Abstract: The invention relates to a diagnostic measuring device for non-invasively collecting at least one physiological parameter of body tissue by way of an optical measuring unit (100), comprising at least one source of radiation (4) for irradiating the body tissue to be examined, and at least one radiation sensor (5) for detecting the radiation scattered and/or transmitted by the body tissue. The invention proposes the arrangement of the at least one source of radiation (4, 702) within a hollow reflector (701).

Abstract: A newborn heart rate monitor is disclosed comprising a sensor integrated into a clamp configured to clamp onto the umbilical cord of a newborn infant. The sensor is configured to detect radial pulsation of the umbilical cord and produce a corresponding electrical signal which can be processed by a processor to calculate the heartbeat of the newborn infant. The heartbeat can be displayed visually or audibly or both. A second reference sensor can be included to detect environmental noise and the processor can be configured to use the detected environmental noise to filter noise from the detected heartbeat. Additional filtering, processing, and alert algorithms can be included for processing and analyzing the detected heartbeat data.

Abstract: A magnetic resonance imaging apparatus includes a first data acquisition unit, a second data acquisition unit and an image data generating unit. The first data acquisition unit acquires first data from a slice to be a target after a first delay time from a reference of a first heart rate in synchronized with an electrocardiogram. The second data acquisition unit acquires second data from the slice after a second delay time from a reference of a second heart rate which is different from the first heart rate. The image data generating unit generates image data with image reconstruction processing using the first data and the second data.

Abstract: Disclosed is a system that includes pressure sensors to assist in monitoring pressure at a selected location. Pressure sensors may be applied to or incorporated into catheters and/or shunts positioned within a patient. A monitoring system may then receive signals from the pressure sensors to monitor pressure at the location over time.

Abstract: Tools and techniques for the rapid, continuous, invasive and/or noninvasive measurement, estimation, and/or prediction of a patient's physiological state. In an aspect, some tools and techniques can estimate predict the onset of conditions intracranial pressure, an amount of blood volume loss, cardiovascular collapse, and/or dehydration. Some tools can recommend (and, in some cases, administer) a therapeutic treatment for the patient's condition. In another aspect, some techniques employ high speed software technology that enables active, long term learning from extremely large, continually changing datasets. In some cases, this technology utilizes feature extraction, state-of-the-art machine learning and/or statistical methods to autonomously build and apply relevant models in real-time.

Abstract: It is disclosed an electronic system to control the acquisition of an electrocardiogram. The system comprises a portable electronic device and a mobile electronic device. The mobile electronic device comprises an optical device for acquiring real-time images of a portion of a human body, a screen and a processing unit. The portable electronic device comprises a first, a second and a third electrode. The processing unit of the mobile electronic device comprises an electrodes placement guiding module for the first, second and third electrode. The screen is configured to display a real-time image representing said portion of the human body and further comprises a first positioning mark, a second positioning mark and a third positioning mark representing the positions wherein to apply the first, second and third electrode respectively.

Abstract: A method and apparatus for the quantitative determination of an individual's risk for sudden cardiac death (SCD) is described. Risk stratification is accomplished (and may have a sensitivity and specificity of greater than about 90%) by determining the presence in any individual being tested for SCD risk of sequences identified herein to correlate quantitatively with SCD risk. Both the number of such sequences present and their alignment scores (similarity) with the SCD risk sequence ensemble are used to calculate quantitative SCD risk.

Abstract: In situations in which an implantable medical device (e.g., a subcutaneous ICD) is co-implanted with a leadless pacing device (LPD), it may be important that the subcutaneous ICD knows when the LPD is delivering pacing, such as anti-tachycardia pacing (ATP). Techniques are described herein for detecting, with the ICD and based on the sensed electrical signal, pacing pulses and adjusting operation to account for the detected pulses, e.g., blanking the sensed electrical signal or modifying a tachyarrhythmia detection algorithm. In one example, the ICD includes a first pace pulse detector configured to obtain a sensed electrical signal and analyze the sensed electrical signal to detect a first type of pulses having a first set of characteristics and a second pace pulse detector configured to obtain the sensed electrical signal and analyze the sensed electrical signal to detect a second type of pulses having a second set of characteristics.

