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Thomas S. Hwang

Publications and source records attributed to Thomas S. Hwang.

10 recordsLinked to original sources

Automated Volumetric Segmentation of Microaneurysms on OCT Using Artificial Intelligence

Purpose: To develop and validate a deep learning-based method for the automated identification and volumetric segmentation of microaneurysms (MAs) in diabetic retinopathy (DR) using OCT. Participants: A total of 125 participants were enrolled, including 20 healthy eyes, 27 with mild NPDR, 30 with moderate NPDR, 30 with severe NPDR, and 18 with PDR. Methods: We obtained multiple repeated 3x3-mm scans from each participant using a commercial 120-kHz spectral-domain OCT system (Solix; Visionix/Optovue, Inc., California, USA), which were registered and averaged to generate high-definition volumes. We developed a 3D deep learning network to segment MAs volumetrically. The input to the network consists of the original OCT volume concatenated with its reflectance-inverted counterpart. Expert graders manually delineated MAs to generate annotations. We evaluated model performance at multiple levels, including voxel-level segmentation, lesion-level detection, and eye-level diagnosis. Results: In the test dataset (20 healthy, 20 DR eyes), the algorithm demonstrated high voxel-level accuracy, with F1 scores of 79.2% on single volumes and 86.1% on averaged volumes. Lesion-level detection reached an F1 score of 96.0% (single) and 97.1% (averaged), while scan-level diagnostic accuracy for MA presence was 97.5% (single and averaged). Conclusions: A deep learning-based method can accurately identify and segment MAs volumetrically on OCT, enabling quantification and characterization, and potentially aiding in the diagnosis, monitoring, and management of DR.

q-bio.QM

Three-Dimensional Retinal Microvasculature Restoration in OCT Angiography

Optical coherence tomographic angiography (OCTA) is a powerful technique for imaging retinal microvasculature. However, acquiring reliable quantification of retinal blood flow and areas of retinal nonperfusion is challenging because of imaging artifacts. Existing methods primarily focus on noise suppression, projection artifact removal, or signal enhancement to improve the image quality of OCTA in cross-sectional or two-dimensional (2D) en face projections, while neglecting the intrinsic three-dimensional vascular architecture. In this study, we propose a deep learning-based algorithm for restoring capillary anatomical vasculature from a single OCTA volume. The network consists of an EfficientNet-B5 encoder and a decoder incorporating concurrent spatial and channel squeeze-and-excitation modules, connected via skip connections to preserve spatial resolution. Three adjacent B-frames are used as input to predict the restored middle B-frame. We evaluated the performance of the model using the peak signal-to-noise ratio (PSNR) and structural similarity index measure (SSIM) against ground truth generated from averaging multiple scans. The results show that the proposed model significantly (both p < 0.001) improved image quality compared with the original single OCTA volume, with a PSNR of 26.16 +/- 1.26 vs. 22.23 +/- 0.78 and an SSIM of 0.91 +/- 0.02 vs. 0.72 +/- 0.03. The proposed model also significantly (p < 0.001) improved microvascular fidelity, measured by the Dice coefficient overlap between the model output and ground truth, in both 2D and 3D by at least 3.8% and 51.2%, respectively, across several different vascular slabs.

cs.CV

Robust Detection of Retinal Neovascularization in Widefield Optical Coherence Tomography

Retinal neovascularization (RNV) is a vision threatening development in diabetic retinopathy (DR). Vision loss associated with RNV is preventable with timely intervention, making RNV clinical screening and monitoring a priority. Optical coherence tomography (OCT) angiography (OCTA) provides high-resolution imaging and high-sensitivity detection of RNV lesions. With recent commercial devices introducing widefield OCTA imaging to the clinic, the technology stands to improve early detection of RNV pathology. However, to meet clinical requirements these imaging capabilities must be combined with effective RNV detection and quantification, but existing algorithms for OCTA images are optimized for conventional, i.e. narrow, fields of view. Here, we present a novel approach for RNV diagnosis and staging on widefield OCT/OCTA. Unlike conventional methods dependent on multi-layer retinal segmentation, our model reframes RNV identification as a direct binary localization task. Our fully automated approach was trained and validated on 589 widefield scans (17x17-mm to 26x21-mm) collected from multiple devices at multiple clinics. Our method achieved a device-dependent area under curve (AUC) ranging from 0.96 to 0.99 for RNV diagnosis, and mean intersection over union (IOU) ranging from 0.76 to 0.88 for segmentation. We also demonstrate our method's ability to monitor lesion growth longitudinally. Our results indicate that deep learning-based analysis for widefield OCTA images could offer a valuable means for improving RNV screening and management.

eess.IV

AI-derived layer-specific OCT biomarkers for classification of geographic atrophy

