Abstract: A computer-assisted method for quantitatively characterizing atrial fibrillation in a patient includes recording time series of bipolar atrial fibrillation signals at multiple sites in a patient's atria using two or more electrodes, calculating a similarity index vector by a computer system based on the bipolar atrial fibrillation signal between a first site and its neighboring sites, constructing an similarity-index vector field based on similarity-index vectors at different sites, calculating Curl and Divergence of the similarity-index vector field, calculating Rotor Identification using Curl and Divergence, calculating Focal Identification using Divergence, and determining one or more critical regions in the patient's atria if Rotor Identification is above a first predetermined threshold and Focal Identification is above a second predetermined threshold.

Abstract: A system for treating medical conditions by neuromodulation of one or more target sites in the nervous system. In certain embodiments, at least one of the target sites is the medial thalamic region, including the intralaminar nucleus and the adjacent white and grey matter. In certain embodiments, where there is more than one target site, the other target sites is elsewhere in the nervous system, including the globus pallidus interna, subthalamic nucleus, corpus callosum, cerebellum, cerebral cortex (including the premotor cortex, motor cortex, and sensory cortex), ventral striatum, lateral thalamus, substantia nigra, and pedunculopontine nuclei. The medical conditions include movement disorders or improvement of movement function, stroke, neuropsychiatric or neuropsychologic disorders, neurodevelopmental disorders, and pain. Methods for treating medical conditions by neuromodulation of the intralaminar nuclei either alone or in combination with another target site(s) is also provided.

Abstract: An exemplary system includes an electro-acoustic stimulation (“EAS”) device, a cochlear implant, an electrode lead comprising a plurality of basal electrodes configured to be disposed within a basal region of a cochlea of a patient and a plurality of apical electrodes configured to be disposed within an apical region of the cochlea; and a loudspeaker communicatively coupled to the EAS device. The EAS device is configured to operate in an EAS mode by 1) disabling the apical electrodes for standard electrical stimulation, 2) detecting, while the apical electrodes are disabled for standard electrical stimulation, audio content presented to the patient and included in an acoustic stimulation frequency range, 3) directing the loudspeaker to apply acoustic stimulation representative of the audio content included in the acoustic stimulation frequency range to the patient, and 4) periodically directing the cochlear implant to apply conditioning stimulation by way of the disabled apical electrodes.

Abstract: Electrical stimulation may be delivered to a patient's heart using a plurality of cardiac electrodes. Each electrode combination may be evaluated based on one or more first parameters and one or more second parameters. In many cases, the one or more first parameters are supportive of cardiac function consistent with a prescribed therapy and the one or more second parameters are not supportive of cardiac function consistent with the prescribed therapy. The electrode combination selected to deliver a cardiac pacing therapy may be more associated with the one or more first parameters supportive of cardiac function consistent with the prescribed therapy and less associated with the one or more second parameters inconsistent with cardiac function.

Abstract: A blood pump includes a hub having an axis of rotation and a generally cylindrical shape. The hub has an upstream end region, a central region, and a downstream end region, and the hub includes a magnetic material. Blades that are disposed on the downstream end region of the hub extend downstream of the hub.

Abstract: A system and method for use during the administration of CPR chest compressions and defibrillating shock on a cardiac arrest victim. The system analyzes compression waveforms from a compression depth monitor to determine the source of chest compressions, and enables the delivery of defibrillating shock during a compression cycle if the compression waveforms are characteristic of an automated CPR chest compression device.

Abstract: Methods and systems of applying treatment to a subject experiencing cardiac distress. In one example, there is provided a defibrillation electrode. The defibrillation electrode includes a non-volatile memory element and a circuit configured to store an indication of a level of energy delivered to a subject during the application of a defibrillation shock to the subject in the non-volatile memory element.

Abstract: Counterpulsation methods and systems for assisting the heart of a patient involve, for example, coordinating the operation of a pulsatile pump to suction blood from an artery through a blood flow conduit while the heart is in systole and expel the blood into the blood flow conduit and the artery while the heart is in diastole.

Abstract: A system includes a medical device lead including a connector at a proximal end of the lead, a conductor electrically connected to the connector at a proximal end of the conductor, and at least one electrode coupled to a distal end of the conductor. The system further includes a device securable to the proximal end of the lead including an inductive element. The device includes a port configured to receive the connector and position the inductive element around at least a portion of the connector.

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: A method of providing therapy to a patient comprising sinking first electrical current into at least a first one of a plurality of electrodes adjacent the spinal cord tissue, thereby providing therapy to a first region of the patient. The method further comprises sinking second electrical current into at least one electrode adjacent peripheral tissue remote from the spinal cord tissue, thereby providing therapy to a second region of the patient. The method further comprises sourcing at least a portion of the first electrical current and at least a portion of the second electrical current into at least a second one of the plurality of electrodes.

