Electrosurgical ablation and aspiration apparatus having flow directing feature and methods related thereto

• US 6,949,096 B2
• Filed: 01/21/2003
• Issued: 09/27/2005
• Est. Priority Date: 01/21/1998
• Status: Expired due to Term

• Current Assignee: ArthroCare Corporation (Smith & Nephew PLC)
• Original Assignee: ArthroCare Corporation (Smith & Nephew PLC)
• Inventors: Woloszko, Jean, Ormsby, Theodore C., Dahla, Robert H., Davison, Terry S.
• Primary Examiner(s): Cohen, Lee S.
• Application Number:
  US10/264,308
• Publication Number:
  US 20030097129A1
• Time in Patent Office: 980 Days
• Field of Search: 606/41, 606 45- 50, 604/35
• US Class Current: 606/41
• CPC Class Codes: A61B 18/14 Probes or electrodes therefor
• CPC Class Codes: A61B 18/148 having a short, rigid shaft for accessing the inner body transcutaneously, e.g. for neurosurgery or arthroscopy
• CPC Class Codes: A61B 2018/00583 Coblation, i.e. ablation using a cold plasma
• CPC Class Codes: A61B 2018/1407 Loop
• CPC Class Codes: A61B 2018/1467 using more than two electrodes on a single probe
• CPC Class Codes: A61B 2018/1472 for use with liquid electrolyte, e.g. virtual electrodes
• CPC Class Codes: A61B 2218/007 Aspiration

Abstract

Electrosurgical methods, systems, and apparatus for the controlled ablation of tissue from a target site of a patient. An electrosurgical apparatus of the invention includes an active electrode assembly having an active electrode screen surrounded by a plurality of flow protectors. Each flow protector defines a shielded region of the active electrode screen, each shielded region of the screen characterized by enhanced plasma formation. The active electrode assembly is adapted for removing tissue from a surgical site, and the active electrode screen is adapted for digesting fragments of resected tissue. In one embodiment, the apparatus is particularly suited to simultaneously removing both hard and soft tissue in, or around, a joint.

Claims

1. An electrosurgical probe for treating a target tissue at a surgical site, comprising:

a shaft having a shalt distal end and a shaft proximal end; and

an active electrode assembly disposed at the shaft distal end, wherein the active electrode assembly includes an electrically insulating electrode support and an active electrode screen, the electrically insulating electrode support including at least one flow protector and a treatment surface, the at least one flow protector protruding from the treatment surface, and the active electrode screen disposed on the treatment surface of the electrically insulating electrode support.

2. The probe of claim 1, further comprising an aspiration unit including a suction cavity and an aspiration lumen, the suction cavity internal to the electrode support, the aspiration lumen in communication distally with the suction cavity, and the aspiration unit adapted for removing ablation by-products from the vicinity of the active electrode assembly via an aspiration stream.

3. The probe of claim 2, wherein the aspiration lumen is coupled at its proximal end to an aspiration tube, and the aspiration tube is adapted for coupling to a vacuum source.

4. The probe of claim 2, wherein the aspiration stream has a flow rare through the aspiration unit in the range of from about 150 to 400 milliliters per minute.

5. The probe of claim 1, wherein the at least one flow protector comprises an electrically insulating material selected from the group consisting of a ceramic, a glass, and a silicone rubber.

6. The probe of claim 1, wherein the at least one flow protector is integral with the electrically insulating electrode support.

7. The probe of claim 1, wherein the at least one flow protector protrudes from the treatment surface by a distance at least twice the thickness of the active electrode screen.

8. The probe of claim 1, wherein the at least one flow protector protrudes from the treatment surface by a distance about three times the thickness of the active electrode screen.

9. The probe of claim 1, wherein each flow protector causes preferential flow of an aspiration stream over an exposed surface of the active electrode screen.

10. The probe of claim 9, wherein each flow protector shields a shielded region of the exposed surface of the active electrode screen from the flow of the aspiration stream, wherein each shielded region lies between a corresponding flow protector and an aspiration port, the aspiration port located within the treatment surface.

11. The probe of claim 10, wherein each flow protector defines a corresponding one of the shielded regions, wherein each shielded region is characterized by a lower flow rate of the aspiration stream than a non-shielded region of the exposed surface of the active electrode screen.

