Estefanía Cobos
Bellvitge University Hospital
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Publication
Featured researches published by Estefanía Cobos.
Retina-the Journal of Retinal and Vitreous Diseases | 2015
Luis Arias; Jose M. Caminal; Marcos J. Rubio; Estefanía Cobos; Pere Garcia-Bru; Alejandro Filloy; Noel Padron; Karol Mejia
Purpose: To evaluate the results of fundus autofluorescence and axial length as prognostic factors for surgical outcome of macular hole retinal detachment in high myopic patients. Methods: This is a retrospective, interventional, nonrandomized study. Patients were treated with posterior vitrectomy, internal limiting membrane peeling, and silicone oil tamponade. Best-corrected visual acuity, axial length, fundus autofluorescence, and spectral domain optical coherence tomography images were obtained. Results: Fifteen eyes from 15 patients (mean age, 69.4 years) were evaluated. The mean refractive error was −19 diopters, and the mean axial length was 29.9 mm. The mean best-corrected visual acuity (logMAR) improved from 2.17 to 1.42 (P = 0.02) after a mean follow-up of 19.3 months. Spectral domain optical coherence tomography scans showed retinal detachment resolution in 13 eyes (86.6%) and macular hole closure in 9 eyes (60%). Fundus autofluorescence showed macular hypoautofluorescence with foveal involvement (mean area of 9.7 mm2) in 10 eyes (66.6%). Postoperative best-corrected visual acuity was significantly worse in these eyes (P = 0.009). Axial length >30 mm was found in the 2 cases with recurrent retinal detachment and in 4 of the 6 cases without macular hole closure (66.6%). Conclusion: Macular hole retinal detachment in high myopic patients can be successfully treated with vitrectomy, internal limiting membrane peeling, and silicone oil. Axial length >30 mm and macular hypoautofluorescence with foveal involvement seem to be prognostic factors for a worse anatomical and visual outcome.
Retina-the Journal of Retinal and Vitreous Diseases | 2015
Jose M. Caminal; Ignacio Flores-Moreno; Luis Arias; C. Gutierrez; Josep M. Piulats; Jaume Català; Marcos J. Rubio; Estefanía Cobos; Pere García; Joan Pera; Joan Giralt; Jorge Arruga
Purpose: To evaluate the efficacy of intravitreal dexamethasone implant 0.7 mg (Ozurdex) in radiation maculopathy secondary to plaque brachytherapy in choroidal melanoma. Methods: Twelve eyes diagnosed of radiation maculopathy secondary to plaque brachytherapy and treated with intravitreal dexamethasone implant were included. Visual acuity, foveal thickness using spectral domain optical coherence tomography, and grade of macular edema, using Horgan classification, were evaluated. Results: Mean age was 65.5 ± 28 years (range, 40–82 years). Mean follow-up was 8.2 ± 7.8 months (range, 2–28 months). Mean visual acuity before treatment was, in logarithm of the minimum angle of resolution scale, 1 ± 0.58 (range, 0.4–2) and mean final visual acuity 0.8 ± 0.58 (range, 0.2–2), showing a nonsignificant trend to improvement (P = 0.091; Wilcoxons test). Foveal thickness before treatment was 416 ± 263 &mgr;m (range, 222–725 &mgr;m) and final foveal thickness 254 ± 170 &mgr;m (range, 145–750), showing a significant decrease (P = 0.016; Wilcoxons test). Referring to Horgan classification, a significant reduction in grades before and after treatment was demonstrated (P = 0.007; Wilcoxons test). Conclusion: Ozurdex is a useful treatment for radiation maculopathy associated to plaque brachytherapy for uveal melanoma, with a significant decrease in foveal thickness and a significant improvement in Horgan classification. This anatomical improvement was correlated with a moderate improvement in visual acuity.
Retina-the Journal of Retinal and Vitreous Diseases | 2017
Daniel Lorenzo; Luis Arias; Netan Choudhry; Eduard Millan; Ignacio Flores; Marcos J. Rubio; Estefanía Cobos; Pere Garcia-Bru; Alejandro Filloy; Josep M. Caminal
Purpose: To study the long-term clinical course of dome-shaped macula in myopic eyes and to evaluate treatment efficacy for subretinal fluid (SRF) as a related complication. Methods: A retrospective, single-center consecutive case series study was conducted. The authors analyzed myopic eyes with dome-shaped macula in patients who presented for evaluation of decreased vision. Dome-shaped macula was defined as a convexity of the retina-choroidal macular complex seen on spectral domain optical coherence tomography images. All patients were followed for at least 12 months (mean, 25 months). Fluorescein angiography and/or indocyanine green angiography were performed in cases with SRF to rule out choroidal neovascularization. Results: A total of 56 dome-shaped macula eyes from 36 patients were included in the study (bilateral in 55% of patients). Mean patient age was 56.9 ± 13.1 years. The mean spherical equivalent was −9.1 ± 6.0 diopters; 53% of eyes were considered highly myopic (>−6 diopters) and 47% of eyes were mildly myopic. In most cases (37 eyes; 66.1%), the dome-shaped macula was detected on vertical spectral domain optical coherence tomography scan patterns. No significant changes (P ≥ 0.1) were observed in mean best-corrected visual acuity or mean central foveal thickness from baseline to final follow-up. Subretinal fluid was present in 29 eyes (51.8%) at baseline, with no differences in best-corrected visual acuity in eyes with and without SRF (P ≥ 0.05). Nineteen of the 29 SRF eyes were treated: 8 underwent low-fluence photodynamic therapy, whereas 7 received bevacizumab, and 4 ranibizumab. No significant differences were found between treated and untreated SRF eyes in best-corrected visual acuity improvement (P ≥ 0.1), or complete resolution of SRF (P ≥ 0.1). Likewise, photodynamic therapy did not yield any significant benefit versus untreated eyes in best-corrected visual acuity or improvement of SRF. Conclusion: Dome-shaped macula is a condition associated with myopic eyes that seems to remain stable over time in terms of vision and macular profiles. It is often associated with chronic SRF, for which no effective treatment is current available. However, SRF does not seem to be a significant cause of visual impairment.
