Oral fundus fluorescein angiogram detects reactivation post anti-VEGF in aggressive retinopathy of prematurity

Objective Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease reactivation in babies treated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) for Aggressive Retinopathy of Prem...

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Published inEye (London) Vol. 39; no. 13; pp. 2540 - 2547
Main Authors Belenje, Akash, Reddy, Rakasi Ugandhar, Padhi, Tapas Ranjan, Jalali, Subhadra
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.09.2025
Nature Publishing Group
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ISSN0950-222X
1476-5454
1476-5454
DOI10.1038/s41433-025-03896-x

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Abstract Objective Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease reactivation in babies treated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) for Aggressive Retinopathy of Prematurity (A-ROP). Methods Eyes clinically suspected to have a possible or definite reactivation after anti-VEGF injection were included in this pilot study. NC-UWF-OFDA was performed in the office setting. Imaging was done prospectively in preterm babies with A-ROP injected with anti-VEGF. OFDA images were analysed for signs of reactivation. Results A total of 20 eyes of 10 preterm babies treated with anti-VEGF underwent NC-UWF-OFDA imaging. The OFDA images were analysed to assess the pattern and dynamics of retinal vasculature with a special focus on detecting the active new vessels through leakage, the pattern of vasculature at the vascular avascular (V-Av) junction, and delineation of the persistent avascular retina (PAR). Seven eyes were confirmed with reactivation of ROP requiring treatment while the rest were followed up. None of the subjects had dye or procedure-related systemic adverse events. Conclusion NC-UWF-OFDA is safe and effective in the diagnosis of reactivation of ROP following anti-VEGF injections. A better appreciation of retinal vascular dynamics with accurate delineation of the posterior extent of capillary non-perfusion areas, PAR, and early definitive detection of active neovascularization helped in formulating the extent of laser treatment needed including intraoperatively. This helped us avoid unnecessary parenteral injections/general anaesthesia for evaluation of disease reactivation and helped avoid over-treatment of cases having clinical suspicion of reactivation during fundoscopy.
AbstractList Objective Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease reactivation in babies treated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) for Aggressive Retinopathy of Prematurity (A-ROP). Methods Eyes clinically suspected to have a possible or definite reactivation after anti-VEGF injection were included in this pilot study. NC-UWF-OFDA was performed in the office setting. Imaging was done prospectively in preterm babies with A-ROP injected with anti-VEGF. OFDA images were analysed for signs of reactivation. Results A total of 20 eyes of 10 preterm babies treated with anti-VEGF underwent NC-UWF-OFDA imaging. The OFDA images were analysed to assess the pattern and dynamics of retinal vasculature with a special focus on detecting the active new vessels through leakage, the pattern of vasculature at the vascular avascular (V-Av) junction, and delineation of the persistent avascular retina (PAR). Seven eyes were confirmed with reactivation of ROP requiring treatment while the rest were followed up. None of the subjects had dye or procedure-related systemic adverse events. Conclusion NC-UWF-OFDA is safe and effective in the diagnosis of reactivation of ROP following anti-VEGF injections. A better appreciation of retinal vascular dynamics with accurate delineation of the posterior extent of capillary non-perfusion areas, PAR, and early definitive detection of active neovascularization helped in formulating the extent of laser treatment needed including intraoperatively. This helped us avoid unnecessary parenteral injections/general anaesthesia for evaluation of disease reactivation and helped avoid over-treatment of cases having clinical suspicion of reactivation during fundoscopy.
Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease reactivation in babies treated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) for Aggressive Retinopathy of Prematurity (A-ROP). Eyes clinically suspected to have a possible or definite reactivation after anti-VEGF injection were included in this pilot study. NC-UWF-OFDA was performed in the office setting. Imaging was done prospectively in preterm babies with A-ROP injected with anti-VEGF. OFDA images were analysed for signs of reactivation. A total of 20 eyes of 10 preterm babies treated with anti-VEGF underwent NC-UWF-OFDA imaging. The OFDA images were analysed to assess the pattern and dynamics of retinal vasculature with a special focus on detecting the active new vessels through leakage, the pattern of vasculature at the vascular avascular (V-Av) junction, and delineation of the persistent avascular retina (PAR). Seven eyes were confirmed with reactivation of ROP requiring treatment while the rest were followed up. None of the subjects had dye or procedure-related systemic adverse events. NC-UWF-OFDA is safe and effective in the diagnosis of reactivation of ROP following anti-VEGF injections. A better appreciation of retinal vascular dynamics with accurate delineation of the posterior extent of capillary non-perfusion areas, PAR, and early definitive detection of active neovascularization helped in formulating the extent of laser treatment needed including intraoperatively. This helped us avoid unnecessary parenteral injections/general anaesthesia for evaluation of disease reactivation and helped avoid over-treatment of cases having clinical suspicion of reactivation during fundoscopy.
Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease reactivation in babies treated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) for Aggressive Retinopathy of Prematurity (A-ROP).OBJECTIVEUtility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease reactivation in babies treated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) for Aggressive Retinopathy of Prematurity (A-ROP).Eyes clinically suspected to have a possible or definite reactivation after anti-VEGF injection were included in this pilot study. NC-UWF-OFDA was performed in the office setting. Imaging was done prospectively in preterm babies with A-ROP injected with anti-VEGF. OFDA images were analysed for signs of reactivation.METHODSEyes clinically suspected to have a possible or definite reactivation after anti-VEGF injection were included in this pilot study. NC-UWF-OFDA was performed in the office setting. Imaging was done prospectively in preterm babies with A-ROP injected with anti-VEGF. OFDA images were analysed for signs of reactivation.A total of 20 eyes of 10 preterm babies treated with anti-VEGF underwent NC-UWF-OFDA imaging. The OFDA images were analysed to assess the pattern and dynamics of retinal vasculature with a special focus on detecting the active new vessels through leakage, the pattern of vasculature at the vascular avascular (V-Av) junction, and delineation of the persistent avascular retina (PAR). Seven eyes were confirmed with reactivation of ROP requiring treatment while the rest were followed up. None of the subjects had dye or procedure-related systemic adverse events.RESULTSA total of 20 eyes of 10 preterm babies treated with anti-VEGF underwent NC-UWF-OFDA imaging. The OFDA images were analysed to assess the pattern and dynamics of retinal vasculature with a special focus on detecting the active new vessels through leakage, the pattern of vasculature at the vascular avascular (V-Av) junction, and delineation of the persistent avascular retina (PAR). Seven eyes were confirmed with reactivation of ROP requiring treatment while the rest were followed up. None of the subjects had dye or procedure-related systemic adverse events.NC-UWF-OFDA is safe and effective in the diagnosis of reactivation of ROP following anti-VEGF injections. A better appreciation of retinal vascular dynamics with accurate delineation of the posterior extent of capillary non-perfusion areas, PAR, and early definitive detection of active neovascularization helped in formulating the extent of laser treatment needed including intraoperatively. This helped us avoid unnecessary parenteral injections/general anaesthesia for evaluation of disease reactivation and helped avoid over-treatment of cases having clinical suspicion of reactivation during fundoscopy.CONCLUSIONNC-UWF-OFDA is safe and effective in the diagnosis of reactivation of ROP following anti-VEGF injections. A better appreciation of retinal vascular dynamics with accurate delineation of the posterior extent of capillary non-perfusion areas, PAR, and early definitive detection of active neovascularization helped in formulating the extent of laser treatment needed including intraoperatively. This helped us avoid unnecessary parenteral injections/general anaesthesia for evaluation of disease reactivation and helped avoid over-treatment of cases having clinical suspicion of reactivation during fundoscopy.
Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease reactivation in babies treated with intravitreal anti-vascular endothelial growth factor (anti-VEGF) for Aggressive Retinopathy of Prematurity (A-ROP).Eyes clinically suspected to have a possible or definite reactivation after anti-VEGF injection were included in this pilot study. NC-UWF-OFDA was performed in the office setting. Imaging was done prospectively in preterm babies with A-ROP injected with anti-VEGF. OFDA images were analysed for signs of reactivation.A total of 20 eyes of 10 preterm babies treated with anti-VEGF underwent NC-UWF-OFDA imaging. The OFDA images were analysed to assess the pattern and dynamics of retinal vasculature with a special focus on detecting the active new vessels through leakage, the pattern of vasculature at the vascular avascular (V-Av) junction, and delineation of the persistent avascular retina (PAR). Seven eyes were confirmed with reactivation of ROP requiring treatment while the rest were followed up. None of the subjects had dye or procedure-related systemic adverse events.NC-UWF-OFDA is safe and effective in the diagnosis of reactivation of ROP following anti-VEGF injections. A better appreciation of retinal vascular dynamics with accurate delineation of the posterior extent of capillary non-perfusion areas, PAR, and early definitive detection of active neovascularization helped in formulating the extent of laser treatment needed including intraoperatively. This helped us avoid unnecessary parenteral injections/general anaesthesia for evaluation of disease reactivation and helped avoid over-treatment of cases having clinical suspicion of reactivation during fundoscopy.
Author Belenje, Akash
Reddy, Rakasi Ugandhar
Jalali, Subhadra
Padhi, Tapas Ranjan
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Snippet Objective Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess...
Utility, safety, and feasibility study of office-based Non-contact Ultra widefield Oral Fundus Fluorescein Dye Angiography (NC-UWF-OFDA) to assess disease...
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Anesthesia
Angiogenesis Inhibitors - therapeutic use
Angiography
Bevacizumab
Birth weight
Disease
Drug dosages
Dyes
Eye
Feasibility Studies
Female
Fluorescein
Fluorescein Angiography - methods
Fundus Oculi
Gestational Age
Histamine
Humans
Infant, Newborn
Infant, Premature
Intravitreal Injections
Laboratory Medicine
Lasers
Male
Medical imaging
Medicine
Medicine & Public Health
Neonates
Ophthalmology
Pediatrics
Pharmaceutical Sciences/Technology
Pilot Projects
Premature babies
Prospective Studies
Pulse oximetry
Retina
Retinal detachment
Retinal Vessels - pathology
Retinopathy
Retinopathy of Prematurity - diagnosis
Retinopathy of Prematurity - drug therapy
Sodium
Surgery
Surgical Oncology
Tomography
Vascular endothelial growth factor
Vascular Endothelial Growth Factor A - antagonists & inhibitors
Vascularization
Title Oral fundus fluorescein angiogram detects reactivation post anti-VEGF in aggressive retinopathy of prematurity
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Volume 39
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