Abstract: An electrode attachment state determination system includes: an electroencephalogram measurement section for measuring an electroencephalogram signal of a user by using at least one set of electrodes including a ground electrode, a reference electrode, and a measurement electrode; a frequency analysis section for performing a frequency analysis of the electroencephalogram signal; an insufficient electrode determination section for extracting at least one parameter of a total frequency power and a noise amount from a result of the frequency analysis, and through a comparison of a value of the parameter against a predetermined threshold value, determining whether the ground electrode, the reference electrode, or the measurement electrode has an insufficient state of attachment; and an output section for, when an insufficient state of attachment is determined, presenting information indicating the insufficient state of electrode attachment to the user.

Abstract: An information processing apparatus includes an acquisition unit, a specification unit, a determination unit, a generation unit, and a display control unit. The acquisition unit acquires a three-dimensional image containing at least a tubular structure. The specification unit specifies a first point inside the tubular structure and specifies a lesion outside the tubular structure in the three-dimensional image. The determination unit determines whether a blood vessel is present in a region between the first point and the lesion based on signal values of voxels of the three-dimensional image in the region between the first point and the lesion. The generation unit generates a two-dimensional image of the tubular structure viewed from the first point based on the three-dimensional image. The display control unit displays information indicating a region of the lesion on the two-dimensional image to be distinguishable in determining whether a blood vessel is present in the region.

Abstract: A method for configuring a presentation of physiological data for a patient includes identifying one or more physiological sensor modules that are connected in a physiological parameter monitoring device. After the physiological sensor modules are identified, the physiological parameter monitoring device is configured so that display areas are allocated on a display screen of the physiological parameter monitoring device for displaying physiological data for the patient. A separate display area is allocated for each identified physiological module. After one or more physiological sensor modules are detected as being connected, the physiological parameter monitoring device is automatically configured to include one or more additional display areas on the display screen for displaying physiological data for the patient. A separate additional display area is allocated for each of the additional physiological sensor modules that is connected.

Abstract: A breath capture device for determining the concentration of acetone in a breath sample from a user. In some embodiments, the device includes a controller programmed to use stored data to control flow of a breath sample into an analysis chamber as the user exhales into a port. In other embodiments, the device includes a switch responsive to an action by the user that is operable between a first orientation in which breath entering the port preferentially travels through a second flow path and a second orientation in which breath entering the port preferentially travels through a first flow path. In still other embodiments, the device includes a flow regulator both responsive to user action and operable from a first position in which breath entering a port preferentially travels through a second flow path to a second position in which breath entering the port preferentially travels through a first flow path.

Abstract: This contact-angle measurement method is a contact-angle measurement method for measuring a contact angle (?) between a droplet that is supplied to a sample curved surface and the sample curved surface. This method includes an apparent contact-angle calculation step of calculating an apparent contact-angle (?) of the droplet by using a captured image of the droplet supplied to the sample curved surface and the sample curved surface; an inclination angle calculation step of calculating an inclination angle (?) of the sample curved surface at an outer periphery portion of a contact portion between the droplet and the sample curved surface by using the captured image; and a contact-angle calculation step of calculating the contact angle (?) by correcting the apparent contact angle (?), using the inclination angle (?).

Abstract: An intravascular measurement system is provided. The system includes a catheter having a plurality of visible markers on a proximal portion that are proportional to a plurality of radiopaque markers on a distal portion. In at least one aspect, the system includes an imaging device adjacent the distal end.

Abstract: One variation of a method for detecting and responding to falls by residents within a facility includes: at a wearable device worn by a resident, writing sensor data from a sensor integrated into the wearable device to a buffer, inputting sensor data into a compressed fall detection model—defining a compressed form of a complete fall detection model and stored locally on the wearable device—to detect a fall event at a first time, and transmitting a corpus of sensor data from the buffer and a cue for confirmation of the fall event to a local wireless hub in response to detecting the fall event; and, remotely from the wearable device, inputting the corpus of sensor data into the complete fall detection model—stored remotely from the wearable device—to confirm the fall event and dispatching a care provider to assist the resident in response to confirming the fall event.

