Abstract: An electrode assembly includes an electrode configured for externally defibrillating a subject. The electrode assembly also includes a camera configured to capture an image of at least a portion of the subject's body. The image has sufficient information to enable the position of the electrode assembly relative to the subject's chest to be determined.

Abstract: This disclosure describes techniques for generating stimulation current pulses that have differing pulse shapes in a medical device. A circuit architecture is described that is configured to charge a capacitor to an initial amount of charge, modulate the amount of charge stored in the capacitor based on a control signal, and generate a stimulation current pulse that has an amplitude based on the amount charge stored in the capacitor. The circuit architecture may be configured to generate complex pulse shapes, such as, e.g., steps, ramps, bursts, and combinations thereof.

Abstract: An electrical stimulation lead includes a plurality of conductive contacts disposed at a distal end and a proximal end of a lead body. The plurality of conductive contacts includes a plurality of electrodes and a plurality of terminals. At least one of the conductive contacts is a first conductive contact that includes at least one adhesive aperture defined between an inner surface and an outer surface of the at least one conductive contact. A plurality of conductors each electrically couple at least one of the electrodes to at least one of the terminals. Each first conductive contact has a conductor associated with, and electrically coupled to that first conductive contact. The adhesive is disposed in proximity to the at least one adhesive aperture of at least one first conductive contact to adhesively couple that first conductive contact to the at least one associated conductor.

Abstract: A treatment system includes: an absorbent member which is arranged to be discharged into the biological tissues as the fusion targets from the first jaw, thermally deformed when the thermal energy is applied thereto; a first energy discharge portion which is configured to discharge the absorbent member toward the second holding surface, and which is configured to supply the high-frequency energy and the thermal energy to the biological tissues; a second energy discharge portion which is configured to come into contact with at least a part of the absorbent member when the absorbent member is discharged, and which is configured to supply the high-frequency energy and the thermal energy to the biological tissues; and a control unit which is configured to control the energy source to supply the thermal energy after discharging the absorbent member to the biological tissues.

Abstract: Systems and techniques for configuring Automated External Defibrillators are described herein. In certain embodiments, a defibrillator may include a memory configured to store a protocol comprising multiple configurations. The defibrillator may also include a computing device configured to send, to a remote database that includes records associated with automated external defibrillator protocols, a request for available protocols for configuring the automated external defibrillator, receive information about one or more available protocols, send, to the remote database, a request to download a particular one of the available protocols, receive from the remote database, configuration information to automatically configure the automated external defibrillator based on the selected protocol, store the received protocol in the memory, and/or configure the automated external defibrillator to operate according to the protocol stored in the memory.

Abstract: A cryotherapeutic device having an integral multi-helical balloon section and methods of making the same. A method of forming the cryotherapeutic device can include forming an extruded integral shaft having first and second substantially parallel lumens. The method can further include twisting a distal section of the shaft such that the first and second lumens form intertwined helical portions. The first and second helical portions can be plastically enlarged to form an inflatable body configured to deliver therapeutically effective cryogenic cooling to a treatment site.

Abstract: Embodiments are directed to various monopolar and bipolar electrosurgical scissor instruments. A monopolar electrosurgical scissor instrument includes one scissor blade that has an electrically conductive tapered edge, where the tapered edge is insufficiently sharp to shear or otherwise mechanically cut tissue. The scissors also include another electrically insulated scissor blade movably mounted to the first scissor blade. The second scissor blade includes a flat contact surface that is aligned with the tapered edge of the first scissor blade. The scissors further include a scissor body that includes a conductor that transfers electrical energy from an energy source to the tapered edge of the first electrically conductive scissor blade to electrically cut interlaying tissue located between the first electrically conductive scissor blade and the second electrically insulated scissor blade.

Abstract: A nerve electrode that is inserted into a living body and that is configured to attach to nerves is provided. The nerve electrode that is inserted into a living body and that is configured to attach to nerves includes: i) a flexible substrate; ii) a plurality of electrodes that are separately positioned on the flexible substrate; and iii) an insulating layer that is positioned at a separation space of the plurality of electrodes and that insulates the plurality of electrodes. The plurality of electrodes include i) at least one linear electrode, and ii) a planar electrode that is separated from the linear electrode. An anti-inflammatory drug transfer layer is positioned on the planar electrode.

Abstract: A medical device lead includes a lead body having a proximal end and a distal end. The proximal end is configured for connection to a pulse generator. One or more electrodes are at a distal end of the lead body, and a lead conductor extends through the lead body and is electrically coupled to at least one of the one or more electrodes. The conductor is configured to deliver electrical signals between the proximal end and the at least one of the one or more electrodes. A sacrificial conductor extends through the lead body adjacent to lead conductor and is configured to fail at a lower stress than the lead conductor.

Abstract: A medical instrument having an elongate frame with proximal and distal ends, an operating assembly at a proximal region of the frame, and a working assembly at a distal region of the frame. The working assembly has a cantilevered tip with a free end and is reconfigurable by an operator through the operating assembly by selectively reorienting the tip relative to: a) the frame; and b) a reference plane extending through the frame orthogonally to the central axis at a location on the frame spaced axially from the working assembly toward the operating assembly. The tip in one position projects in a first axial direction toward the reference plane. The working assembly has at least one cautery component that: a) contacts a human body part at the cutting location; and b) is operable to generate a current that dissects a contacted portion of the human body part.

