Abstract: A sensor for physiology sensing may be configured to generate oscillation signals for emitting radio frequency pulses for range gated sensing. The sensor 402 may include a radio frequency transmitter configured to emit the pulses and a receiver configured to receive reflected ones of the emitted radio frequency pulses. The received pulses may be processed to detect physiology characteristics such as motion, sleep, respiration and/or heartbeat. In some embodiments, the sensor may employ a circuit including a pulse generator configured to generate signal pulses. The circuit may also include a dielectric resonator oscillator configured to generate a radio frequency oscillating signal. A switched oscillation circuit may be coupled to the pulse generator and the dielectric resonator oscillator. The switched circuit may be configured to generate a pulsed radio frequency oscillating signal for emitting the radio frequency pulses.

Abstract: Systems and methods related to the field of cardiac resuscitation, and in particular to devices for assisting rescuers in performing cardio-pulmonary resuscitation (CPR).

Abstract: A method of manufacturing a sensor for in vivo applications includes the steps of providing two wafers of an electrically insulating material. A recess is formed in the first wafer, and a capacitor plate is formed in the recess of the first wafer. A second capacitor plate is formed in a corresponding region of the second wafer, and the two wafers are affixed to one another such that the first and second capacitor plates are arranged in parallel, spaced-apart relation.

Abstract: Example embodiments associated with characterizing a sample using NMR fingerprinting are described. One example NMR apparatus includes an NMR logic that repetitively and variably samples a (k, t, E) space associated with an object to acquire a set of NMR signals that are associated with different points in the (k, t, E) space. Sampling is performed with t and/or E varying in a non-constant way. The NMR apparatus may also include a signal logic that produces an NMR signal evolution from the NMR signals and a characterization logic that characterizes a tissue in the object as a result of comparing acquired signals to reference signals. Example embodiments facilitate distinguishing diseased tissue from healthy tissue based on tissue component fractions identified using the NMR fingerprinting.

Abstract: A method is provided that determines velocity encoding direction of volumetric image data sets comprising three-directional velocity information (V0, V1, V2) of a target volume, which involves: a) defining a coordinate system (X, Y, Z); b) determining all the possible arrangements of the three velocity components (V0, V1, V2) along the three coordinate axes (X, Y, Z); c) determining reference point or points in the target volume either automatically or upon user input; d) determining streamlines for each point for all possible combinations of velocity components as determined in b); and e) considering as velocity encoding direction the arrangement of the three velocity components corresponding to the streamlines having the longest length or a length above a threshold. A corresponding apparatus and computer program are also disclosed.

Abstract: Systems and methods are provided for in vivo measurement of pressure. An implantable sensor assembly includes a pressure sensor configured to provide an analog signal representing pressure and a signal conditioning component configured to convert the pressure sensor output into a digital signal. A transmitter is configured to transmit the digital signal to an external base unit. A power control unit is configured to dynamically allocate power throughout the implantable sensor assembly, such that during an active measurement interval of the implantable sensor assembly, each of the pressure sensor, the signal conditioning component, and the transmitter are powered only for a portion of the active measurement interval necessary to perform a related function.

Abstract: A system for determining T wave bifurcation that includes three or more ECG leads configured to receive an ECG signal and a first computing device including a processor coupled to a memory, the processor and the memory configured to perform operations including: generating at least two orthogonal ECG vectors based on the ECG signal of a patient, processing the at least two orthogonal ECG vectors to determine a loop trajectory of at least a portion of the ECG signal, identifying a trajectory bifurcation by comparing the loop trajectory to a control loop trajectory for a plurality of cardiac cycles, and determining an indicator of a cardiac event based on the trajectory bifurcation.

Abstract: Some embodiments described herein relate to a method that includes defining an electro-anatomical model of a heart. The electro-anatomical model can include conduction patterns for multiple patterns or phases identified by a measurement instrument. The electro-anatomical model can also include a voltage map of the heart. A portion of the heart containing a rotor can be identified based on circulation in one phase of the model. The rotor can be determined to be stable based on that portion of the heart having circulation in another phase of the model. The rotor can be characterized as a substrate rotor based on the rotor being stable and based on the voltage or a change in voltage at the portion of the heart containing the rotor. The rotor can be treated or ablated when the rotor is determined to be a substrate rotor.

