IP Library Granted Patent US 11,129,992
Granted Patent B2
US 11,129,992 · App. 15/922,863 · Granted Sep 28, 2021

Implantable neurostimulator-implemented method for managing bradycardia through vagus nerve stimulation

Inventors: Imad Libbus (St. Paul, MN); Badri Amurthur (Los Gatos, CA); Bruce H. KenKnight (Maple Grove, MN)
Assignee: LivaNova USA, Inc.
A61N1/365A61B5/363A61N1/36114A61N1/36139A61N1/36167A61N1/36175A61N1/36171
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Quick Facts
Patent No.
US 11,129,992
App. No.
15/922,863
Granted
Sep 28, 2021
Kind
B2
Abstract

A method for managing bradycardia through vagus nerve stimulation is provided. An implantable neurostimulator configured to deliver electrical therapeutic stimulation in both afferent and efferent directions of a patient's cervical vagus nerve is provided. An operating mode is stored, which includes parametrically defining a maintenance dose of the electrical therapeutic stimulation tuned to restore cardiac autonomic balance through continuously-cycling, intermittent and periodic electrical pulses. The maintenance dose is delivered via a pulse generator through a pair of helical electrodes via an electrically coupled nerve stimulation therapy lead independent of cardiac cycle. The patient's physiology is monitored, and upon sensing a condition indicative of bradycardia, the delivery of the maintenance dose is suspended. A progressively increasing amount of time is spent waiting via a controller and, upon sensing a condition indicative of an absence or termination of the bradycardia, a progressively increasing partial maintenance dose is delivered via the pulse generator.

Claims (62)

1. A method for managing bradycardia, comprising the steps of:

defining a dose of electrical therapeutic stimulation having a full duty cycle;

delivering the dose to a vagus nerve of a patient;

monitoring the patient's physiology via a physiological sensor;

upon sensing a condition indicative of bradycardia, suspending the delivery of the dose to the vagus nerve, comprising:

initiating a delay;

upon expiry of the delay, checking the patient's physiology via the physiological sensor; and

upon sensing, subsequent to the delay, a condition indicative of an absence or termination of the bradycardia, delivering the dose at a partial duty cycle to the vagus nerve, the partial duty cycle being less than the full duty cycle;

upon sensing, subsequent to delivering the dose at the partial duty cycle, a condition indicative of a continued absence of bradycardia, gradually increasing the duty cycle of the dose to the full duty cycle in response to determining, based on the monitored patient's physiology, that there is a normal sinus rhythm.

2. A method according to claim 1 , wherein the duty cycle is gradually increased while continually monitoring the patient's physiology until a maximum duty cycle is reached.

3. A method according to claim 1 , wherein the delay comprises an amount of time that increases over each previous delay.

4. A method according to claim 1 , further comprising the steps of:

upon sensing a condition indicative of a recurrence of the bradycardia, re-suspending the delivery of the dose to the vagus nerve, comprising:

increasing the delay over a delay most recently used during suspension of the delivery of the dose to the vagus nerve; and

upon expiry of the increased delay, checking the patient's physiology via the physiological sensor.

5. A method according to claim 4 , further comprising the steps of

continuing the re-suspension of the delivery of the dose; and

terminating the delivery of the dose to the vagus nerve once a maximum delay has been reached.

6. A method according to claim 1 , further comprising the step of:

sensing the condition indicative of bradycardia based on at least one of abnormal sinus rhythm and heart rate falling below a threshold.

