Abstract: Ultrasonic energy is used for treating degenerative dementia. A focal point of an ultrasonic transducer beam is directed at a target area of the brain to promote removal of substances that accumulate in the interstitial pathways that are at least partially responsible for the degenerative dementia. In one example, the target area of the brain may comprise the hippocampus and the degenerative dementia may be Alzheimer's disease. The ultrasonic beam may stimulate brain tissue at a frequency that corresponds to a naturally occurring deep sleep burst frequency of neurons and subsequent astrocyte activation patterns that drive a convective process responsible for brain solute disposal. For example, the transducer may generate a burst frequency of between 1-4 hertz to stimulate deep sleep brain functions that help remove amyloid plaque.

Abstract: The present disclosure belongs to the technical field of artificial cardiac pacemakers, and particularly relates to a leadless left-bundle-branch pacemaker. The leadless left-bundle-branch pacemaker comprises a case and an implant core, wherein the implant core is coaxially arranged inside the case, and a head of the implant core can be rotated out from the inside of the case; the implant core has an implant end that can be rotated out from the inside of the case, and the length of the implant end rotated out from the inside of the case is greater than 10 mm; and an end of the case corresponding to the implant end is provided with a fixing end for fixing the pacemaker.

Abstract: A system is provided that includes one or more processors, and a memory coupled to the one or more processors. The memory stores program instructions, and the program instructions are executable by the one or more processors. When executed, the one or more processors obtain cardiac activity (CA) signals for a series of beats, and identify whether a characteristic of interest (COI) from a first segment of the CA signals exceeds a COI limit. The one or more processors also analyze morphology of the CA signals for the series of beats responsive to the first segment of the CA signals exceeding the COI limit, and based on the analyze operation, identify a premature ventricular contraction (PVC) within the series of beats.

Abstract: The present invention relates an implantable pulse generator comprising an electric circuit, wherein the electric circuit comprises: a primary energy store, at least one secondary energy store, and a control unit, wherein the control unit is configured to activate an electric switch in the electric circuit in such a way that, in a first interval of a first phase of a pulse delivery, the primary energy store is discharged via a therapeutic current path, and to activate an electric switch in the electric circuit in such a way that, in a second interval of the first phase of the pulse delivery, the secondary energy store is discharged via the therapeutic current path, wherein the primary energy store and the at least one secondary energy store are fixedly connected, or connectable, in series, and wherein the implantable pulse generator is designed to deliver a shock having an approximately rectangular pulse waveform.

Abstract: A medical device for providing electrical stimulation to a brain of a patient includes one or more processors. The one or more processors are configured to determine a first set of parameters of a first electrical signal that is delivered via a first electrode configured to apply electrical stimulation to a first region of the brain and to determine a second set of parameters of a second electrical signal based on the first set of parameters. The second electrical signal is delivered via a second electrode configured to apply electrical stimulation to a second region of the brain. The one or more processors are further configured to deliver, with the first electrode, the first electrical signal having the first set of parameters and to deliver, with the second electrode, the second electrical signal having the second set of parameters.

Abstract: A ventricular assist device includes a fixation ring set and an inflow cannula designed in a suitable manner to left ventricle diameters and average heart dimensions for an adult woman and an adult man, wherein a surgical suture is not used in the ventricular assist device to provide an implantation facilitation and controlling of bleeding sites.

Abstract: An arrangement for OCT-based laser treatment of vitreous floaters. The arrangement for OCT-based laser vitreolysis includes an OCT system, a laser system having a deflection unit, optical elements that couple the OCT system and the laser system, a display unit and a central control and operating unit. The OCT system is configured to localize the floaters, the laser system is configured to destroy the floaters by application of laser pulses and the central control and operating unit is configured to determine apart from the coordinates of the localized floaters also their distance to structures of the eye, to derive exclusion criteria for the treatment, to align the deflection unit of the laser system to these coordinates and to focus and activate the laser system. The present invention relates to an arrangement for the gentle, low risk and painless laser treatment of vitreous floaters, which enables partially or fully automated therapy.

Abstract: An apparatus for a heart of a patient having a cardiac assist device adapted to be implanted into the patient to assist the heart with pumping blood. The apparatus has a sensor adapted to be implanted into the patient. The sensor in communication with the cardiac assist device and the heart which measures native volume of the heart. The apparatus has a first cardiac assist device and a second cardiac assist device tuned to maximize blood flow to the body of the patient, while resting the heart so the heart may recover function. Alternatively, the sensor monitors the heart based on admittance while the cardiac assist device. Alternatively, the sensor monitors the heart based on impedance.

Abstract: An exemplary electrode lead includes a flexible body formed of a flexible insulating material and that comprises a fantail region that connects to a cochlear implant configured to be implanted within a recipient and that extends to a ground electrode located toward a proximal end of the electrode lead, an electrode contact disposed on a side of the flexible body, a coiled electrode wire provided within the flexible body so as to extend along a length of the flexible body and electrically connect the electrode contact to a signal source, and a coiled reinforcing element provided within the flexible body so as to extend together with the coiled electrode wire along the length of the flexible body. The coiled reinforcing element may only be provided within a proximal portion of the electrode lead. Corresponding methods of manufacturing an electrode lead are also described.