Geographic atrophy (GA) is a key biomarker of dry age-related macular degeneration (AMD) traditionally identified through color fundus photography. Hyper-transmission defects (hyperTDs), a feature highly correlated with GA, have recently gained prominence in optical coherence tomography (OCT) research. OCT offers cross-sectional imaging of the retina, leading to the development of the terms complete retinal pigment epithelium and outer retinal atrophy (cRORA) to describe specific patterns of structural degeneration. Within the definitions of cRORA three critical lesions are implicated: inner nuclear layer and outer plexiform layer (INL-OPL) subsidence, ellipsoid zone and retinal pigment epithelium (EZ-RPE) disruption, and hyperTDs. To enable the automated quantification of retinal atrophy progression, we propose an AI-based model that segments INL-OPL subsidence, EZ-RPE disruption, and hyperTDs. Additionally, we developed an algorithm that leverages these segmentation results to distinguish cRORA from hyperTDs in the absence of GA. We evaluated our approach on a comprehensive dataset of eyes with AMD and healthy eyes, achieving mean voxel-level F1-scores of 0.76/0.13 (mean/standard deviation) for INL-OPL subsidence, 0.64/0.15 for EZ-RPE disruption, and 0.69/0.04 for hyperTDs. For distinguishing cRORA from hyperTDs, we achieved an average pixel-level F1-score of 0.80/0.12 for segment cRORA from hyperTDs. This method demonstrates significant advances in the quantitative analysis of retinal atrophy, offering a promising tool for improved AMD diagnosis and disease progression monitoring.

q-bio.QM

Nonperfused Retinal Capillaries -- A New Method Developed on OCT and OCTA

To develop a new method to quantify nonperfused retinal capillaries (NPCs) by using co-registered optical coherence tomography (OCT) and OCT angiography (OCTA), and to evaluate NPCs in eyes with age-related macular degeneration (AMD) and diabetic retinopathy (DR). Multiple consecutive 3x3-mm OCT/OCTA scans were obtained using a commercial device (Solix; Visionix/Optovue, Inc., California, USA). We averaged multiple registered OCT/OCTA scans to create high-definition volumes. The deep capillary plexus slab was defined and segmented. A novel deep learning denoising algorithm removed tissue background noise from capillaries in the en face OCT/OCTA. The algorithm segmented NPCs by identifying capillaries from OCT without corresponding flow signals in the OCTA. We then investigated the relationships between NPCs and known features in AMD and DR. The denoised en face OCT/OCTA revealed the structure and flow of the capillaries. The automatically segmented NPC achieved an accuracy of 88.2% compared to manual grading of DR. Compared to healthy controls, both the mean number and total length (mm) of NPCs were significantly increased in eyes with AMD and eyes with DR (P < 0.001). Compared to early and intermediate AMD, the number and total length of NPCs were significantly higher in advanced AMD (number: P<0.001, P<0.001; total length: P = 0.002, P =0.003). Geography atrophy, macular neovascularization, drusen volume, and extrafoveal avascular area (EAA) significantly correlated with increased NPCs (P<0.05). In eyes with DR, NPCs correlated with the number of microaneurysms and EAA (P<0.05). The presence of fluid did not significantly correlate with NPCs in AMD and DR. Conclusions A deep learning-based algorithm can segment and quantify retinal capillaries that lack flow using colocalized OCT/OCTA. This novel biomarker may be useful in AMD and DR.

q-bio.QM

Perfused and Nonperfused Microaneurysms Identified and Characterized by Structural and Angiographic OCT

Purpose: Microaneurysms (MAs) have distinct, oval-shaped, hyperreflective walls on structural OCT, and inconsistent flow signal in the lumen with OCT angiography (OCTA). Their relationship to regional macular edema in diabetic retinopathy (DR) has not been quantitatively explored. Participants: A total of 99 participants, including 23 with mild, NPDR, 25 with moderate NPDR, 34 with severe NPDR, and 17 with proliferative DR. Methods: We obtained 3 x 3-mm scans with a commercial device (Solix, Visionix/Optovue) in 99 patients with DR. Trained graders manually identified MAs and their location relative to the anatomic layers from cross-sectional OCT. Microaneurysms were first classified as perfused if flow signal was present in the OCTA channel. Then, perfused MAs were further classified into fully and partially perfused MAs based on the flow characteristics in en face OCTA. The presence of retinal fluid based on OCT near MAs was compared between perfused and nonperfused types. We also compared OCT-based MA detection to fundus photography (FP)- and fluorescein angiography (FA)-based detection. Results: We identified 308 MAs (166 fully perfused, 88 partially perfused, 54 nonperfused) in 42 eyes using OCT and OCTA. Nearly half of the MAs identified in this study straddle the inner nuclear layer and outer plexiform layer. Compared with partially perfused and nonperfused MAs, fully perfused MAs were more likely to be associated with local retinal fluid. The associated fluid volumes were larger with fully perfused MAs compared with other types. OCT/OCTA detected all MAs found on FP. Although not all MAs seen with FA were identified with OCT, some MAs seen with OCT were not visible with FA or FP. Conclusions: OCT-identified MAs with colocalized flow on OCTA are more likely to be associated with DME than those without flow.

