PROSTHETIC CARDIAC VALVE DEVICES, SYSTEMS, AND METHODS
A system for treating a diseased native valve in a patient includes a valve prosthesis and a delivery device. The prosthesis includes an anchor and a frame. The delivery device includes an outer sheath, an inner shaft, an anchor guide, and a tether. The anchor is shaped to encircle chordae or leaflets of a native valve. The frame is configured to sit within the anchor. The inner shaft is positioned within the outer sheath and translatable and rotatable relative to the outer sheath. The anchor guide is attached to a distal end of the inner shaft and has a curved distal section. The tether is configured to detachably couple to the anchor and to longitudinally translate the anchor within the inner shaft and anchor guide. The anchor is configured to be actuated from a delivery configuration to the deployed configuration when the anchor is translated out of the anchor guide.
This application is a continuation application of U.S. application Ser. No. 16/824,576, filed Mar. 19, 2020, entitled “Prosthetic Cardiac Valve Devices, Systems, and Methods”; which claims the benefit of priority to U.S. Provisional Application No. 62/820,570, filed Mar. 19, 2019, entitled “Prosthetic Cardiac Valve Delivery Devices, Systems, and Methods”; U.S. Provisional Application No. 62/828,835, filed Apr. 3, 2019, entitled “Prosthetic Cardiac Valve Devices, Systems, and Methods”; U.S. Provisional Application No. 62/946,602, filed Dec. 11, 2019, entitled “Prosthetic Cardiac Valve Devices, Systems, and Methods”; U.S. Provisional Application No. 62/833,430 filed Apr. 12, 2019, entitled “Prosthetic Cardiac Valve Delivery Devices, Systems, and Methods”; U.S. Provisional Application No. 62/968,909, filed Jan. 31, 2020, entitled “Prosthetic Cardiac Valve Delivery Devices, Systems, and Methods”; U.S. Provisional Application No. 62/872,016, filed Jul. 9, 2019, entitled “Prosthetic Cardiac Valve Delivery Devices, Systems, and Methods”; U.S. Provisional Application No. 62/879,979, filed Jul. 29, 2019, entitled “Prosthetic Cardiac Valve Devices, Systems, and Methods”; U.S. Provisional Application No. 62/984,602, filed Mar. 3, 2020, titled “Prosthetic Cardiac Valve Devices, Systems, and Methods”; the entireties of which are incorporated by reference in their entireties.
This application may also be to U.S. patent application Ser. No. 16/546,901, filed Aug. 21, 2019, entitled “Prosthetic Cardiac Valve Devices, Systems, and Methods; U.S. patent application Ser. No. 16/594,946, filed Oct. 7, 2019, entitled “Prosthetic Cardiac Valve Devices, Systems, and Methods”; International Patent Application No. PCT/US2019/057082, filed Oct. 18, 2019, entitled “Adjustable Medical Device”; U.S. patent application Ser. No. 16/723,537, filed Dec. 20, 2019, entitled “Prosthetic Cardiac Valve Devices, Systems, and Methods”; the entireties of which are incorporated by reference in their entireties.
BACKGROUNDBlood flow between heart chambers is regulated by native valves—the mitral valve, the aortic valve, the pulmonary valve, and the tricuspid valve. Each of these valves are passive one-way valves which open and close in response to differential pressures. Patients with valvular disease have abnormal anatomy and/or function of at least one valve. For example, a valve may suffer from insufficiency, also referred to as regurgitation, when the valve does not fully close and allows blood to flow retrograde. Valve stenosis can cause a valve to fail to open properly. Other diseases may also lead to dysfunction of the valves. While medications may be used to treat the disease, in many cases the defective valve may need to be repaired or replaced at some point during the patient's lifetime. Existing valves and surgical repair and/or replacement procedures may have increased risks, limited lifespans, and/or are highly invasive. Some less-invasive transcatheter options are available, however these generally are limited to aortic valve procedures, are limited in their patient-to-patient flexibility, and often take longer than desired to implant. It would therefore be desirable to provide a less invasive procedure for repair and replacement of heart valves, including the mitral valve, quicker surgical methods, and/or prosthetic valves that can accommodate a variety of individual patients.
Additionally, existing valve repair/replacement procedures are often complicated and time-consuming. Currently available procedures often require the placement of more than one component—for example, a prosthetic valve and a mechanism to anchor it to the native anatomy. Such procedures generally utilize multiple delivery catheters to carry the various components and delivery of each component separately to the valve, which can be time-consuming (particularly if components are delivered sequential), complicated, and/or dangerous. For example, some devices provide rotational anchoring elements to capture the native anatomy such as the chordae tendineae in order to reduce delivery time. However, such anchoring elements, often by design, capture and pull the chordae along during their rotation, which can torque or otherwise stress and damage the chordae during deployment of the anchor elements, resulting in the need for additional medical interventions for the patient. Moreover, such anchoring elements may require extrusion from a low-profile (e.g., elongated) delivery configuration to an expanded configuration at or near the native valve. In at least some instances, extrusion of the anchoring elements can be complicated and may not reliably deploy into the correct expanded configuration relative to the delivery device. Incorrect deployment may result in additional time to retract and re-deploy the anchoring element, more complicated anchoring procedures, and/or damage to the native tissue. It would therefore be desirable to provide quicker, less-complicated, less dangerous, and more reliably deployable valve assemblies for valvular replacement and repair.
SUMMARYThe present disclosure generally relates to treating a diseased native valve in a patient and more particularly relates to prosthetic heart valves.
The present disclosure relates to prosthetic cardiac devices, and in some embodiments, prosthetic heart valves such as catheter-based mitral valves.
The present disclosure generally relates to treating a diseased native valve in a patient and more particularly relates to deployment of prosthetic heart valves and extrusion of anchoring elements from delivery devices.
The present disclosure generally relates to treating a diseased native valve in a patient and more particularly relates to delivery devices, systems, and methods for delivering and deploying a valve prosthesis. The valve prosthesis can include a spiral anchor and a frame structure adjacent the diseased native valve, and the spiral anchor can be deployed around one or more structures of the heart. The anchor can be configured to anchor the frame structure to the native valve when the frame structure is expanded therein.
In general, in one embodiment, a system for treating a diseased native valve in a patient includes an anchor and a tether. The anchor includes a delivery configuration and deployed configuration. The anchor in the deployed configuration is shaped to encircle chordae or leaflets of a diseased native valve in a patient. The tether is detachably coupled to the anchor and configured to longitudinally translate the anchor within a lumen of a delivery device. The anchor is configured to be actuated from the delivery configuration to the deployed configuration when the anchor is translated out of the lumen of the delivery device.
This and other embodiments can include one or more of the following features. The anchor can be configured to be actuated from the delivery configuration to the deployed configuration adjacent a native valve in a patient. The system can further include the delivery device. The delivery device can include an anchor guide having the lumen. The anchor can be configured to be disposed within the lumen of the anchor guide in the delivery configuration. The anchor can be configured to be actuated out of lumen of the anchor guide into the deployed configuration by the tether. The anchor guide can have a curvature that matches a curvature of the anchor in the deployed configuration. The anchor can include an elongated shape in the delivery configuration. The anchor can include a curved shape in the deployed configuration. The curved shape can include a spiral shape. A distal end of the tether can include a preset curved shape. The system can further include a retention wire configured to couple a distal end of the tether to a proximal end of the anchor. The anchor can be configured to wrap at least partially around a frame structure in the deployed configuration. The anchor can include a super-elastic material. The anchor can include nitinol. The system can further include a frame structure having an unexpanded configuration and an expanded configuration. The expanded configuration can be a generally tubular shape. The frame structure can include an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration. The compressed outer periphery can be smaller in diameter than the expanded outer periphery. The system of can further include the delivery device which can include an inner shaft. The anchor can be configured to be disposed in a lumen of the inner shaft and maintained in the delivery configuration by radial constriction from the inner shaft. Advancement of the anchor out of the lumen of the inner shaft by translation of the tether can actuate the anchor into the deployed configuration. The tether can be configured to extend from the anchor to a proximal end of the delivery device. The delivery device can further include an outer sheath. The inner shaft can be disposed within the lumen of the outer sheath. The outer sheath can be steerable. The tether can be configured to advance towards an opening of the lumen of the inner shaft to advance the anchor out of the lumen of the inner shaft and actuate the anchor into the deployed configuration. The anchor can be configured to wrap at least partially around the inner shaft in the deployed configuration. A central axis of the anchor can be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration. A distal end of the inner shaft can include an anchor guide. The anchor guide can be configured to correctly orient the anchor relative the longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is deployed from the delivery configuration to the deployed configuration. A distal end of the tether can have a shape corresponding to a shape of the anchor guide. A distal end of the anchor guide can include a preset curved portion. The tether can include a wire disposed in a housing. The housing can be flexible. A free end of the anchor can extend radially outward from the curved shape. The system can further include a frame structure configured for expanding within the native valve of the patient. The system can further include a frame structure. The anchor can be configured to be fully advanced from an atrial side of the native valve into a ventricle of the heart and anchor the frame structure to the native valve when the frame structure is in an expanded configuration adjacent the native valve. An unexpanded configuration of the frame structure can be sized and dimensioned for percutaneous insertion and the expanded configuration is sized and dimensioned for implantation in the native valve of the patient. The frame structure can include a first and second opposite ends. The first end can be configured to extend above a native valve, and the second end can be configured to extend below the native valve when the frame structure is anchored to the native valve. The frame structure can be configured to sit below the native valve when the frame structure is anchored to the native valve. The system of can further include a frame structure, and a valve segment within the frame structure can include a biocompatible one-way valve. At least a portion of the valve segment can be positioned within at least a portion of the frame structure. The valve segment can include at least one leaflet having an inner layer and an outer layer. The frame structure can be attached to the outer layer at one or more ends of the frame structure. The valve segment can include a plurality of leaflets.
In general, in one embodiment, a method for treating a diseased native valve in a patient includes: (1) Advancing a distal end of a delivery device from a first side of a native valve to a second side of the native valve. The delivery device includes an inner shaft which includes an anchor guide, and an anchor is disposed within a lumen of the inner shaft. The anchor includes a delivery configuration and a deployed configuration; (2) Holding the anchor with within the lumen of the inner shaft with a longitudinally-translatable tether. The anchor is detachably coupled to the tether; (3) Actuating the anchor from the delivery configuration to the deployed configuration adjacent the native valve by translating the tether distally within the lumen of the inner shaft to translate the anchor out of an opening in the delivery device; and (4) Rotating a free end of the deployed anchor around one or more structures on the second side of the native valve.
This and other embodiments can include one or more of the following features. Rotating the free end of the deployed anchor can include rotating the anchor with the anchor guide. The method can further include retracting the anchor guide while holding the anchor with the tether. A distal end of the tether can be coupled to a proximal end of the anchor with a retention wire, and the method can further include releasing the anchor from the tether by de-coupling the retention wire from the anchor. The method can further include steering the distal end of the delivery device such that the distal end of the delivery device points towards the first side of the native valve. The anchor can be configured to wrap at least partially around the delivery device in the deployed configuration. The anchor can be configured to wrap at least partially around a frame structure in the deployed configuration. A central axis of the anchor can be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration. A distal end of the inner shaft can include the anchor guide. The anchor guide can be configured to correctly orient the anchor relative the longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is actuated from the delivery configuration to the deployed configuration. Actuating the anchor can include actuating the anchor from the delivery configuration to the deployed configuration on the first side of the native valve and can further include advancing the anchor in the deployed configuration through the native valve to the second side of the native valve. Advancing the anchor can further include pushing the anchor through the native valve. Advancing the anchor can further include rotating the anchor through the native valve. Actuating the anchor can include positioning the anchor such that it is located only on the second side of the native valve. The distal end of the delivery device can be detachably coupled to a frame structure, and the method can further include expanding the frame structure within the native valve from an unexpanded configuration to an expanded configuration. Expanding the frame structure can occur while holding the anchor with the tether. The frame structure can include a first and second opposite ends, and expanding the frame structure can include expanding the frame structure such that the first end extends above the first side of the native valve and the second end extends below second side of the native valve. Expanding the frame structure can include expanding at least a portion the frame structure within at least a portion of the deployed anchor to anchor the frame structure to the native valve. The method can further include releasing the frame structure from the distal end of the delivery device. Expanding the frame structure and releasing the frame structure can occur simultaneously. The method can further include retracting the delivery device from the patient. The method can further include de-coupling the anchor from the tether. The method can further include retracting the tether from the patient. The one or more structures can include one or more valve leaflets of the native valve. The one or more structures can include one or more chordae of the left ventricle. The native valve ca be in a heart of a patient. The method can further include transseptally inserting the distal end of the delivery device into a left atrium of the heart. The native valve can include a mitral valve. The first side of the native valve can include a left atrium. The second side of the native valve can include a left ventricle.
In general, in one embodiment, a delivery system for delivering a prosthesis to a diseased valve includes an outer sheath, an inner shaft, and an anchor guide. The outer sheath has a central axis. The inner shaft is within the outer sheath and is translatable and rotatable relative to the outer sheath. The anchor guide is attached to a distal end of the inner shaft. The anchor guide includes a proximal section that is on-axis with the central axis and a distal section that curves about the central axis in a tapered spiral.
This and other embodiments can include one or more of the following features. The delivery system can further include a tether configured to extend through the inner shaft and anchor guide to attach to an anchor of the prosthesis. The tether can be further configured to deploy the anchor from the anchor guide. The outer sheath can be steerable. The anchor guide can be configured to correctly orient an anchor of the prosthesis relative to a longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is deployed from the anchor guide. The distal section can transition continuously from a high pitch, low radius curve at a proximal end to a low pitch, high radius curve at a distal end. A distal-most plane of the distal section can be orthogonal to the central axis. A curvature of the distal section can be configured to match a curvature of an anchor of the prosthesis. The inner shaft and the anchor guide can be of unitary construction.
In general, in one embodiment, a delivery system for delivering a prosthesis to a diseased valve includes an outer sheath, an inner shaft, and an anchor guide. The outer sheath has a central axis. The inner shaft is positioned within the outer sheath and is translatable and rotatable relative to the outer sheath. The anchor guide is attached to a distal end of the inner shaft. The anchor guide includes a proximal section that is on-axis with the central axis and a distal section that curves about the central axis. The inner shaft and anchor guide are configured to rotate relative to the outer sheath.
This and other embodiments can include one or more of the following features. The delivery system can further include a tether configured to extend through the inner shaft and anchor guide to attach to an anchor of the prosthesis. The tether can be further configured to deploy the anchor from the anchor guide. The outer sheath can be steerable. The anchor guide can be configured to correctly orient an anchor of the prosthesis relative to a longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is deployed from the anchor guide. The distal section can transition continuously from a high pitch low radius curve at a proximal end to a low pitch, high radius curve at a distal end. A distal-most plane of the distal section can be orthogonal to the central axis. A curvature of the distal section can be configured to match a curvature of an anchor of the prosthesis. The inner shaft and the anchor guide can be of unitary construction.
In general, in one embodiment, a delivery system for delivering a prosthesis to a diseased valve includes an outer sheath, an inner shaft, and an anchor guide. The outer sheath has a central axis. The inner shaft is positioned within the outer sheath and is translatable and rotatable relative to the outer sheath. The anchor guide is attached to a distal end of the inner shaft. The anchor guide includes a proximal section that is on-axis with the central axis and a distal section that curves about the central axis. A distal end of the anchor guide points in a direction that is orthogonal to the axis of the inner shaft.
This and other embodiments can include one or more of the following features. The delivery system can further include a tether configured to extend through the inner shaft and anchor guide to attach to an anchor of the prosthesis. The tether can be further configured to deploy the anchor from the anchor guide. The outer sheath can be steerable. The anchor guide can be configured to correctly orient an anchor of the prosthesis relative to a longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is deployed from the anchor guide. The distal section can transition continuously from a high pitch, low radius curve at a proximal end to a low pitch, high radius curve at a distal end. A distal-most plane of the distal section can be orthogonal to the central axis. A curvature of the distal section can be configured to match a curvature of an anchor of the prosthesis. The inner shaft and the anchor guide can be of unitary construction.
In general, in one embodiment, a method for treating a diseased native valve in a patient includes: (1) Advancing a distal end of a delivery device into a first chamber of a heart. The delivery devices includes an outer sheath and an inner shaft including an anchor guide; (2) Extending the anchor guide out of the outer sheath into the first chamber; (3) Rotating the inner shaft within the outer sheath until the anchor guide is in a desired orientation in the first chamber; (4) Extending an anchor out of a distal end of the anchor guide such that the anchor deploys within the first chamber; (5) moving the delivery device and the deployed anchor into a second chamber of the heart through a native valve annulus; and (6) Rotating the inner shaft within the outer sheath so as to rotate the anchor guide within the second chamber and so as to rotate the deployed anchor about one or more native valve structures.
This and other embodiments can include one or more of the following features. The method can further include retracting the anchor guide while holding the anchor with a tether of the delivery system. A distal end of the tether can be coupled to a proximal end of the anchor with a retention wire, and the method can further include releasing the anchor from the tether by de-coupling the retention wire from the anchor. The method can further include steering the outer sheath such that the distal end of the delivery device points towards the first chamber. The method can further include steering the outer sheath while moving the delivery device and the deployed anchor into the second chamber of the heart. The anchor can be configured to wrap at least partially around the delivery device when the anchor is deployed. A central axis of the anchor can be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration. The anchor guide can be configured to correctly orient the anchor relative the longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is actuated from the delivery configuration to the deployed configuration. The method can further include expanding a frame structure within the native valve from an unexpanded configuration to an expanded configuration. Expanding the frame structure can occur while holding the anchor with the tether. The frame structure can include a first and second opposite ends. Expanding the frame structure can include expanding the frame structure such that the first end extends into the first chamber and the second end extends into the second chamber. Expanding the frame structure can include expanding at least a portion the frame structure within at least a portion of the deployed anchor to anchor the frame structure to the native valve. The one or more structures can include one or more valve leaflets of the native valve. The one or more structures can include one or more chordae of the left ventricle. The method can further include transseptally inserting the distal end of the delivery device into the first chamber. The method can further include counter-rotating the anchor guide to reposition the anchor prior to rotating the anchor guide within the outer sheath so as to rotate the deployed anchor about one or more native valve structures.
In general, in one embodiment, a system for treating a diseased native valve in a patient includes a valve prosthesis and a delivery device. The valve prosthesis includes an anchor and a frame. The delivery device includes an outer sheath, an inner shaft, an anchor guide, and a tether. The anchor has a delivery configuration and deployed configuration. The anchor in the deployed configuration is shaped to encircle chordae or leaflets of a diseased native valve in a patient. The frame is configured to sit within the anchor. The inner shaft is positioned within the outer sheath and is translatable and rotatable relative to the outer sheath. The anchor guide is attached to a distal end of the inner shaft and has a curved distal section. The tether is configured to detachably couple to the anchor and to longitudinally translate the anchor within the inner shaft and anchor guide. The anchor is configured to be actuated from the delivery configuration to the deployed configuration when the anchor is translated out of the anchor guide.
In a another aspect, a system for treating a diseased native valve in a patient is provided. The system comprises an anchor comprising a delivery configuration and deployed configuration and a tether detachably coupled to the anchor and configured to longitudinally translate the anchor within a lumen of a delivery device. The anchor in the deployed configuration is shaped to encircle chordae or leaflets of a diseased native valve in a patient. The anchor is configured to be actuated from the delivery configuration to the deployed configuration when the anchor is translated out of the lumen of the delivery device.
In some embodiments, the anchor may be configured to be actuated from the delivery configuration to the deployed configuration adjacent a native valve in a patient.
In some embodiments, the delivery device may comprise an anchor guide having the lumen, the anchor may be configured to be disposed within the lumen of the anchor guide in the delivery configuration, and the anchor may be configured to be actuated out of lumen of the anchor guide into the deployed configuration by the tether. The tether may be configured to extend out of the anchor guide when the anchor is in the deployed configuration.
In some embodiments, the system may further comprise a core wire disposed within a lumen of the anchor and longitudinally translatable therein. The core wire may comprise a proximal curved portion when unconstrained and a distal tip. The core wire may comprise one or more deflection features disposed adjacent the distal tip and configured to be advanced out of the lumen of the anchor.
In some embodiments, the anchor may comprise an elongated shape in the delivery configuration.
In some embodiments, the anchor may comprise a curved shape in the deployed configuration. In some embodiments, the curved shape may comprise a helical shape. In some embodiments, the curved shape may comprise a spiral shape.
In some embodiments, a distal end of the tether may comprise a curved shape that is discontinuous with the curved shape of the anchor.
In some embodiments, the system may further comprise an engagement wire configured to couple a distal end of the tether to a proximal end of the anchor.
In some embodiments, the anchor may be configured to wrap at least partially around a frame structure in the deployed configuration.
In some embodiments, the anchor may comprise a super-elastic material. For example, the anchor may comprise nitinol.
In some embodiments, the system may further comprise a frame structure having an unexpanded configuration and an expanded configuration. The frame structure may comprise an expandable stent. In some embodiments, the expanded configuration may be a generally tubular expanded shape. In some embodiments, the frame structure may comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration. the compressed outer periphery may be smaller in diameter than the expanded outer periphery. In some embodiments, the frame structure may be balloon-expandable. In some embodiments, the frame structure may be self-expanding.
In some embodiments, the system may further comprise a delivery device. The delivery device may comprise an inner sheath and the anchor may be disposed in a lumen of the inner sheath and maintained in the delivery configuration by radial constriction from the inner sheath. Advancement of the anchor out of the lumen of the inner sheath by translation of the tether may actuate the anchor into the deployed configuration.
In some embodiments, the tether may extend from the anchor to a proximal end of the delivery device.
In some embodiments, the delivery device may further comprise an outer shaft and the inner shaft may be disposed within the lumen of the outer sheath. The outer sheath may be steerable.
In some embodiments, advancement of the tether towards an opening of the lumen of the inner shaft may advance the anchor out of the lumen of the inner shaft and actuate the anchor into the deployed configuration.
In some embodiments, the anchor may be configured to wrap at least partially around the inner shaft in the deployed configuration. Alternatively, or in combination, a central axis of the anchor is co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration.
In some embodiments, the tether may be configured to extend out of the lumen of the inner shaft when the anchor is in the deployed configuration.
In some embodiments, a distal end of the inner shaft may comprise an anchor guide. In some embodiments, the tether may be configured to extend out of a lumen of the anchor guide when the anchor is in the deployed configuration. In some embodiments, the anchor guide may be configured to correctly orient the anchor relative the longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is deployed from the delivery configuration to the deployed configuration. In some embodiments, a distal end of the tether may have a shape corresponding to a shape of the anchor guide. Alternatively, or in combination, a distal end of the anchor guide may comprise one or more deflection features. The one or more deflection features may be configured to interact with an opening of an outer shaft of the delivery device and cause deflection of the distal portion of the anchor guide when the inner shaft is advanced out of a lumen of the outer shaft, thereby facilitating positioning of the anchor relative to the outer shaft during actuation from the delivery configuration to the deployed configuration.
In some embodiments, the system may further comprise a frame structure. Expansion of the frame structure to an expanded configuration may detach the frame structure from the delivery device.
In some embodiments, a free end of the anchor may comprise an atraumatic tip.
In some embodiments, a free end of the anchor may comprise a ball tip.
In some embodiments, a free end of the anchor may comprise a loop.
In some embodiments, a free end of the anchor may be configured for piercing tissue.
In some embodiments, the anchor may comprise a spiral wire.
In some embodiments, the tether may comprise a wire disposed in a housing. The housing may be flexible.
In some embodiments, a free end of the anchor may extend radially outward from the curved shape.
In some embodiments, the system may further comprise a frame structure configured for expanding within the native valve of the patient.
In some embodiments, the system may further comprise a frame structure. The anchor may be configured to be fully advanced from an atrial side of the native valve into a ventricle of the heart and anchor the frame structure to the native valve when the frame structure is in an expanded configuration adjacent the native valve. In some embodiments, an unexpanded configuration of the frame structure may be sized and dimensioned for percutaneous insertion and the expanded configuration is sized and dimensioned for implantation in the native valve of the patient. In some embodiments, the frame structure may comprise a first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the frame structure is anchored to the native valve. In some embodiments, the frame structure may sit below the native valve when the frame structure is anchored to the native valve.
In some embodiments, the system may further comprise a frame structure and a valve segment within the frame structure comprising a biocompatible one-way valve. In some embodiments, at least a portion of the valve segment may be positioned within at least a portion of the frame structure. In some embodiments, the valve segment may comprise at least one leaflet having an inner layer and an outer layer, and the frame structure may be attached to the outer layer at one or more ends of the frame structure. In some embodiments, the valve segment may comprise a plurality of leaflets.
In another aspect, a method for treating a diseased native valve in a patient is provided. The method comprises a) advancing a distal end of a delivery device from a first side of a native valve to a second side of the native valve, wherein the delivery device comprises an inner shaft comprising an anchor guide, wherein an anchor comprising a delivery configuration and a deployed configuration is disposed within a lumen of the inner shaft; b) holding the anchor with within the lumen of the inner shaft with a longitudinally-translatable tether, wherein the anchor is detachably coupled to the tether; c) actuating the anchor from the delivery configuration to the deployed configuration adjacent the native valve by translating the tether distally within the lumen of the inner shaft to translate the anchor out of an opening in the delivery device; and d) rotating a free end of the deployed anchor around one or more structures on the second side of the native valve.
In some embodiments, rotating the free end of the deployed anchor may comprise rotating the anchor with the anchor guide. Optionally, a proximal end of the anchor may coupled to the anchor guide and rotating the anchor may comprise rotating the anchor guide.
In some embodiments, the method may further comprise retracting the anchor guide while holding the anchor with the tether.
In some embodiments, a distal end of the tether may have a curve shape that is discontinuous with a curved shape of the anchor.
In some embodiments, a distal end of the tether may be coupled to a proximal end of the anchor with an engagement wire. The method may further comprise releasing the anchor from the tether by de-coupling the engagement wire from the anchor.
In some embodiments, the method may further comprise steering the distal end of the delivery device such that the distal end of the delivery device points towards the first side of the native valve.
In some embodiments, the anchor may be configured to wrap at least partially around the delivery device in the deployed configuration.
In some embodiments, the anchor may be configured to wrap at least partially around a frame structure in the deployed configuration.
In some embodiments, a central axis of the anchor may be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration.
In some embodiments, a distal end of the inner shaft may comprise the anchor guide.
In some embodiments, the anchor guide may be configured to correctly orient the anchor relative the longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is actuated from the delivery configuration to the deployed configuration.
In some embodiments, a distal end of the tether may have a shape corresponding to a shape of the anchor guide.
In some embodiments, a distal portion of the anchor guide may comprise one or more deflection features. The one or more deflection features may be configured to interact with an opening of an outer shaft of the delivery device and cause deflection of the distal portion of the anchor guide when the inner shaft is advanced out of a lumen of the outer shaft, thereby facilitating positioning of the anchor relative to the outer shaft during actuation from the delivery configuration to the deployed configuration.
In some embodiments, the tether may comprise a wire disposed in a flexible housing.
In some embodiments, actuating the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the first side of the native valve and advancing the anchor in the deployed configuration through the native valve to the second side of the native valve. In some embodiments, advancing the anchor comprises pushing the anchor through the native valve. Advancing the anchor may further comprise rotating the anchor through the native valve.
In some embodiments, actuating the anchor may comprise positioning the anchor such that it is located only on the second side of the native valve.
In some embodiments, the distal end of the delivery device may be detachably coupled to a frame structure. The method may further comprise expanding the frame structure within the native valve from an unexpanded configuration to an expanded configuration. Expanding the frame structure occurs while holding the anchor with the tether. In some embodiments, the frame structure may comprise a first and second opposite ends and wherein the frame structure may comprise expanding the frame structure such that the first end extends above the first side of the native valve and the second end extends below second side of the native valve. Alternatively, or in combination, expanding the frame structure may comprise expanding at least a portion the frame structure within at least a portion of the deployed anchor to anchor the frame structure to the native valve. In some embodiments, the method may further comprise releasing the frame structure from the distal end of the delivery device. In some embodiments, expanding the frame structure and releasing the frame structure may occur simultaneously. In some embodiments, the frame structure may be balloon-expandable and expanding the frame structure may comprise inflating a balloon disposed within the frame structure, wherein inflation of the balloon causes expansion of the frame structure. In some embodiments, the frame structure may be self-expanding and expanding the frame structure may comprise releasing the frame structure from radial constriction by the delivery device. In some embodiments, the frame structure may comprise a valve segment therewithin comprising a biocompatible one-way valve.