Abstract: A catheter adapted for mapping and/or ablation in the atria has a basket-shaped electrode array with two or more location sensors with a deflectable expander. The catheter has comprises a catheter body, a basket electrode assembly at a distal end of the catheter body, and a control handle at a proximal end of the catheter body. The basket electrode assembly has a plurality of electrode-carrying spines and an expander that is adapted for longitudinal movement relative to the catheter body for expanding and collapsing the assembly via a proximal end portion extending past the control handle that can be pushed or pulled by a user. The expander is also adapted for deflection in responsive to an actuator on the control handle that allows a user to control at least one puller wire extending through the catheter body and the expander.

Abstract: A system and method for detecting arrhythmic electrocardiogram (ECG) signals includes defining a plurality of threshold heart rates and rate-dependent sensitivity levels for detecting arrhythmic ECG episodes, wherein more clinically relevant heart rates are assigned rate-dependent sensitivity levels with higher sensitivities. ECG signals are monitored by a medical device, and monitored ECG signals are processed using the plurality of threshold heart rates and rate-dependent sensitivity levels to detect and capture arrhythmic ECG segments.

Abstract: Apparatus for providing information on at least one muscle in a patient, which apparatus comprises: (i) signal providing means for providing measurement-enabling signals for the muscle; (ii) first contact electrodes for enabling the measurement-enabling signals from the signal providing means to be received by the patient; (iii) measurement means for measuring a parameter of the muscle, the parameter being such that it is affected by the measurement-enabling signals, and the parameter being such that it relates to at least one electrical property that is indicative of changes in tissue impedance caused by movement of the muscle; and (iv) a garment which is for being worn over the muscle in the patient and which comprises an array of separate electrically conducting areas. The apparatus optionally includes neuromuscular stimulator means for providing neuromuscular stimulation signals for the muscle.

Abstract: An electrode holding device is described using a headset having a neutral curvature with a radius smaller than a human skull. The headset adapted to provide spring load force against the human skull at the first and the second ends where first and second respective electrode holding panels are attached. The electrode holding panels conform to the human above the ears. The electrode panels are adapted to pivot about pivot points on the ends of the headset. The panels are adapted to contact the human skull under pressure from spring load force generated from the headset bent beyond the neutral curvature of the headset. The headset can in certain examples be further adapted in certain to accommodate an arm having an a third electrode panel that possesses a third electrode assembly, the third electrode assembly adapted to be spring loaded against and in contact with the human forehead.

Abstract: A system and method for imaging a target in a patient's body uses a pre-acquired image of the target and a catheter having a position sensor and an ultrasonic imaging sensor. The catheter is placed in the patient's body and positional information of a portion of the catheter in the patient's body is determined using the position sensor. The catheter is used to generate an ultrasonic image of the target using the ultrasonic imaging sensor. An image processor is used for determining positional information for any pixel of the ultrasonic image of the target and registering the pre-acquired image with the ultrasonic image; and a display is used for displaying the registered pre-acquired image and ultrasonic image.

Abstract: A method and system for assessing electrode-tissue contact before the delivery of ablation energy. The method may generally include determining a difference between a maximum impedance magnitude at a low frequency for a given electrode and an absolute minimum impedance magnitude at the low frequency across all electrodes, determining a difference between a maximum impedance magnitude at a high frequency for a given electrode and an absolute minimum impedance magnitude at the high frequency across all electrodes, and determining a difference between a maximum impedance phase at the high frequency for a given electrode and an absolute minimum impedance phase at the high frequency across all electrodes. These differences may be correlated to one another using a linear model, the results of which determining whether the given electrode is in contact or not in contact with tissue.

Abstract: An in-vivo device includes a first communication circuit to communicate with an external communication device by using a first communication protocol while the in-vivo device is in the gastrointestinal system of a subject, a communication condition monitoring (CCM) circuit to monitor communication conditions for the first communication circuit, a second communication circuit to communicate with the external communication device by using a second communication protocol, and a controller configured to receive, from the communication condition monitoring (CCM) circuit, a signal indicative of a communication condition of the communication via the first communication circuit, to compare the communication condition to prerequisite communication condition(s), and to activate the first communication circuit and concurrently deactivate the second communication circuit, or vice versa, based on the comparison result.

