Abstract: There is provided a fitting device configured to be communicatively connected to first stimulation device comprising an implantable electric stimulation device including a plurality of stimulation channels for electrical stimulation of a patient's ipsilateral ear at various stimulation sites according to a electrical stimulation signal and a second stimulation device selected from the group consisting of a device for acoustic stimulation of the patient's ipsilateral ear and a device for acoustic stimulation of the patient's contralateral ear according to an acoustic stimulation signal for adjusting the first stimulation device and the second stimulation device.

Abstract: A computer-implemented method, computer program product and computing system for receiving a single-lead heartbeat waveform for a user obtained via a differential voltage potential measurement concerning the heart of the user; associating a heart health indicator with the single-lead heartbeat waveform; and providing the heart health indicator to the user.

Abstract: Method for recovering and stabilizing normal heart rate of patients suffering in or being inclined to having atrial fibrillation, comprising the step of sensing primary electrical pulses generated in the right atrium (1), of generating artificial electrical stimulation pulses coordinated with the sensed pulses and stimulating therewith the portion of the left atrium (9) which is remote from the right atrium (1), whereby increasing the areas of the heart muscles that can be reached during a simulation pulse within a predetermined period of time.

Abstract: In some embodiments, a wearable medical device system includes a processor configured to determine whether a patient requires electrical therapy to be provided via a plurality of therapy electrodes, the electrical therapy comprising discharging at least a portion of a stored electrical charge from an energy storage module, and if so, cause a fluid deploying mechanism to deploy a portion of the stored fluid to an interface between at least two therapy electrodes and the patient's skin prior to providing the electrical therapy, the deployed portion of fluid adapted to decrease the impedance measured by an impedance measurement circuit, and cause the fluid deploying mechanism to deploy an additional portion of fluid in response to the impedance measured by the impedance measurement circuit increasing above a threshold during the electrical therapy.

Abstract: The invention relates to a device, a method, a computer program product and an application for establishing a current load level of a user. The device and the method comprise a mobile terminal, which comprises at least one sensor generating signal data and a plurality of available applications for use by the user and also an evaluation unit. According to the invention, provision is made for the mobile terminal to comprise an application, which is configured as further application and establishes a plurality of biometric data in respect of the user, at least from the signal data or from available applications used by the user, and to make said data available to the evaluation unit, and for the evaluation unit to determine the current load level of the user from the biometric data.

Abstract: A hand-held electromechanical surgical device configured to selectively connect with a surgical accessory, is provided and includes a handle assembly having a power pack with a core assembly. The core assembly includes a plurality of motors, with each motor having a rotatable drive shaft extending therefrom, wherein each drive shaft is parallel to one another; a processor connected to and configured to control each motor; and a battery electrically connected to the processor and each motor. The power pack includes an inner housing encasing at least the plurality of motors, the processor, and the battery. The handle assembly includes an outer shell housing configured to selectively encase substantially the entire power pack therein, wherein a rotation from each rotatable drive shaft of each motor is transmitted through the inner housing and the outer shell housing.

Abstract: Methods, systems and devices for applying energy to tissue, and more particularly relates to a system for ablating or modifying structures in a body with systems and methods that generate a flow of vapor at a controlled flow rate for applying energy to the body structure.

Abstract: Devices, methods and systems for predicting and detecting a change in a physiological condition of a subject are disclosed. A device for detecting and predicting a change in physiological condition of a subject may include one or more processors configured to: (i) analyze changes in a heart rhythm of a subject; (ii) analyze a signal from one or more biomarkers that are associated with a physiological condition of the subject; and (iii) determine, based on the changes in the heart rhythm and the signal from the one or more biomarkers, whether there is a change in the physiological condition of the subject during a time period.

Abstract: A detection report data generation method including acquiring event type information of an electrocardiogram event corresponding to electrocardiogram event data, wherein the event data has one or more pieces of event type information; screening the event data according to signal quality evaluation indexes so as to obtain report conclusion data and report entry data; carrying out quality assessment on an event segment included in the event data according to the signal quality evaluation indexes, and determining a pre-selected sample segment according to a quality assessment result; determining position information of an event heart beat in the pre-selected sample segment, and determining segment interception parameters; carrying out interception processing on the pre-selected sample segment according to the segment interception parameters so as to obtain a typical data segment; generating report graphic data according to the typical data segment; and outputting the entry data, the graphic data and the conclusi

Abstract: According to various embodiments, there is provided a probe structure. The probe structure includes a probe configured to emit acoustic energy. The probe structure further includes a load cell underneath and aligned with the probe. The probe structure further includes a probe hub including a cavity for receiving the probe and the load cell.

Abstract: Methods and devices for treating erectile dysfunction are disclosed. Methods are aimed at reducing blood outflow from penile tissue by delivering energy to specific penile tissue that controls blood outflow from the penile tissue and causing remodeling of the specific penile tissue. Devices may be configured to generate RF energy and to apply the generated RF energy to a penis to thereby elevate a temperature of internal penile tissue above a predetermined temperature value while maintaining a penile surface below a predetermined temperature threshold. The predetermined temperature value may be set to initiate synthesis and/or a regeneration of collagen fibers in a collagen-rich penile connective tissue and/or to increase oxygenation of endothelial cells, initiate angiogenesis and neovascularization in a vascular penile tissue. Additionally, electrical penile stimulation is disclosed, possibly applicable in conjuncture with the erectile dysfunction treatment.

