Abstract: A method for instantaneously stimulating a mammalian heart is provided. The mammalian heart includes a first atrium and a second atrium. A commencement signal is received. At least one additional signal is received. A plurality of intervals corresponding to the time between two successive signals is measured. An average interval is calculated. One of the plurality of intervals is compared to the average interval. Finally, a contraction signal is instantly transmitted to the second atrium when a difference between the average interval and one of the plurality of intervals is greater than a predetermined time period, instantaneously transmitting a contraction signal to the second atrium.

Abstract: New methods of characterising ventricular operations by measuring propagation characterisics of the repolarisation wavefront (the T wave) are disclosed, the methods use new descriptions of T wave Morphology Dispersion (TMD), Total Cosin R_ to _T (TCRT) and T wave energy residium to quantify the wavefront characteristics, these descriptors measure the spatial variability of the T wave Morphology, the vector deviations between the depolarisation and repolarisation wavefronts and the energy of the non-dipolar components of the ECG vector respectively. TCRT also provides a responsive descriptor for measuring autonomic tone. As such, has applications for improved pacing and autonomic nervous system monitors.

Abstract: A method for determining a representative noise floor in a cardiac pacing system from which future events are measured is provided. An event amplitude is determined. Pluralities of noise levels are recorded, when each of the plurality of noise levels is less than a predetermined percentage of the event amplitude. The noise floor is determined as an absolute maximum value of the plurality of recorded noise levels.

Abstract: The present invention relates to an intramuscular medical electrical lead, a system for providing electrical stimulation or sensing using such a lead, and methods of implanting, making and using same. The lead includes at least a first fixation member disposed distally or proximally from a sensing or stimulating electrode, and may further include a second fixation member disposed at the opposite end of the electrode form the first fixation member. The fixation members permit the electrode to be reliably and fixedly secured within a patient's muscle tissue at a desired site, and to remain so secured for a predetermined suitable period of time.

Abstract: There is provided an implanted system and method for delivering subsonic mechanical waves to one or more selected patient areas, said areas including the patient's heart and/or lungs. The mechanical waves are delivered for the purpose of treating fibrillation or like arrhythmias, for enhancing lung gas exchange, enhancing cardiac muscle fiber relaxation, and enhancing coronary perfusion. Mechanical waves are generated in a frequency range of about 1,100,000 Hz, and preferably 1-50,000 Hz. The waves may be delivered continuously for short or long time periods, or may be controlled in timing either with respect to detected portions of a patient's heartbeat signal or in response to a detected event such as fibrillation. In one preferred embodiment, the implantable system includes a defibrillation shock generator and control for responding to a defibrillation event by first delivering a sequence of mechanical waves and then delivering an electrical defibrillation shock.

Abstract: There is provided a system and method for continually monitoring the occurrence of contraction during stimulation of skeletal muscle which is employed in a cardiac assist-type system. During delivery of a periodic burst, or train of stimulus pulses, the impedance of the muscle between the electrodes through which the pulses are delivered is monitored, and evaluated to determine whether or not stimulation has been achieved. In a particular embodiment, the impedance and impedance derivative values are accumulated throughout the burst, and assessed to determine whether the impedance change corresponded to a full muscle contraction. In the event of failure to stimulate the muscle to contraction, the system can automatically adjust the pulse output parameters to achieve reliable contraction.

Abstract: Safety adaptors for connecting external medical devices to lead connector elements of temporary medical leads extending percutaneously into a patient's body are disclosed. The safety adaptors comprise a first member attached to but movable in respect of a second member. An elongated bore receives a lead proximal end segment and includes the lead connector elements.

Abstract: A temporary cardiac electrical stimulating lead comprises a stimulating electrode mounted in or on a biodegradable electrode mounting pad disposed at a distal end of the lead. The electrode mounting pad is capable of biodegradably dissolving over time in human body fluids and is loaded with a drug for therapeutically treating a medical condition of a patient's heart. The electrode mounting pad may be loaded with any of a variety of different drugs, such anti-arrhythmia or anti-inflammatory drugs. When the lead body is pulled away from the electrode mounting pad and removed from the patient, any portion of the electrode mounting pad remaining within the patient dissolves over time and disappears.

Abstract: There is provided a pacemaker system which includes intervention for overdriving the patient's natural heart rate in the event of a sensed incipient ventricular arrhythmia condition, and particularly torsades de pointes. The pacemaker continually acquires QT signals and analyzes them for respective properties, updating statistical information relating to the properties. In a preferred embodiment, the pacemaker analyzes QT interval, QT dispersion, time derivative of the QT interval, and/or T-wave amplitude and determines an intervention for pacing therapy based upon changes to these properties. The pacemaker also monitors premature ventricular beats and generates data representative of such occurrences, which data is used alone or in combination with QT data in determining whether intervention is indicated, for adjusting the intervention pacing rate.

Abstract: A low-cost temporary lead for pacing, sensing, monitoring, or defibrillating at least a portion of a human or animal organ, and methods for implanting and making same. The lead has at least two electrodes and distal and proximal ends, and a novel weakened zone disposed between the blunt end of a needle and at least two electrical connectors attached to the proximal end of the lead body. The novel weakened zone permits the needle to be separated from the connectors by application of a sufficiently large bending moment or pulling force thereto. Following separation of the connectors from the needle, the connectors may be attached directly and quickly to an external electrical apparatus.

