Efficacy and safety of intravitreal triamcinolone acetonide in the management of recalcitrant diabetic macular edema

Sathiskumar Rangasami, Subashree Palani, Menaka Chinnappan, S. Radhakrishnan
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引用次数: 1

Abstract

Background: Diabetic macular edema (DME) is the major cause of visual impairment among patients with diabetic retinopathy. The various treatment modalities available for DME are laser photocoagulation, intravitreal injection of anti-vascular endothelial growth factor drugs, and ocular corticosteroids. Usage of intravitreal injections of triamcinolone acetonide has shown to improve vision by reducing macular thickness and the benefits persisted for a longer duration. Aim: The aim is to evaluate the efficacy and safety of intravitreal triamcinolone acetonide in the management of recalcitrant DME. Methodology: A prospective interventional study was performed for 2 years among patients with DME at a tertiary care institute in Tamil Nadu. A total of 35 patients satisfying our inclusion and exclusion criteria were included in the study. Intravitreal injection of 0.05 ml (2 mg) of triamcinolone acetonide was given to all our study participants. The two major outcome parameters were best-corrected visual acuity (VA) and the central foveal thickness (CFT). Patients were followed up for 6 months. Results: Best-corrected visual acuity showed a statistically significant improvement till the end of 3 months, whereas the values measured at the end of 6 months showed no statistically significant difference. The reduction of values in CFT was found to be statistically significant both at the end of 3 months as well as at the end of 6 months. Conclusion: Intravitreal triamcinolone injection showed a significant improvement in VA and a reduction in CFT without an increase in intraocular pressure and in the incidence of cataracts.
玻璃体注射曲安奈德治疗顽固性糖尿病黄斑水肿的疗效和安全性
背景:糖尿病黄斑水肿(DME)是糖尿病视网膜病变患者视力损害的主要原因。DME的各种治疗方式包括激光光凝、玻璃体内注射抗血管内皮生长因子药物和眼部皮质类固醇。玻璃体内注射曲安奈德已被证明可以通过减少黄斑厚度来改善视力,其益处持续时间更长。目的:评价玻璃体内注射曲安奈德治疗顽固性DME的疗效和安全性。方法:在泰米尔纳德邦的一家三级医疗机构对DME患者进行了为期2年的前瞻性介入研究。共有35名符合我们纳入和排除标准的患者被纳入研究。对所有研究参与者进行玻璃体内注射0.05 ml(2 mg)曲安奈德。两个主要的结果参数是最佳矫正视力(VA)和中央凹厚度(CFT)。随访6个月。结果:最佳矫正视力在3个月结束前有统计学意义的改善,而在6个月结束时测量的值没有统计学意义的差异。CFT值的降低在3个月底和6个月底都具有统计学意义。结论:玻璃体内注射曲安奈德可显著改善VA,降低CFT,而不会增加眼压和白内障的发生率。
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27 weeks
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