Abstract: A method for weight and/or fitness management using a metabolic analyzer that measures metabolic data including oxygen and carbon dioxide. The metabolic analyzer includes integrated collection-detection sensors with for high efficiency and collection, high specificity and simultaneous detection of at least two metabolic signatures, including at least oxygen and carbon dioxide, in breath via a porous membrane with high density of sensing binding sites, where the porous membrane includes sensing materials such that the sensing binding sites are specific to the metabolic signatures, and change colors upon interactions with the metabolic signatures. Weight of the subject is measured using a weight measurement device and a recommendation for food intake and/or physical activity is based on at least the readings of the metabolic analyzer and weight of the subject.

Abstract: The invention relates to a length measuring device with a vernier caliper, a hollow profile, on which the vernier caliper is displaceably mounted externally so that it is capable of being brought into contact with an object to be measured in terms of its length, an inner slide, which is displaceably mounted inside the hollow profile, a magnet arrangement, which couples the vernier caliper and inner slide magnetically, so that the inner slide follows every movement of the vernier caliper along the hollow profile, a measuring means for measuring the position of the inner slide along the hollow profile, and a display, visible in the surrounding space of the hollow profile, of the length determined by the measuring means in accordance with the measured position of the inner slide.

Abstract: Disclosed are a system and a method for rehabilitation exercise of hands. The system and the method help a device sense movements of the hands more accurately. The device for rehabilitation exercise of the hands comprising multiple sense parts that are located on each part of a user's hand, and configured to sense movements of the each part; and communication part configured to send movement data sensed by the multiple sense parts to an output device.

Abstract: Patient swallow frequency is automatically determined by collecting patient data, analyzing the patient data to automatically identify swallow events, and automatically calculating the swallow frequency based upon the identified swallow events. In some cases, the patient data is collected by a patient interface that wirelessly transmits the data to a computing device for analysis.

Abstract: The present application relates generally to computer software, mobile electronics, wireless communication links, and wearable monitoring systems. More specifically, techniques, systems, sensors, circuitry, algorithms and methods for wearable monitoring devices and associated exercise apparatus are described. A garment borne sensor system may acquire data on a user's performance during exercise, for example. The data may be analyzed in real time and feedback may be provided to the user based on the analysis. Analysis may be used to alter behavior of the user and/or an apparatus the user is engaged with during an activity, such as exercise, conditioning, therapy, etc. A piece of exercise equipment may be instrumented and in communication with the sensor system or other system and may be controlled in real time to adjust its settings to affect the user during the exercise routine. Communication between the sensor system and other systems may be wireless.

Abstract: A feature-quantity extracting apparatus is provided, which can calculate a proper feature quantity, by performing a simple calculating operation. The apparatus is provided with a code-string acquiring unit for acquiring code strings for every given period from a series of input data, wherein the code string is an arrangement of codes and the code is given to a value of each piece of input data, a code-string pattern frequency counting unit for counting the number of code-string patterns for every code-string pattern among the code strings acquired by the code-string acquiring unit, wherein the code-string pattern represents a code-string whose codes are arranged in accordance with a given order, and a feature-quantity outputting unit for outputting the number of code-string patterns for every code-string pattern counted by the code-string pattern frequency counting unit as a feature quantity of the series of input data.

Abstract: The application relates to a lancing device for obtaining samples of body fluid, said device comprising: a base body which is rotationally symmetrical with relation to the longitudinal axis thereof and on one longitudinal end of which a positioning surface with an exit opening is arranged; a lancet cartridge for receiving a plurality of lancets; a drive device for moving a lancet held in the lancet cartridge back and forth along the longitudinal axis; and a transport device for transporting lancets on a plane perpendicular to the longitudinal axis. The exit opening is located substantially centrally in the positioning surface and the lancet cartridge has a guide track for the lancets, in which track said lancets can be positioned in such a way that their tips can emerge from the exit opening during the movement back and forth.

