Evaluating the Efficacy of Conbercept and Dexamethasone Implants Sequentially in the Treatment of Refractory Macular Edema Secondary to Central Retinal Vein Occlusion (CRVO): A One-Year Follow-Up Study.

Clinical ophthalmology (Auckland, N.Z.) Pub Date : 2024-09-30 eCollection Date: 2024-01-01 DOI:10.2147/OPTH.S487248
Peiyu Xing, Yucheng Zhang, Yong Zhang, Shaowei Wang, Xiaojia Hu, Meihua Wang, Fan Xia, Yang Zhao, Wei Qu, Bo Meng
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Abstract

Purpose: The objective of this research was to assess the effectiveness and safety of using Conbercept injection and dexamethasone implant (DEX I) in sequence for treating refractory macular edema (ME) caused by central retinal vein occlusion (CRVO) in patients.

Methods: A study was conducted on 34 patients with persistent macular edema caused by central retinal vein occlusion, reviewing their medical history and interventions performed. Sequential implantation of DEX I was performed 1 week after the Conbercept injection. OCTA images were used to measure central retinal thickness (CRT), best-corrected visual acuity (BCVA), intraocular pressure (IOP), and pre- and post-treatment vessel density of the superficial capillary plexus (SCP) and deep capillary plexus (DCP), with a 1-year follow-up period.

Results: At the 12-month follow-up, participants demonstrated notable improvements in central retinal thickness and intraocular pressure (p < 0.05). Throughout the monitoring period, no significant differences were found in BCVA improvement or vessel density reduction (p > 0.05). Two patients required topical treatment to lower their intraocular pressure during the study period.

Conclusion: In conclusion, patients experiencing persistent ME due to secondary CRVO may benefit from transitioning to a treatment regimen involving Conbercept and DEX I, potentially resulting in a reduction in CRT. However, no significant improvement was observed in BCVA or deep and superficial capillary plexus vessel density.

评估康柏西普和地塞米松植入剂相继用于治疗继发于视网膜中央静脉闭塞(CRVO)的难治性黄斑水肿的疗效:一年随访研究。
目的:本研究旨在评估依次使用康柏西普注射液和地塞米松植入剂(DEX I)治疗由视网膜中央静脉闭塞(CRVO)引起的难治性黄斑水肿(ME)的有效性和安全性:对34名视网膜中央静脉闭塞引起的持续性黄斑水肿患者进行了研究,回顾了他们的病史和所采取的干预措施。在注射康柏西普一周后,进行了DEX I的序贯植入。OCTA图像用于测量视网膜中央厚度(CRT)、最佳矫正视力(BCVA)、眼压(IOP)以及治疗前后浅层毛细血管丛(SCP)和深层毛细血管丛(DCP)的血管密度,随访期为1年:在为期 12 个月的随访中,参与者的视网膜中央厚度和眼压均有明显改善(P < 0.05)。在整个监测期间,BCVA 的改善和血管密度的降低均无明显差异(P > 0.05)。两名患者在研究期间需要局部治疗以降低眼压:总之,继发性CRVO导致的持续性ME患者可从过渡到使用康柏西普和DEX I的治疗方案中获益,从而有可能减少CRT。然而,在BCVA或深浅毛细血管丛血管密度方面没有观察到明显改善。
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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