71 results about "Chordae tendineae" patented technology

A system and method of repairing a native chordae of a patient using an artificial chordae. The artificial chordae is inserted into the patient in a non-deployed configuration using a delivery system and is delivered to a desired position within the patient. An operator causes the artificial chordae to transition from the non-deployed configuration to a deployed configuration. The artificial chordae is anchored to a myocardium of the patient. The artificial chordae is attached to a leaflet of the native chordae at an attachment location and tuned to a desired tension.

An implantable device or implant is configured to be positioned within anatomy such as a native heart valve to repair the valve. The implantable device or implant is configured to be attached to one or more portions of the anatomy or native heart valve, such as one or more portions thereof can be moved closer together. For example, native valve leaflets, chordae tendinea, papillary muscles, a leaflet cleft, etc. can be moved to prevent or inhibit regurgitant flow through the native valve.

A device for connecting artificial chordae tendineae to the leaflets of an atrioventricular valve, the device comprising: a neochord delivery system comprising a manipulable and pushable catheter that houses a neochord attached to a neochord puncture needle, the catheter being operable to push the puncture needle to puncture and pass the neochord through the papillary muscle of the ventricle; a retriever system comprising a catheter that houses a grasper that is operable to capture the neochord puncture needle after it passes through the papillary muscle and remove the neochord puncture needle and the neochord from the ventricle; and a tissue clamping system comprising a catheter that houses a distal tissue clamp and a proximal tissue clamp that can be deployed to clamp and hold the area of ​​the atrioventricular valve located therebetween so that the area can be punctured by the puncture needle to deliver the neochord through the leaflets and to the papillary muscle.

The present application relates to a kind of trans-catheter heart valve replacement system, which is composed of artificial heart valve and valve anchoring device, wherein the valve anchoring device can be wrapped outside valve chordae tendineae, while capturing native valve leaflet, providing positioning point for subsequent implantation of artificial heart valve;Artificial heart valve can be implanted in heart, and replace the physiological function of native valve.The valve anchoring device and artificial heart valve can be matched and positioned, in order to prevent the two from being too tight and continuous extrusion, friction and causing chordae tendineae rupture, there are two kinds of cooperation between them: the first cooperation state, can let artificial heart valve and valve anchoring device abut each other, ensure the stability of structure and position when the two are matched with each other;Second cooperation state, there is gap between artificial heart valve and valve anchoring device at this time, so that native valve leaflet or chordae tendineae can pass through, to reduce the contact area between valve replacement system and chordae tendineae as much as possible, avoid extruding chordae tendineae.

The present invention discloses a self-expanding atrioventricular valve prosthesis device, comprising: a main body portion, which is a frame structure, and the main body portion is implanted at the native valve annulus of the heart. The main body portion includes an inflow section, an outflow section and a transition section. The inflow section is located at the atrial end, the outflow section is located at the ventricular end, and the transition section is located between the inflow section and the outflow section; it further includes at least one artificial valve leaf, which is fixed to the transition section of the main body portion, and the artificial valve leaf is provided with a connecting portion; it further includes a chordae tendineae portion, one end of which is fixed, and the other end is connected to the artificial valve leaf through the connecting portion. The present invention restricts the movement range of the artificial valve leaf through the chordae tendineae portion, and the connecting portion prevents the chordae tendineae portion from tearing and stress concentration on the valve leaf, thereby increasing the durability of the artificial valve leaf.

This application provides a transcatheter artificial chordae tendineae implantation device and system with easy clamping capability. The transcatheter artificial chordae tendineae implantation device includes a clamp assembly, a drive assembly, a puncture assembly, and a delivery assembly. The clamp assembly includes a first clamp and a second clamp, which are arranged side-by-side along the axial direction of the clamp assembly, with the proximal end of the first clamp movably connected to the proximal end of the second clamp. The drive assembly is connected to the first clamp and / or the second clamp and drives the distal end of the first clamp towards or away from the distal end of the second clamp to clamp the leaflet located between the first and second clamps. The puncture assembly extends from the clamp assembly to puncture the leaflet and implant the artificial chordae tendineae. The delivery assembly delivers the clamp assembly and the puncture assembly. In this application, the first and second clamps achieve relative opening and closing through axial rotation, and the clamping surface of the clamp assembly extends along the axial direction of the clamp assembly, giving the clamp assembly a large clamping area for easy clamping of the leaflet.

