DEVICES AND METHODS FOR CONTROL OF BLOOD PRESSURE

• US 20110077729A1
• Filed: 05/05/2010
• Published: 03/31/2011
• Est. Priority Date: 09/29/2009
• Status: Abandoned Application

• Current Assignee: Vascular Dynamics Inc.
• Original Assignee: Vascular Dynamics Inc.
• Inventors: Weisberg, Ori, Avneri, Itzik, GROSS, Yossi
• Application Number:
  US12/774,254
• Publication Number:
  US 20110077729A1
• Time in Patent Office: Days
• US Class Current: 623/1.1
• CPC Class Codes: A61F 2/06 Blood vessels

Abstract

Apparatus and methods are described, including identifying a subject as suffering from hypertension. In response to the identifying (a) a radius of curvature of a first set of at least three regions of an arterial wall of the subject is increased at a given longitudinal location, while (b) allowing the first set of regions of the arterial wall to pulsate. A device is implanted inside the artery at the longitudinal location such that the device applies pressure to the arterial wall at a second set of at least three regions of the artery, but does not contact the first set of regions, the first set of regions and the second set of regions alternating with each other. Other embodiments are also described.

Claims

1. A method, comprising:

identifying a subject as suffering from hypertension; and

in response to the identifying,

(a) increasing a radius of curvature of a first set of at least three regions of an arterial wall of the subject at a given longitudinal location, while

(b) allowing the first set of regions of the arterial wall to pulsate, by

implanting a device inside the artery at the longitudinal location such that the device applies pressure to the arterial wall at a second set of at least three regions of the artery, but does not contact the first set of regions, the first set of regions and the second set of regions alternating with each other.

2. The method according to claim 1, wherein implanting the device comprises increasing strain in the arterial wall at both the first and the second set of regions, relative to the strain in the arterial wall when the device is absent from the artery.

3. The method according to claim 1, wherein implanting the device comprises increasing a cross-sectional area of the artery.

4. The method according to claim 1, wherein implanting the device comprises implanting a device such that the second set of regions comprises three to six regions at which the device applies pressure to the arterial wall.

14. The method according to claim 1, wherein increasing the radius the curvature of the first set of at least three regions of the arterial wall comprises increasing a systolic radius of curvature at the regions to more than twenty times the systolic radius of curvature of the arterial wall when the device is absent from the artery.

15. The method according to claim 1, wherein implanting the device comprises implanting the device such that each of the regions of the first set of regions is a contiguous region that is able to pulsate, each of the contiguous regions encompassing an angle around a longitudinal axis of the artery of greater than 10 degrees.

17. The method according to claim 15, wherein implanting the device comprises implanting the device such that each of the regions of the first set of regions is a contiguous region that is able to pulsate, each of the contiguous regions encompassing an angle around the longitudinal axis of the artery of greater than 50 degrees.

18. The method according to claim 1, wherein implanting the device comprises implanting the device such that the first set of regions encompass more than 20 percent of a circumference of the arterial wall at the longitudinal location, during systole of the subject.

19. The method according to claim 18, wherein implanting the device comprises implanting the device such that the first set of regions encompass more than 80 percent of the circumference of the arterial wall at the longitudinal location, during systole of the subject.

5-13. -13. (canceled)

16. (canceled)

20. Apparatus for treating hypertension of a subject, comprising:

an implantable device shaped to define at least three separate artery-contacting surfaces, and configured to;

(a) increase a radius of curvature of a wall of the artery at a first set of at least three regions of the arterial wall at a given longitudinal location, while

(b) allowing the first set of regions of the arterial wall to pulsate at the longitudinal location, by

the device being implanted inside the artery at the longitudinal location such that the artery-contacting surfaces contact a second set of at least three regions of the arterial wall, but do not contact the first set of regions of the arterial wall, the first set of regions and the second set of regions alternating with each other.

21. The apparatus according to claim 20, wherein the device is configured such that as the artery-contacting surface apply increasing pressure to the arterial wall, a cross-sectional area of the artery increases.

24. The apparatus according to claim 20, wherein the artery-contacting surfaces comprises three to six artery contacting surfaces.

31. The apparatus according to claim 20, wherein the device has a total cross-sectional area of less than 0.5 sq mm.

32. The apparatus according to claim 20, wherein edges of at least two adjacent artery-contacting surfaces define an angle around a longitudinal axis of the device of greater than 10 degrees.

34. The apparatus according to claim 32, wherein the edges of the two artery-contacting surfaces define an angle around the longitudinal axis of the device of greater than 50 degrees.

22-23. -23. (canceled)

25-30. -30. (canceled)

33. (canceled)

35. A method, comprising:

identifying a subject as suffering from hypertension; and

in response to the identifying,

(a) increasing strain at a first set of regions of an arterial wall of the subject at a given longitudinal location,

(b) while maintaining, at a given stage in a cardiac cycle of the subject, a cross-section of the artery at the longitudinal location that is at least 20 percent of the cross-section of the artery at the longitudinal location, at the given stage in the cardiac cycle, when the device is absent, by

implanting a device outside the artery at the longitudinal location such that the device applies pressure to the arterial wall at the first set of regions of the arterial wall, but does not contact the arterial wall at at least a second set of regions of the arterial wall at the longitudinal location, the first set of regions and the second set of regions alternating with each other.

39. The method according to claim 35, wherein maintaining the cross-section of the artery that is at least 20 percent of the cross-section of the artery at the longitudinal location when the device is absent, comprises maintaining an internal diameter of the artery, in the presence of the device that is at least 30 percent of the diameter of the artery in the absence of the device.

40. The method according to claim 35, wherein maintaining the cross-section of the artery that is at least 20 percent of the cross-section of the artery at the longitudinal location when the device is absent, comprises maintaining a rate of blood flow through the artery that is more than 70 percent of the rate of blood flow through the artery in the absence of the device.

41. The method according to claim 40, wherein maintaining the rate of blood flow through the artery that is more than 70 percent of the rate of blood flow through the artery in the absence of the device, comprises maintaining a rate of blood flow through the artery that is more than 90 percent of the rate of blood flow through the artery in the absence of the device.

42. The method according to claim 35, wherein implanting the device comprises implanting the device such that the arterial wall is able to pulsate at each of the second set of regions.

43. The method according to claim 42, wherein implanting the device, comprises implanting a device outside the artery at the longitudinal location such that the device applies pressure to the arterial wall at a first set of three to six regions of the artery, but does not contact the artery at a second set of three to six regions of the artery.

44. The method according to claim 43, wherein implanting the device comprises implanting a device outside the artery at the longitudinal location such that the device does not contact the artery at at least the second set of regions of the artery, each of the second set of regions being contiguous, and encompassing an angle around a longitudinal axis of the artery of greater than 10 degrees.

46. The method according to claim 44, wherein implanting the device comprises implanting a device such that each of the second set of regions encompasses an angle around the longitudinal axis of the artery of greater than 50 degrees.

48. The method according to claim 35, wherein implanting the device comprises implanting the device such that the device encompasses less than 70 percent of the circumference of the artery.

36-38. -38. (canceled)

45. (canceled)

47. (canceled)

49-51. -51. (canceled)