Two-stage collapsible/expandable prosthetic heart valves and anchoring systems

• US 8,454,686 B2
• Filed: 09/26/2008
• Issued: 06/04/2013
• Est. Priority Date: 09/28/2007
• Status: Active Grant

• Current Assignee: St Jude Medical LLC (Abbott Laboratories)
• Original Assignee: St Jude Medical Incorporated (Abbott Laboratories)
• Inventors: Alkhatib, Yousef F.
• Primary Examiner(s): GHERBI, SUZETTE JAIME J
• Application Number:
  US12/733,758
• Publication Number:
  US 20100204785A1
• Time in Patent Office: 1,712 Days
• Field of Search: 623 21- 237
• US Class Current: 623/2.18
• CPC Class Codes: A61F 2/2403 with pivoting rigid closure members check valves with hinged closure members in general F16K15/03
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/2433 using balloon catheter
• CPC Class Codes: A61F 2210/0014 using shape memory or superelastic materials, e.g. nitinol
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2230/0076 ellipsoidal or ovoid
• CPC Class Codes: A61F 2250/006 modular
• CPC Class Codes: A61F 2250/0069 Sealing means

Abstract

Prosthetic heart valve apparatus is adapted for delivery into a patient in a circumferentially collapsed condition, followed by circumferential re-expansion at the implant site in the patient. The apparatus includes an annular anchoring structure that can be implanted in the patient first. The apparatus further includes an annular valve support structure, which supports a flexible leaflet structure of the valve. The support and leaflet structures are initially separate from the anchoring structure, but they can be implanted in the patient by interengagement of the support structure with the already-implanted anchoring structure.

Claims

1. Apparatus for use as a prosthetic heart valve, comprising:

an annular anchoring structure adapted for (1) delivery into a patient in a circumferentially collapsed condition, and (2) circumferential re-expansion and anchoring engagement with tissue of the patient when at an implant site in the patient, the anchoring structure including a plurality of collapsible cells having a perimeter and an open center;

an annular valve support structure separate from the annular anchoring structure and adapted for (1) delivery into the patient in a circumferentially collapsed condition separate from the anchoring structure, and (2) circumferential re-expansion and interengagement with the anchoring structure in an assembled position, the valve support structure including a plurality of projections, each projection extending radially outwardly into a respective one of the cells in the assembled position; and

a flexible leaflet structure disposed inside the valve support structure.

2. The apparatus defined in claim 1, wherein the plurality of cells are disposed in an array that extends annularly around the anchoring structure.

3. The apparatus defined in claim 1, wherein the valve support structure includes a plurality of circumferentially spaced commissure post structures, and each of the projections is on a respective one of the commissure post structures.

4. The apparatus defined in claim 1, wherein each of the projections includes first and second inclined surfaces that meet at a radially outermost first peak, the first inclined surface inclining from the first peak radially inwardly in a direction toward an inflow end of the apparatus, and the second inclined surface inclining from the first peak radially inwardly in a direction toward an outflow end of the apparatus.

5. The apparatus defined in claim 4, wherein, in the assembled position, the first inclined surface of each projection contacts a first portion of the perimeter of the cell with which the projection is engaged, the first portion being toward the inflow end of the apparatus, and the second inclined surface of each projection contacts a second portion of the perimeter of the cell with which the projection is engaged, the second portion being toward the outflow end of the apparatus.

6. The apparatus defined in claim 5, wherein each of the projections further includes third and fourth inclined surfaces that meet at a radially outermost second peak, the third and fourth inclined surfaces and the second peak being circumferentially spaced from the first and second inclined surfaces and the first peak, respectively, the third inclined surface inclining from the second peak radially inwardly in a direction toward the inflow end, and the fourth inclined surface inclining from the second peak radially inwardly in a direction toward the outflow end.

7. The apparatus defined in claim 6, wherein, in the assembled position, the third inclined surface of each projection contacts a third portion of the perimeter of the cell with which the projection is engaged, the third portion being toward the inflow end, and the fourth inclined surface of each projection contacts a fourth portion of the perimeter of the cell with which the projection is engaged, the fourth portion being toward the outflow end.

8. The apparatus defined in claim 7, wherein, in each of the projections, the first and third inclined surfaces diverge from one another toward the first peak and the second peak, and the second and fourth inclined surfaces diverge from one another toward the first peak and the second peak.

9. The apparatus defined in claim 8, wherein the first and third portions meet at a first point and incline away from one another toward the outflow end, and the second and fourth portions meet at a second point and incline away from one another toward the inflow end.

10. The apparatus defined in claim 1, wherein the anchoring structure includes a plurality of members that are resiliently biased to incline radially outwardly on an inflow side of the patient'"'"'s native heart valve annulus at the implant site.

11. The apparatus defined in claim 1, wherein the anchoring structure includes a plurality of members that are resiliently biased to incline radially outwardly on an outflow side of the patient'"'"'s native heart valve annulus at the implant site.

12. The apparatus defined in claim 11, wherein the members are adapted to push radially outwardly on the patient'"'"'s native heart valve leaflets at the implant site.

13. The apparatus defined in claim 1, wherein the anchoring structure is resiliently biased to circumferentially re-expand.

14. The apparatus defined in claim 1, wherein the valve support structure is resiliently biased to circumferentially re-expand.

15. The apparatus defined in claim 1, wherein the anchoring structure comprises:

an annular inflow portion adapted for inter-engagement with the valve support structure in the assembled position;

an annular outflow portion adapted for disposition in the patient'"'"'s aorta downstream from the patient'"'"'s native aortic valve at the implant site; and

at least one strut connecting the inflow portion to the outflow portion.

16. The apparatus defined in claim 1, wherein the leaflet structure includes a leaflet made of a material selected from the group consisting of biological tissue, metal, polymers and mesh-reinforced polymers.

17. The apparatus defined in claim 1, wherein the leaflet structure includes polymeric leaflets that are integral with the valve support structure.

18. The apparatus defined in claim 1, further comprising:

an annular cuff structure secured to at least one of the anchoring structure and the valve support structure.

19. A method of implanting a prosthetic heart valve in a patient, comprising:

implanting an annular anchoring structure in the patient by delivering the anchoring structure into the patient in a circumferentially collapsed condition and then circumferentially expanding the anchoring structure while in the patient to implant the anchoring structure at an implant site in the patient, the anchoring structure including a plurality of collapsible cells having a perimeter and an open center;

delivering an annular valve support structure into the patient in a circumferentially collapsed condition and separate from the anchoring structure;

circumferentially expanding the valve support structure while in the patient, the expanded valve support structure including a plurality of projections extending radially outwardly; and

interengaging each of the projections with the open center of a respective one of the cells to interlock the expanded valve support structure with the implanted anchoring structure.

20. The method defined in claim 19, wherein the prosthetic heart valve is implanted in the patient so that blood will flow through the prosthetic heart valve in a bloodflow direction, the method further comprising:

inserting the valve support structure into the implanted anchoring structure in the bloodflow direction.

21. The method defined in claim 19, wherein the prosthetic heart valve is implanted in the patient so that blood will flow through the prosthetic heart valve in a bloodflow direction, the method further comprising:

inserting the valve support structure into the implanted anchoring structure in a direction opposite the bloodflow direction.