Methods and devices for performing ablation and assessing efficacy thereof

• US 20070185479A1
• Filed: 02/06/2006
• Published: 08/09/2007
• Est. Priority Date: 02/06/2006
• Status: Abandoned Application

• Current Assignee: Maquet Cardiovascular LLC (Getinge AB)
• Original Assignee: Maquet Cardiovascular LLC (Getinge AB)
• Inventors: Lau, Liming
• Application Number:
  US11/348,177
• Publication Number:
  US 20070185479A1
• Time in Patent Office: Days
• US Class Current: 606/33
• CPC Class Codes: A61B 18/1492 having a flexible, catheter-like structure, e.g. for heart ablation A61B18/1477 takes precedence
• CPC Class Codes: A61B 2018/00351 Heart
• CPC Class Codes: A61B 2018/00875 Resistance or impedance
• CPC Class Codes: A61B 2018/1467 using more than two electrodes on a single probe

Abstract

Devices and methods for performing an ablation procedure. One embodiment of a device includes a main body having proximal and distal end portions and first and second sides extending between the proximal and distal end portions. At least one ablation element is configured to apply an ablation energy or substance to tissue to be ablated. At least one electrode is movably positioned with respect to at least one of the sides of the main body, and each such electrode may be configured to assume a retracted position along that respective side of the main body, and an extended position extending beyond a perimeter of the main body. In one method embodiment, a method of performing ablation includes delivering an ablation energy or substance from an ablation device to a target area of tissue to form a lesion therein; delivering an electrical signal via said ablation device to non-ablated tissue on one side of the lesion; and monitoring non-ablated tissue on an opposite side of the lesion to assess whether electrical conduction through the lesion has occurred.

Claims

1. A device for performing an ablation procedure comprising:

a main body having proximal and distal end portions and first and second sides extending between said proximal and distal end portions;

at least one ablation element configured to apply an ablation energy or substance to tissue to be ablated; and

at least one electrode movably positioned with respect to at least one of said sides, each said electrode configured to assume a retracted position along said respective at least one side, and an extended position extending beyond a perimeter of said main body.

2. The device of claim 1 comprising an array of said ablation elements.

3. The device of claim 1 comprising a plurality of said ablation elements.

4. The device of claim 1, wherein said at least one electrode comprises at least a pair of electrodes, a first electrode of each said pair being positioned along said first side, and a second electrode of each said pair being positioned along said second side, opposite said first electrode, respectively.

5. The device of claim 1, wherein said at least one electrode comprises at least two electrodes, a first electrode of said at least two electrodes being positioned along said first side, and a second electrode of said at least two electrodes being positioned along said second side.

6. The device of claim 1, wherein said main body comprises a channel extending distally therein from an opening in said proximal end portion.

7. The device of claim 6, further comprising a push wire configured to be received in said channel, at least one of said at least one electrodes being mounted on said push wire.

8. The device of claim 7, wherein said push wire is electrically conductive and said at least one electrode is electrically connected to said push wire.

9. The device of claim 7, wherein said push wire is fixed to said main body at a distal end of said channel.

10. The device of claim 7, wherein said push wire is removably received in said channel, a distal end of said channel being closed and providing a stop against which a distal end of said push wire is abuttable against.

11. The device of claim 6, wherein said channel comprises a closed distal end.

12. The device of claim 4, wherein said main body comprises a pair of channels extending distally therein from openings in said proximal end portion, a first channel of said pair extending along and adjacent said first side, and a second channel of said pair extending along and adjacent said second side.

13. The device of claim 12, further comprising a pair of push wires configured to be received in said pair of channels, respectively, at least one of said first electrodes being mounted on a first push wire of said pair of push wires and at least one of said second electrodes being mounted on a second push wire of said pair of push wires.

14. The device of claim 13 comprising a plurality of said pairs of electrodes, each of said first electrodes being mounted on said first push wire and each of said second electrodes being mounted on said second push wire.

15. The device of claim 14, further comprising a plurality of electrically conductive leads, each of said electrodes being electrically connected to one of said electrically conductive leads, respectively, said electrically conductive leads extending proximally out of said main body.

16. The device of claim 13 comprising a plurality of pairs of said push wires, each of said first electrodes being mounted on one of said first push wires, respectively, and each of said second electrodes being mounted on one of said second push wires, respectively, such that only one of said electrodes is mounted on any one of said push wires.

17. The device of claim 16, wherein said push wires are electrically conductive and said electrodes are electrically connected to said push wires.

18. The device of claim 4, wherein said main body comprises a plurality of pairs of channels extending distally therein from openings in said proximal end portion, a first channel of each said pair extending along said first side, and a second channel of each said pair extending along said second side.

19. The device of claim 18, further comprising a plurality of pairs of push wires configured to be received in said plurality of pairs of channels, respectively, said first electrodes being mounted on first push wires of said pairs of push wires and said second electrodes being mounted on second push wires of said pairs of push wires, respectively, wherein only one of said electrodes is mounted on any one of said push wires.

20. The device of claim 19, wherein said push wires are electrically conductive and said electrodes are electrically connected to said push wires.

21. The device of claim 6, further comprising at least one opening in at least one of said first and second sides, connecting with said channel, configured to receive one of said at least one electrodes in said retracted position.