Acta Ophthalmologica | 2018
Estefanía Cobos; Sergio Recalde; Jaouad Anter; Maria Hernandez-Sanchez; Carla Barreales; Leticia Olavarrieta; Alicia Valverde; Marta Suarez-Figueroa; Fernando Cruz; Maximino Abraldes; Julián Pérez-Pérez; Patricia Fernández-Robredo; Luis Arias; Alfredo García-Layana
We sought to determine if specific genetic single nucleotide polymorphisms (SNPs) influence vascular endothelial growth factor inhibition response to ranibizumab in neovascular age‐related macular degeneration (AMD).
Retina-the Journal of Retinal and Vitreous Diseases | 2016
Estefanía Cobos; Marcos J. Rubio; Luis Arias; Jose M. Caminal; Pere Garcia-Bru; Jaume Català; Sara Jordán; Maria Vidal; Laura Gutiérrez
Purpose: To investigate the incidence of postsurgical retinal displacement in patients treated with pars plana vitrectomy for rhegmatogenous retinal detachment and to assess the influence of displacement on macular function. Methods: Observational prospective study of 20 consecutive cases of rhegmatogenous retinal detachment who underwent 23-G pars plana vitrectomy with gas (C3F8 or SF6) tamponade, and prone resting. Three months after surgery, retinal displacement was evaluated by fundus autofluorescence. Macular function was evaluated with optical coherence tomography, multifocal electroretinogram, best-corrected visual acuity, and stereopsis. Results: Postoperative retinal displacement was observed in 60% of cases. No correlation between the type of tamponade used and retinal displacement was observed. Similarly, no association between retinal displacement and postoperative stereopsis or visual acuity was found. A lower amplitude in P1 wave on the multifocal electroretinogram was observed in eyes with rhegmatogenous retinal detachment compared with the contralateral eye. However, no statistically significant differences between groups with or without retinal displacement were found. Conclusion: Retinal displacement in patients who undergo pars plana vitrectomy to treat rhegmatogenous retinal detachment is common. However, this displacement does not seem to affect macular function.
Cancer Research and Treatment | 2017
Daniel Lorenzo; María Ochoa; Josep M. Piulats; Cristina Gutiérrez; Luis Arias; Jaume Català; María Grau; Judith Peñafiel; Estefanía Cobos; Pere Garcia-Bru; Marcos J. Rubio; Noel Padrón-Pérez; Bruno Dias; Joan Pera; Josep M. Caminal
Purpose The purpose of this study was to demonstrate the existence of a bimodal survival pattern in metastatic uveal melanoma. Secondary aims were to identify the characteristics and prognostic factors associated with long-term survival and to develop a clinical decision tree. Materials and Methods The medical records of 99 metastatic uveal melanoma patients were retrospectively reviewed. Patients were classified as either short (≤ 12 months) or long-term survivors (> 12 months) based on a graphical interpretation of the survival curve after diagnosis of the first metastatic lesion. Ophthalmic and oncological characteristicswere assessed in both groups. Results Of the 99 patients, 62 (62.6%) were classified as short-term survivors, and 37 (37.4%) as long-term survivors. The multivariate analysis identified the following predictors of long-term survival: age ≤ 65 years (p=0.012) and unaltered serum lactate dehydrogenase levels (p=0.018); additionally, the size (smaller vs. larger) of the largest liver metastasis showed a trend towards significance (p=0.063). Based on the variables significantly associated with long-term survival, we developed a decision tree to facilitate clinical decision-making. Conclusion The findings of this study demonstrate the existence of a bimodal survival pattern in patients with metastatic uveal melanoma. The presence of certain clinical characteristics at diagnosis of distant disease is associated with long-term survival. A decision tree was developed to facilitate clinical decision-making and to counsel patients about the expected course of disease.
American Journal of Ophthalmology | 2016
Josep M. Caminal; Karol Mejia; Luis Arias; Cristina Masuet-Aumatell; Jon Larrucea-Maseda; Ignasi Modolell; Daniel Lorenzo; Jaume Català; Marc Rubio; Estefanía Cobos; Pere Garcia-Bru; Ignacio Flores; Alejandro Filloy; Jordi Arruga
Annals d'oftalmologia: òrgan de les Societats d'Oftalmologia de Catalunya, Valencia i Balears | 2011
Estefanía Cobos; Nieves Martín Begué; Silvia Muñoz Quiñones; Jorge Arruga Ginebreda
Investigative Ophthalmology & Visual Science | 2017
Jose M. Caminal; Eduard Cabré; Antonia Vinyals; Montse Goma; Josep M. Piulats; Mar Varela; Daniel Lorenzo; Olaia Subira; Maria Jose Paules; Lluis Arias; Marc Rubio; Estefanía Cobos; Pere Garcia-Bru; Bruno Medeiros; Noel Padron; Angels Fabra
Investigative Ophthalmology & Visual Science | 2015
Marcos Javier Rubio Caso; Alex Muñoz Blanco; Ignacio Flores-Moreno; Pere García Bru; Estefanía Cobos; Luis Arias Barquet; Josep Maria Caminal Mitjana