IP Library Granted Patent US 7,539,543
Granted Patent B2
US 7,539,543 · App. 10/320,840 · Granted May 26, 2009

Feedback method for deep brain stimulation with detection of generalized efference copy signals

Assignee: Cornell Research Foundation, Inc.
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Quick Facts
Patent No.
US 7,539,543
App. No.
10/320,840
Granted
May 26, 2009
Kind
B2
Abstract

Disclosed is a method for improving cognitive function or for improving coordination of function across a patient's cortical regions. The method includes applying electrical stimulation to at least a portion of the patient's subcortical structures involved in the generation and control of generalized efference copy signals. Internally generated movement of the patient is then detected and, in response to such internally generated movement, application of electrical stimulation is controlled. The method of the present invention has a number of benefits, including increasing flexibility in identifying targets for stimulation, improving the probability of successfully treating brain injury, and permitting patient biofeedback and self-regulation.

Claims (65)

1. A method of treating a patient suffering from chronic pain and/or generalized seizures, said method comprising:

selecting a patient suffering from chronic pain and/or generalized seizures;

applying electrical stimulation to at least a portion of the patient's subcortical structures involved in the generation and control of generalized efference copy signals under conditions effective to treat the patient's chronic pain and/or generalized seizures;

detecting generalized efference copy signals of the patient; and

controlling said applying electrical stimulation in response to detected generalized efference copy signals of the patient.

2. The method according to claim 1 , wherein the patient is suffering from chronic pain.

3. The method according to claim 1 , wherein the patient is suffering from generalized seizures.

4. The method according to claim 1 , wherein the patient is suffering from chronic pain and generalized seizures.

5. The method according to claim 1 , wherein the subcortical structure is the patient's intralaminar nuclei.

6. The method according to claim 5 , wherein the at least a portion of the patient's intralaminar nuclei comprises paralamellar regions.

7. The method according to claim 5 , wherein electrical stimulation is applied only to at least a portion of the patient's intralaminar nuclei.

8. The method according to claim 1 , wherein electrical stimulation is applied continuously.

9. The method according to claim 1 , wherein electrical stimulation is applied intermittently.

10. The method according to claim 1 , wherein electrical stimulation is applied periodically.

11. The method according to claim 1 , wherein said detecting is carried out by monitoring specific regional or intrahemispheric changes in distribution of power or coherence within a frequency spectrum.

12. The method according to claim 1 , wherein said detecting is carried out by monitoring endogeneous eye movement by indwelling hardware.

13. A method of treating a patient suffering from a brain injury, said method comprising:

selecting a patient suffering from a brain injury;

applying electrical stimulation to at least a portion of the patient's subcortical structures involved in the generation and control of generalized efference copy signals under conditions effective to treat the patient's brain injury;

detecting generalized efference copy signals of the patient; and

controlling said applying electrical stimulation in response to detected generalized efference copy signals of the patient.

14. The method according to claim 13 , wherein the brain injury is produced by stroke.

15. The method according to claim 13 , wherein the brain injury is produced by head trauma.

16. The method according to claim 13 , wherein the brain injury is produced by toxicological agents.

17. The method according to claim 13 , wherein the brain injury is produced by anoxia.

18. The method according to claim 13 , wherein the brain injury is produced by ischemia.

19. The method according to claim 13 , wherein the brain injury is produced by nutritional deficiencies.

20. The method according to claim 13 , wherein the brain injury is produced by developmental diseases.

21. The method according to claim 13 , wherein the brain injury is produced by infectious diseases.

22. The method according to claim 13 , wherein the brain injury is produced by neoplastic diseases.

23. The method according to claim 13 , wherein the brain injury is produced by degenerative diseases.

24. The method according to claim 13 , wherein the subcortical structure is the patient's intralaminar nuclei.

25. The method according to claim 24 , wherein at least a portion of the patient's intralaminar nuclei comprises paralamellar regions.

26. The method according to claim 24 , wherein electrical stimulation is applied only to the at least a portion of the patient's intralaminar nuclei.

27. The method according to claim 13 , wherein electrical stimulation is applied continuously.

28. The method according to claim 13 , wherein electrical stimulation is applied intermittently.

29. The method according to claim 13 , wherein electrical stimulation is applied periodically.

30. The method according to claim 13 , wherein said detecting is carried out by monitoring specific regional or intrahemispheric changes in distribution of power or coherence within a frequency spectrum.

31. The method according to claim 13 , wherein said detecting is carried out by monitoring endogeneous eye movement by indwelling hardware.

32. A method of treating a patient suffering from post-encephalitic parkinsonism, said method comprising:

selecting a patient suffering from post-encephalitic parkinsonism;

applying electrical stimulation to at least a portion of the patient's subcortical structures involved in the generation and control of generalized efference copy signals under conditions effective to treat the patient's post-encephalitic parkinsonism;

detecting generalized efference copy signals of the patient; and

controlling said applying electrical stimulation in response to detected generalized efference copy signals of the patient.

33. The method according to claim 32 , wherein the subcortical structure is the patient's intralaminar nuclei.

34. The method according to claim 33 , wherein at least a portion of the patient's intralaminar nuclei comprises paralamellar regions.

35. The method according to claim 33 , wherein electrical stimulation is applied only to at least a portion of the patient's intralaminar nuclei.

36. The method according to claim 32 , wherein electrical stimulation is applied continuously.

37. The method according to claim 32 , wherein electrical stimulation is applied intermittently.

38. The method according to claim 32 , wherein electrical stimulation is applied periodically.

39. The method according to claim 32 , wherein said detecting is carried out by monitoring specific regional or intrahemispheric changes in distribution of power or coherence within a frequency spectrum.

40. The method according to claim 32 , wherein said detecting is carried out by monitoring endogeneous eye movement by indwelling hardware.

41. A method of treating a patient suffering from oculogyric crises, said method comprising:

selecting a patient suffering from oculogyric crises;

applying electrical stimulation to at least a portion of the patient's subcortical structures involved in the generation and control of generalized efference copy signals under conditions effective to treat the patient's oculogyric crises;

detecting generalized efference copy signals of the patient; and

controlling said applying electrical stimulation in response to detected generalized efference copy signals of the patient.

42. The method according to claim 41 , wherein the subcortical structure is the patient's intralaminar nuclei.

43. The method according to claim 42 , wherein at least a portion of the patient's intralaminar nuclei comprises paralamellar regions.

44. The method according to claim 42 , wherein electrical stimulation is applied only to at least a portion of the patient's intralaminar nuclei.

45. The method according to claim 41 , wherein electrical stimulation is applied continuously.

46. The method according to claim 41 , wherein electrical stimulation is applied intermittently.

47. The method according to claim 41 , wherein electrical stimulation is applied periodically.

48. The method according to claim 41 , wherein said detecting is carried out by monitoring specific regional or intrahemispheric changes in distribution of power or coherence within a frequency spectrum.

49. The method according to claim 41 , wherein said detecting is carried out by monitoring endogeneous eye movement by indwelling hardware.

Assignments (2)
CONFIRMATORY LICENSE Recorded Oct 17, 2017
From: CORNELL UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044217/0967 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Feb 12, 2009
From: CORNELL UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022260/0475 →
Continuity (3)
Continuation 0958925100 · Jun 7, 2000
Provisional Application 6013887300 · Jun 11, 1999
Related Publication 20030097159A1 · May 22, 2003