Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
  • A61F2/2412—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body with soft flexible valve members, e.g. tissue valves shaped like natural valves
  • A61F2/2418—Scaffolds therefor, e.g. support stents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
  • A61F2/2412—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body with soft flexible valve members, e.g. tissue valves shaped like natural valves
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
  • A61F2/2412—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body with soft flexible valve members, e.g. tissue valves shaped like natural valves
  • A61F2/2415—Manufacturing methods
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
  • A61F2/2427—Devices for manipulating or deploying heart valves during implantation
  • A61F2/243—Deployment by mechanical expansion
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
  • A61F2/02—Prostheses implantable into the body
  • A61F2/24—Heart valves ; Vascular valves, e.g. venous valves; Heart implants, e.g. passive devices for improving the function of the native valve or the heart muscle; Transmyocardial revascularisation [TMR] devices; Valves implantable in the body
  • A61F2/2442—Annuloplasty rings or inserts for correcting the valve shape; Implants for improving the function of a native heart valve
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2210/00—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
  • A61F2210/0057—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof stretchable
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2210/00—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
  • A61F2210/0066—Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof shrinkable
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
  • A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
  • A61F2220/0075—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
  • A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
  • A61F2220/0025—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
  • A61F2220/0091—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements connected by a hinged linkage mechanism, e.g. of the single-bar or multi-bar linkage type

Definitions

• the present disclosure concerns embodiments of a prosthetic valve for implantation into body ducts, such as native heart valve annuluses, and methods of implanting the prosthetic valve.
• the human heart can suffer from various valvular diseases. These valvular diseases can result in significant malfunctioning of the heart and ultimately require replacement of the native valve with an artificial valve.
• valvular diseases can result in significant malfunctioning of the heart and ultimately require replacement of the native valve with an artificial valve.
• a prosthetic heart valve is configured to be implanted in a much less invasive procedure by way of catheterization.
• a prosthetic heart valve can be mounted in a crimped state on the distal end of a delivery device and advanced through the patient’s vasculature (e.g., through a femoral artery and the aorta) until the prosthetic valve reaches the implantation site in the heart.
• the prosthetic valve is then expanded to its functional size, for example, by inflating a balloon on which the prosthetic valve is mounted, or by deploying the prosthetic valve from a sheath of the delivery device so that the prosthetic valve can self-expand to its functional size, or by other means.
• Known prosthetic valves can be radially compressible and expandable between a radially compressed state and a radially expanded state.
• the prosthetic valves can be crimped on an implant delivery apparatus in the radially compressed state during delivery, and then expanded to the radially expanded state once the prosthetic valve reaches the implantation site.
• a prosthetic valve typically includes a frame with a valvular structure (e.g., leaflets) mounted therein, an inner skirt secured to the inside of the frame, and optionally, an outer skirt secured to the exterior of the frame.
• the inner skirt can serve several functions.
• the inner skirt can function as a sealing member to prevent (or decrease) paravalvular leakage and to anchor the leaflets to the frame.
• the outer skirt can cooperate with the inner skirt to further reduce or avoid paravalvular leakage after implantation of the valve.
• the inner and outer skirts can be secured to the frame by suturing or stitching the fabric of the respective skirts to the frame.
• the inner skirt desirably comprises a tough, tear resistant material such as
• skirts formed from conventional woven PET or similar fabrics are substantially non elastic, and thus can hardly be stretched.
• the lack of skirt elasticity can create a challenge for crimping the prosthetic valve.
• crimping the prosthetic valve tends to reduce the frame’s diameter while elongate the frame in the axial direction.
• the skirt is usually sutured to the frame, the inelasticity of the skirt can constrain the axial elongation of the frame.
• crimping can create substantial stress of the fabric at the suture points such that it may lead to suture tears, fabric tear, or frame distortion.
• constraint of the skirt during crimping can be localized such that some areas of the skirt may conform to the frame more tightly than other areas. Such non-uniform tightening can lead to undesired uneven attachment of the skirt to the frame, and can further cause tearing of sutures and/or the fabric, or distortion of the frame.
• One possible solution to this problem is to size the skirt such that there is slack in the radial direction when the prosthetic valve is in the radially expanded state. The slack permits axial elongation of the prosthetic valve during the crimping process without being restricted or constrained by the skirt.
• Prosthetic valves disclosed herein can be implanted within any of the native valves of the heart (the aortic, mitral, tricuspid and pulmonary valves).
• the prosthetic valve can be delivered through the vasculature and implanted to the heart of a patient by using a delivery apparatus.
• Certain embodiments of the disclosure concern a prosthetic valve having an annular frame, a valvular structure, and an annular skirt.
• the annular frame can be radially expandable and compressible between a radially compressed configuration and a radially expanded configuration.
• the valvular structure can be positioned within the frame and configured to permit the flow of blood through the prosthetic valve in one direction and block the flow of blood in an opposing direction.
• the annular skirt can have an outer portion covering at least a portion of an outer surface of the frame and an inner portion covering at least a portion of an inner surface of the frame. The skirt can be folded around an inflow end of the frame so as to define a fold between the inner portion and outer portion.
• the skirt can be sized such that when the frame is in the expanded configuration, the outer portion of the skirt conforms to the outer surface of the frame and the inflow end of the frame is axially spaced from the fold to form an axially extending gap between the frame and the fold, and when the frame is radially compressed from the expanded configuration to the compressed configuration, the inflow end of the frame moves axially within the gap closer to the fold.
• the outer portion of the skirt can be secured to a row of stmts defining an outflow end of the frame.
• the outer portion of the skirt can be stretched in a
• the skirt can comprise a non-elastic fabric.
• the fabric can be woven using polyethylene terephthalate fibers in both warp and weft directions.
• the skirt can be woven from a first set of fibers oriented in a first direction and a second set of fibers oriented in a second direction, neither the first nor the second direction being perpendicular to the fold.
• the first direction can be generally perpendicular to the second direction.
• the second direction can form an angle about 45 degrees relative to the fold.
• the valvular structure can include a plurality of leaflets, each leaflet having an inflow edge portion.
• the inflow edge portions of the leaflets can define an undulating shape.
• the inner portion of the skirt can have an undulating outflow edge sutured to the inflow edge portions of the leaflets.
• the prosthetic valve can include a tether coupled to the skirt.
