Abstract: The present disclosure provides an oral data collection device comprising a mouthguard and at least two sensors, a medical analytics system comprising the device, and methods of using the device and system to provide a personalized treatment protocol, stage a health condition, measure a response to therapy, phenotype for selection to participate in drug trials, measure stability of an anatomical structure, or predict a rate of change of a health condition in a subject in need thereof.

Abstract: In some examples, manufacturing techniques for implantable medical devices are described. An example method may including positioning a metal housing component adjacent to a polymer housing component so that there is an interface between the metal housing component and the polymer housing component; and forming a seal at the interface between the metal housing component and the polymer housing component to join the metal housing component and the polymer housing component, wherein the joined metal housing component and the polymer housing component form at least a portion of housing for the implantable medical device, wherein the housing of the implantable medical device contains electronic circuitry.

Abstract: A method includes determining that a portion of a force applied to a sensor system was applied to a non-inclusive region of the sensor system. An activation area of the non-inclusive region may be determined. A force distribution of the non-inclusive region may be determined. A corresponding force measurement of the non-inclusive region based on the activation area and the force distribution may be calculated.

Abstract: A system for a physiological characteristic sensor deployed with a sensor inserter includes an adhesive skin patch coupled to the physiological characteristic sensor. The adhesive patch is to couple the physiological characteristic sensor to an anatomy. The system also includes a gravity resistance system coupled to the adhesive patch and to be coupled to the sensor inserter. The gravity resistance system maintains the adhesive patch substantially perpendicular to a longitudinal axis of the sensor inserter prior to deployment of the physiological characteristic sensor and is removable from the adhesive patch by the sensor inserter upon deployment of the physiological characteristic sensor.

Abstract: A system for a physiological characteristic sensor deployed with a sensor inserter includes an adhesive skin patch coupled to the physiological characteristic sensor. The adhesive patch is to couple the physiological characteristic sensor to an anatomy. The system includes a gravity resistance system coupled to the adhesive patch and to be coupled to the sensor inserter. The gravity resistance system maintains the adhesive patch substantially perpendicular to a longitudinal axis of the sensor inserter prior to deployment of the physiological characteristic sensor and the gravity resistance system is to be removable from the sensor inserter by the adhesive patch upon deployment of the physiological characteristic sensor.

Abstract: Examples of systems and methods described herein may estimate a state of the ear canal of a patient utilizing a smart phone by characterizing acoustic waveforms reflected off the patient's eardrum. Examples may include an acoustic focusing apparatus that may be connected to a smart phone to provide acoustic signals to and receive reflected signals from an ear canal.

Abstract: In some examples, a device includes a catheter insert elongated body defining a body lumen, the catheter insert elongated body being configured to be at least partially inserted to a catheter lumen defined by a catheter without covering a first fluid opening of the catheter and to form a fluidically tight coupling with the catheter, and one or more sensors positioned on the elongated body. At least one of the one or more sensors are configured to sense a substance of interest. The catheter insert elongated body includes a material that is a substantially non-permeable to the substance of interest.

Abstract: In some examples, a medical device includes an elongated body defining an inner lumen. The medical device further includes an anchoring member and a first sensor at a proximal portion of the elongated body, and a second sensor at a distal portion of the elongated body or distal to a distal end of the elongated body. The second sensor is configured to sense a substance of interest and the elongated body comprises a material that is a substantially non-permeable to the substance of interest.

Abstract: Intraocular physiological sensor implants include a physiological sensor and a fluid pathway including a fluid inlet and a fluid outlet. The physiological sensor includes a sensing layer, a coil layer, and an integrated circuit layer. The intraocular pressure sensor provides trabecular bypass flow. The intraocular pressure sensor detects intraocular pressure, to identify patient conditions such as glaucoma.

Abstract: A heart rate correction method and system and a computer readable medium are provided. A heartbeat measurement signal and an acceleration detection signal are collected during a sampling time range. A credibility of an instant heart rate is determined to be credible or incredible based on the acceleration detection signal. An average heart rate is calculated by taking out one or more instant heart rate of which the credibility is determined to be credible. Whether a difference between the average heart rate and a reference heart rate exceeds a variation range is determined. When it is determined that the difference between the average heart rate and the reference heart rate exceeds the variation range, a corrected heart rate is obtained based on a correction value and the reference heart rate, and the corrected heart rate is taken as an output heart rate corresponding to the sampling time range.