Abstract: Systems and methods for a continuous monitoring of analyte values received from an analyte sensor system are provided. One method for a wireless data communication between an analyte sensor system and a mobile device involves storing identification information associated with a transceiver of the analyte sensor system, the identification information entered by a user of the mobile device via a custom application running on the mobile device; causing the custom application to enter a background mode; searching for advertisement signals; receiving an advertisement signal from the transceiver; authenticating the transceiver based on the identification information; prompting the user to bring the custom application to a foreground mode; causing the custom application to request a confirmation from the user that a data connection with the transceiver is desired; receiving the confirmation from the user; and completing the data connection with the transceiver.

Abstract: Disclosed herein are systems and methods for monitoring one or more of cerebral oxygenation and total hemoglobin concentration that can be used to perform accurate, noninvasive measurement of cerebral venous blood oxygen saturation (oxygenation) in neonatal patients. A neonatal cerebral oxygenation detection apparatus comprises a wearable support having a light emitter and an acoustic sensor coupled thereto. The wearable support can be secured onto a head of an infant, and the light emitter can be configured to emit a light toward a superior sagittal sinus of the infant's head. The acoustic sensor can be configured to detect acoustic pressure generated by blood in the superior sagittal sinus when the superior sagittal sinus blood absorbs the light. Cerebral oxygenation and/or total hemoglobin concentration can be determined based on the acoustic pressure detected by the acoustic detector.

Abstract: Methods, device and system for providing a sensor insertion assembly including an inserter housing, an introducer including a body portion having a proximal end and a distal end and a shaft portion comprising a channel and a distal end, the shaft portion extending downwardly from an edge of the body portion, the shaft portion including a holding member disposed along a length of the channel, the holding member configured to substantially releasably retain a sensor, an on-body electronics unit, wherein the introducer is configured for insertion of the sensor through an aperture in the on-body electronics unit prior to insertion through skin and a drive mechanism included in the inserter housing and operatively coupled to the introducer, wherein the drive mechanism drives the introducer and retained sensor through the skin are provided.

Abstract: Disclosed are devices, arrangements and methods for quantifying the concentration of an analyte present in bodily fluid, including: an assay pad having at least one chemical reagent capable of producing a detectable signal in the form of a reaction spot upon reaction with the analyte; a light source; a detector array; a processor; and a memory in communication with the processor, the memory comprising: (a) at least one value indicative of one or more of: (i) the level of hematocrit contained in the sample; (ii) the volume of the sample applied to the assay pad; or (iii) imperfections present in the reaction spot; and (b) at least one algorithm for calculating the concentration of the analyte contained in the sample.

Abstract: A method and apparatus for monitoring a patient for seizure activity including collecting and processing EMG signal data and categorizing the detected data to execute risk stratification. A transmission protocol that is tailored for detected events may be selected and executed.

Abstract: A method of measuring Bone Mineral Density (BMD) including providing a model of a plurality of constituents of at least a portion of a subject body, the model including at least one bone constituent, injecting electric current into the portion of the subject body using a current injection electrode, such that at least part of the current flows through the at least one bone constituent, measuring a value of electric potential at a surface of the subject body using a pickup electrode, using a value of the injected electric current as input to a model of the at least a portion of a subject body, and calculating a value of conductance of the bone constituent corresponding to a value of the injected electric current and the measured value of the electric potential. Related apparatus and methods are also described.

Abstract: A system and method determines a user's compliance with a prescribed therapeutic pneumatic compression treatment by applying external pressure to a body limb using a pneumatic compression sleeve having a pneumatically fillable cell; measuring pneumatic pressure within the pneumatically fillable cell; generating a pressure signal corresponding to the measured pneumatic pressure; determining biological events associated with the user based upon the pressure signal; generating a positive detection signal for each determined biological event associated with the user; and determining a user's compliance with a prescribed therapeutic pneumatic compression treatment when a predetermined number of positive detection signals have been generated within a predetermined time interval.

Abstract: Appurtenances to cavity wound medical dressings are described. In some embodiments, an appurtenance to a cavity wound dressing includes: a substrate including at least one wound-facing surface, the wound-facing surface configured to be oriented facing a wound surface of a cavity wound; and a plurality of sensor units attached to the substrate, the plurality of sensor units oriented and positioned on the substrate relative to the wound surface of the cavity wound.

