Abstract: A biometric feedback system for providing biometric feedback to a subject while the subject performs a controlled physical movement includes an applied-force-recording interface and at least one controller electrically coupled to the applied-force-recording interface. The at least one controller receives applied force from the subject during the controlled physical movement and the applied-force-recording interface records data related to the applied force. The biometric feedback system also includes a dynamic surface electromyograph (“sEMG”) device that detects muscle tension along at least one muscle group of the subject while the subject performs the controlled physical movement and records data related to the muscle tension. A hub receives and processes data from the applied-force-recording interface and the dynamic sEMG device. A visual display displays the processed data from the hub.

Abstract: This invention relates generally to medical devices, and more specifically, to systems and methods for providing a fiducial marker. In one embodiment, a device includes, but is not limited to, one or more markers; and one or more connectors configured to link the one or more markers, wherein at least a portion of the device is detectable via medical imaging.

Abstract: A device for detecting electric potentials includes a plurality of measuring inputs (9) for connecting to measuring electrodes (11), which can be placed on the body of a patient (3), a plurality of measuring amplifiers (Op1, . . . , OpN), and a potential output (27) for connecting to an additional electrode (31), which can be placed on the body of the patient (3), to which a preset voltage can be applied. A summing unit (17) sends a signal, which is an indicator of the mean value of the signals sent by the measuring amplifiers (Op1, . . . , OpN). A current-measuring device (29) sends a current signal, which is proportional to the current flowing through the potential output. An analyzing unit (35) is connected to receive a potential output voltage signal, the summing unit output (19) signal and the current-measuring device signal. The analyzing unit is configured to generate an impedance signal from the fed signals.

Abstract: The invention concerns a rectal coil for magnetic resonance tomography, with a coil for transmitting and/or receiving magnetic resonance tomography electromagnetic signals, an inflatable balloon for securing or positioning the coil in the intestine and a shaft by means of which the coil and balloon are connected and which is used to introduce the rectal coil into the rectum, the coil being attached outside the balloon.

Abstract: According to one embodiment, a magnetic resonance imaging apparatus includes a gantry and a movable bed. A magnet, a gradient coil, and a radio frequency coil are built in the gantry. The movable bed is configured to be positioned to the gantry by a positioning mechanism having different structures at different positions in a longitudinal direction of the bed.

Abstract: Registration is provided for imaging with an intra-patient probe. The intra-patient probe is used for imaging or the imaging is, at least in part, of the intra-patient probe. Either approach for imaging with an intra-patient probe uses active transitions for registration. In one embodiment, one or more markers in the intra-patient probe are moveable relative to the intra-patient probe, allowing avoidance of occlusions and providing more reliable marker detection for registration. In another embodiment, a value of a parameter for imaging with at least one modality is changed so that acceptable or better registration with an image of another modality may be made. The imaging is repeated with differences, such as field-of-view or scale, allowing for registration for different types of modalities.

Abstract: An improved apparatus and method for capturing and analyzing the end-tidal portion of an exhalation. The CO2 level of air drawn into the system (10) is monitored to distinguish inhalation and exhalation of breath. Upon detection of a decrease in the CO2 level in the air drawn into the system (10), indicating a transition between exhalation and inhalation a pair of flow selector valves (26, 28) are operated to capture the end-tidal volume of air drawn into the system (10) immediately prior to the detection of the decrease in the CO2 level. Incoming air is diverted around the captured volume of air, and the CO2 levels are continually monitored to ensure that the captured volume of air corresponds to the end-tidal portion of an exhalation. Once the captured volume of air is positively identified as the end-tidal portion of an exhalation, the captured volume is routed through a gas analyzer (44) for analysis of one or more predetermined gas levels.

Abstract: An alignment system for the muscular-skeletal system is disclosed. The system supports parameter measurement and alignment. The system comprises a sensored device, a reference position tool, and a remote system configured to receive and display sensor data. The sensored device includes a three-axis accelerometer configured to measure position, rotation, and slope. The reference position tool comprises a body, a first arm coupled to a proximal end of the body, and a second arms coupled to a proximal end of the body. The sensored device couples to the reference position tool. The first and second arms of the reference position tool couples to the muscular-skeletal system in predetermined locations to allow a position of the muscular-skeletal system to be referenced. The body of the reference position tool can extend and retract to adapt to different sized muscular-skeletal systems.