In some embodiments, the method may further comprise retracting the delivery device from the patient.
In some embodiments, the method may further comprise de-coupling the anchor from the tether. In some embodiments, the method may further comprise retracting the tether from the patient.
In some embodiments, the one or more structures may comprise one or more valve leaflets of the native valve. Alternatively, or in combination, the one or more structures may comprise one or more chordae of the left ventricle.
In some embodiments, a free end of the anchor may comprise an atraumatic tip. In some embodiments, a free end of the anchor may comprise a ball tip. In some embodiments, a free end of the anchor may comprise a loop.
In some embodiments, a free end of the anchor may be configured for piercing tissue.
In some embodiments, a free end of the anchor may extend radially outward from the curved shape. In some embodiments, the curved shape may be a spiral shape.
In some embodiments, the native valve may be in a heart of a patient. The method may further comprise transseptally inserting the distal end of the delivery device into a left atrium of the heart. In some embodiments, the native valve may comprise a mitral valve, the first side of the native valve may comprise a left atrium, and the second side of the native valve may comprise a left ventricle.
Another aspect of the present disclosure provides a system for treating a diseased native valve in a patient. The system comprises a frame structure having an unexpanded configuration and an expanded configuration and an anchor comprising a coiled wire having a free end and a coiled shape. The anchor comprises a delivery configuration and a deployed configuration. The anchor is configured to be actuated from the delivery configuration to the deployed configuration adjacent a native valve in a patient, The anchor comprises one or more deflection features disposed along the coiled wire. The one or more deflection features comprise one or more kinks along the coiled wire such that at least a first portion of the coiled wire is discontinuous with the coiled shape of the coiled wire.
In some embodiments, the one or more deflection features may be configured to cause deflection of the free end when the anchor is actuated from the delivery configuration to the deployed configuration.
In some embodiments, a proximal end of the anchor may be coupled to a distal end of the frame structure.
In some embodiments, the anchor may comprise an elongated shape in the delivery configuration.
In some embodiments, the anchor may comprise a helical shape in the deployed configuration.
In some embodiments, the anchor may comprise a spiral shape in the deployed configuration.
In some embodiments, the one or more deflection features may comprise one or more pre-formed waves, bends, and/or humps in the coiled wire. For example, the one or more deflection features may comprise a plurality of waves. Alternatively, or in combination, the coiled wire may comprise a plurality of loops and the one or more deflection features may comprise a plurality of waves, each loop comprising a single wave. In some embodiments, the first portion may comprise the free end and the one or more deflection features may comprise a bend near a distal end of the coiled wire such that the free end of the coiled wire is positioned adjacent one or more loops of the coiled wire in the deployed configuration. Alternatively, or in combination, the first portion may comprise the free end and the one or more deflection features may comprise a bend near a free end of the coiled wire such that the free end of the coiled wire angles towards a proximal end of the coiled wire in the deployed configuration.
In some embodiments, the coiled wire may be configured to wrap at least partially around the frame structure in the deployed configuration.
In some embodiments, the anchor may comprise a super-elastic material. For example, the anchor may comprise nitinol.
In some embodiments, the frame structure may comprise an expandable stent.
In some embodiments, the expanded configuration may be a generally tubular expanded shape.
In some embodiments, the frame structure may comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration. The compressed outer periphery may be smaller in diameter than the expanded outer periphery.
In some embodiments, the frame structure may be balloon-expandable.
In some embodiments, the frame structure may be self-expanding.
In some embodiments, the device may further comprise a delivery device. The delivery device may comprise an outer sheath. The anchor may be disposed in a lumen of the outer sheath and maintained in the delivery configuration by radial constriction from the outer sheath. Advancement of the anchor out of the lumen of the outer sheath may actuate the anchor into the deployed configuration. The one or more deflection features disposed along the coiled wire may deflect the free end of the coiled wire as they move past an opening of the lumen of the outer sheath during actuation of the anchor from the delivery configuration to the deployed configuration. In some embodiments, the outer sheath may be steerable.
In some embodiments, the delivery device may further comprise an inner shaft. The inner shaft may be disposed within the lumen of the outer sheath. A proximal portion of the frame structure or a proximal end of the anchor may be coupled to a distal portion of the inner shaft. Advancement of the inner shaft towards an opening of the lumen of the outer sheath may advance the anchor out of the lumen of the outer shaft and may actuate the anchor into the deployed configuration. Alternatively, or in combination, the frame structure may be maintained in the unexpanded configuration by radial constriction from the outer sheath and advancement of the inner shaft out of the lumen of the outer sheath may actuate the frame structure into the expanded configuration. In some embodiments, the coiled wire may be configured to wrap at least partially around the inner shaft in the deployed configuration. Alternatively, or in combination, a central axis of the coiled wire may be co-axial with a longitudinal axis of the inner shaft when the coiled wire is in the deployed configuration. In some embodiments, the frame structure may be detachably coupled to the delivery device in the unexpanded configuration during delivery to the native valve. Expansion of the frame structure to the expanded configuration may detach the frame structure from the delivery device.
In some embodiments, the free end may comprise an atraumatic tip. For example, the free end may comprise a ball tip.
In some embodiments, the free end may be configured for piercing tissue.
In some embodiments, the coiled wire may comprise a spiral wire.
In some embodiments, the coiled wire may comprise a helical wire. Optionally, the anchor may comprise a first portion comprising the helical wire and another portion. Alternatively, or in combination, the anchor may comprise a plurality of helical wires. For example, the anchor may comprise at least two helical wires having different diameters. Alternatively, or in combination, the anchor may comprise at least two helical wires having different winding pitches. In some embodiments, the helical wire may have a generally tubular shape. The free end of the helical wire may extend radially outward from the tubular shape. In some embodiments, the helical wire may have a generally frustoconical shape. The free end of the helical wire may extend radially outward from the frustoconical shape. In some embodiments, the helical wire may have a generally cylindrical shape. The free end of the helical wire may extend radially outward from the cylindrical shape.
In some embodiments, the frame structure may be configured for expanding within the native valve of the patient.
In some embodiments, the anchor may be configured to be fully advanced from an atrial side of the native valve into a ventricle of the heart and anchor the frame structure to the native valve when the frame structure is in the expanded configuration adjacent the native valve. The unexpanded configuration may be sized and dimensioned for percutaneous insertion and the expanded configuration may be sized and dimensioned for implantation in the native valve of the patient. The frame structure may comprise a first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the frame structure is anchored to the native valve. Alternatively, the frame structure may sit entirely below the native valve when the frame structure is anchored to the native valve.
In some embodiments, the device may further comprise a valve segment within the frame structure comprising a biocompatible one-way valve. At least a portion of the valve segment may be positioned within at least a portion of the frame structure. In some embodiments, the valve segment may comprise at least one leaflet having an inner layer and an outer layer, and the frame structure may be attached to the outer layer at one or more ends of the frame structure. The valve segment may comprise a plurality of leaflets.
Another aspect of the present disclosure provides a system for treating a diseased native valve in a patient. The system comprises a frame structure having an unexpanded configuration and an expanded configuration, an anchor comprising a coiled wire having a free end, and an outer sheath comprising a lumen and an opening. The anchor comprises a delivery configuration when disposed within the lumen of the outer sheath and a deployed configuration when advanced out of the lumen of the outer sheath. The anchor comprises one or more deflection features disposed along the coiled wire and configured to interact with the outer sheath and cause deflection of the free end when the anchor is advanced out of the lumen of the outer sheath through the opening to actuate the anchor from the delivery configuration to the deployed configuration. The anchor is configured to be actuated from the delivery configuration to the deployed configuration adjacent a native valve in a patient.
In some embodiments, the one or more deflection features may be configured to cause deflection of the free end when the anchor is actuated from the delivery configuration to the deployed configuration.
In some embodiments, a proximal end of the anchor may be coupled to a distal end of the frame structure.
In some embodiments, the anchor may comprise an elongated shape in the delivery configuration.
In some embodiments, the anchor may comprise a helical shape in the deployed configuration.
In some embodiments, the anchor may comprise a spiral shape in the deployed configuration.
In some embodiments, the one or more deflection features may comprise one or more pre-formed waves, bends, and/or humps in the coiled wire. For example, the one or more deflection features may comprise a plurality of waves. Alternatively, or in combination, the coiled wire may comprise a plurality of loops and the one or more deflection features may comprise a plurality of waves, each loop comprising a single wave. In some embodiments, the first portion may comprise the free end and the one or more deflection features may comprise a bend near a distal end of the coiled wire such that the free end of the coiled wire is positioned adjacent one or more loops of the coiled wire in the deployed configuration. Alternatively, or in combination, the first portion may comprise the free end and the one or more deflection features may comprise a bend near a free end of the coiled wire such that the free end of the coiled wire angles towards a proximal end of the coiled wire in the deployed configuration.
In some embodiments, the coiled wire may be configured to wrap at least partially around the frame structure in the deployed configuration.
In some embodiments, the anchor may comprise a super-elastic material. For example, the anchor may comprise nitinol.
In some embodiments, the frame structure may comprise an expandable stent.
In some embodiments, the expanded configuration may be a generally tubular expanded shape.
In some embodiments, the frame structure may comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration. The compressed outer periphery may be smaller in diameter than the expanded outer periphery.
In some embodiments, the frame structure may be balloon-expandable.
In some embodiments, the frame structure may be self-expanding.
In some embodiments, the anchor may be disposed in a lumen of the outer sheath and maintained in the delivery configuration by radial constriction from the outer sheath. Advancement of the anchor out of the lumen of the outer sheath may actuate the anchor into the deployed configuration. The one or more deflection features disposed along the coiled wire may deflect the free end of the coiled wire as they move past an opening of the lumen of the outer sheath during actuation of the anchor from the delivery configuration to the deployed configuration. In some embodiments, the outer sheath may be steerable.
In some embodiments, the system may further comprise an inner shaft. The inner shaft may be disposed within the lumen of the outer sheath. A proximal portion of the frame structure or a proximal end of the anchor may be coupled to a distal portion of the inner shaft. Advancement of the inner shaft towards an opening of the lumen of the outer sheath may advance the anchor out of the lumen of the outer shaft and may actuate the anchor into the deployed configuration. Alternatively, or in combination, the frame structure may be maintained in the unexpanded configuration by radial constriction from the outer sheath and advancement of the inner shaft out of the lumen of the outer sheath may actuate the frame structure into the expanded configuration. In some embodiments, the coiled wire may be configured to wrap at least partially around the inner shaft in the deployed configuration. Alternatively, or in combination, a central axis of the coiled wire may be co-axial with a longitudinal axis of the inner shaft when the coiled wire is in the deployed configuration. In some embodiments, the frame structure may be detachably coupled to the delivery device in the unexpanded configuration during delivery to the native valve. Expansion of the frame structure to the expanded configuration may detach the frame structure from the delivery device.
In some embodiments, the free end may comprise an atraumatic tip. For example, the free end may comprise a ball tip.
In some embodiments, the free end may be configured for piercing tissue.
In some embodiments, the coiled wire may comprise a spiral wire.
In some embodiments, the coiled wire may comprise a helical wire. Optionally, the anchor may comprise a first portion comprising the helical wire and another portion. Alternatively, or in combination, the anchor may comprise a plurality of helical wires. For example, the anchor may comprise at least two helical wires having different diameters. Alternatively, or in combination, the anchor may comprise at least two helical wires having different winding pitches. In some embodiments, the helical wire may have a generally tubular shape. The free end of the helical wire may extend radially outward from the tubular shape. In some embodiments, the helical wire may have a generally frustoconical shape. The free end of the helical wire may extend radially outward from the frustoconical shape. In some embodiments, the helical wire may have a generally cylindrical shape. The free end of the helical wire may extend radially outward from the cylindrical shape.
In some embodiments, the frame structure may be configured for expanding within the native valve of the patient.
In some embodiments, the anchor may be configured to be fully advanced from an atrial side of the native valve into a ventricle of the heart and anchor the frame structure to the native valve when the frame structure is in the expanded configuration adjacent the native valve. The unexpanded configuration may be sized and dimensioned for percutaneous insertion and the expanded configuration may be sized and dimensioned for implantation in the native valve of the patient. The frame structure may comprise a first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the frame structure is anchored to the native valve. Alternatively, the frame structure may sit entirely below the native valve when the frame structure is anchored to the native valve.
In some embodiments, the device may further comprise a valve segment within the frame structure comprising a biocompatible one-way valve. At least a portion of the valve segment may be positioned within at least a portion of the frame structure. In some embodiments, the valve segment may comprise at least one leaflet having an inner layer and an outer layer, and the frame structure may be attached to the outer layer at one or more ends of the frame structure. The valve segment may comprise a plurality of leaflets.
Another aspect of the present disclosure provides a method for treating a diseased native valve in a patient. The method comprises advancing a distal end of a delivery device from a first side of a native valve to a second side of the native valve, wherein the delivery device comprises an outer sheath comprising an outer sheath comprising a lumen and an opening, wherein the distal end of the delivery device is detachably coupled to an anchor and a frame structure, the anchor comprising a delivery configuration, a deployed configuration, and one or more deflection features disposed along the anchor and configured to deflect a free end of the anchor when the anchor is actuated from the delivery configuration to the deployed configuration; actuating the anchor from the delivery configuration to the deployed configuration adjacent the native valve by (i) advancing the free end of the anchor out of the lumen of the outer sheath through the opening, (ii) deflecting the free end of the anchor by moving the one or more deflection features disposed along the anchor past the opening of the lumen of the outer sheath, and (iii) advancing a remainder of the anchor out of the lumen of the outer shaft through the opening; expanding the frame structure within the native valve from an unexpanded configuration to an expanded configuration; releasing the frame structure from the distal end of the delivery device; and retracting the delivery device from the native valve.
In some embodiments, the method may further comprise steering the distal end of the delivery device such that the distal end of the delivery device points towards the first side of the native valve.
In some embodiments, the anchor may be configured to wrap at least partially around the delivery device in the deployed configuration.
In some embodiments, the anchor may be configured to wrap at least partially around the frame structure in the deployed configuration.
In some embodiments, a central axis of the coiled wire may be co-axial with a longitudinal axis of the inner shaft when the coiled wire is in the deployed configuration.
In some embodiments, actuating the anchor may comprise releasing the frame structure from radial constriction by the delivery device.
In some embodiments, actuating the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the second side of the native valve.
In some embodiments, actuating the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the first side of the native valve and advancing the anchor in the deployed configuration through the native valve to the second side of the native valve. Advancing the anchor may comprise pushing the anchor through the native valve. Alternatively, or in combination, advancing the anchor may comprise rotating the anchor through the native valve.
In some embodiments, actuating the anchor may comprise positioning the anchor such that it is located only on the second side of the native valve.
In some embodiments, the frame structure may comprise a first and second opposite ends and expanding the frame structure may comprise expanding the frame structure such that the first end extends above the first side of the native valve and the second end extends below second side of the native valve.
In some embodiments, expanding the frame structure may comprise expanding at least a portion the frame structure within at least a portion of the deployed anchor to anchor the frame structure to the native valve.
In some embodiments, expanding the frame structure and releasing the frame structure may occur simultaneously.
In some embodiments, the frame structure may be balloon-expandable and expanding the frame structure may comprise inflating a balloon disposed within the frame structure. Inflation of the balloon may cause expansion of the frame structure.
In some embodiments, the frame structure may be self-expanding and expanding the frame structure may comprise releasing the frame structure from radial constriction by the delivery device.
In some embodiments, the anchor may comprise a coiled wire having a free end and the one or more deflection features may comprise one or more pre-formed waves, bends, or humps in the coiled wire. The one or more features may comprise a plurality of waves. For example, the coiled wire may comprise a plurality of loops and the one or more deflection features may comprise a plurality of waves, each loop comprising a single wave. Alternatively, or in combination, the one or more deflection features may comprise a bend near a distal end of the coiled wire such that the free end of the coiled wire is positioned adjacent one or more loops of the coiled wire in the deployed configuration. Alternatively, or in combination, the one or more deflection features may comprise a bend near a free end of the coiled wire such that the free end of the coiled wire angles towards a proximal end of the coiled wire in the deployed configuration.
In some embodiments, the method may further comprise rotating the free end of the deployed anchor around one or more structures on the second side of the native valve. The one or more structures may comprise one or more valve leaflets of the native valve. Alternatively, or in combination, the one or more structures may comprise one or more chordae of the left ventricle.
In some embodiments, the free end may comprise an atraumatic tip. For example, the free end may comprise a ball tip.
In some embodiments, the free end may be configured for piercing tissue.
In some embodiments, the coiled wire may comprise a spiral wire.
In some embodiments, the coiled wire may comprise a helical wire. Optionally, the anchor may comprise a first portion comprising the helical wire and another portion. Alternatively, or in combination, the anchor may comprise a plurality of helical wires. For example, the anchor may comprise at least two helical wires having different diameters. Alternatively, or in combination, the anchor may comprise at least two helical wires having different winding pitches. In some embodiments, the helical wire may have a generally tubular shape. The free end of the helical wire may extend radially outward from the tubular shape. In some embodiments, the helical wire may have a generally frustoconical shape. The free end of the helical wire may extend radially outward from the frustoconical shape. In some embodiments, the helical wire may have a generally cylindrical shape. The free end of the helical wire may extend radially outward from the cylindrical shape.
In some embodiments, the frame structure may comprise a valve segment therewithin comprising a biocompatible one-way valve.
In some embodiments, the native valve may be in a heart of a patient.
In some embodiments, the method may further comprise transseptally inserting the distal end of the delivery device into a left atrium of the heart.
In some embodiments, the native valve may comprise a mitral valve, wherein the first side of the native valve comprises a left atrium, and wherein the second side of the native valve comprises a left ventricle.
In another aspect, a system for treating a diseased native valve in a patient is provided. The system includes: a delivery device comprising: an outer sheath assembly comprising an outer sheath and a distal end, wherein the outer sheath assembly comprises a lumen, an inner shaft within the lumen of the outer sheath assembly, wherein the inner shaft comprises a lumen, and an anchor delivery sheath comprising a lumen configured to maintain an anchor in a delivery configuration; and a valve prosthesis comprising a frame structure and the anchor configured to have the delivery configuration and a deployed configuration, wherein the anchor comprises a spiral band having a free end, and wherein the frame structure is maintained in the delivery configuration by radial constriction from one or more of the outer sheath or the distal end of the outer sheath assembly
In some embodiments, the distal end of the outer sheath assembly can be a soft valve capsule. The soft valve capsule can comprise a cylindrical section and a tapered section. The cylindrical section and the tapered section can comprise a unitary body. The cylindrical section and the tapered section can be permanently attached to one another. The cylindrical section can comprise a flexible material disposed between a proximal ring and a distal ring, wherein the distal ring is attached to the tapered section. The flexible material can comprise a helically wound wire. The flexible material can comprise a series of rings linked by a wire. The cylindrical section and the tapered section can be configured to be separated from one another. The cylindrical section can comprise a flexible material disposed between a first ring and a second ring, wherein the first ring is attached to a proximal end of the flexible material and the second ring is attached to a distal end of the flexible material. The flexible material can further comprise a lumen disposed between a first layer of the flexible material and a second layer of the flexible material.
In some embodiments, the cylindrical section can further comprise a coil wire disposed within the lumen and coupled to the second ring, wherein the coil wire, when translated proximally, is configured to slide the distal ring relative to the proximal ring and collapse the flexible material to separate the cylindrical section from the tapered section. The lumen can comprise an inflatable lumen coupled to the distal ring or the distal end of the flexible material and configured to be deflated in order to collapse the flexible material and separate the cylindrical section from the tapered section. The cylindrical section can be releasably attached to the tapered section.
In some aspects, disclosed herein, the frame structure can be maintained in the delivery configuration by radial constriction from the distal end of the outer sheath assembly, wherein the radial constriction is removed by a separation of the outer sheath from the distal end of the outer sheath assembly. The inner shaft can be coupled to at least a portion of the distal end of the outer sheath assembly such that advancement of the inner shaft distally relative to the outer sheath causes the distal end to separate from the outer sheath. The delivery device can further comprise a guidewire disposed within a lumen of the inner shaft. The anchor can be configured to be released from the delivery configuration into an intermediate configuration and further into a deployed configuration. The anchor can be configured to be released into the intermediate configuration on an atrial side of a valve and subsequently pushed to a ventricle side of the valve. The anchor can be configured to be released into the deployed configuration from the delivery configuration on a ventricle side of a valve. The outer sheath can be configured to be steered to an edge of the valve and advanced along the guidewire into the ventricle side of the valve to position the anchor delivery sheath for delivery of the anchor.
In some embodiments, advancement of the inner shaft out of the lumen of the outer sheath can be configured to expand the frame structure into the expanded configuration. The anchor can comprise a spiral shape in the deployed configuration. The anchor can comprise an elongated shape in the delivery configuration. The anchor can comprise one or more locking mechanisms configured to maintain the anchor in the deployed configuration. The one or more locking mechanisms can comprise a frictional band, a polymer coating, or one or more key and one or more key hole features. The anchor can comprise a first loop, a second loop, and one or more locking mechanisms, and wherein the one or more locking mechanisms are configured to couple the first loop to the second loop when the anchor is in the fully deployed configuration.
In some embodiments, the spiral band can comprise one or more loops. The one or more loops can comprise at least 360 degrees of rotation. The spiral band can comprise a plurality of loops. The spiral band can comprise one or more spaces between the plurality of loops. The plurality of loops can spiral radially outward from a central point.
In some embodiments, the anchor can comprise a super-elastic material. The anchor can comprise nitinol. The frame structure can comprise an expandable stent. The expanded configuration can be a generally tubular expanded shape. The frame structure can comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration, wherein the compressed outer periphery is smaller in diameter than the expanded outer periphery. The frame structure can be balloon-expandable. The frame structure can be self-expanding.
In some embodiments, the free end of the anchor can comprise an atraumatic tip. The free end can comprise a ball tip. The free end can be configured for piercing tissue. The free end can be bent distally. The free end can be bent proximally. The spiral band can comprise a spiral wire. The spiral band can comprise a plurality of spiral wires. The spiral band can comprise a planar spiral band. The spiral band can comprise at least one channel or lumen disposed therein. The spiral band can comprise a hollow spiral band. The at least one channel or lumen can comprise a stiffening member disposed therein. The spiral band can have a circular, tubular, hollow, square, elongated, or triangular cross-section. The spiral band can comprise a tapered spiral band. The tapered spiral band can be configured to taper in height axially.
In some embodiments, the tapered spiral band can be configured to taper from a first end of the tapered spiral band to the free end. The first end can be a proximal end and the free end is a distal end. Subsequent turns of at least a portion of the tapered spiral band nest into each other to reduce a radial footprint of the tapered spiral band. The tapered spiral band can comprise a support structure and a semi-permeable material or impermeable material disposed therein. The semi-permeable material or impermeable material can comprise a webbing material, a fabric, a polymeric material, or an elastomeric material. The free end can be disposed radially outwards from the support structure. The tapered spiral band can further comprise a lumen and a wire disposed within the lumen. The frame structure can be configured for expanding within the native valve of the patient. The unexpanded configuration can be sized and dimensioned for percutaneous insertion and the expanded configuration is sized and dimensioned for implantation in the native valve of the patient.
In some embodiments, the frame structure can comprise a first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the frame structure is anchored to the native valve. The frame structure can sit below the native valve when the frame structure is anchored to the native valve.
In some embodiments, the system can further comprise a valve segment within the frame structure comprising a biocompatible one-way valve. At least a portion of the valve segment can be positioned within at least a portion of the frame structure. The valve segment can comprise at least one leaflet having an inner layer and an outer layer, and wherein the frame structure is attached to the outer layer at one or more ends of the frame structure. The valve segment can comprise a plurality of leaflets.
In another aspect, a method for treating a diseased native valve in a patient is provided. The method includes: advancing a distal end of a guidewire from a first side of a native valve to a second side of the native valve; advancing an outer sheath assembly over the guidewire to a native valve; separating a distal end of the outer sheath assembly from an outer sheath of the outer sheath assembly; advancing an anchor delivery sheath from within the outer sheath to deploy an anchor from the anchor delivery sheath; expanding a frame structure of a valve prosthesis within the native valve from an unexpanded configuration to an expanded configuration; securing the anchor to the native valve; and retracting the guidewire from the native valve. Deploying the anchor from the anchor delivery sheath can be followed by advancing the anchor from a first side of the native valve to a second side of the native valve. The first side of the native valve can be the left atrium and the second side of the native valve is the left ventricle.
In some embodiments, the method can further comprise, in (c), separating the distal end of the outer sheath assembly from the outer sheath to release the valve prosthesis from constraint, wherein the valve prosthesis is maintained within one or more of the outer sheath or the distal end of the outer sheath assembly by radial constriction. Separating of the distal end of the outer sheath assembly from the outer sheath can be caused by pushing an inner shaft through a lumen of the outer sheath. The anchor can be deployed from the anchor delivery sheath from a delivery configuration to an intermediate configuration and further into a deployed configuration. The anchor can be released into the intermediate configuration on the first side of the native valve and subsequently pushed to the second side of the native valve. Separating a distal end of the outer sheath assembly from the outer sheath in (c) can be caused by pushing an inner shaft through the lumen of the outer sheath. The outer sheath can be steerable. Advancing the outer sheath assembly over the guidewire to the native valve in (b) can be followed by steering the outer sheath assembly to an edge of the native valve and advancing the distal end of the outer sheath assembly from the first side of the native valve to the second side of the native valve. The outer sheath assembly can be steered to the edge of the native valve to position the anchor delivery sheath for delivery of the anchor.
In some embodiments, the method can further comprise axially separating the distal end of the outer sheath assembly from the outer sheath after the distal end of the outer sheath assembly is located in the second side of the native valve. The anchor can be deployed from the anchor delivery sheath directly into a deployed configuration such that the anchor is wrapped around the chordae tendineae of the native valve. The anchor can be a spiral band. The spiral band can comprise a free end and anchoring can comprise rotating the free end of the anchor around one or more structures of the native valve. The one or more structures can comprise one or more native chordae tendineae of native valve.
In some embodiments, a central point of the spiral band can be co-axial with a longitudinal axis of the delivery device when the spiral band is in the deployed configuration. The valve prosthesis can comprise a valve segment therewithin comprising a biocompatible one-way valve. The native valve can be in a heart of a patient. The method can further comprise transseptally inserting the distal end of the guidewire into a left atrium of the heart. The native valve can comprise a mitral valve, wherein the first side of the native valve comprises a left atrium, and wherein the second side of the native valve comprises a left ventricle. The first side of the native valve can comprise an atrium of the heart, and the second side of the native valve can comprise a ventricle of the heart.
In another aspect, a device for treating a diseased native valve in a patient is provided. The device comprises an anchor comprising an outer jacket, a first lumen disposed within the outer jacket, and a second lumen disposed within the outer jacket. The first lumen is configured to have at least one support structure fixedly disposed therewithin. The second lumen comprises an open lumen configured to allow one or more elongate members to be disposed and longitudinally translatable therein. The anchor comprises a delivery configuration and a deployed configuration. The anchor in the deployed configuration is shaped to encircle chordae or leaflets of a diseased native valve in a patient.
In some embodiments, the anchor may be configured to be actuated from the delivery configuration to the deployed configuration adjacent the native valve.
In some embodiments, the outer jacket may comprise a flexible material. The flexible material may comprise an extruded plastic or a soft textile. The flexible material may comprise polyethylene terephthalate (PET), polytetrafluoroethylene (PTFE), or pericardium.
In some embodiments, the first lumen and the second lumen may comprise a single lumen configured to remain at least partially open when the at least one support structure fixedly is disposed therewithin.
In some embodiments, the anchor may comprise an elongated shape in the delivery configuration.
In some embodiments, the anchor may comprise a curved shape in the deployed configuration. The curved shape may comprise a helical shape. The curved shape may comprise a spiral shape.
In some embodiments, the device may further comprise the at least one support structure fixedly disposed within the first lumen. The at least one support structure may comprise a wire or a hypotube.
In some embodiments, the device may further comprise the one or more elongate members disposed within the second lumen. The one or more elongate members may comprise a first wire configured to be advanced through the second lumen and out an opening in the free end into a self-assembly configuration. A distal tip of the first wire may be configured to extend radially outward, proximally, or distally of a curved shape of the anchor in the self-assembly configuration, thereby facilitating positioning of the anchor relative to a delivery device during actuation from the delivery configuration to the deployed configuration. The first wire comprises may comprise or more deflection features disposed adjacent the distal tip. The one or more deflection features may be configured to interact with the free end of the anchor and cause deflection of the distal tip when the first wire is advanced out of the second lumen of the anchor into the self-assembly configuration such that it extends radially outward, proximally, or distally of the curved shape of the anchor. In some embodiments, the one or more deflection features may comprise one or more pre-formed waves, bends, kinks, or humps adjacent the distal tip of the first wire. In some embodiments, the one or more deflection features may comprise one or more kinks along the distal tip of the first wire such that at least a portion of the distal tip is discontinuous with a curved shape of a proximal curved portion of the first wire.