Abstract: Provided are a wearable personal digital device and related methods. The wearable personal digital device may comprise a processor, a display, biometric sensors, activity tracking sensors, a memory unit, a communication circuit, a housing, an input unit, a projector, a timepiece unit, a haptic touch control actuator, and a band. The processor may be operable to receive data from an external device, provide a notification to a user based on the data, receive a user input, and perform a command selected based on the user input. The communication circuit may be communicatively coupled to the processor and operable to connect to a wireless network and communicate with the external device. The housing may be adapted to enclose the components of the wearable personal digital device. The band may be adapted to attach to the housing and secure the wearable personal digital device on a user body.

Abstract: A method of monitoring a bone fracture in an individual. The method comprises the steps of: measuring a first parameter indicative of the load on said bone fracture; measuring a second parameter indicative of the activity level of said individual; obtaining a plurality of values for said first and second parameters; correlating said values to determine a measure of bone fracture condition; monitoring a change in said correlation over time; and determining a measure of the change in bone fracture condition over time. A bone fixation system implements this method of monitoring a bone fracture in an individual. The method and system provide a more accurate and reliable measure of bone fracture condition and of the progression of healing of the bone fracture.

Abstract: A coupling portion of a wearable medical monitor may include an attachment member configured to reversibly couple the coupling portion to a body portion of the wearable medical monitor. The wearable medical monitor may be coupled to a sensor via a cable. The coupling portion may also include a cable retention feature including a channel configured to receive the cable. The cable retention feature may be configured to apply a retaining force to the cable when the cable is disposed in the channel.

Abstract: Wearable patches comprising multiple separable adhesive layers. One or more of the layers can comprise electronics, mechanical components, gauze, medicine and/or other types of hardware suitable for the intended use of the patch. In use, a first layer of the patch is adhered to a user. When it is time to change layers, the patch is removed from the user, the first layer is removed from the patch to expose a second adhesive layer, and the second layer is applied to the user. The process may be repeated until the remaining layers of the patch have been used.

Abstract: A system for measuring physiological parameters, including: a portable measurement system, operable to acquire physiological measurement from an examined body location; an external camera operable to capture visible light, oriented toward the examined body location; a synchronization module, operable to receive a triggering indication, and in response to the triggering indication to associate to the physiological measurement a positioning image captured by the camera, the positioning image including at least a part of the portable measurement system adjacent to the examined body location; and a communication module operable to obtain the physiological measurement and the positioning image, and to transmit to a remote system: a physiological measurement record based on the physiological measurement, an orientation image based on the positioning image, and including at least a part of the portable measurement system adjacent to the examined body location, and association data associating the orientation image a

Abstract: A wireless circuit includes a housing having at least one opening, and sensor connected to the housing at the opening. The sensor includes a first layer having a first dimension and a second layer having a second dimension shorter than the first dimension. The second layer may be positioned entirely within the housing and a surface of said first layer may be exposed to an exterior of the housing.

Abstract: Embodiments disclosed herein relate to an interactive surgical drape and system including at least one sensor and at least one controller that operates indicating sensing feedback from the at least one sensor to cause display of information on a dynamic display integrated with the interactive surgical drape. The dynamic display assists the surgical team while performing surgery and can operate to improve the efficiency and/or effectiveness of the surgical team.

Abstract: A method for determining and responding in real-time to an increased risk of death relating to a patient with epilepsy is provided. The method includes receiving cardiac data and determining a cardiac index based upon the cardiac data. The method includes determining an increased risk of death associated with epilepsy if the indices are extreme, issuing a warning of the increased risk of death and logging information related to the increased risk of death. Also presented is a second method for determining and responding in real-time to an increased risk of death relating to a patient with epilepsy comprising receiving at least one of arousal data, responsiveness data or awareness data and determining an arousal index, a responsiveness index or an awareness index, where the indices are based on arousal data, responsiveness data or awareness data respectively.

Abstract: A medical imaging data processing apparatus comprises processing circuitry configured to obtain a first imaging data set comprising a set of pixels or voxels, the first imaging data set being reconstructed from first measurement data representative of measurements of a measurement volume obtained by relative rotation of a medical scanner and the measurement volume by a first range of angles during a first scanning time period; obtain a second imaging data set comprising a set of pixels or voxels, the second imaging data set being reconstructed from second measurement data representative of measurements of the measurement volume obtained by relative rotation of the medical scanner and the measurement volume by a second range of angles during a second scanning time period, wherein the second scanning time period overlaps the first scanning time period such that some angles are included in both the first range of angles and the second range of angles; transform the first imaging data set to obtain a first transf

Abstract: According to one embodiment, an X-ray diagnostic apparatus which can improve operability is provided. This apparatus comprises a top configured to move, a bed including the top, an X-ray tube configured to generate X-rays applied to an object placed on the top, a peripheral unit used around the bed, and control processing circuitry configured to generate a control signal. The peripheral unit moves in a self-propelled manner between a first position and a second position by a motor. The control processing circuitry generates a control signal for controlling the movement of the peripheral unit.

