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Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy

BACKGROUND: There is no consensus on the optimal initial treatment for polypoidal choroidal vasculopathy (PCV). Our study aimed to report the efficacy of repeated injections of intravitreal ranibizumab with or without photodynamic therapy for the treatment of PCV and to determine the possible factor...

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Autores principales: Gu, Xiaoya, Yu, Xiaobing, Dai, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642544/
https://www.ncbi.nlm.nih.gov/pubmed/31324161
http://dx.doi.org/10.1186/s12886-019-1156-4
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author Gu, Xiaoya
Yu, Xiaobing
Dai, Hong
author_facet Gu, Xiaoya
Yu, Xiaobing
Dai, Hong
author_sort Gu, Xiaoya
collection PubMed
description BACKGROUND: There is no consensus on the optimal initial treatment for polypoidal choroidal vasculopathy (PCV). Our study aimed to report the efficacy of repeated injections of intravitreal ranibizumab with or without photodynamic therapy for the treatment of PCV and to determine the possible factors predictive of visual outcomes. METHODS: The results of the initial treatment of 40 patients with PCV with 3 monthly injections of ranibizumab were retrospectively reviewed. We compared the results in terms of the best corrected visual acuity (BCVA), the central retinal thickness (CRT), the number of injections, the regression rates of polyps and the rates of the reduction of subretinal fluid. RESULTS: At the 3-month follow-up, the mean BCVA was significantly increased by 7.3 ± 12.4 letters compared to baseline (p < 0.01). At the 12-month follow-up, the mean BCVA was increased by 3.4 ± 15.4 letters compared to baseline, and there was no significant difference (p > 0.05). The mean CRT at the 12-month follow-up was 593.58 ± 243.64 μm, with an average decrease of 101.55 ± 256.07 μm compared to baseline (p < 0.01). Fifteen eyes (18.8%) showed the complete regression of polyps, and 22 eyes (27.5%) showed a reduction in polyps. The baseline VA, the reduction in subretinal fluids and the greatest lesion diameter were significant independent factors that were predictive of improved VA at the final follow-up. CONCLUSIONS: Three monthly injections of ranibizumab as an initial treatment could significantly improve VA in PCV patients in the short term. At 12 months postinjection, ranibizumab treatment could stabilize VA in most PCV patients. The baseline VA, the reduction in subretinal fluids and the greatest lesion diameter were predictive factors for the relative improvement of VA at the final follow-up.
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spelling pubmed-66425442019-07-29 Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy Gu, Xiaoya Yu, Xiaobing Dai, Hong BMC Ophthalmol Research Article BACKGROUND: There is no consensus on the optimal initial treatment for polypoidal choroidal vasculopathy (PCV). Our study aimed to report the efficacy of repeated injections of intravitreal ranibizumab with or without photodynamic therapy for the treatment of PCV and to determine the possible factors predictive of visual outcomes. METHODS: The results of the initial treatment of 40 patients with PCV with 3 monthly injections of ranibizumab were retrospectively reviewed. We compared the results in terms of the best corrected visual acuity (BCVA), the central retinal thickness (CRT), the number of injections, the regression rates of polyps and the rates of the reduction of subretinal fluid. RESULTS: At the 3-month follow-up, the mean BCVA was significantly increased by 7.3 ± 12.4 letters compared to baseline (p < 0.01). At the 12-month follow-up, the mean BCVA was increased by 3.4 ± 15.4 letters compared to baseline, and there was no significant difference (p > 0.05). The mean CRT at the 12-month follow-up was 593.58 ± 243.64 μm, with an average decrease of 101.55 ± 256.07 μm compared to baseline (p < 0.01). Fifteen eyes (18.8%) showed the complete regression of polyps, and 22 eyes (27.5%) showed a reduction in polyps. The baseline VA, the reduction in subretinal fluids and the greatest lesion diameter were significant independent factors that were predictive of improved VA at the final follow-up. CONCLUSIONS: Three monthly injections of ranibizumab as an initial treatment could significantly improve VA in PCV patients in the short term. At 12 months postinjection, ranibizumab treatment could stabilize VA in most PCV patients. The baseline VA, the reduction in subretinal fluids and the greatest lesion diameter were predictive factors for the relative improvement of VA at the final follow-up. BioMed Central 2019-07-19 /pmc/articles/PMC6642544/ /pubmed/31324161 http://dx.doi.org/10.1186/s12886-019-1156-4 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Gu, Xiaoya
Yu, Xiaobing
Dai, Hong
Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy
title Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy
title_full Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy
title_fullStr Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy
title_full_unstemmed Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy
title_short Therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy
title_sort therapeutic effects of ranibizumab in patients with polypoidal choroidal vasculopathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6642544/
https://www.ncbi.nlm.nih.gov/pubmed/31324161
http://dx.doi.org/10.1186/s12886-019-1156-4
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