Flexible canopy valve repair systems and methods of use

US11026791B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11026791-B2
Application numberUS-201916352963-A
CountryUS
Kind codeB2
Filing dateMar 14, 2019
Priority dateMar 20, 2018
Publication dateJun 8, 2021
Grant dateJun 8, 2021

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A system for treating valvular regurgitation in a heart valve includes a flexible canopy and an elongated tether including an elastic portion and an inelastic portion. When the system is in a deployed configuration, a proximal end of the flexible canopy is coupled to an annulus of the heart valve and a distal end of the elongated tether is coupled to a ventricle. The flexible canopy is configured to overlay a first native leaflet of the heart valve, and tension on the elongated tether is applied and/or adjusted to prevent the first leaflet from prolapsing, to maximize coaptation of the flexible canopy with a second native leaflet of the heart valve, and to minimize regurgitation of the heart valve.

First claim

Opening claim text (preview).

What is claimed is: 1. A system for treating valvular regurgitation in a heart valve, the system including a delivery configuration and a deployed configuration, the system comprising: a flexible canopy including a first surface and a second surface opposite the first surface; an elongated tether configured to be placed under tension in situ, the elongated tether including an elastic portion and an inelastic portion coupled to the elastic portion, wherein the elastic portion is at least as long as the inelastic portion with a ratio of the elastic portion to the inelastic portion being between 50/50 and 70/30 and a proximal end of the elongated tether is attached to a distal end of the flexible canopy; and a distal anchor configured to be embedded into tissue of a ventricle, wherein a distal end of the elongated tether is coupled to the distal anchor, wherein when the system is in the deployed configuration, a proximal end of the flexible canopy is anchored to an annulus of the heart valve and the distal end of the elongated tether is anchored to tissue of a ventricle via the distal anchor such that the first surface of the flexible canopy overlays an underlying first surface of a first leaflet of the heart valve, and the elongated tether is placed under tension such that the system is configured to prevent the first leaflet of the heart valve from prolapsing, and to permit a portion of the second surface of the flexible canopy to coapt with at least an opposing mating portion of a second leaflet of the heart valve. 2. The system of claim 1 , wherein when the first surface of the flexible canopy overlays the first leaflet of the heart valve, the first surface of the flexible canopy is substantially in contact with between forty and ninety percent of the underlying first surface of the first leaflet of the heart valve. 3. The system of claim 1 , wherein the flexible canopy does not extend into the ventricle when the system is in the deployed configuration. 4. The system of claim 1 , wherein the inelastic portion of the elongated tether is positioned distal of the elastic portion of the elongated tether. 5. The system of claim 1 , wherein the elastic portion of the elongated tether is positioned distal of the inelastic portion of the elongated tether. 6. The system of claim 1 , wherein the elastic portion of the elongated tether is longer than the inelastic portion of the elongated tether. 7. The system of claim 1 , wherein the elastic portion of the elongated tether is a spring. 8. The system of claim 1 , further comprising: a frame coupled to a portion of the flexible canopy. 9. The system of claim 8 , wherein the frame does not extend into the ventricle when the system is in the deployed configuration. 10. The system of claim 1 , wherein the flexible canopy is unsupported and does not include a frame coupled thereto. 11. The system of claim 1 , wherein the flexible canopy extends into the ventricle when the system is in the deployed configuration. 12. A system for treating valvular regurgitation in a heart valve, the system including a delivery configuration and a deployed configuration, the system comprising: a flexible canopy including a first surface and a second surface opposite the first surface; and an elongated tether configured to be placed under tension in situ, the elongated tether including an elastic portion and an inelastic portion coupled to the elastic portion, wherein the elastic portion is at least as long as the inelastic portion and a proximal end of the elongated tether is attached to a distal end of the flexible canopy, wherein when the system is in the deployed configuration, a proximal end of the flexible canopy is anchored to an annulus of the heart valve and a distal end of the elongated tether is anchored to tissue of a ventricle such that the first surface of the flexible canopy overlays an underlying first surface of a first leaflet of the heart valve, and the elongated tether is placed under tension such that the system is configured to prevent the first leaflet of the heart valve from prolapsing, and to permit a portion of the second surface of the flexible canopy to coapt with at least an opposing mating portion of a second leaflet of the heart valve, and wherein the first surface of the flexible canopy includes at least one micro-barb and the at least one micro-barb is configured to couple the first surface of the flexible canopy to the underlying first surface of the first leaflet of the heart valve. 13. A system for treating valvular regurgitation in a heart valve, the system including a delivery configuration and a deployed configuration, the system comprising: a flexible canopy including a first surface and a second surface opposite the first surface, wherein the flexible canopy is unsupported and does not include a frame coupled thereto; and an elongated tether configured to be placed under tension in situ, the elongated tether including an elastic portion and an inelastic portion coupled to the elastic portion, wherein a ratio of the elastic portion to the inelastic portion is between 50/50 and 70/30, and wherein a proximal end of the elongated tether is attached to a distal end of the flexible canopy; and a distal anchor configured to be embedded into tissue of a ventricle, wherein a distal end of the elongated tether is coupled to the distal anchor, wherein when the system is in the deployed configuration, a proximal end of the flexible canopy is anchored to an annulus of the heart valve and the distal end of the elongated tether is anchored to tissue of a ventricle via the distal anchor such that the first surface of the flexible canopy overlays an underlying first surface of a first leaflet of the heart valve, and the elongated tether is placed under tension such that the system is configured to prevent the first leaflet of the heart valve from prolapsing, and to permit a portion of the second surface of the flexible canopy to coapt with at least an opposing mating portion of a second leaflet of the heart valve. 14. The system of claim 13 , wherein when the first surface of the flexible canopy overlays the first leaflet of the heart valve, the first surface of the flexible canopy is substantially in contact with between forty and ninety percent of the underlying first surface of the first leaflet of the heart valve. 15. The system of claim 13 , wherein the first surface of the flexible canopy includes at least one micro-tine and the at least one micro-tine is configured to couple the first surface of the flexible canopy to the underlying first surface of the first leaflet of the heart valve. 16. The system of claim 13 , wherein the flexible canopy does not extend into the ventricle when the system is in the deployed configuration. 17. The system of claim 13 , wherein the flexible canopy extends into the ventricle when the system is in the deployed configuration. 18. The system of claim 13 , wherein the inelastic portion of the elongated tether is positioned distal of the elastic portion of the elongated tether. 19. The system of claim 13 , wherein the elastic portion of the elongated tether is positioned distal of the inelastic portion of the elongated tether. 20. The system of claim 13 , wherein the elastic portion of the elongated tether is longer than the inelastic portion of the elongated tether.

Assignees

Inventors

Classifications

  • Chordae tendineae prostheses · CPC title

  • Saddle-shaped · CPC title

  • differing in elasticity, stiffness or compressibility · CPC title

  • cardiac · CPC title

  • Suture anchors, buttons or pledgets, i.e. means for attaching sutures to bone, cartilage or soft tissue; Instruments for applying or removing suture anchors (A61B17/0642 takes precedence; fixation devices for tendons or ligaments A61F2/0811) · CPC title

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What does patent US11026791B2 cover?
A system for treating valvular regurgitation in a heart valve includes a flexible canopy and an elongated tether including an elastic portion and an inelastic portion. When the system is in a deployed configuration, a proximal end of the flexible canopy is coupled to an annulus of the heart valve and a distal end of the elongated tether is coupled to a ventricle. The flexible canopy is configur…
Who is the assignee on this patent?
Medtronic Vascular Inc
What technology area does this patent fall under?
Primary CPC classification A61F2/2454. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jun 08 2021 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).