Table 3. Overview of quantification approaches for fibred endoscopic imaging.
Organ (System) | Quantifying | References | Methodology | Comments |
---|---|---|---|---|
Circulatory | Red blood cell velocity. | Savoire et al. (2004) | Thresholding and line-fitting (M-estimators) translated (through trigonometry) to RBC velocity. | Inventive use of known and quantifiable artefact in raster scanning imaging systems for deriving physiological information. Preliminary results with uncertain clinical relevance. |
Perchant et al. (2007) | ROI tracking and alignment through (i) scanning distortion compensation, and (ii) global affine registration, for blood velocity estimation through spatio-temporal correlation. | Feasibility study. Preliminary results with uncertain clinical relevance. |
||
Oropharyngeal | Epithelial cells in vocal chords. | Mualla et al. (2014) | Watershed segmentation (borders) and local minima detection (location). | Empirical, ad-hoc approach employing off-the-shelf image analysis methods. Limited data can potentially lead to poor generalisation of the proposed methodology. |
Gastro-intestinal | Intestinal crypts in Inflammatory Bowel Disease. (eCLE) | Couceiro et al. (2012) | Detecting (local maxima), segmenting (ellipse fitting on edge detection) and quantifying (number, connectivity). | Empirical, ad-hoc approaches employing off-the-shelf image analysis methods Heuristic parameter estimation, hard thresholds and limited data can potentially lead to poor generalisation of the proposed methodologies. |
Intestinal crypts in colorectal polyps. | Prieto et al. (2016) | Contrast enhancement, thresholding (Otsu’s) and morphological filters (erosion, centre of mass, circularity). | ||
Goblet cells in villi. (eCLE) | Boschetto et al. (2015a) | Detecting (matched filters), segmenting (Voronoi diagrams) cells and identifying (hard threshold) goblet cells within the villi. | ||
Intestinal villi. (eCLE) | Boschetto et al. (2015b) | Detect via morphological filters (top-hat, morphological reconstruction and closing) and quad-tree decomposition. | ||
Boschetto et al. (2016b) | Subdivide to superpixels, extract features and classify through Random Forests to generate a binary segmentation map. | Employing established data driven approaches with reasonable size of data, resulting on better generalisation potential. | ||
Pulmonary | Alveoli sacs in mice distal lung. | Namati et al. (2008) | Segmenting (optimum separation thresholding) and quantifying (8-point connectivity) alveolar sacs. | Limited data and uncertain translatability to human alveoli sacks due to their large size relative to the limited field of view. |
Stained mesenchymal stem cells in rat lungs. | Perez et al. (2017) | Contrast stretch, denoise (opening), threshold and count (connected component analysis). | Empirical, ad-hoc approach employing off-the-shelf image analysis methods. | |
Stained bacteria in distal lung. | Karam Eldaly et al. (2018) | Outlier detection using a hierarchical Bayesian model along with a MCMC algorithm based on Gibbs sampler. | More elaborate approaches, adopting model-based and data-driven methodologies. | |
Stained bacteria and cells in distal lung. | Seth et al., (2017, 2018) | Bacterial and cellular load using spatio-temporal template matching with a radial basis functions network. | They have potential for good generalisation and translation to clinical applications. |