With a deep learning-based approach using TensorFlow™, it is possible to detect AMD in SD-OCT with high sensitivity and specificity. With more image data, an expansion of this classifier for other macular diseases or further details in AMD is possible, suggesting an application for this model as a support in clinical decisions. Another possible future application would involve the individual prediction of the progress and success of therapy for different diseases by automatically detecting hidden image information.
Prior to both qualitative and quantitative analysis, OCT-A images must be carefully reviewed as motion artifacts and segmentation errors in current OCT-A technology are frequent particularly in pathologically altered maculae.
The choriocapillaris (CC) represents a fundamentally important vascular layer that is subject to physiologic changes with increasing age and that is also associated with a wide range of chorioretinal diseases. So far, information on blood flow in this specific layer has remained limited. With the advent of optical coherence tomography angiography (OCTA), new perspectives and possibilities of CC imaging have begun to evolve. This article shall review the opportunities and challenges of applying OCTA technology to the CC layer and summarize the current clinical efforts in OCTA CC imaging exemplarily in dry age-related macular degeneration and central serous chorioretinopathy.
In patients with AMD, active ET technology offers an improved image quality in OCT-A imaging regarding presence of motion artifacts at the expense of higher acquisition time.
Purpose:
To evaluate a deep learning–based method to automatically detect graft detachment (GD) after Descemet membrane endothelial keratoplasty (DMEK) in anterior segment optical coherence tomography (AS-OCT).
Methods:
In this study, a total of 1172 AS-OCT images (609: attached graft; 563: detached graft) were used to train and test a deep convolutional neural network to automatically detect GD after DMEK surgery in AS-OCT images. GD was defined as a not completely attached graft. After training with 1072 of these images (559: attached graft; 513: detached graft), the created classifier was tested with the remaining 100 AS-OCT scans (50: attached graft; 50 detached: graft). Hereby, a probability score for GD (GD score) was determined for each of the tested OCT images.
Results:
The mean GD score was 0.88 ± 0.2 in the GD group and 0.08 ± 0.13 in the group with an attached graft. The differences between both groups were highly significant (P < 0.001). The sensitivity of the classifier was 98%, the specificity 94%, and the accuracy 96%. The coefficient of variation was 3.28 ± 6.90% for the GD group and 2.82 ± 3.81% for the graft attachment group.
Conclusions:
With the presented deep learning-based classifier, reliable automated detection of GD after DMEK is possible. Further work is needed to incorporate information about the size and position of GD and to develop a standardized approach regarding when rebubbling may be needed.
For the first time, this study describes the use of a deep learning-based algorithm to automatically detect and classify GA in FAF. Hereby, the created classifiers showed excellent results. With further developments, this model may be a tool to predict the individual progression risk of GA and give relevant information for future therapeutic approaches.
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