Rishi Pukhraj, Rishi Ekta, Kuniyal Lakshmi, Mathur Gaurav
Shri Bhagwan Mahavir Vitreoretinal Services, Sankara Nethralaya, Chennai, Tamil Nadu, India.
Oman J Ophthalmol. 2012 May;5(2):79-82. doi: 10.4103/0974-620X.99368.
Dexamethasone Posterior-Segment Drug Delivery System is a novel, biodegradable, sustained-release drug delivery system (OZURDEX(®)) for treatment of macular edema following retinal vein occlusion and posterior uveitis. However, its potential role in management of diabetic macular edema has not been reported yet.
The aim was to evaluate the safety and efficacy of (OZURDEX(®)) in patients with recalcitrant diabetic macular edema (DME).
A retrospective, interventional case series from a tertiary eye care center in India is presented. Inclusion criteria comprised patients presenting with recalcitrant DME, 3 or more months after one or more treatments of macular laser photocoagulation and/or intravitreal anti-vascular endothelial growth factor (VEGF) injections. Exclusion criteria included history of corticosteroid-responsive intraocular pressure (IOP) rise, cataract extraction, or other intraocular surgery within 3 months. The main outcome measure was visual acuity at 1 and 4 months after OZURDEX(®) injection. Secondary outcome measures included change in central macular thickness on Optical coherence tomography (OCT) and changes in IOP following intravitreal OZURDEX(®) implant. Of 18 eyes (17 patients) with recalcitrant diabetic macular edema that underwent OZURDEX(®) implant, three eyes (two patients) had follow-up of more than 3 months post-injection.
Mean age of patients was 56 years. Mean duration of diabetes mellitus was 16.6 years. Systemic control of DM was good as assessed by FBS/PPBS and HbA1c. The pre-operative mean central macular thickness was 744.3 μm and improved to 144 and 570 μm at months 1 and 4, respectively. Preoperative mean BCVA was 0.6 logMAR units and improved to 0.3 and 0.46 logMAR units at month 1 and 4, respectively. The mean follow-up was 4.3 months (range 4-5 months).
OZURDEX(®) appears efficacious in management of recalcitrant diabetic macular edema. The results of the ongoing POSURDEX(®) study will elaborate these effects better.
地塞米松眼后段给药系统是一种新型的、可生物降解的缓释给药系统(Ozurdex®),用于治疗视网膜静脉阻塞和后葡萄膜炎后的黄斑水肿。然而,其在糖尿病性黄斑水肿治疗中的潜在作用尚未见报道。
评估Ozurdex®治疗顽固性糖尿病性黄斑水肿(DME)患者的安全性和有效性。
呈现了来自印度一家三级眼科护理中心的回顾性、干预性病例系列研究。纳入标准包括患有顽固性DME的患者,在接受一次或多次黄斑激光光凝和/或玻璃体内抗血管内皮生长因子(VEGF)注射治疗3个月或更长时间后。排除标准包括有糖皮质激素反应性眼压(IOP)升高病史、白内障摘除术或在3个月内进行过其他眼内手术。主要观察指标是Ozurdex®注射后1个月和4个月时的视力。次要观察指标包括光学相干断层扫描(OCT)测量的中心黄斑厚度变化以及玻璃体内植入Ozurdex®后眼压的变化。在18只接受Ozurdex®植入的顽固性糖尿病性黄斑水肿眼(17例患者)中,3只眼(2例患者)在注射后有超过3个月的随访。
患者的平均年龄为56岁。糖尿病的平均病程为16.6年。通过空腹血糖/餐后血糖和糖化血红蛋白评估,糖尿病的全身控制良好。术前中心黄斑平均厚度为744.3μm,在第1个月和第4个月分别改善至144μm和570μm。术前平均最佳矫正视力(BCVA)为0.6 logMAR单位,在第1个月和第4个月分别改善至0.3和0.46 logMAR单位。平均随访时间为4.3个月(范围4 - 5个月)。
Ozurdex®在治疗顽固性糖尿病性黄斑水肿方面似乎有效。正在进行的POSURDEX®研究结果将更好地阐明这些效果。