The present invention discloses a device for repairing tricuspid regurgitation by accordion chordae tendineae, comprising: a chord-gathering member for wrapping around and accordion-gathering the chordae tendineae; a fixing member connected to the chord-gathering member for positioning the device for repairing tricuspid regurgitation by accordion chordae tendineae; and a counterweight block at the connection between the chord-gathering member and the fixing member for stabilizing the chord-gathering member. The present invention effectively prevents the device for repairing tricuspid regurgitation by accordion chordae tendineae from moving upward by adding a counterweight block between the accordion-gathering hollow rod of the chord-gathering member and the fixing member. The position of the counterweight block can be adjusted to adjust the center of gravity of the device for repairing tricuspid regurgitation by accordion chordae tendineae, further stabilizing the device and improving its fit with the heart, such as the atrial wall. Furthermore, the counterweight block is connected to the accordion-gathering hollow rod and the fixing hollow rod via threads, allowing the position of the counterweight block to be adjusted in advance according to the patient's heart shape.

The present disclosure relates generally to the field of medical devices for delivering artificial chordae tendineae in a patient An anchor for engaging a papillary muscle or heart wall is described, wherein the anchor is movable between a delivery configuration and a deployed configuration. When the anchor is in the delivery configuration the anchor has a first outer dimension and when the anchor is in the deployed configuration the anchor has a second outer dimension. The first outer dimension is smaller than the second outer dimension. The anchor is engageable with a papillary muscle or a heart wall when the anchor is in the deployed configuration. The anchor comprises a plurality of arms coupled at a proximal end thereof to a body portion, at least one arm of the plurality of arms movable between a first position and a second position when the anchor moves from the delivery configuration to the deployed configuration. The plurality of arms each have a distal tip for engaging the papillary muscle or heart wall, wherein as the anchor is moved from the delivery configuration to the deployed configuration, the plurality of arms are movable from an elongated shape to a curved shape.

Methods and devices for transvascular prosthetic chordae tendinea implantation are disclosed. A catheter is advanced into the left atrium. From an atrium side, a leaflet connector carried by a distal end of the catheter can be anchored to a superior surface of a mitral valve leaflet. A needle is axially advanceable through the leaflet connector and through the leaflet. A leaflet anchor having a leaflet suture can be advanced out of the needle to secure the mitral valve leaflet to the leaflet suture. A ventricular anchor is anchored to the wall of the ventricle to secure the ventricular wall to a ventricle suture. The leaflet suture and the ventricle suture may be tensioned and connected by a suture lock to form an artificial chordae.

The utility model provides an auxiliary clamping simulation device for treating mitral valve regurgitation. The auxiliary clamping simulation device comprises a water bath, a rotating device arranged on the outer side of the water bath and a cam mechanism connected with the rotating device. The bottom support is fixed in the water bath, the valve ring structure is arranged on the bottom support, and the valve leaflet is connected with the valve ring structure and is connected with the cam mechanism through chordae tendineae. The valve leaflet is of a trumpet-like shell structure, one end of the valve leaflet is flat and provided with a first long-strip-shaped opening, the other end of the valve leaflet is cylindrical and provided with a second round opening, and the first opening and the second opening are communicated with each other. According to the auxiliary clamping simulation device for treating mitral valve regurgitation, training simulation operation can be carried out on the mitral valve repairing process, and experiment / clinical operation risks can be reduced.

This invention provides a cardiac anchor and a corresponding cardiac anchoring system. The cardiac anchor includes a locking assembly and an anchoring member extending distally from the locking assembly. The anchoring member has a connecting end for engagement with cardiac tissue. The locking assembly includes a base and a suture clamping member, the suture clamping member being movably connected to the proximal end of the base. The distal end of the base has a bearing portion, and the suture clamping member has a suture clamping portion. A suture is disposed between the bearing portion and the suture clamping portion. The suture clamping member moves relative to the base to drive the suture clamping portion to move the suture toward the bearing portion and clamp the suture to the bearing portion. This cardiac anchor and cardiac anchoring system not only ensure endothelial overgrafting after the cardiac anchor is anchored to cardiac tissue, but also further avoids damage to the native chordae tendineae, ultimately greatly ensuring and maintaining the therapeutic effect of the surgery.

