Conversion to faricimab after prior anti-vascular endothelial growth factor therapy for persistent diabetic macular oedema

医学 视力 眼科 糖尿病性视网膜病变 不利影响 血管抑制剂 糖尿病 外科 内科学 贝伐单抗 化疗 内分泌学
作者
Asad F. Durrani,Bita Momenaei,Taku Wakabayashi,Sudheshna Vemula,Saagar A. Pandit,Jason Hsu,Allen C. Ho,Marc J. Spirn,Michael A. Klufas,Sunir J. Garg,J.F. Vander,Carl D. Regillo,Allen Chiang,Ajay E. Kuriyan,Yoshihiro Yonekawa
出处
期刊:British Journal of Ophthalmology [BMJ]
卷期号:: bjo-324394 被引量:3
标识
DOI:10.1136/bjo-2023-324394
摘要

Background To assess the anatomical and functional outcomes in eyes with persistent diabetic macular oedema (pDME) on chronic anti-vascular endothelial growth factor therapy switched to intravitreal faricimab. Methods Patients with pDME on chronic anti-vascular endothelial growth factor therapy that were switched to faricimab and received at least three injections at our institution between April 2022 and May 2023 were included in this study. Patients were excluded if they had complete response to previous treatment but were switched to extend treatment intervals if they had steroid or laser treatment for DME within 6 months prior to switch. Clinical and imaging data were extracted from the electronic medical record. Central foveal thickness (CFT) and Snellen visual acuity (VA) were obtained before and after three intravitreal faricimab injections. Generalised estimating equations were used to analyse the change in CFT and VA. Result During the study period, 69 eyes of 53 patients met inclusion criteria. The mean age was 68.6±9.0 years. The mean number of injections prior to switch was 18.1±16.0. Pre-switch mean logarithm of the minimal angle of resolution VA was 0.40±0.30 (Snellen equivalent 20/50) and 0.38±0.27 (Snellen equivalent 20/48) after three faricimab injections (p=0.397). Mean CFT improved from 380±155 microns to 323±147 microns (p<0.001). No ophthalmic or systemic adverse events occurred during the study period. Conclusions Intravitreal faricimab can improve anatomic outcomes while maintaining visual acuity in eyes with pDME previously treated with anti-VEGF therapy.
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