• the tether can be configured to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• Certain embodiments of the disclosure also concern a prosthetic valve having an annular frame, a valvular structure, and an annular skirt.
• the annular frame can have an inflow end and an outflow end, and the frame can be radially expandable and compressible between a radially compressed configuration and a radially expanded configuration.
• the valvular structure can be positioned within the frame and configured to permit the flow of blood through the prosthetic valve in one direction and block the flow of blood in an opposing direction.
• the annular skirt can have a fold extending around the inflow end of the frame so as to cover at least a portion of an outer surface of the frame and at least a portion of an inner surface of the frame.
• an outer portion of the skirt can tightly conform to the outer surface of the frame and the inflow end of the frame can be axially spaced from the fold to form an axially extending gap between the frame and the fold.
• the inflow end of the frame can extend axially so as to at least partially fill the axially extending gap.
• the valvular structure can include a plurality of leaflets, each leaflet having an inflow edge portion, and the inflow edge portions of the leaflets can define an undulating, curved scalloped shape that follows a plurality of interconnected stmt segments of the frame along circumferential direction when the frame is in the radially expanded configuration.
• the outer portion of the skirt can be axially longer than the inner portion of the skirt.
• the outer portion of the skirt can be stretched in a
• the prosthetic valve can include a tether coupled to the skirt and extending at an oblique angle relative to a longitudinal axis of the frame such that the tether can apply a tension to the skirt so as to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• the method can include delivering the prosthetic valve in a radially compressed configuration to a target location, the prosthetic valve including an annular frame and an annular skirt having a fold around an inflow end of the frame so as to cover at least a portion of an outer surface of the frame and at least a portion of an inner surface of the frame.
• the method further includes expanding the prosthetic valve to a radially expanded configuration such that an outer portion of the skirt tightly conforms to the outer surface of the frame, and the inflow end of the frame moves axially away from the fold, thereby forming an axially extending gap between the frame and the fold.
• the prosthetic valve can further include a valvular structure.
• the valvular structure can include a plurality of leaflets, each leaflet having an inflow edge portion, and the inflow edge portions of the leaflets can define an undulating, curved scalloped shape that follows a plurality of interconnected stmt segments of the frame along circumferential direction when the frame is in the radially expanded configuration.
• the outer portion of the skirt can be stretched in a circumferential direction when the frame is in the expanded configuration.
• the inflow end of the frame when the frame is in the radially compressed configuration, can extend axially all the way to the fold so as to completely fill the axially extending gap.
• the prosthetic valve can include a tether coupled to the skirt.
• the tether can be configured to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• a prosthetic valve including an annular frame and an annular skirt covering at least a portion of an outer surface of the frame.
• the annular frame can have an inflow end and an outflow end, and the frame can be radially expandable and compressible between a radially compressed configuration and a radially expanded configuration.
• the lower edge of the skirt can extend over the inflow end of the frame.
• the skirt can be attached to the frame by a plurality of sutures.
• the sutures can be positioned on a plurality of selected struts of the frame such that the sutures form undulating, scallop- shaped suture lines.
• Each of the suture lines can form an about 45-degree angle relative to a longitudinal axis of the frame when the frame is in the radially expanded configuration.
• the skirt can be woven from a first set of non-elastic fibers oriented in a first direction and a second set of non-elastic fibers oriented in a second direction.
• the first direction can be generally perpendicular to the second direction which can form an angle about 45 degrees relative to the lower edge of the skirt.
• the skirt can be sized such it tightly conforms to the outer surface of the frame without any slack when the frame is in the radially expanded configuration.
• the skirt can fold around the inflow end of the frame so that the lower edge of the skirt defines a fold.
• the inflow end of the frame can be axially spaced from the fold to form an axially extending gap between the frame and the fold.
• the inflow end of the frame can move axially within the gap closer to the fold.
• the skirt when the frame is radially compressed, the skirt can billow out to form folded flaps between the scallop-shaped suture lines.
• each flap can be folded over its adjacent flap in a
• a prosthetic valve that includes an annular frame having an inflow end and an outflow end, at least one actuator mounted to the frame, and an annular skirt having a fold extending around the inflow end of the frame so as to cover at least a portion of an outer surface of the frame and at least a portion of an inner surface of the frame.
• the actuator can be configured to radially expand or compress the frame between a radially compressed configuration and a radially expanded configuration.
• an outer portion of the skirt can tightly conform to the outer surface of the frame and the inflow end of the frame can be axially spaced from the fold to form an axially extending gap between the frame and the fold.
• the inflow end of the frame can extend axially so as to at least partially fill the axially extending gap.
• the at least one actuator can be one of a plurality of actuators mounted to and equally spaced around the inner surface of the frame.
• the at least one actuator can include a first anchor attached to a first location of the frame, a second anchor secured to a second location of the frame, and a rod extending through the first anchor and the second anchor.
• the second location can be closer to the inflow end of the frame than the first location.
• the rod can be configured to increase or decrease a distance between the first and second locations so as to radially compress or radially expand the frame, respectively.
• the rod can include external threads that are configured to matingly engage with internal threads of the second anchor.
• the first location can be a junction between two overlaying struts of the frame, and the first anchor can be hingely connected to the junction by a fastener.
• the at least one actuator can include a rod received at least partially within a sleeve, and the axial movement of the rod relative to the sleeve can cause radial expansion or compression of the frame.
• the at least one actuator can include a locking mechanism configured to lock the frame in the radially expanded configuration.
• the at least one actuator can include an attachment member that is configured to form a releasable connection with a corresponding actuation member of a delivery apparatus such that the actuation member of the delivery apparatus can apply force to the at least one actuator for radially compressing or expanding the frame.
• the prosthetic valve can further include a valvular structure positioned within the frame and configured to permit the flow of blood through the prosthetic valve in one direction and block the flow of blood in an opposing direction.
• the valvular structure can include a plurality of leaflets, each leaflet having an inflow edge portion, and the inflow edge portions of the leaflets can define an undulating, curved scalloped shape that follows a plurality of interconnected stmt segments of the frame along circumferential direction when the frame is in the radially expanded configuration.
• the outer portion of the skirt can be axially longer than the inner portion of the skirt.
• the outer portion of the skirt can have about the same axial length as the inner portion of the skirt.
• the outer portion of the skirt can be axially shorter than the inner portion of the skirt.
