Abstract: A balloon catheter comprises a catheter and a balloon located on the distal end of the catheter. A pair of stimulating electrodes for receiving a constant current stimulating signal when the balloon is inflated with an electrically conductive medium and a plurality of sensing electrodes for producing voltage response signals are located on the catheter. The voltage response signals are indicative of the values of the transverse cross-sectional area of the balloon adjacent the sensing electrodes. A first lumen accommodates the inflating medium to and from the balloon, and a second lumen accommodates electrically conductive wires to the stimulating and sensing electrodes. A pressure sensing element is located in a protective housing in the second lumen, and communicates through a communicating opening in the protective housing and through a communicating port in the catheter with a hollow interior region of the balloon.

Abstract: A scapulae position measurement device includes a main body extending in the vertical direction, configured to be positioned to run along the spinal column, having a vertical scale, and a moveable arm, extending in a horizontal direction on the right or left side of the main body, having a horizontal scale. The scapulae position measurement device is capable of measuring position changes of the horizontal direction (X axis) and vertical direction (Y axis) of the scapulae, and capable of displaying the tension/relax state of the surrounding muscles of the scapulae with an objective numerical value.

Abstract: The invention is related to a device and method for monitoring respiration, movements in mechanical ventilation in order to provide a non-pneumatic triggering variable for achieving patient-ventilator asynchrony and continuous measurement of tidal volumes. The method is based on measuring the curvature of the patient's torso surface using a single LPG (Long Period Grating) fiber-optic sensor attached to a surface of the torso in an area having high stiffness of the underlying tissue, such as the area of the lower ribs close to the sternum.

Abstract: A method of method of acoustic screening for processing hearing loss patients utilizes a computing device connected to an audio output device to administer a hearing loss exam to a patient, display an audiogram of their hearing loss to the patient, and attempt to gently guide the patient into undergoing treatment for hearing loss. A correction algorithm is produced from the audiometric data in order to present the patient with comparison scenarios from typical day-to-day sounds with and without being modified by the correction algorithm.

Abstract: An apparatus for acoustic or mechanical stimulation of a cochlea and measurement of acoustically or mechanically evoked electrophysiologic responses from the cochlea is provided. In one example, the apparatus includes an acoustic stimulator for generating an acoustic signal and an electrophysiologic response measuring device positioned proximal the cochlea or within the cochlea for measuring an acoustically evoked electrophysiologic response to the acoustic signal. Methods of utilizing the apparatus for diagnostic and therapeutic procedures related to hearing impairment are also provided.

Abstract: Sensor devices including dissolvable tissue-piercing tips are provided. The sensor devices can be used in conjunction with dissolvable needles configured for inserting the sensor devices into a host. Hardening agents for strengthening membranes on sensor devices are also provided. Methods of using and fabricating sensor devices are also provided.

Abstract: An analyte monitor includes a sensor, a sensor control unit, and a display unit. The sensor has, for example, a substrate, a recessed channel formed in the substrate, and conductive material disposed in the recessed channel to form a working electrode. The sensor control unit typically has a housing adapted for placement on skin and is adapted to receive a portion of an electrochemical sensor. The sensor control unit also includes two or more conductive contacts disposed on the housing and configured for coupling to two or more contact pads on the sensor. A transmitter is disposed in the housing and coupled to the plurality of conductive contacts for transmitting data obtained using the sensor. The display unit has a receiver for receiving data transmitted by the transmitter of the sensor control unit and a display coupled to the receiver for displaying an indication of a level of an analyte.

Abstract: A metabolic physical activity monitor measures metabolic analyte data using one or more wearable analyte sensors. The sensors may be incorporated into a self-contained device or communicatively coupled to an external computing device like a smartphone or computer or both. Sensors may be mounted on any body surface including the skin, under the eyelid or in the mouth. Metabolic Analyte biomarker data may include electrolytes, various metabolites, pCO2 and pO2 in sweat, saliva and tears. Sensor data are used to calculate specific biomarker values, including calorie expenditure. Sensor readings are taken for at least two points during a period of physical activity. Changes in readings are used to determine total and rate of caloric expenditure for the time period. Readings may also be used to evaluate a user's wellness. By using measured changes in relative values complex calibration procedures can be eliminated, while reproducibility is much more easily achieved.

