Abstract: Systems and methods for predicting motion of a target using imaging are provided. In one aspect, a method includes receiving image data, acquired using an imaging system, corresponding to a region of interest (“ROI”) in a subject, and generating a set of reconstructed images from the image data. The method also includes processing the set of reconstructed images to obtain motion information associated with a target in the ROI, and applying the motion information in a motion prediction framework to estimate a predicted motion of the target. The method further includes generating a report based on the predicted motion estimated.

Abstract: The present disclosure provides a vital sign measuring device and method that may measure a heart rate signal of a living body in a motion state. The method comprises detecting two different signals, using an adaptive noise removal algorithm for removing noise from the two signals, and obtaining a more accurate heat rate signal after a certain operation.

Abstract: The invention relates to systems and methods to assist physicians in decision making for stroke patients. In particular the systems and methods can be used to assist physicians to decide on whether a patient with an acute ischemic stroke has a large vessel occlusion (LVO) and should be transferred from a community hospital to a larger hospital to undergo an endovascular thrombectomy procedure.

Abstract: The present invention describes a new functional biomarker of vascular inflammation and its use in predicting all-cause or cardiac mortality. The invention also provides a method for stratifying patients according to their risk of all-cause or cardiac mortality using data gathered from a computer tomography scans of a blood vessel to determine a specific combination of structural and functional biomarkers of vascular inflammation and disease.

Abstract: Systems and methods are described herein for predictive heart valve simulation. The systems and methods described herein can include segmenting anatomical region of a heart of a patient from image data characterizing the heart of the patient. Anatomical model data that can include three-dimensional shapes of the anatomical regions of the heart can be generated based on the image data. The anatomical model data can be used to generate anatomical model data. The analytical model data can include a three-dimensional mesh of the anatomical regions of the heart. A deformed analytical model that can be indicative of a deformed position of the anatomical regions of the heart and a deformed position of the surgical object can be generated based on the analytical model data.

Abstract: Ingestible devices are disclosed that provide very high localization accuracy for the devices when present in the GI tract of a body. Related systems and methods are also disclosed.

Abstract: Methods and apparatus disclosed herein use a filtering technique to improve the accuracy of the results achieved when processing data provided by a physiological sensor. The disclosed filtering technique corrects many of the accuracy problems associated with physiological sensors, particularly PPG sensors. Broadly, the filtering technique adjusts a current filtered estimate of a physiological metric as a function of a rate limit based on a comparison between an instantaneous estimate of the physiological metric and the current filtered estimate.

Abstract: In an ultrasound diagnosis apparatus according to an embodiment, processing circuitry obtains volume data corresponding to at least one cardiac cycle and being taken of a region including the right ventricle of a patient. The processing circuitry estimates motion information of a tissue in the region by using the volume data. The processing circuitry calculates information including at least one selected from between wall motion information and volume information related to the right ventricle, on the basis of the motion information of the tissue. The processing circuitry outputs the calculated information. The processing circuitry corrects first motion information of the right ventricular outflow tract, which is an outflow tract of the right ventricle, by using second motion information of a site that is positioned in the vicinity of the right ventricular outflow tract and exhibits motion similar to that of the right ventricular outflow tract.

Abstract: Systems are provided for generating data representing electromagnetic states of a heart for medical, scientific, research, and/or engineering purposes. The systems generate the data based on source configurations such as dimensions of, and scar or fibrosis or pro-arrhythmic substrate location within, a heart and a computational model of the electromagnetic output of the heart. The systems may dynamically generate the source configurations to provide representative source configurations that may be found in a population. For each source configuration of the electromagnetic source, the systems run a simulation of the functioning of the heart to generate modeled electromagnetic output (e.g., an electromagnetic mesh for each simulation step with a voltage at each point of the electromagnetic mesh) for that source configuration.

Abstract: Embodiments access a set of radiological images acquired from a population of subjects, where a member of the set of radiological images includes a left atrium (LA) region; construct a statistical shape differential atlas from the images; generate a template LA model from the statistical shape differential atlas, where the template LA model includes a site of interest (SOI); acquire a pre-ablation radiological image of a region of tissue in a patient demonstrating atrial fibrillation (AF) pathology; generate a patient LA model from the pre-ablation image; compute a deformation field that registers the SOI to the patient LA model using deformable registration; compute a patient feature vector based on the deformation field; generate an AF probability score for the patient based on the feature vector; generate a classification of the patient based, at least in part, on the AF probability score; and display the classification or the AF probability score.

Abstract: A medical device includes a sheath having a guide wire lumen allowing a guide wire to be inserted therein and an imaging core lumen configured to have an ultrasound transducer inserted therein that acquires image information inside a living body. The medical device includes a rotary shaft that is inserted into the imaging core lumen and is rotatable in order to transmit mechanical drive force to the ultrasound transducer. In the sheath, a circular portion having a constant radii of curvature of the imaging core lumen is formed on a side separated from the guide wire lumen, and a non-circular portion having distances from the center point of the circular portion to the inner surface of the imaging core lumen non-uniform and longer than the radius of the circular portion is formed in at least a part of a side close to the guide wire lumen.

