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US 2022/0015901 A1Published application
Assembly for replacing the tricuspid atrioventricular valve
AssigneeT-Heart SAS
InventorAlain Dibie
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AssigneeT-Heart SAS
InventorAlain Dibie
Estimating the term…
The present invention relates to an assembly for the tricuspid orifice of a human heart, comprising an external frame (100) connected to an internal stent (200) carrying a tricuspid valve bioprosthesis (210) and a sealing skirt (610). The external frame (100) is configured to hold its position in the native tricuspid annulus. The internal stent (200) is connected to the external frame by one or more fixing strands. The sealing skirt (610) covers the interstitial space existing between the external frame (100) and the internal stent (200). Developments are described which comprise in particular the use of a deformable region of the frame, various alternative embodiments of the sealing skirt, the use of a frame composed of multiple sub-sections, the use of fixing strands between the stent and the frame and of fixing elements for fixing the assembly to the native tissue, the use of sensors and/or actuators, and also the use of a stent in the inferior vena cava. Method aspects are described.
An assembly for the tricuspid orifice of the right heart of a human heart, comprising:
The assembly as claimed in one of the preceding claims, wherein the external frame (100) has a deformable region configured to hold the assembly in position inside the native tricuspid annulus.
The assembly as claimed in one of the preceding claims, wherein the external frame (100) has, upstream from the region of the native annulus, a shape configured to reinforce the hold of the assembly in the native tricuspid annulus.
The assembly as claimed in one of the preceding claims, wherein the external frame (100) has, downstream from the region of the native annulus, a shape configured to reinforce the hold of the assembly in the native tricuspid annulus.
The assembly as claimed in any one of the preceding claims, the external frame (100) being connected to the internal stent (200) by one or more strands (411, 412, 413, 414).
The assembly as claimed in any one of the preceding claims, further comprising at least one fixing element (501, 502) for fixing to the native tissue.
The assembly as claimed in any one of the preceding claims, the sealing skirt (610) being composed of several sub-sections and/or of several layers of materials.
The assembly as claimed in any one of the preceding claims, the frame (100) and/or the stent (200) and/or a fixing strand (411, 412, 413, 414) and/or a fixing element (501, 502) being composed of a heat-sensitive and/or shape-memory material.
The assembly as claimed in any one of the preceding claims, further comprising at least one sensor and/or a radiopaque marker.
The assembly as claimed in any one of the preceding claims, further comprising an actuator suitable for modifying the structure of the assembly and/or for adjusting the positioning of a part of the assembly with respect to the native annulus.
The assembly as claimed in any one of the preceding claims, said assembly being connected to a stent (701) suitable for positioning in the inferior vena cava, said stent being connected to the frame of the assembly by a strand made of nitinol.
The assembly as claimed in any one of the preceding claims, said assembly being folded up in a packaged state (800) in a catheter for introduction by a percutaneous route.
Dependencies are inferred from the claim text.