Abstract: Disclosed is a method for measuring the refraction of an individual by a refraction measuring appliance, including: an initial step of determining at least one initial value of a visuo-postural parameter of the individual; a step of processing the initial value in order to deduce at least one initial value of a regulating parameter of the refraction measuring appliance, the regulating parameter being associated with the visuo-postural parameter; a step of regulating the refraction measuring appliance according to the initial value of the regulating parameter; and a step of measuring the refraction of the individual by the measuring appliance regulated in this way. Also disclosed is a method for the optical design of an ophthalmic lens, and to a pair of glasses including such a lens.

Abstract: Systems and methods for assessing the visual acuity of person using a computerized consumer device are described.

Abstract: Disclosed is an apparatus for measuring subjective ocular refraction including a display device configured to display a least one optotype and a refractive optical system arranged between an eye of a viewer and the display device, the refractive optical system having an optical power that can be varied according to a determined minimum step. The display device further includes a unit for varying optical power designed to generate a variation in the spherical and/or cylindrical optical power, such that the display device and the refractive optical system form a first image of the optotype with a first total optical power and, respectively, a second image of the optotype with a second total optical power, the variation in optical power between the first total optical power and the second total optical power being less than the determined minimum step.

Abstract: An image processing device processes an image of a subject eye. The image processing device includes an image acquisition unit that acquires an image of the subject eye, a diagnosis unit that obtains a diagnosis result of the subject eye based on the image acquired by the image acquisition unit, and a display control unit that changes a display mode of a display unit based on the diagnosis result.

Abstract: This patent describes a machine that allows patients with a single, central scotoma to receive an acceptable but sub-optimal refraction for the badThanks. eye based on previous refraction values, current refraction of the Good Eye, cataract characteristics, and subjective judgements of whether the patient can identify optotypes after incremental changes in refraction.

Abstract: Devices and methods for measuring high order aberrations from an eye are described. A method includes obtaining information indicating one or more aberrations of an eye, and obtaining information indicating one or more of a visual axis of the eye, a center of a pupil of the eye, and a corneal vertex of the eye. The information from the optical device is used to modify a design of a contact lens so that a combination of the eye and the modified contact lens has reduced high order aberrations. In some cases, information indicating the orientation of the contact lens positioned on the eye is also used. The optical device may include an aberrometer; a first light source for providing first light toward an eye; a lens assembly for collecting light from the eye; and a first image sensor for receiving light that has been transmitted through the lens assembly.

Abstract: An apparatus includes a stereoscopic image viewer. The stereoscopic image viewer includes a housing, a first lens, a second lens, and an eye-tracking image capture unit. The first lens, the second lens, and the eye-tracking image capture unit are contained in the housing. The eye-tracking image capture unit has a field of view and the eye-tracking image capture unit being is mounted within the housing with the first lens and the second lens within the field of view.

Abstract: Embodiments of the invention relate to a method of extracting eye velocity information from a video footage having a plurality of frames, comprising detecting at least part of an eye in at least two frames of the video footage, applying an optical flow algorithm to the at least two frames of the video footage to extract pixel velocity information, and determining a statistical measure from the pixel velocity information within the detected at least part of the eye. Other embodiments of the invention relate to a method of extracting head image trajectory information from a video footage having a plurality of frames, comprising detecting at least part of a facial region of the head image in at least two frames of the video footage, determining a measure of the movement of the at least part of a facial region between the at least two frames, and determining a transformation map from the measure of the movement.

Abstract: Systems and methods are disclosed for evaluating human eye tracking. One method includes receiving data representing the location of and/or information tracked by an individual's eye or eyes before, during, or after the individual performs a task; identifying a temporal phase or a biomechanical phase of the task performed by the individual; identifying a visual cue in the identified temporal phase or biomechanical phase; and scoring the tracking of the individual's eye or eyes by comparing the data to the visual cue.

Abstract: Virtual reality (VR) technology uses the human eye as a medium to communicate with an individual. It allows for technological access to the wearer's eye which can be inspected to identify health issues to initiate preventative care. Potential health impact of early diagnosis includes reducing 600k deaths due to heart conditions. The foundation of I-Examination is improving the quality of health of those we hold dear, our family and friends. VR is growing in popularity. People use it recreationally, viewing movies, conducting virtual tours, playing games, professionally for training or educational knowledge share. I-Examination, embedded within a VR, would have unlimited opportunities to examine the wearer's eyes. The application could run in the background as the individual engages in work or entertainment. It can also be directly applied during health assessments or routine eye examinations supporting an ophthalmologist to provide faster service effectively.