Abstract: A tremor reduction device has a mechanical flap having a flap portion arranged to apply pressure on part of an inner arm in order to reduce tremor. The pressure can be manually adjusted by moving a rod in a channel in the tremor reduction device. The tremor reduction device has a case for pivotably mounting the mechanical flap and the pressure is at least partly determined by the angle of the mechanical flap relative to the case. The rod has a tapered section and the mechanical flap has a pin in contact the tapered section for changing the angle of the mechanical flap. Optionally a sensor is placed near the pressure applying location to sense the tremor and to provide a sensing signal to a driving mechanism which causes the rod to move in order to adjust the pressure.

Abstract: A system and method are described herein for a sensor device which biomechanically detects in real-time a user's movement state and posture and then provides real-time feedback to the user based on the user's real-time posture. The feedback is provided through immediate sensory feedback through the sensor device (e.g., a sound or vibration) as well as through an avatar within an associated application with which the sensor device communicates. The sensor device detects the user's movement state and posture by capturing data from a tri-axial accelerometer in the sensor device. Streamed data from the accelerometer is normalized to correct for sensor errors as well as variations in sensor placement and orientation. Normalization is based on accelerometer data collected while the user is wearing the device and performing specific actions.

Abstract: Accelerometer data that is received from multiple accelerometers can be synchronized to identify a known movement. This synchronization occurs in real time as the accelerometer data is received from the multiple devices. The orientation of an accelerometer can be compensated for dynamically. By dynamically compensating for the orientation, the user can wear the accelerometers in various orientations without needing to calibrate a portable computing device to account for a particular orientation. Portable devices can have one or more detachable accelerometers. The accelerometers can be detached and placed at virtually any location of a user's body to allow for the detection of custom movements.

Abstract: Techniques for monitoring and detecting ergonomic hot spots associated with movements of subjects are disclosed. For example, data may be collected by way of sensors attached to a plurality of subjects and may be analyzed to determine forces (e.g., vibration, jerks, acceleration, etc.) associated with the movements of the subjects. The analyzed data can be compared to ergonomic conditions to detect the ergonomic hot spots.

Abstract: Embodiments herein provide detection of contamination at one or more contacts of a sensor system. The sensor system includes a sensor assembly and an electronics assembly communicatively coupled together by one or more contacts. The sensor assembly passes a sensor signal to the electronics assembly for further processing. The electronics assembly includes a detection contact for detecting contamination on or near one or more contacts of the sensor assembly and/or the electronics assembly. A switch selectively couples the detection contact to a bias voltage during a measurement mode and to a reference voltage during a detection mode, the reference voltage being different from the bias voltage. A method of contamination detection includes switching the electronics assembly between the measurement mode and the detection mode, and monitoring for a change in the output signal received by the electronics assembly.

Abstract: Perioperative patient blood glucose concentrations are determined by imposing patient effluent ultrafiltrate through a sample cell incorporated in an automated polarimeter. The device includes an optical platform, fluid handling subassembly, controlling electronics, and integration software. A stable collimated light source of known intensity and distinct specified wavelength is passed through an optical platform including a polarizer, retarder, bandpass filters, sample flow cell, analyzer and detector. The angular rotation of the transmitted light resulting from the glucose contained in patient ultrafiltrate collected in the sample flow cell is recorded and provides a measure of the glucose concentration.

Abstract: A device for detection or measurement of a carbohydrate analyte in fluid comprises: an optical sensor comprising components of an assay for carbohydrate analyte, the readout of which is a detectable or measurable optical signal, and a light guide having a distal portion optically coupled to the assay components and a proximal portion; and a reader for interrogating the optical sensor, the reader comprising an assay interrogating system including a lens; and an interface portion forming part of at least one of the optical sensor and the reader, the interface portion being capable of removably constraining the proximal portion of the light guide and the lens of the assay interrogating system in an optically coupled arrangement. The device may be combined with an insulin-infusion system.

