Flexible vascular occluding device

• US 8,617,234 B2
• Filed: 05/24/2006
• Issued: 12/31/2013
• Est. Priority Date: 05/25/2004
• Status: Active Grant

• Current Assignee: Covidien LP (Medtronic Plc)
• Original Assignee: Covidien LP (Medtronic Plc)
• Inventors: Garcia, Adrian, Ye, Ting Tina, Tran, Quang Q, Berez, Aaron L.
• Primary Examiner(s): MCEVOY, THOMAS M
• Application Number:
  US11/420,027
• Publication Number:
  US 20060206201A1
• Time in Patent Office: 2,778 Days
• Field of Search: 606/1.15, 623/1.4, 623/1.15, 623/1.5, 623/1.51, 623/1.53, 623/1.11
• US Class Current: 623/1.15
• CPC Class Codes: A61B 17/12022 Occluding by internal devices, e.g. balloons or releasable wires plugging an opening in the wall of an organ A61B17/0057; occluders for the cervical canal A61F6/146; vas deferens occluders A61F6/20
• CPC Class Codes: A61B 17/12118 for positioning in conjunction with a stent
• CPC Class Codes: A61B 2017/1205 Introduction devices
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/823 Stents, different from stent-grafts, adapted to cover an aneurysm

Abstract

A vascular occluding device for modifying blood flow in a vessel, while maintaining blood flow to the surrounding tissue. The occluding device includes a flexible, easily compressible and bendable occluding device that is particularly suited for treating aneurysms in the brain. The neurovascular occluding device can be deployed using a micro-catheter. The occluding device can be formed by braiding wires in a helical fashion and can have varying lattice densities along the length of the occluding device. The occluding device could also have different lattice densities for surfaces on the same radial plane.

Claims

1. A system, for treatment of an aneurysm, comprising:

a guidewire for guiding the system to an aneurysm;

a tubular-shaped device for positioning by a user within a blood vessel for treatment of an aneurysm, the device including a plurality of braided strands of helically-wound material in a lattice structure, wherein the device is self-expandable to a first expanded tubular configuration, such that the device engages an inner surface of a blood vessel with a surface of the device being apposed to the vessel surface, the first expanded tubular configuration having a first porosity in a first portion and in a second portion along a length of the tubular-shaped device, the second portion being adjustable, after engagement of the device with the vessel surface, along a length of the second portion to change the device into a second expanded tubular configuration based on an input by the user while the device remains engaged with the vessel surface, such that the second portion acquires a second porosity, different from the first porosity, while the first portion maintains the first porosity;

wherein at least two of the braided strands are formed of different metallic materials;

wherein the at least two of the braided strands are of different widths;

wherein one of the materials comprises platinum;

a device adjuster configured to be positioned in the blood vessel, engage an inner surface of the device while at least a portion of the device adjuster is within the tubular-shaped device, and change the device from the first configuration to the second configuration based on the input;

wherein the input comprises movement, by the user, of the device adjuster in contact with the device.

2. The system of claim 1, wherein the first porosity is lower than the second porosity and wherein flow of blood through the lattice structure at the first porosity is higher than flow of blood through the lattice structure at the second porosity.

3. The system of claim 1, wherein a first portion of the lattice structure has the first porosity and a second portion of the lattice structure has the second porosity.

4. The system of claim 3, wherein the first portion of the lattice structure has the first porosity responsive to a delivery device for the tubular-shaped device and the second portion of the lattice structure has the second porosity responsive to said delivery device.

5. The system of claim 3, wherein the first porosity is lower than the second porosity and wherein the second portion of the lattice structure is configured to overlie the aneurysm.

6. The system of claim 5, wherein the first portion of the lattice structure is configured to be spaced from the aneurysm.

7. The system of claim 6, wherein the first portion of the lattice structure is configured to abut a blood vessel lumen.

8. The system of claim 3, wherein the input is configured to change the porosity of the second portion of the tubular-shaped device only.

9. The system of claim 1, wherein the input comprises motion in a longitudinal direction relative to the device.

10. The system of claim 1, wherein the plurality of braided strands of helically-wound material comprises members.

11. The system of claim 10, wherein the helically-wound material comprises less than 16 strands of members.

12. The system of claim 10, wherein each member has a different width.

13. The system of claim 1, wherein the device is radially compressible.

14. The system of claim 1, further comprising longitudinally extending areas of different densities.

15. The system of claim 14, wherein circumferential densities of the longitudinally extending areas vary based on the areas of different densities.

