ENDOVASCULAR PROSTHESIS AND METHOD OF MAKING

• US 20010049554A1
• Filed: 11/18/1998
• Published: 12/06/2001
• Est. Priority Date: 11/18/1998
• Status: Abandoned Application

• Current Assignee: Revasc Corporation
• Original Assignee: Revasc Corporation
• Inventors: DORROS, GERALD, RUIZ, CARLOS E., KRAJCER, ZVONIMIR
• Application Number:
  US09/195,257
• Publication Number:
  US 20010049554A1
• Time in Patent Office: Days
• US Class Current: 623/1.44
• CPC Class Codes: A61F 2/06 Blood vessels
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/852 Two or more distinct overlapping stents
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2002/065 Y-shaped blood vessels
• CPC Class Codes: A61F 2002/077 having means to fill the space between stent-graft and aneurysm wall, e.g. a sleeve
• CPC Class Codes: A61F 2002/826 more than one stent being applied sequentially
• CPC Class Codes: A61F 2220/005 using adhesives
• CPC Class Codes: A61F 2250/0063 Nested prosthetic parts

Abstract

The present invention provides a prosthesis formed from a plurality of tubular layers members deployed in vivo using endovascular techniques and material. The layers define a lumen through a diseased portion of a vascular system. Each layer may be constructed using overlapping tubular members to provide a custom prosthesis. Subsequent prosthesis layers overlapping in the central portion of the lumen strengthen the prosthesis walls and may incorporate biocompatible materials having desirable properties.

Claims

1. A laminated prosthesis for repairing a diseased area in a vessel comprising:

a first tubular layer having a proximal end and distal end defining a lumen through said diseased area, said proximal end engaging a first surface of said vessel upstream of said diseased area and said distal end engaging a second surface of said vessel downstream of said diseased area; and

a second tubular layer disposed in said first tubular layer, said second tubular layer being deployed in said first tubular layer in vivo.

2. A laminated prosthesis as in

claim 1

, wherein said first surface of said vessel is nominally diseased.

3. A laminated prosthesis as in

claim 1

, wherein said second surface of said vessel is nominally diseased.

4. A laminated prosthesis as in

claim 1

, wherein one of said layers is formed from one or more tubular members,

5. A laminated prosthesis as in

claim 4

, wherein one or more of said tubular members is deployed in vivo.

6. A laminated prosthesis as in

claim 4

, wherein at least one of said tubular members are shorter than said layer formed therefrom.

7. A laminated prosthesis as in

claim 1

, wherein at least one of said layers is a mesh scaffolding.

8. A laminated prosthesis as in

claim 7

, wherein said mesh comprises a plurality of longitudinal members interconnected by serpentine transverse members.

9. A laminated prosthesis as in

claim 1

, wherein at least one of said layers includes a material selected from the group consisting of nitinol, stainless steel, synthetic polymers, bipolymers, genetically modified endothelial cells, biocompatible materials, permeable materials, semipermeable materials, and impermeable materials.

10. A laminated prosthesis as in

claim 1

, wherein at least one of said layers expands from a contracted configuration to a fully deployed configuration.

11. A laminated prosthesis as in

claim 1

, wherein at least one of said layers has a portion defining a longitudinally-oriented slot, the longitudinally-oriented slot enabling tissue to grow therethrough to anchor the prosthesis within the vessel.

12. A laminated prosthesis as in

claim 1

, wherein said first layer defines a bifurcated lumen.

13. A laminated prosthesis as in

claim 1

wherein said tubular members are bonded together by an adhesive.

14. A prosthesis for repairing a diseased area in a vessel comprising:

a first tubular member having a proximal end and a distal end, said proximal end engaging a first surface of said vessel outside of said diseased area and said distal end extending into said diseased area; and

one or more overlapping other tubular members, each other tubular member having a proximal end and a distal end, wherein a proximal end of one of said other tubular members being in an overlapping relationship with said first tubular member and a distal end of one of said other tubular members engaging a second surface of said vessel outside of said diseased area, wherein said first and other tubular members define a lumen through said diseased area.

15. A prosthesis as in

claim 14

, wherein one or more of said tubular members are individually deployed in vivo.

16. A prosthesis as in

claim 14

, wherein at least one of said layers is a mesh scaffolding.

17. A prosthesis as in

claim 16

, wherein said mesh scaffolding comprises a plurality of longitudinal members interconnected by serpentine transverse members.

18. A prosthesis as in

claim 14

, wherein said first surface of said vessel is nominally diseased.

19. A prosthesis as in

claim 14

, wherein said second surface of said vessel is nominally diseased.

20. A prosthesis as in

claim 14

, wherein at least one of said tubular members includes a material selected from the group consisting of nitinol, stainless steel, synthetic polymers, bipolymers, genetically modified endothelial cells, biocompatible materials, permeable materials, semipermeable materials, and impermeable materials.

21. A prosthesis as in

claim 14

, wherein at least one of said tubular members expands from a contracted configuration to a fully deployed configuration.

22. A prosthesis as in

claim 14

, wherein at least one of said tubular members has a portion defining a longitudinally-oriented slot, the longitudinally-oriented slot enabling tissue to grow therethrough to anchor the prosthesis within the vessel.

23. A prosthesis as in

claim 14

, wherein at least two of said tubular members are bonded together by an adhesive.

24. A prosthesis as in

claim 14

, wherein said tubular members define a bifurcated lumen.

25. A method of directing flow through a blood vessel, the method comprising steps of:

disposing a first tubular member in a contracted configuration on a delivery system;

advancing the delivery system inside said vessel to dispose the first tubular member at the desired location within the vessel;

actuating the delivery system to deploy the first tubular member at the desired location;

disposing a second tubular member in a contracted configuration on a delivery system;

advancing the delivery system along a guide wire to dispose the second tubular member at the desired location within the vessel; and

actuating the delivery system to deploy the second tubular member in an overlapping relationship with said first tubular member forming a prosthesis having an external wall.

26. The method as defined in

claim 25

further comprising the step of progressively adding additional tubular member in an overlapping relationship, said tubular members forming layers of materials having different properties.

27. The method as defined in

claim 25

further comprising the step of introducing an adhesive to bond said tubular members together.

28. The method as defined in

claim 25

further comprising the step of introducing material inside a cavity between the external wall of the prosthesis and an internal wall of the vessel.

29. The method as defined in

claim 28

, wherein said material is selected from the group consisting of coils, fibers, glues, hydrocarbons, gels, cyanoacrylates.

30. The method as defined in

claim 28

, wherein said material is introduced inside said cavity using a catheter.