US20160256268A1 - Paravalvular leak occlusion device for self-expanding heart valves - Google Patents

Abstract

A system for replacing native valve function includes a prosthetic heart valve having a collapsible and expandable stent, the stent having a plurality of sections, and a valve assembly disposed in the stent. The system further includes an occluder device having an expandable body having a first end and a second end, a fastener coupled to the first end of the body and to a portion of the stent at a first position adjacent a first section of the stent, and a disk coupled to the second end of the body and to a portion of the stent at a second position in a section other than the first section.

Description

BACKGROUND OF THE INVENTION
• The present disclosure relates in general to heart valve replacement and, in particular, to collapsible prosthetic heart valves. More particularly, the present disclosure relates to devices and methods for positioning and sealing of collapsible prosthetic heart valves.
• Prosthetic heart valves that are collapsible to a relatively small circumferential size can be delivered into a patient less invasively than valves that are not collapsible. For example, a collapsible valve may be delivered into a patient via a tube-like delivery apparatus such as a catheter, a trocar, a laparoscopic instrument, or the like. This collapsibility can avoid the need for a more invasive procedure such as full open-chest, open-heart surgery.
• Collapsible prosthetic heart valves typically take the form of a valve structure mounted on a stent. There are two types of stents on which the valve structures are ordinarily mounted: a self-expanding stent or a balloon-expandable stent. To place such valves into a delivery apparatus and ultimately into a patient, the valve must first be collapsed or crimped to reduce its circumferential size.
• When a collapsed prosthetic valve has reached the desired implant site in the patient (e.g., at or near the annulus of the patient's heart valve that is to be replaced by the prosthetic valve), the prosthetic valve can be deployed or released from the delivery apparatus and re-expanded to full operating size. For balloon-expandable valves, this generally involves releasing the entire valve, and then expanding a balloon positioned within the valve stent. For self-expanding valves, on the other hand, the stent automatically expands as the sheath covering the valve is withdrawn.
SUMMARY OF THE INVENTION
• In some embodiments, an occluder device for occluding a gap between a medical device and adjacent body tissue includes an expandable body having a first end and a second end, a fastener coupled to the first end of the body, and an expandable disk coupled to the second end of the body.
• In some embodiments, a method for occluding a gap between a prosthetic heart valve and adjacent body tissue includes delivering an occluder into the interior of the heart valve, the occluder having (i) an expandable body, (ii) a fastener coupled to one end of the body, and (iii) an expandable disk coupled to another end of the body. The occluder is advanced through a cell of the heart valve to the outside of the heart valve. The fastener is coupled to one end of the prosthetic heart valve and the expandable disk is coupled to the prosthetic heart valve at a position spaced from the one end.
BRIEF DESCRIPTION OF THE DRAWINGS
• Various embodiments of the present disclosure are described herein with reference to the drawings, wherein:
• FIG. 1 is a side elevational view of a conventional prosthetic heart valve;
• FIG. 2 is a highly schematic cross-sectional view taken along line A-A ofFIG. 1 and showing the prosthetic heart valve disposed within a native valve annulus;
• FIG. 3A is a side view of a conformable occluder in accordance with one embodiment of the present disclosure;
• FIG. 3B is a side view of the conformable occluder ofFIG. 3A after it has been stretched longitudinally;
• FIG. 3C is a side view of a conformable occluder having a filler in accordance with another embodiment of the present invention;
• FIG. 3D is a side view of a conformable occluder having two fasteners in accordance with another embodiment of the present invention;
• FIGS. 4A-F illustrate the steps used to insert a conformable occluder to seal a prosthetic heart valve within a native valve annulus;
• FIG. 5 is a highly schematic cross-sectional view showing a prosthetic heart valve disposed within a native valve annulus along with a conformable occluder in its fully expanded state;
• FIG. 6A is a side view of a conformable occluder in accordance with another embodiment of the present disclosure;
• FIGS. 6B-D are side, top and bottom views showing the use of the conformable occluder ofFIG. 6A in vitro;
• FIG. 7A is a side view of a conformable occluder in accordance with another embodiment of the present disclosure; and
• FIGS. 7B-D are side, top and bottom views showing the use of the conformable occluder ofFIG. 7A in vitro.
DETAILED DESCRIPTION