Implantable devices formed of materials which are not readily imageable, and which may shift from a delivery configuration to a deployment configuration upon deployment, are delivered and deployed with a deployment / delivery device having sensors generating a signal indicating contact of the delivery / deployment device with tissue to guarantee purchase of the implantable device with tissue upon deployment. The implantable device may be a tissue anchor with talons which shift from a delivery configuration to a deployed configuration. The sensors may be positioned along a distal end of the delivery / deployment device to indicate purchase of the device with tissue, to ensure purchase of the talons with tissue upon deployment. The sensors may include at least three sensors, which may be spaced apart from one another, to indicate full contact of the distal end of the delivery / deployment device with tissue. The sensors may optionally be aligned with the talons.

Apparatus for use with an annuloplasty ring (20), and an atrioventricular valve of a heart of a mammalian subject. A plurality of chord-manipulation arms (26) each include a flexible material and a stiffening element (70), the stiffening elements being configured to provide desired shapes to the chord-manipulation arms (26), when the chord-manipulation arms are disposed in non-radially constrained configurations. The chord-manipulation arms (26) are configured to be deployed among chords of the atrioventricular valve, and subsequently, to cause a size of the valve annulus to decrease, by the chord-manipulation arms (26) being rotated such as to twist the native atrioventricular valve and pull the native atrioventricular valve radially inwards. The stiffening elements (70) are configured to be removed from the flexible material of the chord-manipulation arms and / or de-stiffened, such as to facilitate removal of the chord-manipulation arms (26) from among the chords. Other applications are also described.

A catheter for changing or manipulating a shape of a surrounding anatomical structure or position the catheter in relation to said surrounding anatomical structure has distal and proximal ends. Further the catheter includes at least a first body extending along the catheter in the distal end portion of the catheter, wherein said body has an activated state and inactivated state. In said activated state a second diameter or a second volume of the body is bigger than a first diameter or a first volume of the body in said inactivated state. In addition, in said activated state said body is configured to support the catheter to an anatomical structure surrounded the catheter, such as e.g. chordae, blood vessel or urethra, and thereby change a relative position of the catheter and the surrounding anatomical structure and again to change or manipulate the shape of the surrounding anatomical structure or position the catheter in relation to said surrounding anatomical structure.

Systems and methods of atrioventricular valve replacement are provided. In various embodiments, an arch-like support structure is provided that is insertable and implantable into a heart and is positioned in the mitral annulus to replace a native mitral valve. The support structure is operable to support, and various systems comprise leaflet and chord structures operable to control and regular blood flow between chambers of the heart.

Disclosed are systems and methods of removing heart valve therapy. The systems and methods may include chordae cutting devices having unique shape memory curvature, capture basket catheters with mesh baskets, and leaflet cutting tools with unique shapes that may be pulled through leaflet tissue.

Devices, systems, and method for adjusting and setting tension of an artificial chordae tendineae. The artificial chordae tendineae is coupleable between a leaflet clip and a tissue anchor. A locking assembly, through which the artificial chordae tendineae extends, is shiftable between a tension-adjusting configuration, in which the artificial chordae tendineae is movable to adjust tension on the leaflet, and a tension-setting or locked configuration, in which the artificial chordae tendineae is inhibited or prevented or locked against moving with respect to the locking assembly to set or fix tension on the leaflet.

The invention relates to a laterally deliverable transcatheter prosthetic valve and a method for delivering and anchoring the same. A laterally deliverable prosthetic valve includes an outer frame, a flow control component mounted within the outer frame, and an anchoring element coupled to a distal side of the outer frame. The prosthetic valve is collapsible along the longitudinal axis and compressible along the central axis into a compressed configuration for lateral delivery through the delivery catheter, and is expandable to an expanded configuration when released from the delivery catheter. An end of the anchoring element is configured to engage a guidewire. The anchoring element extends during deployment to allow the anchoring element to capture at least one of the autologous leaflets or chordae and, in response to detachment of the guidewire from the end, transitions to a folded configuration to secure the at least one of the autologous leaflets or chordae between the anchoring element and the distal side of the outer frame.