Abstract: An embodiment in accordance with the present invention provides a non-invasive solution to risk stratify the risk of in arrhythmia in patients with TOF. Currently, no reliable method for non-invasive risk stratification exists. In the realm of congenital heart disease, cardiac MRI is now used routinely for patients with Tetralogy of Fallot (TOF), the most common form of cyanotic congenital heart disease. An innovative platform for using clinical MRI data to create 3D electromechanical models of the heart enables predictions of whether or not patients with ischemic heart disease have the substrate for arrhythmia and what their relative risk for such an event is. An embodiment of the current invention provides a non-invasive solution to risk stratify the risk of arrhythmia in patients with TOF. Currently, no reliable method for non-invasive risk stratification exists.

Abstract: The present invention pertains to methods of determining where, on the skin, a diagnostic, therapeutic, or cosmetic agent is likely to be most effectively applied (e.g., injected), and to methods for monitoring a patient after such an agent has been administered. The monitoring can produce information useful in determining whether a diagnostic, therapeutic (e.g., surgical), or cosmetic regime should be initiated, continued, continued in a modified fashion, or terminated (e.g., for a brief or prolonged period of time). The methods can be repeated periodically and use a non-invasive, in vivo form of digital image speckle correlation (DISC) to track deformation of the skin.

Abstract: A vascular thermography system includes a portable electronic device and a thermal image analyzer in communications therewith. The portable electronic device includes a thermal imager to generate a thermal image of an anatomical area of a patient, a display, a processor configured to display the thermal image on the display, and a transceiver coupled to the processor to transmit the thermal image. The thermal image analyzer receives the thermal image from the portable electronic device, determines an assessment on vascular health of the patient based on comparing the thermal image to a database of thermal images, and transmits the assessment to the portable electronic device.

Abstract: For dead time determination for a gamma camera or other detector, a long-lived point source of emissions is positioned so that the gamma camera detects the emissions from the source while also being used to detect emissions from the patient. The long-lived point source, in the scan time, acts as a fixed frequency source of emissions, allowing for dead time correction measurements that include the crystal detector effects.

Abstract: A garment for bringing an EM transducer to contact with a thoracic skin surface area of a wearer is disclosed. The garment comprises a thoracic garment having a EM transducer placement portion and a pressure applying element associated with the EM transducer placement portion for applying a pressure on an EM transducer secured in an associated the EM transducer placement portion when the thoracic garment is worn by a wearer so that the EM transducer applies a respective pressure on a thoracic skin surface area of the wearer.

Abstract: A non-invasive optical detection system and method are provided. Sample light is delivered into a target volume of interest, whereby the sample light is scattered by the target volume of interest, resulting in a sample light pattern that exits the anatomical structure. Reference light is combined with the sample light pattern to generate at least one interference light pattern, each of which may have a time varying interference component that integrates to a first value in the absence of the physiological event, and that integrates to a second greater value in the presence of the physiological event. Intensities of spatial components of each interference light pattern are detected during a measurement period. A function of the detected spatial component intensities of the interference light pattern(s) is analyzed, and a presence of the physiological event in the target volume of interest is determined based on the analysis.

Abstract: A method for imaging a coronary arterial system of an individual includes releasing, using an actuator, pulses of a radio-opaque dye into a coronary arterial tree of the individual. The method further includes obtaining, using an image capture device, a sequence of invasive coronary x-ray angiogram images over time of the pulses of the radio-opaque dye. The method also includes tracking, using a processor, the pulses through the sequence of invasive coronary x-ray angiogram images and locating the pulses on a three dimensional (3D) structural model of the coronary arterial system to generate a three dimensional (3D) functional model of the coronary arterial system that shows a trajectory of the dye as it flows through different arterial branches.

Abstract: Stimulating cell activity within a tissue is performed by an ultrasound array transducer having a plurality of transducer elements and a controller that actuates a plurality of transducer elements to emit focused acoustic energy to a plurality of focal zone locations in a scan direction at a focal zone scan rate. The actuation of the plurality of transducer elements to emit focused acoustic energy to the plurality of focal zone locations in the scan direction at the focal zone scan rate is repeated for a plurality of sweep cycles at a sweep rate which stimulates cells for optimal tissue growth.

Abstract: A surgical port assembly for use with surgical instruments includes a body including an exterior surface and an interior space defined by an interior surface of the body. The surgical port assembly includes a control interface including a plurality of drive members coupled to the body and controllable to apply a force to a different portion of a shaft of an surgical instrument, when the shaft is disposed within the interior space, to move a distal portion of the surgical instrument to a desired position within a body cavity.