Abstract: A medical device lead includes an insulative lead body, outer and inner conductive coils, and a flexible core assembly. The outer conductive coil extends through the lead body and is coupled to a first electrode at a distal end of the outer conductive coil. The inner conductive coil extends coaxially with the outer conductive coil, is coupled to a second electrode at a distal end of the inner conductive coil, and includes a central lumen. The flexible core assembly is disposed in the central lumen and is comprised of a material that has a saturation magnetization of at least about 1.5 T and a relative permeability of greater than one. The flexible core assembly includes a positioning interface configured for manipulation of the flexible core assembly such that the flexible core assembly translates through the central lumen during insertion and extraction of the flexible core assembly.

Abstract: An implantable or other ambulatory device, such as a pacer, defibrillator, or other cardiac function management device, can use imaging information, such as one or more of cardiac functional magnetic resonance imaging (fMRI) information or cardiac magnetic resonance imaging (MRI) information, such as for helping optimize one or more parameters of the implantable or other ambulatory device.

Abstract: An implantable device, such as a pacer, defibrillator, or other cardiac rhythm management device, can include a failsafe backup, such as a separate and independent safety core that can assume control over operation of the implantable device from a primary controller. In an example, the safety core can include a normal first safety core operating mode and a magnetic resonance imaging (MRI) second safety core operating mode that can provide different functionality from the normal first safety core operating mode.

Abstract: Embodiments of the invention are related to medical systems and methods for controlling authorization of restricted functionality, amongst other things. In an embodiment, the invention includes a medical system including an external medical device programmer comprising control circuitry and a wireless communications module for sending instructions selected from a set of instructions wirelessly to a specific implanted medical device. In an embodiment, the external medical device programmer can be configured to initiate a transfer of verifying data to a remote key authority requesting permission if the user input directs delivery of restricted instructions to the specific implanted medical device, the verifying data including information regarding the specific implanted medical device. Other embodiments are also included herein.

Abstract: An implantable medical device (IMD) includes a lead having one or more sensing electrodes and one or more therapy delivery electrodes, and a sensor configured to detect the presence of static and time-varying scan fields in a magnetic resonance imaging (MRI) environment. A controller, in electrical communication with the lead and the sensor, is configured to process signals related to tachycardia events sensed via the one or more sensing electrodes and to deliver pacing and shock therapy signals via the one or more therapy delivery electrodes. The controller compares the sensed static and time-varying scan fields to static and time-varying scan field thresholds. The controller controls delivery of anti-tachycardia pacing and shock therapy signals as a function of the detected tachycardia events, the comparison of the sensed static scan field to the static scan field threshold, and the comparison of the time-varying scan fields to the time-varying scan field thresholds.

Abstract: This document discusses, among other things, an implantable apparatus comprising a plurality of solid state electronic circuits disposed at a plurality of different locations in the apparatus, a plurality of ionizing radiation exposure sensors disposed at the different locations and configured to generate an indication of a non-single-event-upset (non-SEU) effect to the solid state electronic circuit from an exposure to ionizing radiation, wherein the ionizing radiation exposure sensors respectively monitor at least two different types of operating parameters of respectively correspondingly located solid state circuits, and a controller circuit communicatively coupled to the ionizing radiation exposure sensors, wherein the controller circuit is configured to quantify the effect to the solid state electronic circuits using the different monitored operating parameters.

Abstract: A system and method of enabling detection enhancements selected from a plurality of detection enhancements. In a system having a plurality of clinical rhythms, including a first clinical rhythm, where each of the detection enhancements is associated with the clinical rhythms, the first clinical rhythm is selected. The first clinical rhythm is associated with first and second detection enhancements. When the first clinical rhythm is selected, parameters of the first and second detection enhancements are set automatically. A determination is made as to whether changes are to be made to the parameters. If so, one or more of the parameters are modified under user control.

