Dual-tip Catheter System for Boring through Blocked Vascular Passages

• US 20100125253A1
• Filed: 11/17/2008
• Published: 05/20/2010
• Est. Priority Date: 11/17/2008
• Status: Abandoned Application

• Current Assignee: Avinger Inc.
• Original Assignee: Avinger Inc.
• Inventors: McNall, Charles, Olson, William John
• Application Number:
  US12/272,697
• Publication Number:
  US 20100125253A1
• Time in Patent Office: Days
• US Class Current: 604/267
• CPC Class Codes: A61B 17/320758 with a rotating cutting instrument, e.g. motor driven A61B17/320725, A61B17/32075 and A61B17/320783 take precedence; for removing intra-ocular material A61F9/00763; endoscopic rotatable cutting instruments A61B17/32002
• CPC Class Codes: A61B 2017/22001 Angioplasty, e.g. PCTA
• CPC Class Codes: A61B 2017/22039 eccentric
• CPC Class Codes: A61B 2017/22074 the instrument being only slidable in a channel, e.g. advancing optical fibre through a channel
• CPC Class Codes: A61B 2017/22094 for crossing total occlusions, i.e. piercing
• CPC Class Codes: A61B 2017/320766 eccentric
• CPC Class Codes: A61B 2017/320775 Morcellators, impeller or propeller like means
• CPC Class Codes: A61M 25/01 Introducing, guiding, advancing, emplacing or holding catheters A61M25/10 takes precedence

Abstract

A dual-tip catheter equipped with both a rotating cutting bit and a cavity for a probing guidewire tip for passage through chronic total occlusions or other refractory atherosclerotic plaque from diseased arteries. The catheter'"'"'s guidewire tip and rotating cutting bit reside safely within an outer protective catheter sheath head when not in use, and alternately either the cutting bit or the guidewire tip will protrude out of the same distal opening of the sheath head as needed. By first drilling through refractory occlusions, and then inserting a guidewire tip into the occlusion opening formed by the cutting bit, the catheter can force the guidewire tip past the occlusion. After the guidewire tip has been fully inserted, the dual-tip catheter can be withdrawn, and an alternate catheter inserted and directed up the guidewire to the occlusion site, where the alternate catheter can perform further occlusion enlargement or therapeutic activity.

Claims

1. A catheter comprising

a catheter tube with a proximal end, and a hollow distal end configured to enter a body lumen;

a cavity for a guidewire configured so that a guidewire with a proximal end and a distal tip inserted into the cavity is positionable within the hollow distal end of the catheter tube, and application of force on the proximal end of the guidewire causes the guidewire tip to extend forward at least partially outside of the distal end of the catheter tube; and

a distal rotatable cutting bit positionable within the hollow distal end of the catheter tube and configured to allow force applied to the rotatable cutting bit to cause the cutting bit to extend forward at least partially outside of the distal end of the catheter tube.

2. The catheter of claim 1, in which the application of distally directed linear force on the proximal end of a guidewire inserted into the cavity causes the guidewire tip to extend forward at least partially outside of the distal end of the catheter tube.

3. The catheter of claim 1, in which the application of proximally directed linear force on the proximal end of a guidewire inserted into the cavity causes a guidewire tip that has extended forward at least partially outside of the distal end of the catheter tube to retract back inside the distal end of the catheter tube.

4. The catheter of claim 1, in which torque force in a first direction applied to the rotatable cutting bit causes the rotatable cutting bit to extend forward at least partially outside of the distal end of the catheter tube.

5. The catheter of claim 1, in which torque force in a second direction applied to the rotatable cutting bit causes a rotatable cutting bit that has extended forward at least partially outside of the distal end of the catheter tube to retract back inside the distal end of the catheter tube.

6. The catheter of claim 1, in which the application of distally directed linear force on the rotatable cutting bit causes the rotatable cutting bit to extend forward at least partially outside of the distal end of the catheter tube.

7. The catheter of claim 1, in which the application of proximally directed linear force on the rotatable cutting bit causes a rotatable cutting bit that has extended forward at least partially outside of the distal end of the catheter tube to retract back inside the distal end of the catheter tube.

8. The catheter of claim 1, in which the cutting bit has at least one cutting edge.

9. The catheter of claim 1, in which a guidewire tip from a guidewire inserted into the cavity, and the cutting bit, exit the distal end of the catheter in the same location, and in which only one of the guidewire tip and the cutting bit may extend partially outside of the distal end of the catheter at the same time.

