Device forming an endoluminal intracorporeal endoprosthesis, in particular for the abdominal aorta

• US 6,102,940 A
• Filed: 03/23/1998
• Issued: 08/15/2000
• Est. Priority Date: 02/25/1998
• Status: Expired due to Fees

• Current Assignee: Legona Anstalt
• Original Assignee: Legona Anstalt
• Inventors: Meunier, Jean-Jacques, Robichon, Manuel
• Primary Examiner(s): Willse, David H.
• Application Number:
  US09/046,154
• Time in Patent Office: 876 Days
• Field of Search: 623/1, 623/12
• US Class Current: 623/1.35
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/89 the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/061 provided with means for allowing access to secondary lumens
• CPC Class Codes: A61F 2002/065 Y-shaped blood vessels
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2002/825 having longitudinal struts
• CPC Class Codes: A61F 2220/0058 soldered or brazed or welded
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable

Abstract

The invention relates to a device forming an endoluminal endoprosthesis. The device comprises at least a first segment, and upstream from said segment, at a predetermined distance therefrom, it comprises a "fixing" upstream segment made of a biocompatible material so as to be deployable from a closed or non-deployed position for insertion purposes to a deployed working position, the deployed working position being designed to be located in a healthy zone of blood vessel and being separated from the first segment by a predetermined distance defined by links of predetermined length. The invention makes it easy to recatheterize a blood vessel such as the abdominal aorta suffering from an aneurysm.

Claims

1. An endoluminal endoprosthesis device comprising:

a first element deployable from a closed, non-deployed position for installation purposes to a deployed, working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross-section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, said first element further comprising a third segment connected to and communicating with said downstream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream therefrom, said first element comprising at least one of a wire and tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having shape memory, and said first, second, and third segments being formed by a continuous one of a single meshworking step and a single knitting step of said at least one of a wire and tape such that there are no gaps between the first segment and the second segment and between said second segment and said third segment; and

a second element comprising a leak-proof envelope substantially surrounding said first element including said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element.

2. The device of claim 1, wherein said diameter of said third segment is substantially equal to a diameter of said first segment.

3. The device of claim 1, wherein said third segment is shorter in length than said first segment.

4. The device of claim 1, wherein said first segment is equal in length to or greater than twice said third segment.

5. The device of claim 1, wherein each of said at least two independent trunks is sized for receiving said second endoprosthesis-forming device and effecting a leak-free and non-slip connection therebetween.

6. The device of claim 1, further comprising a radio-opaque marker element mounted at an upstream end of said second segment for facilitating viewing of a position of said second segment.

7. The device of claim 1, wherein said at least one of said wire and tape comprises a bent wire forming substantially annular units, each of said annular units having a plurality of bends, said first, second, and third segments comprising bonding means for connecting said annular units.

8. The device of claim 7, wherein a fraction of the plural bends are connected by said bonding means for facilitating a greater flexibility of said annular units.

9. The device of claim 7, wherein said wire has a non-circular cross-section.

10. The device of claim 1, wherein each of said at least two independent trunks has a constricted blood flow diameter in the deployed state less than half of a diameter of the first segment in the deployed state for facilitating an accelerated blood flow through said second segment thereby promoting increased downstream bloodflow.

11. The device of claim 1, further comprising a fixing segment for connection of said first element to a healthy portion of a blood vessel upstream of said first element and separated from said first element by links of a predetermined length.

12. The device of claim 11, wherein said fixing segment comprises at least another one of a wire and tape, wherein said at least one of another wire and tape is made of a biocompatible alloy having a shape memory.

13. The device of claim 12, wherein said fixing segment comprises a number of rings, the number being within a range including 1 to 3, each of said rings comprising said one of a wire and tape of a biocompatible material bent into a zigzag form and bonding means for connecting adjacent bends of adjacent ones of said rings.

14. The device of claim 1, wherein said envelope does not cover said first element at areas proximate said upstream end and said downstream end of said first element, thereby facilitating connection of said device to the blood vessel of the patient.

15. The device of claim 1, wherein each of said first, second, and third segments is deployable to any overall diameter within a range including 20 to 30 mm.

16. An endoluminal endoprosthesis device comprising:

a first element deployable from a closed or non-deployed position for installation purposes to a deployed, working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, said first element further comprising a third segment connected to and communicating with said down stream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream from said one of said at least two independent trunks, said first element comprising at least one of a wire and tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having a shape memory, and said first, second, and third segments being formed by a continuous one of a single meshworking step and a single knitting step of said at least one of a wire and tape such that there are no gaps between the first segment and the second segment and between said second segment and said third segment;

a second element comprising a leak-proof envelope surrounding said first element including said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element; and

a fixing segment for connection to a healthy portion of a blood vessel upstream of said first segment of said first element and separated from said first segment by links of a predetermined length.

