Two-stage scar generation for treating atrial fibrillation

• US 20060116666A1
• Filed: 10/07/2005
• Published: 06/01/2006
• Est. Priority Date: 10/08/2004
• Status: Abandoned Application

• Current Assignee: Syntach AG
• Original Assignee: Sinus Rhythm Technologies, Inc.
• Inventors: Cornelius, Richard, Sullivan, Daniel, Swanson, William, Shebuski, Ronald
• Application Number:
  US11/246,412
• Publication Number:
  US 20060116666A1
• Time in Patent Office: Days
• US Class Current: 606/1
• CPC Class Codes: A61B 17/08 Wound clamps or clips, i.e. not or only partly penetrating the tissue suture bridges A61B17/0466; Devices for bringing together the edges of a wound
• CPC Class Codes: A61B 17/12 for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord specially adapted for vas deferens or fallopian tubes A61F6/20; materials for ligaturing blood vessels A61L17/00
• CPC Class Codes: A61B 18/14 Probes or electrodes therefor
• CPC Class Codes: A61B 2017/00243 cardiac
• CPC Class Codes: A61B 2017/081 Tissue approximator A61B2017/1103, A61B17/8866 take precedence
• CPC Class Codes: A61B 2018/00375 Ostium, e.g. ostium of pulmonary vein or artery

Abstract

The present invention seeks to provide an implant configured to utilize at least two different scar-generating mechanisms that are generated in sequential or overlapping stages. For example, in one embodiment the present invention provides an expandable device that can be positioned at a desired target location within a patient to generate mechanical ablation damage. After a predetermined amount of mechanical ablation has occurred, additional ablation damage is generated by a different source, such as energy delivery, drug delivery, or inflammatory material delivery. In this respect, the overall ablation scarring can be better controlled by utilizing the ablation techniques that are most appropriate at specific phases of a technique or locations within a patient.

Claims

1. A method of creating a conduction block in tissue comprising:

placing an implant in a target location in a patient, said target location having a wall thickness;

inducing a first scar through at least a portion of said wall thickness using a first scarring mechanism;

inducing a second scar through a remaining portion of said wall thickness using a second scarring mechanism; and

wherein said first scarring mechanism is different than said second scarring mechanism.

2. The method of claim 1, wherein said inducing a first scar through at least a portion of said wall thickness using a first scarring mechanism includes mechanically ablating a target tissue with said implant.

3. The method of claim 2, wherein said inducing a second scar through a remaining portion of said wall thickness using a second scarring mechanism includes delivering a drug.

4. The method of claim 3, wherein said drug is an aklylating agent.

5. The method of claim 3, wherein said drug is an antibiotic.

6. The method of claim 3, wherein said drug is a biodegradable polymer.

7. The method of claim 3, wherein said delivering a drug includes degrading a biodegradable coating prior to releasing said drug.

8. The method of claim 2, wherein said inducing a second scar through a remaining portion of said wall thickness using a second scarring mechanism includes delivering an ablative energy to said implant.

9. The method of claim 8, wherein said delivering an ablative energy to said implant includes supplying ablative energy to a lead wire of said implant.

10. The method of claim 8, wherein said delivering an ablative energy to said implant includes supplying ablative radio frequency energy to a lead wire of said implant.

11. The method of claim 1, wherein said inducing a first scar through at least a portion of said wall thickness using a first scarring mechanism is performed during a first time and inducing a second scar through a remaining portion of said wall thickness using a second scarring mechanism is performed during a second time.

12. The method of claim 11, wherein said first time and said second time are sequential.

13. The method of claim 11, wherein said first time and said second time overlap.

37. A method according to claim 3, wherein the delivering of a drug includes a delayed release of said drug.

14. A prosthesis for generating a scar within a patient comprising:

a prosthesis body having an expanded state and a compressed state;

a first ablation component disposed on said prosthesis so as to induce tissue ablation during a first period of time; and

a second ablation component disposed on said prosthesis so as to induce tissue ablation during a second period of time.

15. The prosthesis of claim 14, wherein the first ablation component is a mechanically ablative component.

16. The prosthesis of claim 14, wherein the second ablation component is a tissue inflaming substance ablative component.

17. The prosthesis of claim 14, wherein the second ablation component element includes an ablative energy supply.

18. The prosthesis of claim 14, wherein said second period of time is consecutive with said first period of time.

19. The prosthesis of claim 14, wherein said second period of time overlaps at least a portion of said first period of time.

