Abstract: The present invention relates to an automated method of determining a kinetic state of a person. The method obtains accelerometer data from an accelerometer worn on an extremity of the person and processes the accelerometer data to determine a measure for the kinetic state. The present invention further relates to a device for determining a kinetic state of a person. The device comprises a processor configured to process data obtained from an accelerometer worn on an extremity of the person and to determine from the data a measure for the kinetic state. In the method and system the kinetic state is at least one of bradykinesia, dyskinesia, and hyperkinesia.

Abstract: Systems, methods, and devices relating to a sensor array for use with a user's finger segment and which indirectly maps the topography of a surface under the finger segment. Each sensor array is worn on a user's finger segment and has multiple sensitive strain gauges as well a positioning sensor. The multiple strain gauges are deployed around the periphery or sides of the finger segment. Each strain gauge measures the deformation of the finger segment pad as the finger segment passes over the surface topography. The relative ratios of the deformation detected indicates the location of a feature or contact point on the topography relative to the group of strain gauges. The positioning sensor determines the array's orientation as well as its location relative to a predetermined global reference frame.

Abstract: Devices and methods are disclosed for quantifying temporal changes in human anterior cruciate ligament (ACL) structural properties, such as Anterior-Posterior tibial shear force (TSF) and Anterior-Posterior tibial shear displacement (TSD) for testing ACL overuse injury during training and minimizing or preventing ACL injury.

Abstract: A stimulation probe device including a first electrode, a stimulation module, a control module and a physical layer module. The stimulation module is configured to (i) wirelessly receive a payload signal from a console interface module or a nerve integrity monitoring device, and (ii) supply a voltage or an amount of current to the first electrode to stimulate a nerve or a muscle in a patient. The control module is configured to generate a parameter signal indicating the voltage or the amount of current supplied to the electrode. The physical layer module is configured to (i) upconvert the parameter signal to a first radio frequency signal, and (ii) wirelessly transmit the first radio frequency signal from the stimulation probe to the console interface module or the nerve integrity monitoring device.

Abstract: Systems for detecting, locating and mitigating impact forces directed towards a person's head are described herein. The systems include devices for wearing on a wearer's head. The devices include a base configured to conform to the wearer's head and retain a plurality of pouches on an outer surface of the base. The plurality of pouches are configured to absorb at least a portion of the impact force directed towards the outer surface of the base, provide an indication when the impact force directed towards the outer surface of the base has a magnitude exceeding a concussion-indicating level of force, and provide a location of impact when the impact force directed towards the outer surface of the base has a magnitude exceeding the concussion-indicating level of force.

Abstract: A wireless intraluminal device (102) and an associated system for treating and diagnosing patients are provided. In one embodiment, the wireless intraluminal device (102) includes a flexible elongate member (158) including a proximal portion (106) and a distal portion (108); a sensor assembly (116) coupled to the distal portion of the flexible elongate member; a cable (117) coupled to the sensor assembly and extending along the flexible elongate member; and a wireless transceiver (252) positioned within the flexible elongate member, wherein the wireless transceiver is in communication with the sensor assembly via the cable. A wireless communication component (104) wirelessly transmits a sensor measurement collected by the sensor assembly to a sensor measurement processing system (132) via a wireless link (150) for physiological data generation at the sensor measurement processing system.

Abstract: Devices, apparatuses, and systems configured to assist in the location of an ABTT terminus and then to measure the temperature of the ABTT terminus.

Abstract: A device mouthpiece is provided wherein the mouthpiece comprises a cylindrical tube and a filter element, wherein the filter element comprises a frame and a filter medium secured to the frame; the frame defines an annular channel which receives therein an end portion of the cylindrical tube; the end portion of the cylindrical tube forms a friction fit within the annular channel; and wherein the filter element is secured to the cylindrical tube via the friction fit.

Abstract: A fall detection and identification system includes a tag worn by a user and a server. The tag collects acceleration data from one or more sensors embedded within the tag and transmits the data to the server. The server receives the data from the tag and performs an analysis on the data to detect and identify a fall. The analysis includes determining a change in acceleration of the user over the time window based on the acceleration data; comparing the change in acceleration of the user against one or more thresholds; and determining a status of the user based on the comparison of the change in acceleration of the user against the one or more thresholds.

Abstract: The disclosure provides tissue force sensor systems and methods for tissues, e.g., laryngeal tissue. The systems include a top housing including on an upper side an attachment mechanism for connecting the top housing to a medical device, e.g., a laryngoscope, and on a lower side a first cavity for receiving a top portion of a force measurement device such as a load cell; a bottom housing including on a lower side an attachment mechanism for connecting the bottom housing to a handle, holding system, or suspension system for holding or supporting the medical device, and on an upper side a second cavity for receiving a bottom portion of the force measurement device; and an attachment device for connecting the top housing to the bottom housing.