Abstract: Methods for bridging brain sites between which there is substantially no effective communication, and associated neural prosthetic devices, are provided. A neural spike in a first neural site in a subject is detected, and a stimulus to a second neural site in the subject is delivered within a defined period of time after the detection of the neural spike, wherein there is substantially no effective communication between the first and second neural sites. The method forms an artificial bridge between the two neural sites, and establishes lasting communication between the two sites. The present disclosure provides, among other things, a neural prosthetic device comprising an integrated circuit that comprises a recording front-end comprising a plurality of recording channels; a processor unit; and a stimulus delivering back-end comprising a plurality of stimulation channels.

Abstract: A method for determining the cause of an irregularity in physiologic data collected by a medical device may include monitoring a collected physiologic characteristic of a patient through the physiologic data, detecting an irregularity in the physiologic data, monitoring position data of the patient, correlating the physiologic data with the position data, and determining the cause of the irregularity in the physiologic data based on correlation of the physiologic data with the position data.

Abstract: Methods and devices for the treatment of chronic pain by modulation of the cholinergic anti-inflammatory pathway. In particular, the methods and systems described herein may be used to enhance chronic pain therapies such as spinal cord stimulation (SCS). Thus, the present invention describes devices and methods for modulation of the cytokine pathway by stimulation of the neuronal cholinergic anti-inflammatory pathway (NCAP) to enhance the treatment of chronic pain by SCS. The use of NCAP in conjunction with SCS may potentiate the effects of SCS and/or prevent the desensitization of the patient to SCS.

Abstract: In a method for the intermittent occlusion of a vein draining the organ system, in which the vein is occluded by an occlusion device, the fluid pressure in the occluded vein is continuously measured and stored, the behavior of the fluid pressure is determined as a function of time, and the occlusion of the vein is triggered and/or released as a function of at least one characteristic value derived from the pressure measurements, pressure is applied during the occlusion in a pulsating manner. The device for the intermittent occlusion of a vein, including an occlusion device, a pressure measuring device for continuously measuring the fluid pressure in the occluded vein, and a memory for storing the fluid pressure behavior as a function of time, means are provided for applying a pulsating pressure in the occluded vein.

Abstract: Systems and techniques that enable a user to selectively extend the time prior to providing an indication of power source depletion, e.g., allow an extended the recommended replacement time (RRT) prior to providing an elective replacement indication (ERI), are described. The user provides input, which may indicate an acceptable level of implantable medical device performance, e.g., that lesser performance for a period between a default RRT and an extended RRT is acceptable. In response to the input, the time until providing an RRT/ERI notification, or some other indication of depletion of the implantable medical device power source, may be extended.

Abstract: A device and method for implanting a catheter between the left atrium and/or left ventricle of the heart from a prepectoral region through a less invasive and lower-risk approach is provided that allows the implantation of the catheter in the left cardiac chambers through a femoral approach atrial transseptal puncture, and the removal of the catheter proximal end by a retrograde venous route. The device includes a transseptal sheath for slidably carrying the catheter, an elongate pulling element attached to a proximal end of the catheter, a runner slidable within the transseptal sheath and operable for biasing against the proximal end of the cardiac catheter, and a loop catheter having a loop formed at one end thereof, wherein the loop is dimensioned for receiving the transseptal sheath and for receiving the elongate pulling element therein when the loop and the elongate pulling element are separated from the transseptal sheath.

Abstract: Selective high-frequency spinal cord modulation for inhibiting pain with reduced side effects and associated systems and methods are disclosed. In particular embodiments, high-frequency modulation in the range of from about 1.5 KHz to about 100 KHz may be applied to the patient's spinal cord region to address low back pain without creating unwanted sensory and/or motor side effects. In other embodiments, modulation in accordance with similar parameters can be applied to other spinal or peripheral locations to address other indications.

Abstract: A probe system for electro-stimulation and bio-feedback training of muscles in the pelvic floor region, in particular for pelvic floor physiotherapy and diagnosis, includes a probe having a probe body which is insertable into a vagina or a rectum, and a plurality of electrodes which are positioned at several locations along the length and around the circumference on the outer surface of the probe, the probe system further includes a control unit, operationally coupled to the probe, adapted for receiving EMG signals from each of the electrodes and for processing each of the signals for mapping the response of the muscles in the pelvic floor region.

Abstract: The present disclosure involves a medical system. The medical system includes a medical device configured to deliver a medical therapy to a patient and store an electronic patient record that includes visual identification information of the patient. The medical system includes a clinician programmer configured to program the medical device. The clinician programmer includes a display screen. The clinician programmer includes a transceiver configured to conduct electronic communication with external devices. The clinician programmer includes a memory storage configured to store machine-readable code. The clinician programmer includes a computer processor configured to execute the machine-readable code to: establish an electronic communication with the medical device via the transceiver; and display the electronic patient record, including the visual identification information of the patient, on the display screen after the electronic communication has been established.

Abstract: An electrosurgical instrument is provided. The electrosurgical instrument includes a housing. An outer shaft extends from the housing. The outer shaft includes a bifurcated distal end having a pair of first spaced-apart members with an elongated slot extending therebetween. The pair of first spaced-apart members configured to receive tissue therebetween. An inner shaft is disposed within the outer shaft and includes a bifurcated distal end having a pair of second spaced-apart members with an elongated slot extending therebetween. The pair of second spaced-apart members is configured to receive tissue therebetween. Each of the pairs of the first and second spaced apart members includes one or more electrodes thereon. The inner shaft is rotatable from an initial configuration for positioning tissue between the pairs of first and second spaced-apart members to a subsequent configuration for compressing the tissue disposed between the pairs of first and second spaced-apart members.