12. The probe of claim 10, wherein each shielded region promotes the generation and maintenance of a plasma thereat.

13. The probe of claim 1, wherein the active electrode screen includes a first screen lead and a second screen lead.

14. The probe of claim 13, wherein the first screen lead terminates in a free end within the electrode support.

15. The probe of claim 14, wherein the second screen lead is coupled to a connection block, the connection block adapted for coupling the active electrode screen to a high frequency power supply.

16. The probe of claim 1, wherein the active electrode screen is disposed on the treatment surface of the electrode support.

17. The probe of claim 1, wherein the active electrode screen has a plurality of voids therein.

18. The probe of claim 1, wherein the active electrode screen comprises an alloy of platinum and iridium.

19. The probe of claim 1, wherein the active electrode assembly further comprises at least one active electrode terminal.

20. The probe of claim 19, wherein the at least one active electrode terminal comprises a material selected from the group consisting of molybdenum, platinum, tungsten, palladium, iridium, titanium, tantalum, stainless steel, and their alloys.

21. The probe of claim 19, wherein the at least one active electrode terminal comprises four active electrode terminals, each active electrode terminal protruding from the treatment surface.

22. The probe of claim 21, wherein the four active electrode terminals are arranged in a substantially rectangular pattern.

23. The probe of claim 19, wherein the at least one active electrode terminal comprises a plurality of active electrode terminals, each of the plurality of active electrode terminals spaced from the at least one flow protector.

24. The probe of claim 19, wherein the at least one active electrode terminal is electrically isolated from the active electrode screen.

25. The probe of claim 19, further comprising an active electrode lead coupled to each active electrode terminal.

26. The probe of claim 19, wherein the at least one active electrode terminal comprises a molybdenum wire having a diameter in the range of from about 0.010 to 0.020 inch.

27. The probe of claim 19, wherein the at least one active electrode terminal comprises a plurality of active electrode terminals, each of the plurality of active electrode terminals arranged orthogonal to the treatment surface of the electrode support.

28. The probe of claim 1, further comprising a return electrode.

29. The probe of claim 28, further comprising an electrically conducting cap at the shaft distal end, wherein the electrode support is mounted in the cap, and wherein the return electrode comprises the cap.

30. The probe of claim 29, wherein the cap is in electrical communication with the shaft.

31. The probe of claim 1, wherein a proximal portion of the shaft is encased within an electrically insulating sleeve.

32. The probe of claim 1, wherein the electrode support includes an internal suction cavity in communication with an aspiration port.

33. The probe of claim 32, wherein the aspiration port comprises a void within the treatment surface.

34. The probe of claim 1, further comprising a connection block adapted for coupling the probe to a high frequency power supply, the connection block independently coupled to a return electrode, the active electrode screen, and at least one active electrode terminal.

35. The probe of claim 34, further comprising a handle, the connection block housed within the handle.

36. The probe of claim 1, wherein the electrode support comprises a ceramic, a glass, or a silicone rubber.

37. The probe of claim 1, wherein the electrode support comprises alumina.

38. An electrosurgical probe, comprising:

a shaft having a shaft distal end and a shaft proximal end;

an electrode support disposed at the shaft distal end, the electrode support including a treatment surface, at least one flow protector protruding from the treatment surface, and a suction cavity within the electrode support;

at least one active electrode terminal protruding from the treatment surface; and

an active electrode screen disposed on the treatment surface.

39. The probe of claim 38, wherein the active electrode screen includes a central portion having at least one screen void.

40. The probe of claim 39, further comprising an aspiration port within the treatment surface, the at least one screen void aligned with the aspiration port.

41. The probe of claim 38, wherein the active electrode screen includes a first side exposed to flow of an aspiration stream and a second side opposing the treatment surface.

42. The probe of claim 41, wherein each flow protector defines a shielded region of the first side of the active electrode screen, wherein each shielded region is adapted for enhanced plasma formation thereat.

43. The probe of claim 38, wherein the at least one active electrode terminal extends beyond the at least one flow protector by a distance in the range of from about 0.003 to 0.010 inch.

44. The probe of claim 38, wherein the at least one active electrode terminal comprises four active electrode terminals.

45. The probe of claim 38, wherein the at least one active electrode terminal has a diameter in the range of from about 0.010 to 0.020 inch.

46. The probe of claim 38, wherein the at least one active electrode terminal comprises molybdenum wire.

47. The probe of claim 38, further comprising a return electrode and an electrically insulating sleeve on a proximal portion of the shaft, wherein the shaft comprises an electrically conducting material, and the return electrode comprises an exposed distal portion of the shaft.