Abstract: Provided is a photoplethysmogram (PPG) sensing module including one or more light sources that emit light to a user; a plurality of optical sensors that receive reflected light from the user and generate sensing signals, each of the sensing signals being generated by one of the optical sensors; a read-out signal generating circuit that receives the sensing signals from the optical sensors and generate read-out signals by performing an analog-to-digital conversion on the sensing signals; and a signal processing circuit that receives the read-out signals, classifies the read-out signals according to one or more movement patterns of the user, measures a movement component of the user based on the classified read-out signals, and generates a PPG signal in which the movement component is removed.

Abstract: [Object] It is an object to provide a determination device capable of determining the health risk of a laborer due to the labor load from the measured biological information only by measuring the biological information including the heart rate of the laborer. [Solution to the problems] In order to solve the above problems, the determination device 1 according to the present invention includes a biological information acquisition unit 3 that acquires biological information including a heart rate of a laborer Wi, a model formula storage unit 4 that stores a model formula for discriminating a health risk due to a labor load based on the biological information, and a determination unit 5 that determines the health risk of the laborer Wi based on the biological information of the laborer Wi and the model formula stored in the model formula storage unit 4.

Abstract: Devices, systems, and methods herein relate to predicting infection of a patient. These systems and methods may comprise illuminating a patient fluid in a fluid conduit from a plurality of illumination directions, measuring an optical characteristic of the illuminated patient fluid using one or more sensors, and predicting an infection state of the patient based at least in part on the measured optical characteristic.

Abstract: Devices, systems, and methods herein relate to predicting infection of a patient. These systems and methods may comprise illuminating a patient fluid in a fluid conduit from a plurality of illumination directions, measuring an optical characteristic of the illuminated patient fluid using one or more sensors, and predicting an infection state of the patient based at least in part on the measured optical characteristic.

Abstract: A photoplethysmography (PPG) circuit obtains PPG signals at a plurality of wavelengths of light reflected from tissue of a user. A processing device generates parameters using the PPG signals to screen the user for an infection, such as sepsis, influenza and/or COVID-19. The processing device may also determine a severity level of the infection and a confidence level in the determination. The parameters may include a measurement of nitric oxide (NO) level, respiration rate, heart rate and/or oxygen saturation.

Abstract: A presymptomatic disease countermeasure system 90 includes a motion measurement unit 91 which obtains motion data that is time-series data representing motion, by measuring the motion of an object, a joint reaction force computation unit 92 which computes joint reaction force at a joint to be evaluated among joints of the object, using the obtained motion data and ground reaction force data that is time-series data representing ground reaction force applied to the object, a feature amount computation unit 93 which computes a feature amount representing a load repeatedly applied to the joint to be evaluated on the basis of the computed joint reaction force, and a determination unit 94 which determines a joint disorder risk indicator that is an indicator representing a joint disorder risk that is the risk of causing joint disorder, on the basis of the computed feature amount.

Abstract: A method for displaying monitoring information includes acquiring measurement data of at least one physiological parameter of a monitored object, obtaining data of at least one physiological parameter within a pre-set time duration, performing distribution statistics on the data within the pre-set time duration based on at least one parameter-value partition, determining a distribution statistic result corresponding to the parameter-value partition where the parameter-value partition represents a numerical interval of the at least one physiological parameter, providing a monitoring interface, generating a measurement data display region and a distribution statistics display region at the monitoring interface, displaying the measurement data of at least one physiological parameter in the measurement data display region of the monitoring interface, and displaying the distribution statistic result in the distribution statistics display region of the monitoring interface.

