Repair Clip For Variable Tissue Thickness
20240277475 ยท 2024-08-22
Assignee
Inventors
Cpc classification
A61F2220/0008
HUMAN NECESSITIES
A61F2/246
HUMAN NECESSITIES
A61F2250/0012
HUMAN NECESSITIES
International classification
Abstract
Fixation device for fixation of heart valve leaflets includes an elongate central member defining a longitudinal axis of the fixation device and first and second arms rotatable about at least one arm hinge point between an open position and a closed position. The fixation device further includes a first gripping element rotatable about a first gripping element axis of rotation to capture a first leaflet of a heart valve between the first gripping element and the first arm, and a second gripping element rotatable about a second gripping element axis of rotation to capture a second leaflet of a heart valve between the second gripping element and the second arm. At least one of the first gripping element axis of rotation and the second gripping element axis of rotation is variably offset from the arm hinge point by an axis offset distance defined along the longitudinal axis.
Claims
1. A fixation device for fixation of leaflets of a heart valve, comprising: a central member defining a longitudinal axis of the fixation device; first and second fixation elements each being moveable between an open position and a closed position and extending outwardly from the central member in the open position, the first and second fixation elements each having a first end, a second end, a tissue engagement surface extending between the first and second ends, and a trough extending into the tissue engagement surface at a location between the first end and the second end; a first gripping element moveable relative to the first fixation element and being disposed in opposition to the tissue engagement surface and trough thereof configured to capture a first leaflet of the heart valve therebetween; and a second gripping element moveable relative to the second fixation element and being disposed in opposition to the engagement surface and trough thereof configured to capture a second leaflet of the heart valve therebetween.
2. The fixation device of claim 1, wherein the trough extends along only a portion of a length of each of the first and second fixation elements, the length extending from the first end to the second end of the respective first and second fixation elements.
3. The fixation device of claim 1, wherein the trough interrupts the tissue engagement surface so that the tissue engagement surface forms a first portion extending between the first end and the trough and a second portion extending between the trough and the second end.
4. The fixation device of claim 1, wherein the trough of each of the first and second fixation elements is located closer to the first end than the second end.
5. The fixation device of claim 4, wherein the first end of the respective first and second fixation elements is rotatably connected to the central member, and the second end is a free end.
6. The fixation device of claim 5, wherein the first gripping element is rotatably connected to the first fixation element, and the second gripping element is rotatably connected to the second fixation element.
7. The fixation device of claim 5, wherein the first and second gripping elements are rotatably connected to the central member.
8. The fixation device of claim 1, wherein the trough of each of the first and second fixation elements is a depression extending into the engagement surface and defines a trough bottom that defines a trough reference plane.
9. The fixation device of claim 8, wherein the first and second fixation elements each define a longitudinal axis extending between the first and second ends thereof, and the trough extends through the respective first and second fixation elements in a direction transverse to the longitudinal axis.
10. The fixation device of claim 8, wherein the trough extends substantially an entire length of the respective first and second fixation elements.
11. The fixation device of claim 8, wherein: the first fixation element includes a first hinge point about which the first fixation element rotates between the open and closed positions, the first hinge point being offset from the trough reference plane of the first fixation element by a first trough offset distance, and the second fixation element includes a second hinge point about which the second fixation elements rotates between the open and closed positions, the second hinge point being offset from the trough reference plane of the second fixation element by a second trough offset distance.
12. The fixation device of claim 11, wherein first and second trough offset distances are fixed.
13. The fixation device of claim 11, wherein the first and second trough offset distance are variable.
14. The fixation device of claim 13, wherein the first and second fixation elements each include an arm flexion portion configured to dynamically adjust the respective first and second trough offsets as the first and second leaflets are captured between the first and second gripping elements and first and second fixation elements, respectively.
15. The fixation device of claim 1, wherein the first and second gripping elements each include friction-enhancing features.