Abstract: This application provides a method of data collection for a pulse oximeter and an improved pulse oximeter device and improved components thereof.

Abstract: A lancet assembly used in a lancing device, includes a launching device for advancing a lancet to be withdrawn to the outside and a lever for stopping and allowing the advance of the lancet or launching device, and includes: a lancet; a lancet body exposing the front of the lancet and coupled to the back of the lancet; and a protective cap enveloping the front of the lancet exposed from the lancet body and closely coupled to the lancet body. The rear end of the lancet body is coupled to the launching device. The lancet body and the protective cap are separated and coupled, allowing loading into the launching device. The lancet body is coupled to and separated from the launching device by an insertion protrusion and a joint, and the lancet body and the protective cap are recoupled by a central groove or protrusion formed in the protective cap.

Abstract: Upon blood collection with a disclosed blood collecting apparatus, a part of a flow path adjacent to a suction drain mechanism is filled with a liquid different from the blood. A gas is inserted in the flow path between the liquid with which the part of the flow path adjacent to the suction drain mechanism is filled and a target blood to be collected. The suction drain mechanism pushes and pulls the gas by pushing and pulling the liquid during a standby time between collection and next collection, thereby controlling movement of the target blood. The suction drain mechanism pushes and pulls the liquid and the gas during the standby time, whereby the target blood is continuously moved. This allows prevention of coagulation of the target blood in the flow path.

Abstract: An allergy testing kit contains a plurality of allergy testing applicators, an allergy testing tray and a plurality of allergen bottles each containing an allergen. Each of the applicators contains an elongated handle, a plurality of arms extending from the elongated handle and disposed in an asymmetrical configuration, and a plurality of legs with tines extending from each of the arms. The allergy testing tray contains a main body having an underside and a top surface, a cover for locking with the main body and a plurality of reservoirs extending from the underside of the main body. The reservoirs each have a chamber with an opening extending from the top surface. The reservoirs are disposed in different groups and each group has an asymmetrical configuration matching that of the applicator.

Abstract: The invention relates to methods for predicting the risk of relapse of cancer patients as well as methods for providing personalized medicine to said patients based on the expression levels of different genes the expression of which is induced in response to TGF-beta stimulation. The invention also relates to kits for carrying out the diagnostic and predictive medicine methods.

Abstract: A device for treating bone in a living body includes (a) comprises an implant configured for attachment to a bone; (b) a first sensor measuring a strain on a first portion of the implant, the first portion of the implant being configured to be mechanically coupled to a weakened portion of a bone when the implant is coupled to the bone in a target position in combination; and (c) a second sensor measuring strain in a non-weakened portion of the bone.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: The present invention is a Miniature Vein Enhancer that includes a Miniature Projection Head. The Miniature Projection Head may be operated in one of three modes, AFM, DBM, and RTM. The Miniature Projection Head of the present invention projects an image of the veins of a patient, which aids the practitioner in pinpointing a vein for an intravenous drip, blood test, and the like. The Miniature projection head may have a cavity for a power source or it may have a power source located in a body portion of the Miniature Vein Enhancer. The Miniature Vein Enhancer may be attached to one of several improved needle protectors, or the Miniature Vein Enhancer may be attached to a body similar to a flashlight for hand held use. The Miniature Vein Enhancer of the present invention may also be attached to a magnifying glass, a flat panel display, and the like.

Abstract: A method to determine a position and a state of a personal activity monitor worn by a user, such personal activity monitor comprising a motion sensor formed as an at least 3-axis accelerometer and a processor unit, the method comprising the steps of determining a number of changes of predominant axis per time period, and comparing it with exceeds a first predetermined threshold in order to infer a wrist worn condition, the method comprising the steps of determining a current level of activity and a temperature criterion to infer that the personal activity monitor is actually worn by the user and that the user has entered a sleep phase, or to infer that the user has emerged from sleep.

Abstract: A sleep detection system and method are provided. In the sleep detection system, a sensor device is configured to measure a heart rate of a user; a measuring device is configured to receive the heart rate, and measure an activity level of the user and calculate an energy-expenditure value according to the heart rate, the activity level and personal parameters of the user; and a receiving device is configured to receive the energy-expenditure value from the measuring device and generate a sleep analysis result according to the energy-expenditure and to display the sleep analysis result.

