Endoprosthesis assembly for percutaneous deployment and method of deploying same

• US 5,843,161 A
• Filed: 06/26/1996
• Issued: 12/01/1998
• Est. Priority Date: 06/26/1996
• Status: Expired due to Term

• Current Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Solovay, Kenneth
• Primary Examiner(s): Willse, David H.
• Assistant Examiner(s): Cuddihy, Francis K.
• Application Number:
  US08/668,345
• Time in Patent Office: 888 Days
• Field of Search: 623/1, 623/11, 623/12, 623/66, 623/900, 623/108, 623/155, 606/191-200, 604/96, 604/104, 600/36, 424/426
• US Class Current: 623/1.13
• CPC Class Codes: A61F 2/0077 Special surfaces of prostheses, e.g. for improving ingrowth A61F2/30767 takes precedence
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/958 Inflatable balloons for placing stents or stent-grafts
• CPC Class Codes: A61F 2002/072 Encapsulated stents, e.g. wire or whole stent embedded in lining

Abstract

The present invention provides an endoprosthesis assembly having a reduced cross sectional profile for percutaneous deployment and implantation within a body passageway such as a blood vessel. The assembly comprises a radially expandable cylindrical frame having first and second ends, and a first unexpanded outer diameter and a second expanded outer diameter. The assembly further comprises a radially expandable elastomeric sleeve surrounding a length of the frame and having first and second ends and a first unexpanded inner diameter and a second expanded inner diameter. The inner diameter of the expanded sleeve is not greater than the outer diameter of the expanded frame. The second expanded inner diameter of the sleeve is in a range from about 60% to about 380% greater than the first unexpanded inner diameter of the sleeve. The assembly of the preferred embodiment is adapted to be deployed through an introducer smaller than 9 French and the sleeve is capable of expanding to an inner diameter of about 12 millimeters.

Claims

1. An endoprosthesis assembly for percutaneous deployment and implantation within a body passageway, comprising:

a radially expandable cylindrical frame having first and second ends, said fame having a first unexpanded outer diameter and a second expanded outer diameter; and

a radially expandable elastomeric sleeve surrounding a length of said frame and having first and second ends, said sleeve having a first unexpanded inner diameter and a second expanded inner diameter;

wherein said second expanded inner diameter of said sleeve is not greater than said second expanded outer diameter of said frame;

wherein said sleeve, when expanded, has a sleeve modulus in a range from about 100 psi to about 6000 psi; and

wherein said second expanded inner diameter of said sleeve is in a range from about 60% to about 380% greater than said first unexpanded inner diameter of said sleeve.

2. The endoprosthesis assembly of claim 1, wherein said first unexpanded inner diameter of said sleeve is not greater than said first unexpanded outer diameter of said frame.

3. The endoprosthesis assembly of claim 1, wherein said second expanded inner diameter of said sleeve is in a range from about 4 mm to about 12 mm.

4. The endoprosthesis assembly of claim 1, wherein said sleeve comprises an elastomer having a percent elongation at break in a range from about 500 to about 585, an ultimate tensile strength in a range from about 4400 psi to about 5300 psi, and a durometer hardness in a range from about 73 (shore A) to about 80 (shore A).

5. The endoprosthesis assembly of claim 2, wherein said sleeve comprises an elastomer having a percent elongation at break in a range from about 500 to about 585, an ultimate tensile strength in a range from about 4400 psi to about 5300 psi, and a durometer hardness in a range from about 73 (shore A) to about 80 (shore A).

6. The endoprosthesis assembly of claim 3, wherein said sleeve comprises an elastomer having a percent elongation at break in a range from about 500 to about 585, an ultimate tensile strength in a range from about 4400 psi to about 5300 psi, and a durometer hardness in a range from about 73 (shore A) to about 80 (shore A).

7. The endoprosthesis assembly of claim 1, wherein said sleeve comprises a polycarbonate polyurethane.

8. The endoprosthesis assembly of claim 2, wherein said sleeve comprises a polycarbonate polyurethane.

9. The endoprosthesis assembly of claim 3, wherein said sleeve comprises a polycarbonate polyurethane.

10. The endoprosthesis assembly of claim 1, wherein said assembly is adapted to be disposed through an introducer having an inner diameter in a range from about 2.5 mm to about 2.7 mm.

