Altering the stiffness, size and/or shape of tissues for breathing disorders and other conditions

• US 20050121039A1
• Filed: 11/04/2004
• Published: 06/09/2005
• Est. Priority Date: 10/04/2002
• Status: Abandoned Application

• Current Assignee: Pavad Medical, Inc.
• Original Assignee: Pavad Medical, Inc.
• Inventors: Brooks, Stephen N., Black, Jed E.
• Application Number:
  US10/982,172
• Publication Number:
  US 20050121039A1
• Time in Patent Office: Days
• US Class Current: 128/863
• CPC Class Codes: A61F 2/00 Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents as cosmetic articles, see the relevant subclasses, e.g. wigs, hair pieces, A41G3/00, A41G5/00; artificial nails A45D31/00; dental prostheses A61C13/00; materials for prostheses A61L27/00; artificial hearts A61M60/00; artificial kidneys A61M1/14
• CPC Class Codes: A61F 2250/0001 Means for transferring electromagnetic energy to implants
• CPC Class Codes: A61F 2250/0018 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 5/56 Devices for preventing snoring by influencing the respiratory system by gas treatment A61M16/00
• CPC Class Codes: A61N 2/004 specially adapted for a specific therapy
• CPC Class Codes: A61N 2/06 using magnetic fields produced by permanent magnets A61N2/12 takes precedence

Abstract

Medical devices, systems, and methods mitigate a variety of disorders, including sleep-related breathing disorders. A stiffness, shape, and/or size of a reinforced tissue structure can be altered by applying a magnetic field and/or electrical field. The upper airway can be remodeled at night while maintaining physiological movement (such as swallowing, speaking, singing, and the like) when awake. Biasing of the tissue structures may also be employed.

Claims

1. A method for treating a sleep-related breathing disorder of a patient, the patient having an anterior pharyngeal wall, a posterior pharyngeal wall, and lateral pharyngeal walls extending therebetween, the method comprising:

attaching a material to the lateral pharyngeal walls;

applying a field to the attached material so that, during nighttime, the attached material inhibits the sleep-related breathing disorder of the patient; and

removing the field from the attached material during daytime.

2. The method of claim 1, wherein the material is attached by implanting the material inside the lateral pharyngeal walls so that the material is embedded beneath a surface of the lateral pharyngeal walls.

3. The method of claim 1, wherein the material is attached by suturing the material to the lateral pharyngeal walls or bonding the material to the lateral pharyngeal walls.

4. The method of claim 1, wherein the material comprises a magnetically susceptible material, the applied field comprising a magnetic field.

5. The method of claim 4, wherein the material comprises a ferromagnetic material.

6. The method of claim 1, further comprising attaching the material to the anterior pharyngeal wall.

7. The method of claim 1, wherein the material has a form comprising plates, discs, spheres, bars, multiple small pieces, or mesh.

8. The method of claim 1, wherein the field is applied from outside the patient.

9. The method of claim 1, wherein the field is applied from within the patient.

10. The method of claim 1, wherein the field is applied so that the attached material inhibits movement of the pharyngeal walls toward closure.

11. The method of claim 1, wherein removal of the field limits effects of the attached material on speaking or swallowing.

12. The method of claim 1, wherein the sleep-related breathing disorder comprises sleep apnea.

13. The method of claim 1, wherein the sleep-related breathing disorder comprises snoring.

21. The method of claim 1, wherein the material comprises a contained polymer, colloid, suspension, gel, or liquid.

22. The method of claim 1, wherein the material comprises a shape memory polymer, electrically activated polymer, or an electro-rheostatic material, and wherein the field comprises an electrical field.

23. The method of claim 1, wherein the material comprises a piezoelectric material.

24. The method of claim 5, wherein the material comprises a magneto-rheostatic material, ferrogel, or ferromagnetic polymer.

27. The method of claim 1, wherein the material comprises a piezoelectric material.

14. A system for treating a sleep-related breathing disorder of a patient, the patient having an anterior pharyngeal wall, a posterior pharyngeal wall, and lateral pharyngeal walls extending therebetween, the system comprising:

a material having a form suitable for attaching to the lateral pharyngeal walls; and

a source for removably applying a field to the lateral pharyngeal walls;

wherein, when the material is attached to the lateral pharyngeal walls;

the material inhibits the sleep-related breathing disorder of the patient when the field is applied, and

removal of the field facilitates speaking or swallowing.

15. The system of claim 14, wherein the material comprises a magnetically susceptible material, the source comprises a magnet, and the field comprising a magnetic field.

16. The system of claim 14, wherein the material has a form comprising plates, discs, spheres, bars, multiple small pieces, or mesh.

17. The system of claim 14, wherein the source is configured to apply the field from outside the patient.

18. The system of claim 14, wherein the source is configured to apply the field from within the patient.

19. The system of claim 14, wherein the field is configured so that the attached material inhibits movement of the pharyngeal walls toward closure when the field is applied.