16. The system of claim 1, wherein the plurality of braided strands of helically-wound material comprises a plurality of woven members, each said member comprising an inner surface and an outer surface configured to be positioned adjacent an inner wall of a vessel and forming a portion of an outer circumference of the device between first and second ends of the device, wherein a plurality of openings extends between the inner surface and the outer surface, the outer surface of the members comprising between about 20 percent and about 50 percent of the total circumferential area of the device.

17. The system of claim 1, wherein the lattice structure at the first porosity restricts fluid flow there through in a direction at an angle to a length of the device and the lattice structure at the second porosity permits greater fluid flow there through relative to the lattice structure at the first porosity.

18. The system of claim 1, wherein the input comprises an applied force at a portion of the device.

19. The system of claim 18, wherein the applied force comprises a rotation force applied to an end portion of said device.

20. The system of claim 1, wherein the input is configured to cause relative movement at crossings of said strands.

21. The system of claim 1, wherein at least one of the first porosity and the second porosity is adjustable based on a second input.

22. The system of claim 1, wherein another of the materials comprises at least one of nitinol and stainless steel.

23. The system of claim 1, wherein the device adjuster comprises an elongate member.

24. The system of claim 1, wherein the device adjuster comprises a lattice density adjusting implement.

25. A system, for treating an aneurysm, comprising:

a guidewire for guiding the system to an aneurysm;

a tubular device having a plurality of crossing strands movable relative to each other and forming a lattice structure, wherein the device is self-expandable to a first configuration, such that the device engages an inner surface of a blood vessel with a surface of the device being apposed to the vessel surface, wherein while in the first configuration, the device has a first porosity in a first portion along a length of the tubular device and the first porosity in a second portion along the length of the tubular device, and wherein the lattice structure is adjustable to a second configuration based on an input by a user while the device remains engaged with the vessel surface, wherein, while in the second configuration, the device has the first porosity in the first portion and a second porosity in the second portion, the second porosity being different than the first porosity;

wherein at least two of the crossing strands are formed of different metallic materials;

wherein the at least two of the crossing strands are of different widths;

wherein one of the materials comprises platinum;

a device adjuster configured to be positioned in the blood vessel, engage an inner surface of the device while at least a portion of the device adjuster is within the tubular device, and change the device from the first configuration to the second configuration based on the input;

wherein the input comprises movement, by the user, of the device adjuster while engaged with the device.

26. The system of claim 25, wherein the crossing strands are closer to each other in the second portion than in the first portion while in the second configuration.

27. The system of claim 25, wherein the crossing strands are further from each other in the second portion than in the first portion while in the second configuration.

28. The system of claim 25, wherein another of the materials comprises at least one of nitinol and stainless steel.

29. The system of claim 25, wherein the device adjuster comprises an elongate member.

30. The system of claim 25, wherein the device adjuster comprises a lattice density adjusting implement.

31. A system, for implanting in a patient'"'"'s vessel, comprising:

a guidewire for guiding the system in the patient'"'"'s vessel;

a stent comprising strands;

a proximal portion having a proximal end;

a distal portion having a distal end;

a stent length extending from the proximal end to the distal end;

a stent wall that defines a lumen extending between the proximal end and the distal end, the stent wall being self-expandable to a self-expanded configuration with a surface of the stent being engaged upon an inner surface of the vessel, the stent wall being further adjustable to an adjusted configuration by mechanical input provided by a user while the surface of the stent remains engaged upon the inner surface of the vessel;

wherein a porosity and a stent length of a discrete portion of the stent wall change as the stent wall adjusts from the self-expanded configuration to the adjusted configuration

wherein at least two of the strands are formed of different metallic materials;

wherein the at least two of the strands are of different widths;

wherein one of the materials comprises platinum;

a stent adjuster configured to be positioned in the patient'"'"'s vessel, engage an inner surface of the stent while at least a portion of the stent adjuster is within the stent, and change the stent from the self-expanded configuration to the adjusted configuration based on the input;

wherein the input comprises movement, by the user, of the stent adjuster relative to the stent.

32. The system of claim 31, wherein, as the stent length is changed, the stent wall porosity changes in the discrete portion relative to the stent wall porosity in at least one of the proximal portion and the distal portion.

33. The system of claim 32, wherein, when the stent length is decreased, the porosity of the stent wall in the discrete portion is reduced relative to the porosity of the stent wall in the proximal portion and the distal portion.

34. The system of claim 31, wherein the stent comprises a first stent length when the stent is in the self-expanded configuration, and a second stent length, shorter than the first stent length, when the stent is in the adjusted configuration.