16. A fixation device for fixation of leaflets of a heart valve, comprising: a central member defining a longitudinal axis of the fixation device; first and second distal elements each being moveable between an open position and a closed position and extending outwardly from the central member in the open position, the first and second fixation elements each having a first end, a second end, a tissue engagement surface extending between the first and second ends, and a trough extending into the tissue engagement surface, the trough defining a trough bottom located closer to the first end than the second end; a first proximal element moveable relative to the first distal element and being disposed in opposition to the tissue engagement surface and trough thereof so as to be configured to capture a first leaflet of the heart valve therebetween; and a second proximal element moveable relative to the second distal element and being disposed in opposition to the engagement surface and trough thereof so as to be configured to capture a second leaflet of the heart valve therebetween.
17. The fixation device of claim 16, wherein the trough bottom extends through the respective first and second distal elements in a direction transverse to a length extending from the first end to the second end.
18. The fixation device of claim 16, wherein the first distal element is rotatably connected to the central member at a first hinge point, and the trough bottom of the first distal element defines a trough reference plane that is offset from the first hinge point by a trough offset.
19. The fixation device of claim 18, wherein the first distal element includes a flexion portion configured to dynamically adjust the trough offset.
20. The fixation device of claim 18, wherein the through offset is fixed.
Description
BRIEF DESCRIPTION OF THE FIGURES
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DETAILED DESCRIPTION
[0034] Reference will now be made in detail to the various exemplary embodiments of the disclosed subject matter, exemplary embodiments of which are illustrated in the accompanying drawings.
[0035] The fixation device for use with the disclosed subject matter provides an edge-to-edge transcatheter valve repair option for patients having various conditions, including regurgitant mitral valves or tricuspid valves. Transcatheter (e.g., trans-septal) edge-to-edge valve repair has been established using a fixation device, such as the MitraClip Transcatheter Mitral Valve Repair device. These fixation devices generally are configured to capture and secure opposing native leaflets using two types of leaflet contacting elements. The first element is a sub-valvular arm (also known as a distal element or fixation element) to contact the ventricular side of a native leaflet to be grasped. With the arm positioned underneath to stabilize the native leaflet in a beating heart, a second gripping element (e.g., a proximal element) can be lowered or moved into contact with the atrial side of the native leaflet to capture the leaflet therebetween. Once each opposing leaflet is captured by a respective arm and gripper element, the fixation device can be closed by raising or moving the arms toward a center of the fixation device such that the leaflets are brought into coaptation, which results in a reduction in valvular regurgitation during ventricular systole. Furthermore, a covering can be provided on the arms and/or gripper elements to facilitate tissue ingrowth with the captured leaflets.
[0036] Additional details of an exemplary fixation device in accordance with the disclosed subject matter are set forth below. Furthermore, a number of patents and publications disclose additional details and aspects of such fixation devices and related operations. See, for example, U.S. Pat. No. 7,226,467 to Lucatero et al.; U.S. Pat. No. 7,563,267 to Goldfarb et al.; U.S. Pat. No. 7,655,015 to Goldfarb et al.; U.S. Pat. No. 7,736,388 to Goldfarb et al.; U.S. Pat. No. 7,811,296 to Goldfarb et al.; U.S. Pat. No. 8,057,493 to Goldfarb et al.; U.S. Pat. No. 8,303,608 to Goldfarb et al.; U.S. Pat. No. 8,500,761 to Goldfarb et al.; U.S. Pat. No. 8,734,505 to Goldfarb et al.; U.S. Pat. No. 8,740,920 to Goldfarb et al.; U.S. Pat. No. 9,510,829 to Goldfarb et al.; U.S. Pat. No. 7,635,329 to Goldfarb et al.; U.S. Patent Application Publication No. 2017/0042546 to Goldfarb et al.; U.S. Patent Application Publication No. 2017/0239048 to Goldfarb et al.; U.S. Patent Application Publication No. 2018/0325671 to Abunassar et al., the entirety of the contents of each of these patents and published applications is incorporated herein by reference.