20. The system of claim 14, further comprising suture or a surgical glue for attaching the material to the lateral pharyngeal walls.

25. The system of claim 14, wherein the material comprises a contained polymer, colloid, suspension, gel, or liquid.

26. The system of claim 14, wherein the material comprises a shape memory polymer, electrically activated polymer, or an electro-rheostatic material, and wherein the field comprises an electrical field.

28. The system of claim 15, wherein the material comprises a magneto-rheostatic material, ferrogel, or ferromagnetic polymer.

29. A method for inhibiting a sleep-related breathing disorder of a patient, the patient having an airway with an airway wall, the method comprising:

attaching a material to the airway wall; and

reversibly stiffening the attached material so that the stiffened attached material mitigates the sleep-related breathing disorder.

30. The method of claim 29, wherein the attached material is plastically deformable.

31. The method of claim 30, wherein the attached material has a liquid or pliable configuration and a stiffened configuration, the attached material in the liquid or pliable configuration having sufficient flexibility to deform with an adjacent region of the airway during physiological movement, the attached material in the stiffened configuration inhibiting hypermobility or resonant movement of the adjacent region sufficiently to mitigate the sleep-related breathing disorder, wherein reversibly stiffening the attached material changes the attached material from the liquid or pliable configuration to the stiffened configuration.

32. The method of claim 31, further comprising changing the attached material from the stiffened configuration to the liquid or pliable configuration.

33. The method of claim 29, wherein the attached material has a shape immediately prior to stiffening, and wherein the stiffening inhibits changes from the shape.

34. The method of claim 33, wherein the stiffening does not impart a desired shape on the attached material so that the attached material does not impose a force against the airway wall after stiffening and prior to movement of the airway wall.

35. The method of claim 29, wherein the material comprises a magneto-rheostatic material and the attached material is stiffened by applying a magnetic field thereto.

36. The method of claim 35, further comprising biasing the attached material with the magnetic field so as to open the airway.

37. The method of claim 29, wherein the material comprises an electro-rheostatic material and wherein the attached material is stiffened by applying an electrical field.

38. The method of claim 29, wherein the material comprises at least one of a superelastic material and a piezoelectric material.

39. The method of claim 29, wherein the material is attached by at least one of suturing the material to the upper airway wall, bonding the material to the upper airway wall, and inserting the material into the upper airway wall.

40. The method of claim 39, wherein the material is attached by inserting the material submucosally into the upper airway wall.

41. The method of claim 40, wherein the material in inserted submucosally by penetrating a mucosa of the airway with a sharp distal tip extending from an insertion shaft, advancing the material distally to a target region using the insertion shaft, detaching the material from the insertion shaft, and withdrawing the insertion shaft proximally from the patient.

42. The method of claim 40, wherein the materially is inserted through a plurality of mucosal penetration sites, the attached material defining a stiffening array.

43. The method of claim 40, wherein the material comprises a film, and further comprising cutting the mucosa with an edge and aligning a major surface of the film along an adjacent surface of the airway.

44. The method of claim 29, further comprising selecting a stiffness from among a plurality of alternatives, the stiffening changing the material to the selected stiffness.

45. The method of claim 44, wherein the stiffness is selected by varying the stiffness while monitoring the sleep-related breathing disorder.

46. The method of claim 29, further comprising implanting an energy supply into the patient, wherein the attached material is stiffened by activating the energy supply.

47. The method of claim 46, wherein activation of the energy supply applies a magnetic field to the attached material.

48. The method of claim 46, wherein activation of the energy supply applies an electrical current or electrical field to the attached material.

49. The method of claim 46, wherein the activation energy supply is coupled to the attached material by a conductor.

50. The method of claim 46, wherein the energy supply is implanted at least in part under a muscle of the neck.

51. The method of claim 46, wherein the energy supply comprises at least one of a battery and an electrical coupler configured for receiving electrical energy through skin.

52. A system for inhibiting a sleep-related breathing disorder of a patient, the patient having an airway with an airway wall, the system comprising:

a material configured to be attached to an adjacent region of the airway wall, the material having a first configuration and second configuration, the material in the first configuration allowing the adjacent region to deform during physiological movement when the material is attached to the airway wall, the attached material in the second configuration having a stiffness inhibiting hypermobility or resonant movement of the adjacent region sufficiently to mitigate the sleep-related breathing disorder; and

a source for generating a field, the field capable of reversibly changing the material between the first configuration and the second configuration.

53. The system of claim 52, wherein the material is plastically deformable.

54. The system of claim 52, wherein the attached material in the first configuration is liquid or pliable.

55. The system of claim 52, wherein the attached material has a shape immediately prior to changing from the first configuration to the second configuration, and wherein the change in configuration inhibits changes from the shape.

56. The system of claim 56, wherein the change in configuration does not impart a desired shape on the attached material so that the attached material does not impose a force against the airway wall after stiffening and prior to movement of the airway wall.

57. The system of claim 56, wherein the material comprises a magneto-rheostatic material, ferromagnetic polymer, or ferrogel, the source comprising a magnetic field source.