• Despite the various improvements that have been made to the collapsible prosthetic heart valve delivery process, conventional devices suffer from some shortcomings For example, with conventional self expanding valves, clinical success of the valve is dependent on accurate deployment and anchoring. Inaccurate deployment and anchoring of the valve increases risks, such as those associated with valve migration, which may cause severe complications and possibly death due to the obstruction of the left ventricular outflow tract. Inaccurate deployment and anchoring may also result in the leakage of blood between the implanted heart valve and the native valve annulus, commonly referred to as paravalvular leakage. This leakage enables blood flow from the aorta back into the left ventricle, reducing cardiac efficiency and putting a greater strain on the heart muscle. Additionally, calcification of the aortic valve may affect performance and the interaction between the implanted valve and the calcified tissue is believed to be relevant to leakage, as will be outlined below.
• Moreover, anatomical variations between patients may require removal of a fully deployed heart valve from the patient if it appears that the valve is not functioning properly. Removing a fully deployed heart valve increases the length of the procedure and increases the risk of infection and/or damage to heart tissue. Thus, methods and devices are desirable that would reduce the likelihood of removal. Methods and devices are also desirable that would reduce the likelihood of valve leakage due to gaps formed between the implanted heart valve and patient tissue known as paravalvular leaks.
• There therefore is a need for further improvements to the devices, systems, and methods for transcatheter delivery and positioning of collapsible prosthetic heart valves. Specifically, there is a need for further improvements to the devices, systems, and methods for accurately implanting a prosthetic heart valve. Among other advantages, the present disclosure may address one or more of these needs.
• Various embodiments of the present invention will now be described with reference to the appended drawings. It is to be appreciated that these drawings depict only some embodiments of the invention and are therefore not to be considered limiting of its scope.
• As used herein, the term “proximal,” when used in connection with a prosthetic heart valve, refers to the end of the heart valve closest to the heart when the heart valve is implanted in a patient, whereas the term “distal,” when used in connection with a prosthetic heart valve, refers to the end of the heart valve farthest from the heart when the heart valve is implanted in a patient. When used in connection with devices for delivering a prosthetic heart valve or other medical device into a patient, the terms “trailing” and “leading” are to be taken as relative to the user of the delivery devices. “Trailing” is to be understood as relatively close to the user, and “leading” is to be understood as relatively farther away from the user.
• The leak occluders of the present invention may be used in connection with collapsible prosthetic heart valves.FIG. 1 shows one such collapsible stent-supportedprosthetic heart valve100 including astent102 and avalve assembly104 as known in the art. Theprosthetic heart valve100 is designed to replace a native tricuspid valve of a patient, such as a native aortic valve. It should be noted that while the inventions herein are described predominately in connection with their use with a prosthetic aortic valve and a stent having a shape as illustrated inFIG. 1, the valve could be a bicuspid valve, such as the mitral valve, and the stent could have different shapes, such as a flared or conical annulus section, a less-bulbous aortic section, and the like, and a differently shaped transition section.
• Prosthetic heart valve100 will be described in more detail with reference toFIG. 1.Prosthetic heart valve100 includesexpandable stent102 which may be formed from, for example, a shape memory material, such as the nickel-titanium alloy known as “Nitinol” or other suitable metals. and in particular, from those materials that are capable of self-expansion.Stent102 extends from proximal orannulus end130 to a distal oraortic end132, and includesannulus section140 adjacentproximal end130,transition section141 and aortic section142 adjacentdistal end132.Annulus section140 has a relatively small cross-section in the expanded condition, while aortic section142 has a relatively large cross-section in the expanded condition. Preferably,annulus section140 is in the form of a cylinder having a substantially constant diameter along its length.Transition section141 may taper outwardly fromannulus section140 to aortic section142. Each of the sections ofstent102 includes a plurality of struts160 forming cells162 connected to one another in one or more annular rows around the stent. For example, as shown inFIG. 1,annulus section140 may have two annular rows of complete cells162 and aortic section142 andtransition section141 may each have one or more annular rows of partial cells162. Cells162 in aortic section142 may be larger than cells162 inannulus section140. The larger cells in aortic section142 better enableprosthetic valve100 to be positioned in the native valve annulus without the stent structure interfering with blood flow to the coronary arteries.