10. The catheter of claim 1, in which said catheter is used to remove material selected from the group consisting of refractory atherosclerotic plaque, chronic total occlusions from coronary arteries, and chronic total occlusions from peripheral limb arteries.

11. A catheter comprising a catheter tube with a proximal end, and a hollow distal end configured to enter a body lumen, a distal rotatable cutting bit, and a cavity for a guidewire with a proximal end and a distal tip;

said rotatable cutting bit and said cavity being configured so that a guidewire tip inserted into the cavity is capable of being positioned within the hollow distal end of the catheter tube;

said cavity and catheter tube being configured to allow application of distally and proximally directed reversible linear force on the proximal end of a guidewire inserted into the cavity to reversibly cause said guidewire tip to extend forward at least partially outside of the distal end of said catheter tube and to retract inside of the distal end of said catheter tube; and

said cutting bit and tube being configured to allow reversible torque force (torque) and optionally linear force reversibly applied to said rotatable cutting bit to cause the cutting bit to reversibly rotate and extend forward at least partially outside of the distal end of the catheter tube and to rotate and retract inside the distal end of the catheter tube.

12. The catheter of claim 11, in which the cutting bit has a first surface, and the distal end of the catheter tube has a complementary second surface configured to allow mechanical interactions between the cutting bit and the catheter tube to translate at least some reversible rotation of the cutting bit into extension of the cutting bit partially outside of the distal end of said catheter tube and to retraction inside the distal end of said catheter tube.

13. The catheter of claim 11, in which a guidewire tip inserted into the cavity and the cutting bit exit the distal end of the catheter in the same location, and in which only one of the guidewire tip and the cutting bit may extend partially outside of the distal end of the catheter at the same time.

14. The catheter of claim 11, in which the forward extension of the cutting bit is restricted by at least one motion stop element on the cutting bit.

15. The catheter of claim 11, wherein said catheter tube is hollow and contains a torque communicating connector, and wherein application of torque to said torque communicating connector causes said rotatable cutting bit to rotate.

16. The catheter of claim 15, wherein the torque is applied to the torque communicating connector by mechanisms selected from the group consisting of manual mechanisms, motors, and feedback controlled electronic motors.

17. The catheter of claim 15, wherein an agent selected from the group consisting of therapeutic agents and visualization dye agents is dispensed through the hollow catheter tube.

18. The catheter of claim 11, in which the cavity is configured so that at least a portion of a guidewire inserted into the cavity resides outside of the catheter for part of the proximal length of the catheter, and in which the guidewire then enters the distal portion of the catheter at least 20 centimeters back from the distal end of the catheter.

19. The catheter of claim 11, in which the cavity is configured so that a guidewire inserted into the cavity resides inside of the entire distal portion of the catheter designed to enter a body lumen.

20. The catheter of claim 11, wherein said rotatable cutting bit has at least one blade edge.

21. The catheter of claim 11, wherein the progress of the extension of said cutting bit outside of said catheter is monitored by a sensor.

22. The catheter of claim 11, wherein the cutting effectiveness of said cutting bit is enhanced by energy selected from the group consisting of ultrasonic vibration energy, radiofrequency (RF) energy, and light energy.

23. The catheter of claim 11, wherein the cutting bit has a radiopaque signature that is different from the radiopaque signature of the catheter.

24. The catheter of claim 11, in which said catheter is used to remove material selected from the group consisting of refractory atherosclerotic plaque, chronic total occlusions from coronary arteries, and chronic total occlusions from peripheral limb arteries.

25. The catheter of claim 11, in which said catheter is used as a pretreatment for a blocked artery, and in which the blocked artery is then subjected to further treatment selected from the group consisting of atherectomy, stenting and balloon angioplasty, following the use of said catheter.