• the outer portion of the skirt can be stretched in a
• an upper edge of the outer portion of the skirt can be generally straight before being attached to the frame. [047] In some embodiments, the upper edge of the outer portion of the skirt can be attached to the frame at a plurality of pivot joints formed by overlapping struts of the frame.
• an upper edge of the outer portion of the skirt can have an undulating shape and is sutured along a row of strut segments of the frame.
• the prosthetic valve can further include a tether coupled to the skirt and extending at an oblique angle relative to the fold such that the tether applies a tension to the skirt so as to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• the oblique angle can range from about 10° to about 80°. In some embodiments, the oblique angle can range from about 30° to about 60°. In some embodiments, the oblique angle can be about 45°.
• a first end of the tether can be located at an outflow edge portion of the outer portion of the skirt, and a second end of the tether can be located adjacent the fold.
• the tether can include a suture that is stitched to the outer portion of the skirt using in-and-out stitches.
• the tether can include an elastic material.
• the tether can be one of a plurality of tethers, each of which can form an oblique angle relative to the fold.
• Certain embodiments of the disclosure also concern a prosthetic valve that includes an annular frame being radially expandable and compressible between a radially compressed configuration and a radially expanded configuration, an annular skirt having an outer portion covering at least a portion of an outer surface of the frame and an inner portion covering at least a portion of an inner surface of the frame, and a tether coupled to the skirt to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• the skirt can be folded around an inflow end of the frame so as to define a fold between the inner portion and outer portion.
• the skirt can be sized such that when the frame is in the expanded configuration, the outer portion of the skirt can conform to the outer surface of the frame and the inflow end of the frame can be axially spaced from the fold to form an axially extending gap between the frame and the fold, and when the frame is radially compressed from the expanded configuration to the compressed configuration, the inflow end of the frame can move axially within the gap closer to the fold.
• the prosthetic valve can further include a valvular structure positioned within the frame and configured to permit the flow of blood through the prosthetic valve in one direction and block the flow of blood in an opposing direction.
• the valvular structure can include a plurality of leaflets, each leaflet having an inflow edge portion, and the inflow edge portions of the leaflets can define an undulating shape.
• the inner portion of the skirt can have an undulating outflow edge sutured to the inflow edge portions of the leaflets.
• the outer portion of the skirt can be secured to a row of stmts defining an outflow end of the frame.
• the outer portion of the skirt can be stretched in a
• the skirt can include a non-elastic fabric.
• the fabric can include polyethylene terephthalate fibers.
• the polyethylene terephthalate fibers can have a thickness of about 20-denier.
• the polyethylene terephthalate fibers can have an inter-fiber spacing ranging from about 155 fibers per inch to about 180 fibers per inch. In some embodiments, the polyethylene terephthalate fibers can have an inter- fiber spacing about 160 fibers per inch.
• the skirt can be woven from a first set of fibers oriented in a first direction and a second set of fibers oriented in a second direction, neither the first nor the second direction being perpendicular to the fold.
• the first direction can be generally perpendicular to the second direction which forms an angle about 45 degrees relative to the fold.
• the first set of fibers can extend generally parallel to a first set of struts of the frame and the second set of fibers can extend generally parallel to a second set of struts of the frame when the frame is in the expanded configuration, and the second set of struts can overlap the first set of struts to form junctions of the frame.
• the tether can extend at an oblique angle relative to the fold and the tether can be configured to apply a tension to the skirt when the frame is in the expanded configuration.
• the oblique angle can be about 45°.
• a first end of the tether can be located at an outflow edge portion of the outer portion of the skirt, and a second end of the tether can be located adjacent the fold.
• the tether can include a suture that is stitched to the outer portion of the skirt using in-and-out stitches.
• the tether can include an elastic material.
• Certain embodiments of the disclosure also concern a prosthetic valve that includes an annular frame being radially expandable and compressible between a radially compressed configuration and a radially expanded configuration, and an annular outer skirt covering at least a portion of an outer surface of the frame. When the frame is in the radially compressed configuration, portions of the outer skirt can billow out to form longitudinally extending folded flaps.
• each flap can be further folded in a circumferential direction so as to maintain a low crimping profile of the prosthetic valve.
• each flap can at least partially overlap an adjacent flap in the circumferential direction.
• the outer skirt can be connected to stmts of the frame along a zig-zag shaped attachment line. [077] In some embodiments, the outer skirt can be connected to the struts of the frame with sutures along the zig-zag shaped attachment line.
• the outer skirt can be not connected to any stmts of the frame or other components of the prosthetic valve at locations not along the zig-zag shaped attachment line.
• the outer skirt can be connected to the frame only along the zig-zag shaped attachment line.
• the prosthetic valve can further include a plurality of leaflets, each leaflet having an inflow edge portion attached to the struts of the frame along the zig zag shaped attachment line.
• the flaps can be V-shaped.
• the prosthetic valve can further include an annular inner skirt covering at least a portion of an inner surface of the frame, and the outer skirt can be connected to the inner skirt via a fold extending around an inflow end of the frame.
• the outer skirt when the frame is in the radially expanded configuration, can be configured to tightly conform to the outer surface of the frame and the inflow end of the frame can be axially spaced from the fold to form an axially extending gap between the frame and the fold, and when the frame is in the radially compressed
• the inflow end of the frame can be configured to extend axially so as to at least partially fill the axially extending gap.
• an axial length of the gap can range from about 4 mm to about 8 mm when the frame is in the radially expanded configuration. In some embodiments, the axial length of the gap can be about 6 mm when the frame is in the radially expanded configuration.
• the inflow end of the frame can extend axially to and completely fill the gap when the frame is in the radially compressed configuration.
• the inner skirt can fold inwardly toward an interior of the frame when the frame is in the radially compressed configuration.
• the prosthetic valve can further include a tether coupled to the outer skirt and extending at an oblique angle relative to the fold such that the tether applies a tension to the outer skirt so as to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• the tether can include a suture that is stitched to the outer skirt using in-and-out stitches.
• the tether can include an elastic material.
• Certain embodiments of the disclosure further concern a method of assembling a prosthetic valve.
• the method can include receiving an annular frame that is radially expandable and compressible between a radially compressed configuration and a radially expanded configuration, and attaching an annular skirt to the frame such that the skirt has an outer portion covering at least a portion of an outer surface of the frame and an inner portion covering at least a portion of an inner surface of the frame.
