Intravitreal Dexamethasone Implant in Anti-Vascular Endothelial Growth Factor Pretreated Diabetic Macular Edema-A Swiss Cohort Study.

IF 4.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Pharmaceuticals Pub Date : 2024-09-19 DOI:10.3390/ph17091235
Ferhat Turgut, Gábor M Somfai, Christoph Tappeiner, Katja Hatz, Irmela Mantel, Aude Ambresin, Guy Donati, Viviane Guignard, Dana Nagyová, Isabel B Pfister, Christine Schild, Justus G Garweg
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引用次数: 0

Abstract

Background/objectives: Diabetic macular edema (DME) is a significant cause of visual impairment, often treated with anti-vascular endothelial growth factor (anti-VEGF) agents. However, some patients do not respond adequately to this treatment. This study aims to evaluate the contribution of the intravitreal dexamethasone (DEX) implant as a second-line treatment in DME patients with insufficient response to anti-VEGF therapy or with high treatment burden.

Methods: This retrospective multicenter cohort study was conducted across seven clinical sites in Switzerland. The study included eyes with active DME that had been pretreated with anti-VEGF for at least six months before receiving DEX therapy. Data were extracted from electronic patient records, focusing on best-corrected visual acuity (BCVA), central subfield thickness (CST), and injection frequency.

Results: A total of 95 eyes from 89 patients (38.8% females, mean age 65.6 ± 9.1 years, follow-up time 80.6 ± 38.5 [13.5-166.7] months) were analyzed. Prior to the first DEX implant, eyes had undergone an average of 16.0 ± 13.3 anti-VEGF injections over 32.5 ± 22.4 months. Post-DEX treatment, 22.1% of eyes received DEX monotherapy, 44.2% received a combination of DEX and anti-VEGF, 25.3% continued with anti-VEGF monotherapy, and 8.4% received no further treatment. The number of anti-VEGF injections decreased significantly from 6.4 ± 3.1 in the year before DEX to 1.6 ± 2.4 in the year after DEX (p < 0.001). BCVA remained stable (0.4 ± 0.3 logMAR at baseline, 0.4 ± 0.5 logMAR at 24 months, p = 0.2), while CST improved from 477.7 ± 141.0 to 320.4 ± 125.5 μm (p < 0.001), and the presence of retinal fluid decreased from 98.0% to 61.1% (p = 0.021). During follow-up, 26.3% of eyes required glaucoma medication, 4.2% underwent glaucoma surgery, and 1.1% needed cataract surgery.

Conclusions: In real-world clinical settings, the addition of DEX to anti-VEGF therapy in DME patients significantly reduces treatment burden and retinal fluid while maintaining visual function. Treatment decisions should balance anatomical and functional outcomes, considering individual patient needs.

抗血管内皮生长因子治疗糖尿病黄斑水肿的静脉内地塞米松植入--瑞士队列研究。
背景/目的:糖尿病黄斑水肿(DME)是视力损伤的重要原因,通常采用抗血管内皮生长因子(anti-VEGF)药物治疗。然而,有些患者对这种治疗方法反应不佳。本研究旨在评估在抗血管内皮生长因子治疗无效或治疗负担较重的 DME 患者中,作为二线治疗手段的玻璃体内植入地塞米松(DEX)的作用:这项回顾性多中心队列研究在瑞士的七个临床机构进行。研究对象包括接受 DEX 治疗前已接受抗血管内皮生长因子治疗至少 6 个月的活动性 DME 患者。研究人员从电子病历中提取数据,重点关注最佳矫正视力(BCVA)、中央子场厚度(CST)和注射频率:共分析了 89 位患者的 95 只眼睛(38.8% 为女性,平均年龄为 65.6 ± 9.1 岁,随访时间为 80.6 ± 38.5 [13.5-166.7] 个月)。在首次植入 DEX 之前,患者平均接受了 16.0 ± 13.3 次抗血管内皮生长因子注射,时间为 32.5 ± 22.4 个月。DEX治疗后,22.1%的眼睛接受了DEX单药治疗,44.2%的眼睛接受了DEX和抗血管内皮生长因子联合治疗,25.3%的眼睛继续接受抗血管内皮生长因子单药治疗,8.4%的眼睛没有接受进一步治疗。抗血管内皮生长因子注射次数从DEX治疗前一年的6.4 ± 3.1次大幅减少到DEX治疗后一年的1.6 ± 2.4次(p < 0.001)。BCVA 保持稳定(基线时为 0.4 ± 0.3 logMAR,24 个月时为 0.4 ± 0.5 logMAR,p = 0.2),CST 从 477.7 ± 141.0 μm 下降到 320.4 ± 125.5 μm(p < 0.001),视网膜积液从 98.0% 下降到 61.1% (p = 0.021)。随访期间,26.3%的眼睛需要服用青光眼药物,4.2%的眼睛接受了青光眼手术,1.1%的眼睛需要接受白内障手术:结论:在真实世界的临床环境中,DME 患者在抗血管内皮生长因子治疗的基础上加用 DEX 可显著减轻治疗负担,减少视网膜积液,同时保持视觉功能。治疗决策应兼顾解剖和功能结果,并考虑患者的个体需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.
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