IP Library Granted Patent US 9,669,220
Granted Patent B2
US 9,669,220 · App. 15/230,023 · Granted Jun 6, 2017

Neurostimulation in a neural fulcrum zone for the treatment of chronic cardiac dysfunction

Inventors: Bruce H. KenKnight (Maple Grove, MN); Jeffrey L. Ardell (Johnson City, TN); Imad Libbus (St. Paul, MN); Badri Amurthur (Los Gatos, CA)
Assignees: CYBERONICS, INC.; EAST TENNESSEE STATE UNIVERSITY
A61N1/36139A61N1/3615A61N1/36053A61N1/36114
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Quick Facts
Patent No.
US 9,669,220
App. No.
15/230,023
Granted
Jun 6, 2017
Kind
B2
Abstract

Systems and methods are provided for delivering neurostimulation therapies to patients for treating chronic heart failure. A neural fulcrum zone is identified and ongoing neurostimulation therapy is delivered within the neural fulcrum zone. This neural fulcrum zone corresponds to a combination of stimulation parameters at which autonomic engagement is achieved, while the tachycardia-inducing stimulation effects are offset by the bradycardia-inducing effects, thereby minimizing side effects such as significant heart rate changes while providing a therapeutic level of stimulation.

Claims (53)

1. A method of operating an implantable medical device (IMD) comprising a neurostimulator coupled to an electrode assembly, the neurostimulator adapted to deliver a stimulation signal to a patient, the method comprising:

activating the IMD to generate a plurality of stimulation signals, each stimulation signal of the plurality of stimulation signals having at least one parameter setting that is different as compared to a corresponding parameter setting of the other stimulation signals of the plurality of stimulation signals;

detecting a heart rate condition of the patient during the generation of the plurality of stimulation signals by:

detecting a tachycardia condition in response to detecting a heart rate increase responsive to a first subset of the stimulation signals;

detecting a bradycardia condition in response to detecting a heart rate reduction of greater than a predefined threshold responsive to a second subset of the stimulation signals; and

detecting a transition heart rate response corresponding to a neural fulcrum zone in response to detecting a heart rate reduction between a baseline heart rate and a predefined threshold responsive to a third subset of the stimulation signals, the transition heart rate response being between a heart rate associated with the tachycardia condition and a heart rate associated with the bradycardia condition.

2. A method according to claim 1 , further comprising:

activating the IMD to chronically deliver the third subset of stimulation signals corresponding to the identified neural fulcrum zone.

3. A method according to claim 2 , wherein the activating the IMD to chronically deliver the third subset of stimulation signals comprises activating the IMD to treat a chronic cardiac dysfunction condition of the patient.

4. A method according to claim 1 , wherein the at least one parameter setting comprises an amplitude setting.

5. A method according to claim 1 , wherein the at least one parameter setting comprises a pulse width setting.

6. A method according to claim 1 , wherein the at least one parameter setting comprises a duty cycle setting.

7. A method according to claim 1 , wherein the at least one parameter setting comprises a frequency setting.

8. A method according to claim 1 , wherein the plurality of stimulation signals includes a series of stimulation signals having a greater amplitude as compared to an immediately previous stimulation signal.

9. A method according to claim 1 , wherein the plurality of stimulation signals is a first plurality of stimulating signals having a first frequency, the method further comprising:

activating the IMD to generate a second plurality of stimulation signals having a second frequency different than the first frequency, each stimulation signal of the second plurality of stimulation signals having at least one parameter setting that is different as compared to a corresponding parameter setting of the other stimulation signals of the second plurality of stimulation signals;

detecting the heart rate condition of the patient during the generation of the second plurality of stimulation signals by:

detecting another tachycardia condition in response to detecting a heart rate increase response to a first subset of the second stimulation signals;

detecting another bradycardia condition in response to detecting a heart rate reduction of greater than the predefined threshold responsive to a second subset of the second stimulation signals; and

detecting another transition heart rate corresponding to a neural fulcrum zone in response to detecting a heart rate reduction between a baseline heart rate and a predefined threshold responsive to a third subset of the second stimulation signals, the another transition response being a heart rate associated with the another tachycardia condition and a heart rate associated with the another bradycardia condition.

10. A method according to claim 9 , further comprising:

activating the IMD to chronically deliver the third subset of stimulation signals corresponding to the another neural fulcrum zone.

11. A method according to claim 10 , wherein the activating of the IMD to chronically deliver the third subset of stimulation signals comprises activating the IMD to treat a chronic cardiac dysfunction condition of the patient.

12. A method according to claim 1 , further comprising:

prior to activating the IMD to generate the plurality of stimulation signals, completing a titration process in which a stimulation intensity is gradually increased over a period of time.

13. A method according to claim 1 , wherein the IMD is adapted to deliver the stimulation signal to a vagus nerve of the patient.