Abstract: One variation of the method for managing blood loss of a patient includes: receiving an image of a physical sample; extracting a feature from an area of the image corresponding to the physical sample; estimating a blood volume indicator of the physical sample according to the extracted feature; estimating a patient blood loss based on the blood volume indicator; estimating a euvolemic patient hematocrit based on an estimated patient blood volume and the estimated patient blood loss; receiving a measured patient hematocrit; and generating a volemic status indicator based on a comparison between the measured patient hematocrit and the estimated euvolemic patient hematocrit.

Abstract: A physiological signal processing apparatus and a method for the same. The physiological signal processing apparatus includes a first light-emitting element, a second light-emitting element, a light control module, an image sensing module and an analyzing module. The light control module is capable of controlling the first light-emitting element to emit a first light beam and the second light-emitting element to emit a second light beam on a light guide panel for a finger to touch. The image sensing module is capable of sensing the first light beam and the second light beam reflected by the light guide panel and acquiring an image signal of the finger. The analyzing module is capable of analyzing the image signal extracted by the first light beam to acquire a first physiological signal and analyzing the image signal extracted by the second light beam to acquire a second physiological signal.

Abstract: A light source emits light into a first portion of a living body. Functionalized particles within the body are configured to specifically bind to a target analyte, and upon receiving the emitted light, undergo a reaction that separates a detectable label from the functionalized particle. A sensor device is configured to detect a response signal from a second portion of the living body that is indicative of an abundance of the detectable label in the second portion. A control system uses the sensor device to obtain sensor data indicative of the response signal from the second portion of the living body detected by the sensor device during a measurement interval, and determines a presence or absence of the target analyte within the first portion of the living body based in part on the obtained data.

Abstract: Devices are provided for measurement of an analyte concentration, e.g., glucose in a host. The device can include a sensor configured to generate a signal associated with a concentration of an analyte; and a sensing membrane located over the sensor. The sensing membrane comprises a diffusion resistance domain configured to control a flux of the analyte therethrough. The diffusion resistance domain comprises one or more zwitterionic compounds and a base polymer comprising both hydrophilic and hydrophobic regions.

Abstract: Methods, systems and devices for providing improved calibration accuracy of continuous and/or in vivo analyte monitoring systems based at least in part on insulin delivery information are provided. Many of the embodiments disclosed herein can determine appropriate conditions for performing a calibration of the analyte sensor in view of the scheduled delivery of insulin or administered insulin amount. One or more other parameters or conditions can also be incorporated to improve calibration accuracy including, for example, the physiological model associated with a patient, meal information, exercise information, activity information, disease information, historical physiological condition information, as well as other types of information. Furthermore, according to some embodiments, calibration of the analyte sensor can be delayed or not performed at all, if appropriate conditions are not met.

Abstract: A testing device according to the present invention includes a housing including a skin surface sheet and an upper surface cover. A hollow needle configured to interlock with the upper surface cover and a testing reagent or equipment are accommodated in the housing. Through deformation of the upper surface cover by application of an external force, the hollow needle perforates the skin. A body fluid flows in the space inside of the housing and is brought into contact with the testing reagent or equipment to acquire information on the body fluid. Through recovery of the upper surface cover to an original shape by elimination of the external force, the hollow needle again becomes accommodated in the housing.

Abstract: The present invention relates to a device (100) for measuring a cycling cadence, a method (500) of operating a device (100) for measuring a cycling cadence, and a cycling cadence computer program. The device (100) comprises a motion sensor (such as, e.g., an accelerometer) for detecting a movement of the device (100) and for generating a motion signal (x, y, z) corresponding to the movement; a cadence determination unit (300) for determining cycling cadence based on the motion signal (x, y, z). The device (100) can be worn on the cyclist's wrist or arm (110). The motion sensor in the device is able to pick up the tiny movements of the arm or wrist that correspond to the cadence. Optionally, an algorithm is applied that can derive the cadence from a noisy signal.

Abstract: The present system is directed in various embodiments to devices, systems and methods for detection, evaluation and/or monitoring olfactory dysfunction by measuring and determining the patient's olfactory detection threshold for the left and the right nostril. More specifically, the present invention relates to devices, systems and methods for detecting an asymmetric differential in a patient's olfactory detection threshold (left vs right nostril) which, when present, may be used as a tool to screen, detect, diagnose and/or monitor relative olfactory deterioration resulting from Alzheimer's disease. A preferred embodiment comprises cascading aromas by serially administering more than one pure odorant to the patient's nostrils, left vs right, with measurement of the time, or numbers of breaths, required to cognitively notice the pure odorants' presence.