[0037] Variations in patient conditions and anatomies can result in leaflet thicknesses varying from relatively thin (e.g., tricuspid leaflets) to relatively thick (e.g., myxotamous thickened mitral valve leaflets). It therefore would be beneficial to provide a leaflet coaptation fixation device to accommodate a range of tissue thickness to increase procedural ease and reduce the likelihood of tissue injury. The disclosed subject matter of herein is directed to a variety of fixation device configurations, features and aspects that enable the treatment of thin and/or thick leaflets, or both, simultaneously. The features and aspects disclosed herein can be incorporated and combined into a variety of tailored fixation device configurations. Furthermore, if desired, a specific design can be specified by a user to enable the safe and easy treatment of a specific valve being evaluated.
[0038] Transcatheter (e.g., trans-septal) edge-to-edge valve repair has been established using a fixation device. These fixation devices are configured to enhance coaptation between opposing leaflets. Such fixation devices generally include two types of leaflet contacting design elements. The first element is a sub-valvular arm also known as a fixation element, configured to contact the ventricular side of a leaflet to be grasped. Once the arms are positioned to stabilize the leaflet in a beating heart, a second element known as a gripping element or proximal element can be lowered into contact with the atrial side of the leaflet to capture the leaflet. Once two opposing leaflets are captured, each between a respective arm or gripping element, the fixation device can be closed with the arms raised or moved reduce the arms angle such that the leaflets are brought into coaptation, which results in a reduction in valvular regurgitation during ventricular systole.
[0039] During this procedure, a fixation device design can utilize a single, central, fixed axis to rotate both the arms (i.e., ventricular contacting elements) and gripping elements (i.e., atrial capture elements), respectfully, to secure leaflets within the fixation device. However, leaflet thickness and characteristics can vary greatly from one patient to another, and even within a single valve. For example, mitral and tricuspid leaflets typically can be thicker at their outermost edge, which is adjacent to a thinner, more central belly region.
[0040] The thickness of leaflets being grasped and captured within a fixation device can vary by valve type and by disease state. For purpose of illustration and not limitation, a commonly treated mitral valve can have leaflets between 0.8 and 2.0 mm thick, however, the thickness of leaflets can vary due to a variety of conditions. For example, leaflet thickness can vary significantly between the anterior mitral leaflet (AML) and the posterior mitral leaflet (PML). Additionally, a patient with a history of rheumatic fever can have leaflets that have thickened up to or beyond 5 mm (Saxena A, Echocardiographic Diagnosis of Chronic Rheumatic Valvular Lesions, Global Heart Volume 8, Issue 3, September 2013, pgs. 203-212). By contrast, tricuspid valve leaflets can be thinner than those of the mitral valve, with a thickness between 0.8 and 1.1 mm (Silver et al., Morphology of the Human Tricuspid Valve, Circulation, Volume XLIII, March 1971). Furthermore, certain leaflet regions can be relatively thicker (i.e., rough zones) proximate their free edges and at chordae attachment zones, whereas leaflets can be relatively thin near the ventral belly region (Pham et al., Material Properties of Aged Human Mitral Valve Leaflets, J Biomed Mater Res A. 2014 August; 102(8): 2692-2703).
[0041] To address these various leaflet parameters, a fixation device is disclosed herein with improved configurations for enhanced performance with regard to device and tissue interaction. For example, since leaflet thickness is known to vary, this disclosure describes a fixation device design for effectively treating a range of known valve thicknesses. Additionally, the various features and aspects as described herein can be combined as desired to provide a tailored fixation device for a desired valve configuration.
[0042] Generally, and as set forth in greater detail below, the disclosed subject matter provided herein includes a fixation device for fixation of leaflets of a heart valve. The fixation device generally includes a central member defining a longitudinal axis of the fixation device, and first and second arms rotatable about at least one arm hinge point between an open position and a closed position. The fixation device further includes a first gripping element rotatable about a first gripping element axis of rotation to capture a first leaflet of a heart valve between the first gripping element and the first arm. The fixation device further includes a second gripping element rotatable about a second gripping element axis of rotation to capture a second leaflet of a heart valve between the second gripping element and the second arm. In accordance with the disclosed subject matter, at least one of the first gripping element axis of rotation and the second gripping element axis of rotation is variably offset from the arm hinge point by an axis offset distance defined along the longitudinal axis.