Abstract: An exemplary cochlear implant system includes a sound processor, a cochlear implant, and equalization circuitry integrated within the sound processor and/or the cochlear implant. The sound processor operates externally to a recipient and is associated with a sound processor coil. The cochlear implant includes a cochlear implant coil larger than the sound processor coil and that is configured to form a transcutaneous narrowband inductive link with the sound processor coil when the cochlear implant is implanted within the recipient. By way of the transcutaneous narrowband inductive link, the cochlear implant receives a forward telemetry signal incorporating power and forward telemetry data. The equalization circuitry facilitates recovery, by the cochlear implant, of the forward telemetry data from the forward telemetry signal by compensating for distortion introduced onto the forward telemetry signal as a result of bandwidth limitations imposed by the transcutaneous narrowband inductive link.

Abstract: A headset for positioning an electronic device against a head of a patient includes a flexible frame configured to surround a portion of the head, the flexible frame defining an interior channel and an exterior slot, a curved structure configured to grasp an ear of the patient, the curved structure being movable within the interior channel of the flexible frame for accommodating a size of the head, and a mount including a support base to which the electronic device can be attached, the mount being slidable along the exterior slot of the flexible frame to position the electronic device along the head.

Abstract: A leadless cardiac pacemaker device is configured to provide HIS bundle pacing and contains a housing having a tip, a first electrode arranged on the housing in the vicinity of the tip, the first electrode being configured to engage with intra-cardiac tissue, and a second electrode arranged on the housing at a distance from the tip of the housing. A processor is enclosed in the housing and operatively connected to the first electrode and the second electrode. The processor is configured to process a reception signal received by at least one of the first electrode and the second electrode and to generate a pacing signal to be emitted using at least one of the first electrode and the second electrode.

Abstract: A medical lead includes a lead body, a lead body helix extending from a distal end of the lead body, wherein the lead body helix is configured to anchor to a patient tissue, and, a cable within the lead body, the cable including a cable conductor, a cable electrode proximate a distal end of the cable conductor, and a cable helix with a blunt tip at a distal end of the cable. The cable is slidable within the lead body to extend and retract the cable electrode along a trajectory extending from the distal end of the lead body.

Abstract: The present invention relates to a catheter that minimizes or eliminates the recirculation of oxygenated blood. The catheter of the present invention can be used to drain blood from multiple points in the patient, namely the superior vena cava, right atrium, and the right ventricle, while returning blood to the patient's pulmonary artery. Further, the catheter of the present invention is less likely to be moved or dislodged than catheters currently available in the art, thus making the catheter particularly useful for portable lung assist devices. The present invention also relates to methods for inserting the catheter into the patient and using the catheter with a lung assist device.

Abstract: In one embodiment, a defibrillation assembly energizable through case opening is provided. The defibrillation assembly includes an electromechanical component; an energy storage element that supplies power to the electromechanical component; circuitry configured to generate a defibrillation waveform, wherein the circuitry is isolated from the energy storage element by the electromechanical component; a housing within which the circuitry is located; and a case within which at least a portion of the housing is located, wherein an opening of the case causes the power to flow to the circuitry through the electro-mechanical component.

Abstract: A defibrillation assembly energizable through pad removal is provided. The defibrillation assembly includes an electromechanical component; an energy storage element that supplies power to the electromechanical component; circuitry configured to generate a defibrillation waveform, wherein the circuitry is isolated from the energy storage element by the electromechanical component; and electrode pads through which the defibrillation waveform is delivered to a patient, wherein a removal of at least one of the electrode pads from an initial position to a further position causes the power to flow to the circuitry through the electro-mechanical component.

Abstract: A multi-label electrocardiogram (ECG) signal classification method based on an improved attention mechanism is provided. A model is constructed for classifying a multi-label (multi-lead) ECG signal. The model has a strong ECG data learning ability, allowing a computer to fully extract a feature of the ECG signal and construct a data processing channel model. Therefore, the multi-label (multi-lead) ECG signal can be effectively classified, improving the accuracy and precision of classification.

Abstract: The present disclosure relates to an optical transfer device for tissue treatment. An optical transfer device of the present disclosure includes an optical probe having a light divergence part at the longitudinal end thereof, and a coating part configured to surround the optical probe, wherein the coating part includes a light diffusion part formed at the end thereof configured to cover the light divergence part, the light diffusion part having multiple grooves formed thereon.

Abstract: Some embodiments of the current disclosure are directed toward defibrillation and defibrillation equipment, and more particularly, an automated external defibrillator (AED) and a non-clinical power adapter therefor. In some embodiments, an AED may include an electrical connector to receive a battery pack, at least one capacitor to store energy, an electrotherapy delivery circuit to deliver the energy externally as electrotherapy, at least one discharge circuit to internally discharge energy stored in the capacitor(s), a non-clinical power adapter to be received by the electrical connector, and at least one processor.

Abstract: Technologies disclosed herein can be used to provide power and data to an implantable device implanted in a recipient, such as when the recipient is not wearing an external device. An example system includes a pillow or other headrest configured as a power and data source for an implanted medical device. Disclosed technologies can be configured to continuously provide power and data to an implantable medical devices over a period of time, such as substantially the entire period of time where the recipient is resting their head on the pillow.