Abstract: Methods and systems are provided for the circulation of blood using a purge-free miniature pump. In one embodiment, a pump is provided that may comprise a housing including a rotor and a stator within a drive unit. In this embodiment, the pump may establish a primary blood flow through the space between the drive unit and the housing and a secondary blood flow between the rotor and stator. In another embodiment, a pump establishes a primary blood flow outside the housing and a secondary blood flow between the rotor and stator. In yet another embodiment, a method is provided for introducing the pump into the body and circulating blood using the pump.

Abstract: The present disclosure generally relates to wearable devices and methods for measuring a photoplethysmographic signal. The wearable devices and methods may include a force sensor that provides input used for motion-noise filtering to obtain improved PPG signals. Feedback from the force sensor may also be used to indicate whether the amount of pressure exerted by the device should be adjusted, or whether the device should be switched to a locked state.

Abstract: A physiological signal detecting device includes a carrier, an electrode layer fixed on the carrier for receiving a physiological signal, and a signal transmitter buckled on the electrode layer and the carrier. The signal transmitter includes a transmitting member and an external connector. The transmitting member includes a first sheet, a column extending from the first sheet, and a thorn curvedly extending from the first sheet. The external connector includes a ring-shaped second sheet and a hollow protrusion extending from an inner edge of the second sheet. The thorn has a sharp end piercing into the electrode layer, the column passes through the electrode layer and the carrier, and a free end portion of the column exposes from the carrier. The protrusion is sleeved at and fastened to the free end portion so that the carrier and the electrode layer are sandwiched between the first and second sheets.

Abstract: An implant including a hermetically tightly sealed housing, wherein a control unit is arranged in the housing, and including a header, which is secured to the housing and includes at least one socket for connection to a plug of an electrode lead, and includes a communication antenna, which is electrically connected to the control unit. To achieve a reliable identification of the electrode lead with a low energy expenditure, the header has, in the region of the at least one socket, at least one electromagnetic transmission element electrically connected to a contact element which is provided on the inner wall of the at least one socket or to the ground of the implant and to the control unit, wherein the electromagnetic transmission element is electromagnetically or inductively coupled to the communication antenna. A corresponding electrode lead and a corresponding method for identifying an electrode lead are also contemplated.

Abstract: A device for neurostimulation has a number N of electrodes. N is equal to or larger than 3. The device is configured to deliver via each electrode therapeutic electric phases of amplitudes I1, I2, . . . IN, with a frequency f and after each therapeutic electric phase a number of N?1 charge balancing electric phases. The charge balancing electric phases of the respective electrode each have a polarity that is opposite the polarity of the preceding therapeutic electric phase of the respective electrode. The device is configured to return for each electrode the current of each therapeutic electric phase in the other N?1 electrodes.

Abstract: Apparatus, systems, and methods for the treatment of bone, cartilage and other types of hard tissue. The treatments, which are suitable for extended treatment, include the treatment and prevention of pathologies through the controllable use of silver, iron, zinc, or magnesium ions. These pathologies may include a pathology which is at least partially induced or aggravated by an infectious disease, for example a bacterial disease. In this case the electrically released ions are silver ions, which are known to have antibacterial properties.

Abstract: Various configurations of systems that employ leadless electrodes to provide pacing therapy are provided. In one example, a system that provides multiple sites for pacing of myocardium of a heart includes wireless pacing electrode assemblies that are implantable at sites proximate the myocardium using a percutaneous, transluminal, catheter delivery system. Also disclosed are various configurations of such systems, wireless electrode assemblies, and delivery catheters for delivering and implanting the electrode assemblies.

Abstract: Systems and methods of performing cardio resynchronization therapy (CRT) on a patient heart include the use of a stimulation system having at least one processor, at least one memory, a pulse generator, a stimulating electrode disposed in proximity to a His bundle of the patient heart, and a sensing electrode adapted to sense electrical activity of the left ventricle (LV) of the patient heart. CRT is provided by applying, using the pulse generator and through the stimulating electrode, a His bundle pacing (HBP) impulse having a first impulse energy. The sensing electrode is then used to measure an LV activation time in response to the HBP impulse. At least one setting of the pulse generator is modified based on the LV activation time such that a subsequent HBP impulse may be provided by the pulse generator via the stimulating electrode using a modified impulse energy.

Abstract: The present invention includes systems and methods directed towards a wearable device (100, 200) that can measure health parameters in two levels. The wearable device can measure a health parameter of a user using an attached sensor (112). This sensor measurement is checked against a threshold database (126, 146, 156) that details an action to be taken if the sensor measurement satisfies a health threshold. The health can be predetermined by the user or by a professional. This action can be a request to the user of the wearable device to move the wearable device to another part of his/her body so that the wearable device can gather a second sensor measurement that can provide more detail or context for the first sensor measurement. The wearable device can thus provide two levels of sensor data measurement, which it can store and synchronize to storage on a network/cloud service (104) or to another electronic device (102).

Abstract: A stimulation lead anchoring system includes a lead anchor and a removable inner core. The lead anchor includes an anchor body that includes a lead lumen that extends longitudinally along the anchor body and is configured and arranged to receive a portion of an electrical stimulation lead. The removable inner core includes a core body that includes an inner lumen that extends longitudinally along the core body. The lead anchor and removable inner core are configured and arranged to expand the anchor body when a portion of the core body is inserted into the lead lumen to facilitate receiving the portion of the electrical stimulation lead into the lead lumen and inner lumen and slidably positioning the lead anchor along the lead. The anchor body is configured and arranged to engage the portion of the electrical stimulation lead upon withdrawal of the core body from the lead lumen.