• Stent102 may also include a plurality of commissure features166 for attaching the commissure between two adjacent leaflets tostent102. As can be seen inFIG. 1, commissure features166 may lie at the intersection of four cells162, two of the cells being adjacent one another in the same annular row, and the other two cells being in different annular rows and lying in end-to-end relationship. Preferably, commissure features166 are positioned entirely withinannulus section140 or at the juncture ofannulus section140 andtransition section141. Commissure features166 may include one or more eyelets which facilitate the suturing of the leaflet commissure to the stent.
• Stent102 may include one or more retaining elements168 atdistal end132 thereof, retaining elements168 being sized and shaped to cooperate with female retaining structures (not shown) provided on the deployment device. The engagement of retaining elements168 with the female retaining structures on the deployment device helps maintainprosthetic heart valve100 in assembled relationship with the deployment device, minimizes longitudinal movement of the prosthetic heart valve relative to the deployment device during unsheathing or resheathing procedures, and helps prevent rotation of the prosthetic heart valve relative to the deployment device as the deployment device is advanced to the target location and the heart valve deployed.
• Prosthetic heart valve100 includesvalve assembly104 preferably positioned inannulus section140 of thestent102 and secured to the stent.Valve assembly104 includes cuff176 and a plurality ofleaflets178 which collectively function as a one-way valve by coapting with one another. As a prosthetic aortic valve,valve100 has threeleaflets178, as well as three commissure features166. However, it will be appreciated that other prosthetic heart valves with which the leak occluders of the present invention may be used may have a greater or lesser number ofleaflets178 and commissure features166.
• Although cuff176 is shown inFIG. 1 as being disposed on the lumenal or inner surface ofannulus section140, it is contemplated that cuff176 may be disposed on the ablumenal or outer surface ofannulus section140 or may cover all or part of either or both of the lumenal and ablumenal surfaces. Both cuff176 andleaflets178 may be wholly or partly formed of any suitable biological material or polymer such as, for example, polytetrafluoroethylene (PTFE).
• Prosthetic heart valve100 may be used to replace a native aortic valve, a surgical heart valve or a heart valve that has undergone a surgical procedure. The prosthetic heart valve may be delivered to the desired site (e.g., near the native aortic annulus) using any suitable delivery device. During delivery,prosthetic heart valve100 is disposed inside the delivery device in the collapsed condition. The delivery device may be introduced into a patient using a transfemoral, transapical, transseptal or any other percutaneous approach. Once the delivery device has reached the target site, the user may deployprosthetic heart valve100. Upon deployment,prosthetic heart valve100 expands so thatannulus section140 is in secure engagement within the native aortic annulus. Whenprosthetic heart valve100 is properly positioned inside the heart, it works as a one-way valve, allowing blood to flow from the left ventricle of the heart to the aorta, and preventing blood from flowing in the opposite direction.
• Problems may be encountered when implantingprosthetic heart valve100. For example, in certain procedures, collapsible valves may be implanted in a native valve annulus without first resecting the native valve leaflets. The collapsible valves may have critical clinical issues because of the nature of the stenotic leaflets that are left in place. Additionally, patients with uneven calcification, bi-cuspid aortic valve disease, and/or valve insufficiency cannot be treated well, if at all, with the current collapsible valve designs.
• The reliance on unevenly calcified leaflets for proper valve placement and seating could lead to several problems, such as paravalvular (also known as perivalvular) leakage (PV leak), which can have severe adverse clinical outcomes. To reduce these adverse events, the optimal valve would anchor adequately and seal without the need for excessive radial force that could harm nearby anatomy and physiology.
• FIG. 2 is a highly schematic cross-sectional illustration ofprosthetic heart valve100 disposed withinnative valve annulus250. As seen in the figure,annulus section140 of thestent102 has a substantially circular cross-section which is disposed within the non-circularnative valve annulus250. At certain locations around the perimeter ofheart valve100, crescent-shaped gaps200 form betweenheart valve100 andnative valve annulus250. Blood flowing through these gaps andpast valve assembly104 ofprosthetic heart valve100 can cause regurgitation and other inefficiencies which reduce cardiac performance Such improper fitment may be due to suboptimal native valve annulus geometry due, for example, to calcification ofnative valve annulus250 or to unresected native leaflets.
