Transcatheter prosthetic heart valve post-dilatation remodeling devices and methods

• US 9,456,899 B2
• Filed: 09/19/2013
• Issued: 10/04/2016
• Est. Priority Date: 04/26/2010
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Yeung, Hubert, Krivoruchko, Mike, Deshmukh, Susheel
• Primary Examiner(s): Miles, Jonathan
• Assistant Examiner(s): Ulsh, George J
• Application Number:
  US14/031,330
• Publication Number:
  US 20140039610A1
• Time in Patent Office: 1,111 Days
• Field of Search: 606/108, 623/1.11, 623/1.12, 623/1.23, 623/2.11
• US Class Current: 1/1
• 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 2/2436 Deployment by retracting a sheath
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61F 2002/9534 for repositioning of stents
• CPC Class Codes: A61F 2230/0054 V-shaped
• CPC Class Codes: A61F 2230/008 paraboloidal
• CPC Class Codes: A61F 2250/0018 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2250/0039 differing in diameter
• CPC Class Codes: A61M 2025/1059 having different inflatable sections mainly depending on the response to the inflation pressure, e.g. due to different material properties with different compartments A61M2025/1072
• CPC Class Codes: A61M 25/1002 characterised by balloon shape A61M25/1006, A61M25/1009 take precedence
• CPC Class Codes: A61M 25/104 used for angioplasty

Abstract

A system and method for restoring (e.g., replacing) a defective heart valve of a patient. A delivery system is manipulated to percutaneously deliver and implant a stented prosthetic heart valve to a native heart valve. A post-dilatation balloon is percutaneously delivered to the implantation site, and a compliant segment thereof is arranged within a region of the implanted prosthesis. The balloon is inflated such that the compliant segment expands and contacts the prosthesis, expanding a remodeling region of the prosthesis to a remodeled state. With these and related techniques, remodeling of an implanted, stented prosthetic heart valve to better match the native valve shape is possible, providing many benefits such as reducing the risk of paravalvular leaks.

Claims

1. A system for percutaneously restoring a native heart valve of a patient, the system comprising:

a stented prosthetic heart valve having a stent frame to which a valve structure is attached, the stent frame configured to radially self-expand from a compressed arrangement;

a delivery device including a delivery sheath sized for percutaneously accessing a heart valve, the delivery device providing a delivery state in which the delivery sheath compressively maintains the stented prosthetic heart valve in the compressed arrangement, and a deployed state in which the delivery sheath is withdrawn from the prosthetic heart valve to permit the prosthetic heart valve to self-expand from the compressed arrangement to a normal, expanded arrangement in which the prosthetic heart valve is completely released from the delivery device; and

a post-dilatation assembly apart from the delivery device, the post-dilatation assembly arranged and configured for percutaneously accessing the stented prosthetic heart valve without the delivery device, the post-dilatation assembly including a catheter and a post-dilatation balloon fluidly attached to the catheter;

wherein a size and shape of the post-dilatation balloon is selected as a function of a size and shape of the stented prosthetic heart valve, the post-dilation balloon including a compliant segment having a longitudinal length not more than 50% of a longitudinal length of the prosthetic heart valve and further wherein with continuous inflation of the post-dilatation balloon at inflation pressures on the order of 0.5-8.0 ATM, a maximum outer diameter of the compliant segment continuously expands and a remainder of the post-dilation balloon does not expand beyond a predetermined shape;

wherein the valve structure includes leaflets that are arranged to establish an outflow region and an inflow region of the prosthetic heart valve, and further wherein a constriction region is formed at a transition from the inflow region to the outflow region, and further wherein the longitudinal length of the compliant segment approximates a longitudinal length of the constriction region; and

wherein in a normal, expanded arrangement, a shape of the outflow region differs from a shape of the inflow region, and further wherein the post-dilatation balloon includes first and second segments at opposite sides of the compliant segment, respectively, and even further wherein a predetermined shape of the first segment upon inflation corresponds with the shape of the inflow region in the normal, expanded arrangement and a predetermined shape of the second segment upon inflation corresponds with the shape of the outflow region in the normal, expanded arrangement.

2. The system of claim 1, wherein the post-dilatation balloon is configured such that in an inflated state, the compliant segment has an obround shape in longitudinal cross-section.

3. The system of claim 1, wherein the post-dilatation balloon further defines a first end segment immediately proximal the compliant segment and a second end segment immediately distal the compliant segment, and further wherein the first and second end segments expand upon inflation of the balloon and are less compliant than the compliant segment.

4. The system of claim 3, wherein the first segment tapers in outer diameter from a maximum diameter to a transition point with the compliant segment.

5. The system of claim 3, wherein in the inflated state, the post-dilatation balloon has a tri-lobed shape.

6. The system of claim 3, wherein a wall thickness of the post-dilatation balloon along the compliant segment is less than a wall thickness of the post-dilatation balloon along the first and second end segments.

7. The system of claim 3, wherein the post-dilatation assembly further includes an engagement feature along an exterior surface of at least one of the first and second end segments, the engagement feature configured to frictionally interface with the stent frame and selected from the group consisting of:

ridges, protrusions, surface roughness, and high friction material.

8. The system of claim 1, wherein the stented prosthetic heart valve and the delivery device are configured to percutaneously deploy and implant the stented prosthetic heart valve without inflation of the post-dilatation balloon.

9. The system of claim 8, wherein the post-dilatation balloon in configured for remodeling a region of the stented prosthetic heart valve following implantation.

10. The system of claim 1, wherein the constriction region is defined between the leaflets and the outflow region, and further wherein the post-dilatation balloon includes first and second segments at opposite sides of the compliant segment, respectively, and even further wherein the post-dilatation balloon is configured such that when located within the stent frame and inflated, the first segment contacts the inflow region, the compliant segment contacts the constriction region, and the second segment contacts the outflow region.