Abstract: This relates to an electronic device with dynamically reconfigurable apertures to account for different skin types, usage conditions, and environmental conditions and methods for measuring the user's physiological signals. The device can include one or more light emitters, one or more light sensors, and a material whose optical properties can be changed in one or more locations to adjust the optical path and the effective separation distances between the one or more light emitters and one or more light sensors or the size, location, or shape of the one or more dynamically reconfigurable apertures. In some examples, the material can be a liquid crystal material, MEMS shutter layer, or light guide, which can form the one or more dynamically reconfigurable apertures. In some examples, the light emitters or light sensors or both can be an array of individually addressable optical components.

Abstract: A measurement sensor package and a measurement sensor reduce susceptibility to noise and enable highly accurate measurement. A measurement sensor package (1) includes a substrate (2), a lid (3), and a ground conductor layer (4). The substrate (2) contains a light emitter and a light receiver, and includes a substrate body (20), a plurality of ground via conductors (21), an frame-shaped ground conductor layer (22), signal wiring conductors (23), and an external connection terminal (24). The ground via conductors (21) are connectable to a ground potential, and are located outward from a first recess (20a) and a second recess (20b) included in the substrate body (20) in a plan view.

Abstract: A non-invasive method of estimating intra-cranial pressure (ICP). The method including the steps of: a. non-invasively measuring pressure pulses in an upper body artery; b. determining central aortic pressure (CAP) pulses that correspond to these measured pressure pulses; c. identifying features of the ICP wave which denote cardiac ejection and wave reflection from the cranium, including Ejection Duration (ED) and Augmentation Index of Pressure (PAIx); d. non-invasively measuring flow pulses in a central artery which supplies blood to the brain within the cranium; e. identifying features of the measured cerebral flow waves which denote cardiac ejection and wave reflection from the cranium as Flow Augmentation Index (FAIx); f. calculating an ICP flow augmentation index from the measured central flow pulses; g.

Abstract: A stereoscopic conductive fabric includes a basement yarn layer, a conductive yarn, and a support yarn. The basement yarn layer includes plural warp yarns arranged coursewise and parallel to each other and plural course yarns arranged warpwise and parallel to each other. The course yarns are interwoven with the warp yarns to form the basement yarn layer. The conductive yarn is arranged coursewise and interwoven with the course yarns in a skip manner to form plural conductive structures protruding from a surface of the basement yarn layer. The support yarn is arranged coursewise and interwoven with the course yarns in a skip manner to form plural pressing structures protruding from another surface of the basement yarn layer. A module for detecting electrical signals from body skin applying the stereoscopic conductive fabric is also disclosed.

Abstract: A magnetic resonance imaging (MRI) visualization method includes identifying a location of a thermally induced lesion in an MRI image by deriving a spatial pattern of MRI pixel values, which represents the lesion as it is expected to appear in the MRI image, as a function of thermal energy applied in creating the lesion. The MRI image is matched with the spatial pattern of pixel values. A local maximum value is found in the matched MRI image, and a location of the local maximum value is presented in the matched MRI image as the location of the lesion.

Abstract: A method comprises advancing a medical instrument and a catheter toward a target tissue within a patient anatomy. The instrument includes a distal sheath marker and is slidably received within the catheter. The distal sheath marker includes a channel and an identification feature. A portion of the instrument is slidably received within the channel. The method further comprises depositing the distal sheath marker at a location at or near the target. The distal sheath marker indicates a farthest advancement point of the instrument within the patient anatomy. The method further comprises: after depositing the distal sheath marker, withdrawing the instrument away from the target; determining an orientation of the distal sheath marker based on the identification feature; and, after withdrawing the instrument, using the location and orientation of the deposited distal sheath marker to determine a trajectory of a distal end of the instrument at or near the target.

Abstract: A laser catheter with a pressure sensor is provided according to embodiments of the invention. The pressure sensor may be coupled with the distal end of the laser catheter and may comprise any of various piezoelectric materials, for example Polyvinylidene Difluoride (PVDF). In various embodiments of the invention the pressure sensor is configured to detect pressure longitudinally and coaxially. The pressure sensor may provide an electric potential that is proportional to the vessel pressure and may be used to monitor and/or adjust laser parameters. In other embodiments the results from the pressure sensor may be used to determine the vessel size and/or the type of material being ablated.