26. A catheter comprising:

a catheter tube with a proximal end, and a distal end configured to enter a body lumen;

a hollow sheath head with a distal opening affixed at the distal end of said catheter tube;

a cavity for a guidewire with a proximal end and a distal tip, said cavity being configured so that a guidewire tip inserted into the cavity is capable of being positioned at least partially inside said hollow sheath head;

a rotatable cutting bit capable of being positioned at least partially inside said hollow sheath head;

said cavity, catheter tube, and hollow sheath head being configured to allow application of distally and proximally directed reversible linear force on the proximal end of a guidewire inserted into the cavity to reversibly cause said guidewire tip to extend forward at least partially outside of the distal opening of said hollow sheath head and to retract inside of the distal opening of said hollow sheath head;

said cutting bit, catheter tube, and hollow sheath head being configured to allow reversible torque force (torque) and optionally linear force reversibly applied to said rotatable cutting bit to cause the cutting bit to reversibly rotate and extend forward at least partially outside of the distal opening of said hollow sheath head and to rotate and retract inside the distal opening of said hollow sheath head.

27. The catheter of claim 26, in which the cutting bit has a first surface, and the interior of the hollow sheath head has a complementary second surface configured to allow mechanical interactions between the cutting bit and the interior of the hollow sheath head to translate at least some reversible rotation of the cutting bit into extension of the cutting bit partially outside of the distal opening of the hollow sheath head and to retraction inside the distal opening of the hollow sheath head.

28. The catheter of claim 27, in which the interior of the hollow sheath head contains an internal sheath head structure with an internal mechanism connected to the interior of the hollow sheath head;

the cutting bit protrudes through the internal mechanism;

and interactions between a first surface on the cutting bit and the internal mechanism translate at least some reversible rotation of the cutting bit into reversible extension of the cutting bit partially outside of the distal opening of the hollow sheath head and to retraction inside the distal opening of the hollow sheath head.

29. The catheter of claim 28, in which the internal mechanism is connected to the interior of the hollow sheath head by connectors selected from the group consisting of flexible supports and hinges.

30. The catheter of claim 26, in which a guidewire tip inserted into the cavity, and the cutting bit, exit the distal opening of the hollow sheath head in the same location, and in which only one of the guidewire tip and the cutting bit may extend partially outside of the distal opening of the hollow sheath head at the same time.

31. The catheter of claim 26, wherein said catheter tube is hollow and contains a torque communicating connector, and wherein application of torque to said torque communicating connector causes said rotatable cutting bit to rotate.

32. The catheter of claim 31, wherein the catheter tube contains a single hollow lumen, and the torque communicating connector and a guidewire inserted into this hollow lumen both reside inside this single hollow lumen for at least a portion of the catheter length.

33. The catheter of claim 31, wherein the catheter tube contains two hollow lumens, and in which the torque communicating connector resides inside a first hollow lumen, and a guidewire inserted into the second hollow lumen resides inside the second hollow lumen for at least a portion of the catheter length.

34. The catheter of claim 31, wherein the torque is applied to the torque communicating connector by mechanisms selected from the group consisting of manual mechanisms, motors, and feedback controlled electronic motors.

35. The catheter of claim 31, wherein an agent selected from the group consisting of therapeutic agents and visualization dye agents is dispensed through the hollow catheter tube.

36. The catheter of claim 31, in which at least a portion of a guidewire inserted into the cavity resides outside of the catheter for part of the proximal length of the catheter, and in which the guidewire then enters the distal portion of the catheter at least 20 centimeters back from the distal end of the catheter.

37. The catheter of claim 31, in which a guidewire inserted into the cavity resides inside the entire distal portion of the catheter designed to enter a body lumen.

38. The catheter of claim 26, wherein said rotatable cutting bit has at least one blade edge.

39. The catheter of claim 26, wherein the progress of the advancement of said cutting bit outside of said hollow sheath head opening is monitored by a sensor.

40. The catheter of claim 26, wherein the cutting effectiveness of said cutting bit is enhanced by energy selected from the group consisting of ultrasonic vibration energy, radiofrequency (RF) energy, and light energy.

41. The catheter of claim 26, wherein the cutting bit has a radiopaque signature that is different from the radiopaque signature of the hollow sheath head.

42. The catheter of claim 26, in which said catheter is used to remove material selected from the group consisting of refractory atherosclerotic plaque, chronic total occlusions from coronary arteries, and chronic total occlusions from peripheral limb arteries.

43. The catheter of claim 26, in which said catheter is used as a pretreatment for a blocked artery, and in which the blocked artery is then subjected to further treatment selected from the group consisting of atherectomy, stenting, and balloon angioplasty, following the use of said catheter.

