Cardiac Pacemakers, Inc.

Douglas J Gifford

William J Linder

David J Ternes

Paul J Huelskamp

Doug M Birkholz

Douglas J Brandner

Scott A Reedstrom

Keith R Maile

Michael John Kane

Scott R Stubbs

Kenneth Paul Hoyme

Thomas J Harris

Hiten J Doshi

Conrad L Sowder

Various implantable device embodiments may comprise a neural stimulator configured to deliver a neurostimulation therapy to stimulate tissue. A prescribed dose of the neurostimulation therapy relates to a therapeutically-effective and safe amount of charge delivered to the stimulated tissue over a period of time. The neural stimulator may include a power supply used to deliver the neurostimulation therapy, and a charge/current monitor configured to monitor a delivered dose of the neurostimulation therapy with respect to the prescribed dose to determine whether the delivered dose is delivering the therapeutically-effective and safe amount of charge to the stimulated tissue over the period of time.

Systems and methods for monitoring neurostimulation dosing

Systems, devices, and methods are disclosed for limiting the duration of elevated pacing rates in an implantable medical device. An illustrative device may include a housing, a plurality of electrodes connected to the housing, and a controller within the housing and connected to the electrodes. The controller may deliver pacing pulses to the electrodes at a base pacing rate, detect a measure of elevated metabolic demand which may vary over time, deliver pacing pulses at an elevated pacing rate based on the measure of elevated metabolic demand. The controller may change a heart stress tracking value (HSTV) when the pacing rate is elevated and may be changed faster during times of relatively higher elevated pacing rates than times of relatively lower elevated pacing rates. The elevated pacing rate may be reduced back toward the base pacing rate after the HSTV crossed a predetermined heart stress threshold.

Devices and methods for adjusting pacing rates in an implantable medical device

Various implantable device embodiments may comprise a neural stimulator configured to deliver a neurostimulation therapy with stimulation ON times and stimulation OFF times where a dose of the neurostimulation therapy is provided by a number of neurostimulation pulses over a period of time. The neural stimulator may be configured to monitor the dose of the delivered neurostimulation therapy against dosing parameters. The neural stimulator may be configured to declare a fault if the monitored dose does not favorably compare to a desired dose for the neurostimulation therapy, or may be configured to record data for the monitored dose of the delivered neurostimulation therapy, or may be configured to both record data fir the monitored dose of the delivered neurostimulation therapy and declare a fault if the monitored dose does not favorably compare to a desired dose for the neurostimulation therapy.

An implantable medical device comprises a non-volatile memory circuit including a configuration memory portion to store auto-configuration data for the IMD, a controller circuit, a reset circuit adapted to generate a reset signal and disable the controller circuit, and a startup circuit adapted to transfer the auto-configuration data from the configuration memory portion to one or more configuration registers in response to the reset signal, wherein values of the one or more configuration registers configure the IMD for a safety mode operation.

Auto-configuration circuit for safety mode operation of implantable medical device

Various implantable device embodiments may comprise a neural stimulator configured to deliver a neurostimulation therapy with stimulation ON times and stimulation OFF times where a dose of the neurostimulation therapy is provided by a number of neurostimulation pulses over a period of time. The neural stimulator may be configured to monitor the dose of the delivered neurostimulation therapy against dosing parameters. The neural stimulator may be configured to declare a fault if the monitored dose does not favorably compare to a desired dose for the neurostimulation therapy, or may be configured to record data for the monitored dose of the delivered neurostimulation therapy, or may be configured to both record data for the monitored dose of the delivered neurostimulation therapy and declare a fault if the monitored dose does not favorably compare to a desired dose for the neurostimulation therapy.

This document discusses, among other things, an 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.

Telemetry during safety mode operation

An apparatus comprises an implantable medical device that includes a storage circuit. The storage circuit includes a first stage circuit configured to receive an input signal and to invert and store information about a data bit received in the input signal, a second stage circuit coupled to the output of the first stage circuit to invert and store information about a data bit received from the first stage circuit, and an error circuit coupled to the output of the first stage circuit and an output of the second stage circuit. The error circuit generates an error indication when the storage circuit outputs match while the first stage circuit and the second stage circuit are in an inactive state.

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Ham Lake, MN, United States of America

Douglas J Gifford