Abstract: Several defibrillators, defibrillator architectures, defibrillator components and methods of operating defibrillators are described. In one aspect, a modular defibrillator architecture is described. A base unit provides a fully functional defibrillator. The functionality of the base unit can be supplemented by attaching an interface unit to the base unit or by connecting a smartphone the base unit. Such devices provide connectivity as well as a screen for displaying supplementary graphics and/or videos which are useful to support both emergency and maintenance & monitoring activities. In some embodiments a battery pack may also or alternatively be coupled to the base unit to prolong the unit's shelf life before recharging or replacement of its batteries is required. If necessary the base unit can be powered from a connected external device such as a mobile communication device.

Abstract: Several defibrillators, defibrillator architectures, defibrillator components and methods of operating defibrillators are described. In one aspect, a modular defibrillator architecture is described. A base unit provides a fully functional defibrillator. The functionality of the base unit can be supplemented by attaching an interface unit to the base unit or by connecting a smartphone the base unit. Such devices provide connectivity as well as a screen for displaying supplementary graphics and/or videos which are useful to support both emergency and maintenance & monitoring activities. In some embodiments a battery pack may also or alternatively be coupled to the base unit to prolong the unit's shelf life before recharging or replacement of its batteries is required. If necessary the base unit can be powered from a connected external device such as a mobile communication device.

Abstract: A defibrillator (AED) using an ECG analysis model or algorithm which can function in two different modes. The ECG analysis model is particularly suited for analysis during periods of CPR. Both modes of operation reach a shock decision in essentially the same way, where one or more ECG data segments indicate a shockable cardiac condition. In one mode of operation, the shock decision is irreversible once made. In another mode of operation, the shock decision is reversible if one or more subsequent ECG data segments indicate a no-shock decision. Improved specificity of the model is obtained without undue degradation of sensitivity to shockable ECG.

Abstract: A urination disorder treatment device includes a pair of body-surface electrode pads to supply an electrical stimulation signal from a back of a sacral bone, a stimulation signal control output circuit from which the pair of body-surface electrode pads supply the stimulation signal, a first measurement portion to measure electrocardiographic data based on a signal of electrical activity of the heart of the person to be treated, and a control portion to control supply of the stimulation signal based on an electrocardiographic waveform measured by the first measurement portion. A heart rate of the person to be treated may be judged to be a normal value from the electrocardiographic data, the control portion may delay timing of an output pulse from the pair of body-surface electrode pads so as not to be synchronized with the atrial systole P or the ventricular systole R of the electrocardiographic waveform.

Abstract: The present invention provides both methods and devices for termination of arrhythmias, such as ventricular or atrial tachyarrhythmias. The device and method involves application of alternating current (AC) for clinically significant durations at selected therapeutic frequencies through the cardiac tissue to a subject experiencing arrhythmia. Methods are also provided to minimize or eliminate pain during defibrillation.

Abstract: Connector enclosure assemblies for medical devices provide an angled lead passageway. The lead passageway which is defined by electrical connectors and intervening seals within the connector enclosure assembly establishes the angle relative to a base plane of the connector enclosure assembly. Various other aspects may be included in conjunction with the angled lead passageway, including an angled housing of the connector enclosure assembly, feedthrough pins that extend to the electrical connectors where the feedthrough pins may include angled sections, and a set screw passageway set at an angle relative to the lead passageway to provide fixation of a lead within the lead passageway.

Abstract: In general, techniques, methods, systems, and devices for delivering high frequency neurostimulation to control one or more pelvic disorders are described. In one example, a method includes identifying, by a medical device configured to be at least partially implanted in a patient, an indication to inhibit bladder activity. The medical device generates, in response to identifying the indication, electrical stimulation therapy comprising first electrical stimulation pulses comprising a first frequency greater than or equal to about 500 Hertz and less than or equal to about 5,000 Hertz. Further, the medical device delivers the electrical stimulation therapy to a target nerve selected from a group consisting of: a sacral nerve, a pelvic nerve, a tibial nerve, and a pudendal nerve of the patient.

Abstract: An apparatus for the treatment of urinary incontinence includes a balloon configured for movement between an inflated state and a deflated state, and the balloon includes bellows. An electrode is coupled to an outer surface of the balloon, and is configured to transmit an electrical pulse to cause a contraction of a muscle in communication with the electrode. A control device is configured to be operable by a user to cause the balloon to selectively move between the inflated state and the deflated state and to cause the electrode to transmit the electrical pulse. The bellows and the electrode are configured to cooperate to maintain the structural integrity of the balloon. The bellows and the electrode are further configured to cooperate to cause the balloon to inflate in a radially non-uniform manner.