A surgical instrument 1 for a valve repair surgery in an animal enables determination of the length of an artificial suture even when the tendinous cord length of a normal tendinous cord is not used as a reference. The surgical instrument 1 for a valve repair surgery in an animal comprises: a support part 20 which is rod-shaped and in which one-side end thereof in the longitudinal direction can abut a ventricle 56 of a heart 50 in an animal; and a suture holding part 30 which is provided at the other-side end of the support part 20, has three projections 32A, 32B, 32C on an end surface, and can abut a valve cusp 52 of the heart 50.

Guide wire apparatuses and methods. Guide wires may be utilized for guiding a delivery apparatus, for example a transcatheter mitral valve delivery apparatus to replace a native mitral valve. A guide wire may include a distal portion. The distal portion may define a central axis and comprise a distal tip. The distal portion may have an undeployed configuration in which the distal tip is contracted medially and centered on the central axis. The distal portion may have a deployed configuration in which the distal tip is expanded radially from the central axis such that, in multiple radial dimensions, the tip is thicker than a size of an opening between adjacent chordae tendineae of the mitral valve. The delivery apparatus may be configured to be passed along the wire to the mitral valve while the distal tip, in the deployed configuration, contacts the adjacent chordae tendineae without passing through the opening.

The application provides a heart valve positioning device which is detachably connected with a delivery system, the heart valve comprises a native valve ring and a native valve leaflet, and the heart valve positioning device comprises: a cylindrical support provided with at least one connecting piece; a plurality of first clamping pieces which are distributed along the outer periphery of the support and are connected with the support; a second clamping piece which is configured to be sleeved on the outer periphery of the first clamping piece; in a delivery state, the heart valve positioning device is contracted in the delivery system, and the connecting piece is connected with the delivery system; in a release state, the connecting piece is separated from the delivery system, the native valve leaflet is clamped between the first clamping piece and the support, and the second clamping piece is folded from the outer periphery of the first clamping piece and clamps the native valve leaflet, so that the native valve leaflet forms a folded structure. The heart valve positioning device of the application can easily pass through chordae tendineae to hook and support the native valve leaflet, and is simple, easy and fast to operate.

This invention provides a valve repair device, a valve repair system, and its operating method. The lifting components are all rigid structures, with the proximal end of each lifting component rotatably connected to the distal end of a stop structure. The distal end of each lifting component is rotatably connected to the distal end of a drive rod, allowing the shape of the lifting components to change through axial movement of the drive rod. This enables the lifting components to lift, clamp, and release chordae tendineae within a 0°–360° range, reducing the number of product specifications and significantly increasing the flexibility and convenience of the surgeon's operation. Furthermore, during surgery, if the valve repair device gets caught on the chordae tendineae, the flexible structure allows for a larger angle and smaller diameter in the open state, making release easier.

A method for treating a patient includes delivering a distal portion of an elongate medical device into a ventricle of a beating closed heart of a subject via a primary skin opening and a secondary puncture, utilizing the distal portion of the elongate medical device to engage a plurality of chordae tendineae extending from a first papillary muscle within the ventricle, at least a first one of the plurality of chordae tendineae attached to a first leaflet of an atrioventricular valve located between the ventricle and an adjacent atrium, and at least a second one of the plurality of chordae tendineae attached to a second leaflet of the atrioventricular valve, approximating the engaged plurality of chordae tendineae to increase an amount of closure possible between the first leaflet and the second leaflet, and locking the plurality of chordae tendineae in their approximated condition.

Various aspects of the present disclosure are directed toward apparatuses, systems, and methods that include device for chordae tendineae repair. The device may include a flexible cord having a first end and a second end; and a helical wire configured to attach to one of the first end and the second end of the flexible cord and anchor the flexible cord to a leaflet of a heart valve; and a capture device having a channel and configured to clamp the leaflet of the heart valve and deliver the flexible cord through the channel to anchor the helical wire to the leaflet.