Abstract: A device may include a display screen and a generally triangular shaped body with first, second, and third sides, where the display screen may be generally parallel with the first side. The device may be configured such that either of the second side and third side may be oriented generally upwards during operation. The device may also include a sensor configured to detect whether the second or the third side is oriented generally upwards, and a computing device configured to orient an image to be displayed on the display screen based on whether the second or the third side is oriented generally upwards.

Abstract: Systems and methods for providing negative-pressure therapy with fluid instillation therapy and, more specifically, scheduling and controlling both the negative pressure therapy and the fluid instillation therapy are described. The method may comprise applying negative pressure to the dressing based on an initial therapy configuration, and monitoring negative pressure parameters associated with the application of negative pressure to the dressing to identify negative pressure alarm conditions. The method may further comprise applying instillation fluid to the dressing based on the initial therapy configuration, and monitoring instillation parameters associated with the application of instillation fluid to the dressing to identify instillation alarm conditions. Both may include modifying the initial therapy configuration to generate a modified therapy configuration in response to the negative pressure and instillation alarm conditions identified.

Abstract: Method and system for providing diabetes management is provided.

Abstract: A magnetic resonance imaging apparatus according to an embodiment includes processing circuitry. The processing circuitry is configured to specify a search start position of a matrix representing inter-regional connectivity between a plurality of regions in a brain based on a result of an analysis on an image of a subject and an attention degree set to each of the regions. The processing circuitry is configured to search the matrix using the search start position.

Abstract: Materials and methods are disclosed for screening advanced glycation end-products from mammalian ocular lens proteins to quantify early biomarkers for the diagnosis of diseases such as diabetes mellitus and to prevent related complications.

Abstract: A method for determining sub-diffuse scattering parameters of a material includes illuminating the material with structured light and imaging remission by the material of the structured light. The method further includes determining, from captured remission images, sub-diffuse scattering parameters of the material. A structured-light imaging system for determining sub-diffuse scattering parameters of a material includes a structured-light illuminator, for illuminating the material with structured light of periodic spatial structure, and a camera for capturing images of the remission of the structured light by the material. The structured-light imaging system further includes an analysis module for processing the images to quantitatively determine the sub-diffuse scattering parameters. A software product includes machine-readable instructions for analyzing images of remission of structured light by a material to determine sub-diffuse scattering parameters of the material.

Abstract: An image processing method for a fluorescence reaction region of teeth. The image processing method includes emitting blue light from a light source to illuminate the teeth in a mouth, so that the teeth generate fluorescence; capturing a first teeth image of the teeth by an image capturing unit; separating the first teeth image into a first red-value image, a first green-value image, and a first blue-value image by a processing unit; transforming the first red-value image into a second red-value image by the processing unit using a pixel value transforming function; and combining the second red-value image, the first green-value image, and the first blue-value image into a second teeth image by the processing unit.

Abstract: An optoacoustic sensor is configured to emit electromagnetic radiation and to detect acoustic waves, and a contact element is configured to be brought into contact with the object, the contact element being spaced from the optoacoustic sensor and being transparent to the electromagnetic radiation and the acoustic waves. Further, a scanning unit is configured to cause a movement of the optoacoustic sensor relative to the contact element, and a sealing element is configured to seal a space between the contact element and the optoacoustic sensor. The sealed space contains an acoustic coupling medium. At least a part of the sealing element is flexible to allow for the movement of the optoacoustic sensor relative to the contact element. Further, the optoacoustic sensor comprises a focused ultrasonic transducer configured to detect the acoustic waves generated in the object, the ultrasonic transducer having an axis of symmetry, and a light-emitting element configured to emit the electromagnetic radiation.

Abstract: A patch-type sensor module is provided. A patch-type sensor module according to one embodiment of the present invention comprises: a base substrate having flexibility and air permeability; an antenna pattern disposed on a first surface of the base substrate; a medicinal solution layer including a functional material and disposed on a second surface of the base substrate; a circuit board electrically connected to the antenna pattern, having at least one driving chip mounted thereon, and disposed on the first surface; and a temperature sensor mounted on the circuit board so as to sense a body temperature of a user.