14. A method of identifying a set of parameter settings for an implantable medical device (IMD) for treating a chronic cardiac dysfunction condition of a patient, the method comprising:

activating the IMD to generate a plurality of stimulation signals at a same frequency, each stimulation signal of the plurality of stimulation signals having at least one parameter setting that is different as compared to a corresponding parameter setting of the other stimulation signals of the plurality of stimulation signals;

detecting a heart rate condition of the patient during the generation of the plurality of stimulation signals by;

detecting a tachycardia condition in response to detecting a heart rate increase responsive to a first subset of the stimulation signals; and

detecting a bradycardia condition in response to a heart rate reduction of greater than a predefined threshold responsive to a second subset of the stimulation signals;

detecting a transition heart rate response corresponding to a neural fulcrum zone in response to detecting a heart rate reduction between a baseline heart rate and a predefined threshold responsive to a third subset of the stimulation signals, the transition heart rate response comprising a heart rate reduction between a baseline heart rate and the predefined threshold; and

identifying the set of parameter settings for treating the chronic cardiac dysfunction condition as the parameters of the third subset of the stimulation signals.

15. A neurostimulation system, comprising:

an electrode assembly; and

a neurostimulator coupled to the electrode assembly, the neurostimulator comprising:

a control circuit; and

a memory operably coupled to the control circuit and comprising instructions that, when executed by the control circuit, cause the control circuit to:

detect a heart rate condition when the IMD generates the plurality of stimulation signals, each stimulation signal of the plurality of stimulation signals having at least one parameter setting that is different as compared to a corresponding parameter setting of the other stimulation signals of the plurality of stimulation signals;

detect a tachycardia condition in response to detecting a heart rate increase responsive to a first subset of the stimulation signals;

detect a bradycardia condition in response to detecting a heart rate reduction of greater than a predefined threshold responsive to a second subset of the stimulation signals; and

detect a transition heart rate response corresponding to a neural fulcrum zone in response to detecting a heart rate reduction between a baseline heart rate and a predefined threshold responsive to a third subset of the stimulation signals, the transition heart rate response being between a heart rate associated with the tachycardia condition and a heart rate associated with the bradycardia condition.

16. A system according to claim 15 , wherein the control system is further programmed to:

activate the neurostimulator to chronically deliver the third subset of stimulation signals corresponding to the neural fulcrum zone.

17. A system according to claim 16 , wherein the control system is programmed to activate the neurostimulator to chronically deliver the third subset of stimulation signals to treat a chronic a cardiac dysfunction condition of the patient.

18. A system according to claim 15 , wherein the at least one parameter setting comprises at least one of an amplitude setting, a pulse width setting, a duty cycle setting, or a frequency setting.

19. A system according to claim 15 , wherein the plurality of stimulation signals includes a series of stimulation signals having a greater amplitude as compared to an immediately previous stimulation signal.

20. A system according to claim 15 , wherein the plurality of stimulation signals is a first plurality of stimulation signals having a first frequency and wherein the control system is further programmed to:

activate the neurostimulator to generate a second plurality of stimulation signals having a second frequency different than the first frequency, each stimulation signal of the second plurality of stimulation signals having at least one parameter setting that is different as compared to a corresponding parameter setting of the other stimulation signals of the second plurality of stimulation signals;

detecting the heart rate condition of the patient during the generation of the second plurality of stimulation signals by:

detecting another tachycardia condition in response to detecting a heart rate increase response to a first subset of the second stimulation signals;

detecting another bradycardia condition in response to detecting a heart rate reduction of greater than the predefined threshold responsive to a second subset of the second stimulation signals; and

detecting another transition heart rate corresponding to a neural fulcrum zone in response to detecting a heart rate reduction between a baseline heart rate and a predefined threshold responsive to a third subset of the second stimulation signals, the another transition response being a heart rate associated with the another tachycardia condition and a heart rate associated with the another bradycardia condition.

Assignments (8)
RELEASE OF SECURITY INTEREST Recorded Sep 20, 2021
From: ACF FINCO I LP
To: LIVANOVA USA, INC.
Reel/Frame 057552/0378 →
SECURITY INTEREST Recorded Aug 16, 2021
From: LIVANOVA USA, INC.
To: GOLDMAN SACHS BANK USA, AS COLLATERAL AGENT
Reel/Frame 057188/0001 →
RELEASE OF SECURITY INTEREST Recorded Aug 16, 2021
From: ARES CAPITAL CORPORATION, AS AGENT FOR THE LENDERS
To: LIVANOVA USA, INC.
Reel/Frame 057189/0001 →
PATENT SECURITY AGREEMENT Recorded Dec 30, 2020
From: LIVANOVA USA, INC.
To: ACF FINCO I LP, AS COLLATERAL AGENT
Reel/Frame 054881/0784 →
CHANGE OF NAME Recorded Jun 29, 2020
From: CYBERONICS, INC.
To: LIVANOVA USA, INC.
Reel/Frame 053306/0229 →
PATENT SECURITY AGREEMENT Recorded Jun 17, 2020
From: LIVANOVA USA, INC.
To: ARES CAPITAL CORPORATION, AS COLLATERAL AGENT
Reel/Frame 053673/0675 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2016
From: ARDELL, JEFFREY L.
To: EAST TENNESSEE STATE UNIVERSITY
Reel/Frame 039704/0220 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2016
From: KENKNIGHT, BRUCE H.; LIBBUS, IMAD; AMURTHUR, BADRI
To: CYBERONICS, INC.
Reel/Frame 039704/0223 →
Continuity (2)
Continuation 14224922 · Mar 25, 2014
Related Publication 20160339252A1 · Nov 24, 2016