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用于治疗糖尿病性视网膜病变和视网膜静脉阻塞继发难治性黄斑水肿的地塞米松植入剂

Dexamethasone implant for refractory macular edema secondary to diabetic retinopathy and retinal vein occlusion.

作者信息

Zhong Yuan-Yuan, Tang Chong, Zhang Lan-Yue, Zhang Xue-Dong, Liu Shu-Lin

机构信息

The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory for the Prevention and Treatment of Major Blinding Eye Diseases, Chongqing 400016, China.

出版信息

Int J Ophthalmol. 2024 Oct 18;17(10):1837-1842. doi: 10.18240/ijo.2024.10.09. eCollection 2024.

Abstract

AIM

To evaluate the efficacy, timing of retreatment and safety of dexamethasone (DEX) implant on macular edema (ME) secondary to diabetic retinopathy (DME) and retinal vein occlusion (RVO-ME) patients who were refractory to anti-vascular endothelial growth factor (VEGF) treatment.

METHODS

This retrospective study included 37 eyes received at least one DEX implant treatment for DME or RVO-ME between January 1, 2019, and January 1, 2023. These refractory DME and RVO-ME cases received at least 5 anti-VEGF injections and failure to gain more than 5 letters or a significant reduction in central retinal thickness (CRT). The best corrected visual acuity (BCVA) and CRT were measured at baseline, and at 1, 3, 4 and 6mo post-DEX implant injection. Adverse events such as elevated intraocular pressure (IOP) and cataract were recorded.

RESULTS

For RVO cases (=22), there was a significant increase in BCVA from 0.27±0.19 to 0.35±0.20 at 6mo post-DEX injection (<0.05) and CRT decreased from 472.1±90.6 to 240.5±39.0 µm at 6mo (<0.0001). DME cases (=15) experienced an improvement in BCVA from 0.26±0.15 to 0.43±0.20 at 6mo post-DEX implant injection (=0.0098), with CRT reducing from 445.7±55.7 to 271.7±34.1 µm at 6mo (<0.0001). Elevated IOP occurred in 45.9% of patients but was well-controlled with topical medications. No cases of cataract or other adverse events were reported.

CONCLUSION

DEX implants effectively improve BCVA and reduce CRT in refractory DME and RVO-ME. Further research with larger cohorts and longer follow-up periods is needed to confirm these findings and assess long-term outcomes.

摘要

目的

评估地塞米松(DEX)植入物对糖尿病性视网膜病变(DME)继发黄斑水肿(ME)以及视网膜静脉阻塞(RVO-ME)且对抗血管内皮生长因子(VEGF)治疗无效患者的疗效、再次治疗时机及安全性。

方法

这项回顾性研究纳入了2019年1月1日至2023年1月1日期间因DME或RVO-ME接受至少一次DEX植入物治疗的37只眼。这些难治性DME和RVO-ME病例至少接受了5次抗VEGF注射,且视力提高未超过5个字母或中心视网膜厚度(CRT)未显著降低。在基线时以及DEX植入物注射后1、3、4和6个月测量最佳矫正视力(BCVA)和CRT。记录眼内压(IOP)升高和白内障等不良事件。

结果

对于RVO病例(n = 22),DEX注射后6个月时BCVA从0.27±0.19显著提高至0.35±0.20(P < 0.05),CRT在6个月时从472.1±90.6降至240.5±39.0 µm(P < 0.0001)。DME病例(n = 15)在DEX植入物注射后6个月时BCVA从0.26±0.15提高至0.43±0.20(P = 0.0098),CRT在6个月时从445.7±55.7降至271.7±34.1 µm(P < 0.0001)。45.9%的患者出现IOP升高,但通过局部用药得到良好控制。未报告白内障或其他不良事件病例。

结论

DEX植入物可有效改善难治性DME和RVO-ME患者的BCVA并降低CRT。需要进行更大样本量队列和更长随访期的进一步研究以证实这些发现并评估长期结果。

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