Abstract: Method and systems are provided for monitoring neuromuscular blockade in patients during surgical procedures. The system and method utilizes a stimulator to provide stimulation to a nerve of the patient, such as train-of-four (TOF). Following such stimulation, the system and method monitors for muscle twitch reaction and, based upon the monitored muscle twitches, the system and method creates a neuromuscular blocking trend curve. The neuromuscular blocking trend curve provides an estimated time of recovery for the patient and provides the estimated recovery time to a clinician. The estimated recovery time allows the clinician to modify treatment of the patient to accelerate recovery if required.

Abstract: The present disclosure includes systems and methods for deriving certain characteristics of the patient's body related to motion from captured motion data. The characteristics may be used to compare the characteristics of the supposed injury to the characteristics of a normally functioning body part as well as the functions of an injured body part. The present disclosure provides a reliable and reproducible way to determine whether a supposed injury is a feigned or exaggerated injury or an actual injury.

Abstract: A medical device and method for determining a dose of insulin to be administered for glycemic control is provided, wherein the dose is stepwise adapted. The method includes determining a blood glucose value, receiving glycemic event information in respect to a predetermined glycemic event, wherein the predetermined glycemic event occurred within a predetermined time interval, receiving a previously adapted dose value stored in a storage unit, and setting an alert based on at least the blood glucose value, the glycemic event information and the previously adapted dose, wherein the alert indicates that the blood glucose value and the predetermined glycemic event are not in a specified relation to the previously adapted dose value.

Abstract: A measuring arrangement for in-vivo determination of the lactate concentration in blood by means of electrochemical impedance spectroscopy, comprising a substantially flat shaped probe having a longitudinal extension, a transverse extension and a thickness, wherein the longitudinal extension and the transverse extension of the probe are each a multiple of the thickness of the probe, an analyzer circuitry connected to the probe, and communication means connected to the analyzer circuitry for transferring data via a WPAN, wherein the substantially flat shaped probe is arranged at an edge of the measuring arrangement, so that the probe, during operation of the measuring arrangement, faces the animal or human body to be examined, in such a manner that the probe is arranged with its longitudinal and transverse extensions approximately parallel to the surface of the body to be examined, a wristband therefor, and a method for the operation thereof.

Abstract: Systems and methods directed to the assessment of tissue vascular health. An optical measurement device includes a light source with one or more wavelengths, configured to illuminate an area of tissue, a detector configured to capture the light reflecting from the tissue at the one or more illumination wavelengths, a processor configured to compute, based on the detected signal, one or more estimates of tissue vascular health, and a display or communication device (e.g., electronic data transfer) configured to store or report the tissue vascular health.

Abstract: Some embodiments relate to a reconfigurable biosensor adapted for performing tests in a plurality of modes or a smartphone or wearable device comprising the reconfigurable biosensor.

Abstract: Method and device for outputting one or more signals associated with a monitored analyte level of an individual, the one or more signals including a substantially real time monitored analyte level and a rate of change information associated with the monitored analyte level, outputting a carbohydrate intake event indication, determining one or more data associated with one or more therapy information related to the monitored analyte level and the meal event indication, and outputting the determined one or more data over the outputted one or more signals associated with the monitored analyte level and the carbohydrate intake event indication are provided.

Abstract: This disclosure relates to a glucose-sensing electrode including a nanoporous metal layer and an electrolyte ion-blocking layer formed over the nanoporous metal layer. The nanoporous metal layer is capable of oxidizing both glucose and maltose without an enzyme specific to glucose in the glucose-sensing electrode. The electrolyte ion-blocking layer is configured to inhibit Na+, K+, Ca2+, Cl?, PO43? and CO32? from diffusing toward the nanoporous metal layer such that there is a substantial discontinuity of a combined concentration of Na+, K+, Ca2+, Cl?, PO43? and CO32? between over and below the electrolyte ion-blocking layer.

Abstract: An apparatus for insertion of a medical device in the skin of a subject is provided.

Abstract: Systems for applying a transcutaneous monitor to a person can include a telescoping assembly, a sensor, and a base with adhesive to couple the sensor to skin. The sensor can be located within the telescoping assembly while the base protrudes from a distal end of the system. The system can be configured to couple the sensor to the base by compressing the telescoping assembly.