[0043] Referring to
[0044] The fixation device of
[0045] With continued reference to
[0046] Further in accordance with the disclosed subject matter, and as depicted in
[0047] As embodied herein, and as further depicted in
[0048] Additionally,
[0049] Further in accordance with the disclosed subject matter, at least one of the first gripping element axis of rotation 127 and the second gripping element axis of rotation 129 can be located at an end of the respective gripper element 116, 118 proximate the elongate central member 111, as depicted in
[0050] In accordance with another aspect of the disclosed subject matter, the fixation device 104 can include selectable offsets wherein a user can select or configure the fixation device 104 to the desired parameters before introduction into the body. For example, if a user is treating a patient valve with relatively thin leaflets (e.g., 0.5 mm-0.8 mm), the user can adjust the axis offset by lowering one or both connector pins 142 toward the arm hinge point such that thin leaflets are secured reliably during the procedure with reduced risk of local injury. Similarly, if a user is intending to treat a myxotamous or rheumatic patient valve with exceptionally thick leaflets (e.g., to 5 mm or 6 mm), the user can adjust the axis offset by moving the connector pins 142 away from the arm hinge point such that the fixation device is tailored to thicker leaflets. Selectable offset can include a single fixation device capable of being reconfigurable by the user (e.g., with a retaining pin). Additionally or alternatively, a plurality of fixation devices 104 can be provided in a kit wherein different fixation devices are provided with differing parameters wherein a selected device is chosen for a given leaflet parameters. A combination of the two is also contemplated. For user-selectable offsets, pre-procedural imaging can be performed to determine leaflet parameters.
[0051] In accordance with the disclosed subject matter, the fixation device 104 can include an individual, independent axis offset for each gripping element to facilitate differing leaflet thicknesses for an opposing anterior mitral leaflet (AML) and posterior mitral leaflet (PML). Individual offsets can be beneficial if prior to surgery a very thick AML (e.g., 4 mm) is observed through imaging while a thin PML (e.g., 1 mm) is observed. In this example, an offset of 4 mm can be selected by the user for one side of the fixation device 104 and a 1 mm offset can be selected for the other side of the fixation device 104.
[0052] With reference now to
[0053] As depicted in
[0054] Referring now to
[0055] As previously noted, and as depicted in
[0056] Referring back to
[0057] Referring now to
[0058] With reference to
[0059] With reference to
[0060] As with previous aspects of the disclosed subject matter, the gripping element 116, 118 having the compliant hinge 145 can be coupled to the elongate central member 111, as shown in
[0061] Referring now to
[0062] For purpose of illustration and not limitation, the embodiment of
[0063] With reference now to
[0064] For purpose of illustration and clarity,
[0065] Further in accordance with the disclosed subject matter, various components and operation of the fixation device 104 in accordance with the disclosed subject matter can be substituted with, or used in combination with, numerous alternative or additional components and operations, such as the components depicted in
[0066] The fixation device 104 can further include two link members or legs 168, each leg 168 having a first end which is rotatably joined with one of the arms 108, 110 and a second end which is rotatably joined with a base 170. The base 170 can be operatively connected with a stud 176 which can be operatively attached to a distal end of a delivery shaft 102. In some embodiments, the stud 176 can be threaded so that the distal end of a delivery shaft 102 can attach to the stud 176 by a screw-type action. Further, the connection point between the stud 176 and the distal end of a delivery shaft 102 can be disposed within the coupling member 174. However, the distal end of a delivery shaft 102 and stud 176 can be operatively connected by any mechanism which is releasable to allow the fixation device 104 to be detached. The stud can be axially extendable and retractable to move the base and therefore the legs 168 which rotate the arms 108, 110 between closed, open and inverted positions. Likewise, immobilization of the stud, such as by a locking mechanism, can hold the legs 168 in place and therefore lock the arms 108, 110 in a desired position. Further details are disclosed in the patents and publications incorporated by reference herein.
