玻璃体内地塞米松植入剂(Ozurdex)与布鲁珠单抗注射液治疗伴有高反光视网膜内点的糖尿病性黄斑水肿的比较分析:一项回顾性研究。

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2024-10-15 eCollection Date: 2024-01-01 DOI:10.2147/OPTH.S484731
Somnath Chakraborty, Jay Umed Sheth
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引用次数: 0

摘要

目的:这项回顾性研究旨在比较玻璃体内地塞米松植入剂(DEX)和布鲁珠单抗注射液治疗伴有高反光性视网膜内点(HRID)的糖尿病性黄斑水肿(DME)的疗效和安全性:在印度进行的一项单中心回顾性研究共纳入了40只眼睛(每组20只),这些患者的糖尿病得到了控制,并通过光学相干断层扫描检查出了HRID。患者接受 DEX 或 Brolucizumab 治疗,并在 24 周内的不同时间间隔进行疗效评估。主要评估指标包括最佳矫正视力(BCVA)、黄斑中心厚度(CMT)和安全性参数:结果:两个治疗组的基线特征相当。在第4、12和24周时,两种治疗方法都能明显改善BCVA,其中DEX植入剂在第12周时的效果明显优于brolucizumab(P=0.04)。在治疗无效的眼球中,所有时间点的BCVA改善情况相似。在难治性 DME 眼中,DEX 在所有时间点的 BCVA 均有显著改善,而布卢单抗仅在第 4 周(P=0.005)和第 24 周(P=0.04)有显著改善。两种治疗方法的CMT也都有所改善,其中DEX在第4周(P=0.003)、第12周(P=0.003)和第24周(P=0.002)分别显示出更好的降低效果。在治疗无效的眼球中,DEX的CMT降低效果一直较好。在难治性 DME 眼睛中,两种治疗方法都能显著减少 CMT,其中 DEX 在第 12 周的疗效更好(P=0.042)。与博路单抗相比,DEX所需的注射次数更少(DEX:1.5±0.61;博路单抗:2.4±0.82;P=0.0002),所需的辅助激光治疗次数更少(DEX:8/20,40%的眼睛;博路单抗:16/20,80%;P=0.01)。两组患者均未出现不良反应:该研究表明,在治疗伴有HRID的DME时,玻璃体内DEX植入剂可能比布卢单抗更有优势。DEX在BCVA和CMT方面表现出持续的积极反应,需要的注射和辅助干预更少。未来的研究应探索延长随访时间、个性化治疗策略和完善生物标志物,以优化 DME 的管理。
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Comparative Analysis of Intravitreal Dexamethasone Implant (Ozurdex) and Brolucizumab Injection in the Treatment of Diabetic Macular Edema with Hyperreflective Intraretinal Dots: A Retrospective Study.

Purpose: This retrospective study aimed to compare the efficacy and safety of intravitreal Dexamethasone Implant (DEX) and Brolucizumab Injection in treating Diabetic Macular Edema (DME) with Hyperreflective Intraretinal Dots (HRID).

Patients and methods: A single-center retrospective study in India included 40 eyes (20 per group) with controlled diabetes and HRID on optical coherence tomography. Patients received either DEX or Brolucizumab, with outcomes assessed at various intervals up to 24 weeks. Primary measures included Best-Corrected Visual Acuity (BCVA), Central Macular Thickness (CMT), and safety parameters.

Results: Both treatment groups demonstrated comparable baseline characteristics. Both treatments significantly improved the BCVA at weeks 4, 12, and 24, with the DEX implant showing significantly better results at week 12 than brolucizumab (P=0.04). In treatment-naïve eyes, BCVA improvements were similar across all time points. In recalcitrant DME eyes, DEX showed significant BCVA improvements at all time points, while brolucizumab showed significant improvements only at weeks 4 (P=0.005) and 24 (P=0.04). The CMT also improved with both treatments, with DEX showing superior reduction at weeks 4 (P=0.003), 12 (P=0.003), and 24 (P=0.002) respectively. In treatment-naïve eyes, DEX showed consistently better CMT reductions. In refractory DME eyes, both treatments significantly reduced CMT, with DEX performing better at week 12 (P=0.042). DEX required fewer injections (DEX: 1.5±0.61; brolucizumab: 2.4±0.82; P=0.0002) and less supplementary laser treatment (DEX:8/20, 40% eyes; brolucizumab: 16/20, 80%; P=0.01) compared to brolucizumab. No adverse events were observed in either group.

Conclusion: The study suggests the potential superiority of intravitreal DEX implant over brolucizumab in managing DME with HRID. DEX exhibited sustained positive responses in BCVA and CMT, requiring fewer injections and supplementary interventions. Future research should explore extended follow-up durations, personalized treatment strategies, and refined biomarkers to optimize DME management.

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