Methods and apparatus for coupling an allograft tissue valve and graft

• US 20060085060A1
• Filed: 10/15/2004
• Published: 04/20/2006
• Est. Priority Date: 10/15/2004
• Status: Abandoned Application

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Campbell, Louis A.
• Application Number:
  US10/966,865
• Publication Number:
  US 20060085060A1
• Time in Patent Office: Days
• US Class Current: 623/1.260
• CPC Class Codes: A61F 2/06 Blood vessels
• CPC Class Codes: A61F 2/2412 with soft flexible valve members, e.g. tissue valves shaped like natural valves check valves with flexible valve members in general F16K15/14

Abstract

Improvements to prosthetic heart valves and grafts for human implantation, particularly to methods and apparatus for coupling a prosthetic heart valve with an artificial graft during a surgical procedure to replace a defective heart valve and blood vessel section, e.g., the aortic valve and a section of the ascending aorta, are disclosed. An annular exterior surface of the prosthetic heart valve is fitted within a vascular graft lumen to dispose the vascular graft proximal end overlying the annular exterior surface, and the proximal end of an elongated vascular graft is compressed against the valve annular exterior surface in a manner that inhibits blood leakage between the vascular graft and the prosthetic heart valve.

Claims

1. A method of coupling an elongated vascular graft having a graft sidewall extending between graft proximal and distal ends with a prosthetic heart valve for replacement of a section of blood vessel and a native heart valve comprising:

fitting an annular exterior surface of the prosthetic heart valve within a vascular graft lumen to dispose the vascular graft proximal end overlying the annular exterior surface; and

clamping the graft proximal end against at least a portion of the annular exterior surface without perforating the vascular graft to couple the vascular graft with the prosthetic heart during chronic implantation and to inhibit blood leakage through the proximal end of an elongated vascular graft.

2. The method of claim 1, further comprising:

providing an expandable compression ring having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to a second ring lumen diameter; and

wherein;

the fitting step further comprises;

expanding the ring lumen to the second ring lumen diameter; and

fitting the graft proximal end overlying the annular exterior surface within the expanded ring lumen; and

the clamping step further comprises halting the expanding to allow the ring lumen to contract toward the first ring lumen diameter, thereby applying compression force of the compression ring against the vascular graft proximal end and at least a portion of the annular exterior surface.

3. The method of claim 2, wherein the prosthetic heart valve comprises a valve body supporting at least one occluding member and an annular, resilient sewing ring disposed about the valve body and the annular exterior surface has an annular surface diameter.

4. The method of claim 3, wherein the providing step comprises providing the expandable compression ring having a first ring lumen diameter sized with respect to the annular surface diameter to provide an interference fit compressing the vascular graft proximal end against the resilient sewing ring.

5. The method of claim 2, wherein the prosthetic heart valve comprises one of a tissue valve and a mechanical valve.

6. The method of claim 2, wherein:

the providing step comprises providing a split ring formed of a biocompatible metal and having an annular channel extending around the circumference of the split ring; and

the clamping step comprises extending a drawstring suture within the annular channel around the circumference of the split ring, tightening the drawstring suture to increase or maintain the compression force, and tying the drawstring suture.

7. The method of claim 2, wherein the providing step comprises providing a split ring formed of a biocompatible metal.

8. The method of claim 2, wherein the providing step comprises providing a garter spring formed of a biocompatible metal.

9. The method of claim 2, wherein the providing step comprises providing an O-ring formed of a biocompatible polymer.

10. The method of claim 2, wherein:

the providing step comprises providing a split ring formed of a biocompatible metal extending between a first split ring end pin receptacle and a second split ring end pin receptacle;

the expanding step comprises expanding the split ring to dispose the first and second split ring receptacles into operative alignment and fitting a locking member into the first and second split ring receptacles to maintain the second ring lumen diameter; and

the halting step comprises removing the locking member from the first and second split ring receptacles.

11. The method of claim 2, wherein:

the providing step comprises providing a split ring formed of a bio-compatible metal extending between a first loop at a first free end of the split ring and a second loop at a second free end of the split ring;

the expanding step comprises expanding the split ring to dispose the first and second loops into operative alignment and fitting a locking pin through the first and second loops to maintain the expanded ring lumen diameter; and

the halting step comprises removing the locking pin from the first and second loops.

