Abstract: A cognitive function evaluation device includes: an obtainment unit that obtains use information indicating a state of use of a toilet by a subject; a calculation unit that calculates a total number of times of use of a toilet by the subject, based on the use information obtained by the obtainment unit; an evaluation unit that evaluates a cognitive function of the subject, based on the total number of times of use calculated by the calculation unit; and an output unit that outputs a result of evaluation performed by the evaluation unit.

Abstract: A system for accessing a patient's uterine cavity and detecting perforations in the uterus includes an elongated probe having a flow channel extending to a terminal outlet in a distal region of the probe. A fluid source is coupled to the flow channel, and a seal on the probe is positionable in an endocervical canal. The probe may be trans-cervically inserted into the uterine cavity, and a fluid may be introduced through the channel to flow outwardly from the terminal outlet into the uterine cavity. A parameter of said fluid flow is monitored to detect a perforation in the uterus.

Abstract: Devices, systems, and methods are disclosed. The devices, systems, and methods detect one or more parameters with respect to movement of a user, cardiac activity of the user, audio associated with the user, or a combination thereof during a sleep session of the user; process the one or more parameters to determine a sleep status of the user, the sleep status being at least one of awake, asleep, or a sleep stage; and calculate an apnea-hypopnea index for the user during the sleep session based, at least in part, on the sleep status.

Abstract: There is presented a wearable device (200) and corresponding system and method for sensing a substance ingested by a subject, for instance an intoxicating substance. The wearable device has a sensing arrangement extending between a first port (205a) and a second port (205b). The sensing arrangement includes two chambers, a pump and two flow-control devices. The first chamber is adapted to collect gas from a skin region of the subject. The second chamber has a sensor to sense the substance. The first flow-control device is provided at the first port (205a) and the second flow-control device is provided at the second port (205b). A controller is provided to control the pump and the sensor. The controller is operable in a first phase to sense a first gas sample from ambient environment, and a second phase to sense a second gas sample from a skin region of the subject.

Abstract: A portable hand-held miniature vein enhancer comprises: a housing, laser, one or more mirrors, mirror drive system, and sensor to determine a distance to the target. The laser emits a beam of light at a selective wavelength that images subcutaneous veins through differential absorption and reflection. The mirror(s) receive the beam of light and create a spot of light on the target, and when driven by the mirror drive system to oscillate, the spot is scanned to form a two-dimensionally shaped pattern of light. The scanned spot of light moves according to a range of angular positions of the mirror(s). When the distance to the target is at or below a threshold distance, the range of angular positions is set to a maximum, producing the largest scan pattern. When the distance increases beyond the threshold, the range of angular positions is reduced proportional to the increased distance.

Abstract: The enclosed describes a sensor pad for wearing on a human body. The sensor pad is configured to be in contact with a substrate having a contoured surface, such as a surface of the body. The sensor pad comprises at least a sensor layer and a stiffener layer. The sensor layer comprises a surface area defining a sensing area configured to measure value at a plurality of locations of the sensing area. The stiffener layer is couples to the surface area of the sensor layer. The stiffener layer has a micro-cut pattern to reduce mechanical resistance of the stiffener layer. The micro-cut pattern facilitates the stiffener layer in stretching or compressing in one or more predefined directions, enabling the stiffener lay to conform to the contoured surface of the substrate.

Abstract: The disclosed computer-implemented method may include (1) sampling an output signal of an amplifier that amplifies a voltage difference between two electrodes, (2) calculating, based on a power spectral density of the output signal, a noise power of the output signal over a predetermined frequency band, (3) estimating an interface impedance of at least one of the two electrodes based on the noise power and a predetermined intrinsic current noise of the amplifier, and (4) performing an operation based at least in part on the estimated interface impedance. Various other methods, systems, and devices are also disclosed.

Abstract: A balloon catheter system has a balloon extending in an axial direction and surrounding a balloon interior. The balloon has an outer side facing away from the balloon interior. A catheter is connected to the balloon and extending in the axial direction, the catheter having a lumen in fluid communication with the balloon interior. First and second annular electrodes are disposed on the outer side, each extending in a circumferential direction of the balloon and being located opposite one another in the axial direction. The electrodes are configured to measure one of more of strain of the balloon in the circumferential direction, strain of the balloon in the radial direction, an impedance of tissue of a patient resting against the electrodes, and a redox potential of tissue of the patient contacting at least one of the electrodes.