Abstract: This disclosure relates to a system and method for drawing blood from a user by skin puncture instead of venous puncture and storing it for analysis. The system includes a receptacle configured to engage an area of skin of the user at a blood draw location and store blood drawn from the user; a lancet device disposed within the receptacle configured to puncture the skin of the user at the blood draw location; a vacuum device configured to reduce a pressure within the receptacle such that the skin at the blood draw location is drawn into the receptacle before the lancet device punctures the skin, and to enhance blood flow while blood is drawn from the user; and a housing configured to house the receptacle, the lancet device, and the vacuum device. The receptacle, the lancet device, and the vacuum device may be modular and removably coupled with the housing.

Abstract: An object of the present invention is to provide a blood test kit and a blood analysis method, which are for performing quantitative analysis of components by precisely obtaining a dilution factor. According to the present invention, provided is a blood test kit for analyzing a concentration of a target component in a blood sample using a normal component which is homeostatically present in blood, the kit including a diluent solution for diluting the blood sample, a first storing instrument for storing the diluent solution, a separation instrument for separating and recovering blood plasma from the blood sample diluted with the diluent solution, a holding instrument for holding the separation instrument, a second storing instrument for storing the recovered blood plasma, and a sealing instrument for keeping the stored blood plasma within the second storing instrument, in which the separation instrument is composed of glass fiber coated with a resin.

Abstract: An improved, injection or blood removal device for intravenous access has a port with a septum at the exterior end of an intravenous catheter, a coupling element having an adhesive surface for securing attachment onto the skin, an injection or blood sampling unit, a connecting cannula piercing the septum of the port, and means to secure functional assembly. Attachment of the device to the skin covering or close to the intravenous puncture site and without long communicating tubes allows ambulant injection of drugs or measuring of concentration-time profiles of exogenous and endogenous analytes to improve treatment modalities on an individualized basis.

Abstract: An intra vaginal device (10) including an elongated hollow body (11) with side wall portions (15, 16 and 24). Secured to each wall portion (15 and 24) is a sensor (19), while secured to the wall portion (16) is a sensor (20). The sensors (19) simply measure forces directly applied by the bi-lateral contraction of the pubococcygeus, while the sensor (20) provides an indication of the puborectalis contraction forces.

Abstract: A mobile device for measuring at least one electrical biosignal. The device comprises a first input and a second input, a measuring circuit part for providing an output signal indicating the electrical biosignal to be measured, the measuring circuit part comprising a first input and a second input, and a charging circuit part for charging a rechargeable battery inserted in the device, the charging circuit part comprising a first input and a second input. The first input of the measuring circuit part and the first input of the charging circuit part are connected to the first input of the mobile device and the second input of the measuring circuit part and the second input of the charging circuit part are connected to the second input of the mobile device.

Abstract: A device for preparing a femur of a patient for receipt of a knee implant in both extension and flexion relative to a resected tibia plateau based on applying tension to medial and lateral collateral ligaments of said patient, comprising a tibial baseplate, a tensioner, the tensioner comprising a tensioner body having a tensioner portion, the tensioner portion affixed to the tibial baseplate, and an expander arm comprising an elongated body portion, a superior side of the elongated body portion having a spiked tip adjacent a posterior end thereof. The spiked tip interacts with an intracondylar notch under tension. The expander arm is operatively connected to the tensioner body via the tensioner portion, the tensioner portion configured for use in selectively raising and lowering the expander arm relative to the tibial baseplate to apply tension to the medial and lateral collateral ligaments in extension or flexion.

Abstract: An information processing device includes: a processor configured to: acquire time series data relating to at least one of acceleration, amounts of activity of a subject whose sleep is to be evaluated, and body positions of the subject, the time series data being measured by a sensor device that the subject wears; obtain a result of evaluation by analyzing a state of the subject that relates to sleep in each of three sections which are obtained by dividing an evaluation period from a getting-into-bed time point or a first onset-of-sleep time point after getting into bed that is specified by the time-series data until a getting-out-of-bed time point or a last waking time point before getting out of bed; and output the result of evaluation so as to identify that the result corresponds to any one of the three sections.

Abstract: An index output device for appropriately evaluating the conditions of the patient under anesthesia. An index output device 100 includes an electric stimulation section 170, an acquisition section 180, a calculation section, and an output section. The electric stimulation section 170 is configured to apply an electric stimulus to a living body. The acquisition section 180 is configured to acquire a plurality of physiological responses from the living body in response to the common electric stimulus applied to the living body by the electric stimulation section 170. The calculation section is configured to calculate, from the plurality of responses of the living body acquired by the acquisition section, an index related to a level of muscular relaxation (TOF) and an index related to a level of analgesia (PIR). The output section is configured to output the indexes calculated by the calculation section.

