Abstract: A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. An evoked stimulation response may be sensed by a sensor near a portion of a subject. The evoked response may be sensed by an electrode and determined with a monitoring system. The evoked response may additionally and/or alternatively be sensed with a motion sensor. A position sensor may be provided to measure or determine whether the sensor has moved during a procedure.

Abstract: A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. An evoked stimulation response may be sensed by a sensor near a portion of a subject. The evoked response may be sensed by an electrode and determined with a monitoring system. The evoked response may additionally and/or alternatively be sensed with a motion sensor. A position sensor may be provided to measure or determine whether the sensor has moved during a procedure.

Abstract: A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. An evoked stimulation response may be sensed by a sensor near a portion of a subject. The evoked response may be sensed by an electrode and determined with a monitoring system. The evoked response may additionally and/or alternatively be sensed with a motion sensor. A position sensor may be provided to measure or determine whether the sensor has moved during a procedure.

Abstract: A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. An evoked stimulation response may be sensed by a sensor near a portion of a subject. The evoked response may be sensed by an electrode and determined with a monitoring system. The evoked response may additionally and/or alternatively be sensed with a motion sensor. A position sensor may be provided to measure or determine whether the sensor has moved during a procedure.

Abstract: A stimulation electrode assembly configured to be positioned relative to a patient for an operative procedure is disclosed. An evoked stimulation response may be sensed by a sensor near a portion of a subject. The evoked response may be sensed by an electrode and determined with a monitoring system. The evoked response may additionally and/or alternatively be sensed with a motion sensor. A position sensor may be provided to measure or determine whether the sensor has moved during a procedure.

Abstract: The present invention relates to the field of ambulatory and non-invasive monitoring of a plurality of physiological parameters of a monitored individual. The invention includes a physiological monitoring apparatus with an improved monitoring apparel, the apparel having sensors for monitoring parameters reflecting pulmonary function and/or parameters reflecting cardiac function and/or parameters reflecting the function of other organ systems. The apparel is preferably also suitable for medical, athletic, and for other uses. The sensors include one or more inductive plethysmographic sensors positioned to monitor at least basic pulmonary parameters, and optionally also basic cardiac parameters. The sensors include one or more ECG sensor electrodes that preferably include a flexible, conductive fabric. The monitoring apparatus also includes an electronic unit for receiving data from the sensors and for storing the data in a computer-readable medium and/or wirelessly transmitted the data.

Abstract: The present invention relates to the field of ambulatory and non-invasive monitoring of a plurality of physiological parameters of a monitored individual. The invention includes a physiological monitoring apparatus with an improved monitoring apparel, the apparel having sensors for monitoring parameters reflecting pulmonary function and/or parameters reflecting cardiac function and/or parameters reflecting the function of other organ systems. The apparel is preferably also suitable for medical, athletic, and for other uses. The sensors include one or more inductive plethysmographic sensors positioned to monitor at least basic pulmonary parameters, and optionally also basic cardiac parameters. The sensors include one or more ECG sensor electrodes that preferably include a flexible, conductive fabric. The monitoring apparatus also includes an electronic unit for receiving data from the sensors and for storing the data in a computer-readable medium and/or wirelessly transmitted the data.

Abstract: A method for determining cardiac parameters of a subject includes receiving a signal from a thoracocardiograph (TCG) sensor. The signal is sensitive to positions and/or motions of an anterior chest wall of the subject and include a cardiac component, a respiratory component, and noise and/or artifact components. The method also includes receiving one or more electrocardiogram (ECG) signals and filtering the received TCG signal to limit one or more of the respiratory component and the noise and/or artifact components. The filtering includes one or more of wavelet de-noising, non-linear filtering, and state space filtering. The method further includes ensemble averaging thefiltered TCG signal. Ensemble members are triggered by occurrence of one or more selected fiducial points determined in the ECG signal. Additionally, the method includes extracting parameters of cardiac functioning from the ensemble averaged signal.

Abstract: A method and an apparatus for projecting an end of service (EOS) and/or an elective replacement indication (ERI) of a component in an implantable device is provided. The method comprises measuring the measured voltage of the energy storage device, and determining whether the measured voltage is less than a transition voltage. When the measured voltage is less than the transition voltage, determining a time period remaining until an end of service of the energy storage device is based upon a function of the measured voltage. When the measured voltage is greater than or equal to the transition voltage, determining a time period remaining until an end of service of the energy storage device is based upon a function of the total charge depleted. The transition voltage is a voltage associated with the transition point of non-linearity in the battery voltage depletion curve.

Abstract: A method and an apparatus for determining a time period remaining in a useful life of an energy storage device in an implantable medical device. The method may include measuring a voltage of the energy storage device to produce a measured voltage, and comparing the measured voltage to a transition voltage. While the measured voltage is greater than or equal to the transition voltage, the time period remaining in the energy storage device's useful life is approximated based upon a function of charge depleted. While the measured voltage is less than the transition voltage, the time period remaining in the energy storage device's useful life is approximated based upon a higher order polynomial function of the measured voltage. The transition voltage corresponds to a predetermined point on a energy storage device voltage depletion curve representing the voltage across the energy storage device over time.