12. The method of claim 2, wherein:

the providing step comprises providing a split ring formed of a bio-compatible metal extending between a first split ring end and a second split ring end; and

the expanding step comprises moving the first and second split ring ends apart to expand the ring lumen to the expanded ring lumen diameter.

13. The method of claim 2, wherein:

the providing step comprises providing a split ring formed of a bio-compatible metal extending between a first split ring end and a second split ring end; and

the expanding step comprises moving the first and second split ring ends apart as the ring lumen is expanded to the expanded ring lumen diameter.

14. The method of claim 2, further comprising the steps of:

wrapping an annular section of the graft proximal end around and over the compression ring disposing the graft proximal end against the graft sidewall; and

securing an edge of the graft proximal end to the graft sidewall.

15. The method of claim 2, wherein the providing step comprises attaching the compression ring around the graft proximal end.

16. The method of claim 15, wherein the providing step comprises forming the compression ring with a plurality of teeth extending inwardly into the graft lumen that may penetrate pores of the sewing ring.

17. The method of claim 15, wherein the providing step comprises forming the compression ring with a plurality of teeth extending inwardly into the graft lumen that may penetrate pores of the sewing ring.

18. The method of claim 1, wherein the prosthetic heart valve comprises one of a tissue valve and a mechanical valve.

19. The method of claim 1, wherein the graft sidewall is formed of a bio-compatible fabric sealed with a sealing material that inhibits loss of blood through fabric pores;

and the prosthetic heart valve comprises a tissue valve packaged in a container with a preservative that preserves the tissue and that would attack the sealing material if the graft was coupled to the tissue valve and packaged in the container.

20. The method of claim 1, wherein the clamping step comprises:

fitting the graft proximal end against at least a portion of the annular exterior surface; and

applying a drawstring suture around the graft proximal end to compress the graft proximal end against the annular exterior surface of the prosthetic heart valve.

21. Apparatus for replacement of a section of blood vessel and a native heart valve comprising:

a prosthetic heart valve having an annular exterior surface;

an elongated vascular graft having a graft sidewall enclosing a vascular graft lumen and extending between graft proximal and distal ends; and

means for clamping the graft proximal end against at least a portion of the annular exterior surface without perforating the vascular graft to couple the vascular graft with the prosthetic heart during chronic implantation and to inhibit blood leakage through the proximal end of an elongated vascular graft.

22. The apparatus of claim 21, wherein said clamping means further comprises an expandable compression ring having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to a second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen, the compression ring adapted to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface when the ring lumen diameter contracts from the second ring lumen diameter toward the first ring lumen diameter.

23. The apparatus of claim 22, wherein the prosthetic heart valve comprises a valve body supporting at least one occluding member and an annular, resilient sewing ring disposed about the valve body and the annular exterior surface has an annular surface diameter.

24. The apparatus of claim 23, wherein the compression ring is formed with a plurality of teeth extending inwardly into the graft lumen that may penetrate pores of the sewing ring.

25. The apparatus of claim 23, wherein the expandable compression ring has a first ring lumen diameter sized with respect to the annular surface diameter to provide an interference fit compressing the vascular graft proximal end against the resilient sewing ring.

26. The apparatus of claim 23, wherein the prosthetic heart valve comprises one of a tissue valve and a mechanical valve.

27. The apparatus of claim 22, wherein the compression ring comprises a split ring formed of a biocompatible metal and having an annular channel extending around the circumference of the split ring adapted to receive a drawstring suture tightened and tied to increase or maintain the compression force.

28. The apparatus of claim 22, wherein:

the compression ring comprises;

a split ring formed of a biocompatible metal extending between a first split ring end pin receptacle and a second split ring end pin receptacle having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to the second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen; and

a locking member fitted into the first and second split ring receptacles to maintain the second ring lumen diameter and adapted to be removed to enable the contraction of the ring lumen diameter from the second ring lumen diameter toward the first ring lumen diameter to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface.

29. The apparatus of claim 22, wherein the compression ring comprises a split ring formed of a biocompatible metal.

30. The apparatus of claim 22, wherein the compression ring comprises a garter spring formed of a biocompatible metal.

31. The apparatus of claim 22, wherein the compression ring comprises an O-ring formed of a biocompatible polymer.

32. The apparatus of claim 22, wherein:

the compression ring comprises a split ring formed of a bio-compatible metal extending between a first loop at a first free end of the split ring and a second loop at a second free end of the split ring having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to the second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen; and

a locking pin fitted into the first and second loops to maintain the second ring lumen diameter and adapted to be removed to enable the contraction of the ring lumen diameter from the second ring lumen diameter toward the first ring lumen diameter to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface.

