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 Science+Business Media]
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.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
上课了没发布了新的文献求助30
刚刚
song完成签到,获得积分10
刚刚
pzt发布了新的文献求助10
1秒前
zypazyp发布了新的文献求助10
2秒前
2秒前
2秒前
剑来不来完成签到,获得积分10
2秒前
勤奋靖易完成签到,获得积分10
2秒前
冯一凡发布了新的文献求助10
2秒前
WW应助谨慎的果汁采纳,获得10
3秒前
3秒前
天天快乐应助璇儿的采纳,获得10
4秒前
Nuyoah发布了新的文献求助10
4秒前
酷波er应助睡眠不足中采纳,获得10
4秒前
h123完成签到,获得积分10
5秒前
纯真乐荷完成签到,获得积分10
5秒前
酷酷珠发布了新的文献求助10
7秒前
7秒前
8秒前
机智臻发布了新的文献求助10
8秒前
11秒前
Sc1ivez发布了新的文献求助10
11秒前
科研通AI2S应助Jin采纳,获得10
11秒前
11秒前
今后应助zmuzhang2019采纳,获得10
11秒前
小马甲应助LeezZZZ采纳,获得10
12秒前
12秒前
12秒前
桐桐应助zhuzhu采纳,获得10
12秒前
鸡腿战神完成签到,获得积分10
13秒前
13秒前
oldblack发布了新的文献求助10
13秒前
白多多完成签到,获得积分10
13秒前
Abruzzi完成签到,获得积分10
13秒前
14秒前
pyh完成签到,获得积分10
14秒前
酷酷珠完成签到,获得积分10
14秒前
小二郎应助飘逸晓博采纳,获得10
14秒前
15秒前
cdercder应助无情的哑铃采纳,获得10
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Cronologia da história de Macau 5000
Braunwald’s Heart Disease, 2 Vol Set A Textbook of Cardiovascular Medicine 13th Edition 1000
Petrology and Plate Tectonics 800
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
Electrode Potentials 550
Handbook Of Synthetic Methodologies And Protocols Of Nanomaterials 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 光电子学 物理化学 电极 基因 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 6994690
求助须知:如何正确求助?哪些是违规求助? 8670532
关于积分的说明 18385324
捐赠科研通 6467116
什么是DOI,文献DOI怎么找? 3098185
关于科研通互助平台的介绍 2160535
邀请新用户注册赠送积分活动 2074566