Abstract: The present disclosure describes a method for determining spinal instability, more particularly, a method for quantifying the type and extent of spinal instability in a standardized way. The disclosure also describes a method comprising measurement of the intervertebral rotation and intervertebral translation between a vertebrae pair using simple images, and from these measurements, determining if one or more vertebrae pair of the spine is unstable. Finally, the disclosure describes software that may be used to quantify the type and extent of spinal instability.

Abstract: A medical imaging device that includes: a press plate that presses a breast; an emitter that radiates radiation onto the breast; an acquisition section that acquires various information indicating a type of an acoustic matching member inserted between the press plate and the breast in cases in which ultrasound imaging of the breast is performed; and a setting section that sets a tube voltage of the emitter to a first tube voltage, in cases in which radiographic imaging of the breast is performed alone, and that sets the tube voltage of the emitter to a second tube voltage that is different from the first tube voltage, by employing the various information acquired by the acquisition section, in cases in which radiographic imaging and ultrasound imaging of the breast are performed consecutively with the acoustic matching member still inserted.

Abstract: A method of identifying a breath comprises sensing a signal generated by a living human or animal body and separating the signal into a plurality of frequency bands to identify a breath candidate.

Abstract: The invention relates to a filtering apparatus (15) for filtering an ultrasound signal, which is influenced by an electrical unit and comprises a first part including information about an object (4) from which the ultrasound signal has been received and a second part not comprising information about the object. A correction signal determination unit (17) determines a correction signal being indicative of the influence of the electrical unit on the ultrasound signal from the second part of the ultrasound signal and a correction unit (18) corrects the first part of the ultrasound signal based on the determined correction signal for filtering the influence of the electrical unit out of the ultrasound signal. Since the correction signal is indicative of the influence of the electrical unit, wherein the correction signal is used for correcting the ultrasound signal, unwanted interference visible in the unfiltered ultrasound signal can be filtered out.

Abstract: Systems and methods for classifying tissue using quantitative ultrasound techniques. Parameters are calculated directly from raw echo signal data acquired from a region-of-interest during an ultrasound scan and parametric maps are produced using these parameters. These parameters can be calculated after normalizing the echo signal data using reference data so as to mitigate the effects of variations in instruments settings, ultrasound beam diffraction, and attenuation effects. First-order and second-order statistical measures are computed from these parametric maps, and are used to classify the tissue or tissues in the region-of-interest. Using these systems and methods, tissue can be classified with different levels of classification. For example, a tissue characterized as malignant cancer can additionally be graded (e.g., Grade I, II, or III).

Abstract: A subject support (114) of an imaging system (100) includes a tabletop (124) that supports a subject or object in an examination region of the imaging system, a base (116), including a mechanical linear actuator (118), and a coupling (128) that mechanically couples the tabletop and the linear mechanical actuator such that the linear mechanical actuator translates the tabletop with respect to the examination region. The coupling rotates in two directions and translates in two directions, thereby providing four degrees of freedom, compensating for at least one of machining inaccuracies or misalignment of the linear mechanical actuator.

Abstract: To provide an ultrasound diagnosis apparatus capable of appropriately assigning a transmission delay time of a group to a transducer without complicated wires. The ultrasound diagnosis apparatus of the embodiment comprises a plurality of transducers, a timing pulse generator, a switch part, and a switch controller. Ultrasound waves are transmitted to the transducers. The timing pulse generator has output terminals for outputting timing pulses based on a delay time to a channel corresponding to each of the transducers, in which a plurality of output terminals are divided into groups and each group has the output terminals of a specific number greater than two. The timing pulse generator then generates the transmission delay time within a predetermined time range for the each group. The switch part selectively connects the channels with the output terminals.