Abstract: Systems, devices, and methods are disclosed herein for monitoring physiological data of subjects seated on a toilet, including systems, devices, and methods for monitoring loads and forces on a toilet seat. In some embodiments, systems, devices, and methods disclosed herein include a set of sensors that can measure loads and forces present at coupling points between a toilet seat and a base or other components of a toilet.

Abstract: A signal acquisition sensor array, an electronic device, and a mattress. The sensor array includes: a connection layer, at least two types of sensor units, a signal acquisition circuit, and a signal line electrically connecting the sensor units with the signal acquisition circuit, where each of the sensor units includes: a first vibration-proof substrate, and a sensor element in one-to-one correspondence with the first vibration-proof substrate and is disposed between the first vibration-proof substrate and the connection layer; and the at least two types of sensor units are arranged in an array at intervals on the connection layer. The solution enables different physiological signals having widely different signal amplitudes to be all accurately detected by the sensor array.

Abstract: A vehicle equipped with a computer system capable of diagnosing a pulseless condition in the driver. The vehicle includes a steering wheel with photoplethysmography sensors positioned around its circumference to measure arteriolo-capillary pulse wave intervals when the driver grips the steering wheel. The computer system is connected to the steering wheel sensors, a proximity sensor system, rear tail lights, a navigation system, and an audio system. The computer system analyzes the time interval between consecutive arteriolo-capillary pulse waves and determines if it exceeds a predetermined time interval. If the predetermined time interval is exceeded, the computer system will perform steps for the safety of the driver.

Abstract: The present invention provides a PHHM for the measurement of a subject's BP and, optionally, one or more other vital signs, comprising a housing located on a PHHCD or a hand-held component of a computing system; a blood flow occlusion means located in the housing such that, when the housing is located on the PHHCD or the hand-held component, an open surface of the blood flow occlusion means is available to be pressed against a body part of the subject or to have a body part of the subject pressed against it; a pressure sensor adapted to provide an electrical signal indicative of the pressure applied to or by the open surface; a means for detecting the flow of blood in the body part of the subject when pressure is applied to or by the open surface; and means for receiving electrical signals from the pressure sensor and the blood flow detecting means and for transmitting electrical signals indicative of the pressure and blood flow to the processor of the PHHCD or the computing system, wherein the processor of t

Abstract: Methods and apparatus are provided for high resolution intravital imaging and for chronic optical imaging of tissues such as lung.

Abstract: This document provides devices and methods for monitoring health patient parameters using a wearable monitoring device. For example, this document provides monitoring devices with multiple sensors, multiple types of sensors, algorithms for managing the multiple sensors to enhance monitor performance, and for detection of health events using health parameter data that is acquired by the monitoring system.

Abstract: The present invention provides a signal quality detection method for an ear-chip physiological measurement device. The signal quality detection method includes receiving a sensing signal from the ear-clip physiological measurement device; filtering the sensing signal to generate a pre-processed signal; calculating a physiological index according to the pre-processed signal; and calculating a similarity of a red light alternating current (AC) component and an infrared light AC component of the pre-processed signal and a plurality of correlation coefficients of the red light AC component, and generating a reliability index of the physiological index accordingly. The reliability index indicates one of a plurality of signal qualities.

Abstract: Disclosed in various embodiments of the present invention are a method and a device comprising: a first electrode, a second electrode and a third electrode which make contact with the body of a user; an instrumentation amplifier for differentially amplifying signals received from the first electrode and the second electrode; a feedback amplifier for feeding back feedback noise to the body of the user through the third electrode; and a control circuit, wherein the control circuit is configured to analyze a noise level by using a biosignal obtained from the instrumentation amplifier, and control the gain of the feedback amplifier on the basis of the result of the analysis. Various embodiments are possible.

Abstract: The present invention relates to a system and method for determining a vital sign of a subject. To improve the detection of electromagnetic radiation reflected from or transmitted through skin of a subject (110) at least two differently modulated radiation sources (112, 114) are used. For both camera and single-element sensors, this allows access (after demodulation) to different mixtures of skin and non-skin reflections/transmissions that can be de-mixed and successively allows the skin-only signal to be used for photo-plethysmography, PPG, extraction. Thus, a sensor (130) detects the reflected or transmitted electromagnetic radiation and a demodulation unit (140) and processing unit (150) enable to determine a vital sign (160) from said detection signal.

