Abstract: An exemplary system includes 1) a cochlear implant module configured to be implanted within a patient and including cochlear implant circuitry configured to apply electrical stimulation representative of one or more audio signals to the patient, 2) a first connector assembly coupled to the cochlear implant module and configured to be implanted within the patient, the first connector assembly including a first induction coil, 3) an implantable module configured to be implanted within the patient, and 4) a second connector assembly coupled to the implantable module and configured to be implanted within the patient, the second connector assembly including a second induction coil. The first connector assembly may be configured to be removably connected to the second connector assembly in order to facilitate inductive transfer of power between the first induction coil and the second induction coil. Corresponding systems are also disclosed.

Abstract: Preferred orientations and placements of an inductor relative to a communication coil in an Implantable Medical Device (IMD) are disclosed. The inductor can comprise part of a boost converter used to generate a power supply voltage in the IMD, which inductor may interfere with the coil. The inductor may have a length defined by its windings around an axis, which axis may be in a plane of the coil or in a plane parallel to the coil. The inductor can be included within the area extent of the coil, and is preferably oriented such that its axis is parallel to a maximum dimension of the coil. Ends of the inductor are further preferably equidistant from the coil. So oriented and placed, the inductor is less prone to interfering with the coil, thus improving communications with the IMD.

Abstract: A system for stimulating the release of satiety hormone in a subject comprises a stimulus device which is implantable in the subject and adapted to apply an electrical stimulus to a tissue of a gastrointestinal system of said subject, and a detection device which is implantable in the subject and adapted to continuously monitoring at least one of a mechanical characteristic and an electrical characteristic of the subject to detect an ingestion of food by said subject, wherein the detection device cooperates with the stimulus device such that the stimulus device applies said electrical stimulus in response to a detected ingestion of food.

Abstract: An system may include an electrode arrangement configured for implantation in an epidural space, a neural modulation generator configured to use electrodes in the electrode arrangement to generate modulation fields, at least one storage and a controller operably connected to the neural modulation generator. The storage(s) may be configured to store supra-perception threshold dorsal root modulation field parameter data and therapeutic modulation field parameter data, where the therapeutic modulation field parameter data may be different than the supra-perception threshold dorsal root modulation field parameter data.

Abstract: A technique for identifying lead-related conditions, such as insulation breaches and/or externalization of lead conductors, includes analyzing characteristics of electrical signals generated on one or more electrode sensing vectors of the lead by a test signal to determine whether a lead-related condition exists. The characteristics of the electrical signals induced on the lead by the test signal may be significantly different on a lead having an insulation breach or externalized conductor than on a lead not having such lead-related conditions. As such, the implantable medical device may be subject to a known test signal and analyze the signals on the lead to detect lead-related conditions.

Abstract: A method of determining health and mortality includes obtaining a ventricular activation (RR) time series from a subject for multiple temporal intervals. The method also includes calculating a cardiac entropy in the RR time series over the temporal intervals using coefficient of sample entropy (COSEn). Additionally, the method includes comparing the cardiac entropy between the intervals to determine health and mortality. The absolute and relative changes in entropy over a patient's follow up period provide dynamic information regarding health and mortality risk. The determination of health and mortality can then be used to create a treatment plan for the subject.

Abstract: System and methods for detecting impedance changes and for adjusting electrical therapy based on impedance changes are disclosed herein. A method in accordance with a particular embodiment includes applying a therapeutic, paresthesia-less electrical signal to a patient via a patient modulation system that includes a signal delivery device in electrical communication with a target neural population of the patient. The method can include monitoring on a periodic basis an impedance of an electrical circuit that includes the signal delivery device. The method can further include detecting a change in the impedance that indicates a fault and providing an indication that the fault exists.

Abstract: Centrifugal deflection device intended to be fitted to a surgical or dental handpiece to prevent the penetration of foreign matter that results from an operation, the centrifugal deflection device including a ring coupled in rotation either directly or via a tool shank to a drive shaft of the handpiece. This device is characterized in that the ring is covered by a sleeve secured to the front end of the body of the handpiece and which, with the ring, delimits an ejection chamber. The ejection chamber includes an inlet that communicates with a rear area of the handpiece and an outlet that communicates with the external environment, the ring having a first diameter at the outlet of the ejection chamber and a second diameter at the inlet of the ejection chamber, the first diameter of the ring being larger than the second diameter of the ring.

Abstract: Architectures for an implantable neurostimulator system having a plurality of electrode-driver integrated circuits (ICs) in provided. Electrodes from either or both ICs can be chosen to provide stimulation, and one of the IC acts as the master while the other acts as the slave. A parallel bus operating in accordance with a communication protocol couples the ICs, and certain functional blocks not needed in the slave are disabled. Stimulation parameters are loaded via the bus into each IC, and a stimulation enable command is issued on the bus to ensure simultaneous stimulation from the electrodes on both ICs. Clocking strategies are also disclosed to allow clocking of the master and slave ICs to be independently controlled, and to ensure that relevant internal and bus clocks used in the system are synchronized.

Abstract: A wearable terminal can include a main body configured to be in contact with a body of a user using one side of the main body, a photo plethysmography including a transmitter combined with one side of the main body and outputs a output signal, and a receiver detecting a reflection signal corresponding to the output signal returned, a cover configured to cover the photo plethysmography and be combined with the main body and a controller configured to measure a heart rate based on a reflection signal measured by the photo plethysmography. The cover is combined with the main body and parts corresponding to the transmitter and the receiver of the photo plethysmography include transparent units through which the output signal and the reflection signal are passing and a barrier unit positioned between the transparent units and shielding the output signal and the reflection signal.