Abstract: A remote patient monitoring system which is particularly well-suited for clinical out of center sleep testing (clinical OCST). Sensor nodes are grouped for wearing on the head, chest, and lower body of the patient. Sensor nodes wirelessly communicate sensor data to a nearby gateway, which communicates this data over a network (e.g., Internet) to one or more servers. The server(s) analyzes the sensor data for usage assurance, and to discern patient sleep patterns and characteristics. Guidance messages are generated by the system based on the analysis. Interfaces are provided to allow the patient to access their own information, and healthcare providers to access information collected regarding their patients.

Abstract: An opto-mechanical system for operation with a container containing a fluid to be administered in an eye or a container such as a syringe for example to administer an insulin injection. The mount of the system is equipped with an optical system and a processing/recording means configured to receive optical data, from light (visual or infra-red) reflected by an area in the vicinity of the eye, which data represents temporal and spatial characteristics of a process of administering drops of the fluid from the container into the eye. Image analysis software or human observation may be used to analyze the recorded images.

Abstract: According to the embodiments described herein, a method for characterizing in vivo operation of a dental prosthetic can include providing subject position data and prosthetic position data. The method may further include transforming the subject position data into a reference three-dimensional coordinate system. The reference three-dimensional coordinate system can be ordered according to a coordinate index. The coordinate index can be based at least in part upon a subject position index of the subject position data. The method may further include comparing, automatically with one or more processors, the prosthetic position data and the reference three-dimensional coordinate system according to a comparison order to characterize the dental prosthetic. The comparison order can be based at least in part upon a prosthetic position index of the prosthetic position data and the coordinate index.

Abstract: System, assembly and method are provided to facilitate reconstruction of cardiac information representing a complex rhythm disorder associated with a patient's heart to indicate a source of the heart rhythm disorder. The complex rhythm disorder can be treated by application of energy to modify the source of the rhythm disorder.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A nutrition and activity management system is disclosed that monitors energy expenditure of an individual through the use of a body-mounted sensing apparatus. The apparatus is particularly adapted for continuous wear. The system is also adaptable or applicable to measuring a number of other physiological parameters and reporting the same and derivations of such parameters. A weight management embodiment is directed to achieving an optimum or preselected energy balance between calories consumed and energy expended by the user. An adaptable computerized nutritional tracking system is utilized to obtain data regarding food consumed, Relevant and predictive feedback is provided to the user regarding the mutual effect of the user's energy expenditure, food consumption and other measured or derived or manually input physiological contextual parameters upon progress toward said goal.

Abstract: A system and method for the biological diagnosis of Post-Traumatic Stress Disorder (PTSD) comprises an electronic device equipped with a built-in or attachable camera, built-in or attachable flash or controllable light source, and a software application. The software application includes a method that records and monitors the diameter of an individual's pupil prior to and after the application of light, using the camera and flash in communication with the electronic device. In another embodiment, the method includes the use of emotionally-charged visual stimuli to increase the accuracy of the diagnosis. In still another embodiment, a heart rate monitor in communication with the electronic device is used to monitor the individual's heart rate variability to further increase the accuracy of the diagnosis. In still another embodiment, the method also measures the auditory startle response. The method analyzes the data collected and determines the likelihood the individual suffers from PTSD.

Abstract: The present invention provides methods, devices, and systems for wireless physiological sensor patches and systems which incorporate these patches. The systems and methods utilize a structure where the processing is distributed asymmetrically on the two or more types of ASIC chips that are designed to work together. The invention also relates to systems comprising two or more ASIC chips designed for use in physiological sensing wherein the ASIC chips are designed to work together to achieve high wireless link reliability/security, low power dissipation, compactness, low cost and support a variety of sensors for sensing various physiological parameters.

Abstract: Intravascular diagnosis apparatus and methods are disclosed. In one aspect of the disclosed technology, a monitoring guidewire includes a core wire having or made of one or more of MP35N, L605, Elgiloy, and an alloy of nickel, cobalt, molybdenum and chromium, a sensor disposed in a distal region of the core wire, and a housing substantially coextensive with the core wire and surrounding the core wire, the housing being more flexible than the core wire for at least the distal portion of the housing.

