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糖尿病性黄斑水肿抗VEGF注射后的玻璃体黄斑界面

Vitreomacular interface after anti-VEGF injections in diabetic macular edema.

作者信息

Veloso Carlos E, Brocchi Daniel N, Singh Rishi P, Nehemy Márcio B

机构信息

Department of Ophthalmology, Federal University of Minas Gerais, Avenida Nossa Senhora do Carmo 90, Savassi, Belo Horizonte, MG, 30330-000, Brazil.

Center for Ophthalmic Bioinformatics, Cole Eye Institute, Cleveland Clinic, Cleveland, OH, USA.

出版信息

Int J Retina Vitreous. 2021 Mar 19;7(1):23. doi: 10.1186/s40942-021-00295-8.

Abstract

BACKGROUND

The purpose of this study was to evaluate the incidence of vitreomacular adhesion (VMA) release after anti-VEGF therapy for the treatment of diabetic macular edema (DME) and to evaluate further changes in outcome.

METHODS

This was a retrospective study that enrolled 66 eyes of 66 patients with DME who presented with VMA diagnosed by spectral-domain optical coherence tomography (OCT) at baseline. VMA was classified as focal (attachment: ≤ 1500 μm) or broad (attachment: > 1500 μm). All patients received at least three monthly intravitreal injections of an anti-VEGF agent. Follow-up visits were performed 1 month after each injection to evaluate the incidence of VMA release.

RESULTS

The mean patient age was 61.4 years (range: 29 to 78 years), and 72.7 % were male. The mean best-corrected visual acuity was 0.62 logMAR, and the mean central retinal thickness (CRT) was 473 μm at baseline. The mean length of follow-up was 18.5 months, and the mean number of injections was 5.8. The intravitreal drugs used were aflibercept (40.9 %), ranibizumab (37.9 %) and bevacizumab (21.2 %). Forty-seven eyes had broad VMA, and 19 had focal VMA. Twenty-two eyes (33.3 %) developed VMA release following a mean of 5.7 injections (range: 3-13). Sixteen eyes (72.7 %) with focal VMA and 6 eyes (27.3 %) with broad VMA at baseline developed VMA release. Twenty-one eyes that developed VMA release showed an improvement in CRT following VMA release (mean: -106 μm; range: 22 to 289 μm).

CONCLUSIONS

VMA release occurs in approximately 1/3 of patients with DME following anti-VEGF therapy. Most of them show a short-term decrease in CRT.

摘要

背景

本研究旨在评估抗血管内皮生长因子(VEGF)治疗糖尿病性黄斑水肿(DME)后玻璃体黄斑粘连(VMA)松解的发生率,并评估治疗效果的进一步变化。

方法

这是一项回顾性研究,纳入了66例DME患者的66只眼,这些患者在基线时经光谱域光学相干断层扫描(OCT)诊断为VMA。VMA分为局限性(粘连:≤1500μm)或广泛性(粘连:>1500μm)。所有患者均接受至少3次每月一次的玻璃体内抗VEGF药物注射。每次注射后1个月进行随访,以评估VMA松解的发生率。

结果

患者平均年龄为61.4岁(范围:29至78岁),男性占72.7%。基线时平均最佳矫正视力为0.62 logMAR,平均中心视网膜厚度(CRT)为473μm。平均随访时间为18.5个月,平均注射次数为5.8次。使用的玻璃体内药物为阿柏西普(40.9%)、雷珠单抗(37.9%)和贝伐单抗(21.2%)。47只眼为广泛性VMA,19只眼为局限性VMA。22只眼(33.3%)在平均5.7次注射(范围:3 - 13次)后发生VMA松解。基线时16只局限性VMA眼(72.7%)和6只广泛性VMA眼(27.3%)发生了VMA松解。21只发生VMA松解的眼在VMA松解后CRT有所改善(平均:-106μm;范围:22至289μm)。

结论

抗VEGF治疗后,约1/3的DME患者会发生VMA松解。其中大多数患者的CRT短期内会下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36cb/7980589/c20d321f0a32/40942_2021_295_Fig1_HTML.jpg

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