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      Incidence and treatment outcomes of secondary epiretinal membrane following intravitreal injection for diabetic macular edema

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          Abstract

          The purpose of this study was to investigate the incidence of secondary epiretinal membrane (ERM) after intravitreal injection and the effect of ERM on visual acuity and central macular thickness (CMT) in patients with diabetic macular edema (DME). We included 147 eyes of 95 patients over 18 years old who were diagnosed with DME from 2012 to 2016, treated with intravitreal injection, and followed-up more than 24 months. Mean CMT in the ERM group was significantly thicker than in the non-ERM group after 9, 12, 18, and 24 months. Secondary ERM developed in 9.5% of patients during follow-up. Compared to other agents, the incidence of secondary ERM was significantly higher after intravitreal injection of dexamethasone implant. Among patients in the ERM group, the mean decrease of CMT between pre-injection and 2 weeks post-injection was significantly less after secondary ERM formation than before ERM formation. Secondary ERM formation was significantly associated with the number of intravitreal injections and the use of dexamethasone implant. Therefore, secondary ERM develops more frequently as the number of intravitreal injections increases and after intravitreal dexamethasone implant injection. The therapeutic effects of intravitreal injections for DME patients decrease after secondary ERM formation.

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          Most cited references22

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          Diabetic retinopathy.

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            The role of cytokines and trophic factors in epiretinal membranes: involvement of signal transduction in glial cells.

            Idiopathic epiretinal membranes (ERMs) in the macular region can cause a reduction in vision and sometimes recurs after surgical removal, but its pathogenic mechanisms are still unknown. On the other hand, the presence of secondary ERMs has been associated with various clinical conditions including proliferative diabetic retinopathy (PDR) and proliferative vitreoretinopathy (PVR). Recent studies have shown a significant association between clinical grades of PDR or PVR, and the expression levels of specific cytokines and/or growth factors in the vitreous fluid. Expression of these factors and their receptors are also observed in secondary ERMs. ERMs are composed of many cell types such as retinal pigment epithelial cells and vascular endothelial cells, however the role of glial cells is yet unclear. Interestingly, glial cells in ERMs express some trophic factor receptors and transcription factors, such as NF-kappaB, suggesting an involvement of glial signal transduction in the pathogenesis of ERMs. In this review, we summarize recent progress regarding the clinical and laboratory findings of ERMs.
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              Management paradigms for diabetic macular edema.

              To provide evidence-based recommendations for diabetic macular edema (DME) management based on updated information from publications on DME treatment modalities.
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                Author and article information

                Contributors
                jps11@hanmail.net
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                17 January 2020
                17 January 2020
                2020
                : 10
                : 528
                Affiliations
                ISNI 0000 0001 0661 1556, GRID grid.258803.4, Department of Ophthalmology, , Kyungpook National University School of Medicine, ; Daegu, 41944 Korea
                Author information
                http://orcid.org/0000-0002-6505-315X
                http://orcid.org/0000-0001-6911-3765
                http://orcid.org/0000-0001-9222-8405
                Article
                57509
                10.1038/s41598-020-57509-6
                6969073
                31953511
                ab5fabe1-8664-4fe3-be6b-ec8575d5286c
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 August 2019
                : 2 January 2020
                Categories
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                © The Author(s) 2020

                Uncategorized
                retinal diseases,outcomes research
                Uncategorized
                retinal diseases, outcomes research

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