Method and apparatus for prevention of arrhythmia clusters using overdrive pacing
First Claim
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1. An implantable medical device, comprising:
- a microprocessor characterizing cardiac activity of a patient, the implantable medical device delivering therapy in response to an identified arrhythmia event; and
a monitor/controller monitoring the characterized cardiac activity and the delivered therapy, determining inter-detection intervals between two or more terminated identified arrhythmia events and controlling subsequent activation of triggered overdrive pacing in response to the determined inter-detection intervals, wherein the monitor/controller determines whether an arrhythmia event has terminated in response to the delivered therapy, determines whether to terminate triggered overdrive pacing in response to triggered overdrive pacing being active, determines whether the arrhythmia event is associated with an arrhythmia cluster in resoonse to the determined inter-detection intervals and triggered overdrive pacing not being active, and activates triggered overdrive pacing in response to the arrhythmia event being associated with an arrhythmia cluster and triggered overdrive pacing being appropriate, and wherein the monitor/controller determines that the arrhythmia event is associated with an arrhythmia cluster in response to an inter-detection interval associated with the arrhythmia event being less than a predetermined time period, a predetermined number of arrhymia events being detected and inter-detection intervals associated with the redetermined number of arrhythmia events corresponding to an arrhythmia cluster.
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Abstract
An implantable medical device that includes a microprocessor that characterizes cardiac activity of a patient to enable the implantable medical device to deliver therapy in response to an identified arrhythmia event. A monitor/controller monitors the characterized cardiac activity and the delivered therapy, and controls activation of triggered overdrive pacing subsequent to the delivered therapy.
57 Citations
19 Claims
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1. An implantable medical device, comprising:
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a microprocessor characterizing cardiac activity of a patient, the implantable medical device delivering therapy in response to an identified arrhythmia event; and a monitor/controller monitoring the characterized cardiac activity and the delivered therapy, determining inter-detection intervals between two or more terminated identified arrhythmia events and controlling subsequent activation of triggered overdrive pacing in response to the determined inter-detection intervals, wherein the monitor/controller determines whether an arrhythmia event has terminated in response to the delivered therapy, determines whether to terminate triggered overdrive pacing in response to triggered overdrive pacing being active, determines whether the arrhythmia event is associated with an arrhythmia cluster in resoonse to the determined inter-detection intervals and triggered overdrive pacing not being active, and activates triggered overdrive pacing in response to the arrhythmia event being associated with an arrhythmia cluster and triggered overdrive pacing being appropriate, and wherein the monitor/controller determines that the arrhythmia event is associated with an arrhythmia cluster in response to an inter-detection interval associated with the arrhythmia event being less than a predetermined time period, a predetermined number of arrhymia events being detected and inter-detection intervals associated with the redetermined number of arrhythmia events corresponding to an arrhythmia cluster. - View Dependent Claims (2, 3, 4, 5, 6, 7)
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8. An implantable medical device, comprising:
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a microprocessor characterizing cardiac activity of a patient, the implantable medical device delivering therapy in response to an identified arrhythmia event; and a monitor/controller monitoring the characterized cardiac activity and the delivered therapy, and controlling activation of triggered overdrive pacing subsequent to the delivered therapy, wherein the monitor/controller determines whether an arrhythmia event has terminated in response to the delivered therapy, determines whether to terminate triggered overdrive pacing in response to triggered overdrive pacing being active, determines whether the arrhythmia event is associated with an arrhythmia cluster in response to triggered overdrive pacing not being active, and activates triggered overdrive pacing in response to the arrhythmia event being associated with an arrhythmia cluster and triggered overdrive pacing being appropriate, the monitor/controller determines one or more of a triggered overdrive pacing rate, a triggered overdrive pacing duration, and a step down period, and the monitor/controller determines whether to terminate friggered overdrive pacing by counting the number of events that have occurred during prior or current triggered overdrive pacing intervals to determine a risk count, determines whether the risk count is greater than a predetermined risk count threshold, and determines whether triggered overdrive pacing adjustments have been exhausted in response to the risk count being greater than the predetermined risk count threshold. - View Dependent Claims (9, 10, 11)
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12. A method for detecting arrhythmias in an implantable medical device, comprising the steps of:
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determining whether an arrhythmia event has terminated in response to a delivered therapy; determining whether triggered overdrive pacing is active; determining whether to terminate triggered overdrive pacing in response to triggered overdrive pacing being active; determining whether the arrhythmia event is associated with an arrhythmia cluster in response to triggered overdrive pacing not being active; determining whether triggered overdrive pacing is appropriate; and delivering triggered overdrive pacing in response to the arrhythmia event being associated with an arrhythmia cluster and triggered overdrive pacing being appropriate, wherein the step of determining whether to terminate triggered overdrive pacing comprises the steps of; counting the number of events that have occurred during prior or current triggered overdrive pacing intervals to determine a risk count; determining whether the risk count is greater than a predetermined risk count threshold; and determining whether triggered overdrive pacing adjustments have been exhausted in response to the risk count being greater than the predetermined risk count threshold. - View Dependent Claims (13, 14, 15)
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16. An implantable medical device, comprising:
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a microprocessor characterizing cardiac activity of a patient, the implantabie medical device delivering therapy in response to an identified arrhythmia event; a monitor/controller monitoring the characterized cardiac activity and the delivered therapy, and controlling activation of triggered overdrive pacing subsequent to the delivered therapy, the monitor/controller determining, prior to activation of triggered overdrive pacing, one or more of a triggered overdrive pacing rate, a triggered overdrive pacing duration, and a step down period; an ischemia detector detecting whether isohemia is present in the patient; and a hemodynamics detector detecting hemodynamics of the patient, wherein the monitor/controller determines whether an arrhythmia event has terminated in response to the delivered therapy, determines whether to terminate triggered overdrive pacing in response to triggered overdrive pacing being active, determines whether the arrhythmia event is associated with an arrhythmia cluster in response to triggered overdrive pacing not being active, and activates triggered overdrive pacing in response to the arrhythmia event being associated with an arrhythmia cluster and triggered overdrive pacing being appropriate, wherein the monitor/controller determines that triggered overdrive pacing is appropriate in response to a heart rate of the patient being less than a first predetermined threshold and ischemia not being present, and wherein, prior to activating the triggered overdrive pacing, the triggered overdrive pacing rate is dynamically adjusted by the monitor/controller based on one of a percentage of a patient'"'"'s heart rate, prior success of triggered overdrive pacing, and the detected hemodynamics of the patient, the triggered overdrive pacing duration is determined as being one of a predetermined time period, automatically adjusted based on prior triggered overdrive pacing, automatically adjusted based on events during or subsequent to the step down period, and a percentage of inter-detection intervals between detected arrhythmia events, and the step down period is calculated as a fraction of a time duration for performing triggered overdrive pacing, wherein the monitor/controller determines whether to terminate triggered overdrive pacing by counting the number of events that have occurred during prior or current triggered overdrive pacing intervals to determine a risk count, determining whether the risk count is greater than a predetermined risk count threshold, and determining whether triggered overdrive pacing adjustments have been exhausted in response to the risk count being greater than the predetermined risk count threshold. - View Dependent Claims (17, 18, 19)
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Specification