q-bio.QM

Interpretable Diabetic Retinopathy Diagnosis based on Biomarker Activation Map

Deep learning classifiers provide the most accurate means of automatically diagnosing diabetic retinopathy (DR) based on optical coherence tomography (OCT) and its angiography (OCTA). The power of these models is attributable in part to the inclusion of hidden layers that provide the complexity required to achieve a desired task. However, hidden layers also render algorithm outputs difficult to interpret. Here we introduce a novel biomarker activation map (BAM) framework based on generative adversarial learning that allows clinicians to verify and understand classifiers decision-making. A data set including 456 macular scans were graded as non-referable or referable DR based on current clinical standards. A DR classifier that was used to evaluate our BAM was first trained based on this data set. The BAM generation framework was designed by combing two U-shaped generators to provide meaningful interpretability to this classifier. The main generator was trained to take referable scans as input and produce an output that would be classified by the classifier as non-referable. The BAM is then constructed as the difference image between the output and input of the main generator. To ensure that the BAM only highlights classifier-utilized biomarkers an assistant generator was trained to do the opposite, producing scans that would be classified as referable by the classifier from non-referable scans. The generated BAMs highlighted known pathologic features including nonperfusion area and retinal fluid. A fully interpretable classifier based on these highlights could help clinicians better utilize and verify automated DR diagnosis.

eess.IV

DcardNet: Diabetic Retinopathy Classification at Multiple Levels Based on Structural and Angiographic Optical Coherence Tomography

Objective: Optical coherence tomography (OCT) and its angiography (OCTA) have several advantages for the early detection and diagnosis of diabetic retinopathy (DR). However, automated, complete DR classification frameworks based on both OCT and OCTA data have not been proposed. In this study, a convolutional neural network (CNN) based method is proposed to fulfill a DR classification framework using en face OCT and OCTA. Methods: A densely and continuously connected neural network with adaptive rate dropout (DcardNet) is designed for the DR classification. In addition, adaptive label smoothing was proposed and used to suppress overfitting. Three separate classification levels are generated for each case based on the International Clinical Diabetic Retinopathy scale. At the highest level the network classifies scans as referable or non-referable for DR. The second level classifies the eye as non-DR, non-proliferative DR (NPDR), or proliferative DR (PDR). The last level classifies the case as no DR, mild and moderate NPDR, severe NPDR, and PDR. Results: We used 10-fold cross-validation with 10% of the data to assess the networks performance. The overall classification accuracies of the three levels were 95.7%, 85.0%, and 71.0% respectively. Conclusion/Significance: A reliable, sensitive and specific automated classification framework for referral to an ophthalmologist can be a key technology for reducing vision loss related to DR.

eess.IV

Automated segmentation of retinal fluid volumes from structural and angiographic optical coherence tomography using deep learning

Purpose: We proposed a deep convolutional neural network (CNN), named Retinal Fluid Segmentation Network (ReF-Net) to segment volumetric retinal fluid on optical coherence tomography (OCT) volume. Methods: 3 x 3-mm OCT scans were acquired on one eye by a 70-kHz OCT commercial AngioVue system (RTVue-XR; Optovue, Inc.) from 51 participants in a clinical diabetic retinopathy (DR) study (45 with retinal edema and 6 healthy controls). A CNN with U-Net-like architecture was constructed to detect and segment the retinal fluid. Cross-sectional OCT and angiography (OCTA) scans were used for training and testing ReF-Net. The effect of including OCTA data for retinal fluid segmentation was investigated in this study. Volumetric retinal fluid can be constructed using the output of ReF-Net. Area-under-Receiver-Operating-Characteristic-curve (AROC), intersection-over-union (IoU), and F1-score were calculated to evaluate the performance of ReF-Net. Results: ReF-Net shows high accuracy (F1 = 0.864 +/- 0.084) in retinal fluid segmentation. The performance can be further improved (F1 = 0.892 +/- 0.038) by including information from both OCTA and structural OCT. ReF-Net also shows strong robustness to shadow artifacts. Volumetric retinal fluid can provide more comprehensive information than the 2D area, whether cross-sectional or en face projections. Conclusions: A deep-learning-based method can accurately segment retinal fluid volumetrically on OCT/OCTA scans with strong robustness to shadow artifacts. OCTA data can improve retinal fluid segmentation. Volumetric representations of retinal fluid are superior to 2D projections. Translational Relevance: Using a deep learning method to segment retinal fluid volumetrically has the potential to improve the diagnostic accuracy of diabetic macular edema by OCT systems.

eess.IV

High-resolution wide-field OCT angiography with a self-navigation method to correct microsaccades and blinks

In this study, we demonstrate a novel self-navigated motion correction method that suppresses eye motion and blinking artifacts on wide-field optical coherence tomographic angiography (OCTA) without requiring any hardware modification. Highly efficient GPU-based, real-time OCTA image acquisition and processing software was developed to detect eye motion artifacts. The algorithm includes an instantaneous motion index that evaluates the strength of motion artifact on en face OCTA images. Areas with suprathreshold motion and eye blinking artifacts are automatically rescanned in real-time. Both healthy eyes and eyes with diabetic retinopathy were imaged, and the self-navigated motion correction performance was demonstrated.

physics.med-ph