Abstract: A microcontroller for recording and storing physiological data includes an analog-to-digital converter for converting analog physiological sensor signals to digital signals, a sample buffer for holding a temporal sequence of the digital signals, a central processing unit (CPU), and a non-volatile memory. The non-volatile memory includes (i) a code storage encoding machine-readable data compression instructions that, when executed by the CPU, control the CPU to (a) transform the temporal sequence of the digital signals to produce transformed physiological data characterized by a set of transformation coefficients and (b) compress the set of transformation coefficients to generate compressed physiological data, and (ii) a data storage configured to contain several different instances of the compressed physiological data respectively associated with several different instances of the temporal sequence of the digital signals.

Abstract: The invention discloses a sparse Bayesian learning (SBL)-based SSR brain source localization method. An SSR record is divided into multiple data segments, frequency-domain information of the data segments is extracted through FFT, and a data matrix is constructed. An automatic iteration stop condition and initial values of a sparse support vector and a spontaneous electroencephalography (EEG)-electrical noise joint power vector are set. The posteriori mean and covariance of SSR components are iteratively estimated and the sparse support vector and the spontaneous EEG-electrical noise joint power vector are updated accordingly. When the iteration ends, the ultimate sparse support vector is used to give a source localization result. An SSR source localization problem is modeled in the frequency domain, the joint sparsity of signals in multiple data segments is involved, and a brain source localization method applicable to various SSRs is given in an SBL framework.

Abstract: System, methods and computer-readable media are provided for facilitating decision support by assessing the severity of injuries and the acute risk of physiologic deterioration and short-term mortality in trauma patients, both on the scene where emergency medical personnel initially evaluate and treat trauma victims and while in-transit to receive care at a health care facility. Embodiments of the invention provide a quantitative numerical score and calculated probabilities of deterioration and/or mortality, based on multi-variable statistical regressions. In some embodiments, fuzzy-set mathematics are employed in the regressions to account for physiologic and epistemologic uncertainty that are inherent in one or more emergency personnel members' observations and recordings of a plurality of measurements periodically during the time on-scene and during transit.

Abstract: An external medical device is provided. The device can include monitoring circuitry configured to sense physiological information of a patient and a controller with one or more input components. The controller can be configured to: detect one or more patient events based, at least in part, on the physiological information; notify the patient of the detection of the one or more patient events; and receive a patient response to the notification. The patient response can include a response activity identifiable by the input component, which is configured to test a psychomotor ability of the patient, cognitive ability of the patient, strength, balance, stability, and flexibility of the patient, and/or to substantially confirm that a person performing the activity is the patient.

Abstract: An optical based patient monitoring system employing an optical sensor and providing an indication of an optical change which does not correlate to a change in a physiological blood parameter and based on that indication, providing a care provider an indication of a condition of a patient. The optical based patient monitoring system providing the indication of the patient condition in relation to a patient using an IV setup.

Abstract: A method for monitoring a patient includes detecting a personal device of the patient, sending an invitation to connect to the personal device, and receiving health data from the personal device when the invitation is accepted. The method further includes determining stabilized values for one or more physiological variables of the patient based on the health data, and adjusting one or more alarm settings based on the stabilized values.

Abstract: A surgical stringer includes a pair of bases, each of the pair of bases having a flat bottom surface, the pair of bases being rotatable with respect to one another, and a pair of poles, each of the pair of poles being coupled to a one of the pair of bases and extending orthogonally thereto, the distance between the pair of poles being variable.

Abstract: A packaged bioprosthetic heart valve comprising a bioprosthetic heart valve, an adaptive seal and a package. The bioprosthetic heart valve comprises an at least partially dehydrated biological tissue leaflet structure coupled to a supporting frame. The bioprosthetic heart valve has a periphery, an inflow portion, and an outflow portion. The adaptive seal is coupled to the bioprosthetic heart valve around at least a portion of the periphery. The adaptive seal comprises an expandable material that expands after exposure to an initiating condition. The bioprosthetic heart valve and the adaptive seal is stored and contained within the package, which does not contain a liquid storage solution in contact with the bioprosthetic heart valve and the adaptive seal.

Abstract: Medical procedure trays and related methods are provided to accommodate joining a first non-sterile medical device with a second sterile medical device and maintaining required sterilization of the second sterile medical device to perform an associated medical procedure. One example of such medical procedures includes biopsy of a bone and/or associated bone marrow using a non-sterile powered driver and a sterile biopsy needle or biopsy needle set. Each medical procedure tray may include a containment bag or sterile sleeve. A coupler assembly, one or more sharps protectors, a biopsy sample ejector and/or associated ejector funnel may also be included. Some medical procedure trays may allow engaging a non-sterile powered driver with one end of a coupler assembly and sealing the non-sterile powered driver in a sterile sleeve or containment bag without compromising sterility of other components in the medical procedure tray.