Abstract: Described is a data processing unit for the telemetric adjustment of an implant and for telemetric communication between the implant and a data device. The data device comprises a control unit for processing the data entered, a memory unit for saving the data supplied, an entry unit for entry of data, a display unit for display of data, a telemetry unit for transfer of data to the implant or vice versa; and at least one reading device to read and/or write on a first and second data carrier, whereby, on the first data carrier, one can store the status data transferred to the implant, and, on the second data carrier, the administrative data pertaining to the implant.

Abstract: A system and method of programming an implantable medical device is disclosed. The system includes a causal model coupled to an implantable medical device and capable of identifying at least one cause of an abnormal condition associated with the implantable medical device or the patient. An abductive inference engine is coupled to the causal model and is capable of identifying a suggested updated setting for the implantable medical device to alleviate the abnormal condition. A display is coupled to the causal model and displays the abnormal behavior and the suggested updated settings to the clinician such that the clinician may implement the suggested updated settings.

Abstract: A medical lead adaptor that provides a rapid, secure, insulated connection of the lead connector end assembly of a cardiac lead having electrodes adapted to be placed in or on the body with an external medical device. The adaptor connector assembly is configured with an elongated receptacle to accept a bipolar, in-line, or a unipolar lead connector end sharing common dimensions. The elongated receptacle includes connector pin and ring receptacle contacts spaced apart from one another therein. In a preferred embodiment, an elongated slot that extends laterally of the elongated receptacle cooperates with a lock mechanism to allow the lateral insertion of the lead connector end assembly, with a stylet wire inserted into the cardiac lead body lumen, into the elongated receptacle. When inserted therein, the lead connector ring and/or pin are nested into contact with the ring and/or pin receptacle contacts and are held there by the lock mechanism.

Abstract: There is provided a telemetry system with a receiver which enables detection of pulsed high frequency data (hf) signals in a manner which suppresses noise which may be present within the high frequency bandwidth. The transmitter carrier, which may be subject to some instability, is encoded at a symbol rate which is generated at a lower frequency than the hf, but which is reliably stable. The receiver detects the phase of each received hf pulse, and generates a phase-locked signal which is synchronized to the transmitter symbol signal. The phase-locked signal in turn is used to demodulate the received pulsed signals. In a specific DSP embodiment, the phase-lock loop has a numerically controlled oscillator which has a center frequency which corresponds to the aliased phase difference between the hf carrier phase and the phase of each pulse, thereby obtaining a signal which carries information as to the exact symbol rate.

Abstract: There is provided an implanted system and method for delivering subsonic mechanical waves to one or more selected patient areas, said areas including the patient's heart and/or lungs. The mechanical waves are delivered for the purpose of treating fibrillation or like arrhythmias, for enhancing lung gas exchange, enhancing cardiac muscle fiber relaxation, and enhancing coronary perfusion. Mechanical waves are generated in a frequency range of about 1,100,000 Hz, and preferably 1-50,000 Hz. The waves may be delivered continuously for short or long time periods, or may be controlled in timing either with respect to detected portions of a patient's heartbeat signal or in response to a detected event such as fibrillation. In one preferred embodiment, the implantable system includes a defibrillation shock generator and control for responding to a defibrillation event by first delivering a sequence of mechanical waves and then delivering an electrical defibrillation shock.

Abstract: An implantable medical device such as a defibrillator is described. The device includes an hermetically sealed housing containing a flat electrolytic capacitor and an energy source such as a battery. The battery is connected to the capacitor and provides charge thereto. The capacitor stores the charge at a relatively high voltage. The charge stored in the capacitor is discharged through a defibrillation lead to a site on or in the heart when fibrillation of the heart is detected by the implantable medical device. Methods of making and using the implantable medical device, the capacitor, and their various components are disclosed.

Abstract: A system and method are provided for anchoring a cranial lead or catheter member within a cranial burr hole in a patient, utilizing a feed-through subassembly which permits a lead to be eccentrically positioned with respect to the center of the burr hole, enabling fixation of the lead to the skull while the lead is maintained stereotactically rigid. The feed-through, or anchoring assembly comprises a burr hole element which is positioned within the burr hole, having a radial slit which extends axially through the piece and has a groove for receiving and containing an O-ring, which O-ring is adjustably positioned radially along the slit in accordance with the target position. The O-ring is made of a compressive material, and has a center orifice which closely receives the lead.

Abstract: An implantable pump apparatus and method of operating the implantable pump for infusing a fluid into a body are described. The implantable pump apparatus includes a support member. A pressure sensitive resistor member is disposed on a first side of the support member. A spring member includes a first end which is adjacent to the pressure sensitive resistor member. An expandable fluid reservoir member includes a first end which is adjacent to a second end of the spring member. The level of fluid within the expandable fluid reservoir member is determined by measuring a force applied to the pressure sensitive resistor member.

Abstract: A prosthetic lamina that replaces a portion of the lamina bone structure. The prosthetic lamina may be configured to deliver a variety of medical therapies, such as electrodes for electrical stimulation, fluid channels for delivering drugs, catheters for dispensing drugs and various systems for healing bone tissue.

Abstract: A self-centering epidural lead is configured to center itself in an optimal location in respect of the midline of the spinal cord for stimulation of the cord. A method for using the lead in spinal cord stimulation is also described. The self-centering epidural lead includes a front side configured to face the spinal cord and a back side to which a pivot member or other self-centering device is operably attached. The pivot member or other self-centering device stabilizes the lead in an optimal position adjacent the spinal cord and aids in preventing spatial migration of the lead.