Abstract: Medical devices, perfusion systems, and methods for detecting a pressure within a space in a subject and for perfusion of fluid into a space in a subject. The space may be a fluid-filled space, or a space that is depleted of fluid due to an obstruction to fluid flow into the space. Methods for forming the medical devices.

Abstract: In certain embodiments, a heater assembly is provided including a water-resistant encapsulating shell. A heating element and/or other electronic components may be sealed in the encapsulating shell, and a catalyst to accelerate hydrogen peroxide decomposition may be coated on or impregnated into an element within the shell. In some embodiments the catalyst to accelerate hydrogen peroxide decomposition may be on the interior surface of the shell. In certain embodiments, the catalyst to accelerate hydrogen peroxide decomposition includes manganese dioxide. The catalyst to accelerate hydrogen peroxide decomposition may also include a binding material such as methyl cellulose.

Abstract: Methods and apparatus are presented for removing motion artifacts from physiological signals produced by a physiological sensor of a wearable device, wherein the physiological sensor includes at least one optical emitter and at least one optical detector. Light emitted by the at least one optical emitter that is scattered by a body of a subject wearing the device is detected, and a physiological information signal therefrom is produced via the at least one optical detector. Light emitted by the at least one optical emitter that is scattered by a light regulating region of the wearable device is detected, and a motion noise information signal is produced via the at least one optical detector. The physiological information signal and the motion noise information signal are processed via at least one processor associated with the wearable device to at least partially remove unwanted motion artifacts from the physiological information signal.

Abstract: Systems and methods for detecting noise episodes and processing analyte sensor data responsive thereto. In some embodiments, processing analyte sensor data includes filtering the sensor data to reduce or eliminate the effects of the noise episode on the signal.

Abstract: A technology for a wearable medical device for monitoring medical parameters. Medical measurement data can be received at the wearable medical device from a medical measurement sensor attached to the wearable medical device or a medical measurement sensor in communication with the wearable medical device. A calibration coefficient can be determined for calibrating the wearable medical device based on the medical measurement data. The wearable medical device can be calibrated based on the calibration coefficient.

Abstract: Systems and methods are disclosed that employ several or numerous factors in the determination of a glycemic urgency index (GUI), which may be based on a measured blood glucose level as well as other factors. The other factors may include time derivatives of the glucose level and/or other factors, e.g., user—entered data, data measured by other sensors or received from a network source, or historical data. The GUI is then presented to the user in an interesting way, e.g., via a background color or other inconspicuous notifier, e.g., on a mobile device such as a smart phone. The GUI may also be employed in the triggering of actionable alerts and alarms on an electronic device for the user. The GUI, or another index calculated from combinations of the variables and parameters described, may further be employed to drive a medicament delivery device such as a pump.

Abstract: The various embodiments herein relate to systems, devices, and methods for tracking abdominal orientation and activity for purposes of preventing or treating conditions of pregnancy or other types of medical conditions. In certain specific embodiments, the system, device, or method relates to identifying abdominal orientation risk values, calculating and updating a cumulative risk value, comparing the cumulative risk value to a threshold, and outputting a warning when the cumulative risk value crosses the threshold.

Abstract: Systems and methods are disclosed that employ several or numerous factors in the determination of a glycemic urgency index (GUI), which may be based on a measured blood glucose level as well as other factors. The other factors may include time derivatives of the glucose level and/or other factors, e.g., user-entered data, data measured by other sensors or received from a network source, or historical data. The GUI is then presented to the user in an interesting way, e.g., via a background color or other inconspicuous notifier, e.g., on a mobile device such as a smart phone. The GUI may also be employed in the triggering of actionable alerts and alarms on an electronic device for the user. The GUI, or another index calculated from combinations of the variables and parameters described, may further be employed to drive a medicament delivery device such as a pump.

Abstract: A monitoring system may include each of a left and a right side EMG detection device and may be configured to detect either seizure activity associated with the left side or right side of a patient's body. The system may further be configured to differentiate symmetric or asymmetric seizure activity. For example, the system may characterize whether left and right side EMG detectors show similar or dissimilar levels of activation during a suspected seizure. In some embodiments, the system may also include one or more orientation and/or position sensors. The system may be configured to determine the orientation and position of the sensor over time and to correlate this data with EMG signals.

