A real-world study assessing the impact of retinal fluid on visual acuity outcomes in patients with neovascular age-related macular degeneration in Korea

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作者
Jae Hui Kim
Min Sagong
Se Joon Woo
Yu Cheol Kim
Heeyoon Cho
Young Hoon Lee
Iksoo Byon
Young Joon Jo
Hee Seung Chin
Youkyung Lee
Jae Eun Chae
Se Woong Kang
机构
[1] Kim’s Eye Hospital,Department of Ophthalmology
[2] Yeungnam University College of Medicine,Department of Ophthalmology
[3] Seoul National University College of Medicine,Department of Ophthalmology, Seoul National University Bundang Hospital
[4] Keimyung University School of Medicine,Department of Ophthalmology
[5] Hanyang University College of Medicine,Department of Ophthalmology, Hanyang University Guri Hospital
[6] Konyang University College of Medicine,Department of Ophthalmology
[7] Pusan National University School of Medicine,Department of Ophthalmology, Pusan National University Hospital
[8] Chungnam National University Hospital,Department of Ophthalmology
[9] Inha University School of Medicine,Department of Ophthalmology
[10] Novartis Korea,Clinical Development and Medical Affairs
[11] LSK Global Pharma Services,Department of Ophthalmology, Samsung Medical Center
[12] Sungkyunkwan University School of Medicine,undefined
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摘要
To evaluate the real-world treatment outcomes in patients with neovascular age-related macular degeneration (nAMD) in Korea, focusing on retinal fluid resolution. This multi-institutional retrospective chart review study, analyzed medical records of patients with nAMD (age ≥ 50 years) who received their first anti-vascular endothelial growth factor (VEGF) treatment in ophthalmology clinics across South Korea between January 2017 and March 2019. The primary endpoint was the proportion of patients with retinal fluid after 12 months of anti-VEGF treatment. The association between fluid-free period and VA gains was also evaluated. A total of 600 patients were enrolled. At baseline, 97.16% of patients had retinal fluid; after 12 months of anti-VEGF treatment, 58.10% of patients had persistent retinal fluid. VA improvements were relatively better in patients with absence of retinal fluid compared with presence of retinal fluid (+ 12.29 letters vs. + 6.45 letters at month 12; P < .0001). Longer duration of absence of retinal fluid over first 12 months correlated with better VA gains at month 12 (P < .01). More than half of the study patients with nAMD had retinal fluid even after 12 months of treatment with their current anti-VEGF. Presence of retinal fluid was associated with relatively worse VA outcomes.
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