Abstract: A system for restoring muscle function to the lumbar spine to treat low back pain is provided. The system may include electrodes coupled to an implantable pulse generator (IPG), a handheld activator configured to transfer a stimulation command to the IPG, and an external programmer configured to transfer programming data to the IPG. The stimulation command directs the programmable controller to stimulate the tissue in accordance with the programming data. The system may include a software-based programming system run on a computer such that the treating physician may program and adjust stimulation parameters.

Abstract: A sensor for contactless electrocardiographic measurement of a person has at least one electrically conductive, planar electrode having a measurement surface facing the person and a connection surface facing away from the person. An electrical terminal for connection with a measurement apparatus is spaced from the connection surface such that the connection surface is only placed in electrical connection with the terminal when pressure of a required magnitude is applied to the measurement. The electrical connection may be achieved by a switching contact disposed between the electrode and the terminal which is brought into contact with both the electrode and the terminal when the electrode is deflected toward the terminal by the pressure. A compressible material is disposed between the electrode and the terminal to allow tuning of the pressure required to achieve electrical contact.

Abstract: A device that monitors and evaluates electrogram signals representing electric activities of a heart chamber, and includes a signal input connected to a mapping catheter, and a signal processing and evaluation unit. The mapping catheter includes one or more electrode poles that pick up electric potentials and generate electrogram signals therefrom.

Abstract: A wearable therapeutic device that includes a garment configured to contain an external defibrillator. The garment is configured to house at least one of an alarm module and a monitor and to house a first therapy electrode and a second therapy electrode. The garment is also configured to releasably receive a receptacle that contains a conductive fluid proximate to at least one of the first therapy electrode and the second therapy electrode, and to electrically couple the receptacle with the garment.

Abstract: Apparatuses (e.g., devices, systems), and methods for transdermal electrical stimulation (TES). Apparatuses described herein can be self-contained, lightweight, and wearable. The apparatus may include a primary unit (TES stimulator) and an electrode portion that includes a first transdermal electrode and a second transdermal electrode and mates with the TES stimulator. The first electrode and secondary electrode are placed at two locations on the skin of a user, for example on the head and/or neck of a user. Electrical stimulation driven between the two electrodes may induce a cognitive effect in a user of the device.

Abstract: Neuromodulation cryotherapeutic devices and associated systems and methods are disclosed herein. A cryotherapeutic device configured in accordance with a particular embodiment of the present technology can include an elongated shaft having distal portion and a supply lumen along at least a portion of the shaft. The shaft can be configured to locate the distal portion intravascularly at a treatment site proximate a renal artery or renal ostium. The supply lumen can be configured to receive a liquid refrigerant. The cryotherapeutic device can further include a cooling assembly at the distal portion of the shaft. The cooling assembly can include an applicator in fluid communication with the supply lumen and configured to deliver cryotherapeutic cooling to nerves proximate the target site when the cooling assembly is in a deployed state.

Abstract: A programming session for an implantable medical device that includes a posture responsive therapy mode includes at least two phases. In a first phase, a first set of therapy parameter values are modified while the posture responsive therapy mode is deactivated. In the posture responsive therapy mode, the medical device automatically selects one or more therapy parameter values that define therapy delivered to a patient based on a detected posture state. In a second phase, the posture responsive therapy mode is activated and a second set of therapy parameter values are adjusted after observing a patient response to the posture responsive therapy delivered with the first set of therapy parameter values selected during the first phase. The second set of therapy parameter values may, for example, define the patient posture states or the modification profiles with which the medical device adjusts therapy upon detecting a posture state transition.

Abstract: A leadless implantable medical device comprises a first electrode configured to deliver electrical pacing energy, a second electrode configured to sense intrinsic electrical cardiac activity, and a third electrode configurable to both deliver electrical pacing energy and sense intrinsic electrical cardiac activity. The first and third electrodes are used for delivering electrical pacing energy and the second and third electrodes are used to sense intrinsic electrical cardiac activity. None of the first, second and third electrodes are incorporated into a lead.

Abstract: A computer-assisted method for quantitative characterizing atrial fibrillation (AF) in a patient includes recording unipolar atrial fibrillation signals from multiple sites in a patient's atria, calculating bipolar electrograms using unipolar AF signals recorded at adjacent sites by a computer system, applying Empirical Mode Decomposition to remove a background from the bipolar electrogram signal to obtain a filtered bipolar electrogram signal, applying Hilbert transform to an envelope function of the filtered bipolar electrogram signal to obtain a time series of instantaneous phases of the filtered bipolar electrogram signal, and identifying a rotor region in patient's atria using the instantaneous phases in the filtered bipolar electrogram signal.