Abstract: A system and a method for assessing a condition in a subject. Phones from speech of the subject are recognized, one or more prosodic or speech-excitation-source features of the phones are extracted, and an assessment of a condition of the subject, is generated based on a correlation between the features of the phones and the condition.

Abstract: Provided is a sleep display program, a sleep display method, and a sleep display device for visualizing an internal clock regarding sleep. The sleep display program is a program for displaying, in a display unit, sleep state data of a user that has been measured and recorded by a sleep evaluation device, the data including at least a wakeup time TW and a bedtime TZ, and the program including a step of obtaining the data from the sleep evaluation device, a step of displaying, in the display unit, a 24-hour circular time display image divided into time periods that each indicate a predetermined span of time, and a step of plotting, on the time periods in the time display image, a set number of days' worth of records of the wakeup times TW and the bedtimes TZ included in the data.

Abstract: In one aspect, the systems, environment, and methods described herein support anticipation and identification of adverse health events and/or atypical behavioral episodes such as Autistic behaviors, epileptic seizures, heart attack, stroke, and/or narcoleptic “sleep attacks” using a portable data collection device. In another aspect, the systems, environment, and methods described herein support measurement of motions and vibrations associated with recurring transitory physiological states and events using a portable data collection device. For example, motion and vibration measurements may be analyzed to identify pronounced head motion patterns indicative of specific heart defects, neurodegenerative conditions, inner ear or other balance problems, or types of cardiac disease.

Abstract: A monitoring device for measuring one or more physiological parameters of a medical patient can include a finger clip sensor connected to a monitor. A placement indicator helps the patient to properly position the sensor. The monitor can display a message alerting the patient to reposition the sensor. The device can delay measurement until the sensor is properly positioned.

Abstract: A method of providing a metal coating on a substrate (10), and electrically insulating sections/parts of the metal coated substrate from each other. A substrate is provided with an insulating material in the substrate, the insulating first material extending through the thickness of the substrate and protruding above one surface of the substrate. It forms an enclosed section/portion (14) of the substrate. A protective structure (15) is provided on the insulating material such that it covers the entire circumference thereof. The insulating material is selectively etched to create an under-etch (18) under the protective structure. Finally conductive material (19) is deposited to provide a metal coating over the substrate, whereby the under-etch will provide a disruption in the deposited metal coating, thereby electrically insulating the enclosed section from the surrounding substrate.

Abstract: Devices, systems, and associated methods for determining heart rate (HR) of a subject from noisy Electrocardiogram (ECG) data are disclosed and described.

Abstract: Self measurements of physiological parameters such as blood pressure are prone to errors and artifacts since they are often not done according to established and standardized protocols i.e., such that predetermined conditions for a reliable measurement are not met. To determine whether the predetermined conditions for a reliable measurement are met one or more physiological and environmental sensors are used to determine a measurement context. The obtained sensor data is compared with predetermined thresholds to determine whether the context allows a reliable self test. In case the predetermined conditions are not met based on the obtained sensor data instructions are given to guide the subject that wants to do a self test.

Abstract: Apparatuses and methods for the prevention of bodily injuries through active monitoring of bodily postures, supporting a body while in or restricting a body from entering predetermined postures which heighten the body's susceptibility to injury, and alerting one or more entities (e.g., an apparatus user) of a body's susceptibility to injury is disclosed herein. In one embodiment, the method may include one or more operations including monitoring one or more bodily postures and/or bodily movements, storing data associated with bodily postures and/or bodily movements, determining a risk of injury associated with bodily postures and/or bodily movements, and alerting one or more entities when a risk of injury associated with bodily postures and/or bodily movements reaches a predetermined level.

Abstract: Methods and systems for the determination and representation of anatomy anatomical information are disclosed herein.

Abstract: Systems and methods are disclosed for monitoring data associated with a plurality of physiological characteristics of a patient, comprising: the methods include generating a set of super-alarm patterns associated with the plurality of physiological conditions, wherein the super-alarm patterns comprising data relating to a combination of at least two individual raw alarms from independent physiological data streams that co-occur within a temporal window, and triggering an alarm if a combination of the input physiological data matches at least a portion of a generated super-alarm pattern.

