Abstract: A medical device detects certain patient activity based on a programmable activity threshold and determines the duration of detected activity. The activity threshold may be optimized by obtaining first and second duration measurements for at least one of a first activity session and second activity session. The first duration measurement is based on the activity threshold, while the second duration measurement is based on actual start and stop of the activity session. An adjustment of the activity threshold is suggested based on a correspondence between the first duration measurement and the second duration measurement of the first activity session, or a correspondence between the first duration measurement and the second duration measurement of the second activity session. One of the first and second activities is non-significant activity expected to be undetected by the device, while the other of the two activities is low-level activity expected to be detected by the device.

Abstract: In one embodiment, an implantable stimulation apparatus includes a vagal nerve stimulator configured to generate electrical pulses below a cardiac threshold of a heart, and an electrode coupled to the vagal nerve stimulator which is configured to transmit the electrical pulses below the cardiac threshold, to a vagal nerve so as to inhibit injury resulting from an ischemia and/or reduce injury resulting from an ischemia. In another embodiment, an implantable stimulation apparatus includes a vagal nerve stimulator configured to generate electrical pulses below a cardiac threshold, and includes an electrode, which is coupled to the vagal nerve stimulator and configured transmit electrical pulses to a vagal nerve so as to reduce a defibrillation threshold of the heart.

Abstract: A morphology discrimination scheme extracts shape characteristics from cardiac signals and identifies an associated cardiac condition based on the shape characteristics. For example, internal data structures may be updated to match the shape characteristics of a known condition (e.g., a patient's normal sinus rhythm). Similarly acquired shape characteristics obtained in conjunction with a later event (e.g., QRS complexes acquired during a tachycardia episode) may be compared with the previously stored shape characteristics to characterize the later event. In some aspects the shape characteristics relate to inflection points of cardiac signals.

Abstract: Implantable systems that can monitor myocardial electrical stability, and methods for use therewith, are provided. Also provided are novel pacing sequences that are used in such monitoring. Such pacing sequences are designed to reveal alternans at low to moderate heart rates.

Abstract: Provided herein are implantable systems, and methods for use therewith, for estimating a level of noise in a signal produced by an implantable sensor that is sensitive to motion induced noise. Sample data is obtained that is representative of a window of a signal produced by the implantable sensor that is sensitive to motion induced noise. Such sample data includes a plurality of samples each having a magnitude (e.g., amplitude). Each of at least some of the samples is assigned to one of a plurality of bins based on the magnitude of the sample, wherein each bin corresponds to a different range of magnitudes. The plurality of bins includes at least a low bin defining a lowest magnitude range and a high bin defining a highest magnitude range. A level of motion induced noise in the sensor signal is estimated based on a distribution of the samples to the bins.

Abstract: An implantable medical device (IMD) is provided. The IMD comprises a sense circuit, a main processing unit coupled to the sense circuit, a memory unit coupled to the main processing unit, and a reconfigurable processor unit coupled to the memory unit and the main processing unit. The reconfigurable processor unit is adapted to receive data, perform a processing function on the data, and return processed data to the memory unit. The memory unit is adapted to store the processed data. The main processing unit is adapted to execute programmed instructions and selectively reconfigure the processing function of the reconfigurable processor unit in response to one of the programmed instructions. Such a configuration can be used to implement a method of efficiently processing data in an IMD.

Abstract: Anode foil, preferably aluminum anode foil, is etched using a process of treating the foil in an electrolyte bath composition comprising a sulfate and a halide, such as sodium chloride. The anode foil is etched in the electrolyte bath composition by passing a charge through the bath. The etched anode foil is suitable for use in an electrolytic capacitor.

Abstract: The present invention provides a method for reforming a capacitor of an implantable medical device, such as an implantable cardioverter defibrillator, wherein the capacitor has a nominal voltage. The method of reforming the capacitor comprises charging the capacitor to a first voltage that is above the nominal voltage of the capacitor, partially discharging the capacitor through system leakage, charging the capacitor to a second voltage that is above the nominal voltage, and discharging the capacitor through system leakage until the charge on the capacitor dissipates. The present invention also provides an implantable medical device having a capacitor reforming circuit for reforming the capacitor. Capacitors reformed according to the present invention have reduced charge time deformation compared to capacitors conventionally reformed at the nominal voltage.

Abstract: Techniques are provided for rapidly optimizing control parameters of pacemakers or implantable cardioverter defibrillators. Briefly, the heart is paced using different sets of control parameters during a sequence of consecutive short evaluation periods of equal duration, which each last only about 5-12 seconds. Transient cardiac performance is monitored during each of the short evaluation phases and optimal parameter settings are then estimated based on changes in the transient cardiac performance from one parameter setting to another. By using a series of consecutive short evaluation periods of equal duration, rather than switching between short test periods and longer baseline periods, the overall duration of the test can be reduced as compared to predecessor techniques that require long intervening baseline periods.