In another aspect, a system for treating a diseased native valve in a patient is provided. The system comprises an anchor comprising an outer jacket and at least two lumens disposed within the outer jacket, the anchor comprising a delivery configuration and a deployed configuration, at least one support structure fixedly disposed within a first lumen of the at least two lumens, a first wire disposed within a second lumen of the at least two lumens, and a second wire disposed within the second lumen, wherein the first and second wires are configured to be longitudinally translatable independent of one another within the second lumen. The anchor in the deployed configuration is shaped to encircle chordae or leaflets of a diseased native valve in a patient.
In some embodiments, the outer jacket may comprise a flexible material. The flexible material may comprise an extruded plastic or a soft textile. The flexible material may comprise polyethylene terephthalate (PET).
In some embodiments, the first wire or the second wire may comprise a super-elastic material. The first wire or the second wire may comprise nitinol.
In some embodiments, the first wire and the second wire may be disposed within a housing. The housing may be flexible and translation of the first wire and the second wire relative to one another may change the curvature of the housing.
In some embodiments, the first wire and the second wire may be coupled to one another at a distal tip.
In some embodiments, the system may further comprise a third wire.
In some embodiments, the first and second wires may comprise pull wires.
In some embodiments, a distal tip of the first wire or the second wire may be configured to be advanced through the second lumen and out an opening in the free end when the first wire or the second wire is in a self-assembly configuration. The first wire or the second wire may be configured to be further advanced through the second lumen into an encircling configuration. The distal tip of the first wire or the second wire may be configured to extend radially outward, proximally, or distally of a curved shape of the anchor in the self-assembly configuration, thereby facilitating positioning of the anchor relative to a delivery device during actuation from the delivery configuration to the deployed configuration. In some embodiments, the distal tip may comprise an atraumatic tip, for example a ball tip. In some embodiments, the distal tip may be configured for piercing tissue.
In some embodiments, the at least one support structure may comprise a wire or a hypotube.
In some embodiments, the at least one support structure may comprise a super-elastic material such as nitinol.
In some embodiments, the anchor may be configured to wrap at least partially around a frame structure in the deployed configuration.
In some embodiments, the system may further comprise a frame structure having an unexpanded configuration and an expanded configuration. The anchor may be configured to wrap at least partially around the frame structure in the deployed configuration. A proximal end of the anchor may be coupled to a distal end of the frame structure. The frame structure may comprise an expandable stent. The frame structure expanded configuration may be a generally tubular shape. In some embodiments, the frame structure may be self-expanding. In some embodiments, the frame structure may be balloon-expandable. The anchor may be configured to be fully advanced from an atrial side of the native valve into a ventricle of the heart and to anchor the frame structure to the native valve when the frame structure is in the expanded configuration adjacent the native valve. A valve segment may be positioned within at least a portion of the frame structure. The valve segment may comprise a biocompatible one-way valve. The valve segment may comprise at least one leaflet having an inner layer and an outer layer, and the frame structure may be attached to the outer layer at one or more ends of the frame structure. In some embodiments, the valve segment may comprise a plurality of leaflets.
In some embodiments, the system may further comprise a delivery device. The delivery device may comprise an outer sheath and the anchor may be disposed in a lumen of the outer sheath and maintained in the delivery configuration by radial constriction from the outer sheath. Advancement of the anchor out of the lumen of the outer sheath may actuate the anchor into the deployed configuration. A pusher portion of the first wire or second wire may extend from a proximal portion of the anchor to a proximal end of the delivery device. The outer sheath may be steerable. In some embodiments, the system may further comprise a frame structure detachably coupled to the delivery device in an unexpanded configuration during delivery to the native valve. In some embodiments, the system may further comprise a frame structure and expansion of the frame structure to an expanded configuration may detach the frame structure from the delivery device. In some embodiments, the delivery device may further comprise an inner shaft. The inner shaft may be disposed within the lumen of the outer sheath. Advancement of the inner shaft towards an opening of the lumen of the outer sheath may advance the anchor out of the lumen of the outer shaft and actuate the anchor into the deployed configuration. In some embodiments, the system may further comprise a frame structure. The frame structure may be maintained in an unexpanded configuration by radial constriction from the outer sheath and advancement of the inner shaft out of the lumen of the outer sheath may actuate the frame structure into an expanded configuration. The anchor may be configured to wrap at least partially around the inner shaft in the deployed configuration. A central axis of the anchor may be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration.
In another aspect, a method for treating a diseased native valve in a patient is provided. The method comprises advancing a distal portion of a delivery device from a first side of a native valve to a second side of the native valve, wherein the distal portion of delivery device is detachably coupled to an anchor, the anchor comprising a delivery configuration, a deployed configuration, an outer jacket, a first lumen disposed within the outer jacket, a free end, and at least one support structure fixedly disposed within the first lumen; actuating the anchor from the delivery configuration to the deployed configuration adjacent the native valve by advancing the free end of the anchor out of the delivery device; and retracting the delivery device from the native valve.
In some embodiments, the anchor may further comprise a second lumen disposed within the outer jacket, the second lumen comprising an open lumen configured to allow one or more elongate members to be disposed and longitudinally translatable therein. The first lumen and the second lumen may comprise a single lumen configured to remain at least partially open when the at least one support structure fixedly is disposed therewithin. In some embodiments, the one or more elongate members may comprise a first wire, and the method may further comprise advancing the first wire through the second lumen and out an opening in the free end. The first wire may comprise one or more deflection features disposed adjacent a distal tip thereof, the one or more defection features may be configured to interact with the free end of the cause deflection of the distal tip when the first wire is advanced out of the second lumen of the anchor into a self-assembly configuration, and the method may further comprise deflecting the distal tip of the first wire by moving the one or more deflection features disposed along the distal tip past the opening of the second lumen into the self-assembly configuration such that it extends radially outward, proximally, or distally of the curved shape of the anchor. In some embodiments, the one or more elongate members may comprise a first wire and a second wire, and the method may further comprise advancing the first wire and the second wire through the second lumen and out an opening in the free end. The first wire and the second wire may be configured to be longitudinally translatable independent of one another. In some embodiments, the first wire and the second wire may be disposed in a housing. The housing may flexible, and the method may further comprise translating the first and second wires relative to one another, thereby changing a curvature of the housing. Alternatively, or in combination, the first wire and the second wire may be coupled to one another at a distal tip, and the method may further comprise translating the first and second wires relative to one another, thereby changing the position of the distal tip. In some embodiments, a third wire may be coupled to the first and second wires at the distal tip. In some embodiments, the method may further comprise deflecting a distal tip of the first wire or second wire into a self-assembly configuration or an encircling configuration. The distal tip of the first wire or second wire to may extend radially outward, proximally, or distally of a curved shape of the anchor in the self-assembly configuration, thereby facilitating positioning of the anchor relative to a delivery device during actuation from the delivery configuration to the deployed configuration. The distal tip may comprise an atraumatic tip, for example a ball tip. The distal tip may be configured for piercing tissue. In some embodiments, the method may further comprise rotating a distal tip of the first wire or second wire in an encircling configuration around one or more structures on the second side of the native valve.
In some embodiments, the method may further comprise rotating the free end of the deployed anchor around one or more structures on the second side of the native valve. The one or more structures may comprise one or more valve leaflets of the native valve. The one or more structures may comprise one or more chordae of the left ventricle.
In some embodiments, the at least one support structure may comprise a wire or a hypotube.
In some embodiments, the method may comprise steering the distal end of the delivery device such that the distal end of the delivery device points towards the first side of the native valve.
In some embodiments, the anchor may be configured to wrap at least partially around the delivery device in the deployed configuration.
In some embodiments, the anchor may be configured to wrap at least partially around a frame structure in the deployed configuration.
In some embodiments, a central axis of the anchor may be co-axial with a longitudinal axis of the distal portion of the delivery device when the anchor is in the deployed configuration. The method may further comprise expanding the frame structure within the native valve from an unexpanded configuration to an expanded configuration. The frame structure may comprise a first and second opposite ends and expanding the frame structure may comprise expanding the frame structure such that the first end extends above the first side of the native valve and the second end extends below second side of the native valve. Expanding the frame structure may comprise expanding at least a portion the frame structure within at least a portion of the deployed anchor to anchor the frame structure to the native valve. The method may further comprise releasing the frame structure from the distal end of the delivery device. Expanding the frame structure and releasing the frame structure may occur simultaneously.
In some embodiments, actuating the anchor may comprise releasing a frame structure detachably coupled to the distal end of the delivery device from radial constriction by the delivery device.
In some embodiments, actuating the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the second side of the native valve.
In some embodiments, actuating the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the first side of the native valve and may further comprise advancing the anchor in the deployed configuration through the native valve to the second side of the native valve. Advancing the anchor may comprise pushing the anchor through the native valve. Advancing the anchor may further comprise rotating the anchor through the native valve.
In some embodiments, the native valve may be in a heart of a patient. The method may further comprise transseptally inserting the distal end of the delivery device into a left atrium of the heart. The native valve may comprise a mitral valve, the first side of the native valve may comprise a left atrium, and the second side of the native valve may comprise a left ventricle.
In another aspect, a system for treating a diseased native valve in a patient is provided. The system comprises an inner shaft and a guidewire comprising a distal end configured to be fully advanced from an atrial side of the native valve into a ventricle of a heart. The inner shaft comprises a lumen. The inner shaft may comprise a guidewire lumen. The inner shaft lumen may comprise an anchor deployment component. The guidewire may be advanceable through the guidewire lumen. A valve prosthesis is coupled to the inner shaft. The valve prosthesis comprises an unexpanded delivery configuration and an expanded configuration. The anchor is coupled to the inner shaft and comprises a spiral band having a free end. The valve prosthesis is configured to be actuated from the unexpanded configuration to the expanded configuration adjacent a native valve in a patient. The anchor is configured to be deployed from an anchor deployment component. The anchor may be configured to be deployed from a lateral opening of the inner shaft. The lateral opening may be a side port of the inner shaft. Alternatively, the anchor deployment component may comprise an anchor drive shaft, deployment drive, and an outer shaft configured to retract along the inner shaft to form the lateral opening. The anchor is configured to secure the valve prosthesis to the native valve when the valve prosthesis is deployed into the expanded configuration adjacent the native valve.
In some embodiments, the anchor may be configured to be fully advanced from an atrial side of the native valve into a ventricle of the heart.
In some embodiments, the anchor comprises a delivery configuration and a deployed configuration. The anchor may comprise a spiral shape in the deployed configuration.
In some embodiments, the anchor is configured to be actuated from the delivery configuration to the deployed configuration adjacent the native valve. The anchor may be configured to be deployed adjacent the native valve.
In some embodiments, the delivery device comprises the inner shaft. The anchor is disposed in the inner shaft and maintained in the delivery configuration by radial constriction from the inner shaft, and wherein advancement of the anchor out of the side port of the inner shaft actuates the anchor into the deployed configuration.
In some embodiments, the valve prosthesis is maintained in the unexpanded configuration by radial constriction from the inner shaft. After the anchor is deployed, advancement of a proximal pusher within the inner shaft deploys the valve prosthesis into the expanded configuration.
In some embodiments, the valve prosthesis is detachably coupled to the proximal pusher in the unexpanded configuration during delivery to the native valve. The expansion of the valve prosthesis to the expanded configuration may detach the valve prosthesis from the proximal pusher.
In some embodiments, the inner shaft is steerable. A central point of the spiral band may be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration. In some embodiments, the spiral band comprises a one or more loops. The one or more loops may comprise at least 360 degrees of rotation. The spiral band may comprise a plurality of loops. There may be one or more spaces between the plurality of loops.
In some embodiments, the anchor comprises a super-elastic material. In some embodiments, the anchor comprises nitinol.
In some embodiments, the valve prosthesis comprises an expandable frame structure. The expanded configuration may be a generally tubular expanded shape. The valve prosthesis may comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration, wherein the compressed outer periphery is smaller in diameter than the expanded outer periphery.
In some embodiments, the valve prosthesis may be balloon-expandable or, alternatively, may be self-expanding.
In some embodiments, the free end of the anchor comprises an atraumatic tip, such as a ball tip. In other embodiments, the free end of the anchor is configured for piercing tissue. Alternatively, or in combination, the free end of the anchor may be bent distally. In some embodiments, the free end of the anchor may be bent proximally.
In some embodiments, the spiral band comprises a spiral wire or a plurality of spiral wires. In some embodiments, the spiral band comprises a planar spiral band. The spiral band may comprise at least one channel or lumen disposed therein. The at least one channel or lumen may comprise a stiffening member disposed therein. In some embodiments, the spiral band comprises a hollow spiral band. In some embodiments, the spiral band has a circular, tubular, hollow, square, elongated, or triangular cross-section. Alternatively, the spiral band may comprise a tapered spiral band. The tapered spiral band may be configured to taper in height axially. The tapered spiral band may be configured to taper from a first end of the tapered spiral band to the free end. In some embodiments, the first end is a proximal end and the free end is a distal end. The free end of the anchor may be disposed radially outwards from the support structure.
In some embodiments, subsequent turns of at least a portion of the tapered spiral band may nest into each other to reduce a radial footprint of the tapered spiral band. The tapered spiral band may comprise a support structure and a semi-permeable material or impermeable material disposed therein. The semi-permeable material or impermeable material may comprise a webbing material, a fabric, a polymeric material, or an elastomeric material. The tapered spiral band can further include a lumen and a wire disposed within the lumen.
In some embodiments, the valve prosthesis is configured for expanding within the native valve of the patient. The unexpanded configuration may be sized and dimensioned for percutaneous insertion and the expanded configuration is sized and dimensioned for implantation in the native valve of the patient. The valve prosthesis may comprise first and second opposite ends, the first end being configured to extend above a native valve and the second end being configured to extend below the native valve when the valve prosthesis is anchored to the native valve. The valve prosthesis may be configured to sit below the native valve when the frame structure is anchored to the native valve.
In some embodiments, a valve segment within the valve prosthesis comprises a biocompatible one-way valve. In some embodiments, at least a portion of the valve segment is positioned within at least a portion of the valve prosthesis. The valve segment may comprise at least one leaflet having an inner layer and an outer layer, and wherein the frame structure is attached to the outer layer at one or more ends of the valve prosthesis. The valve segment may comprise a plurality of leaflets.
In another aspect, a method for treating a diseased native valve in a patient is provided. The method comprises (i) advancing a distal end of a guidewire from a first side of a native valve to a second side of the native valve, (ii) advancing a distal end of an inner shaft over the guidewire to the first side of a native valve, (iii) deploying an anchor from an anchor deployment component of the inner shaft, (iv) securing the anchor to adjacent to the native valve, (v) expanding a valve prosthesis within the native valve from an unexpanded configuration to an expanded configuration, (vi) releasing the valve prosthesis from the inner shaft, (vii) retracting the inner shaft from the native valve, and (viii) retracting the guidewire from the native valve.
In some embodiments, securing the anchor comprises deploying the anchor from a delivery configuration to a deployed configuration. In some embodiments, deploying the anchor comprises actuating the anchor from the delivery configuration to the deployed configuration. Deploying the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the second side of the native valve.
In some embodiments, deploying the anchor comprises deploying the anchor from a side port of the inner shaft. Alternatively, deploying the anchor may comprise actuating an outer shaft, an anchor drive shaft, and a deployment drive.
In some embodiments, anchoring the anchor comprises actuating the anchor from the delivery configuration to the deployed configuration on the first side of the native valve and advancing the anchor in the deployed configuration through the native valve to the second side of the native valve. Advancing the anchor may comprise pushing the anchor through the native valve. Advancing the anchor may further comprise rotating the anchor through the native valve. Securing the anchor may comprise positioning the anchor such that it is located only on the second side of the native valve.
In some embodiments, the valve prosthesis comprises a first and second opposite ends, and wherein expanding the valve prosthesis comprises expanding the valve prosthesis such that the first end extends above the first side of the native valve and the second end extends below second side of the native valve. Expanding the valve prosthesis may comprise expanding at least a portion the valve prosthesis within at least a portion of the deployed anchor to anchor the valve prosthesis to the native valve. Expanding the valve prosthesis and releasing the valve prosthesis may occur simultaneously. The valve prosthesis may be balloon-expandable and expanding the valve prosthesis may comprise inflating a balloon disposed within the inner shaft, wherein inflation of the balloon causes expansion of the valve prosthesis. Alternatively, the valve prosthesis may be self-expanding and expanding the valve prosthesis may comprise releasing the valve prosthesis from radial constriction by the inner shaft using a proximal pusher. In some embodiments, the valve prosthesis may comprise a valve segment therewithin comprising a biocompatible one-way valve.
In some embodiments the anchor may be a spiral band. A central point of the spiral band may be co-axial with a longitudinal axis of the delivery device when the anchor is in the deployed configuration. The spiral band may comprise a free end and anchoring may comprise rotating the free end of the anchor around one or more structures on the second side of the native valve. The one or more structures may comprise one or more native chordae tendineae of the left ventricle. The free end of the spiral band may comprise an atraumatic tip, for example a ball tip. Alternatively, the free end of the spiral band is configured for piercing tissue. In some embodiments, the free end of the spiral band is bent distally. Alternatively, the free end of the spiral band may be bent proximally.
In some embodiments, the spiral band may comprise a spiral wire or a plurality of spiral wires. The spiral band may comprise a planar spiral band. The spiral band may comprise a hollow spiral band. In some embodiments, the spiral band may comprise at least one channel or lumen disposed therein. The at least one channel or lumen may comprise a stiffening member disposed therein. The spiral band may comprise a circular, tubular, hollow, square, elongated, or triangular cross-section. In some embodiments, the spiral band comprises a tapered spiral band.
In some embodiments, advancing the delivery device further comprises transseptally inserting the distal end of the guidewire into a left atrium of the heart.
In some embodiments, the native valve is in a heart of a patient. In some embodiments, the native valve comprises a mitral valve, wherein the first side of the native valve comprises a left atrium, and wherein the second side of the native valve comprises a left ventricle. In some embodiments the first side of the native valve comprises an atrium of the heart, and the second side of the native valve comprises a ventricle of the heart. The first side of the native valve may comprise a ventricle of the heart, and the second side of the native valve may comprise an atrium of the heart. Another aspect of the present disclosure comprises a device for treating a diseased native valve in a patient, the device comprising a guidewire, an inner shaft having a lumen through which the guidewire is advanceable, an anchor, and a valve prosthesis. The anchor may be deployed from the inner shaft through a port located on the side of the inner shaft. Alternatively, the anchor may be deployed by a retraction of an outer shaft followed by a series of rotations of an anchor drive shaft followed by an advancement of the outer shaft, followed by an exposure of a deployment drive. The valve prosthesis may be deployed after the anchor is deployed.
In some embodiments, the valve prosthesis is deployed by a proximal pusher located within the inner shaft. The valve prosthesis may comprise first and second opposite ends, wherein when expanded the first end extends above the first side of the native valve and the second end extends below second side of the native valve. Placement of the valve prosthesis may be facilitated by an opening and closing of the valve during a cardiac cycle.
In some embodiments, the valve prosthesis is detachably coupled to the proximal pusher. In some embodiments, when the valve prosthesis is in the expanded position it is released from the proximal pusher.
In some embodiments, the anchor is a spiral band. The spiral band may comprise a free end. The spiral band may be anchored to one or more native chordae tendinae of the left ventricle. The free end may comprise an atraumatic tip, for example a ball tip. The free end may comprise a key configured to fit into a lock located on the band of the anchor. The spiral band may comprise at least one channel or lumen disposed therein.
In another aspect, a system for treating a diseased native valve in a patient is provided. The system comprises an anchor and a core wire disposed within a lumen of the anchor. The anchor comprises a delivery configuration and deployed configuration. The anchor in the deployed configuration is shaped to encircle chordae or leaflets of a diseased native valve in a patient. The core wire is longitudinally translatable in the lumen of the anchor. The core wire comprises a proximal curved portion when unconstrained and a distal tip. The core wire comprises one or more deflection features disposed adjacent the distal tip and configured to be advanced out of the lumen of the anchor.
In some embodiments, the anchor may be configured to be actuated from the delivery configuration to the deployed configuration adjacent a native valve in a patient.
In some embodiments, a proximal end of the anchor may be coupled to a distal end of a frame structure.
In some embodiments, the anchor may comprise an elongated shape in the delivery configuration.
In some embodiments, the anchor may comprise a curved shape in the deployed configuration. For example, the curved shape may comprise a helical shape. Alternatively, or in combination, the curved shape may comprise a spiral shape. Alternatively, or in combination, the curved shape may comprise a coiled shape. In some embodiments, the proximal curved portion may have a shape which corresponds to the curved shape of the anchor.
In some embodiments, the one or more deflection features may comprise one or more pre-formed waves, bends, kinks, or humps in the distal tip portion of the core wire. The one or more deflection features may, for example, comprise one or more kinks along the distal tip of the core wire such that at least a portion of the distal tip is discontinuous with a curved shape of the proximal curved portion. Alternatively, or in combination, the one or more deflection features may comprise a plurality of waves.
In some embodiments, the core wire may comprise a self-assembly state and an encircling state. The one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire is positioned adjacent one or more loops of the proximal curved portion in the self-assembly state. Alternatively, or in combination, the one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire angles towards the proximal curved portion in the self-assembly state. In some embodiments, the one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire in the encircling state is continuous with a curved shape of the anchor in the deployed configuration. In some embodiments, the one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire angles away from the proximal curved portion in the encircling state.
In some embodiments, the one or more deflection features may be configured to interact with a free end of the anchor and cause deflection of the distal tip when the core wire is advanced out of the lumen of the anchor, thereby facilitating positioning of the anchor relative to a delivery device during actuation from the delivery configuration to the deployed configuration.
In some embodiments, the anchor may be configured to wrap at least partially around a frame structure in the deployed configuration.
In some embodiments, the core wire may comprise a super-elastic material. For example, the core wire may comprise nitinol.
In some embodiments, the system may further comprise a frame structure having an unexpanded configuration and an expanded configuration. The frame structure may comprise an expandable stent. The expanded configuration may have a generally tubular expanded shape. In some embodiments, the frame structure may comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration. The compressed outer periphery may be smaller in diameter than the expanded outer periphery. In some embodiments, the frame structure may be balloon-expandable. In some embodiments, the frame structure may be self-expanding.
In some embodiments, the system may further comprise a delivery device. The delivery device may comprise an outer sheath. The anchor may be disposed in a lumen of the outer sheath and maintained in the delivery configuration by radial constriction from the outer sheath. Advancement of the anchor out of the lumen of the outer sheath may actuate the anchor into the deployed configuration. In some embodiments, a pusher portion of the core wire may extend from the proximal curved portion to a proximal end of the delivery device. Optionally, the delivery device may further comprise an inner shaft disposed within the lumen of the outer sheath. A proximal portion of a frame structure or a proximal end of the anchor may be coupled to a distal portion of the inner shaft. In some embodiments, advancement of the inner shaft towards an opening of the lumen of the outer sheath may advance the anchor out of the lumen of the outer shaft and actuate the anchor into the deployed configuration. In some embodiments, the system may further comprise a frame structure and the frame structure may be maintained in an unexpanded configuration by radial constriction from the outer sheath. Advancement of the inner shaft out of the lumen of the outer sheath may actuate the frame structure into an expanded configuration. In some embodiments, the outer sheath may be steerable. In some embodiments, the anchor may be configured to wrap at least partially around the inner shaft in the deployed configuration. In some embodiments, a central axis of the anchor may be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration. In some embodiments, the system may further comprise a frame structure detachably coupled to the delivery device in an unexpanded configuration during delivery to the native valve. In some embodiments, the system may further comprise a frame structure, wherein expansion of the frame structure to an expanded configuration may detach the frame structure from the delivery device.
In some embodiments, the distal tip may comprise an atraumatic tip. For example, the distal tip may comprise a ball tip.
In some embodiments, the distal tip may be configured for piercing tissue.
In some embodiments, the proximal curved portion may comprise a spiral wire.
In some embodiments, the proximal curved portion may comprise a helical wire.
In some embodiments, the core wire may comprise a first wire and a second wire. The first wire and the second wire may be configured to be longitudinally translatable independent of one another. The first wire and the second wire may be disposed in a housing. The housing may be flexible. Translation of the first and second wires relative to one another may change the curvature of the housing.
In some embodiments, a free end of the anchor may extend radially outward from the curved shape.
In some embodiments, the system may further comprise a frame structure configured for expanding within the native valve of the patient.
In some embodiments, the system may further comprise a frame structure. The anchor may be configured to be fully advanced from an atrial side of the native valve into a ventricle of the heart and anchor the frame structure to the native valve when the frame structure is in an expanded configuration adjacent the native valve. An unexpanded configuration of the frame structure may be sized and dimensioned for percutaneous insertion and the expanded configuration may be sized and dimensioned for implantation in the native valve of the patient. In some embodiments, the frame structure may comprise a first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the frame structure is anchored to the native valve. Alternatively, the frame structure may sit below the native valve when the frame structure is anchored to the native valve.
In some embodiments, the system may further comprise a frame structure and a valve segment within the frame structure comprising a biocompatible one-way valve. At least a portion of the valve segment may be positioned within at least a portion of the frame structure. The valve segment may comprise at least one leaflet having an inner layer and an outer layer, and the frame structure may be attached to the outer layer at one or more ends of the frame structure. Alternatively, or in combination, the valve segment may comprise a plurality of leaflets.
In another aspect, a method for treating a diseased native valve in a patient is provided. The method comprises advancing a distal end of a delivery device from a first side of a native valve to a second side of the native valve, wherein the distal end of the delivery device is detachably coupled to an anchor, the anchor comprising a delivery configuration, a deployed configuration, a lumen, an opening, a free end, and a core wire disposed within the lumen, the core wire comprising a proximal curved portion and a distal tip portion, the distal tip portion comprising a distal tip and one or more deflection features disposed therealong and configured to interact with the free end and cause deflection of the distal tip when the core wire is advanced out of the lumen of the anchor through the opening; actuating the anchor from the delivery configuration to the deployed configuration adjacent the native valve by (i) advancing the free end of the anchor out of delivery device, (ii) deflecting the distal tip of the core wire by moving the one or more deflection features disposed along the distal tip portion past the opening of the lumen of the anchor into a self-assembly state, and (iii) advancing a remainder of the anchor out of the lumen of the outer shaft through the opening; and retracting the delivery device from the native valve.
In some embodiments, the method may further comprise steering the distal end of the delivery device such that the distal end of the delivery device points towards the first side of the native valve.
In some embodiments, the anchor may be configured to wrap at least partially around the delivery device in the deployed configuration.
In some embodiments, the anchor may be configured to wrap at least partially around a frame structure in the deployed configuration.
In some embodiments, a central axis of the anchor may be co-axial with a longitudinal axis of the inner shaft when the anchor is in the deployed configuration.
In some embodiments, actuating the anchor may comprise releasing a frame structure detachably coupled to the distal end of the delivery device from radial constriction by the delivery device.
In some embodiments, actuating the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the second side of the native valve.
In some embodiments, actuating the anchor may comprise actuating the anchor from the delivery configuration to the deployed configuration on the first side of the native valve and may further comprise advancing the anchor in the deployed configuration through the native valve to the second side of the native valve. Advancing the anchor may comprise pushing the anchor through the native valve. Alternatively, or in combination, advancing the anchor may comprise rotating the anchor through the native valve.
In some embodiments, actuating the anchor may comprise positioning the anchor such that it is located only on the second side of the native valve.
In some embodiments, the distal end of the delivery device may be detachably coupled to a frame structure. The method may further comprise expanding the frame structure within the native valve from an unexpanded configuration to an expanded configuration. In some embodiments, the frame structure may comprise a first and second opposite ends and expanding the frame structure may comprise expanding the frame structure such that the first end extends above the first side of the native valve and the second end extends below second side of the native valve. In some embodiments, expanding the frame structure may comprise expanding at least a portion the frame structure within at least a portion of the deployed anchor to anchor the frame structure to the native valve. In some embodiments, the method may further comprise releasing the frame structure from the distal end of the delivery device. Expanding the frame structure and releasing the frame structure may occur simultaneously. In some embodiments, the frame structure may be balloon-expandable and expanding the frame structure may comprise inflating a balloon disposed within the frame structure, wherein inflation of the balloon causes expansion of the frame structure. In some embodiments, the frame structure may be self-expanding and expanding the frame structure may comprise releasing the frame structure from radial constriction by the delivery device. In some embodiments, the frame structure may comprise a valve segment therewithin comprising a biocompatible one-way valve.
