toxoplasmic retinochoroiditis. SD-OCT is superior in evaluating retinal changes associated with ocular toxoplasmosis. Dove Medical Press 2011 2011-05-17 /pmc/articles/PMC3104792/ /pubmed/21629569 http://dx.doi.org/10.2147/OPTH.S20033 Text en © 2011 Diniz et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Diniz, Bruno Regatieri, Caio Andrade, Rafael Maia, Andre Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis |
title | Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis |
title_full | Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis |
title_fullStr | Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis |
title_full_unstemmed | Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis |
title_short | Evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis |
title_sort | evaluation of spectral domain and time domain optical coherence tomography findings in toxoplasmic retinochoroiditis |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3104792/ https://www.ncbi.nlm.nih.gov/pubmed/21629569 http://dx.doi.org/10.2147/OPTH.S20033 |
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