IP Library Granted Patent US 10,660,749
Granted Patent B2
US 10,660,749 · App. 15/407,313 · Granted May 26, 2020

Heart valve prosthesis for percutaneous replacement of a tricuspid valve, and system comprising a heart valve prosthesis of said type

Inventors: Hans Reiner Figulla (Jena, DE); Alexander Lauten (Kleinmachnow, DE)
Assignee: NVT AG
A61F2/2418A61F2/06A61F2/856A61F2002/061A61F2210/0014
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Quick Facts
Patent No.
US 10,660,749
App. No.
15/407,313
Granted
May 26, 2020
Kind
B2
Abstract

The invention relates to a heart valve prosthesis for percutaneous replacement of a tricuspid valve including a stent-type support structure and a biological heart valve; the stent-type support structure can autonomously expand from a radially compressed state into a radially expanded state and includes a fluid-tight cover which extends like a tube over at least some portions of the support structure; the heart valve is arranged in a lateral opening in the support structure. Embodiments further relate to a system including a heart valve prosthesis of said type.

Claims (27)

1. A heart valve prosthesis, for the percutaneous supplementation or replacement of an organic tricuspid valve, the heart valve prosthesis having an overall tubular form and comprising:

a stent-type support structure and a biological heart valve,

the stent-type support structure configured to autonomously expand from a radially compressed state into a radially expanded state; and

a fluid-tight tubular covering extending over a circumference of at least longitudinally central portions of the stent-type support structure, wherein

the biological heart valve is disposed in a lateral opening formed in a common tubular wall plane of both the stent-type support structure and the fluid-tight tubular covering, the lateral opening extending through a tubular wall of the stent-type support structure and the fluid-tight tubular covering to form an exit from an inner tubular lumen of the heart valve prosthesis,

the biological heart valve is disposed within the lateral opening and occluding the lateral opening;

the heart valve prosthesis is configured to form an overall tubular connection extending between the superior vena cava and the inferior vena cava of an organic heart, and

when the stent-type support structure is in the radially expanded state, a circumference of the stent-type support structure at one or more of an end of the heart valve prosthesis corresponding to the superior vena cava and an end of the heart valve prosthesis corresponding to the inferior vena cava is at least as large as a transverse circumference of the stent-type support structure and the fluid-tight tubular covering both immediately above the lateral opening and Immediately below the lateral opening.

2. The heart valve prosthesis according to claim 1 , characterized in that the lateral opening, arranged in the plane with the tubular wall, follows a curvature of the tubular wall or a course of the common wall plane.

3. The heart valve prosthesis according to claim 1 , characterized in that the stent-type support structure comprises two axially longitudinal-axially end sections adapted respectively to anchoring in the superior vena cava and inferior vena cava of the organic heart.

4. The heart valve prosthesis according to claim 3 , characterized in that the stent-type support structure comprises an atrium section that extends between the axially longitudinal end sections.

5. The heart valve prosthesis of claim 4 , characterized in that the atrium section is of a length that corresponds to a distance between the superior vena cava and the inferior vena cava of the organic heart.

6. The heart valve prosthesis according to claim 4 , characterized in that the lateral opening, corresponding to the biological heart valve, is arranged in the atrium section of the stent-type support structure.

7. The heart valve prosthesis according to claim 1 , characterized in that the stent-type support structure comprises a wire mesh and/or laser-cut lattice structure respectively enclosing closed meshes or cells.

8. The heart valve prosthesis according to claim 1 , characterized in that the stent-type support structure comprises a segment without any tubular covering and permeable to blood, disposed at least at one axially longitudinal-end.

9. The heart valve prosthesis according to claim 8 , wherein the stent-type support structure comprises wire mesh and/or laser-cut lattice structure, and characterized in that the segment without any tubular covering and permeable to blood comprises a wire mesh and/or laser-cut lattice structure of a larger mesh size than a mesh size of other wire mesh and/or laser-cut lattice structures of the stent-type support structure.

10. The heart valve prosthesis according to claim 1 , characterized in that the biological heart valve is firmly attached to the stent-type support structure within the lateral opening.

11. The heart valve prosthesis according to claim 10 , characterized in that the fluid-tight tubular covering is attached in a fluid-tight manner to the biological heart valve fixed in the lateral opening.

12. The heart valve prosthesis according to claim 1 , characterized in that the stent-type support structure comprises a shape-memory material and/or a superelastic material.

13. The heart valve prosthesis according to claim 12 , characterized in that the shape-memory material and/or the superelastic material comprises a nickel-titanium alloy.

14. The heart valve prosthesis according to claim 13 , characterized in that the nickel-titanium alloy comprises Nitinol.

15. The heart valve prosthesis according to claim 1 in combination with a catheter,

wherein the heart valve prosthesis is configured to be inserted in the radially compressed state by the catheter to position the heart valve prosthesis in the radially compressed state, wherein the heart valve prosthesis is implantable into an organic heart by the catheter percutaneously, and

wherein there is a diameter ratio between the radially compressed state and the radially expanded state.

16. The heart valve prosthesis according to claim 15 , characterized in that the heart valve prosthesis is implantable into the organic heart transluminally.

17. The heart valve prosthesis according to claim 16 , characterized in that the heart valve prosthesis is implantable into the organic heart transfemorally.

18. A method of using the heart valve prosthesis of claim 15 , comprising implanting the heart valve prosthesis into the organic heart by the catheter.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2020
From: NVT AG
To: MEDIRA AG
Reel/Frame 053013/0972 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2018
From: LAUTEN, ALEXANDER; FIGULLA, HANS REINER
To: NVT AG
Reel/Frame 045698/0852 →
Continuity (2)
Continuation PCTEP2014065294 · Jul 16, 2014
Related Publication 20170165061A1 · Jun 15, 2017