[0067] In each of the embodiments disclosed herein, the fixation device 104 can be releasably coupled to the distal end of a delivery shaft 102.
[0068] The embodiments illustrated herein are adapted for repair of a heart valve, such as a mitral valve, using an antegrade approach from a patient's left atrium. For some embodiments (e.g., embodiments requiring user input) imaging can be performed prior to a procedure to anticipate a patient's tissue thickness and assist a user in selecting a fixation device having the desired parameters. After imaging, a user can select an appropriate fixation device 104 (e.g., from a kit, as described above). Additionally or alternatively, a user can adjust the parameters of a fixation device 104 (e.g., a user-selectable axis offset). The desired fixation device 104 can be introduced in a femoral vein and advanced through the inferior vena cava into the heart, across a penetration in the interatrial septum. For mitral valve repair, the fixation device 104 can be advanced through the mitral valve from the left atrium to the left ventricle. The arms 108, 110 can be oriented to be perpendicular to a line of coaptation and then positioned so that the arms 108, 110 contact the ventricular surface of the valve leaflets, thereby grasping the leaflets. The gripping elements 116, 118 can remain on the atrial side of the valve leaflets so that the leaflets lie between the gripping elements 116, 118 and the arms 108, 110. The fixation device 104 can be repeatedly manipulated to reposition the device so that the leaflets are properly grasped at a desired location. Repositioning is achieved with the fixation device 104 in the open position. In some circumstances, regurgitation of the valve can also be checked while the fixation device 104 is in the open position. If regurgitation is not satisfactorily reduced, the fixation device 104 can be repositioned and regurgitation checked again until the desired results are achieved.
[0069] Once the fixation device 104 has been positioned in a desired location relative to the valve leaflets, the leaflets can then be captured between the gripping elements 116, 118 and the arms 108, 110. At this time, the gripping elements 116, 118 can be lowered toward the arms 108, 110 so that the leaflets are held therebetween. The arms 108, 110 can be closed to an angle selectable by the user and locked to the prevent the arms 108, 110 from moving toward an open position. The fixation device 104 can then be detached from the distal end of the delivery shaft 102. After detachment, the repair of the leaflets or tissue can be observed by non-invasive visualization techniques, such as echocardiography, to ensure the desired outcome. If the repair is not desired, the fixation device 14 can be retrieved. If the repair is satisfactory, the gripper element lines can be disconnected and the fixation device can be released for implantation.
[0070] While the embodiments disclosed herein utilize a push-to-open, pull-to-close mechanism for opening and closing arms it should be understood that other suitable mechanisms can be used, such as a pull-to-open, push-to-close mechanism. A closure bias may be included in the design using a compliant mechanism such as a linear spring, helical spring, or leaf spring. Likewise, other actuation elements can be used for deployment of the gripper elements.
[0071] While the disclosed subject matter is described herein in terms of certain preferred embodiments for purpose of illustration and not limitation, those skilled in the art will recognize that various modifications and improvements can be made to the disclosed subject matter without departing from the scope thereof. Moreover, although individual features of one embodiment of the disclosed subject matter can be discussed herein or shown in the drawings of one embodiment and not in other embodiments, it should be readily apparent that individual features of one embodiment can be combined with one or more features of another embodiment or features from a plurality of embodiments.
[0072] In addition to the specific embodiments claimed below, the disclosed subject matter is also directed to other embodiments having any other possible combination of the dependent features claimed below and those disclosed above. As such, the particular features presented in the dependent claims and disclosed above can be combined with each other in other possible combinations. Thus, the foregoing description of specific embodiments of the disclosed subject matter has been presented for purposes of illustration and description. It is not intended to be exhaustive or to limit the disclosed subject matter to those embodiments disclosed.
It will be apparent to those skilled in the art that various modifications and variations can be made in the method and system of the disclosed subject matter without departing from the spirit or scope of the disclosed subject matter. Thus, it is intended that the disclosed subject matter include modifications and variations that are within the scope of the appended claims and their equivalents.