• the skirt can be folded around an inflow end of the frame so as to define a fold between the inner portion and outer portion.
• the skirt can be sized such that when the frame is in the expanded configuration, the outer portion of the skirt can conform to the outer surface of the frame and the inflow end of the frame can be axially spaced from the fold to form an axially extending gap between the frame and the fold, and when the frame is radially compressed from the expanded configuration to the compressed configuration, the inflow end of the frame can move axially within the gap closer to the fold.
• attaching the annular skirt to the frame can include suturing an upper edge of the inner portion of the skirt to a selected row of stmt segments of the frame from inside the frame.
• attaching the annular skirt to the frame can include suturing the outer portion of the skirt to a row of struts defining an outflow end of the frame.
• the method can further include attaching a valvular structure to the frame.
• the valvular structure can be configured to permit the flow of blood through the prosthetic valve in one direction and block the flow of blood in an opposing direction.
• the valvular structure can include a plurality of leaflets, each leaflet having an inflow edge portion. The inflow edge portions of the leaflets can define an undulating shape. Attaching the valvular structure to the frame can include suturing the inflow edge portions of the leaflets from inside the frame to a row of interconnected strut segments of the frame along circumferential direction.
• the method can further include coupling a tether to the skirt in an oblique angle relative to the fold so as to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• Certain embodiments of the disclosure further concern a method including receiving a prosthetic valve comprising an annular frame that is radially expandable and compressible between a radially compressed configuration and a radially expanded configuration and an annular skirt that covers at least a portion of an outer surface of the frame, compressing the frame to the radially compressed configuration so that portions of the skirt billow out to form longitudinally extending folded flaps, and folding the flaps in a circumferential direction.
• the skirt can be sutured to struts of the frame along a zig-zag shaped attachment line.
• the prosthetic valve can include a plurality of leaflets, and each leaflet can have an inflow edge portion being attached to the struts of the frame along the zig zag shaped attachment line.
• the skirt can cover at least a portion of an inner surface of the frame and form a fold around an inflow end of the frame.
• the skirt can be sized such that when the frame is in the expanded configuration, the inflow end of the frame can be axially spaced from the fold to form an axially extending gap between the frame and the fold, and when the frame is radially compressed from the expanded configuration to the compressed configuration, the inflow end of the frame can move axially within the gap closer to the fold.
• the prosthetic valve can further include a tether coupled to the skirt at an oblique angle relative to the fold so as to prevent the fold from moving inside the frame when the frame is radially expanded from the compressed configuration to the expanded configuration.
• the method can further include loading the prosthetic valve into a sheath of a delivery apparatus, inserting the prosthetic valve into a patient, advancing the prosthetic valve through the patient’s vasculature to an implantation site, and radially expanding the prosthetic valve at the implantation site.
• radially expanding the prosthetic valve can cause the flaps to unfold.
• the skirt when the frame is in the radially expanded configuration, the skirt can tightly conform to the outer surface of the frame.
• FIG. 1 shows a perspective view of a prosthetic valve, according to one embodiment.
• FIG. 2A shows the frame of the prosthetic valve of FIG. 1 shown in a radially compressed configuration.
• FIG. 2B shows the frame of the prosthetic valve of FIG. 1 shown in a partially radially expanded configuration.
• FIG. 2C shows the frame of the prosthetic valve of FIG. 1 shown in a fully radially expanded configuration.
• FIG. 3 shows a side elevational view of the prosthetic valve depicted in FIG. 1 in a radially compressed configuration, the valve further comprising a skirt attached to the frame.
• FIG. 4 shows a side elevational view of the prosthetic valve depicted in FIG. 3 in a radially expanded configuration.
• FIG. 5 shows a side cross sectional view of the prosthetic valve when it is fully expanded.
• FIG. 6 shows a side cross sectional view of the prosthetic valve when it is partially compressed.
• FIG. 7 shows a side cross section of an outermost portion of the prosthetic valve when it is fully compressed.
• FIG. 8 shows a flattened view of the skirt.
• FIG. 9 shows a prospective view of a prosthetic valve, according to an alternative embodiment.
• FIG. 10 shows a prospective view of a radially expanded frame of a prosthetic valve, according to another embodiment.
• FIG. 11 shows the frame of FIG. 10 being partially compressed and the outer portion of the skirt folds outwardly.
• FIG. 12A shows the prosthetic valve of FIG. 9 being fully compressed and the outer portion of the skirt billows out to form folded flaps.
• FIG. 12B shows the fully compressed prosthetic valve of FIG. 12A wherein the flaps are circumferentially folded.
• FIG. 12C shows a cross-sectional view of the fully compressed prosthetic valve depicted in FIG. 12B.
• FIG. 1 shows an exemplary prosthetic valve 10, according to one embodiment.
• the prosthetic valve 10 can be implanted within the native aortic annulus, although it also can be implanted at other locations in the heart, including within the native mitral valve, the native pulmonary valve, and the native tricuspid valve.
• the prosthetic valve 10 can include an annular stent or frame 12 having an inflow end 14 and an outflow end 16.
• the prosthetic valve 10 can also include a valvular structure 18 which is coupled to and supported inside of the frame 12. The valvular structure 18 is configured to regulate the flow of blood through the prosthetic valve 10 from the inflow end 14 to the outflow end 16.
• the prosthetic valve 10 can further include one or more actuators 50 mounted to and equally spaced around the inner surface of the frame 12.
• Each of the actuators 50 can be configured to form a releasable connection with one or more respective actuators of a delivery apparatus, as further described below.
• the valvular structure 18 can include, for example, a leaflet assembly comprising one or more leaflets 20 made of a flexible material.
• the leaflets 20 can be made from in whole or part, biological material, bio-compatible synthetic materials, or other such materials. Suitable biological material can include, for example, bovine pericardium (or pericardium from other sources).
• the leaflets 20 can be secured to one another at their adjacent sides to form commissures 22, each of which can be secured to a respective actuator 50 or the frame 12.
• the valvular structure 18 comprises three leaflets 20, which can be arranged to collapse in a tricuspid arrangement.
• Each leaflet 20 can have an inflow edge portion 2E
• the inflow edge portions 21 of the leaflets 20 can define an undulating, curved scalloped shape that follows or tracks a plurality of interconnected stmt segments of the frame 12 in a circumferential direction when the frame 12 is in the radially expanded configuration.