Abstract: Methods and devices for the diagnosis and treatment of diabetes are disclosed in which an analyte concentration within a peritoneal fluid of a human subject may be determined by implanting an analyte sensor apparatus in the subject where the apparatus may comprise a housing and a flexible sensing catheter which has a lumen with a plurality of apertures and an exterior surface with an analyte sensor affixed thereto. The catheter may comprise a proximal end attached to the housing and the remaining end may be positioned freely within the peritoneal space to contact peritoneal fluid where an analyte concentration in the peritoneal fluid may be sensed. The housing may be anchored at a subcutaneous site proximate the peritoneal space. The sensed analyte concentration may then be transduced into a transmittable electrical signal.

Abstract: Methods and apparatus for providing data processing and control for use in a medical communication system are provided.

Abstract: Devices and methods are described for providing continuous measurement of an analyte concentration. In some embodiments, the device has a sensing mechanism and a sensing membrane that includes at least one surface-active group-containing polymer and that is located over the sensing mechanism. The sensing membrane may have a bioprotective layer configured to substantially block the effect and/or influence of non-constant noise-causing species.

Abstract: Methods and devices are provided for transporting fluid between a body and an external source. More particularly, the methods and devices provided can be used to transport blood from a body. In one exemplary embodiment, a system is provided for transporting fluid between a body and an external source. The system can include a collection catheter that is sized to fit inside a catheter that is placed in the body and configured to have its distal end extend beyond a distal end of the catheter that is placed in the body. Various methods for transporting fluid from the body to an external source are also provided.

Abstract: Blood sample optimization systems and methods are described that reduce or eliminate contaminates in collected blood samples, which in turn reduces or eliminates false positive readings in blood cultures or other testing of collected blood samples. A blood sample optimization system can include a blood sequestration device located between a patient needle and a sample needle. The blood sequestration device can include a sequestration chamber for sequestering an initial, potentially contaminated aliquot of blood, and may further include a sampling channel that bypasses the sequestration chamber to convey likely uncontaminated blood between the patient needle and the sample needle after the initial aliquot of blood is sequestered in the sequestration chamber.

Abstract: A device and method yielding a blood analysis employable in combination with an introducer for a catheter for a concurrent testing of blood from the introducer flash chamber during placement of a venous catheter. The device employs a colorimetric blood analysis to provide the user a visually discernable alert to the results of tested blood concurrent with the placement of the catheter with the introducer.

Abstract: An individual can exhibit one or more mental states when reacting to a stimulus. A camera or other monitoring device can be used to collect, on an intermittent basis, mental state data including facial data. The mental state data can be interpolated between the intermittent collecting. The facial data can be obtained from a series of images of the individual where the images are captured intermittently. A second face can be identified, and the first face and the second face can be tracked.

Abstract: Patients afflicted by a seizure may be monitored for the presence of post-ictal motor manifestations that may indicate that the patient is at heightened risk of adverse effects of a seizure, including, for example, risk of sudden explained death in epilepsy. If the patient is deemed to be at risk of experiencing adverse effects of a seizure, one or more system responses may be initiated as appropriate for the at-risk patient.

Abstract: A method for characterization of a patient's esophagus may include receiving data measured by an impedance and high resolution manometry catheter in an esophagus in which the data may be representative of a pressure and/or an impedance associated with a swallowing event. The method may also include determining a cross-sectional area of the esophagus based on the received data and a pre-determined amount of a bolus consumed during the swallowing event. Systems and apparatus for characterizing a patient's esophagus may also include measuring data with a high resolution manometry catheter to determine the cross-sectional area, work, and compliance of the esophagus as a function of time during a swallowing event. Averaged data may establish a database of normal values for work done and compliance and allow for comparison of a patient to normal pathology.

Abstract: There is provided an arrangement (100) for enabling assessment of scoliosis. The arrangement (100) is configured to obtain at least one x-ray image by means of one or more photon-counting x-ray detectors. The arrangement (100) is further configured to determine at least one characteristic of the spine of a patient having possible scoliosis based on said at least one x-ray image obtained by means of the photon-counting x-ray detector(s) to enable assessment of scoliosis.

Abstract: The system of the present invention is intended to provide a simple, out-of-clinic sleep disorders testing tool. It can be used for pretest screening and diagnosis, and post therapy follow-up of patients. The hardware component comprises a disposable sensor pack containing a PVDF airflow sensor and a PVDF pulse wave sensor, each of which is permanently connected to a signal conditioning and communications module configured to communicate with a patient's smartphone via a Bluetooth circuit. An APP stored in the smartphone allows a patient to initiate a diagnostic recording, collect and store digitized data onto the phone and, subsequently, upload data to a secure server for analysis on a host computer following completion of the test.