58. The system of claim 57, wherein the field is sufficient to induce biasing of the attached material so as to open the airway.

59. The system of claim 57, wherein the source comprises an implantable magnetic field source for removably transmitting the magnetic field to the attached material from inside the patient body.

60. The system of claim 57, wherein the source comprises an external magnetic source, and further comprising a support removably mounting the source outside the patient body.

61. The system of claim 57, wherein the material comprises an electro-rheostatic material and wherein the attached material is stiffened by applying an electrical field.

62. The system of claim 57, wherein the material comprises at least one of a superelastic material and a piezoelectric material.

63. The system of claim 57, further comprising at least one of suture for suturing the material to the upper airway wall, adhesive for bonding the material to the upper airway wall, and a probe for inserting the material into the upper airway wall.

64. The system of claim 63, wherein the probe comprises a shaft supporting a sharp distal tip for penetrating a mucosa of the airway passage under visual guidance, the material advancable with the shaft and releasable submucosally.

65. The system of claim 64, wherein the materially comprises a plurality of separate bodies insertable through a plurality of mucosal penetration sites, so that the attached material defines a stiffening array.

66. The system of claim 63, wherein the material comprises a film, and further comprising an edge for cutting the mucosa, the film alignable with a major surface of the film extending along an adjacent surface of the airway within the airway wall.

67. The method of claim 57, wherein the source comprises a variable source and generates a variable field, a stiffness of the material in the second configuration varying in response to the field so as to provide a plurality of alternative stiffness configurations.

68. The system of claim 57, wherein the source has an input for varying the stiffness while monitoring the sleep-related breathing disorder.

69. The system of claim 57, wherein the source comprises an energy supply implantable into the patient, wherein activation of the energy supply stiffens the material when the material is attached to the airway passage.

70. The system of claim 69, wherein activation of the energy supply applies a magnetic field to the material.

71. The system of claim 69, wherein activation of the energy supply applies an electrical current or electrical field to the attached material.

72. The system of claim 71, wherein the energy supply is coupled to the attached material by a conductor.

73. The system of claim 69, wherein the energy supply is implanted at least in part under a muscle of the neck.

74. The system of claim 69, wherein the energy supply comprises at least one of a battery and an electrical coupler configured for receiving electrical energy through skin.

75. The system of claim 57, wherein the material comprises at least one of a plate, a bar, a sphere, and a plurality of pieces.

76. The system of claim 57, wherein the material comprises a mesh.

77. The system of claim 57, wherein the material comprises at least one of a contained colloid, suspension, contained gel, or contained liquid.

78. The system of claim 77, wherein the contained colloid, suspension, gel, or liquid comprises an electro-rheostatic material or a magneto-rheostatic material, and further comprising a biocompatible polymer encasing the material.

79. A method for treating a sleep-related breathing disorder of a patient, the patient having pharyngeal walls, the method comprising:

attaching a magneto-rheostatic material to the pharyngeal walls;

applying a magnetic field to the attached material so that, during nighttime, stiffening of the attached material inhibits the sleep-related breathing disorder of the patient; and

removing the magnetic field from the attached material during daytime.

80. A method for treating a patient, the patient having a tissue, the method comprising:

attaching a magneto-rheostatic material to the tissue; and

reversibly stiffening the attached material by applying a magnetic field to the attached material.

81. The method of claim 80, wherein the tissue comprises a penile tissue.

82. A system comprising:

a material configured to be attached to a tissue of a patient, the material comprising a magneto-rheostatic material having a first configuration and a second configuration, the material in the first configuration having sufficient flexibility to deform with physiological movement when the material is attached to the tissue, the attached material in the second configuration having a stiffness that is greater than in the first configuration; and

a source generating a magnetic field, the field capable of reversibly changing the material between the first configuration and a second configuration when the material is attached to the tissue.

83. The method of claim 82, wherein the material comprises at least one of a contained polymer, colloid, suspension, gel, or liquid, and further comprising a biocompatible polymer encasing the material.

84. A method for inhibiting a sleep-related breathing disorder of a patient, the patient having an airway with an airway wall, the method comprising:

attaching a material to the airway wall;

monitoring breathing of the patient; and

reversibly stiffening, re-sizing, or re-shaping the attached material in response to the monitoring so that the attached material mitigates the sleep-related breathing disorder.

85. A system for inhibiting a sleep-related breathing disorder of a patient, the patient having an airway with an airway wall, the system comprising:

a sensor for monitoring the patient;

a material configured to be attached to the airway wall, the material having a first configuration and second configuration, the material in the first configuration facilitating physiological movement when the material is attached to the airway wall, the attached material in the second configuration having a stiffness, shape, or size inhibiting hypermobility or resonant movement of the adjacent region sufficiently to mitigate the sleep-related breathing disorder; and

a source coupled to the sensor, the source generating a field.capable of reversibly changing the material between the first configuration and the second configuration in response to the monitored patient.