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Outcomes after switching eyes that were stable on aflibercept to ranibizumab versus continuing aflibercept in neovascular age-related macular degeneration

阿柏西普 血管抑制剂 医学 黄斑变性 眼科 脉络膜新生血管 验光服务 贝伐单抗 外科 化疗
作者
Mirataollah Salabati,Anthony Obeid,Raziyeh Mahmoudzadeh,Omesh P. Gupta,Allen Chiang,Marc J. Spirn,Michael A. Klufas,Jason Hsu
出处
期刊:Graefes Archive for Clinical and Experimental Ophthalmology [Springer Nature]
被引量:1
标识
DOI:10.1007/s00417-022-05601-0
摘要

PurposeTo describe outcomes of neovascular age-related macular degeneration (nAMD) eyes that were stable on aflibercept but switched to ranibizumab compared to eyes maintained on aflibercept over the same period.MethodsIn this retrospective cohort study, eyes switched from aflibercept to ranibizumab due to intraocular inflammation (IOI) concerns with aflibercept were identified. Data was gathered from 3 visits pre-switch, switch visit (Sw), and 3 visits post-switch (P1, P2, P3). Similar data was gathered on eyes eligible to switch but continued on aflibercept with the middle visit considered the “presumed switch.” Outcome measures included visual acuity (VA) and central foveal thickness (CFT).ResultsA total of 142 eyes were analyzed with 71 in each of the switch and aflibercept groups. In the switch group, mean CFT increased from 165.7 µm at Sw to 184.7 µm at P1 (p = 0.009), 180.9 µm at P2 (p = 0.007), and 183.3 µm at P3 (p = 0.004). VA changed from logMAR 0.43 (20/54) at Sw to 0.49 (20/61) at P1 (p = 0.02), 0.54 (20/69) at P2 (p = 0.008), and 0.53 (20/68) at P3 (p = 0.04). In the aflibercept group, no significant change in CFT was found over the same period. VA changed from logMAR 0.56 (20/72) at the “presumed switch” to 0.58 (20/76) at P1 (p = 0.085), 0.62 (20/83) at P2 (p = 0.001), and 0.59 (20/77) at P3 (p = 0.14).ConclusionsnAMD eyes that were stable or improving on aflibercept but were switched to ranibizumab worsened, while those in a comparable group maintained on aflibercept remained fairly stable, suggesting a potential efficacy difference between the two drugs.
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