Abstract: Some embodiments of the current disclosure are directed toward physiological monitoring of patients, and more particularly, systems, devices and methods for physiological monitoring of patients with a continuous or near-continuous transmission and analysis of monitored physiological data during the monitoring process. In some embodiments, a physiological patient monitoring system is provided which includes a physiological monitoring device which comprises a housing disposed on a patch, and the patch is configured for removable attachment to or proximate the skin of a patient, the housing including at least one memory. Antenna disposed on the housing transmit radio-frequency (RF) waves towards a targeted portion of an internal tissue of the patient and receive reflected RF waves from the internal tissue. RF circuitry in communication with the at least one memory perform an RF-based measurement of a lung fluid level of the patient during a predetermined time period.

Abstract: The present invention provides advancements in the art of cardiac pacemakers. The invention provides a pacemaker system that comprises at least one pacemaker and that is, to a large extent, self-controlled, allows for long-term implantation in a patient, and minimizes current inconveniences and problems associated with battery life. The invention further includes a mechanism in which at least two pacemakers are implanted in a patient, and in which the pacemakers communicate with each other at the time of a given pacing or respiratory event, without any required external input, and adjust pacing parameters to respond to the patient's need for blood flow. The invention further provides a design for a pacemaker in which the pacemaker electrode is connected to the pacemaker body by a lead that is configured to allow the pacemaker to lie parallel to the epicardial surface and to reduce stress on the pacemaker and heart tissue.

Abstract: Generally discussed herein are systems, devices, and methods for providing a therapy or data signal using an implantable device.

Abstract: Generally discussed herein are systems, devices, and methods for providing a therapy (e.g., stimulation) and/or data signal using an implantable device. Systems, devices and methods for interacting with (e.g., communicating with, receiving power from) an external device are also provided. A system can include an external power source that propagates a field within tissue and an at least partially implantable device configured to receive the propagated field from the external power source, the implantable device including circuitry, a first antenna electrically coupled to the circuitry, a second antenna electrically coupled to the first antenna, and an electrode electrically connected to the circuitry.

Abstract: An operating room cable assembly for electrically coupling at least one implantable electrical stimulation lead to a trial stimulator includes an elongated body; a trial stimulator connector disposed at one end of the elongated body; and a lead connector disposed at another end of the elongated body. The lead connector can include one or more buttons that can be pushed to load a lead into the lead connector and released to retain the lead. Alternatively, the lead connector can include a lever that can be operated to load the lead. A further alternative is a slider with a lead engagement element that can be slid between positions allowing loading of a lead and engagement of the lead. Other alternatives include a lead connector with doors that can swing open to allow loading of a lead or a collet/sleeve that can be tightened on the lead.

Abstract: One of the methods includes positioning the physiological data acquirer on the body of a mammal with the electrodes exposed to the body; activating a data acquisition mode of operation of the physiological data acquirer and acquiring physiological data from the user when in said data acquisition mode. Another one of the methods includes extracting the acquired data using a data extraction device.

Abstract: Electrical non-invasive brain stimulation (NIBS) delivers weak electrical currents to the brain via electrodes that are affixed to the scalp. NIBS can excite or inhibit the brain in areas that are impacted by that electrical current during and for a short time following stimulation. Electrical NIBS can be used to change brain structure in terms of increasing white matter integrity as measured by diffusion tensor imaging. Together the electrical NIBS can induce changes in brain structure and function. The present methods and devices are adaptable to and configurable for facilitating the enhancement of brain performance, and the treatment of neurological diseases and tissues. The present methods and devices are advantageously designed to utilize modern electrodes deployed with, inter alia, various spatial arrangements, polarities, and current strengths to target brain areas or networks to thereby enhance performance or deliver therapeutic interventions.

Abstract: Certain aspects of the disclosure are directed to an apparatus including a scale. The scale includes a platform in which a plurality of electrodes are integrated and configured and arranged for engaging a user and processing circuitry. The processing circuitry is electrically integrated with the plurality of electrodes to process user-corresponding data with physiologic parameter data obtained while the user is standing on the platform and therefrom derive and output derivation data indicative of a physiologic status of the user for assessment of a condition or treatment of the user that corresponds with the physiologic status, and store, in response to the derived derivation data, additional data in the memory circuit to supplement the user-corresponding data with information corresponding to the physiologic parameter data obtained while the user is standing on the platform.

Abstract: Devices and methods obtain and use endovascular electrograms in a number of clinical applications and settings. In one embodiment, methods for triggering analysis of an endovascular ECG waveform are based on the detection of a peak in a skin-based ECG waveform in order to determine a location of an indwelling medical device, such as a catheter. In another embodiment, the position of a catheter or other medical device within the vasculature can be determined by analysis of the energy profile of a detected P-wave. In yet other embodiments, magnetic connecting devices are used for establishing an operable connection through a sterile field.

Abstract: A phototherapy device for promoting wound healing and treating pain associated with soft-tissue and musculo-skeletal injuries is presented. The phototherapy device may deliver therapeutic light outputs that are variable, in real time, based in part on morphologic data of the patient measured by the device in real-time.

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.