Abstract: A patient monitoring device includes at least one physiological sensor (32) configured to acquire at least one measured value for a patient of at least one monitored physiological variable. A cardiovascular (CV), pulmonary, or cardiopulmonary (CP) modeling component (42) includes a microprocessor pro-programmed to: receive the measured values of the at least one monitored physiological variable; receive a value for at least one patient-specific medical image parameter generated from at least one medical image of the patient; compute values for the patient of unmonitored physiological variables based on the measured values for the patient of the monitored physiological variables and the patient-specific medical image parameter; and at least one of (1) display the computed values and (2) control a therapy device delivering therapy to the patient based on the computed values.

Abstract: This system for identifying information represented by biological signals is configured so as to detect biological signals (S501), analyze the detected biological signals and then output feature data (S502), determine the respective similarities between the feature data and a plurality of teaching data (S503), store the similarities per time in a time series (S504), and determine information represented by the biological signals on the basis of the plurality of similarities within a prescribed period among the stored similarities in the time series (S505).

Abstract: In part, the disclosure relates to computer-based methods, devices, and systems suitable for pre-stent planning, stent planning and post-stent planning using one or more computing devices. In one embodiment, a method generates one or more stent profiles, such as a target stent profile, that are user configurable during a pre-stent planning stage by selecting one or more frames. The method performs a comparative analysis of the previously set target stent profile relative to a vessel lumen region post stent deployment. The method and related user interfaces can alert a user to move, remove, reposition, or inflate a stent. The location of jailed side branches can also be identified and displayed based upon the comparative analysis. Parameters that change based on the outcome of the stent deployment can be displayed in terms of the predicted parameter value and the value that is measured or determined after stent deployment.

Abstract: An electric toothbrush includes a brush head at an end of a handle, an acceleration sensor and/or a rotation sensor that detect(s) movement parameters of the electric toothbrush, a wireless communication interface that wirelessly transmits recorded data comprising the detected movements parameters of the electric toothbrush in a processed state and receives treatment mode data for operating the electric toothbrush, a pressure sensor that detects a contact pressure applied by the brush head to teeth and/or gums, at least one first outputting device that visually outputs signals or commands in accordance with the detected contact pressure or in accordance with the detected movement parameters, and at least one second outputting device that haptically outputs signals or commands, in the form of vibrations, in accordance with the detected contact pressure or in accordance with the detected movement parameters.

Abstract: To better understand the impact that meals have on the blood glucose level, some individuals with diabetes have begun recording meals consumed over time. However, the relationship between meals consumed by an individual and the glycemic health state of the individual has been difficult to understand. Introduced here are computer programs and associated computer-implemented techniques for utilizing information regarding the meals consumed by an individual to manage the blood glucose level of the individual in a personalized manner. By consistently and properly attributing physiological responses represented as excursions in blood glucose measurements to meals, the relationship between these meals and the glycemic health state can be better understood. For example, by examining this relationship, a diabetes management platform may be able to identify appropriate recommendations for monitoring, managing, and/or improving the glycemic health state of an individual.

Abstract: A method for detecting evidence of a stroke in a patient may involve securing a volumetric integral phase-shift spectroscopy (VIPS) device to the patient's head, transmitting a first signal from a first transmitter of the VIPS device through a left hemisphere of the patient's brain to a receiver of the VIPS device, transmitting a second signal from a second transmitter of the VIPS device through a right hemisphere of the patient's brain to the receiver, and detecting the evidence of the stroke, with the VIPS device.

Abstract: A nerve mapping system includes an energy based dissection device, a plurality of beacons, and a processing device. The plurality of beacons are disposed in a tissue of a patient. Each beacon is adapted to transmit one or more first electrical signals within the body and receive one or more second energy signals. The processing device is adapted to determine first locations associated with the plurality of beacons, a second location associated with the energy based dissection device, and a third location associated with a nerve within the tissue, based on the one or more second signals, generate a mapping of the first locations, second location, and third location, and cause the first locations, second location, and third location to be displayed on a display device.

Abstract: One variation of a system for collecting biosignal data includes: a left junction; a right junction; a first band spanning the left and right junctions; a first band adjuster configured to adjust a length of the first band between the left and right junctions; a second band spanning the left and right junctions and radially offset from the first band about a lateral axis spanning the left and right junctions; a second band adjuster configured to adjust a length of the second band between the left and right junctions; a first electrode fixedly mounted to the first band and centered between the left and right junctions; a second electrode mounted to the first band offset from the first electrode and laterally-adjustable along the length of the first band; and a third electrode mounted to the second band and laterally-adjustable along the length of the second band.

