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玻璃体内单次注射地塞米松作为糖尿病性黄斑水肿初始治疗的长期结果。

Long-term results of a single injection of intravitreal dexamethasone as initial therapy in diabetic macular edema.

机构信息

Chief Medical Officer and Vitreoretinal Surgeon, JPM Rotary Club of Cuttack Eye Hospital and Research Institute, Cuttack, Odisha, India.

Ophthalmology Resident, JPM Rotary Club of Cuttack Eye Hospital and Research Institute, Cuttack, Odisha, India.

出版信息

Indian J Ophthalmol. 2020 Mar;68(3):490-493. doi: 10.4103/ijo.IJO_620_19.

Abstract

PURPOSE

To evaluate the long-term safety and efficacy of the intravitreal dexamethasone implant in the treatment of diabetic macular edema (DME) as initial therapy.

METHODS

A hospital-based prospective, non-comparative case study of recently detected DME patients was conducted between July 2016 and December 2017, in which30 eyes of 30 patients were studied. Presenting vision, age, gender, duration of diabetes, general and ocular examination, intraocular pressure, indirect ophthalmoscopy, fundus fluorescein angiography, optical coherence tomography (OCT), and blood sugar levels were noted. Patients with increased central macular thickness (CMT) received an intravitreal dexamethasone implant as initial therapy. All were followed up at 1 week, 1 month, 3 months, 6 months, and 1 year, and the findings were recorded and analyzed using SPSS software.

RESULTS

30 eyes of 30 patients were studied which included 22 males and 8 females. The mean age of presentation was 58.7 ± 4.45 years. The mean decrease in CMT following intravitreal dexamethasone was 269.27 ± 112.002, 253.5 ± 108.294, and 286.73 ± 143.395 μm at the end of 3, 6, and 12 months, respectively, and the mean improvement in visual acuity (VA) was 2.27 ± 1.70 lines at 3 months, 2.27 ± 1.83 lines at 6 months, and 1.17 ± 2.00 lines at 12 months. Out of 30 cases, 4 had persistent DME and 6 had recurrence of DME at completion of 1 year of follow-up.

CONCLUSION

Intravitreal dexamethasone as initial therapy in the treatment of DME is both safe and efficacious in the reduction of CMT and improvement of vision and can be considered as primary therapy for DME.

摘要

目的

评估玻璃体内注射地塞米松植入物作为初始治疗糖尿病黄斑水肿(DME)的长期安全性和疗效。

方法

2016 年 7 月至 2017 年 12 月,对新诊断的 DME 患者进行了一项基于医院的前瞻性、非对照病例研究,共纳入 30 例 30 只眼的患者。记录了患者的视力、年龄、性别、糖尿病病程、一般和眼部检查、眼压、间接检眼镜检查、眼底荧光素血管造影、光学相干断层扫描(OCT)和血糖水平。所有中央黄斑厚度(CMT)增加的患者均接受玻璃体内注射地塞米松植入物作为初始治疗。所有患者均在 1 周、1 个月、3 个月、6 个月和 1 年进行随访,并使用 SPSS 软件记录和分析结果。

结果

研究纳入 30 例 30 只眼的患者,其中男 22 例,女 8 例。就诊时的平均年龄为 58.7±4.45 岁。玻璃体内注射地塞米松后 CMT 平均降低 269.27±112.002、253.5±108.294 和 286.73±143.395μm,分别在 3、6 和 12 个月时,视力(VA)平均改善 2.27±1.70 行,在 3 个月时,2.27±1.83 行,在 6 个月时,1.17±2.00 行,在 12 个月时。30 例中,4 例持续性 DME,6 例 DME 复发,1 年随访结束。

结论

玻璃体内注射地塞米松作为 DME 的初始治疗,在降低 CMT 和改善视力方面既安全又有效,可作为 DME 的主要治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1bad/7043155/f0d0c75600bb/IJO-68-490-g001.jpg

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