• FIGS. 3A and 3B illustrate one embodiment ofconformable occluder300 intended to fill irregularities betweenheart valve100 andnative valve annulus250 shown inFIG. 2. As will be described in more detail below,conformable occluder300 allows for superior sealing between the perimeter ofheart valve100 andnative valve annulus250 while affording a low radial outward force.FIG. 3A, showsconformable occluder300 in a relaxed and expanded configuration whileFIG. 3B showsconformable occluder300 in a stretched and partially elongated configuration.Conformable occluder300 has aleading end302 and a trailingend304, and may generally includebody310,fastener320, anddisk330.
• Body310 may be a metallic structure that may be longitudinally stretched in the direction of arrows S from a relaxed condition shown inFIG. 3A to a stretched condition shown inFIG. 3B. In the relaxed condition,body310 may have a cross-section that is greater in size than it is in the stretched condition. Thus,body310 ofconformable occluder300 may be flexible and capable of contracting in the radial direction when a force is applied thereto to conform to the shape of the annulus in which it will be implanted. Moreover, the ability ofbody310 to longitudinally stretch in the direction of arrow S will allow the occluder to be delivered through a small diameter catheter and to be secured between two attachment points as will be seen below with reference toFIGS. 4A-4F.
• Occluder300 may be formed from a tubular section of braided fabric comprising a plurality of braided strands. The strands forming the braid may have a predetermined relative orientation with respect to one another (e.g., a helical braid). The ends of the strands may be located at leadingend302 and trailingend304 and affixed to prevent unraveling by any suitable means such as solder, braze, weld, coat, glue, clamp, tie, or clamp. Moreover,occluder300 may comprise a plurality of layers of braided fabric and/or other occluding material (e.g. seefiller345 inFIG. 3C) such thatoccluder300 is capable of at least partially inhibiting blood flow therethrough in order to facilitate the formation of thrombus and epithelialization.
• Occluder300 may be formed, for example, of a braided fabric mesh of a shape-memory material, of a super-elastic material, of a bio-compatible polymer, or of another material that is capable of collapsing and expanding. In the embodiments depicted inFIGS. 3A-3C,occluder300 comprises a braided metal fabric that is both resilient and capable of heat treatment to substantially set a desired preset shape (e.g. the relaxed configuration shown inFIG. 3A). One class of materials which meets these qualifications is shape memory alloys. One example of a shape memory alloy is Nitinol. It is also understoodoccluder300 may comprise various materials other than Nitinol that have elastic and/or memory properties, such as spring stainless steel, trade named alloys such as Elgiloy®, Hastelloy®, CoCrNi alloys (e.g., trade name Phynox), MP35N®, CoCrMo alloys, or a mixture of metal and polymer fibers. Depending on the individual material selected, strand diameter, number of strands, and pitch may be altered to achieve the desired properties ofoccluder300.
• As further described below,body310 may be collapsed during delivery into the patient and re-expanded after delivery to occlude gaps between a prosthetic heart valve and the native valve annulus to one side of the valve. Whilebody310 is shown inFIG. 3A as having an elliptical longitudinal cross-section in the expanded condition, it will be understood that the body may be constructed with various shapes and/or sizes. For example,body310 may have a circular, oval, polygonal, square, diamond, triangular or other shape in longitudinal cross-section when expanded.Body310 may also include two or more segments. Additionally,body310 may be formed of multiple layers of braid to decrease occlusion time.
• Body310 may be connected tofastener320 at leadingend302 ofconformable occluder300.Fastener320 may be formed of a suture, polymeric fiber, metallic filament, such as a flexible stranded stainless steel cable or loop of nitinol wire, or other suitable material, and may be configured to secureconformable occluder300 toprosthetic heart valve100 as will be described in greater detail below. Thoughfastener320 is shown inFIG. 3A as a loop, it will be understood that a simple hook, clasp or other similar structure capable of grasping, clipping, or hookingconformable occluder300 to strut160 ofprosthetic heart valve100 may be used.
• Body310 may further be coupled todisk330 at trailingend304 ofconformable occluder300. In the depicted embodiment,body310 is coupled todisk330 by a small diameter waist.Disk330 may be an ovular or spherical body sized to coupleconformable occluder300 to a cell of a prosthetic heart valve. Specifically,disk330 may be sized larger than cell162 ofstent102 such that it is incapable of passing through the cell (seeFIG. 1).Disk330 may be formed of the same material asbody310 or from a different material. For example,disk330 may be formed of a braided nitinol mesh or other shape-memory mesh. It is also contemplated thatdisk330 may be constructed from a bio-compatible polymer material.Disk330 may include a lip having a greater cross-sectional dimension thandisk330.Female component335 connected todisk330 at trailingedge335 may be used to coupleconformable occluder300 to a delivery device to position and deliverconformable occluder300.Female component335 may include an internally threaded screw attachment, a ring, or any other suitable means for coupling with a delivery device.
