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Dexamethasone intravitreal implant for treatment of uveitic persistent cystoid macular edema in vitrectomized patients

机译:地塞米松玻璃体内植入物治疗玻璃体切除患者葡萄膜持续性囊样黄斑水肿

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PURPOSE: To evaluate the safety and efficacy of Ozurdex (dexamethasone intravitreal implant) 0.7 mg in the treatment of uveitic macular edema in vitrectomized eyes. METHODS: Data from 13 patients (17 eyes) with persistent uveitic cystoid macular edema and a history of pars plana vitrectomy in the study eyes that were treated with intravitreal injection of 0.7-mg dexamethasone implant were reviewed retrospectively. Main outcome measures were changes in central retinal thickness measured by optical coherence tomography and changes in best-corrected visual acuity. RESULTS: The median age of patients was 61 years (range, 19-81 years). The median duration of uveitic macular edema was 12 months (range, 2-72 months). The mean baseline central retinal thickness (95% confidence interval) was 461.6 μm (403.8-519.4), decreased to 277.2 μm (244.6-309.8) at 4 weeks (P < 0.01), remained low at 349.9 μm (281.8-418.0) at 3 months (P = 0.01), and then reached 394.1 μm (328.3-459.8) at 6 months (P = 0.14). After 3 months, there was a median improvement of 2 lines of best-corrected visual acuity, with 52.9% of eyes gaining 2 lines or more (P < 0.01). At 6 months, there were 5 eyes that maintained the 2 lines gain and none had lost >1 line from baseline (P = 0.03). In 8 eyes (47.1%), reinjection of the implant was performed at a mean of 6.5 months. Ocular hypertension (47.1%), hypotony (11.8%), anterior chamber displacement of the implant (5.9%), and glaucoma, which required filtration surgery (5.9%), were the most common adverse events. Mean follow-up was 9.6 months (range, 6-17 months). CONCLUSION: In this small case series of eyes with limited follow-up, treatment with dexamethasone intravitreal implant injection for uveitic macular edema in vitrectomized eyes was associated with favorable visual outcomes and had an acceptable safety profile.
机译:目的:评估0.7 mg Ozurdex(地塞米松玻璃体内植入物)在玻璃体切割术中治疗葡萄膜黄斑水肿的安全性和有效性。方法:回顾性分析了经玻璃体腔注射0.7 mg地塞米松植入物治疗的13例持续性葡萄膜囊样黄斑水肿和扁平玻璃体切除术史的患者的数据。主要结果指标是通过光学相干断层扫描测量的视网膜中央厚度的变化和最佳矫正视力的变化。结果:患者的中位年龄为61岁(范围19-81岁)。葡萄膜黄斑水肿的中位持续时间为12个月(范围2-72个月)。基线中央视网膜平均厚度(95%置信区间)为461.6μm(403.8-519.4),在第4周时降至277.2μm(244.6-309.8)(P <0.01),在349.9μm(281.8-418.0)时保持较低3个月(P = 0.01),然后在6个月时(P = 0.14)达到394.1μm(328.3-459.8)。 3个月后,最佳矫正视力的2线改善了中位数,有52.9%的眼睛获得2线或以上(P <0.01)。在6个月时,有5只眼睛维持了2条线的增益,并且没有一条线从基线丢失> 1条线(P = 0.03)。在8只眼(47.1%)中,平均6.5个月进行了植入物的再注射。最常见的不良事件是高眼压(47.1%),低渗(11.8%),植入物的前房移位(5.9%)和青光眼,需要进行滤过手术(5.9%)。平均随访9.6个月(6-17个月)。结论:在这种眼部随访情况不多的小病例中,地塞米松玻璃体内植入物治疗玻璃体切除的眼睛葡萄膜黄斑水肿具有良好的视觉效果,并且具有可接受的安全性。

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