Abstract: A system for detecting disposal of metallic objects into an opening of a medical waste container, including: an indicator for indicating passage of metallic objects through the opening, a pair of receive coils and a transmit coil spaced therebetween shaped for receiving waste therethrough adjacent to the opening, and a controller in electrical communication with the coils. The controller generates and communicates a transmit signal to the transmit coil, which generates a magnetic field that induces voltage in each of the receive coils, which each generate a receive signal. The controller generates a waveform based on the receive signals with a baseline corresponding to absence of metallic objects, and analyzes the waveform with respect to opposite first and second thresholds. The controller activates the indicator in response to metallic objects passing through the coils when the waveform first exceeds the first threshold and then subsequently exceeds the second threshold.

Abstract: The present invention relates to an X-ray anti-scatter grid (10). The anti-scatter grid comprises a plurality of primary septa walls (20), and a plurality of secondary septa walls (30). The plurality of primary septa walls comprise an X-ray absorbing material. The plurality of primary septa walls are substantially parallel to one another. The plurality of secondary septa walls are located between adjacent pairs of walls of the plurality of primary septa walls such that each secondary septa wall is located between an adjacent pair of walls of the plurality of primary septa walls. Each secondary septa wall of the plurality of secondary septa walls is formed from a plurality of columnar structures (40) extending between the plurality of primary septa walls. The plurality of columnar structures comprise an X-ray absorbing material.

Abstract: The display controller displays a first tomographic image of a three-dimensional image consisting of a plurality of tomographic images on a display unit. A first correction unit corrects the boundary of a first region of interest extracted from the first tomographic image, by a correction instruction using a correction instruction region for the boundary of the first region of interest. The first instruction region setting unit sets a first instruction region on a second tomographic image of the plurality of tomographic images. The second correction unit corrects the boundary of a second region of interest extracted from the second tomographic image by setting a second instruction region on the second tomographic image.

Abstract: Methods and systems are provided for assessing the presence of functionally significant stenosis in one or more coronary arteries, further known as a severity of vessel obstruction. The methods and systems can implement a prediction phase that comprises segmenting at least a portion of a contrast enhanced volume image data set into data segments corresponding to wall regions of the target organ, and analyzing the data segments to extract features that are indicative of an amount of perfusion experiences by wall regions of the target organ. The methods and systems can obtain a feature-perfusion classification (FPC) model derived from a training set of perfused organs, classify the data segments based on the features extracted and based on the FPC model, and provide, as an output, a prediction indicative of a severity of vessel obstruction based on the classification of the features.

Abstract: Disclosed is an X-ray imaging device, which is capable of providing a tomographic image of an image layer disposed between an axis of rotation and an X-ray source. The imaging device according to the present invention includes a radiography unit having an X-ray source and an X-ray sensor disposed to face each other with a rotating axis therebetween, wherein the X-ray sensor configured to obtain X-ray transmission images, a driver configured to rotate the X-ray source and the X-ray sensor about the rotating axis, and an image processor configured to provide a two-dimensional tomographic image of an image layer disposed between the rotating axis and the X-ray source, by shifting and overlapping the X-ray transmission images after reversing left and right at least some of the X-ray transmission images.

Abstract: The method may include obtaining a first set of imaging data affording a sagittal view relating to a subject and a first couch supporting the subject. The first couch may have a plurality of first positions reflected in the first set of imaging data as a first conformation. The method may also include determining a displacement field associated with a first set of imaging data with respect to the reference conformation based on the first conformation and a reference conformation. The method may further include adjusting the first set of imaging data with respect to the reference conformation based on the displacement field. In some embodiments, the method may include obtaining an image of the subject with respect to the reference conformation based on the adjusted first set of imaging data.

Abstract: The invention relates to an interventional system comprising an introduction element (4) like a catheter for being introduced into an object (9), for instance, a person. A moving unit (2) like a robot moves the introduction element within the object, wherein a tracking image generating unit (3) generates tracking images of the introduction element within the object and wherein a controller (8) controls the tracking image generating unit depending on movement parameters of the moving unit, which are indicative of the movement, such that the tracking images show the introduction element. This control can be performed very accurately based on the known real physical movement of the introduction element such that it is not necessary to, for instance, irradiate a relatively large area of the object for ensuring that the introduction element is really captured by the tracking images, thereby allowing for a reduced radiation dose applied to the object.