48. The probe of claim 38, wherein the shaft comprises a material selected from the group consisting of stainless steel, molybdenum, platinum, tungsten, palladium, iridium, titanium, tantalum, stainless steel and their alloys.

49. An electrosurgical probe, comprising:

a shaft having a shaft distal end and a shaft proximal end;

an electrode support disposed at the shaft distal end, the electrode support including a treatment surface, and at least one flow protector protruding from the treatment surface;

an aspiration unit including a suction cavity and an aspiration port, the suction cavity internal to the electrode support, and wherein a void in the treatment surface defines the aspiration port;

at least one active electrode terminal protruding from the treatment surface; and

an active electrode screen disposed on the treatment surface, wherein each flow protector defines a shielded region of the active electrode screen, the shielded region adapted for promoting plasma formation by the active electrode screen.

50. The probe of claim 49, wherein the at least one active electrode terminal is substantially cylindrical in shape.

51. The probe of claim 49, wherein the at least one active electrode terminal comprises a length of molybdenum wire.

52. The probe of claim 49, wherein the active electrode screen comprises a platinum/iridium alloy plate having at least one void therein.

53. The probe of claim 49, wherein the at least one flow protector comprises a protrusion of the treatment surface.

54. The probe of claim 49, wherein each flow protector is integral with the electrode support.

55. The probe of claim 49, wherein each flow protector comprises an electrically insulating material.

56. The probe of claim 49, wherein each flow protector extends from the treatment surface by a distance in the range of from about 0.006 to 0.020 inch.

57. The probe of claim 49, wherein each flow protector is arranged substantially orthogonal to the treatment surface.

58. An electrosurgical system, comprising:

an electrosurgical probe including a shalt having a shaft distal end and a shaft proximal end, an active electrode assembly disposed at the shaft distal end, and a return electrode, the active electrode assembly comprising an electrically insulating electrode support having a treatment surface, an active electrode screen disposed on the treatment surface, and at least one active electrode terminal protruding from the treatment surface, the at least one active electrode terminal electrically isolated from the active electrode screen, and the electrode support including at least one flow protector protruding from the treatment surface; and

a high frequency power supply independently coupled to the active electrode screen and to the at least one active electrode terminal.

59. An active electrode assembly, comprising:

an electrode support having a treatment surface;

an active electrode screen disposed on the treatment surface;

at least one flow protector protruding from the treatment surface, the at least one flow protector extending beyond the active electrode screen; and

at least one active electrode terminal protruding from the treatment surface, the at least one active electrode terminal electrically isolated from the active electrode screen.

60. The active electrode assembly of claim 59, wherein the active electrode screen has a thickness, Ts, and the at least one flow protector extends from the treatment surface by a distance, Hp, wherein the ratio Hp:

Ts is in the range of from about 3;

1 to 5;

1.

61. The active electrode assembly of claim 59, wherein each active electrode terminal and the at least one flow protector extend from the treatment surface by distances Ht and Hp, respectively, wherein Ht is greater than Hp.

62. The active electrode assembly of claim 61, wherein the distance Ht is about 0.005 inch greater than the distance Hp.

63. The active electrode assembly of claim 60, wherein the thickness, Ts of the active electrode screen is in the range of from about 0.002 to 0.005 inch.

64. The active electrode assembly of claim 59, wherein the treatment surface has a void therein, and the void defines an aspiration port.

65. The active electrode assembly of claim 64, further comprising a suction cavity within the electrode support, wherein the suction cavity is in communication with the aspiration port.

66. The active electrode assembly of claim 59, wherein the electrode support comprises a material selected from the group consisting of a ceramic, a glass, and a silicone rubber.

67. The active electrode assembly of claim 59, wherein the at least one active electrode terminal is arranged substantially orthogonal to the treatment surface.

68. The active electrode assembly of claim 59, wherein the at least one active electrode terminal comprises a material selected from the group consisting of molybdenum, platinum, tungsten, palladium, iridium, titanium, tantanlum, stainless steel and their alloys.

69. The active electrode assembly of claim 59, wherein the at least one active electrode terminal comprises a plurality of active electrode terminals.

70. The active electrode assembly of claim 69, wherein each of the plurality of active electrode terminals comprises molybdenum wire.