Abstract: A graphical representation may be displayed including at least a plurality of transducer graphical elements, each transducer graphical element of the plurality of transducer graphical elements representative of a respective transducer of a plurality of transducers of a transducer-based device. A set of user input may be received including an instruction set to reposition a first transducer graphical element in a state in which the first transducer graphical element is located at a first location in the graphical representation and a second transducer graphical element is located at a second location in the graphical representation, the second location closer to a predetermined location in the graphical representation than the first location. In response to conclusion of receipt of the set of user input, the first transducer graphical element may be repositioned from the first location in the graphical representation to the predetermined location in the graphical representation.

Abstract: A method is for generating an X-ray image dataset via an X-ray detector having a converter element and a multiplicity of pixel elements. In an embodiment, the method includes first counting of at least one quantity of count signals dependent upon the incident X-ray radiation in each pixel element of the multiplicity of pixel elements; second counting of at least one quantity of coincidence count signals in each pixel element of the subset of pixel elements with at least one further pixel element of the multiplicity of pixel elements; and generating an X-ray image dataset based upon the at least one quantity of count signals counted in each pixel element of the multiplicity of pixel elements and upon the at least one quantity of coincidence count signals counted in each pixel element of the subset of pixel elements.

Abstract: A photon-counting X-ray detector is for acquiring an X-ray image data set of an object penetrated by X-ray radiation. The detector includes a converter element, designed to convert incident X-ray radiation into an electrical signal; and a matrix with a plurality of pixel elements. At least a partial number of the plurality of pixel elements receive a signal input and at least one configurable counter is coupled to the at least a partial number of the plurality of pixel elements, for signaling. Further, the at least one configurable counter is designed to count either a pixel count signal, based on a signal directly received in each respective pixel element, or a coincidence count signal, based on the signal received directly in the respective pixel element and on a coincident signal of at least one further pixel element.

Abstract: A travel handle (20) is provided with a pair of support plates (22) and a gripping bar (21) extended between the support plates (22). The pair of support plates (22) has a groove-like shape and is engaged with a slider (25) provided to a main body so that the support plates are reciprocally guided in a longitudinal direction inclined relative to the horizontal direction, and the reciprocal motion ends of the support plate in the reciprocating direction are regulated. The slider (25) is provided with a braking roller in contact with a groove portion side surface of the support plate (22) of the travel handle (20) and a braking control mechanism (26) for performing control such that the braking force by the travel handle (20) against the upward/downward movement of the travel handle (20) in the inclined direction is increased when the travel handle (20) is moved downward and decreased when the travel handle (20) is moved upward.

Abstract: Various embodiments discussed herein utilize a C-shaped imager to provide images with a minimal footprint, such as may be suitable in a surgical context. In addition the systems and methods described herein allow for suitable angular (i.e., azimuthal) scan coverage about the patient. To provide real-time 3D imaging, multiple X-ray tubes or a distributed X-ray source may be employed, coupled with an extended detector or multiple detectors. To reconstruct high-quality volumes, in some implementations reconstruction techniques may be employed that utilize pre-operative (pre-op) computed tomography (CT), magnetic resonance imaging (MRI), ultrasound (U/S), or other suitable modality images or data as prior information.

Abstract: A radiographic image display apparatus 3 included in a radiographic imaging system 100 includes a hardware processor that obtains an image data item on each of the frame images generated by the radiographic imaging apparatus 2, detects a situation of the subject at least at a time point in the dynamic imaging, associates the detected situation of the subject with the obtained image data items, and issues a specific output for notification that the subject is in a specific situation when the subject is in a state of a specific frame image fs, in a case where the display is caused to display the specific frame image fs, this specific frame image fs being taken when it is detected that the situation of the subject is the specific situation.

Abstract: A system, device, and method for visualizing vascular structures is disclosed. According to some implementations, in order to provide further improved digital subtraction angiography, a device for visualizing vascular structures is provided that includes a data provision processor, an image processor, and an output. The data provision processor is configured to provide a first sequence of non-contrast X-ray images of a region of interest of a patient for use as raw X-ray mask images. The data provision processor is also configured to provide a second sequence of contrast X-ray images of the region of interest of a patient for use as raw X-ray live-images. The image processor is configured to perform a first spatial subtraction for the first sequence of non-contrast X-ray images resulting in a first sequence of spatial-subtracted mask images.