Abstract: A PPG system for determining a stroke volume of a patient includes a PPG sensor configured to be secured to an anatomical portion of the patient. The PPG sensor is configured to sense a physiological characteristic of the patient. The PPG system may include a monitor operatively connected to the PPG sensor. The monitor receives a PPG signal from the PPG sensor. The monitor includes a pulse trending module determining a slope transit time of an upslope of a primary peak of the PPG signal. The pulse trending module determines a stroke volume of the patient as a function of the slope transit time.

Abstract: A device includes a substrate, an electrode, an electrical pad, and a signal line. The signal line is coupled to the substrate and covered by an insulation layer. The signal line is coupled to the electrical pad and the electrode. At least one of the electrode and the signal line includes a diamagnetic material and paramagnetic material, wherein a ratio of the diamagnetic material and the paramagnetic material is selected based on the susceptibility properties of a physiological tissue. The term paramagnetic herein refers to magnetic susceptibility greater than that of the surrounding tissue and diamagnetic refers to magnetic susceptibility lower than that of the tissue.

Abstract: A system and method for creating and presenting a rolling severity of illness acuity score are comprised of two phases. The first phase analyzes historical physiologic and clinical data from a hospital's EMR system and discovers data patterns that presage a deleterious outcome. These data patterns are stored in a first database. Once these patterns have been revealed, the second phase involves embedding these patterns into a hospital's EMR, collecting data on new patients in near-real time, matching up this data against the patterns uncovered in Phase One, and producing a score based on how many of these deleterious patterns a patient is exhibiting. This score is updated continuously, weighting the current value higher than previous scores. If this rolling score surpasses a specific value, an alert is generated. The alert, in one example a color-coded signal, is then sent to a mobile device or tablet of the clinicians caring for the patient.

Abstract: A method, including obtaining information indicative of a phenomenon sensed at a read electrode of a cochlear implant electrode array relative to a reference and/or at a read electrode remote from the electrode array relative to a reference, where one of the electrodes of the cochlear implant electrode array was energized executing a first analysis of the information to identify one or more first meanings from among a first group of meanings of the sensed phenomenon, conditioning the obtained information based on the identified one or more first meanings, and executing a second analysis of the conditioned information to identify one or more second meanings from among a second group of meanings of the sensed phenomenon.

Abstract: A method for performing CPR with a mobile defibrillator (AED) unit can include detecting, via an application on a user device, a connection of a mobile AED unit to the user device; detecting, via the application, that pads have been attached to a subject, the pads comprising at least one accelerometer; recording, via the application, EKG measurements of the subject made by the pads; receiving accelerometer data from the at least one accelerometer; analyzing the accelerometer data to determine a breathing pattern of the subject; and based on the determined breathing pattern, initiating a CPR protocol.

Abstract: Examples of the present disclosure are related to devices in the field of transcutaneous electrical nerve stimulation and neuromuscular electrical stimulation. More specifically, embodiments are related to devices that are configured to automatically detect the stimulation intensity range and the motor point to generate a high efficiency, low intensity electrical stimulation treatment.

Abstract: The present invention provides materials and methods for using electrical stimulation to treat a mammal having a proteinopathy (e.g., neurodegenerative diseases) or at risk of developing a proteinopathy are provided. For example, the present invention provides materials and methods for modulating glymphatic clearance (e.g., enhancing glymphatic clearance) of pathogenic proteins.

Abstract: Persons with sleep disordered breathing (SDB) may, or may not, recognize that they have symptoms of SDB, and/or that they may be at-risk of, or suffering certain health problems associated with SDB, including death. The disclosed Energy Conversion Monitor (ECM) sensor, when embodied, for example, in a wearable upper-armband format, has been demonstrated to be more sensitive and responsive than pulse oximetry monitoring of blood oxygen saturation as an indication of hypoxic stress induced by SDB, and is compatible with: (1) inclusion in sleep laboratory polysomnograph (PSG) testing instrumentation, (2) home-based diagnostic testing for SDB, (3) control of home-use airway therapy devices, (4) continuous remote surveillance and refinement of airway therapy, and (5) spot-check and continuous surveillance of sleep quality in the general population. The disclosed ECM also provides new measurements of physiologic stress during and following exercise.

Abstract: A method and a medical device for implementing a dual-chamber pacing mode without ventricular pacing are disclosed. The method includes: obtaining pacing mode information configured by a user; controlling a dual-chamber pacemaker to operate in an ADD mode and detecting whether there is a need for delivering a pace; and performing a predetermined interruption process if a need for delivering a pace is detected. The predetermined interruption process includes: 2041) determining whether a chamber to be subsequently paced is a ventricle; 2042) if it is determined that the chamber to be subsequently paced is a ventricle, determining whether there is a need for delivering a real ventricular pace; 2043) if delivery of a real ventricular pace is not needed, delivering a virtual ventricular pace VVP and resetting a first atrial escape interval; and returning after the predetermined interruption process is terminated.