Abstract: An implantable medical device (IMD) may include a lead circuit including a first node configured to be coupled to a first lead that may be coupled to a first target tissue and including a second node configured to be coupled to a second lead that may be coupled to a second target tissue. The IMD may include an impedance unit that may determine at least one characteristic of coupled energy associated with the lead circuit, where the coupled energy may be produced by a source external to the IMD. The impedance unit may provide an impedance between the first node and the second node, where the impedance is selected based at least in part on a characteristic of the coupled energy. The impedance is selected to reduce the coupled energy or a negative effect associated with functionality of the IMD induced by the coupled energy.

Abstract: An electrode assembly includes an electrode adapted to at least partially surround a first longitudinal portion of a target nerve or nerve bundle. The electrode includes an inner surface adapted to contact an outer surface of the target nerve or nerve bundle. The electrode also includes a plurality of fiber elements each having a proximal end and a distal end. The fiber elements are coupled at the proximal ends to the inner surface of the electrode and the distal ends of the fiber elements are operative to penetrate the outer surface of the target nerve or nerve bundle.

Abstract: An implantable medical device (IMD) may include a lead circuit including a first node configured to be coupled to a first lead that may be coupled to a first target tissue and including a second node configured to be coupled to a second lead that may be coupled to a second target tissue. The IMD may include an impedance unit that may determine at least one characteristic of coupled energy associated with the lead circuit, where the coupled energy may be produced by a source external to the IMD. The impedance unit may provide an impedance between the first node and the second node, where the impedance is selected based at least in part on a characteristic of the coupled energy. The impedance is selected to reduce the coupled energy or a negative effect associated with functionality of the IMD induced by the coupled energy.

Abstract: A method, system, and apparatus are provided for using an electrode for delivering an electrical signal to a first tissue of a patient's body. An electrode system comprises a lead and an electrode coupled to the lead. The electrode includes a stimulation portion that couples to the first tissue to deliver an electrical signal to the first tissue. The electrode also includes a dissipation portion that does not interface with the first tissue. The dissipation portion is adapted to dissipate thermal energy from the electrode.

Abstract: A method, system, and apparatus for implementing a safe mode operation of an implantable medical system using impedance adjustment(s) are provided. A first impedance is provided to a lead. An indication of a possibility of a coupled energy is received. Based upon said indication, a second impedance associated with the lead to reduce the coupled energy is provided.

Abstract: A method, system, and apparatus for implementing a safe mode operation of an implantable medical system using impedance adjustment(s) are provided. A first impedance is provided to a lead. An indication of a possibility of a coupled energy is received. Based upon said indication, a second impedance associated with the lead to reduce the coupled energy is provided.

Abstract: An electrode assembly includes an electrode adapted to at least partially surround a first longitudinal portion of a target nerve or nerve bundle. The electrode includes an inner surface adapted to contact an outer surface of the target nerve or nerve bundle. The electrode also includes a plurality of fiber elements each having a proximal end and a distal end. The fiber elements are coupled at the proximal ends to the inner surface of the electrode and the distal ends of the fiber elements are operative to penetrate the outer surface of the target nerve or nerve bundle.

Abstract: An apparatus and system are provided for employing an electrode for delivering an electrical signal to a portion of a tissue of a patient's body. The electrode includes a first surface to electrically couple to the portion of an outer layer of the tissue. The electrode also includes a plurality of fibers or longitudinal elements coupled to the outer surface. The plurality of fibers or longitudinal elements are adapted to migrate to an interior portion of the tissue.

Abstract: The present invention relates to the field of ambulatory and non-invasive monitoring of a plurality of physiological parameters of a monitored individual. The invention includes a physiological monitoring apparatus with an improved monitoring apparel, the apparel having sensors for monitoring parameters reflecting pulmonary function and/or parameters reflecting cardiac function and/or parameters reflecting the function of other organ systems. The apparel is preferably also suitable for medical, athletic, and for other uses. The sensors include one or more inductive plethysmographic sensors positioned to monitor at least basic pulmonary parameters, and optionally also basic cardiac parameters. The sensors include one or more ECG sensor electrodes that preferably include a flexible, conductive fabric. The monitoring apparatus also includes an electronic unit for receiving data from the sensors and for storing the data in a computer-readable medium and/or wirelessly transmitted the data.

Abstract: A method and an apparatus for projecting an end of service (EOS) and/or an elective replacement indication (ERI) of a component in an implantable device is provided. The method comprises measuring the measured voltage of the energy storage device, and determining whether the measured voltage is less than a transition voltage. When the measured voltage is less than the transition voltage, determining a time period remaining until an end of service of the energy storage device is based upon a function of the measured voltage. When the measured voltage is greater than or equal to the transition voltage, determining a time period remaining until an end of service of the energy storage device is based upon a function of the total charge depleted. The transition voltage is a voltage associated with the transition point of non-linearity in the battery voltage depletion curve.