Incidence of Total Blindness After Central Retinal Artery Occlusion With Ocular Neovascularization.
Harshvardhan ChawlaHayley J RedrickJoshua T PannellNathaniel P GoldblattD Anthony MazzullaJoseph D BeneventoSidharth PuriPublished in: Journal of vitreoretinal diseases (2023)
Purpose: To determine the time-based incidence of total blindness after central retinal artery occlusion (CRAO) with secondary ocular neovascularization (ONV). Methods: In this retrospective cohort study, electronic records were queried using ICD-9 and ICD-10 codes to identify patients with secondary ONV post-CRAO. Patients with possible alternative ONV etiologies, previous panretinal photocoagulation (PRP), and/or previous antivascular endothelial growth factor (anti-VEGF) therapy were excluded. Clinical data included demographics, medical comorbidities, ONV manifestations, medical/surgical management, and best-corrected visual acuity (BCVA). Kaplan-Meier analysis was performed with total blindness (defined as a BCVA of no light perception) as the outcome of interest. Results: Of 345 eyes with CRAO, 34 met the inclusion criteria with a mean (±SD) follow-up of 22.0 ± 26.2 months. ONV management included PRP (70.6%), glaucoma drainage implant surgery or transscleral cyclophotocoagulation (32.4%), and intravitreal anti-VEGF therapy (mean 2.8 ± 5.6 injections per patient). The cumulative incidence of total blindness was 49.4% (95% confidence interval, 27.2%-71.6%) at 24 months, with 53.3% of cases occurring within 4 months of ONV onset. Conclusions: Post-CRAO ONV is associated with a high risk for progression from severe vision loss to total blindness. Neovascular glaucoma can present up to 4 months after CRAO, challenging the paradigm of "30-day-glaucoma." Routine gonioscopy should extend through this period, while glaucoma surgery can delay further vision loss. These findings can be used to counsel patients on the importance of follow-up adherence.
Keyphrases
- diabetic retinopathy
- optic nerve
- vascular endothelial growth factor
- optical coherence tomography
- growth factor
- endothelial cells
- risk factors
- minimally invasive
- healthcare
- coronary artery bypass
- platelet rich plasma
- ejection fraction
- end stage renal disease
- cataract surgery
- newly diagnosed
- age related macular degeneration
- surgical site infection
- stem cells
- bone marrow
- artificial intelligence
- tyrosine kinase
- mesenchymal stem cells
- coronary artery disease
- glycemic control
- percutaneous coronary intervention
- soft tissue