20. The prosthesis of claim 14, wherein said prosthesis body includes a plurality of struts connected to a circular wire and positioned to contact an adjacent strut.

38. A prosthesis according to claim 16, wherein said tissue inflaming substance ablative component is a delayed release drug.

21. A method of creating a conduction block in tissue comprising:

placing an implant in a target location in a patient, said target location having a tissue thickness;

damaging at least a portion of said tissue thickness using a first ablating mechanism;

damaging a remaining portion of said tissue thickness using a second ablating mechanism; and

wherein said first ablating mechanism is different than said second ablating mechanism.

22. The method of claim 21, wherein said damaging at least a portion of said tissue thickness using a first ablating mechanism occurs during a first time period and wherein said damaging a remaining portion of said tissue thickness using a second ablating mechanism occurs during a second time period.

23. The method of claim 22, wherein said first time period and said second time period are sequential.

24. The method of claim 22, wherein said first time period and said second time period overlap.

25. The method of claim 21, wherein said damaging at least a portion of said tissue thickness using a first ablating mechanism includes applying a mechanical pressure against said tissue thickness.

26. The method of claim 21, wherein said damaging at least a portion of said tissue thickness using a first ablating mechanism includes delivering a drug to said tissue thickness.

27. The method of claim 21, wherein said damaging at least a portion of said tissue thickness using a first ablating mechanism includes applying an ablative energy to said implant.

28. The method of claim 21, wherein said damaging a remaining portion of said tissue thickness using a second ablating mechanism includes applying a mechanical pressure against said tissue thickness.

29. The method of claim 21, wherein said damaging a remaining portion of said tissue thickness using a second ablating mechanism includes delivering a drug to said tissue thickness.

30. The method of claim 21, wherein said damaging a remaining portion of said tissue thickness using a second ablating mechanism includes applying an ablative energy to said implant.

31. The method of claim 21, wherein said placing an implant in a target location in a patient includes positioning said implant at least partially within a pulmonary vein.

39. A method according to claim 26, wherein said delivering a drug to said tissue thickness includes a delivering said drug through delayed delivery.

32. A method of creating a conduction block in tissue comprising:

placing an implant in a target location in a patient, said target location having a wall thickness;

reducing said wall thickness with a first tissue disruption mechanism of said implant;

damaging a remaining thickness of said target location with a second tissue disruption mechanism; and

wherein a tissue disruption capability of said second tissue disruption mechanism is inversely related to a tissue disruption capability of said first disruption mechanism.

33. A method according to claim 32, wherein said first tissue disruption mechanism is a mechanical disruption mechanism.

34. A method according to claim 33, wherein said second tissue disruption mechanism includes an ablative drug.

35. A method according to claim 34, wherein a greater reduction in said wall thickness achieved by said mechanical disruption mechanism reduces the amount of ablative drug required in said second tissue disruption mechanism.

36. A method according to claim 34, wherein said damaging of said remaining thickness is achieved through delayed release of said ablative drug.

40. A method of creating scar lines through the wall of tissue of a pulmonary vein comprising:

providing a prosthesis having an expanded state and a compressed state;

pressing a portion of said prosthesis into tissue around an ostium of said pulmonary vein when said prosthesis is in its expanded state;

allowing a neointimal layer to substantially cover said portion of said prosthesis; and

releasing a substantial portion of an ablative material disposed in said portion of said prosthesis only after a formation of said neointimal layer.

41. A method according to claim 40, wherein an initial portion of ablative material is released prior to the releasing of a substantial portion of said ablative material.

42. A method according to claim 40, wherein said ablative material is a scar generating medical substance.

43. A device for creating scar lines through a tissue wall of a pulmonary vein comprising:

a support structure having an expanded state and a compressed state;

a tissue engagement structure disposed on said support structure;

said tissue engagement structure being loaded with an ablative material; and

said tissue engagement structure having a barrier structure preventing release of a substantial portion of said ablative material until after a neointimal layer is formed on said tissue engagement structure.

44. A device according to claim 43, wherein said barrier allows release of an initial portion of said ablative material prior to formation of said neointimal layer, said initial portion being less than said substantial portion.

45. A device according to claim 43, wherein said ablative material is a scar generating medical substance.