Abstract: Systems, methods and devices for controlled sympathectomy procedures for neuromodulation in the treatment of subjects having neoplastic conditions are disclosed. Systems, methods, and devices for interventionally treating a cancerous tumor and cancer related pain are disclosed.

Abstract: Dietary intake regulating devices that can assist a user in measuring his or her dietary intake and optionally his or her physical activity are disclosed.

Abstract: A method is described to facilitate behavioral nudging. The method includes receiving sensory data from one or more wearable devices, determining a context for a user wearing the one or more wearable devices based on the sensory data, determining a mechanism to nudge the user to reinforce user behavior based on stored preferences and policies and transmitting a nudging stimulus to at least one of the wearable devices via the determined mechanism to provide a notification to the user.

Abstract: A wireless communication method, a wearable device, a mobile terminal, and a system are provided. In the technical solution of the present disclosure, a mobile terminal sends frequency band information to a wearable device; the mobile terminal receives a second signal sent by the wearable device, converts the second signal into a second baseband signal, receives a third signal that is sent by a base station and corresponds to the frequency band information, and coverts the third signal into a third baseband signal; and the mobile terminal acquires a radio signal corresponding to the frequency band information according to the second baseband signal and the third baseband signal. In this way, data can be received through multiple paths by using communication capabilities of multiple wearable devices, and the receiving capability of a mobile phone can be greatly improved.

Abstract: Systems are described for monitoring extremities for injury following an impact. A system embodiment includes, but is not limited to, a device including a deformable substrate integrated with a textile; a sensor assembly coupled to the deformable substrate, the sensor assembly configured to generate one or more sense signals based on detection of a physical impact to a body portion and based on detection of a physiological parameter; circuitry operably coupled to the sensor assembly and configured to receive the one or more sense signals based on detection of the physical impact and to determine whether the physical impact exceeds a threshold impact value, the circuitry configured to instruct the sensor assembly to detect one or more physiological parameters of the body portion when the physical impact exceeds the threshold impact value; and a reporting device operably coupled to the circuitry; and an external device communicatively coupled with the device.

Abstract: An implantable medical device includes a sensing module configured to receive a cardiac electrical signal via electrodes carried by a medical electrical lead coupled to the implantable medical device and a control module configured to detect a lead issue. The sensing module is configured to produce cardiac sensed event signals and spike detect signals. The control module is configured to determine event intervals defined by consecutive ones of the received cardiac sensed event signals and the received spike detect signals and identify one or more received spike detect signals as lead issue spikes based on at least one of the determined event intervals.

Abstract: In one embodiment of the invention, an interactive vital signs scanning method is disclosed including concurrently scanning for a plurality of vital signs with a portable vital signs scanner; detecting movement of the portable vital signs scanner during the scanning for the plurality of vital signs; and determining a measure of quality of the scanning for the plurality of vital signs with the portable vital signs scanner. In another embodiment, a method of improving the quality of vital signs data is disclosed including concurrently sensing data from a plurality of vital signs sensors over a period of time with a portable vital signs scanner; determining a plurality of vital sign values for a respective plurality of vital signs in response to the sensed data from the plurality of vital signs sensors over the period of time; and fusing at least two vital sign values of the plurality of vital sign values for the respective plurality of vital signs.

Abstract: Systems and methods for providing sensitive and specific alarms indicative of glycemic condition are provided herein. In an embodiment, a method of processing sensor data by a continuous analyte sensor includes: evaluating sensor data using a first function to determine whether a real time glucose value meets a first threshold; evaluating sensor data using a second function to determine whether a predicted glucose value meets a second threshold; activating a hypoglycemic indicator if either the first threshold is met or if the second threshold is predicted to be met; and providing an output based on the activated hypoglycemic indicator.

Abstract: The present approach includes, in one implementation, a direct drive motor for use in a CT gantry and having a segmented motor stator assembly. The stator segments are connected in series. The stator segments are not independently operable and are instead connected in series to, and operated by, a single frequency controller.