Abstract: An embodiment in accordance with the present invention provides a method for applying task-based performance predictors (measures of noise, spatial resolution, and detectability index) based on numerical observer models and approximations to the local noise and spatial resolution properties of the CBCT reconstruction process (e.g., penalized-likelihood iterative reconstruction). These predictions are then used to identify projections views (i.e., points that will constitute the scan trajectory) that maximize task performance, beginning with the projection view that maximizes detectability, proceeding to the next-best view, and continuing in an (arbitrarily constrained) orbit that can be physically realized on advanced robotic C-arm platforms.

Abstract: According to the present invention, improved methods and apparatus are provided for providing cushioning and other ergonomic surfaces on devices requiring the patient or tissue to be compressed, such as radiography machines, fluoroscopy units, mammography units and the like. In particular a radiolucent pad element is provided for releasable attachment to at least one surface of a compression device to be used under x-ray, for example, during mammography. The pad element of the present invention can be disposable or constructed to be reusable and in some cases may be applied directly to the patient's breast. Furthermore, a cushioned paddle is provided wherein the compression paddle and the cushion can be separately or integrally formed.

Abstract: A system and method of X-ray imaging includes an X-ray emitter that projects X-rays. An X-ray receiver receives X-rays from the X-ray emitter to produce a plurality of projection images. A filter with at least one filter leaf absorbs at least a portion of the X-rays from the X-ray emitter to define a limited field of view within a full field of view, wherein the X-rays are attenuated in at least one attenuated portion of the full field of view. A processor reconstructs a three dimensional image based upon the projection images of the full field of view. The limited field view is located within the reconstructed three dimensional image. At least one corrective parameter is determined from the reconstructed three dimensional image. A three dimensional image is reconstructed based upon the limited field of view and the at least one corrective parameter.

Abstract: A control apparatus for an X-ray imaging system obtains examination information including a plurality of imaging techniques and a plurality of imaging conditions corresponding to the plurality of imaging techniques. When the content of a condition item of the imaging condition selected from the plurality of imaging conditions is changed in accordance with an operation input from the operator, the control apparatus applies the change to an imaging condition other than the selected imaging condition of the plurality of imaging conditions.

Abstract: A medical image processing apparatus according to the embodiments includes a memory circuitry that stores a program, and a processing circuitry that reads out the program from the memory circuitry and executes the program. The processing circuitry sets a region of interest to be observed and a region of non-interest that is different from the region of interest based on volume data, and determines a trajectory of an arm that holds an X-ray irradiator that irradiates X-rays and a detector that detects the irradiated X-rays based on a relative positional relationship between the region of interest and the region of non-interest.

Abstract: Disclosed herein are an X-ray imaging apparatus and a control method thereof in which a clear 3D volume of an object may be acquired when the 3D volume of the object is reconstructed from X-ray images acquired by radiating X-rays to the object. The X-ray imaging apparatus includes an image processing unit configured to acquire a plurality of X-ray images of an object from converted electrical signals, group the plurality of X-ray images into groups of X-ray images acquired from the same cardiac phase, and perform image reconstruction of each of the groups acquired as a result of the grouping.

Abstract: Disclosed is a method and apparatus for determining a tumor ablation margin. The method includes acquiring an angiography image before tumor ablation and an angiography image after tumor ablation when tumor ablation is performed, registering the angiography image before tumor ablation and the angiography image after tumor ablation, and determining the tumor ablation margin according to the relative positions of the tumor area in the angiography image before tumor ablation and the ablation area in the angiography image after tumor ablation after registration. Using an embodiment, one directly determines the tumor ablation margin during tumor ablation, thus improving the efficiency and success rate of tumor ablation.

Abstract: In image data obtained, the radius and the ulna, and interosseous soft tissue between two bones are identified. A midpoint (Ygk) of the length of the interosseous soft tissue in a Y axis direction in (Xk) coordinates is determined. This midpoint is determined in multiple coordinates, and an approximate straight line of these midpoints is determined and set as a reference line. The foot of the perpendicular from the ulna styloid process to the reference line is set as a reference position. A region of interest is set in a position at a predetermined distance from the reference position along the reference line.