33. The apparatus of claim 22, wherein the compression ring comprises a split ring formed of a bio-compatible metal extending between a first split ring end and a second split ring end adapted to be engaged and moved apart to expand the ring lumen to the expanded ring lumen diameter.

34. The apparatus of claim 22, wherein the compression ring comprises a split ring formed of a bio-compatible metal extending between a first split ring end and a second split ring end, the first and second split ring ends movable apart as the ring lumen is expanded to the expanded ring lumen diameter.

35. The apparatus of claim 21, wherein the prosthetic heart valve comprises one of a tissue valve and a mechanical valve.

36. The apparatus of claim 21, wherein said clamping means further comprises an expandable compression ring fixedly attached to the graft proximal end having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to a second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen, the compression ring adapted to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface when the ring lumen diameter contracts from the second ring lumen diameter toward the first ring lumen diameter.

37. The apparatus of claim 35, wherein the expandable compression ring further comprises a plurality of teeth extending inwardly into the graft lumen that may penetrate pores of the sewing ring.

38. The apparatus of claim 21, wherein the graft sidewall is formed of a bio-compatible fabric sealed with a sealing material that inhibits loss of blood through fabric pores;

and the prosthetic heart valve comprises a tissue valve packaged in a container with a preservative that preserves the tissue and that would attack the sealing material if the graft was coupled to the tissue valve and packaged in the container.

39. The apparatus of claim 21, wherein the clamping means comprises a slip ring having a slip ring lumen sized with respect to the annular exterior surface enabling the fitting of the graft proximal end overlying the annular exterior surface within the slip ring lumen, whereby a drawstring suture can be tied adjacent the slip ring to apply compression force against the vascular graft proximal end adjacent the solid ring and at least a portion of the annular exterior surface when the drawstring suture is drawn tight.

40. The apparatus of claim 21, wherein the graft is formed having a proximal annular section having a radially expandable graft sidewall and a distal annular section having a longitudinally extendable graft sidewall.

41. Apparatus for replacement of a section of blood vessel and a native heart valve comprising:

a prosthetic heart valve having an annular exterior surface;

an elongated vascular graft having a graft sidewall enclosing a vascular graft lumen and extending between graft proximal and distal ends; and

an expandable compression ring having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to a second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen, the compression ring adapted to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface when the ring lumen diameter contracts from the second ring lumen diameter toward the first ring lumen diameter.

42. The apparatus of claim 41, wherein the prosthetic heart valve comprises a valve body supporting at least one occluding member and an annular, resilient sewing ring disposed about the valve body and the annular exterior surface has an annular surface diameter.

43. The apparatus of claim 42, wherein the providing step comprises forming the compression ring with a plurality of teeth extending inwardly into the graft lumen that may penetrate pores of the sewing ring.

44. The apparatus of claim 42, wherein the compression ring has a first ring lumen diameter sized with respect to the annular surface diameter to provide an interference fit compressing the vascular graft proximal end against the resilient sewing ring.

45. The apparatus of claim 42, wherein the prosthetic heart valve comprises one of a tissue valve and a mechanical valve.

46. The apparatus of claim 41, wherein the compression ring comprises a split ring formed of a biocompatible metal.

47. The apparatus of claim 41, wherein the compression ring comprises a garter spring formed of a biocompatible metal.

48. The apparatus of claim 41, wherein the compression ring comprises an O-ring formed of a biocompatible polymer.

49. The apparatus of claim 41, wherein the compression ring comprises a split ring formed of a biocompatible metal and having an annular channel extending around the circumference of the split ring adapted to receive a drawstring suture tightened and tied to increase or maintain the compression force.

50. The apparatus of claim 41, wherein the compression ring comprises:

a split ring formed of a biocompatible metal extending between a first split ring end pin receptacle and a second split ring end pin receptacle having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to the second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen; and

further comprising;

a locking member fitted into the first and second split ring receptacles to maintain the second ring lumen diameter and adapted to be removed to enable the contraction of the ring lumen diameter from the second ring lumen diameter toward the first ring lumen diameter to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface.

