Method and system for adjusting a stimulation rate of an implantable medical device

• US 8,588,905 B2
• Filed: 05/28/2010
• Issued: 11/19/2013
• Est. Priority Date: 05/28/2010
• Status: Active Grant

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Inventors: Williamson, Richard
• Primary Examiner(s): DIETRICH, JOSEPH M
• Application Number:
  US12/790,056
• Publication Number:
  US 20110295334A1
• Time in Patent Office: 1,271 Days
• Field of Search: 607/9, 607/25, 607/26, 607/27
• US Class Current: 607/9
• CPC Class Codes: A61B 5/364 Detecting abnormal ECG interval, e.g. extrasystoles, ectopic heartbeats
• CPC Class Codes: A61N 1/3622 comprising two or more electrodes co-operating with different heart regions
• CPC Class Codes: A61N 1/365 controlled by a physiological parameter, e.g. heart potential evoked response A61N1/371

Abstract

An implantable medical device includes a lead, a pulse generator, a cardiac signal module, a fusion detection module and a rate modification module. The lead includes electrodes that are configured to be positioned within a heart to sense cardiac signals of the heart. The pulse generator delivers stimulus pulses to the heart through at least one of the electrodes. The cardiac signal module monitors the cardiac signals and directs the pulse generator to deliver one or more of the stimulus pulses to the heart at a stimulation rate based on the cardiac signals. The fusion detection module identifies a presence of fusion-based behavior of the heart that is associated with delivery of the one or more of the stimulus pulses. The rate modification module then adjusts the stimulation rate based on the presence of the fusion-based behavior.

Claims

1. An implantable medical device comprising:

a lead including electrodes configured to be positioned within a heart to sense cardiac signals of the heart;

a detector to analyze the cardiac signals of the heart and detect atrial arrhythmias;

a pulse generator electrically coupled to the lead and adapted to deliver stimulus pulses to the heart through at least one of the electrodes;

a cardiac signal module to monitor the cardiac signals and direct the pulse generator to deliver one or more of the stimulus pulses to the heart at a stimulation rate based on the cardiac signals during a detected atrial arrhythmia;

a fusion detection module to identify a presence of fusion-based behavior of the heart that is associated with delivery of the one or more of the stimulus pulses during the detected atrial arrhythmia; and

a rate modification module to adjust the stimulation rate based on the presence of the fusion-based behavior.

2. The implantable medical device of claim 1 wherein the rate modification module increases the stimulation rate when the presence of fusion-based behavior is identified in the heart.

3. The implantable medical device of claim 1, wherein the cardiac signal module determines if consecutive cardiac events occur within an escape interval.

4. The implantable medical device of claim 3, wherein each of the consecutive cardiac events includes at least one of an intrinsic contraction and a paced contraction of one or more chambers of the heart.

5. The implantable medical device of claim 3 wherein the rate modification module adjusts the stimulation rate by modifying the escape interval.

6. The implantable medical device of claim 1 wherein the rate modification module adjusts the stimulation rate based on an event interval extending between delivery of the one or more of the stimulus pulses and identification of the fusion-based behavior.

7. The implantable medical device of claim 1 wherein the rate modification module adjusts the stimulation rate based on a paced contraction time of the heart.

8. The implantable medical device of claim 1, wherein the cardiac signal module measures an event interval elapsing between consecutive cardiac events and wherein the rate modification module adjusts the stimulation rate based on the event interval.

9. The implantable medical device of claim 8, wherein the rate modification module compares the event interval to a predetermined minimum interval and adjusts the stimulation rate based on the predetermined minimum interval when the predetermined minimum interval exceeds the event interval.

10. A method for adjusting a stimulation rate at which an implantable medical device applies stimulus pulses to a heart during an atrial arrhythmia, the method comprising:

monitoring cardiac signals of the heart;

analyzing the cardiac signals to detect the atrial arrhythmia;

delivering one or more stimulus pulses to the heart during the atrial arrhythmia at the stimulation rate based on the cardiac signals;

identifying a presence of fusion-based behavior of the heart that is associated with delivery of the one or more of the stimulus pulses during the atrial arrhythmia; and

adjusting the stimulation rate based on the presence of the fusion-based behavior.

11. The method of claim 10, wherein the adjusting operation comprises increasing the stimulation rate when the presence of fusion-based behavior is identified in the heart.

12. The method of claim 10, wherein the monitoring operation comprises determining if consecutive cardiac events occur within an escape interval.

13. The method of claim 12, wherein each of the consecutive cardiac events includes at least one of an intrinsic contraction and a paced contraction of one or more chambers of the heart.

14. The method of claim 12, wherein the adjusting operation comprises modifying the stimulation rate by adjusting the escape interval.

15. The method of claim 12, wherein the delivering operation comprises delivering the one or more of the stimulus pulses to the heart when the consecutive cardiac events occur outside of the escape interval.

16. The method of claim 10, wherein the adjusting operation comprises modifying the stimulation rate based on an event interval extending between delivery of the one or more of the stimulus pulses and identification of the fusion-based behavior.

17. The method of claim 10, wherein the monitoring operation comprises measuring an event interval elapsing between consecutive cardiac events, further wherein the adjusting operation comprises modifying the stimulation rate based on the event interval.

18. The method of claim 17, wherein the adjusting operation comprises comparing the event interval to a predetermined minimum interval and modifying the stimulation rate based on the predetermined minimum interval when the predetermined minimum interval exceeds the event interval.

19. The method of claim 10, wherein the adjusting operation comprises modifying the stimulation rate based on the presence of the fusion-based behavior during an atrial arrhythmia.

20. A computer readable storage medium for use in an implantable medical device having a lead including electrodes configured to be positioned within a heart, a pulse generator configured to deliver stimulus pulses to the heart, and a microcontroller, the computer readable storage medium comprising instructions to direct the microcontroller to:

monitor cardiac signals of the heart using one or more of the electrodes;

detect atrial arrhythmias from the cardiac signals;

instruct the pulse generator to deliver one or more stimulus pulses to the heart at a stimulation rate using at least one of the electrodes when consecutive cardiac events occur outside of an escape interval during the atrial arrhythmia;

identify a presence of fusion-based behavior of the heart that is associated with delivery of the one or more of the stimulus pulses; and

adjust the stimulation rate based on the presence of the fusion-based behavior.