• In one example, as shown inFIG. 3C,body310′ may be hollow and may be at least partially filled withfiller345 of a fabric or fibers of materials that are intertwined within the mesh ofconformable occluder300′ to assist with sealing, occlusion and healing. For example,body310′ may includefiller345 of polyester threads or polyester fabric, as well as any suitable fiber material to increase density and/or promote tissue growth.Filler345 may also be in the form of a foam material, such as a closed cell sponge. The density ofbody310′ may be such that it impedes the flow of blood through it. Inclusion offiller345 inbody310′ may speed occlusion time forconformable occluder300′.
• In an alternative embodiment, shown inFIG. 3D,occluder300″ has leadingend302 and trailingend304, and may generally includebody310 extending entirely from leadingend302 to the trailingend304. As seen inFIG. 3D,occluder300″ includesfirst fastener320 at leadingend302. Instead of a disk on the opposite end (seedisk335 inFIGS. 3A-3C),occluder300″ includessecond fastener320′ disposed near trialingend304. In this embodiment,occluder300″ may be coupled to select struts160 ofstent102 via first andsecond fasteners320,320′ without the need fordisk335.
• FIGS. 4A-F illustrate the steps used to insert conformable occluder300 (orconformable occluder300′ orconformable occluder300″) to sealheart valve100 withinnative valve annulus250. As seen inFIG. 4A,heart valve100 has been implanted in a patient withannulus portion140 thereof positioned innative valve annulus250. Gap G may be formed betweenheart valve100 andnative valve annulus250 to one side ofheart valve100.
• As an initial step to seal gap G,conformable occluder300 may be disposed within delivery system400 (FIG. 4A) in a collapsed condition, such as the stretched or elongated configuration shown inFIG. 3B.Delivery system400 may includeouter sheath410 andinner wire420 havingmale component425.Male component425 may include a conventional screw attachment, a terminal hook or other suitable structure for mating withfemale component335.Male component425 is configured to couple withfemale component335 of conformable occluder300 (elements shown uncoupled inFIG. 4F).Outer sheath410 is slidable relative toinner wire420.Delivery system400 may be inserted into the patient and advanced toward the implantedheart valve100 in the direction of arrow X. As it reachesheart valve100,delivery system400 may be advanced into theheart valve100 ataortic end132 and out therefrom throughcell162bin transition section141 (shown inFIG. 4A).Delivery system400 may then be further advanced through gap G towardannulus end140 of implantedheart valve100, as shown inFIG. 4B. Ifheart valve100 ordelivery system400 includes echogenic materials, such materials may be used to guidedelivery system400 to the appropriate position using the assistance of three-dimensional echocaradiography to visualizeheart valve100 within the patient.
• Oncedelivery system400 has reached the desired site of sealing (e.g. gap G) as shown inFIG. 4C,outer sheath410 may be retracted slightly in the direction of arrow R (toward the trailing end of delivery system400) to expose fastener320 (shown inFIG. 4D).Conformable occluder300 remains coupled toinner wire420 at this stage and trailingedge304 ofoccluder300 remains housed bydelivery system400.
• Delivery system400 may be manipulated by gently twisting and/or tiltingdelivery system400 to positionfastener320 over the apex ofcell162aatannulus end130 ofheart valve100. Oncefastener320 has latched onto or been looped around apex ofcell162a,outer sheath410 may be further retracted in the direction of arrow R to exposebody310 ofconformable occluder300. Asouter sheath410 is further retracted, more ofoccluder body310 is exposed andoccluder300 expands within the gap G betweenheart valve100 and native valve annulus250 (FIGS. 4D and 4E). As seen inFIGS. 4D-4F,body310 is positioned parallel toannulus section140 andtransition section141. In this intermediate stage of deployment,body310 has expanded to its relaxed state and contacted the walls ofnative valve annulus250, and substantially fills gap G.
• Outer sheath410 may then be fully retracted to exposedisk330 and allow it to expand nearcell162b.In the depicted embodiment,disk330 is located on the interior ofheart valve100, although other in other embodiments,disk330 is located on the exterior ofheart valve100. In either instance,disk330 is spaced away fromvalve assembly104 so as not to impedenormal leaflet178 function.Disk330 then expands to a size small enough fordisk300 to project partially out of or intocell162b,but remains too large to pass through that cell. The interference ofdisk330 withcell162bcreates a second attachment region forconformable occluder300. Thus,conformable occluder300 is stretched between the two attachment regions—the interference betweendisk330 andcell162band the connection betweenfastener320 andcell162a.Fastener320 preventsoccluder300 from migrating into the aorta, whiledisc330 preventsoccluder300 from migrating back into the heart. Alternatively, in embodiments having two fasteners instead ofdisk330 such as that shown inFIG. 3D,first fastener320 may be coupled to the apex ofcell162a,whilesecond fastener320′ may be likewise coupled over the apex of a cell at theaortic end132 ofstent100.