Abstract: A method for 3D image reconstruction includes the steps of radiating an X-ray source at a predetermined angle to a photographing subject and acquiring a plurality of two-dimensional image images received through a detector, generating an image population by scaling the obtained plurality of two-dimensional image images, generating a virtual image using a pixel average between two-dimensional images from the plurality of scale-corrected two-dimensional images, and adding the virtual image to the image population, repeatedly generating a virtual image using a pixel average between two-dimensional images included in the image population until a two-dimensional image larger than a predetermined number P is generated in the image population, and generating a 3D video image using the generated 2D video image.

Abstract: A medical imaging apparatus is provided. The medical image apparatus includes an output unit; and a controller configured to control the output unit to display an image obtained by photographing an object and to display, over the image, a top indicator for setting a top limit for an area to be X-rayed and at least one guideline indicating a bottom limit for the area to be X-rayed according to the top indicator and the number of partial photographing operations.

Abstract: The present invention relates to a method for the evaluation of tissue gadolinium deposition that offers advantages compared with known methods. Comparison of different gadolinium-based contrast agents (GBCAs) based on retention, organ distribution, washout and safety is facilitated using the methods of the present invention.

Abstract: A method for characterization of coronary plaque tissue data and perivascular tissue data using image data gathered from a computed tomography (CT) scan along a blood vessel, the image information including radiodensity values of coronary plaque and perivascular tissue located adjacent to the coronary plaque, the method comprising quantifying radiodensity in regions of coronary plaque, quantifying, radiodensity in at least one region of corresponding perivascular tissue adjacent to the coronary plaque, determining gradients of the quantified radiodensity values within the coronary plaque and the quantified radiodensity values within the corresponding perivascular tissue, and determining a ratio of the quantified radiodensity values within the coronary plaque and the corresponding perivascular tissue; and characterizing the coronary plaque by analyzing a gradient of the quantified radiodensity values in the coronary plaque and the corresponding perivascular, and/or the ratio of the coronary plaque radiodensity

Abstract: A medical system according to an embodiment is a system in which at least one medical image diagnosis apparatus and a server are connected via a network and the medical system includes a storage circuit, a processing circuit, and a display circuit. The storage circuit stores information on examinations that are performed by the at least one medical image diagnosis apparatus. The processing circuit generates proposal information based on information on the examinations. The display circuit displays the proposal information.

Abstract: Various methods and systems are provided for workflow monitoring during x-ray mammography and related procedures. In one example, a vision system is utilized to monitor an x-ray mammography system, accessories associated with the system, and surrounding environment. Based on the detection and user indications, via a user interface for example, one or more of a current mode of operation of the x-ray system, a current workflow step in the current mode, and one or more errors may be identified using the vision system, and one or more of indications to the user and system adjustments may be performed based on the identification.

Abstract: The invention relates to a data processor (1) for processing 3D radiographic imaging data. The processor comprises an input (2) for receiving the imaging data and for providing a motion signal indicative of a motion of the imaged subject. The processor comprises an image segmenter (4) for segmenting a body part of interest in a first image included in or derived from the imaging data, and a gating function calculator (5) for calculating temporal gating functions for voxels that belong to the body part taking the motion signal into account. The processor comprises an image reconstructor (3) for reconstructing the imaging data into reconstructed three-dimensional images, by taking the temporal gating functions into account such as to associate each of the reconstructed three-dimensional images with a corresponding phase of the motion.

Abstract: To provide a technique with which dose indices can be managed for body parts in a range to be imaged on a body part-by-body part basis, an X-ray CT apparatus comprises: image producing unit (51) for producing a scout image (10) of a patient; defining unit (52) for defining a range (11) to be imaged in the scout image (10); segmenting unit (53) for segmenting the range (11) to be imaged into two body parts; identifying unit (54) for identifying which one of body parts (12) included in a human body each of the two body parts corresponds to; and calculating unit (55) for calculating a dose index for each of the two body parts.

Abstract: A radiographic imaging system includes a radiographic detector having a scanning device to obtain patient identifying information. The detector is programmed to display the patient identifying information in human readable form and to access additional information about the patient stored in networked databases.