Abstract: A system for evaluating breast cancer risk in a user includes: a temperature-sensing brassiere including: a first sensor mesh comprising: a first flexible mesh defining a mesh pattern and extending across a first breast region of the user; a first set of temperature-sensing assemblies arranged at intersections in the first flexible mesh; and for each temperature-sensing assembly in the first set of temperature-sensing assemblies, an electrical trace in the first mesh electrically coupling the temperature-sensing assembly to a controller; a brassiere structure configured to locate the first sensor mesh across the first breast region of the user; and the controller configured to: sample each temperature-sensing assembly in the first set of temperature-sensing assemblies during a data collection period to generate a series of temperature data; and store the series of temperature data.

Abstract: A system for distributed heat flux sensing of body tissue includes a distributed sensor, a thermal energy source, and one or more processors. The distributed sensor provides a plurality of temperature measurements corresponding to a plurality of points in a measurement range. The thermal energy source applies thermal energy to the body tissue along the measurement range. The one or more processors are configured to receive the plurality of temperature measurements from the distributed sensor, determine an amount of thermal energy applied by the thermal energy source at each of the plurality of points, and determine heat flux at each of the plurality of points based on the plurality of temperature measurements and the amount of thermal energy applied by the thermal energy source. The plurality of temperature measurements correspond to the plurality of points.

Abstract: Soft capacitive pressure sensors for continuous wearable health monitoring applications are described herein. Wrinkled gold thin films on elastomeric substrates are used as robust parallel plate electrodes to create a robust integration with the polymer, allowing repeated normal force to deform the thin film without failure. By incorporating micro-ridged structures that support the counter electrodes to create air cavities within the elastomeric dielectric layer, pressure sensitivity is further increased. The pressure sensors are configured to measure human physiological signals such as pressure exerted from a radial pulse on a skin's surface. The radial pulse pressure detected by the sensor can be correlated to an arterial blood pressure. Calibration of said pressure sensors using a neural network allows for determination of absolute blood pressure.

Abstract: A method of controlling a gas delivery apparatus including an apparatus controllable variable using an iterative algorithm to deliver a test gas (TG) for non-invasively determining a subject's pulmonary blood flow comprising iteratively generating and evaluating test values of a iterated variable based on an iterative algorithm in order output a test value of the iterated variable that meets a test criterion wherein iterative algorithm is characterized in that it defines a test mathematical relationship between the at least one apparatus controllable variable, the iterated variable and an end tidal concentration of test gas attained by setting the apparatus controllable variable, such that the iterative algorithm is determinative of whether iteration on the test value satisfies a test criterion or iteratively generates a progressively refined test value.

Abstract: A method for monitoring autoregulation includes, using a processor, using a processor to execute one or more routines on a memory. The one or more routines include receiving one or more physiological signals from a patient, determining a correlation-based measure indicative of the patient's autoregulation based on the one or more physiological signals, and generating an autoregulation profile of the patient based on autoregulation index values of the correlation-based measure. The autoregulation profile includes the autoregulation index values sorted into bins corresponding to different blood pressure ranges. The one or more routines also include designating a blood pressure range encompassing one or more of the bins as a blood pressure safe zone indicative of intact regulation and providing a signal to a display to display the autoregulation profile and a first indicator of the blood pressure safe zone.

Abstract: Systems and methods for performing and assessing neuromodulation therapy are disclosed herein. One method for assessing the efficacy of neuromodulation therapy includes positioning a neuromodulation catheter at a target site within a renal blood vessel of a human patient and delivering neuromodulation energy at the target site with the neuromodulation catheter. The method can further include obtaining a measurement related to a blood flow rate through the renal blood vessel via the neuromodulation catheter. The measurement can be compared to a baseline measurement related to the blood flow rate through the renal blood vessel to assess the efficacy of the neuromodulation therapy. In some embodiments, the baseline and post-neuromodulation measurements are obtained by injecting an indicator fluid into the renal blood vessel upstream of the target site and detecting a transient change in vessel impedance caused by the indicator fluid.

Abstract: The invention relates to a method of scanning for vascular ill health using a data set from an in vivo scan, the method including the steps of: (1) extracting blood vessel location data and blood vessel size data from the scan data set; (2) selecting a region in the extracted vessel location data; and (3) comparing the size data in the selected region to size data in a corresponding region of a normative data set to determine vascular health.