In some embodiments, the one or more deflection features may comprise one or more pre-formed waves, bends, kinks, or humps in the distal tip portion of the core wire. The one or more deflection features may, for example, comprise one or more kinks along the distal tip of the core wire such that at least a portion of the distal tip is discontinuous with a curved shape of the proximal curved portion. Alternatively, or in combination, the one or more deflection features may comprise a plurality of waves.
In some embodiments, the core wire may comprise a self-assembly state and an encircling state.
In some embodiments, the one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire is positioned adjacent one or more loops of the proximal curved portion in the self-assembly state.
In some embodiments, the one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire angles towards the proximal curved portion in the self-assembly state.
In some embodiments, the one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire in the encircling state is continuous with a curved shape of the anchor in the deployed configuration.
In some embodiments, the one or more deflection features may comprise a bend near the distal tip of the core wire such that the distal tip of the core wire angles away from the proximal curved portion in the encircling state.
In some embodiments, the method may further comprise rotating the distal tip of the core wire around one or more structures on the second side of the native valve.
In some embodiments, the method may further comprise rotating the free end of the deployed anchor around one or more structures on the second side of the native valve. The one or more structures may comprise one or more valve leaflets of the native valve. Alternatively, or in combination, the one or more structures may comprise one or more chordae of the left ventricle.
In some embodiments, the distal tip may comprise an atraumatic tip. For example, the distal tip may comprise a ball tip.
In some embodiments, the distal tip may be configured for piercing tissue.
In some embodiments, the proximal curved portion may comprise a spiral wire.
In some embodiments, the proximal curved portion may comprise a helical wire.
In some embodiments, the core wire may comprise a first wire and a second wire. The first wire and the second wire may be configured to be longitudinally translatable independent of one another. The first wire and the second wire may be disposed in a housing. The housing may be flexible. The method may further comprise translating the first and second wires relative to one another, thereby changing a curvature of the housing.
In some embodiments, a free end of the anchor may extend radially outward from the curved shape.
In some embodiments, the native valve may be in a heart of a patient. In some embodiments, the method may further comprise transseptally inserting the distal end of the delivery device into a left atrium of the heart. In some embodiments, the native valve may comprise a mitral valve, the first side of the native valve may comprise a left atrium, and the second side of the native valve may comprise a left ventricle.
These and other embodiments are described in further detail in the following description related to the appended drawing figures.
INCORPORATION BY REFERENCEAll publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference.
The novel features of the present disclosure are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present disclosure will be obtained by reference to the following detailed description that sets forth illustrative embodiments, in which the principles of the present disclosure are utilized, and the accompanying drawings of which:
In the following detailed description, reference is made to the accompanying figures, which form a part hereof. In the figures, similar symbols typically identify similar components, unless context dictates otherwise. The illustrative embodiments described in the detailed description, figures, and claims are not meant to be limiting. Other embodiments may be utilized, and other changes may be made, without departing from the scope of the subject matter presented herein. It will be readily understood that the aspects of the present disclosure, as generally described herein, and illustrated in the figures, can be arranged, substituted, combined, separated, and designed in a wide variety of different configurations, all of which are explicitly contemplated herein.
Although certain embodiments and examples are disclosed below, inventive subject matter extends beyond the specifically disclosed embodiments to other alternative embodiments and/or uses, and to modifications and equivalents thereof. Thus, the scope of the claims appended hereto is not limited by any of the particular embodiments described below. For example, in any method or process disclosed herein, the acts or operations of the method or process may be performed in any suitable sequence and are not necessarily limited to any particular disclosed sequence. Various operations may be described as multiple discrete operations in turn, in a manner that may be helpful in understanding certain embodiments, however, the order of description should not be construed to imply that these operations are order dependent. Additionally, the structures, systems, and/or devices described herein may be embodied as integrated components or as separate components.
For purposes of comparing various embodiments, certain aspects and advantages of these embodiments are described. Not necessarily all such aspects or advantages are achieved by any particular embodiment. Thus, for example, various embodiments may be carried out in a manner that achieves or optimizes one advantage or group of advantages as taught herein without necessarily achieving other aspects or advantages as may also be taught or suggested herein.
The present disclosure is described in relation to deployment of systems, devices, or methods for treatment of a diseased native valve of the heart, for example a mitral valve, aortic valve, or tricuspid. However, one of skill in the art will appreciate that this is not intended to be limiting and the devices and methods disclosed herein may be used in other anatomical areas and in other surgical procedures.
For convenience in explanation and accurate definition in the appended claims, the terms “up” or “upper”, “down” or “lower”, “inside” and “outside” are used to describe features of the present disclosure with reference to the positions of such features as displayed in the figures.
In many respects the modifications of the various figures resemble those of preceding modifications and the same reference numerals followed by subscripts “a”, “b”, “c”, and “d” designate corresponding parts. It will be understood by one of ordinary skill in the art that modifications of corresponding parts of the various figures are interchangeable with one another between embodiments to arrive at multiple combinations with multiple modified parts.
While preferred embodiments of the present disclosure have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents be covered thereby.
In various embodiments, the unexpanded configuration may be 18Fr or smaller. In various embodiments, the unexpanded configuration may be 20Fr or smaller. In various embodiments, the unexpanded configuration may be 22Fr or smaller. In various embodiments, the unexpanded configuration may be 24Fr or smaller. In various embodiments, the unexpanded configuration may be 26Fr or smaller. In various embodiments, the unexpanded configuration may be 27Fr or smaller. In various embodiments, the unexpanded configuration may be 28Fr or smaller. In various embodiments, the unexpanded configuration may be 29Fr or smaller. In various embodiments, the unexpanded configuration may be 30Fr or smaller. In various embodiments, the unexpanded configuration may be sized and dimensioned for transseptal access. In various embodiments, the unexpanded configuration may be sized and dimensioned for femoral access.
Referring to
The valve segment 14 can be similar to existing transcatheter valves. The valve segment 14 can be similar to existing surgical tissue valves, and mechanical valves. At least a portion of the valve segment 14 may be positioned within at least a portion of the valve prosthesis 10, for example with the frame structure 12 of the valve prosthesis 10. The valve segment 14 may include leaflets formed of multi-layered materials for preferential function. The valve segment 14 may comprise at least one leaflet having an inner layer and an outer layer. The valve segment 14 may be attached directly to the valve prosthesis 10. Alternatively, the valve segment 14 may be attached to an intermediate valve structure that is in turn connected to the valve prosthesis 10. The valve segment 14 may be connected to the valve prosthesis 10 before or after the valve prosthesis 10 has been deployed adjacent a native valve. The valve prosthesis 10 may be attached to a leaflet of the valve segment 14, for example an outer layer of a leaflet, at one or more ends of the valve prosthesis 10. The valve prosthesis 10 may be attached to a leaflet of the valve segment 14, for example an outer layer of a leaflet, at one or more intermediate portions of the valve prosthesis 10. The valve segment may comprise a plurality of leaflets. The valve segment 14 may comprise a biocompatible one-way valve. Flow in one direction may cause the leaflet(s) to deflect open and flow in the opposite direction may cause the leaflet(s) to close.
The frame structure 12 may be configured like a stent. The frame structure 12 may, for example, comprise a scaffold in a diamond pattern formed from a shape memory material (e.g., NiTi). One of ordinary skill in the art will appreciate that many other structures, materials, and configurations may be employed for the frame structure 12. For example, the frame structure 12 may be formed of a polymer of sufficient elasticity. The frame structure 12 may be formed of a combination of metal and polymer, such as metal (e.g., shape memory material) covered in polymer. The frame structure 12 may include a variety of patterns besides diamond shapes. In some embodiments, frame structure 12 is a closed frame such that blood flow is forced through valve segment therein. One or more skirts and/or seals may help force blood through valve segment.
The anchor can be configured to fix the prosthesis 10 in place within the body (e.g., within a cardiac valve).
One of ordinary skill in the art will recognize based on the description herein that any of the valve prostheses described herein may comprise any of the frame structure shapes, frame structure designs, frame structure materials, anchor shapes, anchor windings, anchor materials, free end tips, leaflet(s) configurations, or any other of the variable features described herein in any combination thereof as desired.
The valve prosthesis may additionally or alternatively include any of the features of any of the valve prostheses described in PCT/US2019/047542, PCT/US2019/055049, PCT/US2019/057082, and PCT/US2019/068088, the entireties of which are incorporated by reference herein.
Referring to
The anchor 15 may comprise a delivery (e.g., elongated) configuration (shown in
Although referred to as an anchor, one will appreciate that anchor 15 does not require performing an anchor function in the traditional sense. As will be described in more detail below, the anchor 15 can guide valve prosthesis 10 into a desired position within a native valve. The anchor 15 may also mitigate against undesired entanglement and disturbances to the chordae tendineae and valve leaflets of the cardiac valve, such as the mitral valve.
In some embodiments, the anchor 15 may be configured to wrap at least partially around a distal portion of the delivery device 30, for example around the inner shaft 52, in the deployed configuration.
In some embodiments, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a first side of the native valve prior to being advanced to a second side of the native valve. For example, the anchor 15 may be deployed in a left atrium of a heart prior to being advanced to a left ventricle of the heart as described herein.
Alternatively, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a second side of the native valve after being advanced to the second side from a first side of the native valve. For example, anchor 15 may be advanced from a left atrium of a heart prior to being deployed in a left ventricle of the heart.
The anchor 15 may be detachably coupled to a proximal or distal portion of the frame structure 12. Alternatively, or in combination, the anchor 15 may be detachably coupled to the delivery device 30 in the delivery configuration during delivery to the native valve. For example, the proximal end 57 of the anchor 15 may be detachably coupled to the inner shaft 52 of the delivery device 30 and/or a tether 78 (see, e.g.,
The anchor 15 may be configured to rotate when the inner shaft 52 or other element of the delivery device 30 is rotated. Rotation of the anchor 15 may aid in advancement of the anchor 15 to the second side of the native valve. Alternatively, or in combination, rotation of the anchor 15 may aid in capture of one or more structures on the second side of the native valve by the free end 22 as described herein. By capturing one or more structures on the second side of the native valve, the anchor 15 may maintain its position relative to the native valve and provide an anchor point for the frame structure 12 when in the expanded configuration.
The wire 20 of anchor 15 may comprise a curved wire in the deployed configuration, for example a coiled wire or band, a helical wire or band, or a spiral wire or band as described herein. The wire 20 may be shaped to encircle chordae and/or leaflets of a diseased native valve. In various embodiments, the wire 20 may have a curved shape in the deployed configuration and an elongated—rather than curved—shape in the delivery configuration. For example, the wire 20 may be elongated into a straight shape within the delivery device 30. In various embodiments, a portion of the wire 20 may have a curved encircling shape. In various embodiments, a substantial portion of the wire or band 20 may have a curved encircling shape. In various embodiments, the wire 20 may be formed as a flat curve (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis). In various embodiments, the wire may be formed as a three-dimensional curve (in the deployed configuration) whereby the loops generally are positioned out of plane with one another.
The wire 20 may comprise a helical wire in the deployed configuration. As used herein, a helix or helical shape may comprise a curve for which the tangent at any point along the curve makes a constant angle with a fixed line (e.g., a central axis). The curve may turn around an axis at a constant or continuously varying distance while moving parallel to the axis. In some embodiments, the wire 20 may comprise one or more helical portions as described herein.
In various embodiments, free end 22 extends radially outward from frame structure 12, and in particular the remainder of wire 20. As will be described below, the free end 22 is configured to encircle a larger radius than the main coils of the wire 20. When the main coils of wire 20 have a generally curved shape (e.g., spiral, helical, tubular, frustoconoical, etc.), the free end 22 may extend radially outward from the curved shape. For example, when the main coils of wire 20 have a generally spiral shape, the free end 22 may extend radially outward from the spiral shape. When the main coils of wire 20 have a generally tubular shape, the free end 22 may extend radially outward from the tubular shape. When the main coils of wire 20 have a generally helical shape, the free end 22 may extend radially outward from the helical shape. When the main coils of wire 20 have a generally frustoconical shape, the free end 22 may extend radially outward from the frustoconical shape. When the main coils of wire 20 have a generally cylindrical shape, the free end 22 may extend radially outward from the cylindrical shape. The free end 22 may be configured to encircle a larger radius than the main coils of the helical wire 20. The larger diameter facilitates capturing of the valve leaflets and/or chordae tendineae within the sweep of the free end 22 when rotated as described herein.
In various embodiments, the wire or band 20 may have a generally helical shape in the deployed configuration. In various embodiments, the wire or band 20 may be elongated—rather than helix-shaped—in the delivery configuration. For example, the wire or band 20 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the wire or band 20 may have a helical shape. In various embodiments, a substantial portion of the wire or band 20 may have a helical shape. In various embodiments, the helical wire or band 20 may be formed as a three-dimensional helix (in the deployed configuration) whereby the loops generally are positioned around the same axis (for example, a longitudinal axis of the delivery device 30).
Optionally, the anchor 15 may comprise a first portion comprising the helical wire 20 and another portion. Alternatively, or in combination, the anchor 15 may comprise a plurality of helical wires 20. For example, the anchor 15 may comprise at least two helical wires 20 having the same or different diameters. Alternatively, or in combination, the anchor 15 may comprise at least two helical wires 20 having the same or different winding pitches.
The wire 20 may comprise a spiral wire or band in the deployed configuration. As used herein, a spiral or spiral shape may comprise a curve which emanates from a point (e.g., a central point) having a continuously increasing or decreasing distance from the point. The spiral or spiral shape may be two-dimensional (e.g., planar) or three-dimensional. In some embodiments, the wire or band 20 may comprise one or more spiral portions as described herein.
In various embodiments, the anchor and/or core wire may have a spiral-shaped deployed configuration. In various embodiments, spiral refers to a shape with windings about a central axis. The spiral may be continuous. The windings may gradually widen (or tighten) along the length. The spiral may be formed in a flat plane perpendicular to the central axis. In various embodiments, the anchor and/or core wire may have a deployed configuration that is not formed in a flat plane, or in other words the deployed shape is formed in a three-dimensional and/or non-degenerate space. In various embodiments, the anchor and/or core wire may have a conical-shaped deployed configuration including, but not limited to, tubular, conical, frustoconical, and/or helical shapes.
In various embodiments, the anchor 15 may comprise a flat spiral shape. Loops of the flat spiral shaped anchor may be generally positioned within the same plane (the plane being perpendicular to a longitudinal axis of a delivery device) as described herein.
The free end 22 of the spiral band or wire 20 may extend radially outward from the frame 12, and in particular from the remainder of the spiral band or wire 20. The other end of the spiral band or wire 20 may be coupled to the top or bottom of the frame structure 12 as described herein. Alternatively, or in combination, the other end of the spiral band or wire 20 may not be attached to the frame structure 12 as described herein. The free end 22 of the spiral band or wire 20 may facilitate capturing of the valve leaflets and/or chordal tendineae within the sweep of the free end during rotation as described herein. During rotation of the spiral band or wire 20, the leaflets and/or chordae tendineae may be captured by the free end 22 and trapped between the valve frame structure 12 and an interior surface of the spiral band or wire 20.
In various embodiments, the wire or band 20 may have a generally spiral shape in the deployed configuration. In various embodiments, the wire or band 20 may be elongated—rather than spiral-shaped—in the delivery configuration. For example, the wire or band 20 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the wire or band 20 may have a spiral shape. In various embodiments, a substantial portion of the wire or band 20 may have a spiral shape. In various embodiments, the spiral wire or band 20 may be formed as a flat spiral (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis).
Optionally, the anchor 15 may comprise a first portion comprising the spiral wire 20 and another portion. Alternatively, or in combination, the anchor 15 may comprise a plurality of spiral wires 20. For example, the anchor 15 may comprise at least two spiral wires 20 having the same or different diameters. Alternatively, or in combination, the anchor 15 may comprise at least two spiral wires 20 having the same or different winding pitches.
The wire 20 may comprise one or more loops. For example, the wire 20 may comprise a plurality of loops, which may increase the radial strength of the anchor by increasing friction and addition structural support. The one or more loops of the wire 20 may be substantially cylindrical around a central axis of the wire 20, for example along an axis which is coaxial with a longitudinal axis of a delivery device 30. The one or more loops of the wire 20 may be substantially helical around a central axis or helical axis of the wire 20, for example along an axis which is coaxial with a longitudinal axis of a delivery device. The one or more loops of the wire 20 may spiral radially outward from a central point or central axis of the wire 20, for example along an axis which is coaxial with a longitudinal axis of a delivery device 30 such that the wire 20 lies approximately along a plane perpendicular to the longitudinal axis of the delivery device 30.
The one or more loops (also referred to herein as coils or turns) of the wire or band 20 may comprise a curved shape that bends around back towards its origin (for example, an arc, ellipsoid, circle, or the like). In some embodiments, a loop may comprise a curved shape that bends back towards its origin but does not cross itself, making a rotation within a range of about 180 degrees to about 360 degrees. For example, a loop may comprise a curve or an arc having a central angle within a range of about 180 degrees to about 360 degrees. In at least some embodiments, the one or more loops may comprise an arc. In some embodiments, a loop may comprise a shape that bends back towards and crosses itself, making at least a 360 degree rotation. In at least some embodiments, the one or more loops may comprise a 360 degree rotation (for example, a circle). In some embodiments, the one or more loops may comprise a 360 degree to 720 degree rotation (for example, a loop crossing itself once and rotating further towards a second crossing and formation of a second 360 loop).
The one or more loops may comprise any number of loops desired, for example, one, two, three, four, five, six, seven, eight, nine, or ten loops. The one or more loops may comprise a rotation within a range of about 180 degrees to about 3600 degrees. The one or more loops may comprise a rotation within a range bounded by any of the following values: 180 degrees, 270 degrees, 360 degrees, 450 degrees, 540 degrees, 630 degrees, 720 degrees, 810 degrees, 900 degrees, 990 degrees, 1080 degrees, 1170 degrees, 1260 degrees, 1350 degrees, 1440 degrees, 1530 degrees, 1620 degrees, 1710 degrees, 1800 degrees, 1890 degrees, 1980 degrees, 2070 degrees, 2160 degrees, 2250 degrees, 2340 degrees, 2430 degrees, 2520 degrees, 2610 degrees, 2700 degrees, 2790 degrees, 2880 degrees, 2970 degrees, 3060 degrees, 3150 degrees, 3240 degrees, 3330 degrees, 3420 degrees, 3510 degrees, or 3600 degrees.
Interaction of the frame structure 12 with the one or more loops of the anchor 15 may create opposing forces therebetween that provide mechanical leverage for anchoring the frame structure 12 to the one or more anatomical structures. In some embodiments, the one or more loops may comprise at least 360 degrees of rotation when deployed such that the loops wrap around one another and provide additional mechanical leverage against the frame structure 12 in order to facilitate anchoring of the frame structure 12 as described herein. Additional loops or partial loops may provide additional mechanical strength and/or leverage.
In some embodiments, the one or more loops of the wire or band 20 may comprise one or more spaces therebetween. The spaces may facilitate movement of the captured tissue (e.g. chordae and/or leaflets) from the free end 22 to the center of the spiral structure during rotation of the anchor 15 as described herein.
The wire 20 may be configured to wrap at least partially around the frame structure 12 in the deployed configuration.
In some embodiments, the wire 20 may be configured to wrap at least partially around a distal portion of the delivery device 30, for example around the inner shaft, in the deployed configuration.
The free end 22 of the wire 20 may be sized and dimensioned for insertion through the native valve, for example through tissue at or near a commissure of the native valve or through the valve opening itself. In some embodiments, the free end 22 of the wire 20 may comprise an atraumatic tip to avoid reduce risk of injury to the native valve tissue and leaflets. For example, the free end may comprise a blunt end, a ball tip, a curved tip (e.g., J-tip or pigtail), or other atraumatic shapes. Alternatively, the free end 22 of the wire 20 may be configured for piercing tissue.
In various embodiments, the free end 22 is separate from and extends outward from the main coils of the anchor 15. In various embodiments, the main body coils of the anchor 15 circumscribe an area (in the case of a spiral coil) or a volume (in the case of a helical coil) having a diameter, and the free end 22 extends to a radius greater than the diameter of the anchor 15. In various embodiments, the free end 22 extends to a radius substantially greater than the diameter of the anchor 15. In various embodiments, the free end 22 is configured to circumscribe a larger diameter than the anchor 15. In various embodiments, the free end 22 is configured to circumscribe all of the chordae tendineae of the native valve to be treated.
In various embodiments, the free end 22 may be shaped and configured to reduce the risk of counter-rotation. For example, the tip 22 may have a curled end to cause the free end 22 to snag chordae if it is rotated in a direction opposite the anchoring rotation.
The free end 22 of the wire or band 20 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The wire or band 20 and/or free end 22 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the wire or band 20 and/or free end 22 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the wire or band 20. For example, the wire or band 20 may comprise one or more spaces between loops of the curved wire or band which facilitate radially-inward movement of the captured tissue (e.g. chordae and/or leaflets) from the free end 22 to the center of the curved structure with little or no torque and/or rotation of the structures during rotation of the wire or band 20 as described herein. Alternatively or in combination, the wire or band 20 may be configured such that, when fully deployed none of the structures reside between the loops of the curved encircling shape. Instead, the one or more structures may sit radially inward of the loops in order to facilitate capture of the one or more structures between the wire or band 20 and the expanded frame structure 12. The one or more structures may retain or nearly retain their normal anatomical position when the wire or band 20 is fully deployed.
Wire 20 may be formed of a material having sufficient rigidity to hold a predetermined shape. The wire may, for example, be formed of a shape memory material (e.g., NiTi). It may be desirable for at least an end portion (e.g., free end 22) to be relatively rigid such that it can exert a force to move chordal tendineae, while still retaining flexibility to be collapsed within a delivery device. In various embodiments, the end portion only needs sufficient rigidity to hold its shape and will deform under a load. For example, the end portion may be configured with a similar rigidity to a guidewire, or slightly stiffer.
In various embodiments, wire 20 has varying stiffness along its length. The wire 20 may have two or more segments of differing stiffness and/or the stiffness may transition over its length. In various embodiments, wire 20 is attached to frame 12 at multiple points such that free end 22 is relatively flexible and the wire 20 is more rigid along portions where it is attached to the frame structure 12.
The anchor 15 may be configured to taper in height axially. For example, the anchor 15 may be configured to taper in height from a first end of the anchor 15, which may be coupled to a delivery device and/or frame structure as described herein, to a free end 22 of the anchor 15. In some embodiments, the anchor 15 may taper in height from a proximal end to a distal end. Alternatively, the anchor 15 may taper in height from a distal end to a proximal end. The anchor 15 may be tapered such that subsequent turns of the tapered anchor 15 nest into each other so as to reduce a radial footprint of the tapered anchor 15. The anchor 15 may, for example, comprise a solid wire-like spiral band with a taper as described herein. In some embodiments, the anchor 15 may comprise a plurality of spiral support wires.
The spiral band 17 may be configured to anchor the frame structure 12 to the native valve when the frame structure 12 is in the expanded configuration adjacent the native valve. The frame structure 12 may be configured to be actuated from the unexpanded configuration to the expanded configuration adjacent a native valve in a patient. The spiral band 17 may be configured to be fully advanced from a first side of a native valve in a patient (e.g. an atrial side) to a second side of the native valve (e.g. into a ventricle of the heart) and anchor the frame structure 12 to the native valve when the frame structure 12 is in the expanded configuration adjacent the native valve as described herein.
During deployment and/or rotation of the spiral band 17, the leaflets and/or chordae tendineae may be captured by the free end 22 and trapped between the valve frame structure 12 and an interior surface of the spiral band 17. The free end 22 and the spiral band 17 may optionally rotated around one or more structures on the second side of the native valve such that the one or more valve structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The spiral band 17 and/or free end 22 may be configured such that minimal torque is applied to the one or more valve structures. Alternatively, or in combination, the spiral band 17 and/or free end 22 may be configured such that the one or more valve structures are not rotated, or are minimally rotated, during rotation of the spiral band 17. For example, the spiral band 17 may comprise one or more spaces 18 between loops of the spiral band 17, which facilitate movement of the captured tissue (e.g. chordae and/or leaflets) from the free end 22 to the center of the spiral band 17 with little or no torque and/or rotation of the structures during rotation of the spiral band 17. Alternatively, or in combination, the spiral band 17 may be configured such that, when fully deployed (for example, as shown in
The spiral band 17 may comprise a delivery (e.g. an elongated) configuration and a deployed configuration. The spiral band 17 may be configured to be actuated from the delivery configuration to the deployed configuration adjacent a native valve in a patient. In various embodiments, the spiral band 17 may have a generally spiral shape in the deployed configuration. In various embodiments, the spiral band 17 may be elongated—rather than spiral-shaped—in the delivery configuration. For example, the spiral band 17 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the band 17 may have a spiral shape. In various embodiments, a substantial portion of the spiral band 17 may have a spiral shape. In various embodiments, the spiral band 17 may be formed as a flat spiral (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis).
Spiral band 17 may be formed of a material having sufficient rigidity to hold a predetermined shape. The wire may, for example, be formed of a shape memory material (e.g. NiTi). It may be desirable for at least an end portion (e.g. free end 22) to be relatively rigid such that it can exert a force to move chordal tendineae, while still retaining flexibility to be collapsed within a delivery device. In various embodiments, the end portion only needs sufficient rigidity to hold its shape and will deform under a load. For example, the end portion may be configured with a similar rigidity to a guidewire, or slightly stiffer.
The one or more loops (also referred to herein as coils or turns) of the spiral band 17 may comprise a shape that bends around back towards its origin (for example, an arc, ellipsoid, circle, or the like). In some embodiments, a loop may comprise a shape that bends back towards its origin but does not cross itself, making a rotation within a range of about 180 degrees to about 360 degrees. For example, a loop may comprise an arc having a central angle within a range of about 180 degrees to about 360 degrees. In at least some embodiments, the one or more loops may comprise an arc. In some embodiments, a loop may comprise a shape that bends back towards and crosses itself, making at least a 360 degree rotation. In at least some embodiments, the one or more loops may comprise a 360 degree rotation (for example, a circle). In some embodiments, the one or more loops may comprise a 360 degree to 720 degree rotation (for example, a loop crossing itself once and rotating further towards a second crossing and formation of a second 360 loop).
The spiral band 17 may comprise a spiral wire. The spiral band 17 may comprise a plurality of spiral wires as described.
In some embodiments, the spiral band 17 may be configured to wrap at least partially around a distal portion of the delivery device 30, for example around the inner shaft, in the deployed configuration.
The spiral band 17 may comprise one or more loops. For example, the spiral band 17 may comprise a plurality of loops, which may increase the radial strength of the anchor by increasing friction and additional structural support. The one or more loops of the spiral band 17 may be spiral radially outward from a central point or central axis of the spiral, for example along an axis which is coaxial with a longitudinal axis of a delivery device 30 such that the spiral band 17 lies approximately along a plane perpendicular to the longitudinal axis of the delivery device 30.
The outer jacket 80 may be configured to provide circumferential constraint to the one or more support structures 81 and/or other structures (e.g., longitudinally translatable core wires 74 as shown and described with respect to
In some embodiments, the anchor 15 may comprise a single lumen 71 within the outer jacket 80. The single lumen 71 may comprise one or more support structures 81 disposed therein. Alternatively, or in combination, the first lumen 71 may comprise one or more translatable and/or removable core wires 74 (e.g., as shown in
In some embodiments, the anchor 15 may comprise at least two lumens 71. For example, the anchor 15 may comprise a first lumen 71 and a second lumen 71. In some embodiments, the anchor 15 may further comprise a third lumen 71, for example as shown in
It will be understood by one of ordinary skill in the art based on the teachings herein that the anchor 15 may comprise any number of lumens 71 desired. For example, the anchor 15 may comprise 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more lumens 71 disposed within the outer jacket 80.
In some embodiments, the one or more support structures 81 may comprise one or more stiffening members, wires, hypotubes, guidewires, or the like, or any combination thereof. The one or more support structures 81 may comprise a super-elastic material such as nitinol. The one or more support structures 81 may be shaped to correspond to the shape of the outer jacket 80 of the anchor 15.
