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      A Randomized Trial Comparing Suprachoroidal and Intravitreal Injection of Triamcinolone Acetonide in Refractory Diabetic Macular Edema due to Epiretinal Membrane

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          Abstract

          Purpose

          To compare the efficacy and safety of suprachoroidal and intravitreal injection of triamcinolone acetonide in pseudophakic patients with refractory diabetic macular edema (DME) due to epiretinal membrane (ERM). Study Design. This study is a randomized clinical trial (RCT). Participants. Twenty-three nonvitrectomized pseudophakic eyes of 23 subjects (9 M and 14 F with mean age: 54.8 years) with refractory DME due to ERM.

          Methods

          The eyes were randomized to suprachoroidal triamcinolone acetonide injection 4 mg/0.1 ml (SCTA) ( n = 13 eyes) or intravitreal triamcinolone acetonide 4 mg/0.1 ml (IVTA) ( n = 10 eyes) and were evaluated at baseline and 1 and 3 months after injection to assess outcome measures. Main Outcome Measures. Changes in best-corrected visual acuity (BCVA) (primary outcome), central foveal thickness (CFT) by optical coherence tomography (OCT), and intraocular pressure (IOP) measurement (secondary).

          Results

          Baseline median BCVA (logMAR) was 1.0 (range 0.8–1.0) in both groups, improved within the SCTA group to 0.8 on the 1 st and 3 rd months, while in the IVTA group, median BCVA changed to 0.8 and 0.9 on the 1 st and 3 rd months, respectively. No significant differences were noted between groups regarding BCVA at baseline ( P=0.927), and 1 st ( P=0.605) and 3 rd months ( P=0.313). Regarding mean CFT, no significant differences were observed at baseline ( P=0.353) and at the first month ( P=0.214) between both groups, while at the third month, CFT was significantly higher in the IVTA group (385 um) than in the SCTA group (323 um) ( P=0.028). Mean IOP was significantly higher in the IVTA group (15 mmHg) on 1 st month than in the SCTA group (12 mmHg) ( P=0.011); after 3 rd month, IOP was significantly higher within the IVTA group (18 mmHg) than SCTA (14 mmHg) ( P=0.028). No significant difference was noted between both groups at baseline IOP ( P=0.435).

          Conclusions

          Both SCTA and IVTA are effective in reduction of CFT and improvement of patients' visual acuity, but with a higher recurrence rate and rise in IOP after IVTA when compared to SCTA. Both treatments have temporary effects with the possibility of recurrence of DME and the need for retreatment.

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          Most cited references20

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          Diabetic retinopathy.

          Diabetic retinopathy is a common and specific microvascular complication of diabetes, and remains the leading cause of preventable blindness in working-aged people. It is identified in a third of people with diabetes and associated with increased risk of life-threatening systemic vascular complications, including stroke, coronary heart disease, and heart failure. Optimum control of blood glucose, blood pressure, and possibly blood lipids remains the foundation for reduction of risk of retinopathy development and progression. Timely laser therapy is effective for preservation of sight in proliferative retinopathy and macular oedema, but its ability to reverse visual loss is poor. Vitrectomy surgery might occasionally be needed for advanced retinopathy. New therapies, such as intraocular injection of steroids and antivascular endothelial growth-factor agents, are less destructive to the retina than are older therapies, and could be useful in patients who respond poorly to conventional therapy. The outlook for future treatment modalities, such as inhibition of other angiogenic factors, regenerative therapy, and topical therapy, is promising. Copyright 2010 Elsevier Ltd. All rights reserved.
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            Aflibercept, Bevacizumab, or Ranibizumab for Diabetic Macular Edema: Two-Year Results from a Comparative Effectiveness Randomized Clinical Trial.

            To provide 2-year results comparing anti-vascular endothelial growth factor (VEGF) agents for center-involved diabetic macular edema (DME) using a standardized follow-up and retreatment regimen.
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              • Record: found
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              Inflammation in diabetic retinopathy.

              Diabetes causes a number of metabolic and physiologic abnormalities in the retina, but which of these abnormalities contribute to recognized features of diabetic retinopathy (DR) is less clear. Many of the molecular and physiologic abnormalities that have been found to develop in the retina in diabetes are consistent with inflammation. Moreover, a number of anti-inflammatory therapies have been found to significantly inhibit development of different aspects of DR in animal models. Herein, we review the inflammatory mediators and their relationship to early and late DR, and discuss the potential of anti-inflammatory approaches to inhibit development of different stages of the retinopathy. We focus primarily on information derived from in vivo studies, supplementing with information from in vitro studies were important. Copyright © 2011 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                Journal
                J Ophthalmol
                J Ophthalmol
                JOPH
                Journal of Ophthalmology
                Hindawi
                2090-004X
                2090-0058
                2022
                21 January 2022
                : 2022
                : 7947710
                Affiliations
                Department of Ophthalmology, Faculty of Medicine, Benha University, Farid Nada St., Banha 13511, Egypt
                Author notes

                Academic Editor: Alessandro Meduri

                Author information
                https://orcid.org/0000-0003-1435-3918
                Article
                10.1155/2022/7947710
                8799353
                35096422
                4acd5b23-fcae-4714-85d6-3e1edf33806a
                Copyright © 2022 Ahmed Abdelshafy Tabl et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 September 2021
                : 5 January 2022
                Categories
                Research Article

                Ophthalmology & Optometry
                Ophthalmology & Optometry

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