Abstract: A calibration phantom for radiometric characterization and/or radiotherapy dose calculation of a subject is provided, which includes an ellipsoid base having a primary volume defining a plurality of cylindrical voids, each of said cylindrical voids configured to receive a cylindrical insert having a diameter, wherein the ellipsoid base, the primary volume, and each of said inserts are formed from a tissue substitution material independently selected to approximate a radiological property of an anatomical feature of the subject to which the ellipsoid base, the primary volume, and each of said inserts corresponds, wherein the radiological property of the tissue substitution material, the diameter of each of said inserts, and a location of each of said inserts within the ellipsoid base are selected to mimic beam hardening upon exposure of the calibration phantom to a radiation beam. Optionally, one or more peripheral rings are disposed concentrically about the ellipsoid base.

Abstract: An X-ray imaging device may comprise: a radiation unit configured to preheat a filament and radiate an X-ray; a detection unit configured to detect shake of the radiation unit and generate information on the shake of the radiation unit; and a controller configured to determine a degree of the shake based on the information on the shake received from the detection unit and control an operation of the radiation unit depending on the determined degree of the shake. Therefore, the device can acquire a clear X-ray image without blur, and furthermore has effect in that unnecessary radiation exposure by re-photographing due to the blur of the X-ray image can be minimized.

Abstract: A system for monitoring health during a water birth includes a health sensor configured to be coupled to a mother. The health sensor includes a first sensor configured to measure one or more health parameters of a mother, a fetus within the mother or both, a second sensor configured to generate a submerged signal representing whether the health sensor is at least partially submerged in water, and a transmitter configured to transmit communication signals representing data collected by the first sensor. One or more parameters of the communication signals change depending on whether the submerged signal represents that the health sensor is at least partially submerged.

Abstract: The disclosed non-invasive blood pressure systems and methods measure a patient's blood pressure without restricting blood flow. Other sensors, such as physiological sensors, sensors that sense data about the NIBP system components, and/or environment sensors sense data that is combined with the NIBP signal. The combined NIBP and sensor signals are used to measure a patient's non-invasive blood pressure.

Abstract: An ultrasound imaging system including an image processor configured to receive input data for capturing ultrasound images of a region of interest. The ultrasound images are taken along a first plane; and the input data further includes an indication that a needle will be inserted into the region of interest. The system can capture a plurality of ultrasound images of the region of interest along the first plane. The system can determine one or more high-confidence areas of the region of interest where the needle will intersect the first plane. Each high-confidence area is based on a probability that the needle will intersect the first plane at any portion of the high-confidence area; and display one or more on-screen markers corresponding to the one or more high-confidence areas in conjunction with the plurality of ultrasound images on the display.

Abstract: A computer based method for classifying a mass of an organ such as a cyst is provided. The computer based method provides a class indicating a presence of a serum and a solid in the cyst and a subclass indicating a presence of one or more serous loculi or one or more solid loculi in the cyst. The computer based method is advantageous applications for a diagnosis of ovarian cysts.

Abstract: Systems and methods for automated physiological parameter estimation from ultrasound image sequences are provided. An ultrasound system includes an ultrasound imaging device configured to acquire a sequence of ultrasound images of a patient. An anatomical structure recognition module includes processing circuitry configured to receive the acquired sequence of ultrasound images from the ultrasound imaging device, and automatically recognize an anatomical structure in the received sequence of ultrasound images. A physiological parameters estimation module includes processing circuitry configured to automatically estimate one or more physiological parameters associated with the recognized anatomical structure.

Abstract: An analyzing apparatus according to an embodiment includes processing circuitry. The processing circuitry acquires a plurality of time-series medical images. The processing circuitry calculates, for each of image pairs each formed of two medical images included in the medical images, a first index value indicating similarity between image signals in the two medical images. The processing circuitry also calculates, on the basis of a plurality of the first index values calculated for the respective image pairs, a second index value corresponding to a statistical value in a time direction of the first index values.

Abstract: Intravascular devices, systems, and methods are disclosed. In some instances, a method for treating a vessel of a patient includes collecting intravascular ultrasound imaging data of the placement of the stent using the intravascular ultrasound imaging device, estimating, using a processing device, a restenosis probability value based on the intravascular ultrasound imaging data of the placement of the stent and communicating the estimated restenosis probability value to a clinician. Associated devices and systems are also provided.