51. The apparatus of claim 41, wherein the compression ring comprises:

a split ring formed of a bio-compatible metal extending between a first loop at a first free end of the split ring and a second loop at a second free end of the split ring having a ring lumen adapted to be expanded from a first ring lumen diameter sized with respect to the annular exterior surface to the second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen; and

further comprising;

a locking pin fitted into the first and second loops to maintain the second ring lumen diameter and adapted to be removed to enable the contraction of the ring lumen diameter from the second ring lumen diameter toward the first ring lumen diameter to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface.

52. The apparatus of claim 41, wherein the compression ring comprises a split ring formed of a bio-compatible metal extending between a first split ring end and a second split ring end adapted to be engaged and moved apart to expand the ring lumen to the expanded ring lumen diameter.

53. The apparatus of claim 41, wherein the compression ring comprises a split ring formed of a bio-compatible metal extending between a first split ring end and a second split ring end, the first and second split ring ends movable apart as the ring lumen is expanded to the expanded ring lumen diameter.

54. The apparatus of claim 41, wherein the prosthetic heart valve comprises one of a tissue valve and a mechanical valve.

55. The apparatus of claim 41, wherein said compression ring is fixedly attached to the graft proximal end.

56. The apparatus of claim 55, wherein the compression ring further comprises a plurality of teeth extending inwardly into the graft lumen that may penetrate pores of the sewing ring.

57. The apparatus of claim 41, wherein the graft sidewall is formed of a bio-compatible fabric sealed with a sealing material that inhibits loss of blood through fabric pores;

and the prosthetic heart valve comprises a tissue valve packaged in a container with a preservative that preserves the tissue and that would attack the sealing material if the graft was coupled to the tissue valve and packaged in the container.

58. The apparatus of claim 41, wherein the graft is formed having a proximal annular section having a radially expandable graft sidewall and a distal annular section having a longitudinally extendable graft sidewall.

59. Apparatus for replacement of a section of blood vessel and a native heart valve comprising:

a prosthetic heart valve having an annular exterior surface;

an elongated vascular graft having a graft sidewall enclosing a vascular graft lumen and extending between graft proximal and distal ends, the graft distal end formed with a compression ring having a ring diameter adapted to fit over the annular exterior surface to enable application of a drawstring suture around the graft proximal end to compress the graft proximal end against the annular exterior surface of the prosthetic heart valve.

60. The apparatus of claim 59, wherein the compression ring is expandable from a first ring lumen diameter sized with respect to the annular exterior surface to a second ring lumen diameter enabling the fitting of the graft proximal end overlying the annular exterior surface within the expanded ring lumen, the compression ring adapted to apply compression force against the vascular graft proximal end and at least a portion of the annular exterior surface when the ring lumen diameter contracts from the second ring lumen diameter toward the first ring lumen diameter.

61. The apparatus of claim 59, wherein the compression ring is formed with a plurality of teeth extending inwardly into the graft lumen that may penetrate pores of the sewing ring.

62. The apparatus of claim 59, wherein the compression ring is a slip ring having a slip ring lumen sized with respect to the annular exterior surface enabling the fitting of the graft proximal end overlying the annular exterior surface within the ring lumen, whereby the drawstring suture applies compression force against the vascular graft proximal end adjacent the solid ring and at least a portion of the annular exterior surface when the drawstring is drawn tight.

63. The apparatus of claim 59, wherein the graft is formed having a proximal annular section having a radially expandable graft sidewall and a distal annular section having a longitudinally extendable graft sidewall.

66. The apparatus of claim 59, wherein the graft is formed having a proximal annular section having a radially expandable graft sidewall and a distal annular section having a longitudinally extendable graft sidewall.

64. Apparatus for replacement of a section of blood vessel and a native heart valve comprising:

a prosthetic heart valve having an annular exterior surface;

an elongated vascular graft having a graft sidewall enclosing a vascular graft lumen and extending between graft proximal and distal ends, the graft distal end adapted to fit over the annular exterior surface; and

a slip ring having a slip ring diameter sized with respect to the annular exterior surface enabling the fitting of the graft proximal end overlying the annular exterior surface within the slip ring lumen, to enable application of a drawstring suture around the graft proximal end to compress the graft proximal end adjacent the slip ring against the annular exterior surface of the prosthetic heart valve.

65. The apparatus of claim 64, wherein the slip ring is attached to the graft proximal end.