44. A catheter comprising:

a hollow catheter tube with a proximal end, and a distal end configured to enter a body lumen;

a hollow sheath head with a distal opening affixed at the distal end of said catheter tube;

a cavity for a guidewire with a proximal end and a distal tip, said cavity being configured so that the distal tip of a guidewire inserted into the cavity can be positioned at least partially inside said hollow sheath head;

a rotatable cutting bit with at least one blade edge that is capable of being positioned at least partially inside said hollow sheath head;

and a torque communicating connector, wherein application of torque to said torque communicating connector causes said rotatable cutting bit to rotate;

said guidewire cavity, catheter tube, and hollow sheath head being configured to allow application of distally and proximally directed reversible linear force on the proximal end of a guidewire inserted into the cavity to reversibly cause said guidewire tip to extend forward at least partially outside of the distal opening of said hollow sheath head and to retract inside of the distal opening of said hollow sheath head;

said cutting bit, catheter tube, and hollow sheath head being configured to allow reversible torque force (torque) and optionally linear force reversibly applied to said rotatable cutting bit to cause the cutting bit to reversibly rotate and extend forward at least partially outside of the distal opening of said hollow sheath head and to rotate and retract inside the distal opening of said hollow sheath head;

in which a guidewire tip inserted into the cavity and the cutting bit exit the distal opening of the hollow sheath head in the same location, and in which only one of the guidewire tip and the cutting bit may extend partially outside of the distal opening of the hollow sheath head at the same time.

45. The catheter of claim 44, in which the cutting bit has a first surface, and the interior of the hollow sheath head has a complementary second surface configured to allow mechanical interactions between the cutting bit and the interior of the hollow sheath head to translate at least some reversible rotation of the cutting bit into extension of the cutting bit partially outside of the distal opening of the hollow sheath head and to retraction inside the distal opening of the hollow sheath head.

46. The catheter of claim 45, in which the interior of the hollow sheath head contains an internal sheath head structure with an internal mechanism connected to the interior of the hollow sheath head;

the cutting bit protrudes through the internal mechanism;

and interactions between a first surface on the cutting bit and the internal mechanism translate at least some reversible rotation of the cutting bit into reversible extension of the cutting bit partially outside of the distal opening of the hollow sheath head and to retraction inside the distal opening of the hollow sheath head.

47. The catheter of claim 46, in which the internal mechanism is connected to the interior of the hollow sheath head by connectors selected from the group consisting of flexible supports and hinges.

48. The catheter of claim 44, wherein the catheter tube contains a single hollow lumen, and the torque communicating connector and a guidewire inserted into the lumen both reside inside this single hollow lumen for at least a portion of the catheter length.

49. The catheter of claim 44, wherein the catheter tube contains two hollow lumens, and in which the torque communicating connector resides inside a first hollow lumen, and the a guidewire inserted into the second hollow lumen resides inside the second hollow lumen for at least a portion of the catheter length.

50. The catheter of claim 44, wherein the torque is applied to the torque communicating connector by mechanisms selected from the group consisting of manual mechanisms, motors, and feedback controlled electronic motors.

51. The catheter of claim 44, wherein an agent selected from the group consisting of therapeutic agents and visualization dye agents is dispensed through the hollow catheter tube.

52. The catheter of claim 44, in which at least a portion of a guidewire inserted into the cavity resides outside of the catheter for part of the proximal length of the catheter, and in which the guidewire then enters the distal portion of the catheter at least 20 centimeters back from the distal end of the catheter.

53. The catheter of claim 44, in which a guidewire inserted into the cavity resides inside the entire distal portion of the catheter designed to enter a body lumen.

54. The catheter of claim 44, wherein the progress of the advancement of said cutting bit outside of said hollow sheath head opening is monitored by a sensor.

55. The catheter of claim 44, wherein the cutting effectiveness of said cutting bit is enhanced by energy selected from the group consisting of ultrasonic vibration energy, radiofrequency (RF) energy, and light energy.

56. The catheter of claim 44, wherein the cutting bit has a radiopaque signature that is different from the radiopaque signature of the hollow sheath head.

57. The catheter of claim 44, in which said catheter is used to remove material selected from the group consisting of refractory atherosclerotic plaque, chronic total occlusions from coronary arteries, and chronic total occlusions from peripheral limb arteries.

58. The catheter of claim 44, in which said catheter is used as a pretreatment for a blocked artery, and in which the blocked artery is then subjected to further treatment selected from the group consisting of atherectomy, stenting, and balloon angioplasty following the use of said catheter.