• Male component425 may be disconnected fromfemale component335 by manipulating (e.g., rotating)wire420. Alternatively,inner wire420 may comprise a suture tied tofemale component335, and the suture may be simply cut to releaseconformable occluder300 fromdelivery system400. In another example, male and female components may be threaded anddelivery system400 may be twisted relative to occluder300 to decouple the two from one another. Accordingly, many mating solutions betweendelivery system400 andoccluder300 would serve the intended purpose for deployment ofoccluder300.FIG. 4F illustratesheart valve100 in its fully expanded state withconformable occluder300 fully filling the gap G betweenheart valve100 andnative valve annulus250.Delivery system400 may then be withdrawn in the direction of arrow R and removed from the patient, leavingconformable occluder300 in place to sealvalve100 withinnative valve annulus250.
• FIG. 5 is a highly schematic cross-sectional view showingconformable occluder300 in its relaxed state withbody310 fully radially expanded to fill crescent-shaped gap200 shown inFIG. 2. The mesh ofconformable occluder300 may be capable of promoting tissue growth betweenheart valve100 andnative valve annulus250. For example,conformable occluder300 may be treated with a biological or chemical agent to promote tissue growth on the conformable occluder, further sealing the heart valve within the native valve annulus. Alternatively,conformable occluder300 may be sufficiently dense through the use of polyester fibers or polyester fabric to adequately seal the heart valve without the need for major tissue growth throughoutgap G. Occluder300 may also be double-layered and/or may include tighter braiding to more quickly occlude the space betweenheart valve100 andnative valve annulus250. Whenconformable occluder300 is functioning properly,heart valve100 will be adequately sealed withinnative valve annulus250 so that blood flows throughvalve assembly104 and passing through leaflets108, while limiting or at least reducing blood flow through any gaps formed betweenheart valve100 andnative valve annulus250.
• FIG. 6A illustrates another embodiment ofconformable occluder600.Conformable occluder600 extends betweenleading end602 and trailingend604, and may generally include atubular body610 anddisk630.Disk630 includes an enlargedouter rim632 and is coupled toconnector635 for mating with a delivery system (not shown). As seen inFIG. 6A, reduceddiameter neck portion640 connectsbody610 todisk630. A fastener (not shown) may be attached to joint650 at leadingend602 to connectoccluder600 to an apex of a cell162 as described above with reference toFIGS. 4A-4F.
• FIGS. 6B-D are side, top and bottom end views illustrating the use ofoccluder600. Specifically,FIG. 6B shows a side view of the system whileFIG. 6C illustrates a top view (e.g., as seen fromaortic end132 of stent102) andFIG. 6D illustrates a bottom view (e.g., as seen fromannulus end130 of stent102). In these figures,container670 approximates the native valve annulus andstent102 is disposed therein to simulate aprosthetic heart valve100. A valve assembly is not shown attached to thestent102 for the sake of clarity. As seen inFIGS. 6B-D occluder600 is coupled tostent102 and shown to fill a gap betweenstent102 and the native valve annulus, approximated by the walls ofcontainer670. Specifically,disk630 is shown disposed within the interior of stent102 (FIG. 6C) andbody610 is disposed outside of stent102 (FIG. 6D). Though a fastener is not shown, it will be understood that a fastener may attach to joint650 andcouple leading end602 ofoccluder600 to an apex of a cell atannulus end130 ofstent102.Occluder600 may be delivered and positioned in a manner similar to that described above with reference toFIGS. 4A-F.
• FIGS. 7A illustrates another embodiment ofconformable occluder700.Conformable occluder700 extends betweenleading end702 and trailingend704, and may generally include abody710 formed of twobody segments712,712′, anddisk730. Thoughoccluder700 is shown having twosegments712,712′ it will be understood that three or more segments may be employed in constructingoccluder700. In some instances, it may be helpful to usemultiples segments712,712′ as opposed to a single unitary body to improve occlusion. For example,first segment712 may expand to a small radius, while asecond segment712′ may expand to a larger radius to accommodate a non-uniform native valve annulus and fill multiple gaps at varying longitudinal extents.
• Disk730 includes an enlargedouter rim732 and is coupled toconnector735 for mating with a delivery system (not shown). As seen inFIG. 7A, two reduceddiameter neck portions740,740′ connectbody disk730 tofirst segment712 andfirst segment712 tosecond segment712′, respectively. A fastener (not shown) may be attached to joint750 at leadingend702 to connectoccluder700 to an apex of a cell162 as described above with reference toFIGS. 4A-4F.