The present application provides an artificial chord implantation device, comprising a conveying mechanism, a chord assembly, a clamping assembly, and a puncture assembly. The clamping assembly and the puncture assembly are fixed by a multi-lumen tube of the conveying mechanism. In the chord assembly, the two free ends of the artificial chord after being folded in half are connected to a fastener. The first clamp of the clamping assembly has a first pre-buried groove arranged in a ring shape, and the second clamp has a second pre-buried groove connected to the first pre-buried groove. The fastener is placed in the second pre-buried groove, and the annular portion of the artificial chord after being folded in half is sleeved in the first pre-buried groove. The puncture assembly has a fastener portion. After the puncture assembly passes through the annular portion and the leaflet in sequence, the fastener portion is engaged with the fastener. Then, the puncture assembly is pulled back to pass the fastener through the annular portion to complete the intracardiac knotting of the artificial chord. The artificial chord implantation device provided by the present application can simultaneously complete the intracardiac suturing and knotting of the artificial chord, thereby improving the efficiency of the operation. It also makes the artificial chord more securely fixed on the leaflet, thereby improving the success rate of the operation.

A method for treating a patient includes delivering a distal portion of an elongate medical device into a ventricle of a beating closed heart of a subject via a primary skin opening and a secondary puncture, utilizing the distal portion of the elongate medical device to engage a plurality of chordae tendineae extending from a first papillary muscle within the ventricle, at least a first one of the plurality of chordae tendineae attached to a first leaflet of an atrioventricular valve located between the ventricle and an adjacent atrium, and at least a second one of the plurality of chordae tendineae attached to a second leaflet of the atrioventricular valve, approximating the engaged plurality of chordae tendineae to increase an amount of closure possible between the first leaflet and the second leaflet, and locking the plurality of chordae tendineae in their approximated condition.

Methods and devices for transvascular prosthetic chordae tendinea implantation are disclosed. A catheter is advanced into the left atrium. From an atrium side, the catheter can be anchored to a superior surface of a mitral valve leaflet and a leaflet anchor can be advanced into the mitral valve leaflet to secure the mitral valve leaflet to a leaflet suture. A ventricular anchor is anchored to the wall of the ventricle to secure the ventricular wall to a ventricle suture. The leaflet suture and the ventricle suture may be tensioned and connected by a suture lock to form an artificial chorda.

Mitral valve prolapse and mitral regurgitation can be treating by implanting in the mitral annulus a transvalvular intraannular band. The band is positioned so that it extends transversely across a coaptive edge formed by the closure of the mitral valve leaflets, to inhibit prolapse into the left atrium. At least one marginal chordae is severed, to permit leaflet closure against the band.

The present disclosure relates generally to the field of medical devices for delivering artificial chordae tendineae in a patient. A system for adjusting tension in an artificial chordae tendineae includes an artificial chordae tendineae coupleable between a clip and an anchor. The clip is engageable with a leaflet of a heart valve while the anchor is engageable with a papillary muscle or heart wall. The anchor includes a body portion, and a locking portion coupleable with the artificial chordae tendineae and configured to allow movement of the artificial chordae tendineae in a first direction while preventing movement of the artificial chordae tendineae in a second direction opposite the first direction. An actuator is coupled to the locking portion for selectively releasing the locking portion to enable selective movement of the artificial chordae tendineae in the second direction.

This application provides an artificial chordae tendineae implantation device, comprising a leaflet capturing assembly and an artificial chordae tendineae implantation assembly. The leaflet capturing assembly includes a first clamping member, a second clamping member, and a transmission assembly. Driven by the transmission assembly, the second clamping member can open relative to the first clamping member to form an angle, or close to capture and clamp the leaflet of a valve between the first and second clamping members. One of the first and second clamping members has a protruding convex component, and the other has a groove. When the first and second clamping members are closed relative to each other and the leaflet is not located between the convex component and the groove, the convex component is received in the groove. The artificial chordae tendineae implantation assembly includes a puncture needle and a pushable artificial chordae tendineae housed within the puncture needle. After the leaflet capturing assembly captures and clamps the leaflet, the puncture needle punctures the leaflet, and the artificial chordae tendineae is pushed to the other side of the leaflet. After the artificial chordae tendineae is pushed to the other side of the leaflet, the leaflet capturing assembly separates from the leaflet and withdraws.