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Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy
OBJECTIVE: To evaluate the short- and long-term outcomes of half-dose verteporfin with photodynamic therapy (PDT) in the treatment of chronic central serous retinopathy (CSR). DESIGN: Retrospective case series. PARTICIPANTS: 45 eyes in 39 patients with chronic CSR were included. Diagnosis of chronic...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724425/ https://www.ncbi.nlm.nih.gov/pubmed/29263642 http://dx.doi.org/10.2147/OPTH.S151933 |
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author | Dhirani, Nadeem Ali Yang, Yelin Somani, Sohel |
author_facet | Dhirani, Nadeem Ali Yang, Yelin Somani, Sohel |
author_sort | Dhirani, Nadeem Ali |
collection | PubMed |
description | OBJECTIVE: To evaluate the short- and long-term outcomes of half-dose verteporfin with photodynamic therapy (PDT) in the treatment of chronic central serous retinopathy (CSR). DESIGN: Retrospective case series. PARTICIPANTS: 45 eyes in 39 patients with chronic CSR were included. Diagnosis of chronic CSR was confirmed by fluorescein angiography and persistence of subretinal fluid by optical coherence tomography for a minimum of 3 months duration. METHODS: Each patient underwent treatment with half-dose verteporfin with full-fluence PDT; initial follow-up was defined as a 6–8 week visit following the treatment, and final follow-up ranged from 5 to 70 months. RESULTS: The average follow-up period for treatment was 19.3 months. Best-corrected visual acuity increased from logMAR means of 0.52 to 0.42 (p<0.05). Central retinal thickness and choroidal thickness also significantly decreased at last follow-up (p<0.05). Eight of 45 eyes (18%) demonstrated a recurrence of CSR following treatment within the follow-up period. At the final follow-up, 41 out of the 45 eyes (91%) had complete resolution of subretinal fluid accumulation. CONCLUSION: Half-dose PDT is an effective treatment option for chronic CSR in a Canadian population, and it is both safe and durable. The positive treatment effect is realized rapidly, with the initial 6-week result highly correlated with the final follow-up result. |
format | Online Article Text |
id | pubmed-5724425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57244252017-12-20 Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy Dhirani, Nadeem Ali Yang, Yelin Somani, Sohel Clin Ophthalmol Original Research OBJECTIVE: To evaluate the short- and long-term outcomes of half-dose verteporfin with photodynamic therapy (PDT) in the treatment of chronic central serous retinopathy (CSR). DESIGN: Retrospective case series. PARTICIPANTS: 45 eyes in 39 patients with chronic CSR were included. Diagnosis of chronic CSR was confirmed by fluorescein angiography and persistence of subretinal fluid by optical coherence tomography for a minimum of 3 months duration. METHODS: Each patient underwent treatment with half-dose verteporfin with full-fluence PDT; initial follow-up was defined as a 6–8 week visit following the treatment, and final follow-up ranged from 5 to 70 months. RESULTS: The average follow-up period for treatment was 19.3 months. Best-corrected visual acuity increased from logMAR means of 0.52 to 0.42 (p<0.05). Central retinal thickness and choroidal thickness also significantly decreased at last follow-up (p<0.05). Eight of 45 eyes (18%) demonstrated a recurrence of CSR following treatment within the follow-up period. At the final follow-up, 41 out of the 45 eyes (91%) had complete resolution of subretinal fluid accumulation. CONCLUSION: Half-dose PDT is an effective treatment option for chronic CSR in a Canadian population, and it is both safe and durable. The positive treatment effect is realized rapidly, with the initial 6-week result highly correlated with the final follow-up result. Dove Medical Press 2017-12-06 /pmc/articles/PMC5724425/ /pubmed/29263642 http://dx.doi.org/10.2147/OPTH.S151933 Text en © 2017 Dhirani et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Dhirani, Nadeem Ali Yang, Yelin Somani, Sohel Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy |
title | Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy |
title_full | Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy |
title_fullStr | Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy |
title_full_unstemmed | Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy |
title_short | Long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy |
title_sort | long-term outcomes in half-dose verteporfin photodynamic therapy for chronic central serous retinopathy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724425/ https://www.ncbi.nlm.nih.gov/pubmed/29263642 http://dx.doi.org/10.2147/OPTH.S151933 |
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