Abstract: A system and method for providing a set of anatomical subdermal tags configured to form part of a local positioning system (in contrast to an operating room-wide global reference system) used in obscured visualization/localization of anatomical structures, locations, and components, as well as visualization/localization/orientation of implant(s) into referenced anatomical structures.

Abstract: A system for deploying needles in tissue includes a controller and a visual display. A treatment probe has both a needle and tines deployable from the needle which may be advanced into the tissue. The treatment probe also has adjustable stops which control the deployed positions of both the needle and the tines. The adjustable stops are coupled to the controller so that the virtual treatment and safety boundaries resulting from the treatment can be presented on the visual display prior to actual deployment of the system.

Abstract: Disclosed herein is a system and method for detecting the proximity of a needle to an ultrasound probe. The system can include an ultrasound system having a probe, including a body and a magnetic sensor, the magnetic sensor capable of detecting a magnetic field generated by or associated with the needle. The system can also include logic stored on non-transitory computer-readable medium that, when executed by one or more processors, causes performance of operations which can include: receiving an indication that the magnetic field has been detected including a strength of the magnetic field, determining a distance between a distal tip of the needle and the probe based on the strength of the magnetic field, and in response to the distance being within a first threshold, generating a first alert. The ultrasound system can further include a console apparatus communicatively coupled to the probe that includes the non-transitory computer-readable medium.

Abstract: A catheter-based ultrasound imaging system configured to provide a full circumferential 360-degree view around an intra-vascular/intra-cardiac imaging-catheter-head by generating a three-dimensional view of the tissue surrounding the imaging-head over time. The ultrasound imaging system can also provide tissue-state mapping capability. The evaluation of the vasculature and tissue characteristics include path and depth of lesions during cardiac-interventions such as ablation. The ultrasound imaging system comprises a catheter with a static or rotating sensor array tip supporting continuous circumferential rotation around its axis, connected to an ultrasound module and respective processing machinery allowing ultrafast imaging and a rotary motor that translates radial movements around a longitudinal catheter axis through a rotary torque transmitting part to rotate the sensor array-tip.

Abstract: Apparatuses, systems, and methods are provided herein to control movement of a patient's eyelid during a diagnostic procedure such as scanning the patient's eye with an ultrasound or optical imaging device. Strips having a non-adhesive portion and an adhesive portion are attached to each eyelid. The patient can then pull on distal ends of the strip to open the patient's eye and press the strips into an eyepiece to hold the patient's eyelids and keep the patient's eye open.

Abstract: An assembly and method for positioning a fetal heart transducer against skin. The assembly includes a strip having first and second ends and openings along its length, first and second fixation devices, each device having first and second surfaces, the first surface having adhesive thereon. A protuberance extends outwardly from the second surface. The assembly includes a fetal heart transducer. The first fixation device is secured to the skin at a first location and the protuberance of the first fixation device is received into a first opening on the first end of the strip. The first surface of the second fixation device is secured to the skin at a second location and the protuberance of the second fixation device is received into a second opening on the second end of the strip. The fetal heart transducer is secured between first and second fixation devices and beneath the strip.

Abstract: A method of visualizing a surgical site includes scanning a surgical site with an ultrasound system, marking a first area or point of interest within a cross-sectional view of the surgical site with a first tag, viewing the surgical site with a camera, and showing an image of the surgical site captured by the camera on a second display. The second display displays a first indicia representative of the first tag on the image of the surgical site captured by the camera.

Abstract: A backing 20 includes a lead array 24a that electrically connects each vibration element 12 and a plurality of ICs 32. Each bump 42 provided at a lower end portion of each lead 24 is connected to a conductor pad on an upper side surface of a relay substrate 26, and a ball-shaped terminal 44 of each IC 32 is connected to a lower surface of the relay substrate 26. The lower end portions of the leads 24 are grouped into a plurality of dense groups 46 corresponding to each IC 32 in a longitudinal direction (X-axis direction) by wiring patterns of the leads.

Abstract: An ultrasound probe comprises an air chamber unit that includes a transducer slot, where the transducer slot is configured to receive a transducer assembly, the air chamber unit comprises at least one sealed cavity and each of the at least one sealed cavity is filled with one or more gases, and the transducer assembly comprises transducer elements configured to perform one or both of transmitting and receiving acoustic energy.