In some embodiments, the one or more support structures 81 may comprise one or more stiffening members. The stiffening members may be configured to provide stiffness to the anchor 15. In some instances, providing one or more support structures 81 to the anchor 15 may make the anchor 15 radially stiffer than an anchor 15 that does not include a support structure 81 (e.g., that is only made up of a single band or wire 20). This may advantageously result in fewer anchor turns or loops being required to maintain sufficient engagement of the anchor 15 with the frame structure 12. It will be understood by one of ordinary skill in the art based on the teachings herein that the stiffness of the anchor 15 may be adjusted based on the material of the support structure(s) and/or number of support structure(s) disposed within the outer jacket 80.
The one or more support structures 81 may be fixedly disposed within a lumen 71 (or lumens) of the anchor 15. It will be understood by one of ordinary skill in the art based on the teachings herein that the any number of support structures 81 may be disposed within the anchor 15 as desired. For example, there may be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more support structures 81 disposed within one or more lumens 71 of the anchor 15 as desired.
The one or more support structures 81 may be formed of a material having sufficient rigidity to hold a predetermined shape. The one or more support structures 81 may, for example, be formed of a shape memory material (e.g., NiTi). It may be desirable for at least a distal end portion of the support structure 81 to be relatively rigid such that it can exert a force to move chordal tendineae, while still retaining flexibility to be collapsed within a delivery device 30. In various embodiments, the distal end portion of the support structure 81 has sufficient rigidity to hold its shape, but can be configured to deform under a load. For example, the end portion of the support structure 81 may be configured with a similar rigidity to a guidewire, or slightly stiffer.
The outer jacket 80 and/or support structures 81 of the anchor 15 may comprise a curved shape in the deployed configuration, for example a coiled shape, a helical shape, or a spiral shape as described herein. The outer jacket 80 and/or support structures 81 may be shaped to encircle chordae and/or leaflets of a diseased native valve. In various embodiments, the outer jacket 80 and/or support structures 81 may have a curved shape in the deployed configuration. In various embodiments, the outer jacket 80 and/or support structures 81 may be elongated—rather than curved—in the delivery configuration. For example, the outer jacket 80 and/or support structures 81 may be elongated into a straight shape within the delivery device 30. In various embodiments, a portion of the outer jacket 80 and/or support structures 81 may have a curved encircling shape. In various embodiments, a substantial portion of the outer jacket 80 and/or support structures 81 may have a curved encircling shape. In various embodiments, the outer jacket 80 and/or support structures 81 may be formed as a flat curve (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis). In various embodiments, the outer jacket 80 and/or support structures 81 may be formed as a three-dimensional curve (in the deployed configuration) whereby the loops generally are positioned out of plane with one another.
The outer jacket 80 and/or support structures 81 may comprise a helical shape in the deployed configuration. In some embodiments, the outer jacket 80 and/or support structures 81 may comprise one or more helical portions as described herein.
The free end 22 of the anchor 15 may extend radially outward from the frame structure 12, and in particular from the remainder of the outer jacket 80. In some embodiments, the helical outer jacket 80 may have a generally tubular shape. The free end may extend radially outward from the tubular shape. In some embodiments, the helical outer jacket 80 may have a generally frustoconical shape. The free end 22 may extend radially outward from the frustoconical shape. In some embodiments, the helical outer jacket 80 may have a generally cylindrical shape. The free end 22 may extend radially outward from the cylindrical shape. The free end 22 may be configured to encircle a larger radius than the main coils (also referred to herein as loops or turns) of the helical outer jacket 80. The larger diameter may facilitate capturing of one or more structures, for example the valve leaflets of the chordal tendineae within the sweep of the free end 22 when rotated as described herein.
In various embodiments, the outer jacket 80 and/or support structures 81 may have a generally helical shape in the deployed configuration. In various embodiments, the outer jacket 80 and/or support structures 81 may be elongated—rather than helix-shaped—in the delivery configuration. For example, the outer jacket 80 and/or support structures 81 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the outer jacket 80 and/or support structures 81 may have a helical shape. In various embodiments, a substantial portion of the outer jacket 80 and/or support structures 81 may have a helical shape. In various embodiments, the helical outer jacket 80 and/or support structures 81 may be formed as a three-dimensional helix (in the deployed configuration) whereby the loops generally are positioned around the same axis (for example, a longitudinal axis of the delivery device 30).
The outer jacket 80 and/or support structures 81 may comprise a spiral shape in the deployed configuration. In some embodiments, the outer jacket 80 and/or support structures 81 may comprise one or more spiral portions as described herein.
In various embodiments, the outer jacket 80 and/or support structures 81 may have a spiral-shaped deployed configuration. In various embodiments, spiral refers to a shape with windings about a central axis. The spiral may be continuous. The windings may gradually widen (or tighten) along the length. The spiral may be formed in a flat plane perpendicular to the central axis. In various embodiments, the outer jacket 80 and/or support structures 81 may have a deployed configuration that is not formed in a flat plane, or in other words the deployed shape is formed in a three-dimensional and/or non-degenerate space. In various embodiments, the outer jacket 80 and/or support structures 81 may have a conical-shaped deployed configuration including, but not limited to, tubular, conical, frustoconical, and/or helical shapes.
The free end 22 of the outer jacket 80 may extend radially outward from the frame structure 12, and in particular from the remainder of the spiral outer jacket 80. The other end of the spiral outer jacket 80 may be coupled to the top or bottom of the frame structure 12 as described herein. Alternatively, or in combination, the other end of the spiral outer jacket 80 may not be attached to the frame structure 12 as described herein. The free end 22 of the spiral outer jacket 80 may facilitate capturing of the valve leaflets and/or chordal tendineae within the sweep of the free end during rotation as described herein. During rotation of the spiral outer jacket 80, the leaflets and/or chordae tendineae may be captured by the free end 22 and trapped between the valve frame structure 12 and an interior surface of the spiral outer jacket 80.
In various embodiments, the outer jacket 80 and/or support structures 81 may have a generally spiral shape in the deployed configuration. In various embodiments, the outer jacket 80 and/or support structures 81 may be elongated—rather than spiral-shaped—in the delivery configuration. For example, the outer jacket 80 and/or support structures 81 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the outer jacket 80 and/or support structures 81 may have a spiral shape. In various embodiments, a substantial portion of the outer jacket 80 and/or support structures 81 may have a spiral shape. In various embodiments, the spiral outer jacket 80 and/or support structures 81 may be formed as a flat spiral (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis).
The free end 22 and/or the outer jacket 80 may be sized and dimensioned for insertion through the native valve, for example through tissue at or near a commissure of the native valve or through the valve opening itself. In some embodiments, the free end 22 may comprise an atraumatic tip to avoid reduce risk of injury to the native valve tissue and leaflets. For example, the free end may comprise a blunt end, a ball tip, a curved tip (e.g., J-tip or pigtail), or other atraumatic shapes. Alternatively, the free end 22 may be configured for piercing tissue.
The outer jacket 80 and/or free end 22 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The outer jacket 80 and/or free end 22 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the outer jacket 80 and/or free end 22 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the outer jacket 80. For example, the outer jacket 80 may comprise one or more spaces between loops to facilitate radially-inward movement of the captured tissue (e.g. chordae and/or leaflets) from the free end 22 to the center of the curved structure with little or no torque and/or rotation of the structures during rotation of the outer jacket 80 as described herein. Alternatively or in combination, the outer jacket 80 may be configured such that, when fully deployed none of the structures reside between the loops of the curved encircling shape. Instead, the one or more structures may sit radially inward of the loops in order to facilitate capture of the one or more structures between the outer jacket 80 and the expanded frame structure 12. The one or more structures may retain or nearly retain their normal anatomical position when the outer jacket 80 is fully deployed.
The outer jacket 80 and/or support structures 81 may comprise one or more loops. For example, the outer jacket 80 and/or support structures 81 may comprise a plurality of loops, which may increase the radial strength of the anchor by increasing friction and addition structural support. The one or more loops of the outer jacket 80 and/or support structures 81 may be substantially cylindrical around a central axis of the outer jacket 80 and/or support structures 81, for example along an axis which is coaxial with a longitudinal axis of a delivery device 30. The one or more loops of the outer jacket 80 and/or support structures 81 may be substantially helical around a central axis or helical axis of the outer jacket 80 and/or support structures 81, for example along an axis which is coaxial with a longitudinal axis of a delivery device. The one or more loops of the outer jacket 80 and/or support structures 81 may spiral radially outward from a central point or central axis of the outer jacket 80 and/or support structures 81, for example along an axis which is coaxial with a longitudinal axis of a delivery device 30 such that the outer jacket 80 and/or support structures 81 lies approximately along a plane perpendicular to the longitudinal axis of the delivery device 30.
The one or more loops (also referred to herein as coils or turns) of the outer jacket 80 and/or support structures 81 may comprise a curved shape that bends around back towards its origin (for example, an arc, ellipsoid, circle, or the like). In some embodiments, a loop may comprise a curved shape that bends back towards its origin but does not cross itself, making a rotation within a range of about 180 degrees to about 360 degrees. For example, a loop may comprise a curve or an arc having a central angle within a range of about 180 degrees to about 360 degrees. In at least some embodiments, the one or more loops may comprise an arc. In some embodiments, a loop may comprise a shape that bends back towards and crosses itself, making at least a 360 degree rotation. In at least some embodiments, the one or more loops may comprise a 360 degree rotation (for example, a circle). In some embodiments, the one or more loops may comprise a 360 degree to 720 degree rotation (for example, a loop crossing itself once and rotating further towards a second crossing and formation of a second 360 loop).
Interaction of the frame structure 12 with the one or more loops of the outer jacket 80 and/or support structures 81 may create opposing forces therebetween that provide mechanical leverage for anchoring the frame structure 12 to the one or more anatomical structures. In some embodiments, the one or more loops may comprise at least 360 degrees of rotation when deployed such that the loops wrap around one another and provide additional mechanical leverage against the frame structure 12 in order to facilitate anchoring of the frame structure 12 as described herein. Additional loops or partial loops may provide additional mechanical strength and/or leverage.
In some embodiments, the one or more loops of the outer jacket 80 may comprise one or more spaces therebetween. The spaces may facilitate movement of the captured tissue (e.g. chordae and/or leaflets) from the free end 22 to the center of the spiral structure during rotation of the anchor 15 as described herein.
The outer jacket 80 and/or support structures 81 may be configured to wrap at least partially around the frame structure 12 in the deployed configuration.
In some embodiments, the outer jacket 80 and/or support structures 81 may be configured to wrap at least partially around a distal portion of a delivery device (e.g., delivery device 30 of
The one or more core wires 74 may comprise a shape memory material or super-elastic material such as nitinol. In some embodiments, the one or more core wires 74 may be made of a heat treatable material. The one or more core wires 74 may be formed of a material having sufficient rigidity to hold a predetermined shape. It may be desirable for at least the distal section 77 of the one or more core wires 74 to be relatively rigid such that it can exert a force to move chordal tendineae, while still retaining flexibility to be collapsed within the delivery device 30. In various embodiments, the distal portion 77 has sufficient rigidity to hold its shape, but is configured to deform under a load. For example, the distal section 77 may be configured with a similar rigidity to a guidewire or slightly stiffer.
The one or more core wires 74 may comprise one or more sections of wire having the same or different pre-formed shapes to facilitate deployment within the lumen(s) 71 of the anchor 15. For example, the distal section 77 can have a preformed shape (e.g., include one or more deflection features as described herein). The one or more core wires 74 may also comprise a proximal curved (or looped) section 76 proximal to the distal section 77. The curved shape of the proximal curved section 76 may be substantially similar to the curved shape of the anchor 15 in order to provide robust rotational constraint to the one or more core wires 74 so that the distal tip 75 of the one or more core wires does not rotate relative to the anchor 15 as the distal tip is translated. Alternatively, the proximal curved section 76 may be configured with a different shape or curvature that the anchor 15 in order to induce rotation in the distal tip 75 during translation as desired.
The one or more core wires 74 may comprise one or more pull-wires.
The one or more core wires 74 may be translatably disposed within an open lumen 71 (or lumens) of the anchor 15. It will be understood by one of ordinary skill in the art based on the teachings herein that the any number of core wires 74 may be disposed within the anchor as desired. For example, there may be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or more core wires 74 disposed within one or more lumens 71 of the anchor 15 as desired.
The one or more core wires 74 may be translatable. The one or more core wires 74 may translate distally and proximally within the lumen 71 of the anchor 15. The one or more core wires 74 may be longitudinally translatable independent of one another. In some embodiments, the one or more core wires 74 may comprise a plurality of wires which may be translated relative to one another in order to change the shape of a distal section 77 and deflect the distal tip 75 of the wires 74 to facilitate wrapping of the wires 74 and/or anchor 15 around the delivery device 30 and/or one or more native structures of the valve as described herein. For example, the one or more core wires 74 may comprise a first wire 74a and a second wire 74b. The first and second wires 74a, 74b may be longitudinally translatable independent of one another within the lumen 71 of the anchor 15. In some embodiments, the one or more core wires 74 may further comprise a third wire 74c. The third wire 74 may be longitudinally translatable independent of the first and/or second wires 74a, 74b.
The anchor 15 with outer jacket 80, support structures 81, and/or core wires 74 may be detachably coupled to the delivery device 30 (see
In some embodiments, deployment of the anchor 15 may be facilitated by longitudinal translation of the one or more core wires 74 within the lumen(s) 71 in order to advance or retract the distal tip 75 of the one or more core wires 74 away from or towards the free end 22 of the anchor 15 in order to change the shape of the distal portion of the anchor 15.
The one or more core wires 74 may be translated within the lumen(s) 71 of the anchor 15 before, during, or after deployment of the anchor 15 from the undeployed configuration to the deployed configuration. For example, the one or more core wires 74 may be translated within the anchor 15 before deployment of the anchor 15 into a self-assembly state in order to facilitate wrapping of the anchor 15 around the delivery device 30 (e.g., by extending past the free end 22 of the anchor 15). Alternatively, or in combination, the one or more core wires 74 may be translated within the lumen(s) 71 of the anchor 15 during deployment of the anchor 15 in order to actively or reactively “wiggle” or deflect the angle of the free end and/or distal tip as it deploys as described herein. Alternatively, or in combination, the one or more core wires 74 may be translated with the anchor 15 into an encircling state in order to facilitate grasping of and rotation of the anchor 15 around the one or more native valve structures as described herein.
The one or more core wires 74 may facilitate deployment of the anchor 15 from the delivery configuration to the deployed configuration. For example, the one or more core wires 74 may be configured to be advanced through the one or more lumens 71 of the outer jacket 80 and out an opening in the free end 22 of the anchor 15 into a self-assembly configuration. A distal tip 75 of one or more of the core wires 74 (e.g., a distal tip of a first wire and/or a second wire) may be configured to extend radially outward, proximally, or distally of a curved shape of the anchor 15 in the self-assembly configuration. The self-assembly configuration may facilitating positioning of the anchor relative to a delivery device during actuation from the delivery configuration to the deployed configuration.
The distal tip 75 of the one or more core wires 74 may be advanced into a self-assembly configuration prior to or during deployment of the anchor 15 from the delivery device 30 in order to facilitate wrapping of the one or more core wires 74 and anchor 15 around the delivery device 30 into the correctly deployed configuration. In the self-assembly state, the distal tip 75 may be deflected prior to or during deployment of the anchor 15 such that the distal tip 75 overlaps with one or more turns of the anchor 15 in order to ensure that the free end 22 wraps back around the delivery device 30.
In the self-assembly state, the distal tip 75 of the one or more core wires 74 may be deflected or angled proximally (e.g., towards a proximal portion of the anchor 15 and a distal end of the delivery device 30), distally (e.g., away from a proximal portion of the anchor 15 and towards a proximal portion of the delivery device 30), and/or radially (e.g., radially outwards or inwards from the main body of the anchor 15 and away from or towards the delivery device 30). In some embodiments, for example, the distal tip 75 may be positioned adjacent one or more loops of the anchor 15 when the anchor 15 is in the deployed configuration. Alternatively, or in combination, the distal tip 75 may be positioned such that it angles towards a proximal end of the anchor 15 when the anchor 15 is in the deployed configuration. Alternatively, or in combination, the distal tip 75 may be positioned such that it angles towards a distal end of the delivery device 30 when the anchor 15 is in the deployed configuration.
In at least some instances, it may be sufficient to initially advance the distal tip 75 into the self-assembly configuration during wrapping as described herein in order to form the first loop of the anchor 15 around the delivery device 30. Once the first loop as wrapped around the delivery device 30, the remaining loops may be more inclined or biased to wrap correctly around the delivery device 30 without additional deflection or manipulation. The one or more core wires 74 may remain in the self-assembly configuration for the entirety of the deployment of the anchor 15 from the delivery device 30. Alternatively, once the free end 22 has made a first loop around the delivery device 30 facilitated by the distal tip 75, the distal tip 75 may be translated proximally and retracted at least partially back into the anchor 15 for the remainder of the deployment of the anchor 15.
Alternatively, or in combination, the one or more core wires 74 may facilitate capture of and rotation of the anchor 15 around the one or more structures as described herein. For example, during and/or following core wires 74 may be configured to be advanced (or further advanced from the self-assembly configuration) into an encircling configuration. A distal tip 75 of the one or more core wires 74 (e.g., a first wire and/or a second wire) may be configured to angle away from the anchor 15 in the encircling configuration.
In the encircling configuration, the distal tip 75 of the one or more core wires 15 may be configured to deflect or angle proximally (e.g., towards a proximal portion of the anchor 15 and a distal end of the delivery device 30), distally (e.g., away from a proximal portion of the anchor 15 and towards a proximal portion of the delivery device 30), and/or radially (e.g., radially outwards or inwards from the main body of the anchor 15 and away from or towards the delivery device 30, respectively).
In at least some instances, deflection (e.g., angling proximally, distally, and/or radially outward) of the distal tip 75 away from the loops of the anchor 15 may aid in capture of the one or more structures by forming a “grabber” arm. For example, during rotation of the anchor 15, the grabber arm distal tip 75 may be rotated to capture the one or more structures of the native valve.
The distal tip 75 of the one or more core wires 74 may optionally rotated around one or more structures on the second side of the native valve such that the one or more native valve structures (e.g., chordae, leaflets, and/or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The distal tip 75, anchor 15, and/or free end 22 may be configured such that minimal torque is applied to the one or more native structures. Alternatively, or in combination, the distal tip 75, anchor 15, and/or free end 22 may be configured such that the one or more native valve structures are not rotated, or are minimally rotated, during rotation of the anchor 15.
Following deployment of the anchor 15 and/or rotation of the free end 22 (optionally facilitated by distal tip 75 as described herein) around the one or more structures of the native valve and/or expansion of the frame structure 12 within the anchor 15 adjacent the native valve, the one or more core wires 74 may be removed from the system, leaving the composite anchor 15 wrapped around the frame structure 12 at the native valve. By removing the one or more core wires 74 from the system following correct deployment of the valve prosthesis 10, potential complications related to having a discontinuously shaped distal end and/or translatable element left within the native valve may be reduced. Alternatively, the one or more core wires 74 may be fixed and left in the system following correct deployment if desired.
In various embodiments, the one or more core wires 74 may have a spiral-shaped deployed configuration. In various embodiments, spiral refers to a shape with windings about a central axis. The spiral may be continuous. The windings may gradually widen (or tighten) along the length. The spiral may be formed in a flat plane perpendicular to the central axis. In various embodiments, the one or more core wires 74 may have a deployed configuration that is not formed in a flat plane, or in other words the deployed shape is formed in a three-dimensional and/or non-degenerate space. In various embodiments, the one or more core wires 74 may have a conical-shaped deployed configuration including, but not limited to, tubular, conical, frustoconical, and/or helical shapes.
The distal tip 75 of the one or more core wires 74 may extend radially outward from the frame structure 12, and in particular from the remainder of the spiral one or more core wires 74 and/or anchor 15. The distal tip 75 of the one or more core wires 74 may facilitate capturing of the valve leaflets and/or chordal tendineae within the sweep of the free end during rotation as described herein. During rotation of the anchor 15 and one or more core wires 74 extending distally therefrom, the leaflets and/or chordae tendineae may be captured by distal tip 75 and trapped between the valve frame structure 12 and an interior surface of the anchor 15 and/or one or more core wires 74.
In various embodiments, the one or more core wires 74 may have a generally spiral shape in the deployed configuration. In various embodiments, the one or more core wires 74 may be elongated—rather than spiral-shaped—in the delivery configuration. For example, one or more core wires 74 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the one or more core wires 74 may have a spiral shape. In various embodiments, a substantial portion of the one or more core wires 74 may have a spiral shape. In various embodiments, the spiral one or more core wires 74 may be formed as a flat spiral (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis).
The distal tip 75 of the one or more core wires 74 may be sized and dimensioned for insertion through the native valve, for example through tissue at or near a commissure of the native valve or through the valve opening itself. In some embodiments, the distal tip 75 of the one or more core wires 74 may comprise an atraumatic tip to avoid reduce risk of injury to the native valve tissue and leaflets. For example, the distal tip 75 may comprise a blunt end, a ball tip, a curved tip (e.g., J-tip or pigtail), or other atraumatic shapes. Alternatively, the distal tip 75 of the one or more core wires 74 may be configured for piercing tissue.
In various embodiments, the distal tip 75 may be shaped and configured to reduce the risk of counter-rotation. For example, the distal tip 75 may have a curled end to cause the distal tip 75 to snag chordae if it is rotated in a direction opposite the anchoring rotation.
The distal tip 75 of the one or more core wires 74 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The distal tip 75 of the one or more core wires 74 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the distal tip 75 of the one or more core wires 74 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the anchor 15.
In some embodiments (e.g., instead of or in addition to having multiple core wires 74), one or more of the core wires 74 and/or distal end of the anchor 15 may comprise one or more deflecting features such that, when advanced distally past the free end 22 of the anchor 15, a distal tip of the one or more core wires 74 may be caused to “wiggle” or deflect away from the curvature of the anchor body 15 and change the deployment angle of the distal tip out of the anchor body 15 in order to facilitate wrapping of the anchor 15 around the delivery device 30 as described herein (e.g., radially outward, proximally, or distally of the curved shape of the anchor). The deflecting features may, for example, comprise one or more pre-formed waves, bends, kinks, or humps adjacent the distal tip 75 of the one or more core wires 74. For example, the one or more deflection features may comprise one or more kinks along the distal tip 75 of one or more of the core wires 74 such that at least a portion of the distal tip 75 is discontinuous with a curved shape of a proximal curved portion of the one or more core wires 74. The movable core wires 74 may be translated within the anchor 15 before, during, or after deployment of the anchor 15 from the undeployed configuration to the deployed configuration. For example, the one or more core wires 74 may be translated within the lumen(s) 71 of the anchor 15 before deployment of the anchor into a self-assembly state in order to facilitate wrapping of the anchor 15 around the delivery device (e.g., by extending past the free end 22 of the anchor 15 and acting similarly to the free end 22 comprising the deflecting features described herein). Alternatively, or in combination, one or more core wires 74 may be translated within the lumen(s) 71 of the anchor 15 during deployment of the anchor 15 in order to actively or reactively “wiggle” or deflect the angle of the distal tip as it deploys. Alternatively, or in combination, the one or more core wires 74 may be translated with the lumen(s) 71 of the anchor 15 into an encircling state in order to facilitate grasping of and rotation of the anchor 15 around the one or more native structures as described herein. By utilizing movable core wires 74 comprising one or more deflecting features, the anchor 15 may comprise a relatively simpler shape compared to an anchor having one or more deflecting features itself, which may facilitate design and fabrication of the anchor. For example, the anchor 15 may have a shape with a substantially continuous curvilinear shape and/or the reduction of complex bends. Alternatively, or in combination, the behavior of the free end 22 of the anchor 15 and/or the free end 75 of the core element 74 may be optimized to facilitate various deployment and/or implantation steps of the anchor. The lumen 71 of the anchor 15 may be sized and dimensioned to match or be slightly larger than the diameter of the one or more core wires 74 in order to enable translation therein. In some embodiments, the one or more core wires 74 may be made of a shape memory material such as nitinol in order to allow shaping of the one or more core wires 74. In some embodiments, the one or more core wires 74 may be made of a heat treatable material in order to allow shaping thereof. The anchor 15 may be relatively stiffer than the core wire 74. The anchor 15 may be sufficiently stiffer than the one or more core wires 74 such that the core wire 74 anchor 15 experiences little or no deflection itself when the one or more core wires 74 are disposed therein. The anchor 15 may be relatively stiffer than the one or more core wires 74 in order to prevent or reduce deflection of the anchor body when the movable core element is disposed in a lumen thereof. In some embodiments, the one or more core wires 74 may comprise a relatively more complex shape compared to the anchor in order to guide and the free end 22 of the relatively stiffer anchor 15.
The one or more core wires 74 may comprise a plurality of wires which may be translated relative to one another in order to change the shape of a distal tip portion 77 and deflect the distal tip 75 of the wires 74 to facilitate wrapping of the wires 74 and/or anchor 15 around the delivery device 30 and/or one or more native structures as described herein. For example, the one or more core wires 74 may comprise a first wire 74a and a second wire 74b. The first and second wires 74a, 74b may be longitudinally translatable independent of one another within the lumen 71 of the anchor 15. In some embodiments, the one or more core wires 74 may further comprise a third wire 74c. The third wire 74 may be longitudinally translatable independent of the first and/or second wires 74a, 74b. Translation of the first, second, and/or third wires 74a, 74b, 74c may facilitate deployment of the anchor 15 and/or capture of the chordae as described herein.
In some embodiments, the one or more core wires 74 (e.g., wires 74a, 74b, 74c) may comprise a proximal pusher section 73 proximal to the proximal curved section 76 which extends from the proximal curved section 76 to a proximal end of the delivery device 30. The proximal pusher section 73 may act as an actuation mechanism and facilitate longitudinal translation of the one or more core wires 74 within the lumen 71 of the anchor 15. For example, the proximal end of the proximal pusher section 73 may be coupled to an actuation mechanism in/on the delivery device 30 in order to translate the one or more core wires 74. Alternatively, the proximal end of the proximal pusher section 73 may be manually manipulated by at or near a proximal end of the delivery device in order to translate the one or more core wires 74. The proximal pusher section 73 of the first and second wires 74a, 74b74b (and the third wire 74c, a fourth wire, etc.) may or may not be disposed within the housing. For example, the proximal pusher portion 73 be disposed within the housing between the proximal end of the anchor and the distal end of the frame structure 12.
The core wires 74a, 74b, 74c may extend through and towards a proximal end of the delivery device 30. The wires 74a, 74b, 74c may be coupled to one or more actuation mechanisms in/on the delivery device in order to translate the wires 74a, 74b, 74c relative to one another and/or the anchor 15. Alternatively, the wires 74a, 74b, 74c may be manually manipulated by at or near a proximal end of the delivery device in order to translate the core wires 74a, 74b, 74c. The wires 74a, 74b, 74c may be independently translated in order to generate additive curvatures. The wires 74a, 74b, 74c may be pulled/pushed distally or proximally relative to one another to cause the distal tip portion 77 to deflect in any number and manner of shapes or curvatures desired.
In some embodiments, the first wire 74a and the second wire 74b (and the third wire 74c, a fourth wire, etc.) may be coupled to one another at the distal tip 75. Translation of the first and second wires 74a, 74b relative to one another may change the curvature of the distal section 77, thereby deflecting the distal tip 75 of the core wires 74 in order to facilitate anchor deployment and/or wrapping of the anchor 15 around one or more structures of the native valve as described herein. By providing two or more wires 74a, 74b coupled to one another at a distal tip 75, the distal tip 75 of the core wire 74 may be deflected into more complex and/or varying shapes than may be possible with a deflection feature disposed on or along the one or more core wires 74 or a single wire as described herein. The two wires 74a, 74b may be independently translated in order to generate additive curvatures. The wires 74a, 74b may be pulled/pushed distally or proximally relative to one another to cause the entire “grabber arm” of the distal section 77 to deflect in any number and manner of shapes or curvatures desired. In this way, the wires 74a, 74b may act as pull wires for the grabber arm of the distal section 77 and alter the shape thereof.
For example, the distal tip 75 may be deflected proximally or distally as shown in
In some embodiments, the first wire 74a and the second wire 74b (and the third wire 74c, a fourth wire, etc.) may be disposed within a housing. The housing may comprise a flexible material. Translation of the first and second wires 74a, 74b relative to one another may change the curvature of the housing, thereby deflecting the distal tip 75 of the core wires 74 in order to facilitate anchor deployment and/or wrapping of the anchor 15 around one or more structures of the native valve as described herein. By providing two or more wires 74a, 74b within a housing, the distal tip 75 of the core wire 74 may be deflected into more complex and/or varying shapes than may be possible with a deflection features disposed on or along the one or more core wires 74 described herein. The two wires 74a, 74b may be independently translated in order to generate additive curvatures. The wires 74a, 74b may be pulled/pushed distally or proximally relative to one another to cause the housing of the distal tip portion 77 to deflect in any number and manner of shapes or curvatures desired. In some embodiments, the entire “grabber arm” of the distal tip portion 77 may be made up of wires.