Abstract: An X-ray imaging apparatus can include an X-ray detector configured to acquire X-ray data by detecting X-rays and an image processor configured to segment a first image generated based on the acquired X-ray data into two or more segmentation regions, to identify one or more materials present in one segmentation region of the two or more segmentation regions, and to acquire an image relating to an object which includes abnormal materials.

Abstract: An X-ray apparatus includes: a collimator for adjusting an X-ray irradiation region; a data obtainer for obtaining position information of a target in an object based on an electrode signal sensed from electrodes attached to the object; and a controller for setting first coordinates indicating a position of the target on a first coordinate system with respect to the object based on the position information, transforming the first coordinates to second coordinates on a second coordinate system with respect to an X-ray image of the object, and adjusting a position of the collimator based on the second coordinates.

Abstract: An apparatus, method, and computer program product for calibrating a CT scan without the use of an external calibration phantom, to enable quantitative assessment of internal body tissues and organs and additionally for any application that would benefit from a calibration of the scan attenuation data, such as viewing CT images in a consistent fashion. Embodiments are described with applications to quantitative assessment of bone density in the spine and hip, mineral content in blood vessels, hepatic-fat content in the liver, and gray-to-white matter ratio in the brain. The primary advantages of the method are that it does not require the use of an external calibration phantom, it is robust across different CT machines and scanner settings, and it is also highly precise, lending itself to a high degree of automation.

Abstract: A phantom assembly for testing x-ray equipment comprising a phantom assembly for testing x-ray equipment comprising at least one image plate made of at least one image plate material, at least one base member made of at least one base material, at least one step surface formed in the base member, and at least one mesh insert. The at least one base material is selected, sized, and dimensioned such that base member yields a transmitted reference signal in addition to at least one transmitted energy test spectrum associated with the at least one step surface. The at least one mesh insert is selected, sized, and dimensioned such that the at least one mesh insert yields a transmitted energy resolution signal.

Abstract: A method and system are disclosed for a compact, inexpensive ultrasound system using an off-the-shelf personal digital assistant (PDA) device interfacing to a hand-held probe assembly through a standard digital interface. The hand-held probe assembly comprises a detachable transducer head attached to a beamforming module that performs digital beamforming. The PDA runs Windows applications and displays menus and images to a user. The PDA also runs ultrasound data processing software to support a plurality of imaging modes. An internal battery is provided in the PDA to power the system. The transducer head is detachable from the beamforming module.

Abstract: A surgical retractor device for retaining and/or moving internal organs during minimally invasive or laparoscopic surgery is provided. The surgical retractor can be a single continuous structure that includes a shaft. The shaft can branch into a first elongate finger with a first distal end opposite the shaft and a second elongate finger with a second distal end opposite the shaft. The retractor can further include a resilient lattice structure disposed between the first elongate finger and the second elongate finger. The retractor can have an expanded configuration and a collapsed configuration based on relative distance between the first distal end and the second distal end. When the retractor is in the collapsed configuration, spring force energy can be stored in the resilient lattice structure.

Abstract: In intervertebral operative spinal procedures, using separate or pre-attached spreader blocks to control the directional growth of a distracting balloon.

Abstract: The present disclosure relates to an anchor assembly. The anchor assembly includes an anchor defining a cavity and an opening to the cavity; and a headless insertion member configured for arrangement within the anchor cavity, the insertion member including a body having a threaded proximal portion, a non-threaded distal portion, and a cannulation extending a partial length of the insertion member. Other anchor assemblies, anchors, and delivery devices are also disclosed.

Abstract: A method for securing a suture to bone can include loading the suture in a distal opening of an inserter of an assembly. The suture can be coupled to soft tissue. The assembly can include the inserter, an anchor carried by the inserter, a distal tip and a driver each coupled to the inserter. A hole can be formed in the bone with the distal tip, and the distal opening and a portion of the suture can be positioned in the hole. The driver can be actuated to allow movement relative to the inserter and can be advanced in a first direction to drive the anchor about the inserter into the hole to secure the distal tip, anchor and suture to the bone with an absence of a knot. The driver can be moved in a second direction to remove the inserter from the distal tip, anchor and suture.