Abstract: A method and system for acquiring a series of medical images includes receiving medical imaging data corresponding to photons emitted from a subject having received a dose of a radiotracer. Determining, from the medical imaging data, coincidence events including photon coincidence events involving two photons and photon coincidence events involving more than two photons. The photon coincidence events involving two photons and photon coincidence events involving more than two photons are processed and use to reconstruct a series of medical images of the subject.

Abstract: Described herein is an approach to determine a deflection of a portion of an imaging system tabletop located at iso-center utilizing a tabletop deflection determiner with a least a first portion located on a rotating gantry portion of the imaging system. In one non-limiting instance, an imaging system includes a rotating gantry portion (606) with an aperture defining an examination region, a tabletop (620) that supports a subject or object in the examination region, wherein the tabletop cantilevers into and deflects in the examination region, and a tabletop deflection determiner (622) that determines a deflection of the tabletop in the examination region, wherein a first portion (702, 706) of the tabletop deflection determiner is located on the rotating gantry portion.

Abstract: The invention relates to a medical computed tomography imaging apparatus which is especially designed to enable cranial imaging. The structure of the apparatus includes a gantry (2) comprising imaging means (21, 22) and a positioning support (8) which positioning support (8) is arranged to position the patient's cranium for exposure such that, when exposed, the cranium is scanned by a radiation beam substantially parallel with a plane formed by the facial area of the cranium and substantially only in an area on the facial side of the cranium.

Abstract: Methods and apparatus for integrating a table with at least one X-ray source for medical imaging of patients. The apparatus comprises a table on which a patient may be placed, at least one X-ray source configured to generate X-rays at a plurality of X-ray source locations along a linear direction, wherein the at least one X-ray source is arranged to generate the X-rays such that at least some of the X-rays pass through a portion of the table in addition to passing through a portion of a patient placed on the table, and at least one detector array comprising a plurality of detector elements and arranged to detect the at least some of the X-rays passed through the portion of the patient placed on the table, wherein the at least one detector array comprises detector elements arranged in a two-dimensional configuration. Iterative reconstruction techniques may be used to reconstruct an image from X-ray data detected using the at least one detector.

Abstract: According to one embodiment, a medical imaging diagnosis apparatus includes a top-plate, a bed, a first gantry, a second gantry and a moving assembly. The top-plate places a subject thereon. The bed supports the top-plate. The first gantry includes an X-ray generator and an X-ray detector which revolve around the top-plate. The second gantry includes a gamma ray detector which detects gamma rays emitted from the subject. The moving assembly moves, based on a first position indicative of a center position of an effective view field in the first gantry and a second position indicative of a center position of an effective view field in the second gantry, the top-plate relative to the second position.

Abstract: Examples include an envelope for an imaging plate. The envelope can include an opaque film partially hermetically sealed with a transparent film defining a cavity between the opaque film and the transparent film; the cavity configured to receive an imaging plate; an adhesive disposed on the opaque film or the transparent film along an unsealed portion of the opaque film and the transparent film; and a notch defined by the opaque film and the transparent film along a tab portion of the opaque film and transparent film that is hermetically sealed.

Abstract: An X-ray diagnostic apparatus in embodiments includes a calculating module, a generator, and a changing module. The calculating module calculates feature quantity concerning a flow of a contrast material for each pixel in a predetermined section based on temporal transition in signal intensity of the contrast material in a predetermined section of a plurality of X-ray images radiographed with time by using the contrast material. The generator generates a first color image in which color information corresponding to the feature quantity concerning the flow of the contrast material in a first section as the predetermined section is reflected in each pixel. The changing module changes the predetermined section to a second section that is within the first section.

Abstract: A set of first modality data (e.g., MR or CT) is provided. The set of first modality data comprises a plurality of mu-maps, a plurality of motion vectors and a plurality of gated data. Each of the mu-maps corresponds to one of the beds. A set of second modality data (e.g., PET/SPECT) is provided. The set of second modality data comprises a plurality of frames for each of the beds. Each of the plurality of frames is warped by one or more motion vectors of the plurality of motion vectors. A single-bed image is generated for each bed by summing the frames corresponding to the bed. A whole body image is generated by summing the single-bed images for each of the beds.