In medical image processing, many filters have been developed to enhance certain structures in 3-D data. In this paper, we propose to use pattern recognition techniques to design more optimal filters. The essential difference with previous approaches is that we provide a system with examples of what it should enhance and suppress. This training data is used to construct a classifier that determines the probability that a voxel in an unseen image belongs to the target structure(s). The output of a rich set of basis filters serves as input to the classifier. In a feature selection process, this set is reduced to a compact, efficient subset. We show that the output of the system can be reused to extract new features, using the same filters, that can be processed by a new classifier. Such a multistage approach further improves performance. While the approach is generally applicable, in this work the focus is on enhancing pulmonary fissures in 3-D computed tomography (CT) chest scans. A supervised fissure enhancement filter is evaluated on two data sets, one of scans with a normal clinical dose and one of ultra-low dose scans. Results are compared with those of a recently proposed conventional fissure enhancement filter. It is demonstrated that both methods are able to enhance fissures, but the supervised approach shows better performance; the areas under the receiver operating characteristic (ROC) curve are 0.98 versus 0.90, for the normal dose data and 0.97 versus 0.87 for the ultra low dose data, respectively.
The malignancy of lung nodules is most often detected by analyzing changes of the nodule diameter in follow-up scans. A recent study showed that comparing the volume or the mass of a nodule over time is much more significant than comparing the diameter. Since the survival rate is higher when the disease is still in an early stage it is important to detect the growth rate as soon as possible. However manual segmentation of a volume is time-consuming. Whereas there are several well evaluated methods for the segmentation of solid nodules, less work is done on subsolid nodules which actually show a higher malignancy rate than solid nodules. In this work we present a fast, semi-automatic method for segmentation of subsolid nodules. As minimal user interaction the method expects a user-drawn stroke on the largest diameter of the nodule. First, a threshold-based region growing is performed based on intensity analysis of the nodule region and surrounding parenchyma. In the next step the chest wall is removed by a combination of a connected component analyses and convex hull calculation. Finally, attached vessels are detached by morphological operations. The method was evaluated on all nodules of the publicly available LIDC/IDRI database that were manually segmented and rated as non-solid or part-solid by four radiologists (Dataset 1) and three radiologists (Dataset 2). For these 59 nodules the Jaccard index for the agreement of the proposed method with the manual reference segmentations was 0.52/0.50 (Dataset 1/Dataset 2) compared to an inter-observer agreement of the manual segmentations of 0.54/0.58 (Dataset 1/Dataset 2). Furthermore, the inter-observer agreement using the proposed method (i.e. different input strokes) was analyzed and gave a Jaccard index of 0.74/0.74 (Dataset 1/Dataset 2). The presented method provides satisfactory segmentation results with minimal observer effort in minimal time and can reduce the inter-observer variability for segmentation of subsolid nodules in clinical routine.
Abstract.A method for automatic extraction and labeling of the airway tree from thoracic CT scans is presented and extensively evaluated on 150 scans of clinical dose, low dose and ultra-low dose data, in inspiration and expiration from both relatively healthy and severely ill patients. The method uses adaptive thresholds while growing the airways and it is shown that this strategy leads to a substantial increase in the number, total length and number of correctly labeled airways extracted. From inspiration scans on average 170 branches are found, from expiration scans 59.
Airway wall thickening in cigarette smokers is thought to be a result of inflammatory changes and airway remodeling. This study investigates if CT-derived airway wall thickening associates to disease severity in smokers with and without COPD and if airway wall thickening is reversible by smoking cessation. We examined 2000 smokers and 46 never-smokers who returned for a 5-year follow-up visit in the COPDGene-study. Multivariable regression analyses were performed at visit 1 to associate airway wall thickness (expressed as Pil0) with percent predicted forced expiratory volume in one second (FEV1%-predicted), 6-minute walking distance (6MWD), and St. George Respiratory Questionnaire (SGRQ). Longitudinal analyses were performed to assess the effect of smoking cessation on Pi10 using linear mixed models. A higher Pi10 was significantly associated with worse FEV1%-predicted, 6MWD, and SGRQ in all GOLD-stages. Longitudinal analyses showed that subjects that quit smoking significantly decreased in Pil0 (ΔPil0=−0.18mm, p<0.001). Subjects that started smoking had a significant increase in Pil0 (ΔPil0=0.14mm, p<0.001). Pil0 is a clinically relevant biomarker of smoking-related airway injury in smokers with and without COPD. The change in Pil0 with change in smoking status suggests that it can quantify a reversible component of smoking-related airway inflammation.
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