A Spatiotemporal Illumination Model for 3D Image Fusion in Optical Coherence Tomography

Optical coherence tomography (OCT) is a non-invasive, micrometer-scale imaging modality that has become a clinical standard in ophthalmology. By raster-scanning the retina, sequential cross-sectional image slices are acquired to generate volumetric data. In-vivo imaging suffers from discontinuities between slices that show up as motion and illumination artifacts. We present a new illumination model that exploits continuity in orthogonally raster-scanned volume data. Our novel spatiotemporal parametrization adheres to illumination continuity both temporally, along the imaged slices, as well as spatially, in the transverse directions. Yet, our formulation does not make inter-slice assumptions, which could have discontinuities. This is the first optimization of a 3D inverse model in an image reconstruction context in OCT. Evaluation in 68 volumes from eyes with pathology showed reduction of illumination artifacts in 88\% of the data, and only 6\% showed moderate residual illumination artifacts. The method enables the use of forward-warped motion corrected data, which is more accurate, and enables supersampling and advanced 3D image reconstruction in OCT.

Unsupervised detection of small hyperreflective features in ultrahigh resolution optical coherence tomography

Recent advances in optical coherence tomography such as the development of high speed ultrahigh resolution scanners and corresponding signal processing techniques may reveal new potential biomarkers in retinal diseases. Newly visible features are, for example, small hyperreflective specks in age-related macular degeneration. Identifying these new markers is crucial to investigate potential association with disease progression and treatment outcomes. Therefore, it is necessary to reliably detect these features in 3D volumetric scans. Because manual labeling of entire volumes is infeasible a need for automatic detection arises. Labeled datasets are often not publicly available and there are usually large variations in scan protocols and scanner types. Thus, this work focuses on an unsupervised approach that is based on local peak-detection and random walker segmentation to detect small features on each B-scan of the volume.

Retinal blood flow speed quantification at the capillary level using temporal autocorrelation fitting OCTA

Optical coherence tomography angiography (OCTA) can visualize vasculature structures, but provides limited information about the blood flow speeds. Here, we present a second generation variable interscan time analysis (VISTA) OCTA, which evaluates a quantitative surrogate marker for blood flow speed in vasculature. At the capillary level, spatially compiled OCTA and a simple temporal autocorrelation model, {\rho}({\tau}) = exp(-{\alpha}{\tau}), were used to evaluate a temporal autocorrelation decay constant, {\alpha}, as the blood flow speed marker. A 600 kHz A-scan rate swept-source provides short interscan time OCTA and fine A-scan spacing acquisition, while maintaining multi mm2 field of views for human retinal imaging. We demonstrate the cardiac pulsatility and repeatability of {\alpha} measured with VISTA. We show different {\alpha} for different retinal capillary plexuses in healthy eyes and present representative VISTA OCTA of eyes with diabetic retinopathy.