• FIGS. 7B-D are side, top and bottom end views illustrating the use ofoccluder700 within an approximatingcontainer770 as described above with reference toFIGS. 6B-6D. As seen inFIGS. 7B-D occluder700 is coupled tostent102 and shown to fill a gap betweenstent102 and the native valve annulus, approximated by the walls ofcontainer770. Specifically,disk730 is shown disposed within the interior of stent102 (FIG. 6C) andsegments712,712′ are disposed outside of stent102 (FIG. 6D). Though a fastener is not shown, it will be understood that a fastener may attach to joint750 to couple leadingend702 ofoccluder700 to an apex of a cell atannulus end130 ofstent102.Occluder700 may be delivered and positioned in a manner similar to that described above with reference toFIGS. 4A-F.
• While the inventions herein have been described for use in connection with heart valve stents having a particular shape, the stent could have different shapes, such as a flared or conical annulus section, a less-bulbous aortic section, and the like, and a differently shaped transition section. Additionally, thoughconformable occluder300 has been described in connection with expandable transcatheter aortic valve replacement, it may also be used in connection with surgical valves, sutureless valves and other devices in which it is desirable to create a seal between the periphery of the device and the adjacent body tissue. Additionally, though the deployment ofoccluder300 has been described usingdelivery system400 that deploysfastener320 first, followed bybody310 and finallydisk330, it will be understood that, through a different delivery approach, such as, for example, a transapical route,disk330 may be deployed first, followed bybody310 and thenfastener320.
• It will also be understood that while the preceding disclosure has illustrated the use of a single occluder to fill gaps to one side of a prosthetic heart valve, it will be understood that multiple occluders may be deployed around the perimeter of a heart valve. Such occluders may be delivered successively to each gap formed between the prosthetic heart valve and the native valve annulus. Conversely, multiple occluders may be delivered simultaneously using a large single outer sheath having two or more male components or other connectors. Additionally, multiple occluders may be simultaneously deployed by using multiple delivery systems each having a male component or other connector.
• Moreover, although the disclosure herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present disclosure. It is therefore to be understood that numerous modifications may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the present disclosure as defined by the appended claims.
• For examples, the occluder may be deployed for use with a prosthetic heart valve having a collapsible and expandable stent forming cells, and a valve assembly disposed in the stent for controlling the flow of blood through the stent. The disk is expandable from a collapsed configuration to a relaxed configuration, the disk in the relaxed configuration having a size larger than the size of at least some of the cells of the stent. The stent may include a plurality of struts and the fastener is coupleable to at least one of the plurality of the struts. The body may include at least one of a metallic mesh or a shape-memory material. The body may have an elliptical longitudinal cross-section. The body may include a metal mesh and polyester fiber intertwined with the metal mesh to increase the density of the body. The fastener may include a loop for coupling to the medical device. The disk may include at least one of a metallic mesh or a shape-memory material.
• The device may also include a female component or other connected attached to the disk for coupling to a delivery device. The body may include an agent for promoting tissue growth. A system for occluding a gap between a medical device and adjacent body tissue may include the occluder and a delivery system including an outer sheath, an inner wire disposed within and translatable with respect to the outer sheath, and a male component or other connector attached to the inner wire, the male component or other connector being configured to couple the inner wire to the expandable disk of the occluder. The outer sheath may be adapted to house the occluder in a contracted configuration, the medical device is a prosthetic heart valve having a collapsible and expandable stent forming cells and a valve assembly disposed in the stent for controlling the flow of blood through the stent, and the outer sheath is sized to pass through a cell of the expandable stent.
• In the methods described above, the fastener may be a loop and the step of coupling the fastener may include positioning the loop around an apex of a cell at the one end of the prosthetic heart valve. The body may have a substantially elliptical longitudinal cross-section in an expanded condition.
• It will be appreciated that the various dependent claims and the features set forth therein can be combined in different ways than presented in the initial claims. It will also be appreciated that the features described in connection with individual embodiments may be shared with others of the described embodiments.