71. A method for removing a target tissue at a surgical site, comprising:

a) providing an electrosurgical probe having an active electrode assembly and a return electrode, the active electrode assembly comprising an active electrode screen disposed on a treatment surface of an electrically insulating electrode support, at least one flow protector protruding from the treatment surface, and a plurality of active electrode terminals protruding from the treatment surface, each of the plurality of active electrode terminals electrically isolated from the active electrode screen;

b) positioning the active electrode assembly in at least close proximity to the target tissue; and

c) applying a high frequency voltage between the active electrode screen and the return electrode and between the plurality of active electrode terminals and the return electrode, wherein at least a portion of the target tissue is ablated or modified.

72. The method of claim 71, wherein said step c) comprises applying the high frequency voltage concurrently to both the active electrode screen and to the plurality of active electrode terminals.

73. The method of claim 72, wherein during said step c) at least about 65% of the power is applied to the active electrode screen.

74. The method of claim 71, wherein during said step c) the active electrode screen is adapted for removing soft tissue from a patient.

75. The method of claim 74, wherein the plurality of active electrode terminals are adapted for aggressively removing the target tissue, and the active electrode screen is further adapted for digesting resected fragments of the target tissue.

76. The method of claim 71, wherein during said step c) the active electrode terminals are adapted for ablating connective tissue selected from the group consisting of ligament, cartilage, tendon, and bone.

77. The method of claim 71, further comprising:

d) aspirating unwanted materials from the surgical site in an aspiration stream.

78. The method of claim 77, wherein the aspiration stream flows at a volume in the range of from about 150 to 400 milliliters per minute.

79. The method of claim 77, wherein the probe includes an aspiration unit, and the unwanted materials are aspirated from the surgical site via the aspiration unit.

80. The method of claim 79, wherein the aspiration unit includes an aspiration port within the treatment surface, a suction cavity located within the electrode support, the aspiration port leading to the suction cavity, and an aspiration lumen in communication distally with the suction cavity.

81. The method of claim 80, wherein the aspiration lumen is coupled proximally to a vacuum source.

82. The method of claim 77, wherein the at least one flow protector defines a shielded region of the active electrode screen, wherein a first flow rate of the aspiration stream over the shielded region is lower than a second flow rate of the aspiration stream over a non-shielded region of active electrode screen.

83. The method of claim 82, wherein a relatively low flow rate of the aspiration stream in the shielded region promotes generation and maintenance of a plasma at the shielded region upon application of the high frequency voltage of said step c).

84. The method of claim 71, wherein the at least one active electrode terminal is adapted for ablating the target issue via molecular dissociation of components of the target tissue.

85. The method of claim 71, further comprising:

e) during said step c), manipulating the active electrode assembly with respect to the target tissue wherein the target tissue is ablated.

86. The method of claim 71, further comprising:

f) prior to or during said step c), delivering an electrically conductive fluid to the active electrode assembly or to the surgical site.

87. The method of claim 71, wherein the high frequency voltage applied in said step c) in the range of from about 200 volts RMS to 1800 volts RMS.

88. The method of claim 71, wherein during said step c) the target tissue is exposed a temperature in the range of from about 400 C to 900 C.

89. A method for ablating a target tissue at a surgical site of a patient, comprising:

a) providing an electrosurgical probe including a return electrode and an active electrode assembly, the active electrode assembly including at least one active electrode terminal and an active electrode screen, the active electrode screen disposed on a treatment surface of an electrically insulating electrode support, the electrode support including a flow protection unit for providing differential flow of an aspiration stream on a first side of the active electrode screen;

b) positioning the active electrode assembly in at least close proximity to the target tissue;

c) applying a high frequency voltage concurrently to the at least one the active electrode terminal and to the active electrode screen, the high frequency voltage sufficient to ablate at least a portion of the target tissue; and

d) aspirating unwanted materials from the surgical site, wherein the unwanted materials are aspirated via an aspiration port and a suction cavity, the aspiration port within the treatment surface and the suction cavity internal to the electrode support.

90. The method of claim 89, wherein the surgical site lies within a synovial joint.

91. The method of claim 89, wherein the surgical site lies within the vertebral column.

92. The method of claim 89, further comprising:

e) during said step c), reciprocating the active electrode assembly with respect to the target tissue, wherein the target tissue is ablated.

93. The method of claim 89, wherein the target tissue comprises a material selected from the group consisting of cartilage, ligament, tendon, and bone.