Abstract: Disclosed are methods, materials and devices for approximation of blood volume in a fluid, such as in a biological fluid collected during a surgical procedure. The method and devices include the use of a RBC flocculant, such as polyDADMAC, and an approximate blood hematocrit for the type of animal, as well as a calculated RBC packing ratio corresponding to the collection device being used. Also provided is a Blood Indicator Panel (BIP), comprising a series of markings calculated from an observed red blood settlement volume, the average animal type hematocrit, and a calculated RBC packing ratio “?” value for the collection device. Pediatric (about 200 ml or 250 ml size container), adult human (about 1,000 ml-1,500 ml) and veterinary (about 500 ml-2,500 ml) collection containers are also disclosed, that include a RBC flocculant, for use in approximating blood volume in a fluid. Methods of detecting blood in a sample, such as a fluid sample, and kits for performing the methods, are also provided.

Abstract: According to one embodiment, a sensor includes a structure body including a deforming portion, and a first sensing element provided at the deforming portion. The first sensing element includes first to fourth magnetic layers and a first intermediate layer. The first magnetic layer is provided between the second and third magnetic layers. The fourth magnetic layer is provided between the first and third magnetic layers. The first intermediate layer is provided between the second and first magnetic layers. The third magnetic layer includes at least one of a first material or a second material. The first material includes at least one selected from the group consisting of Ir—Mn, Pt—Mn, Pd—Pt—Mn, and Ru—Rh—Mn. The second material includes at least one of CoPt, (CoxPt100-x)100-yCry, or FePt. A crystallinity of at least a portion of the fourth magnetic layer is higher than a crystallinity of the first magnetic layer.

Abstract: A smart watch and a method for measuring a pulse information are provided in the present disclosure. The smart watch includes a dial, a watchband, a blood vessel information collecting apparatus, and a processing apparatus. The watchband is connected with the dial. The blood vessel information collecting apparatus is disposed in the watchband and is configured to collect a blood vessel information from an inner side of a wrist of a user. The processing apparatus is connected with the blood vessel information collecting apparatus and is configured to receive and process the blood vessel information to obtain the pulse information of the user.

Abstract: Disclosed are a heart rate detection system and a wearable device using the same. The heart rate detection system includes a light emitting unit, a light sensor and a processor. The light emitting unit emits a light to a human body. The light sensor senses a reflected light of the light and accordingly generates a first electric signal. The processor calculates the low-frequency noise signal and the high-frequency noise signal of the first electric signal, and removes them. After that, the processor executes a peak detection with respect to the first electric signal to calculate peak values of the first electric signal, and calculate a heart rate based on the time intervals among the peak values.

Abstract: Improved assemblies, systems, and methods provide safeguarding against tissue injury during surgical procedures and/or identify nerve damage occurring prior to surgery and/or verify range of motion or attributes of muscle contraction during reconstructive surgery. A stimulation control device may incorporate a range of low and high intensity stimulation to provide a stimulation and evaluation of both nerves and muscles. A stimulation control device is removably coupled to a surgical device or is imbedded within the medical device to provide a stimulation and treatment medical device. A disposable hand held stimulation system includes an operative element extending from the housing, the housing includes a visual indication to provide feedback or status to the user.

Abstract: An electrocardiography device is provided, including an adhesive assembly, a printed circuit board, two electrodes, a power supply assembly, and a sensing assembly. The printed circuit board is disposed on the adhesive assembly. The electrodes are connected to the circuit board and arranged along a first direction. The power supply assembly and the sensing assembly are disposed on the adhesive assembly and arranged along a second direction. The first direction is different from the second direction, and the power supply assembly is separate from the sensing assembly.

Abstract: The present disclosure provides methods for diagnosing and determining the disease progression of neurodegenerative disorders in patients using neurophysiological biomarkers.

Abstract: Electrocardiography (ECG) signals contain important markers for Coronary Heart Disease (CHD). State of the art systems and methods rely on clinically available multi-lead ECG for CHD classification which is not cost effective. Moreover the state of the art methods are applied on digital ECG time series data only. Also, discriminative HRV markers are not often present in short ECG recordings necessitating long hours of ECG data to analyze. In accordance with the present disclosure, systems and methods described hereinafter extract ECG time series from ECG images obtained from commercially available low-cost single lead ECG devices through a combination of image and signal processing steps including Histogram analysis, Morphological operation-thinning, Extraction of lines, Extraction of Reference Pulse, Extraction of ECG and interpolating missing data.