11. The endoprosthesis assembly of claim 10, wherein said second expanded inner diameter of said sleeve is in a range from about 4 mm to about 7 mm.

12. The endoprosthesis assembly of claim 10, wherein said second expanded inner diameter of said sleeve is in a range from about 7 mm to about 12 mm.

13. The endoprosthesis assembly of claim 1, wherein said sleeve is braided from yarn spun from elastomeric material.

14. The endoprosthesis assembly of claim 1, wherein said sleeve is knitted from yarn spun from elastomeric material.

15. The endoprosthesis assembly of claim 1, wherein said sleeve is woven from yarn spun from elastomeric material.

16. The endoprosthesis assembly of claim 13, wherein said yarn has a denier in a range from about 10 to about 70.

17. The endoprosthesis assembly of claim 14, wherein said yarn has a denier in a range from about 10 to about 70.

18. The endoprosthesis assembly of claim 15, wherein said yarn has a denier in a range from about 10 to about 70.

19. The endoprosthesis assembly of claim 1, wherein said sleeve, when unexpanded, has a wall thickness in a range from about 0.002 inches to about 0.005 inches and wherein said frame has a hoop strength in a range from about 6 psi to about 30 psi.

20. A method of percutaneously deploying an endoprosthesis assembly for implantation at a treatment site within a body passageway of a patient, comprising the steps of:

(a) forming said assembly by surrounding a length of an unexpanded cylindrical fame having a first unexpanded outer diameter with an elastomeric sleeve having a first unexpanded inner diameter;

(b) inserting said assembly into said body passageway;

(c) threading said assembly through said body passageway until said assembly reaches said treatment site; and

(d) expanding said frame to a second expanded outer diameter such that said sleeve is expanded to a second expanded inner diameter not greater than said second expanded outer diameter of said frame and such that said sleeve is expanded to a second expanded outer diameter not less than an inner diameter of said body passageway at said treatment site, wherein said sleeve, when expanded, has a sleeve modulus in a range from about 100 psi to about 6000 psi and wherein said second expanded inner diameter of said sleeve is in a range from about 60% to about 380% greater than said first unexpanded inner diameter of said sleeve.

21. The method of claim 20, wherein said inserting step (b) comprises the step of pushing said assembly through an introducer.

22. The method of claim 21, wherein said introducer has an inner diameter in a range from about 2.5 mm to about 2.7 mm.

23. The method of claim 20, wherein said expanding step (d) comprises the step of inflating a balloon disposed inside said frame.

24. The method of claim 22, wherein said introducer is a 7.5 French introducer and wherein said second expanded inner diameter of said sleeve is in a range from about 4 mm to about 7 mm.

25. The method of claim 22, wherein said introducer is an 8 French introducer and wherein said second expanded inner diameter of said sleeve is in a range from about 8 mm to about 12 mm.

26. The method of claim 20, wherein said first unexpanded inner diameter of said sleeve is not greater than said first unexpanded outer diameter of said frame.

27. The method of claim 20, additionally comprising the step of crimping said assembly onto a first end of an elongated flexible tube for insertion of said assembly into said body passageway and for threading said assembly through said body passageway.

28. The method of claim 20, wherein said sleeve comprises an elastomer having a percent elongation at break in a range from about 500 to about 585, an ultimate tensile strength in a range from about 4400 psi to about 5300 psi, and a durometer hardness in a range from about 73 (shore A) to about 80 (shore A).

29. The method of claim 20, wherein said sleeve comprises a polycarbonate polyurethane.

30. The method of claim 20, wherein said sleeve is braided, knitted, or woven from yarn spun from elastomeric material.

31. The method of claim 30, wherein said yarn has a denier in a range from about 10 to about 70.

32. The method of claim 20, wherein said sleeve, when unexpanded, has a wall thickness in a range from about 0.002 inches to about 0.005 inches and wherein said frame has a hoop strength in a range from about 6 psi to about 30 psi.