Claims (21)

1. (canceled)

2. A system for replacing native valve function, the system comprising:

a prosthetic heart valve having a collapsible and expandable stent, the stent having a plurality of sections, and a valve assembly disposed in the stent; and

an occluder device comprising an expandable body having a first end and a second end, a fastener coupled to the first end of the body and to a portion of the stent at a first position adjacent a first section of the stent, and a disk coupled to the second end of the body and to a portion of the stent at a second position in a section other than the first section.

3. The system ofclaim 2, wherein the stent includes an annulus section, a transition section, and an aortic section.

4. The system ofclaim 2, wherein the disk is expandable from a collapsed configuration to a relaxed configuration.

5. The system ofclaim 4, wherein the stent includes a plurality of cells, and the disk, in the relaxed configuration, has a size larger than a size of at least some of the cells of the stent and incapable of passing therethrough.

6. The system ofclaim 2, wherein the stent includes a plurality of struts and the fastener is coupled to at least one of the plurality of the struts.

7. The system ofclaim 2, wherein the body includes at least one of a metallic mesh or a shape-memory material.

8. The system ofclaim 2, wherein the body has an elliptical longitudinal cross-section.

9. The system ofclaim 2, wherein the body includes a metal mesh and polyester fiber intertwined with the metal mesh.

10. The system ofclaim 2, wherein the fastener includes a loop of wire.

11. The system ofclaim 2, wherein the disk is expandable and includes at least one of a metallic mesh or a shape-memory material.

12. The system ofclaim 2, further comprising:

a connector attached to the disk for coupling to a delivery device.

13. The system ofclaim 2, wherein the body includes multiple segments, each segment being capable of independent radial expansion from the other segments.

14. The system ofclaim 2, further comprising:

a delivery system including an outer sheath, an inner wire disposed within and translatable with respect to the outer sheath, and a connector attached to the inner wire, the connector being configured to couple the inner wire to the disk of the occluder device.

15. The system ofclaim 14, wherein the outer sheath is adapted to house the occluder device in a contracted configuration, and the outer sheath is sized to pass through a cell of the expandable stent.

16. A method for occluding a gap between a prosthetic heart valve and adjacent body tissue, the method comprising:

delivering an occluder to the heart valve, the occluder including (i) an expandable body, (ii) a fastener coupled to one end of the body, and (iii) an expandable disk coupled to another end of the body;

coupling the fastener to one end of the prosthetic heart valve; and

coupling the expandable disk to the prosthetic heart valve at a position spaced from the one end.

17. The method ofclaim 16, wherein the step of coupling the fastener includes positioning a loop around an apex of a cell at the one end of the prosthetic heart valve.

18. The method ofclaim 16, wherein the step of coupling the disk includes disposing the disk on an outside of at least one cell of the stent such that the disk cannot pass therethrough.

19. The method ofclaim 16, wherein delivering the occluder comprises disposing the occluder within a delivery system and advancing the delivery system to the heart valve.

20. The method ofclaim 19, further comprising:

coupling the expandable disk to an inner wire of the delivery system.

21. The method ofclaim 20, further comprising:

decoupling the expandable disk from the inner wire after coupling the expandable disk to the heart valve.

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