Alternatively, or in combination, at least a portion of the anchor 15 may include a support covering and/or band material disposed on or around the anchor 15. The anchor 15 material may comprise a permeable, semi-permeable, or impermeable material while the support covering or band material may be flexible, semi-flexible, or rigid. In some embodiments, the anchor 15 material may be relatively soft so as to reduce the risk of injury to the one or more structures during rotation of the anchor 15. The anchor 15 material may, for example, comprise a webbing material, a fabric, a polymeric material, an elastomeric material, or the like. The anchor 15 material may fully span the support covering so as to reduce leakage therethrough. Alternatively, or in combination, the anchor 15 material may be configured to improve alignment of the support covering. It will be understood by one of ordinary skill in the art from the description herein that any of the anchors 15 described herein may comprise a support covering and/or a material disposed therein or thereon.
In some embodiments, the support covering may comprise one or more channels or lumens disposed therein. The support covering may comprise a hollow, tubular cross-section.
In some embodiments, the support covering may, for example, comprise a hypotube. The lumen of the support covering may be configured to pass another component (e.g. a wire, guidewire, etc.) therethrough. The support covering may, for example, comprise an upper (proximal) wire and a lower (distal) wire. The upper and lower wires may be coupled to one another at a proximal attachment point and/or a distal attachment point. The wires may be round wires or have other cross-sectional shapes. In various embodiments, the support covering may comprise a scaffold such as a laser-etched Nitinol scaffold or a mesh. The anchor 15 may be tapered such that subsequent turns of the anchor 15 and support covering nest into each other so as to reduce a radial footprint of the anchor 15. The upper and lower wires of the support covering may be configured to nest with one another when the in the deployed configuration.
In some embodiments, the upper wire and lower wires of the support covering may be bundled together during deployment from an undeployed configuration to an intermediate deployed configuration. The intermediate configuration may be configured to reduce the size the size of the lumen and/or aperture in or through which, respectively, the anchor 15 may travel (for example, a lumen or aperture of the delivery device) during deployment. The anchor 15 may be maintained in the intermediate configuration during rotation around the one or more native valve structures as described herein. In at least some instances, coupling the upper and lower wires of the support covering together into an intermediate configuration may facilitate alignment of the wires of the support covering. After delivery from the delivery device 30 and/or rotation around one or more native valve structures, the anchor 15 may be fully deployed into the deployed configuration by releasing the bundle and allowing the upper and lower wires to “spring out” into the deployed configuration. In some embodiments the anchor and/or upper and lower wires “spring out” or expand into the deployed configuration. In some embodiments, the anchor 15 is pushed out of the delivery device into the deployed configuration. The support covering may have a band material disposed therein or thereon as described herein. The band material may span the distance between upper and lower wires in order to couple the wires to one another. The band material may span the structural support so as to reduce leakage therethrough as described herein. Alternatively, or in combination, the band material may be configured to improve alignment of the support covering upper and lower wires such that they maintain a desired relative position to one another.
In some embodiments, the support covering may comprise one or more channels or lumens disposed therein. For example, one or more of the wires may comprise one or more channels or lumens. One or more of the wires may comprise a hollow, tubular cross-section. The support covering or anchor 15 may, for example, comprise a hypotube. The lumen of the spiral band may be configured to pass another component (e.g. a wire, guidewire, etc.) therethrough. The channels or lumens may for example be left as open lumens. Alternatively, or in combination, the channels or lumens may be filled, for example with one or more stiffening members.
Any of the free ends 22 of the anchors 15 described herein can include a “grabber” arm extending therefrom. The grabber arm can be configured to extend radially outwards from the rest of the anchor 15 to help capture one or more native valve structures as the anchor 15 is rotated. For example,
Referring to
In some embodiments, the anchor 15 may comprise one or more locking mechanisms configured to maintain the anchor 15 in the deployed configuration. The one or more locking mechanisms may be any of the locking mechanisms described herein or understood by one of ordinary skill in the art from the description herein. In various embodiments, one or more loops may be nested with each other when the anchor is in the deployed configuration.
Referring to
The valve prosthesis 10 may comprise first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the valve prosthesis 10 is anchored to the native valve. Alternatively, the valve prosthesis 10 may be configured to sit entirely below the native valve when the valve prosthesis 10 is anchored to the native valve.
In some embodiments, the valve prosthesis 10 may comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration. The compressed outer periphery may be smaller in diameter than the expanded outer periphery.
In some embodiments, at least a portion of the valve prosthesis 10 may be actuated from the unexpanded configuration to the expanded configuration on a first side of the native valve prior to being advanced to a second side of the native valve. For example, the valve prosthesis 10 may be expanded in a left atrium of a heart prior to being advanced to a left ventricle of the heart as described herein.
Alternatively, or in combination, at least a portion of the valve prosthesis 10 may be actuated from the unexpanded configuration to the expanded configuration on a second side of the native valve after being advanced to the second side from a first side of the native valve. For example, valve prosthesis 10 may be advanced from a left atrium of a heart prior to being expanded in a left ventricle of the heart.
Delivery device 30 may refer to various components in certain embodiments. For example, delivery device 30 may refer to a steerable catheter for transseptal delivery. Delivery device 30 may refer to a catheter for delivery of the replacement valve, frame structure, and/or anchor. In some embodiments, delivery device 30 may refer to a first delivery device component detachably coupled to the anchor and a second delivery device component detachably coupled to the frame structure. In some embodiments, one or more valve prosthesis components may be different delivery devices or different components of a delivery device system.
Referring to
The valve prosthesis 10 may be operably coupled to the delivery device 30 as described herein. In some embodiments, at least a portion of the valve prosthesis 10 may be directly coupled to the inner shaft 52 (or tether 78). Alternatively, or in combination, at least a portion of the valve prosthesis 10 may be indirectly coupled to the inner shaft 52 (or tether 78). For example, at least a portion of the valve prosthesis 10 may be coupled to a torque hub or other connector, which may be coupled to the inner shaft 52.
The valve prosthesis 10 may be detachably coupled to the delivery device 30 in the unexpanded configuration during delivery to the native valve. Expansion of the valve prosthesis 10 to the expanded configuration may detach (i.e. release) the valve prosthesis 10 from the delivery device 30.
The valve prosthesis 10 may be balloon-expandable, self-expanding, or otherwise expansible as will be understood to one of ordinary skill in the art from the description herein.
For example, the delivery system 30 may comprise an inflatable balloon (for example, as shown in
Alternatively, or in combination, the valve prosthesis 10 may be self-expandable. The valve prosthesis 10 may be maintained in the unexpanded configuration by radial constriction from the outer sheath of the delivery device 30 when disposed in a lumen of the outer sheath. Advancement of the inner shaft 52 out of the lumen of the outer sheath may actuate the valve prosthesis 10 into the expanded configuration. Stated another way, retraction of the outer sheath away from the valve prosthesis 10 may actuate the valve prosthesis 10 into the expanded configuration.
The anchor 15 of the prosthesis 10 may be directly coupled to the frame structure 12 (or tether 78), for example at a proximal or distal end thereof. Alternatively, or in combination, the anchor 15 may be detachably coupled to the delivery device 30 prior to deployment at the native valve. For example, a proximal end 57 (see
The frame structure 12 may have an unexpanded configuration (for example, as shown in
The frame structure 12 may comprise a first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the frame structure 12 is anchored to the native valve. Alternatively, the frame structure 12 may be configured to sit entirely below the native valve when the frame structure 12 is anchored to the native valve.
In some embodiments, the frame structure 12 may comprise an expanded outer periphery in the expanded configuration and a compressed outer periphery when subject to an external radial force in the unexpanded configuration. The compressed outer periphery may be smaller in diameter than the expanded outer periphery.
The frame structure 12 may be balloon-expandable, self-expanding, or otherwise expansible as will be understood by one of ordinary skill in the art. The frame structure 12 may, for example, comprise an expandable stent.
The delivery system 30 may comprise an inflatable balloon (for example as shown in
In some embodiments, the delivery device 30 may be configured to carry the anchor 15 in an undeployed configuration and deploy the anchor 15 into a deployed configuration as the desired location as described herein.
The delivery device 30 may additionally or alternatively include any of the features of the delivery devices described in PCT/US2019/047542, PCT/US2019/055049, PCT/US2019/057082, and PCT/US2019/068088, the entireties of which are incorporated by reference herein.
In use, a valve prosthesis 10 may be loaded onto the delivery device 30. The valve system may optionally be primed before or after loading onto the delivery device 30. The delivery device 30 may be inserted through an introducer into a vessel. The delivery device 30 can be guided over a guidewire to a target location using the Seldinger technique.
The distal end of the delivery device 30 may be configured to be advanced from a first side of a native valve to a second side of the native valve. For example, the distal end of the delivery device 30 may be advanced from a left atrial side of a mitral valve to a left ventricular side of a mitral valve. In some instances, the distal end of the delivery device 30 may be transseptally inserted into the left atrium of the heart prior to advancement into the left ventricle. Alternatively, or in combination, the distal end of the delivery device 30 may be steerable such that it is positionable to point towards the first side of the native valve before being advanced to the second side of the native valve.
After advancing to the second side of the native valve, the anchor 15 may be fully deployed on the second side of the native valve. Fully deploying the anchor 15 may comprise actuating the anchor 15 from an elongated delivery configuration as shown in
In some embodiments, fully deploying the anchor 15 may comprise actuating the anchor 15 from an elongated delivery configuration to a deployed configuration on the first side of the native valve and advancing the anchor 15 in the deployed configuration through the native valve to the second side of the native valve. Advancing the anchor 15 may comprise pushing the anchor through the native valve. Advancing the anchor 15 may further comprise rotating the anchor 15 through the native valve.
In some embodiments, fully deploying the anchor 15 may comprise positioning the anchor 15 such that it is located only on the second side of the native valve.
In some embodiments, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a first side of the native valve prior to being advanced to a second side of the native valve. For example, the anchor 15 may be deployed in a left atrium of a heart prior to being advanced to a left ventricle of the heart as described herein.
Alternatively, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a second side of the native valve after being advanced to the second side from a first side of the native valve. For example, anchor 15 may be advanced from a left atrium of a heart prior to being deployed in a left ventricle of the heart.
The free end 22 of the deployed anchor 15 may optionally be rotated around one or more structures on the second side of the native valve. The one or more structures may comprise one or more valve leaflets of the native valve. Alternatively, or in combination, the one or more structures may comprise one or more chordae of the left ventricle.
The free end 22 of the deployed anchor 15 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The anchor 15 and/or free end 22 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the anchor 15 and/or free end 22 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the anchor 15.
In some embodiments, the valve prosthesis 10, for example anchor 15, may be counter-rotated in order to reposition the anchor 15 with respect to the one or more structures of the native valve before continuing the rotation in the first direction. For example, counter-rotation may be applied if the one or more structures are caught by the free end of the anchor 15 (or another part of the valve prosthesis 10 or delivery device 30) during the initial rotation. In such instances, counter-rotation may enable to the clinician to disengage some or all of the one or more structures to reduce the stress or torque on the one or more structures (e.g., by adjusting the position of the valve prosthesis 10) before resuming rotation. Rotation and counter-rotation may be applied as many times as desired by the clinician in order to properly position the anchor 15 around the one or more structures of the native valve.
The anchor 15 may then be released from the distal end of the delivery device 30. The anchor 15 may be released from the distal end of the delivery device 30 on the second side of the native valve.
The frame structure 12 may be expanded within the native valve from an unexpanded configuration to an expanded configuration. The valve prosthesis 10 is finally anchored when the frame structure 12 is expanded within the native valve 4. The frame structure 12 dilates the valve leaflets 14 and the compressive force fixes the valve prosthesis 10 into position. Thereafter tissue ingrowth ensures the valve prosthesis 10 remains seated and does not migrate.
The frame structure 12 may be released from the distal end of the delivery device 30. In some embodiments, at least a portion the frame structure may be expanded within at least a portion of the deployed anchor to anchor the frame structure to the native valve.
In some embodiments, expanding the frame structure and releasing the frame structure may occur simultaneously.
Finally, the delivery device 30 may be retracted from the native valve.
The valve devices described herein in accordance with the present disclosure provides several advantages over conventional valve systems. Embodiments described herein provide an easy-to-use, repositionable device. Unlike conventional valve systems, the valve prosthesis described herein reduces the risk of injuring or tearing chordae. Typical mitral valve replacement systems involve implanting a prosthetic annulus or ring around the valve. The ring increases the circumference of the valve and risks occluding the entry to the aortic valve. The valve device described herein overcomes these and other problems.
While the method shown in
As shown in
In some instances, advancing the anchor 15 through the native valve 4 may cause the anchor 15 to be stretched or elongated as shown in
In some embodiments, the anchor 15 may be advanced into the ventricle after being fully deployed from the delivery (e.g., elongated) configuration to the deployed configuration.
In some embodiments, the anchor 15 may be advanced into the ventricle before being deployed from the delivery (e.g., elongated) configuration to the deployed configuration.
Rotation of the valve prosthesis 10, for example, rotation of the anchor 15 and/or frame structure 12, may be facilitated by the delivery device 30 described herein. For example, the inner shaft 52 may be rotated and rotational motion may be transmitted from the inner shaft 52 to the valve prosthesis 10 in order to rotate the valve prosthesis 10 around one or more of the structures on the ventricle side of the mitral valve 4 as described herein.
In some embodiments, the valve prosthesis 10, for example anchor 15, may be counter-rotated in order to reposition the anchor 15 with respect to the chordae tendineae 40 before continuing the rotation in the first direction. For example, counter-rotation may be applied if the chordae tendineae 40 are caught by the free end of the anchor 15 (or another part of the valve prosthesis 10 or delivery device 30) during the initial rotation. In such instances, counter-rotation may enable to the clinician to disengage some or all of the chordae tendineae 40 to reduce the stress or torque on the chordae tendineae 40 (e.g., by adjusting the position of the valve prosthesis 10) before resuming rotation. As another example, the anchor 15 may encounter friction or other resistance to rotation. In this case the clinician may counter-rotate the anchor 15 to return to the original position and then begin rotating the anchor 15 to re-start and/or continue encircling chordae tendineae 40. Rotation and counter-rotation may be applied as many times as desired by the clinician in order to properly position the anchor 15 around the valve structures.
In some embodiments, the anchor 15 may be deployed such that at least a portion of the anchor 15 resides within a subvalvular plane. For example, at least 50%, 60%, 70%, 80%, 90%, 100% of the anchor 15 may reside within the subvalvular plane after being deployed. The subvalvular plane may be located at the posterior valve annulus, below the valve annulus and around the native valve leaflets 42, and/or parallel to a plane within at least three points of the plane in which the valve annulus resides. In some instances, the anchor 15 may be rotated in the subvalvular plane around the chordae tendineae 40. In some instances, the anchor 15 may be rotated in a plane below to the subvalvular plane in order to encircle the chordae tendineae 40 before the anchor 15 is moved into the subvalvular plane (e.g., by pulling the anchor 15 into the sub-annular space).
Once the anchor 15 has been anchored adjacent to the native valve 4, the frame structure 12 and prosthetic valve segment 14 may be expanded at least partially within the anchor 15 as described herein. The frame structure 12 and the valve segment 14 may be deployed (e.g., expanded) simultaneously. Alternatively, or in combination, the frame structure 12 and the valve segment 14 may be deployed sequentially, for example by first expanding the frame structure 12 and then receiving the prosthetic valve segment 14 therein.
The valve prosthesis 10 may then be released from the delivery device 30. In some embodiments, releasing the valve prosthesis 10 may comprise releasing the anchor 15 and/or the frame structure 12. Releasing the valve prosthesis 10 from the delivery device 30 may comprise expanding the valve prosthesis 10 from the unexpanded configuration to the expanded configuration. For example, expanding the frame structure 12 and releasing the frame structure 12 may occur simultaneously as described herein. Alternatively, the frame structure 12 may be released prior to or after being expanded.
Although the steps above show a method of deploying a valve prosthesis 10 within a native valve 4 in accordance with embodiments, a person of ordinary skill in the art will recognize many variations based on the teaching described herein. The steps may be completed in a different order. Steps may be added or deleted. Some of the steps may comprise sub-steps. Many of the steps may be repeated as often as necessary to assemble at least a part of an article.
For example, in some embodiments, deploying the valve prosthesis 10 may occur in multiple steps such that a portion of the valve prosthesis 10 (e.g., anchor 15) may be deployed before another portion the valve prosthesis 10 (e.g., frame structure 12). Alternatively, or in combination, in some embodiments, deploying the anchor 15 may occur in multiple steps such that a portion of the anchor 15 may be deployed before being advanced through the native valve 4 and another portion of the anchor 15 may be deployed after being advanced through the native valve 4. Alternatively, or in combination, the delivery device 30 may be advanced from the left atrium 25 to the left ventricle 26 with the valve prosthesis 10 undeployed. In many embodiments, the frame structure 12 may be self-expanding and the balloon 48 may not be necessary for expansion of the frame structure 12. Alternatively, or in combination, the anchor 15 may be released after the frame structure 12 has been expanded within it.
Although shown and described with respect to a mitral valve, one of ordinary skill in the art will understand that the principles described herein may be applied equally to other atrioventricular valves. Aspects of the procedure, delivery tool, and implanted valve prosthesis are similar to those described in U.S. Pat. Nos. 9,034,032; 9,005,273; 8,323,336; 8,075,615; 7,621,948; and 7,175,656 and U.S. Pub. No. 2011/0288637, which are incorporated herein for all purposes in their entirety.
In some embodiments, any of the valve prostheses 10 described herein may be deployed to replace a diseased mitral valve. The first side of the native valve may comprise a left atrium and the second side of the native valve may comprise a left ventricle.
In some embodiments, any of the valve prostheses 10 described herein may be deployed to replace a diseased tricuspid valve. The first side of the native valve may comprise a right atrium and the second side of the native valve may comprise a right ventricle.
In some embodiments, any of the valve prostheses 10 described herein may be deployed to replace a diseased aortic valve. The first side of the native valve may comprise a left ventricle and the second side of the native valve may comprise an aorta.
The valve prosthesis device and implant method described herein in accordance with the present disclosure may provide many advantages as will be understood by one of ordinary skill in the art. The overall device and method may provide a simpler way to approach the native valve compared to existing devices. The system may enable a transcatheter approach through the septal wall compared to more invasive transapical approaches. The device may provide a consistent and relatively easy mechanism for anchoring to the native valve. Clinicians need only use the common technique of inserting the device through the valve and then rotating the anchor. The coil may provide preliminary anchoring in the native valve. If desired, the clinician can readjust the anchor and/or retrieve the anchor (e.g. by counterrotation). The device is then easily set by expanding within the native valve leaflets. The device and methods in accordance with the present disclosure may also address unmet clinical needs with atrioventricular repair and replacement. Existing devices face challenges with the complex anatomy of the mitral and tricuspid valves, for example. The present disclosures address these complications by reshaping the native valve annulus to a conventional round shape and providing a robust, yet simple, anchoring mechanism.
After the anchor 15 has been deployed from the delivery device 30, the frame structure 12 may be at least partially deployed from the delivery device 30 (for example as shown in
After the anchor 15 has been deployed from the delivery device 30 in the configuration shown in
In some embodiments, the delivery system 30 can include an anchor guide 153 and/or a tether 78. For example, an anchor guide 153 is shown in
Referring to
In some embodiments (as best shown in
The distal section 162 of the anchor guide 153 may direct the anchor 15 out of the guide 153 in an initial direction that is transverse to the longitudinal axis of the inner shaft 52 and/or proximal section 161. As the anchor 15 is rotated, however, the spiral can form about the longitudinal axis of the inner shaft 52 and/or proximal section 161. The anchor guide 153 may thus be shaped to act as a throwdown arm and may be configured to correctly orient the anchor 15 relative to the chordae tendineae and/or prevent twisting of the anchor 15 during deployment and/or rotation, as well as ensure that the anchor 15 will self-assemble around the inner shaft 52 and/or frame structure 12, after the outer sheath 50 is advanced through the native valve. During anchor deployment, translation and/or rotation of the inner shaft 52 and anchor guide 153 may provide control over the direction and orientation of anchor self-assembly. During encircling of the chordae tendineae, the axial position of the inner shaft 52 and anchor guide 153 may control the height of the anchor relative to the valve annulus, and rotation of the inner shaft 52 and anchor guide 153 may be translated to the anchor 15 to provide encircling motion thereto as described herein.
In some embodiments, the anchor guide 153 may be held in a relatively straight collapsed configuration when positioned within the lumen of the outer sheath 50 (e.g., by radial constriction from the sheath 50). The anchor guide 153 may be shape-set such that distal translation of the anchor guide 153 relative to the distal tip of the outer sheath 50, and release of radial constriction therefrom, allows the anchor guide 153 to bend at the distal section 162. In some embodiments, the anchor guide 153 can be retracted into the outer sheath 50 (i.e., return to the collapsed configuration) after deployment of the anchor 15. The anchor guide 153 can thus be an extendable and retractable anchor guide 153.
In some embodiments, the anchor guide 153 may comprise one or more deflection features, similar to as described herein for other elements, in order to facilitate delivery of the anchor 15 to the native valve. The one or more deflection features may help provide the anchor guide 153 with a shape configured to correctly orient the anchor 15 relative the longitudinal axis of the inner shaft 52 in order to facilitate concentric wrapping of the anchor 15 around the inner shaft 52 as the anchor 15 is deployed from the delivery configuration to the deployed configuration.
Referring to
In some embodiments, the anchor guide 153 can be designed such that the distal end thereof overlaps with a proximal end of the anchor 15 even when the anchor 15 is fully deployed, thereby increasing torsional and bending stiffness of the anchor. Further, in some embodiments, the distal end of the anchor guide 153 can be tapered to minimize the step size between the anchor guide 153 and the anchor 15, thereby reducing the chances of the anchor guide 153 getting stuck on native valve structures during deployment.
The anchor guide 153 can advantageously ensure deployment of the anchor 15 in a concentric direction with the delivery device 30, avoiding tangling of the anchor 15 with the delivery device 30. Additionally, the anchor guide 153 can advantageously provide a stable support for the anchor 15 after the anchor 15 has been advanced and as the anchor 15 is rotated about the native valve structures.
In some embodiments, the inner shaft 52 and anchor guide 153 may be translated (or “wiggled”) within the outer sheath 50 prior to, during, or after deployment of the anchor 15 in order to actively or reactively move the distal tip 156 of the anchor guide 153. Translating the inner shaft 52 and anchor guide 153 back-and-forth during deployment of the anchor 15 may correspondingly adjust the angle of the anchor 15 and/or free end 22 of the anchor 15 as it deploys. This may facilitate deployment of the anchor 15 in tight spaces and/or facilitate encircling of the chordae tendineae (e.g., by adjusting the orientation and/or location of the free end 22). In some embodiments, the anchor guide 153 can be moved with respect to the sheath 50 to change the shape or length of the anchor guide 153 during deployment of the anchor 15.
In some embodiments, the anchor guide 153 is a unitary construct with the distal end of the inner shaft 52. Referring to
Referring to
Referring to
The anchor 15 may comprise a delivery (e.g., elongated, radially collapsed, or unexpanded) configuration and a deployed configuration. In various embodiments, the anchor 15 may be self-expanding and may move to the deployed configuration as it is deployed (e.g., pushed out from the anchor guide 153 by the tether 78). In various embodiments, the anchor 15 may be configured to self-assemble when it is deployed in the heart cavity (e.g., left ventricle or left atrium). The anchor 15 may be actuated from the delivery configuration to the deployed configuration adjacent the native valve using any method or mechanism understood by one of ordinary skill in the art from the description herein. Advancement of the inner shaft 52 and guide 153 out of the lumen of the outer sheath 50 may actuate the anchor 15 into the deployed configuration as described herein.
Referring to
In some embodiments, and as shown in
A proximal end of the anchor 15 may be detachably coupled to the tether 78. The tether 78 may be disposed within a lumen of the delivery device 30 (e.g., within a lumen of the inner shaft 52 and anchor guide 153) and may operably couple the anchor 15 to the delivery device 30. The tether 78 may act as an actuation mechanism and facilitate longitudinal translation of the anchor 15 through the delivery device 30 during deployment. For example, a proximal end of the tether 78 may be coupled to an actuation mechanism in/on the delivery device 30 in order to translate the anchor 15. Alternatively, the proximal end of tether 78 may be manually manipulated by, at, or near a proximal end of the delivery device 30 in order to translate the anchor 15.
The tether 78 may comprise a flexible advancement member housed and translatable within the inner shaft 52. The tether 78 may comprise a flexible shaft or stylet, for example, in the form of a wire or a metal wire, and/or flexible hypotube with a lumen to accommodate a guidewire. The tether 78 may be sufficiently flexible to allow for easy rotation within the deflectable delivery device 30. The tether 78 may be comprise a release actuation mechanism (e.g., retention wire 88).
In various embodiments, the anchor 15 may be self-expanding and may move to the deployed configuration as it is deployed (e.g., pushed out) from the anchor guide 153 by the tether 78. The anchor 15 may be rotated by the rotating the inner shaft 52 (and anchor guide 153) and/or the tether 78. In some embodiments, the tether 78 may be rotated, and rotational motion may be translated from the tether 78 to the anchor 15. Rotation of the anchor 15 via the anchor guide 153 and/or tether 78 can enable the anchor 15 to wrap around the one or more native valve structures on the ventricle side of the mitral valve as described herein.
The anchor 15 may be disposed in the inner shaft 52 (and anchor guide 153) and maintained in the delivery configuration by radial constriction from the inner shaft 52 and anchor guide 153. Advancement of the anchor 15 out of the inner shaft 52 may actuate the anchor 15 into the deployed configuration. The proximal end 57 of the anchor 15 may be detachably coupled to the tether 78 within the lumen of the inner shaft 52 as described herein. Although the anchor 15 is described as being pushed out of the inner shaft 52 in some embodiments, one will appreciate from the description herein that different mechanisms may be employed to deploy the anchor depending on the anchor 15 and/or inner shaft 52 design. In some respects, pushing is used somewhat interchangeably with rotation in reference to deployment of the anchor 15. For example, the anchor 15 can be rotated out of a lateral opening with a rotational action.
The tether 78 may be coupled to the anchor 15 by a retention wire 88. The retention wire 88 may run the length of the tether 78 from the connection point 300 to the proximal end. A distal end of the retention wire 88 may be threaded through a hole 304 spanning at least a portion of both the anchor 15 and the tether wire 78 when aligned in the delivery configuration. When threaded as such, the retention wire 88 may act as an engagement pin to keep the anchor 15 and tether wire 78 together during deployment of the anchor 15. Once the anchor 15 is deployed, the proximal end of the retention wire 88 may be translated proximally in order to disengage the retention wire 88 from the anchor 15 and release the anchor 15 from the tether 78. The proximal end of the retention wire 88 may be coupled to an actuation mechanism in/on the delivery device in order to translate the retention wire 88. Alternatively, the proximal end of the retention wire 88 may be manually manipulated by, at, or near a proximal end of the delivery device in order to translate the retention wire 88. Once disengaged, the tether 78 may be retracted from the body, leaving the deployed anchor 15 adjacent the native valve as described herein.
Advancing the anchor 15 may comprise pushing the anchor 15 through the native valve 4. Advancing the anchor 15 may further comprise rotating the anchor 15 through the native valve 4.
The free end 22 of the deployed anchor 15 may optionally be rotated around one or more structures on the second side of the native valve 4. The one or more structures may comprise one or more valve leaflets 42 of the native valve 4. Alternatively, or in combination, the one or more structures may comprise one or more chordae tendineae 40 of the left ventricle 23.
The free end 22 of the deployed anchor 15 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The anchor 15 and/or free end 22 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the anchor 15 and/or free end 22 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the anchor 15.
In some embodiments, the anchor 15 may be counter-rotated in order to reposition the anchor 15 with respect to the one or more structures of the native valve before continuing the rotation in the first direction. For example, counter-rotation may be applied if the one or more structures are caught by the free end of the anchor 15 (or another part of the valve prosthesis 10 or delivery device 30) during the initial rotation. In such instances, counter-rotation may enable to the clinician to disengage some or all of the one or more structures to reduce the stress or torque on the one or more structures (e.g., by adjusting the position of the valve prosthesis 10) before resuming rotation. Rotation and counter-rotation may be applied as many times as desired by the clinician in order to properly position the anchor 15 around the one or more structures of the native valve.