• the inflow edges of the leaflets can be referred to as a“scallop line.”
• the inflow edge portions 21 of the leaflets 20 can be sutured to the struts generally along the scallop line.
• each leaflet 20 By forming the leaflets 20 with this scalloped geometry, stresses on the leaflets 20 are reduced, which in turn improves durability of the valve 10. Moreover, by virtue of the scalloped shape, folds and ripples at the belly of each leaflet 20 (the central region of each leaflet), which can cause early calcification in those areas, can be eliminated or at least minimized.
• the scalloped geometry also reduces the amount of tissue material used to form valvular structure 18, thereby allowing a smaller, more even crimped profile at the inflow end 14 of the valve 10.
• transcatheter prosthetic heart valves including the manner in which the valvular structure can be coupled to the frame 12 of the prosthetic valve 10, can be found, for example, in U.S. Patent Nos. 6,730,118, 7,393,360, 7,510,575, 7,993,394 and 8,652,202, and U.S. Patent Application No. 15/978,459, all of which are incorporated herein by reference in their entireties.
• the prosthetic valve 10 can be radially compressible and expandable between a radially compressed configuration and a radially expanded configuration. FIGS.
• FIG. 2A-2C show the bare frame 12 of the prosthetic valve 10 (without the leaflets and other components) for purposes of illustrating expansion of the prosthetic valve 10 from the radially compressed configuration to the radially expanded configuration.
• FIG. 2A shows the frame 12 in the radially compressed configuration
• FIG. 2B shows the frame 12 in a partially expanded configuration
• FIG. 2C shows the frame 12 in the fully radially expanded configuration.
• the prosthetic valve 10 can be mechanically expanded from the radially configuration to the radially expanded configuration.
• the prosthetic valve 10 can be radially expanded by maintaining the inflow end 14 of the frame 12 at a fixed position while applying a force (F) in the axial direction against the outflow end 16 toward the inflow end 14.
• the prosthetic valve 10 can be expanded by applying an axial force against the inflow end 14 while maintaining the outflow end 16 at a fixed position, or by applying opposing axial forces to the inflow and outflow ends 14, 16, respectively.
• each of the actuators 50 can comprise a screw or threaded rod 52, a first anchor in the form of a cylinder or sleeve 54, and a second anchor in the form of a threaded nut 56.
• the rod 52 extends through the sleeve 54 and the nut 56.
• the sleeve 54 can be secured to the frame 12, such as with a fastener that forms a hinge at the junction between two struts.
• Each actuator 50 is configured to increase the distance between the attachment locations of a respective sleeve 54 and nut 56, which causes the frame 12 to elongate axially and compress radially, and to decrease the distance between the attachment locations of a respective sleeve 54 and nut 56, which causes the frame 12 to foreshorten axially and expand radially.
• each rod 52 can have external threads that engage internal threads of the nut 56 such that rotation of the rod causes corresponding axial movement of the nut 56 toward or away from the sleeve 54 (depending on the direction of rotation of the rod 52).
• the actuators 50 can be reciprocating type actuators configured to apply axial directed forces to the frame to produce radial expansion and compression of the frame.
• the rod 52 of each actuator can be fixed axially relative to the sleeve 56 and slidable relative to the sleeve 54.
• moving the rod 52 distally relative to the sleeve 54 and/or moving the sleeve 54 proximally relative to the rod 52 radially compresses the frame.
• moving the rod 52 proximally relative to the sleeve 54 and/or moving the sleeve 54 distally relative to the rod 52 radially expands the frame.
• the prosthetic valve can also include one or more locking mechanisms that retain the frame in the expanded state.
• the locking mechanisms can be separate components that are mounted on the frame apart from the actuators, or they can be a sub-component of the actuators themselves.
• Each rod 52 can include an attachment member 58 along a proximal end portion of the rod 52 configured to form a releasable connection with a corresponding actuator of a delivery apparatus.
• the actuator(s) of the delivery apparatus can apply forces to the rods for radially compressing or expanding the prosthetic valve 10.
• the attachment member 58 in the illustrated configuration comprises a notch 60 and a projection 62 that can engage a corresponding projection of an actuator of the delivery apparatus.
• the prosthetic valve 10 includes three such actuators 50, although a greater or fewer number of actuators could be used in other embodiments.
• the leaflets 20 can have commissure attachments members 64 that wrap around the sleeves 54 of the actuators 50. Further details of the actuators, locking mechanisms and delivery apparatuses for actuating the actuators can be found in U.S. Patent Application Nos.
• the frame 12 can be made of any of various suitable materials, such as stainless steel, a cobalt chromium alloy, or a nickel titanium alloy (“NiTi”), for example Nitinol.
• the frame 12 can include a plurality of interconnected stmts 24 arranged in a lattice-type pattern.
• the struts 24 are shown as positioned diagonally, or offset at an angle relative to, and radially offset from, a longitudinal axis 26 of the prosthetic valve 10 when the prosthetic valve 10 is in the expanded configuration.
• the stmts 24 can be offset by a different amount than depicted in FIGS. 2B and 2C, or some or all of the stmts 24 can be positioned parallel to the longitudinal axis 26 of the prosthetic valve 10.
• the stmts 24 are pivotably coupled to one another at one or more pivot joints along the length of each stmt.
• the stmts 24 are pivotably coupled to one another at one or more pivot joints along the length of each stmt.
• each of the stmts 24 can be formed with apertures at opposing ends of the stmt and apertures spaced along the length of the stmt.
• Respective hinges can be formed at the locations where stmts 24 overlap each other via fasteners, such as rivets or pins 28 that extend through the apertures. The hinges can allow the stmts 24 to pivot relative to one another as the frame 12 is radially expanded or compressed, such as during assembly, preparation, or implantation of the prosthetic valve 10.
• the stmts 24 are arranged in five rows (I, II, III, IV and V) from the inflow end 14 to the outflow end 16.
• Each row is defined by the stmt segments extending in a zig-zag pattern between adjacent circumferential rows of hinges 28.
• the first row I is defined by stmt segments 25 extending between a first row of hinges 28a at the inflow end of the frame and an adjacent row of hinges 28b.
• segments of the stmts 24 can be arranged in different number of rows.
• the frame 12 can be constructed by forming individual components (e.g., the stmts and fasteners of the frame) and then mechanically assembling and connecting the individual components together.
