Objective Evaluation of Proliferative Diabetic Retinopathy Using OCT.
Schwartz Roy, Khalid Hagar, Sivaprasad Sobha, Nicholson Luke, Anikina Evgenia, Sullivan Paul, Patel Praveen J, Balaskas Konstantinos, Keane Pearse A
AI Summary
OCT and OCTA objectively assessed PDR. Structural OCT best detected new neovascularization, while B-scan OCTA excelled at monitoring regression/reactivation, improving PDR management.
Abstract
Purpose
To present the routine use of OCT and OCT angiography (OCTA) for the objective diagnosis and monitoring of proliferative diabetic retinopathy (PDR).
Design
Retrospective, observational case series.
Participants
Patients with diabetic retinopathy imaged using a standardized PDR protocol.
Methods
Patients routinely imaged with a standardized PDR protocol between March 2017 and January 2019 were included. This included a 12×9-mm structural OCT volume centered on the macula and a 6×6-mm OCTA scan centered on the optic nerve head obtained using a Topcon swept-source system (DRI OCT-1 Triton, Topcon, Tokyo, Japan). Ultra-widefield fluorescein angiography (FA) was also performed when clinically indicated. The ground truth for each case was determined by merging the findings from biomicroscopy and imaging modalities to generate the maximum level of detection for each finding.
Main outcome measures
Detection rates of new-onset, regression, and reactivation of neovascularization of the disc (NVD) and neovascularization elsewhere (NVE) using different modalities (biomicroscopy/color photography, structural OCT, B-scan OCTA, en face OCTA). Detection of progression of tractional retinal detachment (TRD).
Results
A total of 383 eyes of 204 patients were evaluated. After excluding patients without PDR or with insufficient image quality, 47 eyes of 35 patients were included. For the detection of new-onset NVD and NVE, structural OCT had the highest detection rate (100%) of all modalities. However, for the detection of regression or reactivation of neovascularization (NV), B-scan OCTA had the highest detection rate (100%). Structural OCT detected regression only in 45.5% of cases, resulting in a low detection rate of reactivation (12.5%). Among 10 eyes with TRD, OCT detected fovea-threatening TRD during follow-up in 7 eyes, resulting in vitrectomy.
Conclusions
This study demonstrates the utility of novel multimodal imaging in the daily management of patients with PDR. Posterior pole structural OCT had the best detection rate for NV, and B-scan OCTA showed the most potential for objective monitoring of disease after treatment.
MeSH Terms
Shields Classification
Key Concepts5
In a retrospective, observational case series of 47 eyes of 35 patients with proliferative diabetic retinopathy (PDR), structural OCT had the highest detection rate (100%) for new-onset neovascularization of the disc (NVD) and neovascularization elsewhere (NVE) among all modalities (biomicroscopy/color photography, structural OCT, B-scan OCTA, en face OCTA).
In a retrospective, observational case series of 47 eyes of 35 patients with proliferative diabetic retinopathy (PDR), B-scan OCTA had the highest detection rate (100%) for regression or reactivation of neovascularization (NV).
In a retrospective, observational case series of 47 eyes of 35 patients with proliferative diabetic retinopathy (PDR), structural OCT detected regression of neovascularization in only 45.5% of cases, resulting in a low detection rate of reactivation (12.5%).
In a retrospective, observational case series of 10 eyes with tractional retinal detachment (TRD) in patients with proliferative diabetic retinopathy (PDR), OCT detected fovea-threatening TRD during follow-up in 7 eyes, leading to vitrectomy.
A retrospective, observational case series evaluated 383 eyes of 204 patients with diabetic retinopathy, ultimately including 47 eyes of 35 patients with proliferative diabetic retinopathy (PDR) and sufficient image quality, using a standardized PDR protocol including a 12x9-mm structural OCT volume and a 6x6-mm OCTA scan, with ultra-widefield fluorescein angiography (FA) performed when clinically indicated.
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