In some embodiments, the anchor 15 may be deployed towards the apex of the ventricle 26 in order to avoid interference with motion of the native leaflets 42 during positioning. In some embodiments, the anchor 15 may then be pulled upwards to seat the anchor 15 adjacent the native leaflets 42.
The frame structure 12 may deployed before, during, or after retraction of the anchor guide 153 and/or outer sheath 50.
Referring to
The valve capsule 154 may comprise a flexible material or a rigid material. The valve capsule 154 may be relatively rigid such that it can exert a compression force on a frame structure 12 delivered within the valve capsule 154 while still retaining flexibility to deform under an external force. The valve capsule 154 may comprise a soft or flexible material.
As described herein, the inner shaft 52 may be disposed within a lumen of the outer sheath assembly 155, and a guidewire 54 may be disposed adjacent to the inner shaft 52 within a lumen of the outer sheath assembly 155. Alternatively, the guidewire 54 may be disposed in a lumen of inner shaft 54. The guidewire 54 may optionally comprise a nosecone to facilitate guidance of the guidewire 54 to the native valve. A proximal end of the valve prosthesis 10 may be operably coupled to the inner shaft 52 (or tether 78, such as described with respect to
In some embodiments, the valve capsule 154 of the outer sheath assembly 155 may be steerable. The valve capsule 154 of the outer sheath assembly 155 may be steered prior to or after separation of the valve capsule 154 from the outer sheath 50 such that the valve capsule 154 points towards the native valve.
The valve prosthesis 10 may be operably coupled to the delivery device 30 as described herein. In some embodiments, at least a portion of the valve prosthesis 10 may be directly coupled to the inner shaft 52 (or tether 78). Alternatively, or in combination, at least a portion of the valve prosthesis 10 may be indirectly coupled to the inner shaft 52. For example, at least a portion of the valve prosthesis 10 may be coupled to a torque hub or other connector, which may be coupled to the inner shaft 52.
In some embodiments, the anchor 15 may be partially deployed to an intermediate deployed configuration in the left atrium before being advanced through the native valve into the left ventricle. In the intermediate deployed configuration, the anchor 15 may be wrapped at least partially around the inner shaft 52.
In some embodiments, the anchor 15 may be fully deployed from the anchor guide 153 into a deployed configuration within the left atrium prior to being advanced into the left ventricle.
The anchor 15 may comprise a delivery (e.g., elongated, radially collapsed, or unexpanded) configuration and a deployed configuration. A frame structure of the valve prosthesis (e.g., frame structure 12 shown in
In some embodiments, the anchor 15 may be actuated from the delivery configuration to the deployed configuration (or intermediate configuration) on a first side of the native valve prior to being advanced to a second side of the native valve. For example, the anchor 15 may be deployed in a left atrium of a heart prior to being advanced to a left ventricle of the heart as described herein (e.g. as shown in
Advancement of the anchor guide 153 as the outer sheath 50 is brought into alignment with the mitral valve and/or advanced through the mitral valve may expose a bend in the anchor guide 153. The bend in the anchor guide 153 can act as a throwdown arm and may be configured to correctly orient the anchor 15 relative to the chordae tendineae 40 and/or prevent twisting of the anchor 15 during deployment and/or rotation, as well as ensure that the anchor 15 will self-assemble around the inner shaft 52 and/or frame structure 12, after the outer sheath 50 is straightened.
In some embodiments, the valve capsule 154 of the outer sheath assembly 155 may comprise a soft valve capsule as described herein.
The separation of the valve capsule 154 of the outer sheath assembly 155 from the outer sheath 50 may be facilitated by advancement of an inner shaft 52 through the lumen of the outer sheath 50. In some embodiments, the frame structure 12 may be housed within the valve capsule 154 of the outer sheath assembly 155 and can be maintained in the delivery configuration by radial constriction from one or more of the valve capsule 154 or by the outer sheath 50.
FIGS. 6A3-64C sequentially describe a method of deploying a valve prosthesis within the native valve, in accordance with many embodiments.
The outer sheath assembly 155 may be steerable as described herein. The outer sheath assembly 155 may be steered through the native valve such that the valve capsule 154 is positioned on below the native valve and the outer sheath 50 is positioned above the native valve. Steering of the valve capsule 154 of the outer sheath assembly 155 may be accomplished by a guidewire 54 with a deflection element such as a rigid bend. The anchor guide 153 may also position the anchor 15 for attachment to the chordae tendineae 40 as described herein. A proximal pusher arm or tether within the anchor guide 153 may position the anchor 15 for attachment to the chordae tendineae 40 as described herein. Alternatively, or in combination, the distal end of the anchor 15 may comprise a deflection element to steer the anchor 15 as it is released from the radial constriction of the anchor guide 153. The outer sheath 50 and the valve capsule 154 may be separated to form an opening therebetween and expose an inner shaft 52 of the delivery device 30 as described herein. The outer sheath 50 and the valve capsule 154 may be separated from one another such that the opening spans the native valve. The outer sheath 50 and the valve capsule 154 may be separated from one another such that the opening entirely on the second side of the native valve (e.g., on a ventricular side of the native valve).
The anchor 15 may be detachably coupled to a proximal or distal portion of the frame structure 12 as described herein. Alternatively, or in combination, the frame structure 12 may be detachably coupled to the delivery device 30 in the delivery configuration during delivery to the native valve. For example, the proximal end of the frame structure 12 may be detachably coupled to the inner shaft 52 of the delivery device 30 by radial constriction from the outer sheath 50 or the valve capsule 154. Retraction of the outer sheath 50 away from the proximal end of the frame structure 12 (or, similarly, extrusion of the distal end of the frame structure 12 out of an opening in the outer sheath) may detach the frame structure 12 from the delivery device 30. Alternatively, or in combination, the proximal end of the frame structure 12 may be detachably coupled to the inner shaft 52 of the delivery device 30 by an attachment element. Alternatively, or in combination, the proximal end of the frame structure 12 may be detachably coupled to the inner shaft 52 of the delivery device 30 by a weak adhesive.
The valve capsule 154 may comprise a cylindrical proximal section 220 and a tapered distal section 219. In some embodiments, the valve capsule 154 may comprise a single unitary construction (i.e., the cylindrical proximal section 220 and a tapered distal section 219 can be of single unitary construction). In some embodiments, the cylindrical section 220 and the tapered distal section 219 may comprise different structural features or elements (for example, as shown in
During use of any of the delivery devices 30 of
The delivery device 30 may be advanced into the heart over the guidewire 54 (e.g., as shown in
The valve capsule 154 may be separated from the outer sheath 50 adjacent the native valve to form the opening and expose the inner shaft 52 and anchor guide 153. The opening may be formed prior to, during, or after advancing the distal end of the delivery device 30 from the first side of the native valve to the second side of the native valve.
In some embodiments, the distal end of delivery device 30 may be advanced from the first side of the native valve to the second side of the native valve after at least partially deploying the anchor 15 (e.g., as shown in
After advancing to the second side of the native valve, the anchor 15 may be fully deployed from the anchor guide 153 on the second side of the native valve (e.g., as shown in
In some embodiments, fully deploying the anchor 15 from the anchor guide 153 may comprise actuating the anchor 15 from an elongated delivery configuration to a deployed configuration on the first side of the native valve (e.g., as shown in
In some embodiments, fully deploying the anchor 15 from the anchor guide 153 may comprise positioning the anchor 15 such that it is located only on the second side of the native valve as can be seen in
In some embodiments, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a first side of the native valve prior to being advanced to a second side of the native valve (e.g., as shown in
Alternatively, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a second side of the native valve after being advanced to the second side from a first side of the native valve (e.g., as shown in
The free end of the deployed anchor 15 may optionally be rotated around one or more native valve structures on the second side of the native valve. The one or more native valve structures may comprise one or more valve leaflets of the native valve. Alternatively, or in combination, the one or more native valve structures may comprise one or more chordae of the left ventricle.
The free end of the deployed anchor 15 may optionally rotated around one or more native valve structures on the second side of the native valve such that the one or more native valve structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor and/or towards the longitudinal axis of the delivery device. The anchor and/or free end may be configured such that minimal torque is applied to the one or more native valve structures. Alternatively, or in combination, the anchor 15 and/or free end may be configured such that the one or more native valve structures are not rotated, or are minimally rotated, during rotation of the anchor.
In some embodiments, rotation of the free end may occur simultaneously with deployment of the anchor 15 from the anchor delivery sheath.
The anchor 15 may then be released from the anchor guide 153. The anchor 15 may be released from the anchor guide 153 on the second side of the native valve.
The frame structure 12 may be expanded within the native valve from an unexpanded configuration to an expanded configuration (e.g., as shown in
The frame structure 12 may be released from the distal end of the delivery device.
The frame structure 12 may be held within the valve capsule 154. In some embodiments, the cylindrical proximal section 220 and the tapered distal section 219 of the valve capsule 154 may be permanently attached to one another (e.g., as shown in
In some embodiments, at least a portion the frame structure 12 may be expanded within at least a portion of the deployed anchor 15 to anchor the frame structure 12 to the native valve.
In some embodiments, expanding the frame structure 12 and releasing the frame structure 12 may occur simultaneously.
In some embodiments, the frame structure 12 may be self-expanding and may be maintained in the unexpanded configuration by radial constriction from one or more of the outer sheath 50 of the delivery device 30 or by the valve capsule 154 of the outer sheath assembly 155. Advancement of the inner shaft 52 out of the lumen of the outer sheath 50 may actuate the frame structure 12 into the expanded configuration. Advancement of the inner shaft 52 out of the lumen of the outer sheath assembly 155 may actuate the frame structure 12 into the expanded configuration by the separation of the valve capsule 154 of the outer sheath assembly 155 from the outer sheath 50.
Finally, the delivery device 30 may be retracted from the native valve as shown in
While
The delivery device 30 may comprise an optional outer sheath 50 (e.g., an outer catheter) and an inner shaft 52 (e.g., a delivery tube) disposed within a lumen of the outer sheath 5-. A proximal end of the valve prosthesis 10 may be operably coupled to the inner shaft 52 during delivery to the native valve as described herein. The outer sheath 50 may be steerable. The inner shaft 52 may be steerable and may include the side opening 215.
The valve prosthesis 10 may be similar to any of the valve prostheses described herein. For example, the valve prosthesis may include a frame structure 12 and an anchor 15. The anchor 15 may be directly coupled to the frame structure 12, for example at a proximal or distal end thereof. Alternatively, or in combination, the anchor 15 may be detachably coupled to the delivery device 30 prior to deployment at the native valve. The anchor 15 may comprise a deployed configuration (for example, as shown in
The frame structure 12 may comprise a first and second opposite ends, the first end extending above a native valve and the second end extending below the native valve when the frame structure 12m is anchored to the native valve. Alternatively, the frame structure 12 may be configured to sit entirely below the native valve when the frame structure 12 is anchored to the native valve.
The frame structure 12 may be self-expanding and may be maintained in the unexpanded configuration by radial constriction from the outer shaft 54 or inner shaft 52 of the delivery device 30. In some embodiments, advancement of the inner shaft 52 out of the lumen of the outer shaft may actuate the frame structure 12 into the expanded configuration. In some embodiments, advancement of the frame structure 12 out of the lumen of the inner shaft 52, for example with the aid of a proximal pusher 78 (see
In some embodiments, the anchor 15 may be detachably coupled to and/or disposed within the delivery device 30 at a location proximal to the frame structure 12. In some embodiments, the anchor 15 may be detachably coupled to and/or disposed within the delivery device 30 at a location distal to the frame structure 12. In some embodiments, at least a portion of the anchor 15 may be detachably coupled to and/or disposed within the delivery device 30 at a location adjacent (e.g., around) the frame structure 12. In some embodiments, the anchor 15 may be disposed in a lumen of the inner shaft 52. The anchor 15 may or may not be coupled to the inner shaft 52. The anchor 15 may be maintained in the delivery configuration by radial constriction from the inner shaft 52. Advancement of the anchor 15 out of the inner shaft 52, for example out of the side port 215 of the inner shaft 52, may actuate the anchor 15 into the deployed configuration. The proximal end 57 of the anchor 15 may be detachably coupled to an actuation arm (e.g., proximal pusher 78 shown in
The anchor 15 may comprise a curved wire in the deployed configuration, for example a coiled wire or band, a helical wire or band, or a spiral wire or band as described herein. In various embodiments, the anchor 15 may have a curved shape in the deployed configuration. In various embodiments, the anchor may be elongated—rather than curved—in the delivery configuration. For example, the anchor 15 may be elongated into a straight shape within the delivery device 30. In various embodiments, a portion of the anchor 15 may have a curved shape. In various embodiments, a substantial portion of the anchor 15 may have a curved shape. In various embodiments, the anchor 15 may be formed as a flat curve (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis). In various embodiments, the anchor 15 may be formed as a three-dimensional curve (in the deployed configuration) whereby the loops generally are positioned out of plane with one another.
The anchor 15 may comprise a spiral wire or band in the deployed configuration. As used herein, a spiral or spiral shape may comprise a curve which emanates from a point (e.g., a central point) having a continuously increasing or decreasing distance from the point. The spiral or spiral shape may be two-dimensional (e.g., planar) or three-dimensional. In some embodiments, the anchor 15 may comprise one or more spiral portions as described herein. In various embodiments, the anchor 15 may have a spiral-shaped deployed configuration. In various embodiments, spiral refers to a shape with windings about a central axis. The spiral may be continuous. The windings may gradually widen (or tighten) along the length. The spiral may be formed in a flat plane perpendicular to the central axis. In various embodiments, the anchor 15 may have a deployed configuration that is not formed in a flat plane, or in other words the deployed shape is formed in a three-dimensional and/or non-degenerate space. In various embodiments, the anchor 15 may have a conical-shaped deployed configuration including, but not limited to, tubular, conical, frustoconical, and/or helical shapes.
The anchor 15 may comprise one or more loops. For example, the anchor 15 may comprise a plurality of loops, which may increase the radial strength of the anchor by increasing friction and addition structural support. The one or more loops of the anchor 15 may be spiral radially outward from a central point or central axis of the spiral, for example along an axis which is coaxial with a longitudinal axis of a delivery device 30 such that the anchor 15 lies approximately along a plane perpendicular to the longitudinal axis of a delivery device. In some embodiments, the one or more loops of the anchor 15 may comprise one or more spaces therebetween. The spaces may facilitate movement of the captured tissue (e.g. chordae and/or leaflets) from the free end 22 to the center of the anchor 15 during rotation of the anchor 15 as described herein.
The free end 22 of the anchor 15 may extend radially outward from the frame 12, and in particular from the remainder of the spiral band or wire 20. The other end of the anchor 15 may be coupled to the top or bottom of the frame structure 12 as described herein. Alternatively, or in combination, the other end of the anchor 15 may not be attached to the frame structure 12 as described herein. The free end 22 of the anchor 15 may facilitate capturing of the valve leaflets and/or chordal tendineae within the sweep of the free end during rotation as described herein. During rotation of the anchor 15, the leaflets and/or chordae tendineae may be captured by the free end 22 and trapped between the valve frame structure 12 and an interior surface of the anchor 15.
The anchor 15 (e.g., including a tapered spiral band) may comprise a delivery (e.g., elongated) configuration and a deployed configuration (and optional intermediate configurations) as described herein. The anchor 15 may be configured to be actuated from the elongated configuration to the deployed configuration adjacent a native valve in a patient. The anchor 15 may be delivered to the native valve by a delivery device in the elongated configuration as described herein. The anchor 15 may be coupled to the delivery device and/or a frame structure of a valve prosthesis as described herein, for example at a proximal portion (e.g. adjacent proximal attachment point on an interior of the spiral) or distal portion (e.g. adjacent distal attachment point on an exterior of the spiral) thereof. The anchor 15 may be deployed adjacent the native valve substantially similarly to other anchor embodiments as described herein.
After extending out of the side opening 215, the free end 22 of the anchor 15 may optionally rotated around one or more native valve structures on the second side of the native valve such that the one or more native valve structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The anchor 15 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the anchor 15 may be configured such that the one or more native valve structures are not rotated, or are minimally rotated, during rotation of the anchor 15. For example, the anchor 15 may comprise one or more spaces between loops of the anchor 15 which facilitate movement of the captured tissue (e.g. chordae and/or leaflets) from the free end 22 to the center of the spiral structure with little or no torque and/or rotation of the native valve structures during rotation of the tapered spiral band as described herein. Alternatively or in combination, the anchor 15 may be configured such that, when fully deployed, none of the native valve structures reside between the loops of the spiral. Instead, the one or more native valve structures may sit radially inward of the loops in order to facilitate capture of the one or more structures between anchor 15 and the expanded frame structure 12 as described herein. The one or more native valve structures may retain or nearly retain their normal anatomical position when the spiral band is fully deployed. The free end 22 may be disposed radially outwards from the remainder of the anchor 15. Disposing the free end 22 radially outward from the remainder of the anchor 15 may, for example, aid in deployment of the anchor 15 from the delivery device and/or capture of the one or more native valve structures as described herein. The free end 22 may be angled proximally (e.g., towards a proximal portion of the anchor 15 and a distal end of the delivery device 30) or distally (e.g., away from a proximal portion of the anchor 15 and towards a proximal portion of the delivery device 30) from the rest of the anchor 15. Angling the free end 22 proximally or distally towards or away from the delivery device 30 may, for example, aid in deployment of the anchor 15 from the side opening 215 delivery device and/or capture of the one or more native valve structures as described herein.
The distal end of the delivery device 30 may be configured to be advanced from a first side of a native valve to a second side of the native valve. For example, the distal end of the delivery device 30 may be advanced from a left atrial side of a mitral valve to a left ventricular side of a mitral valve. In some instances, the distal end of the delivery device 30 may be transseptally inserted into the left atrium of the heart prior to advancement into the left ventricle. Alternatively, or in combination, the distal end of the delivery device 30 may be steerable such that it is positionable to point towards the first side of the native valve before being advanced to the second side of the native valve.
After advancing to the second side of the native valve, the anchor 15 may be fully deployed on the second side of the native valve. In some embodiments, fully deploying the anchor 15 may comprise positioning the anchor 15 such that it is located only on the second side of the native valve. One will appreciate from the description here, that alternatively the anchor may be deployed on the first side of the valve (e.g., in one of the atria) and then pushed through the respective valve and subsequently rotated to anchor to the chordae and/or native valve.
Advancing the anchor 15 may comprise pushing the anchor through the native valve. Advancing the anchor 15 may further comprise rotating the anchor 15 through the native valve.
In some embodiments, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a first side of the native valve prior to being advanced to a second side of the native valve. For example, the anchor 15 may be deployed in a left atrium of a heart prior to being advanced to a left ventricle of the heart as described herein.
Alternatively, the anchor 15 may be actuated from the delivery configuration to the deployed configuration on a second side of the native valve after being advanced to the second side from a first side of the native valve. For example, anchor 15 may be advanced from a left atrium of a heart prior to being deployed in a left ventricle of the heart by the retreat of an outer sheath 50 or advancement out of an inner shaft 52.
The free end 22 of the deployed anchor 15 may optionally be rotated around one or more structures on the second side of the native valve. The one or more structures may comprise one or more valve leaflets of the native valve. Alternatively, or in combination, the one or more structures may comprise one or more chordae of the left ventricle.
The free end 22 of the deployed anchor 15 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15m and/or towards the longitudinal axis of the delivery device 30. The anchor 15 and/or free end 22 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the anchor 15 and/or free end 22 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the anchor 15.
The anchor 15 may then be released from the distal end of the delivery device 30. The anchor 15 may be released from the distal end of the delivery device 30 on the second side of the native valve.
The frame structure 12 may be expanded within the native valve from an unexpanded configuration to an expanded configuration.
The frame structure 12 may be released from the distal end of the delivery device 30. In some embodiments, at least a portion the frame structure 12 may be expanded within at least a portion of the deployed anchor 15 to anchor the frame structure 12 to the native valve.
In some embodiments, expanding the frame structure 12 and releasing the frame structure 12 may occur simultaneously.
Finally, the delivery device 30 may be retracted from the native valve.
As noted,
While the method shown in
Returning to
The distal end of the delivery device 30 and/or valve prosthesis 10 may be configured to be advanced from a first side of a native valve to a second side of the native valve. For example, the distal end of the delivery device 30 and/or valve prosthesis 10 may be advanced from a left atrial side of a mitral valve 4 to a left ventricular side of a mitral valve 4.
Rotation of the valve prosthesis 10, for example, rotation of the anchor 15 and/or frame structure 12, may be facilitated by the delivery device 30 described herein. For example, the inner shaft 52 may be rotated and rotational motion may be transmitted from the inner shaft 52 or the anchor guide 153 to the valve prosthesis 10 in order to rotate the valve prosthesis 10 around one or more of the structures on the ventricle side of the mitral valve 4 as described herein. Alternatively, or in combination, a proximal portion of the anchor 15 may be detachably coupled to a tether 78 that extends through a lumen of the inner shaft 52 to a distal end thereof. The tether 78 may be rotated and rotational motion may be translated from the tether 78 to the anchor 15 in order to rotate the anchor 15 around the one or more structures on the ventricle side of the mitral valve 4 as described herein.
Once the anchor 15 has been anchored adjacent to the native valve 4, the valve prosthesis 10 comprising the frame structure 12 and prosthetic valve segment 14 may be expanded at least partially within the anchor 15 as described herein. The frame structure 12 and the valve segment 14 may be deployed (e.g., expanded) simultaneously. Alternatively, or in combination, the frame structure 12 and the valve segment 14 may be deployed sequentially, for example by first expanding the frame structure 12 and then receiving the prosthetic valve segment 14 therein.
In some embodiments, the frame structure 12 and the anchor 15 may be located within the same lumen of the delivery device 30 prior to deployment. In some embodiments, the frame structure 12 and the anchor 15 may be located within different lumens of the delivery device 30.
In some embodiments, the frame structure 12 and the anchor 15 may be deployed from the same opening (e.g., the side port 215) in the delivery device 30. In some embodiments, the frame structure 12 and the anchor 15 may be deployed from different openings in the delivery device 30.
The valve prosthesis 10 may then be released from the delivery device 30. Releasing the valve prosthesis 10 from the delivery device 30 may comprise expanding the valve prosthesis 10 from the unexpanded configuration to the expanded configuration. For example, expanding the frame structure 12 and releasing the frame structure 12 may occur simultaneously as described herein. Alternatively, the frame structure 12 may be released prior to or after being expanded.
After the frame structure 12 has been expanded and anchored to the native valve 4 as described herein, the proximal pusher 72 may be retracted. The delivery device 30, comprising the guidewire 54, may then be removed from the heart 2.
Although the steps above show a method of deploying a valve prosthesis 10 within a native valve 4 in accordance with embodiments, a person of ordinary skill in the art will recognize many variations based on the teaching described herein. The steps may be completed in a different order. Steps may be added or deleted. Some of the steps may comprise sub-steps. Many of the steps may be repeated as often as necessary to assemble at least a part of an article.
For example, in some embodiments deploying the valve prosthesis 10 may occur in multiple steps such that a portion of the valve prosthesis 10 (e.g., anchor 15) may be deployed before another portion the valve prosthesis 10 (e.g., frame structure 12). Alternatively, or in combination, in some embodiments, deploying the anchor 15 may occur in multiple steps such that a portion of the anchor 15 may be deployed before being advanced through the native valve 4 and another portion of the anchor 15 may be deployed after being advanced through the native valve 4. Alternatively, or in combination, the delivery device 30 may be advanced from the left atrium 25 to the left ventricle 26 with the valve prosthesis 10 undeployed. In many embodiments, the frame structure may 12 be balloon-expandable and the delivery device may comprise a balloon instead of or in addition to the proximal pusher 72 in order to expand the frame structure 12. Alternatively, or in combination, the anchor 15 may be released after the frame structure 12 has been expanded within it.
As shown in
The delivery device 30 may further comprise the anchor drive shaft 82. The anchor 15 may be disposed on or around the anchor drive shaft 82 in a screw-like undeployed configuration.
Deployment of the anchor 15 from the delivery device 30 may be facilitated by combined retraction of at least a portion of the outer sheath 50 relative to the inner shaft 52 to form or expose a lateral opening in the delivery device 30 and rotation of an anchor drive shaft 82 relative to the outer sheath 50 and/or inner shaft 52. The anchor 15 may be actuated from a delivery configuration (shown in
In some embodiments, the outer sheath 50 may be moved back and forth over the anchor drive shaft 82 prior to, during, or after rotation of the anchor drive shaft 82 in order to “ratchet” incremental portions of the anchor 15 out of the delivery device 30 and away from the inner shaft 52. For example, the anchor 15 may be deployed by a retraction of the inner shaft 52 followed by a series of rotations of the anchor drive shaft 82 followed by an advancement of the anchor drive shaft 82, which may be repeated as needed to deploy the full anchor 15.
The anchor 15 may be releasably coupled to the deployment drive 83. Once the anchor 15 is in the deployed configuration, the deployment drive 83 may remain connected until the anchor 15 is fully secured around the diseased valve and fully deployed implant valve. The deployment drive 83 may be used to translate the anchor 15 distally such that it sits at least partially around the frame structure 12 (as shown in
The anchor 15 may be deployed from the delivery device 30 in the left atrium of the heart and advanced into the left ventricle through the diseased mitral valve as described herein. Alternatively, the anchor 15 may be deployed from the delivery device 30 in the left ventricle of the heart as described herein. Alternatively, the anchor 15 may be partially deployed in the left atrium, advanced into the left ventricle, and then fully deployed in the left ventricle as described herein.
In some embodiments, deployment of the anchor 15 and capture of the one or more structure of the native valve may occur in a stepwise fashion. For example, the anchor 15 may be deployed before being rotated to capture the one or more structures.
In some embodiments, deployment of the anchor 15 and capture of the one or more structure of the native valve may occur simultaneously. For example, rotation of the anchor drive shaft 82 may rotate the anchor 15 out of the delivery device 30. If deployed in the left ventricle, the free end 22 of anchor 15 may be rotated around the one or more native valve structures as the anchor 15 is rotated out of the delivery device.
The distal free end 22 of the anchor may comprise a key 84 configured to slide into a complementary lock 85 located on the band of the anchor 15. When the anchor 15 is fully deployed and wrapped around the frame structure 12 and the diseased valve, the key 84 may slide over the band of the anchor 15 until it falls into place within the lock 85. Once engaged, the key 84 and lock 85 may hold the anchor 15 in place against the one or more structures of the native valve. The respective locations of key 84 and lock 85 may be configured to lock the anchor 15 into the fully deployed configuration, the fully undeployed configuration, or any intermediate configuration therebetween. Any number of key 84 and lock 85 elements may be placed on the anchor 15 in order to allow for one or more locked configurations as desired. The key 84 and lock 85 may be replaced with or combined with other locking mechanisms. For example, a frictional band may replace or be added to the key 84 and lock 85 locking mechanism.
Referring to
In some embodiments, the anchor 15 may comprise a helical or spiral shape in the deployed configuration as described herein. The deflection feature 23 may be comprise one or more bends or kinks along the helical anchor which are discontinuous with the helical shape. In some embodiments, the deflection features 23 may be attached (fixedly or detachably) to the helical or spiral shape, for example in the form of a tab or a wing or the like. Alternatively or in combination, the deflection features 23 may comprise discontinuities in the helical or spiral shape, for example in the form of bends, kinks, waves, humps, bumps, or the like in the helical wire itself. In some embodiments, the deflection features 23 may position a portion of the wire inside, outside, above, below, or at an angle to the otherwise relatively continuous helical or spiral shape of the anchor 15.
The one or more deflection features 23 may be configured so as to resist straightening of the bends when the anchor 15 is in the elongated configuration. The one or more deflection features 23 may be configured interact with the frame structure 12 to facilitate anchoring. The one or more deflection features 23 may be configured not to interact with the frame structure 12 in order to facilitate anchoring. The one or more deflection features may be introduced to the anchor 15 without adding substantial circumferential compliance into the coil.
In at least some instances, it may be sufficient to initially deflect the free end 22 during wrapping as described herein in order to form the first loop around the delivery device 30. Once the first loop as wrapped around the delivery device 30, the remaining loops may be more inclined or biased to wrap correctly around the delivery device 30 without additional deflection or manipulation.
In at least some instances, deflection (e.g., angling proximally, distally, and/or radially outward) of the free end 22 away from the loops of the proximal portion of the anchor 15 may aid in capture of the one or more structures by forming a “grabber” arm.
In at least some instances, the absence of additional deflection features 23 on the loops of the anchor 15 may facilitate rotation of the loops around the one or more structures as described herein. Alternatively, or in combination, the absence of additional deflection features 23 on the loops may enhance the circumferential strength of the loops of the anchor 15.