Abstract: Systems and methods are disclosed that provide for regular, periodic or continuous monitoring of fluid volume based on direct measurement of an inferior vena cava (IVC) physical dimension using a wireless measurement sensor implanted in the IVC. By basing diagnostic decisions and treatments on changes in an IVC physical dimension, information on patient fluid state is available across the entire euvolemic range of fluid states, thus providing earlier warning of hypervolemia or hypovolemia and enabling the modulation of patient treatments to permit more stable long-term fluid management.

Abstract: The invention relates to methods and compositions for restoring normal microbiota in pre-term newborns or newborns delivered by Cesarean section and methods for preventing or ameliorating diseases associated with delivery by Cesarean section or pre-term birth comprising administering to said newborns at the time of birth or shortly thereafter an effective amount of a vaginal microbiota inoculum obtained from the newborn's mother or a donor or an effective amount of a probiotic composition. The invention also relates to a device for collecting maternal vaginal microbiota from the vaginal canal of a patient. The device can have a housing forming a cavity, an absorbent material removable disposed within the cavity, and a deployment element disposed in the housing and movable along a length of the housing. The movement of the deployment element can displace the absorbent material out of the cavity and in to the vaginal canal.

Abstract: A method for determining the dry weight of a patient after dialysis therapy, wherein the patient's blood volume is monitored and blood volume values are output. The blood volume values are recorded and evaluated for a predetermined period of time after reaching an ultrafiltration volume appropriately predetermined for the patient, wherein the dry weight of the patient then is determined on the basis of the rate of change of the blood volume during the predetermined period of time.

Abstract: A gait motion display system including: a triaxial accelerometer, attached to the subject, that measures acceleration data of a subject in walking; an imaging unit that takes images of the subject in walking to obtain moving image data showing gait motions of the subject; a recording unit that records the acceleration data and the moving image data in synchronization with each other; an identification unit that converts the acceleration data recorded by the recording unit into horizontal displacement data and vertical displacement data, and identifies, from the moving image data, a representative image corresponding to a representative motion in a gait cycle, based on the horizontal displacement data or the vertical displacement data; and a display that displays an image illustration of the representative motion in the gait cycle, with the representative image identified by the identification unit.

Abstract: A hollow stranded wire (2) has a first layers (4) and second layers (6). The second layer is located outside the first layer. The first layer is formed by twisting eight first element wires (8) which are flat wires. The second layer is formed by twisting eight second element wires (10) which are flat wires. A ratio (Ww/Tw) of a width Ww to a thickness Tw of each flat wire is from 2 to 11. A twisting direction of the second element wires is opposite that of the first element wires. A twisting angle of each first element wire is not greater than 85°. A twisting angle of each second element wire is not greater than 85°. A ratio (D/T) of an average diameter D to a thickness T of the hollow stranded wire is not less than 5 and not greater than 20.

Abstract: In various embodiments, the invention teaches systems and methods for magnetic resonance imaging. In some embodiments, the invention teaches systems and methods for determining the source of pain in intervertebral discs by measuring one or more physiological biomarkers associated with disc pain and/or disc degeneration.

Abstract: A catheter system includes an elongated tube structure configured for insertion into a luminal space, such as the vasculature, of a body. The catheter is conductive and configured to conduct electrical signals. The catheter includes one or more power and data coupling devices configured to send and receive power and/or data signals, such as from an underlying guidewire disposed within a lumen of the catheter. One or more sensors are coupled to a distal section of the catheter and are electrically connected to the one or more power and data coupling devices.

Abstract: A biological fluid collection system that receives a sample and provides flow-through blood stabilization technology and a precise sample dispensing function for point-of-care and near patient testing applications is disclosed. A biological fluid collection system of the present disclosure is able to effectuate distributed mixing of a sample stabilizer within a blood sample and dispense the stabilized sample in a controlled manner. In this manner, a biological fluid collection system of the present disclosure enables blood micro-sample management, e.g., passive mixing with a sample stabilizer and controlled dispensing, for point-of-care and near patient testing applications.

Abstract: The present disclosure provides alert implants that comprise a medical device and an implantable reporting processor (IRP), where one example of such a medical device includes a component for a total knee arthroplasty (TKA) such as a tibial extension, a femoral component for hip replacements, a breast implant, a distal rod for arm or leg breakage repair, a scoliosis rod, a dynamic hip screw, a spinal interbody spacer, and tooling and methods that may be used to form the alert implant, and uses of such alert implants in the health maintenance of patients who receive the implant.

Abstract: A blood pressure measuring device includes a device main body; a curler configured to bend along a circumferential direction of a wrist of a living body, and configured to come into contact with a portion of the wrist at least between a dorsal side and a palmar side; a strap on the device main body, configured to cover an outer surface of the curler; a sensing cuff arranged in a region of the wrist where arteries exist; a rubber plate on a side of the sensing cuff nearer to the curler and configured to elastically deform; a pressing cuff between the curler and the rubber plate and configured to press the sensing cuff; and a cuff on a side of the curler nearer to the living body and arranged on the dorsal side of the wrist.