Abstract: A system for acquiring an electrical signal comprises: a plurality of electrodes, a plurality of signal quality detectors, each detector, being configured to detect a signal from a pair of electrodes and each detector comprising an analog-to-digital converter for providing a digital representation of a first resolution of the detected signal; a signal selection logic for determining at least one quality measure of each of the digital representations for selecting a pair of electrodes for signal acquisition; a multiplexer for selecting a pair of electrodes for signal acquisition based on a control signal from the signal selection logic; and a signal processing unit for performing analog-to-digital conversion on the selected signal and providing a digital representation having a second resolution, which is higher than the first resolution.

Abstract: A neural implant system for communicating neural impulses generated by a brain of a patient having a body includes a neural implant electrode system that is configured to be implanted in a selected site of the patient's brain. A wireless power receiver and communication circuit is in communication with the neural implant electrode and is configured to be disposed within the patient's body at a predetermined location. An external telemetry and power unit is configured to provide power to and to communicate with the wireless power receiver and communication circuit. The wireless power source and transceiver circuit is configured to operate outside of the patient's body.

Abstract: Methods, systems, and techniques for providing neurofeedback and for training brain wave function are provided. Example embodiments provide a Brain Training Feedback System (“BTFS”), which enables participants involved in brain training activities to learn to evoke/increase or suppress/inhibit certain brain wave activity based upon the desired task at hand. In one embodiment, the BTFS provides a brain/computer interaction feedback loop which monitors and measures EEG signals (brain activity) received from participant and provides feedback to participant. The BTFS may use an FFT based system or machine learning engines to deconstruct and classify brain wave signals. The machine learning based BTFS enable optimized feedback and rewards, adaptive feedback, and an ability to trigger interventions to assist in desired brain transitions.

Abstract: Methods, systems, and techniques for providing neurofeedback and for training brain wave function are provided. Example embodiments provide a Brain Training Feedback System (“BTFS”), which enables participants involved in brain training activities to learn to evoke/increase or suppress/inhibit certain brain wave activity based upon the desired task at hand. In one embodiment, the BTFS provides a brain/computer interaction feedback loop which monitors and measures EEG signals (brain activity) received from participant and provides feedback to participant. The BTFS may use an FFT based system or machine learning engines to deconstruct and classify brain wave signals. The machine learning based BTFS enable optimized feedback and rewards, adaptive feedback, and an ability to trigger interventions to assist in desired brain transitions. In addition, synchrony only based training is supported with the use of surround sound.

Abstract: Computerized systems, methods, and computer-readable storage media storing code for implementing the methods are described for providing dynamically-updated musculoskeletal information. One such system includes a processor is programmed to: provide, as an input to a trained inference model, information based on a plurality of neuromuscular signals from a user and information based on at least one image of the user; determine, based on an output of the trained inference model, position information describing a spatial relationship between two or more connected musculoskeletal segments of the user and/or force information describing a force exerted by at least one musculoskeletal segment of the user; and output the position information and/or the force information.

Abstract: Computerized systems, methods, and computer-readable storage media storing code for implementing the methods are provided for training an inference model used to generate a musculoskeletal representation. One such system includes a processor programmed to: determine, based on information obtained from at least one image, position information describing a spatial relationship between two or more connected musculoskeletal segments of a user; determine, based on a plurality of neuromuscular signals, force information; associate the position information with the force information; train an inference model to output a musculoskeletal representation consistent with the position information and/or the force information when neuromuscular input signals provided to the inference model have at least one predetermined characteristic, to produce an updated inference model; and cause the updated inference model to be stored in a memory.

Abstract: According to at least one example, an ambulatory medical device is provided. The device includes a plurality of electrodes disposed at spaced apart positions about a patient's body and a control unit. The control unit includes a sensor interface, a memory and a processor. The sensor interface is coupled to the plurality of electrodes and configured to receive a first ECG signal from a first pairing of the plurality of electrodes and to receive a second ECG signal from a second pairing of the plurality of electrodes. The memory stores information indicating a preferred pairing, the preferred pairing being either the first pairing or the second pairing. The processor is coupled to the sensor interface and the memory and is configured to resolve conflicts between interpretations of first ECG signal and the second ECG signal in favor of the preferred pairing.

Abstract: Certain examples of the present invention relate to a multi-electrode device for use with a user's body part. Certain examples provide an apparatus (100) comprising: a plurality of electrodes (101); a signal line (102) for conveying electrical signals to or from the plurality of electrodes (101); wherein the plurality of electrodes (101) and the signal line (102) are integrally formed in the apparatus (100), and wherein the apparatus (100) is configured such that a user is able to selectively electrically couple one or more of the plurality of electrodes (101) to the signal line (102).

