Minimally invasive heart valve replacement

Claim 2

An anchoring device for securing a percutaneously implantable replacement heart valve in an existing valve in the human heart, which device comprises: a framework of generally tubular shape which is constructed of shape-memory material and includes a central portion, a distal portion and a proximal portion that are integral with one another, said distal portion comprising a plurality of individually controllable distal linear arms which are each connected at only one end to said central portion and have a free opposite end, which distal linear arms evert as a result of temperature change and wrap around the free ends of native leaflets of a stenotic or malfunctioning valve to contact downstream surfaces of the valve leaflets, said proximal portion of said framework comprising a plurality of individually controllable, proximally extending proximal linear arms which are each connected at only one end to said central portion and have a free opposite end, which proximal linear arms are constructed to swing radially outward at their free ends toward said everted distal arms and contact upstream-facing surfaces of the native leaflets and secure said framework within the human heart valve, and said distal and proximal linear arms having means at each said opposite end which allows attachment of cords to individually control and retract each of said linear arms.

Claim 3

The anchoring device according to claim 1 wherein the shape-memory of said central portion of said framework causes it to radially expand while said proximal arms swing outward to contact upstream surfaces of the native leaflets and sandwich the native valve leaflets between them and said everted distal arms so as to provide a secure anchor for a replacement valvular device to be mounted interior thereof.

Claim 4

The anchoring device according to claim 2 wherein said central portion is formed with a surface with a shape that is complementary to and that will securely interengage with a portion of a stent for a replacement valvular device having a complementary shape.

Claim 5

The anchoring device according to claim 3 wherein said central portion comprises a ring section having a generally annular surface of inwardly convex shape which accommodates string loop means used to control its radial expansion and to collapse said ring section if desired.

Claim 6

The anchoring device according to claim 4 wherein an exterior covering of biocompatible sheet material surrounds said framework, and said central portion has the general shape of a section of a torus.

Claim 7

The anchoring device according to claim 1 in combination with a hollow delivery implement, wherein the device is disposed about the exterior surface of said hollow implement through which a plurality of cords are routed that individually control the distally-extending and proximally extending linear arms and that also control the expansion of the anchoring device as its shape-memory alloy material tends to revert to its desired “memory” shape upon warming to body temperature, and wherein a temporary valve element is carried within said hollow delivery implement which valve element can be deployed once said anchoring device is in place so as to serve as a temporary functioning valve.

Claim 8

The combination of a hollow delivery implement and an anchoring device, which combination comprises: a collapsible-expandable anchoring device having a framework of generally tubular shape which is constructed of shape-memory material and includes a central portion, a distal portion and a proximal portion that are integral with one another, said distal portion comprising a plurality of individually controllable distal linear arms which are each connected at only one end to said central portion and have a free opposite end with an opening through which a cord can be passed, which distal linear arms evert as a result of temperature change and wrap around the free ends of native leaflets of a stenotic or malfunctioning valve to contact downstream surfaces of the valve leaflets, and said proximal portion of said framework comprising a plurality of individually controllable, proximal linear arms which are each connected at only one end to said central portion and have a free opposite end with an opening through which a cord can be passed, said proximal linear arms being constructed to swing radially outward at their free ends toward said everted distal arms and contact upstream-facing surfaces of the native leaflets and secure said framework within the human heart valve, a hollow delivery implement for passage through a cannula inserted in the chest of a patient about the exterior surface of which the anchoring device is disposed, and a plurality of cords are routed through said hollow implement individually control the distal and proximal arms by passage through said openings at the end of each said linear arm and also control the expansion of the anchoring device as its shape-memory alloy material tends to revert to its desired “memory” shape upon warming to body temperature.

Claim 9

The combination of a hollow delivery implement and an anchoring device, which combination comprises: a collapsible-expandable anchoring device having a framework of generally tubular shape which is constructed of shape-memory material and includes a central portion, a distal portion and a proximal portion that are integral with one another, said distal portion comprising a plurality of individually controllable distal linear arms which are each connected at only one end to said central portion and have a free opposite end with an opening through which a cord can be passed, which distal linear arms evert as a result of temperature change and wrap around the free ends of native leaflets of a stenotic or malfunctioning valve to contact downstream surfaces of the valve leaflets, and said proximal portion of said framework comprising a plurality of individually controllable, proximal linear arms which are each connected at only one end to said central portion and have a free opposite end with an opening through which a cord can be passed, said proximal linear arms being constructed to swing radially outward at their free ends toward said everted distal arms and contact upstream-facing surfaces of the native leaflets and secure said framework within the human heart valve, a hollow delivery implement for passage through a cannula inserted in the chest of a patient about the exterior surface of which the anchoring device is disposed, and a plurality of cords are routed through said hollow implement individually control the distal and proximal arms by passage through said openings at the end of each said linear arm and also control the expansion of the anchoring device as its shape-memory alloy material tends to revert to its desired “memory” shape upon warming to body temperature.