• the stmts 24 are not coupled to each other with respective hinges but are otherwise pivotable or bendable relative to each other to permit radial expansion and contraction of the frame 12.
• the frame 12 can be formed (e.g., via laser cutting, electroforming or physical vapor deposition) from a single piece of material (e.g., a metal tube). Further details regarding the construction of the frame and the prosthetic valve are described in U.S. Patent Applications Nos.
• the frame can be made of any of various suitable plastically-expandable materials (e.g., stainless steel, cobalt-chromium alloys, etc.) or self expanding materials (e.g., Nitinol) as known in the art.
• plastically-expandable materials e.g., stainless steel, cobalt-chromium alloys, etc.
• self expanding materials e.g., Nitinol
• the frame (and thus the valve) can be crimped to a radially compressed configuration on a delivery apparatus and then expanded inside a patient by an inflatable balloon or another suitable expansion mechanism.
• the frame (and thus the valve) can be crimped to a radially compressed
• valve can be advanced from the delivery sheath, which allows the valve to expand to its functional size.
• the prosthetic valve 10 can further include an annular skirt 30 that is attached to the frame 12. A flattened view of the skirt 30 is shown in FIG. 8.
• the skirt 30 in the illustrated embodiment can have an inner portion 32 and an outer portion 34. Specifically, the skirt 30 can extend along an inner surface of the frame 12, around the inflow end 14 of the frame 12, and then along the outer surface of the frame so as to define a fold 36 between the inner portion 32 and outer portion 34.
• the inner portion 32 can cover at least a portion of an inner surface of the frame 12
• the outer portion 34 can cover at least a portion of an outer surface of the frame 12.
• the inner portion 32 of the skirt 30 can function as a sealing member to prevent or decrease paravalvular leakage and to anchor the leaflets 20 to the frame 12.
• the outer portion 34 of the skirt 30 can function as a sealing member for the prosthetic valve 10 by sealing against the tissue of the native valve annulus and helping to reduce paravalvular leakage past the prosthetic valve 10.
• the upper edge 38 of the inner portion 32 (which is the outflow edge of the inner portion in the illustrated embodiment) can have an undulating shape that generally follows the shape of a selected row of strut segments 22 of the frame 12 when the frame 12 is in the expanded configuration. In this manner, the upper edge 38 of inner portion 32 can be tightly secured to the selected row of strut segments 22 with sutures.
• the upper edge 38 of the inner portion 32 can be sutured to row II of stmts segments. In other embodiments, the upper edge 38 of the inner portion 32 can be sutured to row III of stmts segments.
• the suture(s) used to secure the upper edge 38 extends only around the stmt segments that are aligned with the scallop line defined by the leaflets 20 (the line that tracks the inflow edge portions 21 of the leaflets).
• the upper edge 38 of the inner portion 32 is“sandwiched” between the frame 12 and the leaflets 20.
• the inflow edge portions 21 of the leaflets can overlap a portion of the inner surface of the inner portion 32 along the upper edge 38 and the leaflets can be secured to the inner portion 32 with sutures extending through the inner surface of the inner portion 32.
• the upper edge 40 of the outer portion 34 (which is the outflow edge of the outer portion in the illustrated embodiment) is generally straight and can be attached to the frame at the pivot joints just below row V of stmt segments (see e.g., FIG. 4).
• the upper edge 40 of the outer portion 34 can also have an undulating shape (similar to the upper edge of the inner portion 32) so that it can be sutured along the stmt segments of a selected row (e.g., row V of stmt segments).
• the outer portion 34 of the skirt 30 is axially longer than the inner portion 32 of the skirt 30, i.e., the upper edge 40 of the outer portion 34 extends closer to the outflow end 16 of the frame than the upper edge 38 of the inner portion 32.
• the axial length of the outer portion 34 can be the same as or substantially the same as that of the inner portion 32.
• the outer portion 34 can be axially shorter than the inner portion 32, i.e., the upper edge 38 of the inner portion 32 can extend closer to the outflow end 16 of the frame than the upper edge 40 of the outer portion 34.
• the frame 12 is radially expanded to a larger diameter (i.e., the deployment diameter).
• the deployment diameter can be within a working range of diameters defined between a smallest deployment diameter and a largest deployment diameter. In one exemplary but non-limiting embodiment, the smallest deployment diameter is about 26 mm and the largest deployment diameter is about 29 mm.
• the outer portion 34 of the skirt 30 when the frame 12 is radially expanded (see e.g., FIGS. 4- 5), the outer portion 34 of the skirt 30 can be slightly stretched in a circumferential direction.
• the skirt 30 can be sized such that when the frame 12 is expanded to a diameter within the working range, the outer portion 34 of the skirt 30 can be stretched so as to tightly or snugly conform to the outer surface of the frame 12, i.e., no slack is formed in the outer portion 34 around the circumferential periphery of the frame 12.
• the skirt 30 can be sutured to the frame 12 when it is expanded to its smallest deployment diameter.
• the skirt 30 can be sized such that the outer portion 34 tightly conforms to the outer surface of the frame 12 without any slack in the radial direction when the frame 12 is expanded to its smallest deployment diameter.
• Such tight conformation of the skirt 30 on the outer surface of the frame 12 can inhibit the skirt 30 from protruding through the frame cells, thus preventing abrasion of the leaflets 20.
• the outer portion 34 of the skirt 30 can further tighten on the frame 12.
• the skirt 30 in order to ensure that the outer portion 34 fits tightly around the frame 12 at its smallest deployment diameter, the skirt 30 can be cut to a smaller size and the skirt 30 can be mounted on the frame 12 (at its smallest deployment diameter) with some stretching in the circumferential direction.
• the skirt 30 can be sized to fit snugly around the frame without stretching of the skirt in any direction and without any slack in the radial direction when the frame 12 is expanded to its smallest deployment diameter. When the frame is radially expanded to a larger diameter within the working range, the skirt 30 can stretch slightly and tighten around the frame.
• a prosthetic valve may have only one deployment diameter.
• the skirt 30 can be sized to fit snugly around the frame without stretching of the skirt in any direction and without any slack in the radial direction when the frame 12 is expanded to the deployment diameter.
• the skirt 30 can be sized such that it is slightly stretched in the circumferential direction when the frame is expanded to the deployment diameter.