17. The device of claim 16, wherein said diameter of said third segment is substantially equal to a diameter of said first segment.

18. The device of claim 17, wherein said third segment is shorter in length than said first segment.

19. The device of claim 16, wherein said first segment is equal in length to or greater than twice said third segment.

20. The device of claim 16, wherein each of said at least two independent trunks is sized for receiving said second endoprosthesis-forming device and effecting a leak-free and non-slip connection therebetween.

21. The device of claim 16, further comprising a radio-opaque marker element mounted at an upstream end of said second segment for facilitating viewing of a position of said second segment.

22. The device of claim 16, wherein said at least one of said wire and tape comprises a bent wire forming substantially annular units, each of said annular units having a plurality of bends, said first, second, and third segments comprising bonding means for connecting said annular units.

23. The device of claim 22, wherein a fraction of the plural bends are connected by said bonding means for facilitating a greater flexibility of said annular units.

24. The device of claim 22, wherein said wire has a non-circular cross-section.

25. The device of claim 16, wherein said fixing segment comprises at least another one of a wire and tape, wherein said at least another one of said wire and tape is made of a biocompatible alloy having a shape memory.

26. The device of claim 25, wherein said fixing segment comprises a number of rings, the number being within a range including 1 to 3, each of said rings comprising said at least another one of a wire and tape bent into a zigzag form and bonding means for connecting adjacent bends of adjacent ones of said rings.

27. The device of claim 16, wherein said envelope does not cover said first element at areas proximate said upstream end and said downstream end of said first element, thereby facilitating connection of said device to the blood vessel of the patient.

36. The device of claim 16, wherein each of said first, second, and third segments is deployable to any overall diameter within a range including 20 to 30 mm.

28. An endoluminal endoprosthesis device comprising:

a first element deployable from a closed or non-deployed position for installation purposes to a deployed working position and having an upstream end and a downstream end, said first element comprising a first segment having first and second end openings and sized for filling a cross-section of a blood vessel in which said first element is to be incorporated when said first element is in said deployed, working position, said first element further comprising a second segment connected to one of said first and second end openings of said first segment and forming at least two independent trunks, each of said at least two independent trunks having an upstream first opening communicating with said first segment and a downstream second opening, each of said at least two independent trunks having a constricted blood flow diameter in the deployed state that is less than half of a diameter of the first segment in the deployed state for facilitating accelerated blood flow through said second segment thereby promoting increased downstream bloodflow, said first element further comprising a third segment connected to and communicating with said down stream second opening of said each of said at least two independent trunks of said second segment, said third segment having a diameter in said deployed state for facilitating access of a second endoprosthesis-forming device through said third segment into engagement in one of said at least two independent trunks for treating a blood vessel downstream from said one of said at least two independent trunks, said first element comprising at least one of a wire and a tape, wherein said at least one of said wire and tape is made of a biocompatible alloy having a shape memory, said first, second, and third segments being formed by means of a continuous one of a single meshworking step and a single knitting step of said at least one of said wire and tape such that there are no gaps between said first and second segments and said second and third segments; and

a second element comprising a leak-proof envelope surrounding said first element and said at least two independent trunks of said second segment, said envelope providing a leak-proof fluid seal about said first element and permitting fluid flow from said upstream end to said downstream end of said first element.

29. The device of claim 28, wherein said at least one of said wire and said tape comprises a bent wire forming substantially annular units, each of said annular units having a plurality of bends, and said first, second, and third segments comprising bonding means for connecting adjacent ones of said annular units.

30. The device of claim 29, wherein a fraction of the plural bends are connected by said bonding means for facilitating a greater flexibility of said annular units.

31. The device of claim 29, wherein said wire has a non-circular cross-section.

32. The device of claim 28, further comprising a fixing segment for connection of said first element to a healthy portion of a blood vessel upstream of said first element and separated from said first element by links of a predetermined length.

33. The device of claim 32, wherein said fixing segment comprises at least another one of a wire and tape, wherein said at least one of another wire and tape is made of a biocompatible alloy having a shape memory.

34. The device of claim 33, wherein said fixing segment comprises a number of rings, the number being within a range including 1 to 3, each of said rings comprising said one of a wire and tape of a biocompatible material bent into a zigzag form and bonding means for connecting adjacent bends of adjacent ones of said rings.

35. The device of claim 28, wherein said envelope does not cover said first element at areas proximate said upstream end and said downstream end of said first element, thereby facilitating connection of said device to the blood vessel of the patient.

37. The device of claim 28, wherein each of said first, second, and third segments is deployable to any overall diameter within a range including 20 to 30 mm.