Abstract: A wrist-type body composition measuring apparatus is provided to measure body composition conveniently. The wrist-type body composition measuring apparatus includes a main body comprising a measurer configured to measure body impedance of a user, and an analyzer configured to analyze a body composition of the user based on the measured body impedance; a strap connected to the main body and configured to be flexible; a first inner electrode and a second inner electrode which are provided on a rear surface of the main body to be in direct contact with the user; and a first outer electrode and a second outer electrode which are provided on a surface of the main body to be in contact with the user during measurement of the body composition, wherein the first outer electrode and the second outer electrode are each formed as a half ring and face each other with a gap therebetween.

Abstract: Methods and apparatuses are provided for measuring a vital signal. An application is executed to output vital information of a user wearing an electronic device. Instructions are output that guide inhalation and exhalation of the user based on the executed application. At least one vital signal for the user is obtained while outputting the instructions. Vital information corresponding to the obtained at least one vital signal is output.

Abstract: This medical device measures blood flow rate through the renal artery after a kidney transplant in real time. The device utilizes a force sensing resistor (FSR) to detect the amount of blood and the given blood pressure at any instantaneous point in time. The FSR wraps around the renal artery after transplantation and should remain connected for five to seven days for optimal kidney blood flow and kidney functioning detection. This will be achieved by measuring the flow rate, estimating blood pressure, and beats per minute this device should alert doctors if irregular kidney function should occur for fast and immediate surgical or bedside intervention. Our goal is to detect post-transplant kidney rejection in real-time. The device is biocompatible and sterile, easily removed from the renal artery, and smaller than 5 mm in diameter.

Abstract: The disclosed systems and methods for monitoring a patient in a medical setting may include various types of sensors that obtain data indicative of one or more patient parameters and one or more environmental parameters. One or more processors may process the data to identify a correlation, or causal relationship, between the one or more patient parameters and the one or more environmental parameters. Thus, the systems and methods may be used to identify particular environmental parameters that affect a particular patient to facilitate creation of a suitable environment for the particular patient. The disclosed monitoring systems and methods may be especially useful for sensitive, high-risk, and/or non-verbal patients, such as infants in a neonatal intensive care unit (NICU).

Abstract: A method for clip selection includes receiving through an interface to a medical imaging device, a selection of a diagnostic procedure and a target portion of a mammalian body. Thereafter, the device acquires video clip imagery of the target portion and stores the video clip imagery in an image store. Each video clip of the video clip imagery is then image processed to determine a view and a quality of each video clip and a rule is retrieved from a rules base corresponding to the selected diagnostic procedure and target portion. In this regard, the rule specifies a requisite view and quality of the video clip imagery. Finally, the retrieved rule is applied to the video clip imagery as a filter to produce a subset of video clip imagery satisfying the specified requisite view and quality and the subset of video clip imagery is stored in the image store.

Abstract: Devices and methods for detecting an event using a variable threshold. A patient monitoring system can receive physiologic information and compare the information to an onset threshold. When the onset threshold is exceeded, the system shifts to a reset threshold that is different than the onset threshold. When the reset threshold is crossed, the system shifts back to the onset threshold.

Abstract: An X-ray CT system according to one embodiment includes a top plate on which a subject is laid, a driver configured to drive the top plate in a lateral direction of the top plate, a frame provided on both sides of the top plate in the lateral direction, and a cover provided between the frame and the top plate, respectively. The top plate and the cover are arranged so that the top plate does not come in contact with the cover in a drive range of the top plate by the driver in the lateral direction.

Abstract: Systems and methods for securely positioning a patient's head during medical imaging are presented. A fixation device includes a headrest which may be provided with inflatable chambers to adjust the headrest to the patient's head, a neck section which may be adjustable, and a base designed to couple to a patient bed or gurney forming part of a medical imaging system. The fixation device allows adjustment of the patient's head to an orientation which may variously minimize scanning time, improve imaging results, and/or protect sensitive tissues from unnecessary irradiation.

Abstract: A system for medical imaging is provided. The system includes a scanning device configured with a scanning cavity, a control device, and an output device configured within the scanning cavity. The control device is configured to obtain one or more scan protocols and acquire at least one guide instruction corresponding to the one or more scan protocols. The output device is configured to obtain guide information corresponding to the at least one guide instruction and present the guide information. The scanning device is configured to scan a subject with the presentation of the guide information according to the one or more scan protocols.