Abstract: An ultrasound transceiver that overcomes many of the deficiencies of conventional ultrasound transceivers by providing the ability to transmit high power and high frequency arbitrary waveforms with low distortion and with the ability to monitor the transmit signals through the receiver during the transmit period, the transceiver circuit having a transducer element to emit an ultrasound signal and to receive a reflected ultrasound signal, a transformer circuit having a transformer with a secondary winding coupled to the transducer element and a primary winding, an H-Bridge transmit waveform circuit coupled to the primary winding of the transformer to generate a transmit waveform signal to the transducer element via the transformer, an FET clamp coupled to the secondary winding of the transformer, and a receiver circuit having an input coupled to the FET clamp.

Abstract: The present application provides an ultrasound probe comprising a housing that includes a coupling interface having a sinusoidal geometry. The housing is formed by a first body (300) and a second body having opposite and corresponding sinusoidal geometries. The first body includes a first proximal portion (105) and a first distal portion (107). The first proximal portion comprises a first sinusoidal shape (326). The second body includes a second proximal portion and a second distal portion. The second proximal portion comprises an opposite second sinusoidal shape. The first body and the second body are coupled to form a handle having a sinusoidal interface. Further, the first distal portion and the second distal portion form a head portion at which the ultrasound transducer assembly is disposed.

Abstract: Non-destructive testing scanner devices are disclosed to enable examination of portions of a part to be examined that presently-available scanners are not designed for. A scanner may include a central shaft having an assembly of engagement members adapted to engage an inner bore of a part and thereby support the central shaft along a central axis of the bore. An encoder may be supported by the central shaft. An ultrasonic probe may also be supported by the central shaft. The probe may be positioned on a surface of the part to be examined and moved in a circular path around the central shaft, and in so doing may cause a drive shaft on the encoder to rotate. The probe and encoder may be electrically connected to an instrument to convey data from the probe and from the encoder representative of characteristics of the surface being examined to the instrument.

Abstract: An elasticity comparative measuring method includes: controlling an ultrasound probe to transmit a first ultrasound wave to a region of interest in a biological tissue when the biological tissue is deformed; receiving echoes of the first ultrasound wave to obtain a first echo signal; controlling the ultrasound probe to transmit a second ultrasound wave to the region of interest when the biological tissue is deformed; receiving echoes of the second ultrasound wave to obtain a second echo signal; obtaining a first elasticity result corresponding to a first cross section in the region of interest according to the first echo signal; obtaining a second elasticity result corresponding to a second cross section in the region of interest according to the second echo signal; outputting, via a display, the first elasticity result and the second elasticity result.

Abstract: For ultrasound imaging with an ultrasound scanner, fat fraction of the tissue is measured. The fat fraction may be measured without access to channel data, such as from beamformed data. The speed of sound varies with the fat fraction of tissue, so the fat fraction is used to set the speed of sound in beamforming. Imaging the tissue using the fat fraction-based optimization for speed of sound may provide better images than imaging with an assumed speed.

Abstract: Systems and methods for estimating acoustic properties in a region-of-interest in a subject or other object being imaged using a reference frequency method (“RFM”) is described. Using this RFM technique, ultrasound data acquired at a given frequency are normalized by ultrasound data acquired at different frequencies (e.g., adjacent frequencies or otherwise) in order to provide estimations of the acoustic properties (e.g., attenuation coefficient, a backscatter coefficient, or both) that are independent of the ultrasound system used to acquire the underlying data. For instance, the amplitude of each frequency component can be normalized by a different frequency in the power spectrum to cancel out the system-dependent effects. Because the methods described in the present disclosure are system independent, they can be applied to any transducer geometry (e.g., linear or curved arrays) and using any beam pattern (e.g., focused or unfocused).

Abstract: Methods and systems are provided for fusing tissue characterization information into ultrasound images. In one example, a method includes obtaining first image data of an anatomical region of interest (ROI) of a patient, the first image data including tissue characterization information and acquired with a first imaging modality; obtaining second image data of the anatomical ROI of the patient, the second image data acquired with a second imaging modality; registering the first image data and the second image data; adjusting the second image data based on the tissue characterization information and the registration, wherein the adjusting includes filtering, adjusting colorization, adjusting brightness, and/or adjusting material appearance properties of one or more aspects of the second image data; generating a fused image from the adjusted second image data; and outputting the fused image for display and/or storage.

Abstract: The present disclosure relates to the technical field of image processing, in particular to an ultrasound imaging device and system and a breast ultrasound apparatus.