• the inflow end 14 of the frame 12 can be axially spaced from the fold 36 to form an axially extending gap 42 between the inflow end 14 of frame 12 and the fold 36 (see e.g., FIG. 5).
• the gap 42 can have a length (L) ranging from about 4 mm to about 8 mm.
• the length L of the gap 42 can be about 6 mm.
• the inflow end 14 of the frame 12 can move axially within the gap 42 closer to the fold 36.
• the inflow end 14 of the frame 12 can extend all the way to the fold 36 such that the frame 12 completely fills the gap 42.
• the outer portion 34 of the skirt 30 can form longitudinal pleats as illustrated in FIG. 3. Meanwhile, the inner portion 32 of the skirt 30 can fold inwardly toward the interior of the frame 12.
• the skirt 30 can be formed from any of various suitable biocompatible materials, including any of various synthetic materials (e.g., PET) or natural tissue (e.g., pericardial tissue).
• the skirt 30 is generally non-elastic.
• the skirt 30 can be woven using PET fibers or yarns in both the warp (longitudinal) and weft
• the skirt can be assembled on the frame such that the warp fibers extend in the axial direction of the frame and the weft fibers extend in the circumferential direction of the frame.
• the skirt can be assembled on the frame such that the weft fibers extend in the axial direction of the frame and the warp fibers extend in the circumferential direction of the frame.
• the skirt 30 can be elongated in both the radial and axial directions to certain degrees even if it is still woven using non-elastic fibers. Such pseudo elasticity can be achieved, for example, by orienting the fibers at angles relative to the height of the skirt and/or increasing the spacing between fibers.
• the skirt 30 can be woven from a first set of fibers (or yarns or strands) extending in a first direction 44, and a second set of fibers (or yams or strands) extending in a second direction 46, wherein neither the first direction 44 nor the second direction 46 being perpendicular to the fold 36.
• the first direction 44 can be generally perpendicular to the second direction 46, and the second direction can extend at an angle a of about 45 degrees (e.g., between 15-75 degrees or between 30-60 degrees) relative to the fold 36.
• the first direction 44 extends parallel or substantially parallel to outer struts 24a and the second direction 46 extends parallel or substantially parallel to inner stmts 24b when the frame 12 is in its radially expanded state.
• the spacing between the woven fibers (or yarns or strands) can be increased to facilitate elongation of the skirt 30 in both radial and axial directions.
• the yam density can be about 15% to about 30% less than a conventional PET skirt.
• the yarn spacing of the skirt 30 can be from about 155 yarns per inch to about 180 yarns per inch, such as about 160 yams per inch, whereas in a conventional PET skirt the yarn spacing can be from about 217 yams per inch to about 247 yams per inch.
• the fibers can be oriented so that they are parallel or substantially parallel to the stmts and/or increasing the spacing between the fibers can allow the skirt 30 to elongate in the axial and/or circumferential direction by up to about 40%.
• rotation of the fibers and/or increasing the spacing between the fibers can allow the skirt 30 to elongate in the circumferential direction from the smallest deployment diameter up to the largest deployment diameter.
• the outer portion 34 of the skirt 30 does not constrain axial elongation of the frame 12 when the frame is radially compressed.
• the frame 12 is free to move axially within the axially extending gap 42 toward the fold 36 during crimping. Consequently, relatively low crimping forces are needed to crimp the prosthetic valve 10 and overstretching of the skirt 30 can be avoided.
• a tether 48 can be coupled to the skirt 30 to prevent the fold 36 from moving inside the frame 12 when the frame 12 is radially expanded from the
• the skirt 30 can include a tether 48 extending diagonally from a first end 48a to a second end 48b located at or near the fold 36 such that the tether 48 forms an oblique angle relative to the fold 36 (see e.g., FIG. 3).
• the angle between the tether 48 and the fold 36 can range from about 10° to about 80°.
• the angle between the tether 48 and the fold 36 can range from about 30° to about 60°. In one specific embodiment, the angle between the tether 48 and the fold 36 can be about 45°.
• the first end 48a can be located at the upper edge 40 of the outer portion 34. In another embodiment, the first 48a can be spaced from the upper edge 40. In alternative embodiments, the first end 48a can be attached to an upper portion of the frame 12. In some embodiments (not shown), more than one tether 48 can be coupled to the skirt 30, with each tether 48 extending at an oblique angle relative to the fold 36.
• the tether 48 can be formed from a suture that is stitched to the outer portion 34 of the skirt using, for example, in-and-out stitches, as depicted in FIGS. 3 and 4. Due to the in-and-out stitches, the length of the suture can be longer than the distance traveled by the suture such that the suture line can be elongated if stretched. In this manner, the suture can function similar to a coil, which returns to its original length after being stretched.
• the tether 48 can be formed from an elastic material (e.g., an elastic fabric) that can be stretched longitudinally when tension is applied along its length and then return to its original length when tension is removed.
• the tether 48 when the frame 12 is radially expanded from the compressed configuration to the expanded configuration, the tether 48 can be stretched in the lengthwise direction of the tether due to radial expansion of the outer portion 34 of the skirt. As a result, the tether 48 is relatively taut and can hold the fold 36 in place against hemodynamic forces. Thus, the tether 48 can prevent the fold 36 from moving inside the frame 12 when the frame 12 is in the expanded configuration, which may otherwise obstruct the fluid inflow through the valve 10. When the frame 12 is radially compressed, the tether 48 can return to its original length.
• the prosthetic valve 10 described above can be mounted on a delivery apparatus and delivered to a target location within the patient.
• Various embodiments of the delivery apparatus and methods of delivering the prosthetic valve have been described, e.g., in U.S. Patent Application Publication Nos. 2013/0030519, 2010/0049313, 2009/0281619,
• the prosthetic valve 10 can be crimped onto a shaft of the delivery apparatus.
• the diameter of the frame 12 decreases while the axial length of the frame 12 elongates.
• the skirt 30 can elongate in the axial direction.
• the frame 12 is not constrained by the outer portion 34 of the skirt 30, the frame 12 is free to elongate in the axial direction and the inflow end 14 of the frame 12 can extend into the gap 42 during crimping.
• the outer portion 34 of the skirt 30 can form longitudinal pleats and the inner portion 32 of the skirt 30 can fold inwardly.