Abstract: Ultrasound scanners that are initialized and placed to the side in a sterile bag for use in a sterile environment may suffer overheating and cut out early, because the bag represents a poor cooling environment. The rate of increase in temperature of a scanner is monitored and a determination is made as to whether the scanner is in a regular environment or a poor cooling environment. If the scanner is in a poor cooling environment, the scanner is switched from a regular state of operation to a poor cooling state of operation. In the poor cooling state of operation, the scanner settings consume less power and generate less heat on the whole than the regular scanner settings. The scanner reverts to higher power settings as and when needed to perform the desired scan. The user interface on an associated display device also changes in response to the scanner entering the poor cooling state of operation.

Abstract: Provided is a method for displaying an ultrasonic image, the method comprising: acquiring data by transmitting ultrasound pulses to a subject and receiving echo signals reflected from the subject; detecting microcalcified tissues in the subject by analyzing the acquired data; and displaying an image representing the detected microcalcified tissues.

Abstract: The present disclosure provides a new concept of fusion imaging device for simultaneously providing anatomical information and functional/biochemical information of human bodies, to accurately localize lesions in the pre-operative process and measure in real time, thereby ensuring the stability of patients with lower radiation doses than the existing fusion imaging devices such as positron emission tomography (PET)/computed tomography (CT) and single photon emission computed tomography (SPECT)/CT, and includes: a transducer to transmit and receive an ultrasound; a matching layer positioned on top of the transducer to reduce a difference in acoustic resistance between the transducer and an affected part, to support an ultrasound beam to be smoothly transmitted into tissues and a reflected beam to be received with high sensitivity; a backing member to absorb the ultrasound on an opposite side of the affected part with respect to the transducer; and a scintillator to detect gamma rays which are radiation, wherei

Abstract: Systems, methods and devices for providing combined ultrasound, electrocardiography, and auscultation data are provided. One such system includes an ultrasound sensor, an electrocardiogram (EKG) sensor, an auscultation sensor, and a computing device. The computing device includes memory and a processor, and the processor receives signals from the ultrasound sensor, the EKG sensor, and the auscultation sensor. Artificial intelligence techniques may be employed for automatically analyzing the data obtained from the ultrasound sensor, the EKG sensor, and the auscultation sensor and producing a clinically-relevant determination based on a combined analysis of the data.

Abstract: An ultrasound diagnostic apparatus includes: a hardware processor that search for a blood vessel position of a subject in a tomographic image and automatically setting a region corresponding to the blood vessel position detected in the tomographic image as a measurement region for generating a Doppler image. In a case where a measurement region has been already set or in a case where a specified position specified by a user exists when the hardware processor automatically sets the measurement region, the hardware processor executes processing of searching for the blood vessel position such that the measurement region is automatically set near the measurement region that has been already set or the specified position.

Abstract: An ultrasound system includes a computing device, a transducer configured to angulate through a scan region in response to a mechanical drive system that converts rotational motion generated by a motor into angular motion that angulates the transducer through the scan region, and an encoder configured to detect a rotational position of a shaft of the motor. The computing device is configured to determine an angular position of the transducer within the scan region based on the rotational position of the shaft detected by the encoder, and control generation of scan lines from the transducer based on a pulse firing pattern of scan lines to produce a predefined sequence of scan line densities across the scan region and the determined angular position of the transducer.

Abstract: An endoscope (1) having a suction channel and a suction connector in communication with said suction channel, and a working channel through which a liquid may pass. A valve for diverting the suction through the sampling device through a sample container is provided. The endoscope (1) further includes an actuator (7) for propelling the liquid through said working channel.

Abstract: A sweat collection device includes a flexible body having a first, outwardly facing surface and a second, skin-facing surface, and a sweat collection channel formed in the body, the sweat collection channel having a first end defining a sweat inlet port, and a second end defining a sweat outlet port. The sweat inlet port and the sweat outlet port are configured to be closed and sealed such that the sweat collection device and the collected sweat therein may be stored and shipped.