Abstract: Enclosures for implantable medical devices are machined from biocompatible materials using processes such as electric discharge machining and/or milling. Material is machined to create an enclosure. The enclosure may include an enclosure sleeve that has top and bottom caps added where the enclosure sleeve is machined either as a whole or as two separate halves that are subsequently joined together. During construction, circuitry is installed and where the enclosure includes an enclosure sleeve, the open top and bottom may be closed by caps while a connector block module may be mounted to the complete enclosure. The machining process allows materials that are typically difficult to stamp, such as grade 5 and 9 titanium and 811 titanium, that are beneficial to telemetry and recharging features of an implantable medical device to be used while allowing for an enclosure with a relatively detailed geometry and relatively tight tolerances.

Abstract: Provided is a wire fixing device for a cardiac pacemaker electrodes, including: an electrode fixator having an electrode clamping component, first hooks and second hooks; the electrode clamping component includes a first clamping piece and a second clamping piece that are semicircular cylindrical, the first clamping piece and the second clamping piece are connected by a clamp hinge connector, and a circular tube is formed when the electrode clamping component is closed; first hooks are provided on the back of the first clamping piece, second hooks are provided on the back of the second clamping piece, and hook tips of the first and second hooks are all bent towards a rotation direction of the electrode clamping component during closing; and the first and second hooks can be interlaced with each other when the electrode clamping component is closed, and can be separated when the electrode clamping component is open.

Abstract: The present disclosure is directed to a robotic surgical system. The robotic surgical system includes at least one robot arm, a camera, and a console. The console includes a first handle, a second handle, and a selector switch configured to select between a robotic control mode and a camera control mode. In the system the first handle or the second handle control the at least one robot arm in the robotic control mode and the first handle and the second handle control the camera in the camera control mode.

Abstract: An external defibrillator system may include processing circuitry; signal generation circuitry communicatively coupled to the processing circuitry; and a plurality of electrodes, each including an electrode body electrically coupled to the signal generation circuitry and configured to deliver an electrical pulse therapy to a patient; and an electrolyte dispersal pad that includes a substrate defining a plurality of wells, each defining an opening; an electrolyte material, e.g., fluid, disposed within at least a portion of the plurality of wells; and a conductive material disposed over at least a portion of the openings and configured to retain the electrolyte material within the plurality of wells, where the processing circuitry is configured control the signal generation circuitry to pass a current pulse through a portion of the conductive material to fuse the portion of the conductive material to release the electrolyte material from at least one of the wells.

Abstract: A sheath assembly for the insertion of a percutaneous pump includes a tubular sheath body dimensioned for insertion into a blood vessel through a vessel aperture. The tubular sheath body includes a wall having a proximal end portion, a distal end portion, a longitudinal axis, an outer surface, an inner surface defining a first lumen substantially parallel to the longitudinal axis, and a second lumen disposed within the wall between the inner surface and the outer surface and extending from the proximal end portion to the distal end portion. The first lumen is dimensioned to allow passage of a portion of the percutaneous pump, and the second lumen is dimensioned for passage of a guidewire. A stylet is removably positioned to substantially occlude the second lumen. The stylet has a proximal end releasably secured to the sheath assembly.

Abstract: A system and method of fitting an Electric Acoustic Stimulation (EAS) system of a patient that has binaural hearing is provided. The patient has an ipsilateral ear and a contralateral ear opposite the ipsilateral ear, with the EAS system associated with the ipsilateral ear of the patient. Stimulation parameters of the EAS system are developed unilaterally while taking into account hearing abilities of the contralateral ear. The EAS system is configured based on the developed stimulation parameters.

Abstract: Systems and methods for setting one or more parameters for a multi-test-period titration for oral appliance therapy are described herein. A method can include performing a titration for oral appliance therapy during a first test period, identifying a variable associated with the titration performed during the first test period, and setting a parameter for a titration for oral appliance therapy to be performed during a second test period. The parameter can be dependent on the variable associated with the titration performed during the first test period. The method can also include performing the titration for oral appliance therapy during the second test period, and establishing an outcome of oral appliance therapy based on the titrations performed during the first and second test periods.

Abstract: A system and associated method for determining whether a signal is ambiguous, wherein the system includes a plurality of electrodes configured to be located proximate tissue of a patient. A display apparatus thereof includes a graphical user interface configured to present information to a user. A computing apparatus thereof is configured to determine maximums for beats of signals from the electrodes.

Abstract: A monitoring system (10) includes at least one video camera (14), a motion unit (40), and a segmentation unit (42). The at least one video camera (14) is configured to continuously receive video of a subject in normal and darkened room conditions. The motion unit (40) identifies clusters of motion of the subject based on respiratory and body part motion in the received video of the subject. The segmentation unit (42) segments body parts of the subject based on the identified clusters of subject motion.

Abstract: The present disclosure generally relates to wearable devices and methods for measuring a photoplethysmographic (PPG) signal. The wearable devices and methods described herein are capable of obtaining PPG signals by employing a PPG sensor array configured to receive light at angles associated with a high perfusion index. Viewing components may be coupled to the PPG sensor array to effect transmission of light at these preferential angles.