Disparities in Retinal Vein Occlusion Presentation and Initiation of Anti-VEGF Therapy An Academy IRIS® Registry Analysis

被引:1
|
作者
Haller, Julia A. [1 ,2 ,3 ,4 ,5 ,6 ]
Tomaiuolo, Maurizio [2 ,3 ,4 ,5 ,6 ]
Lucas, Mary M. [7 ]
Yang, Christopher C. [7 ]
Hyman, Leslie [2 ,4 ,5 ,6 ]
机构
[1] Univ Washington, Seattle, WA USA
[2] Massachusetts Eye & Ear Harvard Ophthamol, Boston, MA USA
[3] Stanford Univ, Stanford, CA USA
[4] Wills Eye Hosp & Res Inst, Philadelphia, PA USA
[5] Wills Eye Hosp & Res Inst, Vickie & Jack Farber Vis Res Ctr, 840 Walnut St,Suite 1530, Philadelphia, PA 19107 USA
[6] Thomas Jefferson Univ, Dept Ophthalmol, Sidney Kimmel Med Coll, Philadelphia, PA USA
[7] Drexel Univ, Coll Comp & Informat, Philadelphia, PA USA
来源
OPHTHALMOLOGY RETINA | 2024年 / 8卷 / 07期
基金
美国国家科学基金会;
关键词
Retinal vein occlusion; Anti-VEGF; Disparities; MACULAR EDEMA; INTRAVITREAL AFLIBERCEPT; UNITED-STATES; RANIBIZUMAB; OUTCOMES;
D O I
10.1016/j.oret.2024.01.017
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective: Investigate disparities in retinal vein occlusion (RVO) presentation and initiation of anti-VEGF treatment. Design: Retrospective cohort study. Subjects: Patients in the American Academy of Ophthalmology IRIS (R) (Intelligent Research in Sight) Registry database (2015-2021) with branch or central RVO and macular edema (ME). Methods: The association of demographic characteristics and presenting visual acuity (VA) with anti-VEGF treatment initiation were quantified using multivariable logistic regression. Main Outcome Measures: Treatment with > 1 anti-VEGF injection within 12 months after RVO diagnosis. Results: A total of 304 558 eligible patients with RVO and ME were identified. Age at presentation varied by race, ethnicity, sex, and RVO type (all P values < 0.001). Within the first year after RVO presentation, 192 602 (63.2%) patients received >= 1 anti-VEGF injection. In a multivariable regression model adjusting for relevant covariates, female (vs. male) patients had lower odds of receiving injections (odds ratio [OR], 0.95; 95% confidence interval [CI], 0.93-0.96; P < 0.0001) as did Black/African American (vs. White) patients (OR, 0.90; 95% CI, 0.88-0.92; P < 0.0001) and Asian (vs. White) patients (OR, 0.95; 95% CI, 0.91-0.99; P = 0.02), whereas older patients (vs. patients aged < 51 years) had higher odds (61-70 years: OR, 1.20; 95% CI, 1.16-1.24; 71-80 years: OR, 1.20; 95% CI, 1.16-1.24; > 80 years: OR, 1.15; 95% CI, 1.11-1.18; all P values < 0.0001). Hispanic (vs. non-Hispanic) patients had a small increased odds of treatment initiation (OR, 1.08; 95% CI, 1.04-1.11; P < 0.0001). Results were similar in the subset of 226 143 patients with VA data. In this subset, patients with presenting VA < 20/40 to 20/200 were most frequently treated in the first year after diagnosis (w 70%) and patients with light perception/no light perception (LP-NLP) vision or VA of 20/20 or better were treated least frequently (36.9% and 41.9%, respectively). Conclusions: In this large national clinical registry, 37% of RVO patients with ME had no anti-VEGF treatment documented in the first year after diagnosis. Black/African American, Asian, and female patients and patients with VA of LP-NLP were least likely to receive treatment. Awareness of this undertreatment and these disparities highlight the need for initiatives to ensure all RVO patients receive timely anti-VEGF injections for optimized visual outcomes. (c) 2024 by the American Academy of Ophthalmology
引用
收藏
页码:657 / 665
页数:9
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