A system and method are provided for medical imaging that includes acquiring, during a common imaging acquisition process, rotational, x-ray volume image data and x-ray tomosynthesis image data from a subject. The method includes reconstructing a time-resolved three-dimensional (3D) image volume from the rotational, x-ray volume image data and producing a four-dimensional (4D) image series of the subject with resolved overlapping features by selectively combining the time-resolved 3D image volume and the x-ray tomosynthesis imaging data.

A stroke detection system analyzes images of a person's face over time to detect asymmetric changes in the position of certain reference points that are consistent with sagging or drooping that may be symptomatic of a stroke or TIA. On detecting possible symptoms of a stroke or TIA, the system may alert caregivers or others, and log the event in a database. Identifying stroke symptoms automatically may enable more rapid intervention, and identifying TIA symptoms may enable diagnostic and preventative care to reduce the risk of a future stroke.

Methods are provided for operating a medical X-ray device to improve the image quality of an X-ray examination. In one example, the method includes recording at least one first X-ray image of a body region as a mask image; providing a first subsequent image and recording a second X-ray image of the body region, wherein the second X-ray image represents the body region at a later recording time than the first subsequent image; determining a degree of deviation relating to a deviation between the first subsequent image and the second X-ray image; determining an averaging amount in dependence on the degree of deviation; generating a second subsequent image from the second X-ray image or from the first subsequent image together with the second X-ray image, wherein the averaging amount specifies the proportions in which the first subsequent image and the second X-ray image are mixed; and forming an overall image from the mask image and the second subsequent image.

Disclosed are systems and methods for clinical trial assessment of skin disease treatment. The disclosure includes obtaining a series of digital images over a period of time, wherein each digital image includes an affected area of the subject; identifying characteristic morphologies and lesions in the affected area of the subject in each of the digital images; classifying each of the detected and segmented morphologies and lesions into one or more identified categories for each of the digital images; assigning a global score to each of the digital images based on a count of the detected and segmented characteristic morphologies and lesions in each of the one or more identified categories; analyzing the global scores of each of the digital images; and making an assessment of the clinical trial based on the analysis of the global scores of each of the digital images.

A method includes, following specification of an initial transformation as a test transformation that is to be optimized, determining a 2D gradient x-ray image and a 3D gradient dataset of the image dataset, carrying out, for each image element of the gradient comparison image, a check for selection as a contour point, and determining an environment best corresponding to a local environment of the contour point and extending around a comparison point in the gradient x-ray image for all contour points in the at least one gradient comparison image. Local 2D displacement information is determined by comparing the contour points with the associated comparison points, and motion parameters of a 3D motion model describing a movement of the target region between the acquisition of the image dataset and the x-ray image are determined from the displacement information and a registration transformation describing the registration.

A tomographic image generation device includes a projection image acquisition section configured to acquire plural projection images obtained by radiating radiation onto a breast in sequence from plural radiation angles and by performing imaging at each of the plural radiation angles; a mammary gland density acquisition section configured to acquire a mammary gland density of the breast; a derivation section configured to derive a slice thickness that decreases as the mammary gland density acquired by the mammary gland density acquisition section increases; and a generation section configured to generate a tomographic image at the slice thickness derived by the derivation section based on the plural projection images acquired by the projection image acquisition section.

A method and system for monitoring a retail environment by performing video content analysis based on two-dimensional image data and depth data are disclosed. Accuracy in customer actions to provide assistance, change marketing behavior, safety and theft, for example, is increase by analyzing video containing two-dimensional image data and associated depth data. Height data may be obtained from depth data to assist in object detection, object classification (e.g., detection a customer or inventory) and/or event detection.

An embodiment in accordance with the present invention provides a method for non-invasively determining the functional severity of coronary artery stenosis. The method includes gathering patient-specific data related to concentration of a contrast agent within a coronary artery of a patient using a coronary computed tomography angiography scan (CCTA). The patient-specific data is used to calculate a patient-specific transluminal attenuation gradient for the coronary artery of the patient. The patient specific transluminal attenuation gradient is used to determine an estimate of a coronary flow velocity, pressure gradient, loss coefficient, coronary flow reserve, and/or fractional flow reserve for the patient. Coronary flow velocity, pressure gradient, loss coefficient, coronary flow reserve, and fractional flow reserve can then be used to estimate the functional severity of coronary artery stenosis.

A system and method is provided for automated polyp detection in optical colonoscopy images. The system includes an input configured to acquire a series of optical images, and a processor configured to process the optical images. Processing steps include performing a boundary classification with steps comprising locating a series of edge pixels using at least one acquired optical image, selecting an image patch around each said edge pixel, performing a classification threshold analysis on each image patch of said edge pixels using a set of determined boundary classifiers, and identifying, based on the classification threshold analysis, polyp edge pixels consistent with a polyp edge. Processing steps for the processor also include performing a vote accumulation, using the identified polyp edge pixels, to determine a polyp location. The system also includes an output configured to indicate potential polyps using the determined polyp location.

The present invention relates to a cell peeling recognizing device and a cell peeling recognizing method. When a moving part (robot 6) moves culture vessel 5, imaging device 14 images an interior of culture vessel 5 a plurality of times as the cells move inside the culture vessel due to the moment of inertia, and recognizing part 10a recognizes the peeled state of cells C by comparing various sets of the captured imaging data. The peeled state of cells in the culture vessel can be determined with high precision.