Abstract: Disclosed is a method and corresponding system for correcting the pileup effect in energy-discriminating photon-counting detectors. According to a first aspect, there is provided a method for pileup correction in a non-paralyzable energy-discriminating photon-counting x-ray detector operating based on a number of energy bins. The method includes adding, for each of a number of energy bins, a correction term to the detected signal of the energy bin, the correction term being a product of two separable parameterized functions, each of which includes at least one parameter, where a first parameterized function depends on a weighted sum of the detected signal over the energy bins, and where a second parameterized function depends on the detected signal(s) in one or several energy bin(s). By assuming separability and ignoring any cross correlations, the number of parameters and the complexity of the pileup correction algorithm are reduced substantially.

Abstract: A variable PET apparatus allows structural changes of detector modules in transversal and longitudinal directions to correspond to various imaging purposes and a cross-sectional diameter of a subject while maintaining an arrangement of the detector modules to be close to a true circle. The variable PET apparatus includes: a gantry having an opening on a longitudinal axis; and detector modules supported on the gantry and arranged a predetermined distance apart from each other such that a detection ring is configured with a diameter in a circumferential direction, wherein the gantry is driven by a gantry drive member, and the detector modules are driven by a detector module drive member. According to the present invention, structural changes of the detector modules in the PET apparatus is possible to correspond to a cross-sectional diameter of a subject without additional devices, thereby improving the spatial resolution and sensitivity.

Abstract: A radiation detector according to an embodiment includes a plurality of radiation detector modules and a fixing frame. When a radiation detector module is attached to the fixing frame, a guiding part with a groove shape formed at an end of a support member of the radiation detector module on a side of the fixing frame is fitted to a guiding pin provided to an end of the fixing frame, so that the radiation detector module is positioned in a radiation irradiation direction while a movement thereof in a channel direction and a row direction is restricted.

Abstract: The invention comprises a method and apparatus for imaging a tumor with X-rays while, simultaneously or alternatingly, treating or imaging the tumor with positively charged particles. An X-ray imaging system, such as one or two sets of a cone beam X-ray source coupled to an X-ray detector, is rotatable about a first axis and a patient. The X-ray imaging system is positioned off axis a path of charged particles delivered through an exit port of a nozzle system from a synchrotron and does not block a path of the positively charged particles from the exit nozzle to the patient or an imaging path from the patient to a scintillation detector. Fiducial indicators are used to confirm an unobstructed path of the positively charged particles in a treatment room comprising many movable elements, such as the X-ray imaging system and a patient positioning system/couch.

Abstract: In an X-ray imaging apparatus an image processor is configured to generate a phase contrast image based on a plurality of first images acquired by a first detection region (R1) at a plurality of relative positions of the first detection region with respect to a subject (T) to be imaged, and to generate an absorption image based on a plurality of second images acquired by a second detection region (R2) at a plurality of relative positions of the second detection region with respect to the subject.

Abstract: A method, system and computer readable storage media for segmenting individual intra-oral measurements and registering said individual intraoral measurements to eliminate or reduce registration errors. An operator may use a dental camera to scan teeth and a trained deep neural network may automatically detect portions of the input images that can cause registration errors and reduce or eliminate the effect of these sources of registration errors.

Abstract: A computer-implemented method and system for providing a dynamic mask image, including receiving projection images that image an examination region containing at least one vessel from at least two different projection directions, receiving a static mask image, initializing the dynamic mask image, determining exclusive rays that extend in each case parallel to one of the projection directions and correspond to a respective image value in the associated projection image, wherein at least one of the exclusive rays in each case extends through precisely one of the unmasked image areas of the static mask image, identifying and masking contrasted and uncontrasted vessels in the static mask image, annotating the contrasted and uncontrasted vessels in the dynamic mask image, determining and masking an imaging of the contrasted vessels in the projection images, repeating certain steps until an abort condition occurs, and providing the dynamic mask image.

Abstract: An imaging apparatus and associated methods are provided to receive measured projection data in a primary region and correct for scatter by processing the imaging data as two separate components: non-scatter-corrected data and scatter-only data. Separate image processing (e.g., reconstruction) allows for the use of individualized data processing, including filters, suited to the source data, thereby focusing on specific aspects of the source data, including, for example, noise and artifact reduction, resolution, edge preservation, etc. Combining the separately processed data results in an optimized balance of these aspects with improved image quality.