Xing Peiyu, Zhang Yucheng, Zhang Yong, Wang Shaowei, Hu Xiaojia, Wang Meihua, Xia Fan, Zhao Yang, Qu Wei, Meng Bo
Department of Ophthalmology, China Medical University the Fourth People's Hospital of Shenyang, Shenyang, People's Republic of China.
Department of Ophthalmology, The 2nd Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.
Clin Ophthalmol. 2024 Sep 30;18:2721-2730. doi: 10.2147/OPTH.S487248. eCollection 2024.
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.
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.
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.
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.
本研究的目的是评估序贯使用康柏西普注射液和地塞米松植入剂(DEX I)治疗视网膜中央静脉阻塞(CRVO)患者难治性黄斑水肿(ME)的有效性和安全性。
对34例因视网膜中央静脉阻塞导致持续性黄斑水肿的患者进行了一项研究,回顾了他们的病史和所进行的干预措施。在注射康柏西普1周后序贯植入DEX I。使用光学相干断层扫描血管造影(OCTA)图像测量视网膜中央厚度(CRT)、最佳矫正视力(BCVA)、眼压(IOP)以及治疗前后浅表毛细血管丛(SCP)和深层毛细血管丛(DCP)的血管密度,随访期为1年。
在12个月的随访中,参与者的视网膜中央厚度和眼压有显著改善(p < 0.05)。在整个监测期内,BCVA改善或血管密度降低方面未发现显著差异(p > 0.05)。两名患者在研究期间需要局部治疗来降低眼压。
总之,因继发性CRVO而出现持续性ME的患者可能受益于转换为涉及康柏西普和DEX I的治疗方案,这可能导致CRT降低。然而,BCVA以及深层和浅表毛细血管丛血管密度未观察到显著改善。