Abstract: An ultrasound imaging system includes at least one transducer element. The ultrasound imaging system further includes a console with a transducer controller that controls the at least one element, a transducer processor that processes information detected by the at least one element, and a display controller that controls display of the processed information. The ultrasound imaging system further includes a display monitor with a first image display region. The ultrasound imaging system further includes a touch screen keyboard with a second image display region, wherein the display monitor and the touch screen keyboard are separate devices.

Abstract: In an ultrasonic diagnostic apparatus according to an embodiment, a separator separates an arbitrary region of a displayed object represented from image data, in a depth direction, based on a characterizing quantity included in the image data. An image generation controller generates an image to be displayed in which depth direction information is reflected on the arbitrary region of the displayed object, separated by the separator. A display controller causes a monitor being capable of providing a stereoscopic vision to display the image to be displayed generated by the image generation controller.

Abstract: The invention relates to a brachytherapy instrument comprising a body, wherein the body is provided with at least one marker comprising a material suitable to be visualized using an ultrasonic and/or magnetic resonance imaging technique. The invention further relates to an image acquisition system and a method of image acquisition.

Abstract: Provided is an ultrasound diagnostic apparatus that measures the modulus of elasticity of a vascular wall, wherein only M-mode images for heartbeats necessary for the measurement are displayed. The problem is solved by, when freeze is implemented during a B/M-mode display, displaying an M-mode image after discarding a heartbeat at the time of freeze and possibly also a heartbeat immediately before freeze.

Abstract: A method of full-field or “ping-based” Doppler ultrasound imaging allows for detection of Doppler signals indicating moving reflectors at any point in an imaging field without the need to pre-define range gates. In various embodiments, such whole-field Doppler imaging methods may include transmitting a Doppler ping from a transmit aperture, receiving echoes of the Doppler ping with one or more separate receive apertures, detecting Doppler signals and determining the speed of moving reflectors. In some embodiments, the system also provides the ability to determine the direction of motion by solving a set of simultaneous equations based on echo data received by multiple receive apertures.

Abstract: The present invention provides a method and a system for medical imaging and information display. According to an aspect of the present invention, there is proposed a method (10) of medical imaging and information display, comprising: acquiring (11) imaging data of each point of a plurality of points in an imaging plane or imaging volume of a subject in each mode of a plurality of different imaging modes of a medical imaging apparatus; deriving (12), for said each point, a value by applying the imaging data of the point in said each mode and the imaging data of at least one other point of said plurality of points adjacent to the point in said each mode to a predetermined model, wherein the predetermined model is selected in accordance with a clinical medical application related to the subject; constructing (13) an image based on all the derived values; and displaying (14) the constructed image to a user.

Abstract: Adjustment of operation of an ultrasound imaging system may be based at least in part on one or more characteristics represented in ultrasound return signals from two or more sample volumes. Adjustment may include adjusting a principal sample volume location or selecting a new principal sample volume. For example, a location of a principal sample volume may be adjusted or new principal sample volume selected so as to remain focused on an identified region of interest or to maintain the principal sample volume relative to some structure or reference. The principal sample volume may be maintained in the center or along a centerline of an artery or other structure, as the transducer array is moved along the artery or structure.

Abstract: An ultrasonic diagnosis apparatus includes an ultrasonic probe, an image generation unit, a display unit, and a control unit. The image generation unit generates image data from a reflected wave received from the ultrasonic probe. The display unit displays the image data. The ultrasonic probe includes a plurality of temperature sensors that measure the temperature of the ultrasonic probe and a switching circuit that is connected to the respective temperature sensors and switches connection to any one of the temperature sensors to a valid state to output data from the temperature sensors to a temperature detector. The control unit includes an instruction unit that instructs the switching circuit to switch connection to any one of the temperature sensors to a valid state at a predetermined time interval and a determination unit that determines whether a temperature measured by the temperature detector is within a set temperature range.

Abstract: Embodiments of the present invention relate to non-invasive methods and compositions for collecting detecting, measuring, and identifying target molecules. In some embodiments, methods and compositions relate to target molecules in gastrointestinal lavage fluid or feces.

Abstract: The present disclosure relates to adapter assemblies for use with and to electrically and mechanically interconnect electromechanical surgical devices and surgical loading units, and to surgical systems including handheld electromechanical surgical devices and adapter assemblies for connecting surgical loading units to the handheld electromechanical surgical devices.