22. A method of performing ablation, said method comprising the steps of:

delivering an ablation energy or substance from an ablation device to a target area of tissue to form a lesion therein;

delivering an electrical signal via said ablation device to non-ablated tissue on one side of the lesion; and

monitoring non-ablated tissue on an opposite side of the lesion to assess whether electrical conduction through the lesion has occurred.

23. The method of claim 22, wherein said monitoring comprises visual monitoring of the non-ablated tissue on the opposite side.

24. The method of claim 22, wherein said monitoring comprises contacting an electrode of said ablation device to the non-ablated tissue on the opposite side and interpreting any receipt of the electrical signal or lack thereof via monitoring equipment electrically connected to said electrode.

25. The method of claim 22, wherein said delivering further comprises extending at least one electrode beyond a perimeter of a main body of said ablation device to extend over the lesion and contact the non-ablated tissue, wherein said at least one electrode is electrically connected to a power source.

26. The method of claim 25, further comprising retracting said at least one electrode after a determination that no electrical conduction through the lesion has occurred.

27. The method of claim 22, further comprising re-applying the ablation energy or substance from said ablation device when said monitoring has determined that conduction across the lesion has occurred.

28. The method of claim 27, further comprising repeating said delivering and monitoring steps to assess whether electrical conduction through the lesion has occurred, and repeating said re-applying, delivering and monitoring steps if electrical conduction through the lesion continues.

29. The method of claim 22, wherein said delivering an electrical signal and said monitoring are carried out concurrently with said delivering an ablation energy or substance, said method further comprising ceasing said delivering an ablation energy or substance when it is determined by said monitoring that the lesion has formed sufficiently to create a conduction block.

30. The method of claim 29, wherein said monitoring comprises monitoring an electrogram of said electrical signal as received on the opposite side.

31. The method of claim 22, wherein said delivering an electrical signal and said monitoring are carried out after ceasing said delivering an ablation energy or substance, said method further comprising re-applying the ablation energy or substance from said ablation device when said monitoring has determined that blocking of conduction across the lesion is insufficient.

32. A method of assessing the efficacy of an ablation procedure, said method comprising the steps of:

contacting an electrode, extending from a device used to perform an ablation, to non-ablated tissue on one side of a target area for lesion formation by the ablation procedure;

delivering an electrical signal via said electrode to the non-ablated tissue contacted by the electrode; and

monitoring non-ablated tissue on an opposite side of the target area to assess electrical conduction from said electrode to said non-ablated tissue on the opposite side of the target area.

33. The method of claim 32, wherein said monitoring comprises visual monitoring of the non-ablated tissue on the opposite side.

34. The method of claim 32, wherein said monitoring comprises contacting a second electrode, extending from said ablation device on a side opposite of said electrode delivering the electrical signal, to the non-ablated tissue on the opposite side and interpreting any receipt of the electrical signal or lack thereof via monitoring equipment electrically connected to said second electrode.

35. The method of claim 32, further comprising applying ablation energy or substance from said ablation device when said monitoring has determined that electrical conduction across the target area has occurred.

36. The method of claim 35, wherein said ablation device remains in position for application of ablation energy or substance during said contacting, delivering and monitoring steps, so that said ablation device does not need to be repositioned for said applying ablation energy.

37. The method of claim 35, further comprising repeating said delivering and monitoring steps to assess whether electrical conduction through the lesion formed at the target area has occurred, and repeating said applying, delivering and monitoring steps if electrical conduction through the lesion continues.

38. The method of claim 32, further comprising applying ablation energy or substance from said ablation device to the target area during said delivering and monitoring, said method further comprising ceasing said applying ablation energy or substance when it is determined by said monitoring that the lesion has formed sufficiently.

39. The method of claim 38, wherein said monitoring comprises monitoring an electrogram of said electrical signal as received on the opposite side.

40. A method of performing atrial ablation, said method comprising the steps of:

delivering an ablation energy or substance from an ablation device to a target area of tissue to form one or more lesions to surround one or more pulmonary vein ostia;

delivering an electrical signal via said ablation device to non-ablated tissue on one side of the lesion formation made by said one or more lesions; and

monitoring non-ablated tissue on an opposite side of the lesion formation to assess whether electrical conduction across at least one of the lesions, or through a gap between lesions has occurred.

41. The method of claim 40, wherein said monitoring comprises visual monitoring of the non-ablated tissue on the opposite side.

42. The method of claim 40, wherein said monitoring comprises contacting a second electrode, extending from said ablation device on a side opposite of said electrode delivering the electrical signal, to the non-ablated tissue on the opposite side and interpreting any receipt of the electrical signal or lack thereof via monitoring equipment electrically connected to said second electrode.

43. The method of claim 40, further comprising re-applying ablation energy or substance from said ablation device when said monitoring has determined that electrical conduction has occurred to the opposite side.

44. The method of claim 40, wherein said delivering an electrical signal and said monitoring are carried out concurrently with said delivering an ablation energy or substance, said method further comprising ceasing said delivering an ablation energy or substance when it is determined by said monitoring that the lesion has formed sufficiently.

45. The method of claim 44, wherein said monitoring comprises monitoring an electrogram of said electrical signal as received on the opposite side.

46. The method of claim 40, wherein said delivering an electrical signal and said monitoring are carried out after cessation of said delivering an ablation energy or substance, said method further comprising reapplying said delivering an ablation energy or substance when it is determined by said monitoring that the lesion has not formed sufficiently.