7. A method according to claim 1 , wherein the duty cycle is in a range of 2% to 89%.

8. A method according to claim 7 , wherein the duty cycle is in a preferred range of 4% to 36%.

9. A method for managing bradycardia, comprising the steps of:

defining a dose of electrical therapeutic stimulation, wherein the electrical therapeutic stimulation comprises a pulsed electrical signal comprising:

a signal ON time;

a signal OFF time;

an output current;

a signal frequency;

a pulse width; and

a duty cycle defined by dividing the signal ON time by the sum of the signal ON time and signal OFF time, the duty cycle of the defined dose being a full duty cycle;

delivering the dose to a vagus nerve of a patient;

monitoring the patient's physiology via a physiological sensor;

upon sensing a condition indicative of bradycardia, suspending the delivery of the dose to the vagus nerve, comprising:

initiating a delay;

upon expiry of the delay, checking the patient's physiology via the physiological sensor; and

upon sensing, subsequent to the delay, a condition indicative of an absence or termination of the bradycardia, delivering the dose at a partial duty cycle to the vagus nerve, the partial duty cycle being less than the full duty cycle;

upon sensing, subsequent to delivering the dose at the partial duty cycle, a condition indicative of a continued absence of bradycardia, gradually increasing the duty cycle of the dose to the full duty cycle in response to determining, based on the monitored patient's physiology, that there is a normal sinus rhythm.

10. A method according to claim 9 , wherein the duty cycle is gradually increased while continually monitoring the patient's physiology until a maximum duty cycle is reached.

11. A method according to claim 9 , wherein the delay comprises an amount of time that increases over each previous delay.

12. A method according to claim 9 , further comprising the steps of:

upon sensing a condition indicative of a recurrence of the bradycardia, re-suspending the delivery of the maintenance dose to the vagus nerve, comprising:

increasing the delay over a delay most recently used during suspension of the delivery of the dose to the vagus nerve; and

upon expiry of the increased delay, checking the patient's physiology via the physiological sensor.

13. A method according to claim 12 , further comprising the steps of:

continuing the re-suspension of the delivery of the dose; and

terminating the delivery of the dose to the vagus nerve once a maximum delay has been reached.

14. A method according to claim 9 , further comprising the step of:

sensing the condition indicative of bradycardia based on at least one of abnormal sinus rhythm and heart rate falling below a minimum threshold.

15. A method according to claim 9 , wherein the pulsed electrical signal further comprises a signal ramp-down time.

16. A method according to claim 9 , wherein the pulsed electrical signal further comprises a signal ramp-up time.

17. A method according to claim 9 , wherein the pulsed electrical signals propagate in both an efferent and afferent direction.

18. A method according to claim 9 , wherein the duty cycle is in a range of 2% to 89%.

19. A method according to claim 18 , wherein the duty cycle is in a preferred range of 4% to 36%.

20. A non-transitory computer readable storage medium storing code for executing by a processor, the processor configured to perform the steps of:

defining a dose of electrical therapeutic stimulation having a full duty cycle;

delivering the dose to a vagus nerve of a patient;

monitoring the patient's physiology via a physiological sensor;

upon sensing a condition indicative of bradycardia, suspending the delivery of the dose to the vagus nerve, comprising:

initiating a delay;

upon expiry of the delay, checking the patient's physiology via the physiological sensor; and

upon sensing, subsequent to the delay, a condition indicative of an absence or termination of the bradycardia, delivering the dose at a partial duty cycle to the vagus nerve, the partial duty cycle being less than the full duty cycle;

upon sensing, subsequent to delivering the dose at the partial duty cycle, a condition indicative of a continued absence of bradycardia, gradually increasing the duty cycle of the dose to the full duty cycle in response to determining, based on the monitored patient's physiology, that there is a normal sinus rhythm.

Assignments (7)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 23, 2020
From: LIBBUS, IMAD; AMURTHUR, BADRI; KENKNIGHT, BRUCE H.
To: CYBERONICS, INC.
Reel/Frame 053859/0767 →
CHANGE OF NAME Recorded Sep 23, 2020
From: CYBERONICS, INC.
To: LIVANOVA USA, INC.
Reel/Frame 053859/0904 →
PATENT SECURITY AGREEMENT Recorded Jun 17, 2020
From: LIVANOVA USA, INC.
To: ARES CAPITAL CORPORATION, AS COLLATERAL AGENT
Reel/Frame 053673/0675 →