Abstract: Provided is a method of providing location information regarding a location of a target object through a medical apparatus. The method includes setting photographing conditions about the target object, acquiring current location information of the target object, acquiring recommended location information of the target object according to the photographing conditions, outputting the acquired recommended location information, comparing the current location information with the recommended location information, and outputting additional information about a current location of the target object, according to a comparison result.

Abstract: An X-ray diagnostic device has an attachment-and-detachment detection element that detects an attachment-and-detachment of the attachment-and-detachment member, a rotation detection element that detects the rotation of the motor, a torque adjustment element that adjusts the torque of the motor, and a torque detection element that detects the torque when the rotation of the motor suspends; wherein when attachment-and-detachment is detected, the brake is released; when the brake is released, the rotation of the motor due to an out of balance condition between the up-and-down moving element and the counterweight is detected and the motor torques is adjusted so as to suspend the detected rotation of the motor; the torque when the rotation of the motor suspends is continuously provided, so that the balance between the up-and-down moving element and the counterweight can be kept positioned.

Abstract: One aspect of the present disclosure relates to a system that can employ multi-modal imaging to provide an image with an enhanced resolution. In some instances, the multi-modal imaging can allow an operator to determine and control a tissue margin without the need for intra-operative tissue pathology. The system can include an imaging system that includes a gamma camera to detect a gamma image and an optical imaging modality to detect an optical image. The system can also include a display device to display an enhanced gamma image created based on a function of the optical image. The enhanced gamma image illustrates a characteristic of a disease in the field of view (e.g., a lymphatic pathway, a sentinel lymph node target, or a satellite disease state).

Abstract: A medical image processing apparatus, includes: a reconstructed moving image obtainer that obtains a reconstructed moving image; a focus region identifier that identifies a first focus region corresponding to the designated focus; a fluoroscopic moving image obtainer that obtains at least one-period data on a fluoroscopic moving image; a second characteristics identifier that identifies each of two or more second characteristics regions corresponding to the internal body portion; a comparison selector that compares the two or more first characteristic regions; a conversion parameter calculation unit that calculates a conversion parameter for converting the first characteristic region.

Abstract: An X-ray apparatus includes an image separator configured to separate an X-ray image of an object into material images representing materials in the object; a parameter determiner configured to determine a width of a material of interest (MOI) based on the material images, and determine an enhancement parameter configured to enhance contrast of the MOI according to the width of the MOI; and an image enhancer configured to separate the X-ray image into detailed images respectively including spatial frequencies of different frequency bands, enhance each of the detailed images according to the enhancement parameter, and synthesize the enhanced detailed images to generate an enhanced image.

Abstract: A computed tomography (CT) apparatus includes a reconstruction unit which reconstructs a first CT image corresponding to a field of view (FOV) by using a first sinogram acquired by a CT scan of an object; and a correction unit which acquires a second sinogram by performing forward projection on the first CT image and acquires a second CT image by using the second sinogram and a third sinogram representing a portion of the object that is not included in the FOV. Thus, the CT apparatus reduces generation of image errors to thereby provide a high-quality reconstructed CT image.

Abstract: The invention relates to an imaging system (17) like a computed tomography system for generating an image of an object. Spectral measured projection data and non-spectral measured projection data are generated by a detector (6) having spectral detection elements and non-spectral detection elements, and spectral estimated projection data are estimated by using a model material distribution which could have caused the non-spectral measured projection data and by simulating a measurement of the spectral estimated projection data based on the model material distribution. An image is reconstructed based on the measured and estimated spectral projection data. Using the spectral estimated projection data in addition to the spectral measured projection data can lead to high quality spectral imaging, especially high quality spectral computed tomography imaging, which uses a simplified detector not only having generally more complex spectral detection elements, but also having simpler non-spectral detection elements.

Abstract: A radiation imaging system includes an imaging unit, a detection unit, a change determination unit and a control unit. The imaging unit emits radiation and images a dynamic state of a subject, thereby taking a plurality of frame images of the dynamic state of the subject. The detection unit detects the dynamic state of the subject being imaged and generates detection information on the dynamic state. The change determination unit determines whether change of the dynamic state being imaged is within a predetermined range based on the generated detection information. The control unit controls capturing of the taken frame images according to a result of the determination of the change determination unit.