Termination of respiratory oscillations characteristic of Cheyne-Stokes respiration

• US 7,421,296 B1
• Filed: 01/26/2004
• Issued: 09/02/2008
• Est. Priority Date: 01/26/2004
• Status: Active Grant

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Inventors: Benser, Michael, Bornzin, Gene A.
• Primary Examiner(s): Getzow; Scott M
• Application Number:
  US10/765,624
• Time in Patent Office: 1,681 Days
• Field of Search: 600/529, 607/20, 607/42
• US Class Current: 607/42
• CPC Class Codes: A61N 1/3601 of respiratory organs
• CPC Class Codes: A61N 1/36514 controlled by a physiological quantity other than heart potential, e.g. blood pressure controlled by two or more physical parameters A61N1/36585

Abstract

An exemplary method includes sensing respiratory information related to tidal volume, based at least in part on the respiratory information, determining if tidal volume is less than a limit and, if the tidal volume is less than the limit, calling for diaphragm activation at a stimulation power based on a nondecreasing monotonic relationship with respect to increasing tidal volume. Other exemplary methods, devices, systems, etc., are also disclosed.

Claims

1. A method comprising:

sensing respiratory information during a respiratory cycle related to tidal volume and upper airway patency;

based at least in part on the respiratory information, determining if tidal volume is less than a limit;

based at least in part on the respiratory information, determining if upper airway patency is inadequate;

if the tidal volume is less than the limit and upper airway patency is not inadequate, calling for diaphragm activation at a stimulation power based on an increasing monotonic relationship with respect to increasing tidal volume; and

if the tidal volume is less than the limit but upper airway patency is inadequate, inhibiting diaphragm activation.

2. The method of claim 1 wherein the diaphragm activation includes a member selected from the group consisting of phrenic nerve stimulation and diaphragm stimulation.

3. The method of claim 1 further comprising delivering stimulation to induce diaphragm activation.

4. The method of claim 3 wherein stimulation is delivered approximately at the end of expiration of the respiratory cycle.

5. The method of claim 3 wherein stimulation is delivered approximately at the beginning of the inspiratory phase of a next respiratory cycle.

6. The method of claim 1 wherein the limit relies on historical respiratory information unaffected by Cheyne-Stokes respiration.

7. The method of claim 1 wherein the respiratory information includes information selected from the group consisting of impedance information, plethysmography information, intracardiac electrogram (IEGM) information, neural activity information, pressure information, blood oxygen information, and blood carbon dioxide information.

8. The method of claim 1 wherein the calling for diaphragm activation increases tidal volume.

9. The method of claim 8 wherein the calling for diaphragm activation increases tidal volume to a tidal volume based at least in part on the historical respiratory information.

10. The method of claim 1 further comprising if diaphragm activation is called for, continuing to monitor for inadequate airway patency and adjusting diaphragm stimulation power based at least in part on information related to upper airway patency.

11. An implantable apparatus comprising:

an input to receive information related to tidal volume;

an input to receive information related to upper airway patency; and

a microprocessor configured to use the information to determine if tidal volume is less than a limit and if upper airway patency is inadequate, and if the tidal volume is less than the limit and upper airway patency is not inadequate to call for diaphragm activation at a stimulation power based on an increasing monotonic relationship with respect to increasing tidal volume, and if the tidal volume is less than the limit but upper airway patency is inadequate, to inhibit diaphragm activation.

12. The implantable apparatus of claim 11 wherein the input includes a connector to connect a lead to the apparatus.

13. The implantable apparatus of claim 11 wherein the information related to tidal volume comprises information selected from the group consisting of impedance information, plethysmograph information, intracardiac electrogram (IEGM) information, neural activity information, pressure information, blood oxygen information, and blood carbon dioxide information.

14. The implantable apparatus of claim 11 wherein the limit relies on historical information related to tidal volume unaffected by Cheyne-Stokes respiration.

15. The implantable apparatus of claim 11 further comprising a pulse generator responsive to the call for diaphragm activation.

16. The implantable apparatus of claim 11 further comprising an output to deliver the stimulation power.

17. The implantable apparatus of claim 16 wherein the output includes a connector to connect a lead to the apparatus.

18. The implantable apparatus of claim 11 further comprising a pulse generator responsive to the call for diaphragm activation, a lead bearing one or more electrodes electrically connectable to the pulse generator and positionable proximate to a phrenic nerve.

19. The implantable apparatus of claim 11 further comprising a pulse generator responsive to the call for diaphragm activation, a lead bearing one or more electrodes electrically connectable to the pulse generator and positionable proximate to a hemidiaphragm.

20. The implantable apparatus of claim 11 wherein the microprocessor is further configured to adjust the stimulation power based at least in part on the information related to upper airway patency.

21. The implantable apparatus of claim 11 further comprising an output to deliver cardiac stimulation.

22. A method comprising:

sensing respiratory information related to tidal volume;

based at least in part on the respiratory information, determining if tidal volume is between an upper limit and a lower limit; and

if the tidal volume is between the upper limit and the lower limit, calling for diaphragm activation at a stimulation power based on a decreasing monotonic relationship with respect to increasing tidal volume and, if the tidal volume is less than the lower limit, calling for diaphragm activation at a stimulation power based on an increasing monotonic relationship with respect to increasing tidal volume.

23. A method comprising:

sensing respiratory information during a respiratory cycle related to inspiratory flow and expiratory flow;

determining if inspiratory flow exceeds a first inspiratory limit and expiratory flow exceeds a first expiratory limit;

determining if inspiratory flow exceeds a second inspiratory limit and expiratory flow exceeds a second expiratory limit;

if inspiratory flow exceeds the second inspiratory limit but fails to exceed the first inspiratory limit, and expiratory flow exceeds the second expiratory limit but fails to exceed the first expiratory limit, calling for diaphragm activation at a stimulation power that is proportional to one or more of inspiratory flow and expiratory flow; and

if inspiratory flow does not exceed the second inspiratory limit and expiratory flow does not exceed the second expiratory limit, inhibiting diaphragm activation.