35. The system of claim 34, wherein the porosity of the stent can be reduced in the discrete portion by decreasing the stent length to less than the second stent length.

36. The system of claim 31, wherein another of the materials comprises at least one of nitinol and stainless steel.

37. The system of claim 31, wherein the stent adjuster comprises an elongate member.

38. The system of claim 31, wherein the stent adjuster comprises a lattice density adjusting implement.

39. A system, for implanting a stent in a patient'"'"'s vessel, comprising:

a guidewire for guiding the system in the patient'"'"'s vessel;

a stent adjuster being configured to extend within a blood vessel of a patient; and

a stent comprising strands and being self-expandable from a compressed configuration to a self expanded configuration such that the stent engages an inner surface of a blood vessel with a surface of the stent being apposed to the vessel surface, the stent having a proximal end, a distal end, a stent lumen extending from the proximal end to the distal end, and a stent wall that has, in the self-expanded configuration, an adjustable porosity after engagement of the stent with the vessel surface;

wherein at least two of the strands are formed of different metallic materials;

wherein the at least two of the strands are of different widths;

wherein one of the materials comprises platinum;

wherein, when the distal end of the stent is in the self-expanded configuration, the adjustable porosity is adjustable by advancing or withdrawing the proximal end of the stent relative to the distal end of the stent by providing an input from a user while the stent remains engaged with the vessel surface;

wherein the stent adjuster is configured to be positioned in the blood vessel, engage an inner surface of the stent while at least a portion of the stent adjuster is within the stem, and adjust the device stem from the self-expanded configuration based on the input;

wherein the input comprises movement, by the user, of the stent adjuster in contact with the stent.

40. The system of claim 39, wherein the adjustable porosity is adjustable in multiple discrete locations along a length of the stent wall.

41. The system of claim 39, wherein, when the stent is in the self-expanded configuration, the adjustable porosity is decreasable in discrete, spatially separate sections of the stent wall as the proximal end of the stent is advanced toward the distal end of the stent.

42. The system of claim 41, wherein, when the stent is in the self-expanded configuration, the adjustable porosity is increasable in the discrete, spatially separate sections of the stent wall as the proximal end is withdrawn from the distal end of the stent.

43. The system of claim 39, wherein another of the materials comprises at least one of nitinol and stainless steel.

44. The system of claim 39, wherein the stent adjuster comprises an elongate member.

45. The system of claim 39, wherein the stent adjuster comprises a lattice density adjusting implement.

46. A system, for implanting a stent in a body lumen of a patient, comprising:

a guidewire for guiding the system through the body lumen;

a stent comprising strands and having a proximal portion and a distal portion;

the stent having a stent wall that defines a lumen extending from the proximal portion to the distal portion, the stem wall having a compressed configuration and a self-expanded configuration wherein the stem engages an inner surface of a blood vessel with a surface of the stent being apposed to a surface of the vessel;

wherein at least two of the strands are formed of different metallic materials;

wherein the at least two of the strands are of different widths;

wherein one of the materials comprises platinum;

wherein, from the self-expanded configuration, the stem wall has a variable porosity that is adjustable by relative movement of the proximal portion with respect to the distal portion in response to a mechanical input provided by a user while the surface of the stent remains engaged upon the inner surface of the vessel;

a stent adjuster configured to be positioned in the blood vessel, engage an inner surface of the stent while at least a portion of the stent adjuster is within the stent, and change the stent from the self-expanded configuration based on the input;

wherein the input comprises movement, by the user, of the stent adjuster in contact with the stent.

47. The system of claim 46, wherein the porosity of the stent wall is adjustable in a plurality of spatially separated locations between the proximal and distal portions.

48. The system of claim 46, wherein the porosity of the stent wall is decreased when a length of the stent, extending from the proximal portion to the distal portion, is decreased.

49. The system of claim 46, wherein, when a length of the stent, extending from the proximal portion to the distal portion, is changed, a porosity of the stent wall in a first region, located between the proximal portion and the distal portion, changes relative to a porosity of the stent wall in a second region, located in at least one of the proximal portion and the distal portion.

50. The system of claim 49, wherein, when the length of the stent is decreased, the porosity in the first region is reduced relative to the porosity in the second region.

51. The system of claim 46, wherein another of the materials comprises at least one of nitinol and stainless steel.

52. The system of claim 46, wherein the stent adjuster comprises an elongate member.

53. The system of claim 46, wherein the stent adjuster comprises a lattice density adjusting implement.