Abstract: Systems and methods for arrhythmia therapy in MRI environments are disclosed. Various systems disclosed utilize ATP therapy rather than ventricular shocks when patients are subjected to electromagnetic fields in an MRI scanner bore and shock therapy is not available. As the patient is moved out from within the scanner bore and away from the MRI scanner, the magnetic fields diminish in strength eventually allowing a high voltage capacitor within the IMD to charge if necessary. The system may detect when the electromagnetic fields no longer interfere with the shock therapy and will transition the IMD back to a normal operational mode where shock therapy can be delivered. Then, if the arrhythmia still exists, the system will carry out all of the system's prescribed operations, including the delivery of electric shocks to treat the arrhythmia.

Abstract: Systems and methods for checking the connection of a lead to an implantable medical device implanted within a patient's body are disclosed. An illustrative method includes measuring at least one characteristic associated with the lead connection to the implantable medical device prior to an MRI scan. The method further includes comparing the at least one measured characteristic with a threshold parameter programmed within the implantable medical device. The method further includes setting a flag in the implantable medical device upon the at least one measured characteristic satisfying at least one condition associated with the threshold parameter for a predetermined period of time. The flag indicates a disconnection of the lead from the implantable medical device.

Abstract: Energy delivered from an implantable medical device to stimulate tissue within a patient's body is controlled. An electrical signal used to stimulate the tissue is changed from a first energy state to a second energy state during a magnetic resonance imaging (MRI) scan. The energy delivered is maintained at the second energy state after the MRI scan. A capture threshold of the tissue is then measured, and the energy delivered to the tissue is adjusted based on the measured capture threshold of the tissue.

Abstract: Embodiments herein generally relate to implantable medical devices and, specifically, to a system and method for providing fault tolerant processing in an implantable medical device. In an embodiment a system for providing fault tolerant processing in an implantable medical device is provided. The system can include an implantable medical device comprising a processor and memory store configured to execute a plurality of threads, temporal and spatial constraints assigned to one or more of the threads, and a kernel. The kernel can include a scheduler and a thread monitor configured to monitor execution of threads against the temporal and spatial constraints, and further configured to issue a response upon violation of either of the constraints by one of the plurality of threads. In an embodiment a method for providing fault tolerant processing in an implantable medical device is provided. Other embodiments are also included herein.

Abstract: A system and method for providing fault resilient processing in an implantable medical device is provided. A processor and memory store are provided in an implantable medical device. Separate times on the processor are scheduled to a plurality of processes. Separate memory spaces in the memory store are managed by exclusively associating one such separate memory space with each of the processes. Data is selectively validated prior to exchange from one of the processes to another of the processes during execution in the separate processor times.

Abstract: This document discusses, among other things, an implantable apparatus comprising a solid state electronic circuit and a sensor. The sensor is configured to detect an exposure of the solid state electronic circuit to ionizing radiation, and generate an indication of a non-single-event-upset (non-SEU) effect to the solid state electronic circuit from the exposure to ionizing radiation.

Abstract: This document discusses, among other things, n implantable device comprising a communication circuit configured to communicate with an external device, a logic circuit communicatively coupled to the communication circuit, and a processor, communicatively coupled to the logic circuit and the communication circuit. The processor is configured to communicate information with the external device, via the communication circuit and the logic circuit, using a set of communication messages. While in a device safety mode, the processor is held in an inactive state and the logic circuit is configured to communicate with the external device using a subset of the set of communication messages.

Abstract: To provide a positive indication that a medical lead terminal is properly secured within the longitudinal bore in the header of an implantable medical device there is provided a force sensor (strain gauge) positioned within the device's lead receiving bore and cooperating with the lock mechanism to provide an indication of the amount of force being exerted on the lead terminal to retain it in place. The force sensor provides an output signal through the device's feedthrough wires to the electronic circuit contained within a hermetically sealed housing and is compared by a microprocessor to preprogrammed values. The results of the comparison may then be telemetered to an external programmer device for analysis by a physician.

Abstract: To provide a positive indication that a medical lead terminal is properly secured within the longitudinal bore in the header of an implantable medical device there is provided a force sensor (strain gauge) positioned within the device's lead receiving bore and cooperating with the lock mechanism to provide an indication of the amount of force being exerted on the lead terminal to retain it in place. The force sensor provides an output signal through the device's feedthrough wires to the electronic circuit contained within a hermetically sealed housing and is compared by a microprocessor to preprogrammed values. The results of the comparison may then be telemetered to an external programmer device for analysis by a physician.