Claim 10

The combination of claim 7 wherein said central portion comprises a ring section having, when expanded, a generally annular surface of inwardly convex shape which is proportioned to securely interengage with a portion of a stent for a replacement valvular device having a complementary shape.

Claim 11

The combination of claim 7 , wherein said hollow delivery implement has a plurality of holes in the sidewall thereof through which said cords pass that control said proximal arms.

Claim 12

The combination of claim 7 wherein a temporary valve element is carried within said hollow delivery implement, which valve element is designed to be deployed from an open end of said hollow delivery implement once said anchoring device is in place so as to serve as a temporary functioning valve.

Claim 13

A collapsed anchoring device for securing a percutaneously implantable replacement heart valve within the confines of an existing valve in the human heart that has become stenotic or malfunctioning following its insertion into the body via a catheter, which device comprises: a framework of generally tubular shape which is constructed of shape-memory material and includes a central portion, a distal portion and a proximal portion that are integral with one another, said distal portion comprising a plurality of individually controllable distal linear arms which are each connected at only one end to said central portion and which have openings at opposite free ends thereof through which cords can be passed, which distal linear arms evert as a result of temperature change and individually wrap around the free ends of native leaflets of a stenotic or malfunctioning valve to contact downstream surfaces of the valve leaflets, and said central portion being expandable radially outward within the orifice of the native valve as a result of its shape memory, and said proximal portion of said framework comprising a plurality of individually controllable, proximal linear arms which are each connected at only one end to said central portion and which have openings at opposite free ends through which cords can be passed, said proximal linear arms being constructed to swing radially outward at their free ends toward said everted distal linear arms and contact upstream-facing surfaces of the native leaflets and secure said framework within the human heart valve, whereby said distal and proximal linear arms are individually controllable via cords that are passed through said openings at said respective free ends thereof.

Claim 14

A collapsed anchoring device for securing a percutaneously implantable replacement heart valve within the confines of an existing valve in the human heart that has become stenotic or malfunctioning following its insertion into the body via a catheter, which device comprises: a framework of generally tubular shape which is constructed of shape-memory material and includes a central portion, a distal portion and a proximal portion that are integral with one another, said distal portion comprising a plurality of individually controllable distal linear arms which are each connected at only one end to said central portion and which have openings at opposite free ends thereof through which cords can be passed, which distal linear arms evert as a result of temperature change and individually wrap around the free ends of native leaflets of a stenotic or malfunctioning valve to contact downstream surfaces of the valve leaflets, and said central portion being expandable radially outward within the orifice of the native valve as a result of its shape memory, and said proximal portion of said framework comprising a plurality of individually controllable, proximal linear arms which are each connected at only one end to said central portion and which have openings at opposite free ends through which cords can be passed, said proximal linear arms being constructed to swing radially outward at their free ends toward said everted distal linear arms and contact upstream-facing surfaces of the native leaflets and secure said framework within the human heart valve, whereby said distal and proximal linear arms are individually controllable via cords that are passed through said openings at said respective free ends thereof.

Claim 15

The device according to claim 11 wherein said framework comprises at least three of said distal linear arms and at least three of said proximal linear arms made of shape-memory material, which at least six linear arms have circular eyelets at the free ends thereof to provide said openings through which cords are passed to facilitate individual control of each arm.

Claim 16

The device according to claim 11 wherein said central portion of said framework is formed with a C-shaped outwardly concave axial cross section and has openings through which additional cords can be routed to both control such shape-memory expansion of said framework and to effect reduction of the diameter thereof.

Claim 17

The device according to claim 13 wherein said central portion comprises a ring section having a generally annular surface of inwardly convex shape which is proportioned to securely interengage with a portion of a stent for a replacement valvular device having a complementary outwardly concave peripheral shape.