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玻璃体内注射地塞米松植入物治疗持续性糖尿病性黄斑水肿患者

Dexamethasone intravitreal implant for treatment of patients with persistent diabetic macular edema.

作者信息

Dutra Medeiros Marco, Postorino Maurizio, Navarro Rafael, Garcia-Arumí José, Mateo Carlos, Corcóstegui Borja

机构信息

Instituto de Microcirugia Ocular, Barcelona, Spain.

出版信息

Ophthalmologica. 2014;231(3):141-6. doi: 10.1159/000356413. Epub 2013 Dec 19.

Abstract

PURPOSE

To report the 6-month anatomical and best-corrected visual acuity (BCVA) response after primary intravitreal dexamethasone implantation (Ozurdex®) in patients with refractory diabetic macular edema (DME).

METHODS

Retrospective review of the medical records of 58 patients with decreased visual acuity, due to refractory DME, who underwent a single injection of Ozurdex between November 2010 and January 2012, at the Instituto de Microcirurgia Ocular, Barcelona, Spain.

RESULTS

At baseline, the mean foveal thickness (FT) was 543.24 ± 156.51 μm. Mean (±SD) values of FT did decrease to 346.82 ± 123.74 μm at month 1 and 341.12 ± 129.64 μm at month 3. Data on the 6-month follow-up showed a mild increase to 420.16 ± 152.15 μm. All of the FT reduction outcomes were statistically significant, with respect to baseline data (p = 0.0001). The baseline BCVA data was 0.66 ± 0.36 logarithm of the minimum angle of resolution (logMAR). The mean BCVA improved to 0.52 ± 0.32 logMAR (p = 0.0001) and 0.44 ± 0.27 logMAR (p = 0.0001) after 1 and 3 months, respectively. At the last visit (6-month follow-up), the mean BCVA increased to 0.51 ± 0.31 logMAR (p = 0.0001).

CONCLUSIONS

In this study, intravitreal treatment with a dexamethasone implant safely reduced DME and improved visual acuity in a difficult-to-treat patient population with long-standing refractory DME.

摘要

目的

报告难治性糖尿病性黄斑水肿(DME)患者初次玻璃体内注射地塞米松植入剂(Ozurdex®)后6个月的解剖学和最佳矫正视力(BCVA)反应。

方法

回顾性分析2010年11月至2012年1月期间在西班牙巴塞罗那眼显微外科研究所因难治性DME导致视力下降而接受单次Ozurdex注射的58例患者的病历。

结果

基线时,平均黄斑中心凹厚度(FT)为543.24±156.51μm。FT的平均值(±标准差)在第1个月降至346.82±123.74μm,在第3个月降至341.12±129.64μm。6个月随访数据显示轻度增加至420.16±152.15μm。所有FT降低结果与基线数据相比均具有统计学意义(p = 0.0001)。基线BCVA数据为最小分辨角对数(logMAR)0.66±0.36。平均BCVA在1个月和3个月后分别提高到0.52±0.32 logMAR(p = 0.0001)和0.44±0.27 logMAR(p = 0.0001)。在最后一次随访(6个月随访)时,平均BCVA增加到0.51±0.31 logMAR(p = 0.0001)。

结论

在本研究中,玻璃体内注射地塞米松植入剂可安全降低DME,并改善长期难治性DME这一难以治疗的患者群体的视力。

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