Abstract: According to one embodiment, a magnetic resonance imaging apparatus includes processing circuitry. The processing circuitry collects magnetic resonance data in accordance with a pulse sequence. The processing circuitry determines image quality based on the magnetic resonance data. The processing circuitry selects a re-collection pulse sequence when it is determined that the image quality does not satisfy criteria, the re-collection pulse sequence having at least one of a type of sequence or an imaging condition differing from that of the pulse sequence.

Abstract: The present disclosure provides methods for targeting a biomedical system. Aspects of the subject methods include determining the trajectory of a targeting device using magnetic resonance imaging (MRI) of a MRI-visible style of a trajectory guide that is compatible with the targeting device. Targeted biomedical systems may be utilized for a variety of purposes including targeted delivery of a therapeutic, holding a therapeutic device, positioning of a therapeutic device and other uses. Also provided are devices and systems that can be used in practicing the described methods including but not limited to trajectory guides and adjustable targeting systems, as well as non-transitory computer readable medium storing instructions that, when executed by a computing device, cause a computing device to perform steps of the described methods.

Abstract: The present disclosure provides systems and methods for measuring a concentration of a contrast agent using magnetic resonance imaging (MRI). The method includes acquiring pre- and post-contrast data from a volume of a subject, where the pre-contrast data is acquired before a contrast agent is administered and the post-contrast data is acquired after the contrast agent is administered. A pre- and post-contrast resonance frequency map are then computed, where the pre-contrast frequency map is based on one or more pre-contrast resonance frequency values, and the post-contrast resonance frequency map is based on one or more post-contrast resonance frequency values. The pre- and post-contrast frequencies maps are then used to generate a resonance frequency change map that is subsequently used to generate a contrast agent concentration map that indicate a concentration of the contrast agent that was present at each voxel in the volume at the second time.

Abstract: Devices, systems, and methods for the localization of body lumen junctions and other intraluminal structure are disclosed. Various embodiments permit clinicians to identify and locate lesions and/or anatomical structures within a lumen and accurately place leads and/or devices within a lumen, through determining the intralumen conductance and/or cross-sectional area at a plurality of locations within the body lumen.

Abstract: A catheter-based tracking system includes one or more field generators and a processor. The one or more field generators, located adjacent to a Magnetic Resonance Imagining (MRI) system, are configured to apply Alternating Current (AC) magnetic fields. The processor is configured to receive signals, which are produced responsively to the AC magnetic fields in a single axis sensor (SAS) that is fitted at a distal end of a catheter inserted into an organ of a patient, to calculate, based on the signals received from the SAS, a direction of the distal end, to receive from a Hall effect sensor that is fitted at the distal end of the catheter a sensed component of a Direct Current (DC) magnetic field of the magnetic resonance imagining (MRI) system, and, based on the calculated direction and the sensed component of the DC magnetic field, to calculate a roll-angle of the distal end inside the organ.

Abstract: A portable device for receiving pulmonary function test data and displaying and analyzing same with both real-time and recorded patient clinical data such as that obtained with ultrasound and/or an electronic stethoscope.

Abstract: In one example, an apparatus. includes a shoe having a sole with at least a portion of foam replaced with a composite polymeric foam, at least one probe disposed in the composite polymeric foam, a voltage detector coupled to the probe that detects voltage data generated by the composite polymeric foam, and a transformation module that converts voltage data generated by the composite polymeric foam in response to deformation events into GRF, acceleration, or pressure data. In another example, a method includes receiving voltage data produced by composite polymeric foam, the composite polymeric foam providing support and padding in the sole of a shoe, converting the voltage data to force data, comparing the force data to a profile, and transmitting, when the force data fails to fall within a threshold of the profile, a feedback signal to a physical feedback device, the feedback signal indicating a difference with the profile.

Abstract: A valve sizer for determining an appropriate replacement valve size when performing a heart valve replacement procedure is provided. In one version the valve sizer has a hollow shaft with proximal and distal ends. A movable sizing element couples to the distal end of the shaft and is radially expandable between first, contracted and second, expanded positions. An actuator assembly on a handle includes an actuator coupled to a clutch member via a ball-spring-detent clutch. A rod extends through the shaft and maintains a fixed distance between the handle and a distal hub in the sizing element. Movement of the actuator causes axial movement of the shaft, thereby causing radial expansion of sizing petals relative to the hub. The clutch slips when a predetermined reaction force from the surrounding valve annulus is met by the petals.