• the prosthetic valve 10 After being delivered to the target location, the prosthetic valve 10 can be expanded until the diameter of the frame 12 is within its working range. During expansion, the diameter of the frame 12 increases while the axial length of the frame 12 shortens. When the prosthetic valve 10 is in the radially expanded configuration, the outer portion 34 of the skirt 30 in particular embodiments can be stretched circumferentially such that it can tightly conform to the outer surface of the frame 12 without any slack in the radial direction.
• the inflow end 14 of the frame 12 can move away from the fold 36 to form an axially extending gap 42 between the frame 12 and the fold 36.
• one or more tethers 48 can be coupled to the skirt 30 to prevent the fold 36 from moving inside the frame 12 during valve expansion.
• FIG. 9 shows a prosthetic valve 110, according to another embodiment.
• the prosthetic valve 110 includes a frame 112 that can be radially expandable and compressible between a radially compressed configuration and a radially expanded configuration. Similar to the prosthetic valve 10, the prosthetic valve 110 can include a valvular structure 118 attached to the frame 112, and the valvular structure 118 can include a plurality of leaflets 120 having scalloped geometry (three leaflets are shown in FIG. 9).
• the prosthetic valve 110 can further include an outer skirt 130 that covers at least a portion of the outer surface of the frame 112.
• the lower edge 136 of the skirt 130 (the inflow edge in the illustrated embodiment) can extend from the inflow end 114 of the frame 112, whereas an upper edge 140 of the skirt 130 (the outflow edge in the illustrated embodiment) can be offset from an outflow end 116 of the frame 112.
• the frame 112 has five rows of strut segments, and only the row of stmt segments defining the outflow end 116 is not covered by the skirt 130.
• the skirt 130 can be sized to cover a different portion of the outer surface of the frame than shown in FIG. 9 or it can extend over the entire outer surface of the frame 112. In some embodiments, the skirt 130 can fold around the inflow end 114 of the frame to form a gap similar to the axially extending gap 42 depicted in FIG. 5.
• the skirt 130 can be sutured to the stmt segments 124 of the frame 112 along the scallop line 121 defined by the inflow edges of the leaflets 120.
• the scallop line 121 is a zig-zag shaped attachment line for the skirt 130 and the inflow edges of the leaflets 120.
• the sutures 122 can be positioned to wrap around a plurality of stmts so that the sutures 122 are positioned along a path that generally follows the scallop line 121. As shown in FIG.
• each segment of the scallop line 121 (where the inflow edges of the leaflets 120 attach to the frame 112) forms an approximately 45-degree angle relative to the longitudinal axis 126 of the frame 112 when the frame 112 is in the expanded configuration.
• the stmt segments along the scallop line 121 move inwardly.
• those suture 122 along the scallop lines 121 do not impose stress to the skirt 130.
• some of the sutures 122 along the scallop line 121 are configured to be slidable along the struts. Such sliding sutures can further reduce the stress to the skirt 130 when the frame 112 is radially compressed or expanded.
• the outer skirt 130 is connected to the frame only along the attachment line 121; that is, the outer skirt is not connected to any struts of the frame or other components of the prosthetic valve at locations not along the attachment line 121.
• the outer skirt 130 is connected to the struts of the frame along the attachment line 121, while the inflow edge portions of the leaflets 120 need not be connected to the frame along the attachment line 121.
• FIG. 10 shows a prosthetic valve 210, according to another embodiment. Similar to the valve 110 discussed above, the valve 210 includes a radially compressible and expandable frame 212 and an outer skirt 230 covering at least a portion of the outer surface of the frame 212. Like valve 110, the skirt 230 can be secured to the frame 212 with sutures 222 along a predefined scallop line 221 (which is a zig-zag shaped attachment line for the skirt in the illustrated embodiment). The valvular structure is not shown in FIG. 10 so that the suture lines 221 in the back of the frame 212 can be clearly seen. The frame 212 in the illustrated embodiment has four rows of strut segments, and the two rows of strut segments closest to near the outflow end 216 are not covered by the skirt 230.
• the fabric of skirt 130 or 230 can be woven using non-elastic fibers that are rotated (e.g., 45 degrees), and optionally with increased spacing between fibers, so that the skirt 130 or 230 can accommodate certain degree of elongation in both radial and axial directions.
• the skirt 130 or 230 can be sized such it tightly conforms to the outer surface of the respective frame 112 or 212 without any slack when the respective frame 112 or 212 is expanded to its smallest working diameter.
• Fig. 12A shows that when the frame 112 is radially compressed, portions of the skirt 130 can billow out to form V-shaped, longitudinally extending folded flaps 150 between adjacent sections of the scallop-shaped suture line 121.
• each flap 150 can be further folded in a circumferential direction so as to maintain a low crimping profile of the valve 110.
• each flap 150 can partially overlap an adjacent flap in a circumferential direction.
• FIGS. 12B- 12C show that the flaps 150 are folded in a clockwise direction (viewed from the outflow end), although it should be understood that the flaps 150 can also be folded in a counter clockwise direction.
• the skirt 230 can billow out to form V-shaped, longitudinally extending folded flaps 250 between adjacent sections of the suture line 221.
• the inflow and outflow edges of the skirt 130 and skirt 230 are not connected to the frame or other components of the prosthetic valve except along the attachment line 121, 221 which forms a plurality of first V-shaped flaps opening toward the outflow end of the prosthetic valve alternating with a plurality of second V-shaped flaps opening toward the inflow end of the prosthetic valve around a circumference of the frame (as best shown in FIG. 11).
• the disclosed embodiments can be adapted to deliver and implant prosthetic devices in any of the native annuluses of the heart (e.g., the pulmonary, mitral, and tricuspid annuluses), and can be used with any of various delivery approaches (e.g., retrograde, antegrade, transseptal, transventricular, transatrial, etc.).
• native annuluses of the heart e.g., the pulmonary, mitral, and tricuspid annuluses
• delivery approaches e.g., retrograde, antegrade, transseptal, transventricular, transatrial, etc.
• the singular forms“a,”“an,” and“the” include the plural forms unless the context clearly dictates otherwise.
• the term “includes” means“comprises.”
• the terms“coupled” and“connected” generally mean electrically, electromagnetically, and/or physically (e.g., mechanically or chemically) coupled or linked and does not exclude the presence of intermediate elements between the coupled or associated items absent specific contrary language.

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• 2020
  • 2020-01-23 CN CN202080020800.3A patent/CN113613594B/zh active Active
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