Abstract: The present specification discloses devices and methodologies for the treatment of transient lower esophageal sphincter relaxations (tLESRs). Individuals with tLESRs may be treated by implanting a stimulation device within the patient's lower esophageal sphincter and applying electrical stimulation to the patient's lower esophageal sphincter, in accordance with certain predefined protocols. The presently disclosed devices have a simplified design because they do not require sensing systems capable of sensing when a person is engaged in a wet swallow and have improved energy storage requirements.

Abstract: In one aspect, an ingestible, electrical device, comprises one or more electrodes comprising a biocompatible conducting material and a biocompatible insulating material; a generator connected to the one or more electrodes; and an outer casing enclosing the one or more electrodes and the generator, the outer casing configured to dissolve in an aqueous environment of the organism; wherein the one or more electrodes have a first form factor when enclosed in the outer casing and a second form factor following a dissolution of the outer casing, the first form factor is a form factor that is collapsed an increased amount relative to an amount that the second form factor is collapsed, and the second form factor is a form factor that is collapsed a decreased amount relative to an amount that the first form factor is collapsed.

Abstract: A microwave applicator device comprising a probe (11) for ablating the body of a human or animal, a cooling passage sage (20, 21) extending through the probe (11) and arranged to carry a cooling fluid, a pump (71) for pumping the fluid through the probe (11), and an elongate flexible duct (104) extending between the pump (71) and one end of the cooling passage (20, 21), the pump comprising a pump body (73) including a motor (120) and a pump head (72) detachably mounted to the pump body (73), the pump head (72) comprising a first port (86) connected to a proximal end of the elongate flow duct (104), a second port (85) and fluid propulsion means (84, 92) for creating a flow of fluid between the ports (85, 86) and along the elongate flow duct 104 upon energization of the motor (120), the pump head (72) being arranged to sealingly contain the fluid.

Abstract: A method can include storing a plurality of data sets including values computed for each of a plurality of points for a given spatial region of tissue, the values in each of the data sets characterizing electrical information for each respective point of the plurality of points for a different time interval. The method can also include combining the values computed for each of a plurality of points in a first interval, corresponding to a first map, with the values for computed for each of the respective plurality of points in another interval and to normalize the combined values relative to a common scale. The method can also include generating a composite map for the given spatial region based on the combined values that are normalized.

Abstract: An axial-flow blood pump includes a housing having an inlet and an outlet opposite therefrom. An impeller located within the housing is suspended during operation by magnetic forces between magnets or magnetized regions of the impeller and a motor stator surrounding the housing, and hydrodynamic thrust forces generated by a flow of blood between the housing and a plurality of hydrodynamic thrust bearing surfaces located on the impeller. A volute may be in fluid-tight connection with the outlet of the housing for receiving blood in the axial direction and directing blood in a direction normal to the axial direction. The volute has a flow-improving member extending axially from the volute and into the housing in a coaxial direction of the housing.

Abstract: Devices, systems and methods are provided for treating migraine headaches and other conditions by non-invasive electrical stimulation of nerves and other tissue. A hand-held device includes a housing with a controller having a signal generator, an electrode for delivering electrical signals, and a conductive surface configured as a return path for the electrical signals. In certain implementations, the electrode is repositionable with respect to the housing. The patient can self-apply the hand-held device by pressing it against areas in need of pain relief. The device may include a pressure-sensitive gating switch to control delivery of the stimulation therapy. In certain embodiments, the electrode is a rollerball electrode. The device may include a chamber for retaining and dispensing conductive gel to the therapy site. In certain approaches, the device includes an electrode support for coupling an electrical stimulation system to the head for hands-free electrical stimulation therapy.

Abstract: A removable wrist device in a continuous physiological monitoring system includes a mounting fixture with a pair of rails to securely retain another device, such as a battery, a watch, or a display. The rails may be curved to secure the device against displacement during purely translational movement while conveniently conforming to the shape of a wrist. At the same time, the rails can permit movement around the axis of the wrist (where significant rotational forces are not regularly encountered) to permit convenient attachment and removal of the other device to the wrist-mounted device through a rotational, sliding motion. This configuration provides an advantageous combination of ease of use (sliding on and off in a natural motion), mounting tenacity, and comfort.

Abstract: The current technology is relevant to a system having a programming device capable of communication with an implantable medical device, where the programming device is configured to identify a patient condition comprising the patient's inability to exercise to a desired capacity, configured to notify a clinical user of the identified condition and configured to identify a therapy appropriate for the identified condition.

Abstract: A neurostimulation paddle lead, method of neurostimulation, and neurostimulation system are provided. The neurostimulation paddle lead carries a plurality of electrodes comprising at least four columns of electrodes having a spacing between two inner electrode columns less than a spacing between the inner electrode columns and adjacent outer electrode columns. The inner electrode columns may also be longitudinally offset from the outer electrode columns. The methods and neurostimulation systems steer current between the electrodes to modify a medial-lateral electrical field created adjacent spinal cord tissue.

Abstract: Disclosed is a plug-in accessory for operating a mobile device as an external controller for an Implantable Medical Device (IMD). The accessory includes a connector insertable into a port on the mobile device. Accessory circuitry can be powered by a battery or by the mobile device. An application on the mobile device in conjunction with the accessory configures the mobile phone for immediate use as an IMD external controller. When the accessory is inserted into the port or a switch on the accessory pressed, the application operates to validate the accessory; to unlock the phone; to secure the mobile device; and to render a graphical user interface on the mobile device for communicating with the IMD. The accessory can additionally include telemetry circuitry and an antenna for communicating with the IMD, rather than using short-range communication means provided in the mobile device itself.