In some embodiments, the anchor 15 may comprise a flat spiral shape in the deployed configuration as described herein. The deflection feature 23 may be comprise one or more bends or kinks along the spiral anchor which are discontinuous with the spiral shape. In some embodiments, the deflection features 23 may be attached (fixedly or detachably) to the spiral shape, for example in the form of a tab or a wing or the like. Alternatively or in combination, the deflection features 23 may comprise discontinuities in the spiral shape, for example in the form of bends, kinks, waves, humps, bumps, or the like in the spiral wire itself. In some embodiments, the deflection features 23 may position a portion of the wire radially inside, radially outside, above, below, or at an angle to the otherwise relatively continuous spiral shape of the anchor 15.
In at least some instances, the absence of additional deflection features 23 on the loops of the anchor 15 may facilitate rotation of the loops around the one or more structures as described herein. Alternatively, or in combination, the absence of additional deflection features 23 on the loops may enhance the circumferential strength of the loops of the anchor 15.
While the one or more deflection features have been described herein with reference to changing the angle of a free end of an anchor of a valve prosthesis during deployment from a delivery device, it will be understood by one of ordinary skill in the art that such features may be used in a variety of settings.
Alternatively, or in combination with, the deflection feature(s) 23 built into the anchor 15, the anchor 15 may include a movable core wire (e.g., wire or rod) therein configured to change the shape of the distal portion of the anchor assembly. For example,
In various embodiments, the anchor 15 and/or core wire 74 may have a spiral-shaped deployed configuration. In various embodiments, spiral refers to a shape with windings about a central axis. The spiral may be continuous. The windings may gradually widen (or tighten) along the length. The spiral may be formed in a flat plane perpendicular to the central axis. In various embodiments, the anchor 15 and/or core wire 74 may have a deployed configuration that is not formed in a flat plane, or in other words the deployed shape is formed in a three-dimensional and/or non-degenerate space. In various embodiments, the anchor 15 and/or core wire 74 may have a conical-shaped deployed configuration including, but not limited to, tubular, conical, frustoconical, and/or helical shapes.
In various embodiments, the core wire 74 may be configured to be removed from the valve prosthesis (e.g., translated proximally out of the body) after the anchor 15 has been deployed. The core wire 74 may be removed with the delivery device as will be understood by one of ordinary skill in the art based on the disclosure herein.
In various embodiments, the core wire 74 may be configured to remain within the anchor 15 after the anchor 15 has been deployed. A proximal end of the core wire 74 may be released from the delivery device 30 as will be understood by one of ordinary skill in the art based on the disclosure herein.
In various embodiments, a proximal end of the core wire 74 may be directly manipulated by a user outside the body in order to translate the core wire 74 within the anchor 15. In various embodiments, a proximal end of the core wire 74 may be indirectly manipulated by a user, for example, with a translatable pusher section 73 (as described elsewhere herein) disposed within the delivery device and coupled to the proximal end of the core wire 74 adjacent the anchor 15, in order to translate the core wire within the anchor.
The anchor 15 may be relatively stiffer than the core wire 74. The anchor 15 may be sufficiently stiffer than the core wire 74 such that the core wire 74 anchor 15 experiences little or no deflection itself when the core wire 74 is disposed therein.
In some embodiments, the distal tip 75 may comprise an elongated delivery configuration as described herein. The deflection feature 33 may comprise one or more bends or kinks along the length of the elongated distal tip 75. The elongated distal tip 75 may be substantially straight along a longitudinal axis thereof (for example, substantially co-axial with a longitudinal axis of the delivery device 30 as described herein). The deflection feature 33 may comprise one or more bends that position at least a portion of the core wire 74 discontinuous with the rest of the core wire 74, for example along an axis other than the longitudinal axis. For example, the deflection feature 33 may comprise a bend at an angle relative to the longitudinal axis or a plurality of bends to form a portion (for example, a wave, bump, hump, or the like) which starts and ends along the longitudinal axis but which is disposed off-axis (e.g., parallel to or at an angle to the longitudinal axis) along at least a portion of the deflection feature 33. In some embodiments, the deflection features 33 may be attached (fixedly or detachably) to the distal tip 75, for example in the form of a tab or a wing or the like.
In some embodiments, at least a portion of the core wire 74 may comprise a curved shape when the anchor 15 is in the deployed configuration. The curved shape may, for example, comprise a coil, a helix, or a spiral as described herein. The curved shape may be configured to encircle one or more structures of the native valve. The curved shape may correspond to the curved shape of the anchor 15 in the deployed configuration. The deflection feature 33 may be comprise one or more bends or kinks along the core wire 74 which are discontinuous with the curved shape. In some embodiments, the deflection features 33 may be attached (fixedly or detachably) or adjacent to the curved shape, for example in the form of a tab or a wing or the like. Alternatively or in combination, the deflection features 33 may comprise discontinuities in the curved shape, for example in the form of bends, kinks, waves, humps, bumps, or the like in the curved wire itself. In some embodiments, the deflection features 33 may position a portion of the wire inside, outside, above, below, or at an angle to the otherwise relatively continuous curved shape of the core wire 74.
It will be understood by one of ordinary skill in the art that the number of bends, the angle of each bend, the length, the shape, the location, and/or the orientation of the deflection feature 33, the number of deflection features 33, and/or the diameter and/or material of the core wire 74 and/or anchor 15 may be adjusted in order to effect a desired amount and orientation of the deflection of the distal tip 75 of the core wire 74 and/or free end 22 of the anchor 15.
In various embodiments, the anchor 15 may have a generally helical shape in the deployed configuration. In various embodiments, the anchor 15 may be elongated—rather than helix-shaped—in the delivery configuration. For example, the anchor 15 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the anchor 15 may have a helical shape. In various embodiments, a substantial portion of the anchor 15 may have a helical shape. In various embodiments, the helical anchor 15 may be formed as a three-dimensional helix (in the deployed configuration) whereby the loops generally are positioned around the same axis (for example, a longitudinal axis of the delivery device 30).
Optionally, the anchor 15 may comprise a first portion comprising the helical shape and another portion. Alternatively, or in combination, the anchor 15 may comprise a plurality of helical portions. For example, the anchor 15 may comprise at least two helical portions having the same or different diameters. Alternatively, or in combination, the anchor 15 may comprise at least two helical portions having the same or different winding pitches.
The free end 22 of the anchor 15 may extend radially outward from the frame structure 12, and in particular from the remainder of the anchor 15 (for example, as shown in
The anchor 15 may comprise a movable core wire 74 disposed within a lumen or channel of the anchor 15 as described herein. A distal tip portion of the core wire 74 may comprise one or more deflection features 33 disposed thereon or therealong as described herein. For example the distal tip portion may comprise a single deflection feature 33. The core wire 74 may be translatable. The core wire 74 may translate distally and proximally within the lumen 71 of the anchor 15. Translation of the core wire 74 within the lumen 71 of the anchor 15 may cause the one or more deflection features 33 to deflect the distal tip 75 of the core wire 74 as it moves in or out of the anchor 15. For example, when advanced distally past the free end 22 of the anchor 15, a distal tip 75 of the core element 74 may be caused to “wiggle” or deflect away from the curvature of the curved anchor body 15 and change the deployment angle of the distal tip 75 of the core wire 74 out of the anchor body 15 in order to facilitate wrapping of the anchor 15 around the delivery device 30 as described herein.
The movable core wire 74 may be translated within the anchor 15 before, during, or after deployment of the anchor 15 from the undeployed configuration to the deployed configuration. For example, the movable core wire 15 may be translated within the anchor 15 before deployment of the anchor 15 into a self-assembly state (e.g., as shown in
Deflection of the core wire 74 and distal tip 75 may be adjusted and/or optimized for various steps during deployment of the valve prosthesis 10 as described herein. For example, the distal tip 75 may be advanced into a self-assembly state prior to or during deployment of the anchor 15 from the delivery device 30 in order to facilitate wrapping of the core wire 74 and anchor 15 around the delivery device 30 into the correctly deployed configuration as described herein. In the self-assembly state, the distal tip 75 may be deflected prior to or during deployment of the anchor 15 such that the distal tip 75 overlaps with one or more turns of the anchor 15 in order to ensure that the free end 22 wraps back around the delivery device 30.
The deflection feature 33 in the self-assembly state may, for example, be configured to deflect the distal tip 15 proximally (e.g., towards a proximal portion of the anchor 15 and a distal end of the delivery device 30), distally (e.g., away from a proximal portion of the anchor 15 and towards a proximal portion of the delivery device 30), and/or radially (e.g., radially outwards or inwards from the main body of the anchor 15 and away from or towards the delivery device 30, respectively). In some embodiments, for example, the deflection feature 33 may be configured to position the distal tip 75 adjacent one or more loops of the anchor 15 when the anchor 15 is in the deployed configuration. Alternatively, or in combination, the deflection feature 33 may be configured to position the distal tip 75 such that it angles towards a proximal end of the anchor 15 when the anchor 15 is in the deployed configuration. Alternatively, or in combination, the deflection feature 33 may be configured to position the distal tip 75 such that it angles towards a distal end of the delivery device 30 when the anchor 15 is in the deployed configuration.
In at least some instances, it may be sufficient to initially deflect the distal tip 75 during wrapping as described herein in order to form the first loop of the anchor 15 around the delivery device 30. Once the first loop as wrapped around the delivery device 30, the remaining loops may be more inclined or biased to wrap correctly around the delivery device 30 without additional deflection or manipulation. The core wire 74 may remain in the self-assembly for the entirety of the deployment of the anchor 15 from the delivery device 30. Alternatively, once the free end 22 of the anchor 15 has made a first loop around the delivery device 30 facilitated by the distal tip 75 of the core wire 74, the distal tip 75 of the core wire 74 may be translated proximally and retracted at least partially back into the anchor 15 for the remainder of the deployment of the anchor 15.
The deflection feature 33 in the encircling state may, for example, be configured to deflect the distal tip 15 proximally (e.g., towards a proximal portion of the anchor 15 and a distal end of the delivery device 30), distally (e.g., away from a proximal portion of the anchor 15 and towards a proximal portion of the delivery device 30), and/or radially (e.g., radially outwards or inwards from the main body of the anchor 15 and away from or towards the delivery device 30, respectively).
In at least some instances, deflection (e.g., angling proximally, distally, and/or radially outward) of the distal tip 75 of the core wire 74 away from the loops of the anchor 15 may aid in capture of the one or more native valve structures by forming a “grabber” arm. For example, during rotation of the anchor 15, the grabber arm distal tip 75 of the core wire 74 may be rotated as shown to capture the one or more structures of the native valve.
The distal tip 75 of the core wire 74 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, and/or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The core wire 74, distal tip 75, anchor 15, and/or free end 22 may be configured such that minimal torque is applied to the one or more native valve structures. Alternatively, or in combination, the core wire 74, distal tip 75, anchor 15, and/or free end 22 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the anchor 15.
The distal tip 75 of the core wire 74 may optionally rotated around one or more structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The core wire 74, distal tip 75, anchor 15, and/or free end 22 may be configured such that minimal torque is applied to the one or more native valve structures. Alternatively, or in combination, the core wire 74, distal tip 75, anchor 15, and/or free end 22 may be configured such that the one or more native valve structures are not rotated, or are minimally rotated, during rotation of the anchor 15.
The anchor 15 may comprise a single lumen or channel 71. The anchor 15 may comprise a plurality of lumens or channels 71. For example, the anchor 15 may comprise one, two, three, four, five, six, seven, eight, nine, or ten lumens of channels 71 disposed therethrough. It will be understood to one of ordinary skill in the art based on the teachings herein that any number of channels may be utilized as desired. The channels 71 may for example be left as open lumens (e.g., for placement of one or more core wires 74 therethrough). Alternatively, or in combination, the channels may be filled, for example with one or more stiffening members.
The anchor 15 may comprise a round cross-section. The anchor 15 may comprise a non-round cross section. The anchor 15 may have a cross-section of any shape desired, for example a circular, tubular, hollow, square, elongated, ovoid, triangular, or any other shaped cross-section. The cross-sectional shape of the anchor 15 may, for example, be selected to facilitate deployment from the delivery device. Alternatively, or in combination, the shape of the anchor 15 may be selected to reduce pulling, torqueing, or otherwise damaging the one or more native valve structures as it is rotated therearound. Alternatively, or in combination, the shape of the anchor 15 may be selected to provide sufficient radial strength when a frame structure 12 is expanded therein to anchor the frame structure 12 to the one or more native valve structures therebetween.
The anchor 15 may comprise or more loops. For example, the anchor 15 may comprise a plurality of loops, which may increase the radial strength of the anchor by increasing friction and addition structural support. The one or more loops of the anchor 15 may be substantially cylindrical around a central axis of the anchor 15, for example along an axis which is coaxial with a longitudinal axis of a delivery device 30. The one or more loops of the anchor 15 may be substantially helical around a central axis or helical axis of the anchor 15, for example along an axis which is coaxial with a longitudinal axis of a delivery device. The one or more loops (also referred to herein as coils or turns) of the anchor 15 may comprise a curved shape that bends around back towards its origin (for example, an arc, ellipsoid, circle, or the like). In some embodiments, a loop may comprise a curved shape that bends back towards its origin but does not cross itself, making a rotation within a range of about 180 degrees to about 360 degrees, as described herein. In some embodiments, a loop may comprise a shape that bends back towards and crosses itself, making at least a 360 degree rotation, as described herein. The one or more loops may comprise any number of loops desired, for example, one, two, three, four, five, six, seven, eight, nine, or ten loops. The one or more loops may comprise a rotation within a range of about 180 degrees to about 3600 degrees as described herein. The one or more loops may comprise a rotation within a range bounded by any of the following values: 180 degrees, 270 degrees, 360 degrees, 450 degrees, 540 degrees, 630 degrees, 720 degrees, 810 degrees, 900 degrees, 990 degrees, 1080 degrees, 1170 degrees, 1260 degrees, 1350 degrees, 1440 degrees, 1530 degrees, 1620 degrees, 1710 degrees, 1800 degrees, 1890 degrees, 1980 degrees, 2070 degrees, 2160 degrees, 2250 degrees, 2340 degrees, 2430 degrees, 2520 degrees, 2610 degrees, 2700 degrees, 2790 degrees, 2880 degrees, 2970 degrees, 3060 degrees, 3150 degrees, 3240 degrees, 3330 degrees, 3420 degrees, 3510 degrees, or 3600 degrees.
Interaction of the frame structure 12 with the one or more loops of the anchor 15 may create opposing forces therebetween that provide mechanical leverage for anchoring the frame structure 12 to the one or more anatomical structures as described herein. In some embodiments, the one or more loops may comprise at least 360 degrees of rotation when deployed such that the loops wrap around one another and provide additional mechanical leverage against the frame structure 12 in order to facilitate anchoring of the frame structure as described herein. Additional loops or partial loops may provide additional mechanical strength and/or leverage.
In some embodiments, the core wire 74 may comprise a helical shape in the deployed configuration as described herein. The deflection feature 33 may be comprise one or more bends or kinks along the distal section 77 which are discontinuous with the helical shape of the proximal curved section 76. In some embodiments, the deflection feature 33 may be attached (fixedly or detachably) to the distal section 77, for example in the form of a tab or a wing or the like. Alternatively or in combination, the deflection feature 33 may comprise a discontinuity in the helical shape, for example in the form of bends, kinks, waves, humps, bumps, or the like in the wire itself.
In some embodiments, the core wire 74 may comprise a spiral shape in the deployed configuration as described herein (e.g., as shown in
In some embodiments, one or more deflection features 33 may be positioned along the length of the distal section 77 at one or more locations such that deflection of the distal tip 75 is “timed” to occur with the distal tip 75 and/or free end 22 wrapping back towards the delivery device 30 as described herein. The distal tip 75 may, for example, be deflected each time it wraps back towards the delivery device 30 as described herein. In some embodiments, the deflection features 33 may position the distal tip portion 77 of the core wire 74 inside, outside, above, below, or at an angle to the otherwise relatively continuous curved shape of the proximal curved section 76.
The one or more deflection features 33 may be configured so as to resist straightening of the bends when the anchor is in the elongated configuration. The one or more deflection features 33 may be configured interact with the frame structure 12 to facilitate anchoring. The one or more deflection features 33 may be configured not to interact with the frame structure in order to facilitate anchoring. The one or more deflection features 33 may advantageously avoid a need for substantial circumferential compliance into the curved shape of the anchor 15.
The core wire 74 may be formed of a material having sufficient rigidity to hold a predetermined shape. The core wire 74 may, for example, be formed of a shape memory material (e.g., NiTi). It may be desirable for at least an end portion (e.g., a distal section 77 as described herein) to be relatively rigid such that it can exert a force to move chordal tendineae, while still retaining flexibility to be collapsed within the anchor 15 and/or a delivery device 30. In various embodiments, the distal section 77 only needs sufficient rigidity to hold its shape and will deform under a load. For example, the distal section 77 may be configured with a similar rigidity to a guidewire, or slightly stiffer.
The distal tip 75 of the core wire 74 may be sized and dimensioned for insertion through the native valve, for example through tissue at or near a commissure of the native valve or through the valve opening itself. In some embodiments, the distal tip 75 may comprise an atraumatic tip to avoid reduce risk of injury to the native valve tissue and leaflets. For example, the distal tip 75 may comprise a blunt end, a ball tip, a curved tip (e.g., J-tip or pigtail), or other atraumatic shapes. Alternatively, the distal tip 75 may be configured for piercing tissue.
In various embodiments, the distal tip 75 may be shaped and configured to reduce the risk of counter-rotation. For example, the distal tip 75 may have a curled end to cause the distal tip 75 to snag chordae if it is rotated in a direction opposite the anchoring rotation.
The distal tip 75 may optionally rotated around one or more native valve structures on the second side of the native valve such that the one or more structures (e.g., chordae, leaflets, or annulus) are pulled radially inwards towards the longitudinal axis of the anchor 15 and/or towards the longitudinal axis of the delivery device 30. The distal tip 75 and/or free end 22 may be configured such that minimal torque is applied to the one or more structures. Alternatively, or in combination, the distal tip 75 and/or free end 22 may be configured such that the one or more structures are not rotated, or are minimally rotated, during rotation of the anchor 15. For example, the anchor 15 may comprise one or more spaces between loops of the curved shape of the anchor 15 which facilitate movement of the captured tissue (e.g. chordae and/or leaflets) from the distal tip 75 and/or free end 22 to the center of the curved structure with little or no torque and/or rotation of the structures during rotation of the anchor 15 as described herein. The one or more native valve structures may sit radially inward of the loops in order to facilitate capture of the one or more native valve structures between the distal tip 75 and/or anchor 15 and the expanded frame structure 12. The one or more native valve structures may retain or nearly retain their normal anatomical position when the anchor 15 is fully deployed.
The free end 22 of the anchor 15 may extend radially outward from the frame structure, and in particular from the remainder of the anchor 15. The other end of the spiral band or wire 20 may be coupled to the top or bottom of the frame structure as described herein. Alternatively, or in combination, the other end of the anchor 15 may not be attached to the frame structure 12 as described herein. The free end 22 of the anchor 15 may facilitate capturing of the valve leaflets and/or chordal tendineae within the sweep of the free end during rotation as described herein. During rotation of the anchor 15, the leaflets and/or chordae tendineae may be captured by the free end 22 and trapped between the valve frame structure and an interior surface of the anchor 15.
In various embodiments, the anchor 15 may have a generally spiral shape in the deployed configuration. In various embodiments, the anchor 15 may be elongated—rather than spiral-shaped—in the delivery configuration. For example, the anchor 15 may be elongated into a straight shape within the delivery device. In various embodiments, a portion of the anchor 15 may have a spiral shape. In various embodiments, a substantial portion of the anchor 15 may have a spiral shape. In various embodiments, the anchor 15 may be formed as a flat spiral (in the deployed configuration) whereby the loops generally are positioned within the same plane (the plane being perpendicular to a longitudinal axis).
Optionally, the anchor 15 may comprise a first portion comprising the spiral portion and another portion. Alternatively, or in combination, the anchor 15 may comprise a plurality of spiral portions. For example, the anchor 15 may comprise at least two spiral portions having the same or different diameters. Alternatively, or in combination, the anchor 15 may comprise at least two spiral portions having the same or different winding pitches.
The anchor 15 may comprise a movable core element 74 disposed within a lumen or channel 71 of the anchor 15 as described herein. A distal section 77 of the core wire 74 may comprise one or more deflection features 33 disposed thereon or therealong as described herein. For example the distal tip portion may comprise a single deflection feature 33. The core wire 74 may be translatable. The core wire 74 may translate distally and proximally within the lumen 71 of the anchor 15. Translation of the core wire 74 within the lumen 71 of the anchor 15 may cause the one or more deflection features 33 to deflect the distal tip 75 of the core wire 74 as it moves in or out of the anchor 15. For example, when advanced distally past the free end 22 of the anchor 15, a distal tip 75 of the core element 74 may be caused to “wiggle” or deflect away from the curvature of the curved anchor body 15 and change the deployment angle of the distal tip 75 out of the anchor body 15 in order to facilitate wrapping of the anchor 15 around the delivery device 30 as described herein.
The movable core wire 74 may be translated within the anchor 15 before, during, or after deployment of the anchor 15 from the undeployed configuration to the deployed configuration. For example, the movable core wire 74 be translated within the anchor 15 before deployment of the anchor 15 into a self-assembly state (e.g., as shown in
While the one or more deflection features 23, 33 have been described herein with reference to changing the angle of a distal tip 75 of a core wire 74 and/or free end 22 of an anchor 14 of a valve prosthesis 10 during deployment from a delivery device 30, it will be understood by one of ordinary skill in the art that such deflection features 23, 33 may be used in a variety of settings.
The core wire 74 may comprise one or more sections of wire having the same or different pre-formed shapes to facilitate deployment within the lumen of the anchor. For example, the core wire 74 may comprise a distal wire section 77 comprising the distal tip 75 and one or more deflection features as described herein. The core wire 74 may also comprise a proximal curved section 76 proximal to the distal section 77 which comprises a curved shape. The curved shape may be substantially similar to the curved shape of the anchor in order to provide robust rotational constraint to the core wire 74 so that the distal tip 75 does not rotate relative to the anchor as it is translated. Alternatively, the curved shape may be configured with a different shape or curvature that the anchor in order to induce rotation in the distal tip 75 during translation as desired. In some embodiments, the core wire 74 may comprise a tether 78 or proximal pusher section proximal to the proximal curved section 76 which extends from the proximal curved portion 76 to a proximal end of the delivery device. The proximal pusher section or tether 78 may act as an actuation mechanism and facilitate longitudinal translation of the core wire 74 within the lumen 71 of the anchor 74. For example, a proximal end of the proximal pusher section or tether 78 may be coupled to an actuation mechanism in/on the delivery device 30 in order to translate the core wire 74. Alternatively, the proximal end of the proximal pusher section or tether 78 may be manually manipulated by at or near a proximal end of the delivery device in order to translate the core wire 74.
Rather than providing a core wire 74 comprising a single wire and one or more deflection features 33 disposed thereon or therealong (e.g., as shown in
In some embodiments, the first wire 74a and the second wire 74b may be disposed within a housing 79. The housing 79 may comprise a flexible material. Translation of the first and second wires 74a, 74b relative to one another may change the curvature of the housing 79, thereby deflecting the distal tip 75 of the core wire 74 in order to facilitate anchor deployment and/or wrapping of the anchor 15 around one or more structures of the native valve in a manner substantially similar to that described with respect to the deflecting features described herein. By providing two or more wires 74a, 74b within a housing 79, the distal tip 75 of the core wire 74 may be deflecting into more complex and/or varying shapes than may be possible with a deflection features disposed on or along the core wire 74. In some embodiments, the entire “grabber arm” of the distal section 77 may be made up of wires.
It should be understood that any feature described with respect to one embodiment may be combined with or substituted for any feature described with respect to another embodiment.
Although the method steps described herein are described sequentially in accordance with certain embodiments, a person of ordinary skill in the art will recognize many variations based on the teaching described herein. The steps may be completed in a different order. Steps may be added or deleted. Some of the steps may comprise sub-steps. Many of the steps may be repeated as often as necessary ensure correct placement of the delivery device and deployment of the valve prosthesis components.
Not necessarily all such aspects or advantages are achieved by any particular embodiment. Thus, various embodiments may be carried out in a manner that achieves or optimizes one advantage or group of advantages taught herein without necessarily achieving other aspects or advantages as may also be taught or suggested herein.
When a feature or element is herein referred to as being “on” another feature or element, it can be directly on the other feature or element or intervening features and/or elements may also be present. In contrast, when a feature or element is referred to as being “directly on” another feature or element, there are no intervening features or elements present. It will also be understood that, when a feature or element is referred to as being “connected”, “attached” or “coupled” to another feature or element, it can be directly connected, attached or coupled to the other feature or element or intervening features or elements may be present. In contrast, when a feature or element is referred to as being “directly connected”, “directly attached” or “directly coupled” to another feature or element, there are no intervening features or elements present. Although described or shown with respect to one embodiment, the features and elements so described or shown can apply to other embodiments. It will also be appreciated by those of skill in the art that references to a structure or feature that is disposed “adjacent” another feature may have portions that overlap or underlie the adjacent feature.
Terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. For example, as used herein, the singular forms “a”, “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. It will be further understood that the terms “comprises” and/or “comprising,” when used in this specification, specify the presence of stated features, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, steps, operations, elements, components, and/or groups thereof. As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items and may be abbreviated as “/”.
Spatially relative terms, such as “under”, “below”, “lower”, “over”, “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. It will be understood that the spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if a device in the figures is inverted, elements described as “under” or “beneath” other elements or features would then be oriented “over” the other elements or features. Thus, the exemplary term “under” can encompass both an orientation of over and under. The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly. Similarly, the terms “upwardly”, “downwardly”, “vertical”, “horizontal” and the like are used herein for the purpose of explanation only unless specifically indicated otherwise.
Although the terms “first” and “second” may be used herein to describe various features/elements (including steps), these features/elements should not be limited by these terms, unless the context indicates otherwise. These terms may be used to distinguish one feature/element from another feature/element. Thus, a first feature/element discussed below could be termed a second feature/element, and similarly, a second feature/element discussed below could be termed a first feature/element without departing from the teachings of the present invention.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word “comprise”, and variations such as “comprises” and “comprising” means various components can be co-jointly employed in the methods and articles (e.g., compositions and apparatuses including device and methods). For example, the term “comprising” will be understood to imply the inclusion of any stated elements or steps but not the exclusion of any other elements or steps.
As used herein in the specification and claims, including as used in the examples and unless otherwise expressly specified, all numbers may be read as if prefaced by the word “about” or “approximately,” even if the term does not expressly appear. The phrase “about” or “approximately” may be used when describing magnitude and/or position to indicate that the value and/or position described is within a reasonable expected range of values and/or positions. For example, a numeric value may have a value that is +/−0.1% of the stated value (or range of values), +/−1% of the stated value (or range of values), +/−2% of the stated value (or range of values), +/−5% of the stated value (or range of values), +/−10% of the stated value (or range of values), etc. Any numerical values given herein should also be understood to include about or approximately that value, unless the context indicates otherwise. For example, if the value “10” is disclosed, then “about 10” is also disclosed. Any numerical range recited herein is intended to include all sub-ranges subsumed therein. It is also understood that when a value is disclosed that “less than or equal to” the value, “greater than or equal to the value” and possible ranges between values are also disclosed, as appropriately understood by the skilled artisan. For example, if the value “X” is disclosed the “less than or equal to X” as well as “greater than or equal to X” (e.g., where X is a numerical value) is also disclosed. It is also understood that the throughout the application, data is provided in a number of different formats, and that this data, represents endpoints and starting points, and ranges for any combination of the data points. For example, if a particular data point “10” and a particular data point “15” are disclosed, it is understood that greater than, greater than or equal to, less than, less than or equal to, and equal to 10 and 15 are considered disclosed as well as between 10 and 15. It is also understood that each unit between two particular units are also disclosed. For example, if 10 and 15 are disclosed, then 11, 12, 13, and 14 are also disclosed.
While preferred embodiments of the present invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions will now occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed in practicing the invention. It is intended that the following claims define the scope of the invention and that methods and structures within the scope of these claims and their equivalents be covered thereby.
Claims
1-25. (canceled)
26. A delivery system for delivering a prosthesis to a diseased valve, the delivery system comprising:
- an outer sheath;
- an inner shaft within the outer sheath, the inner shaft translatable and rotatable relative to the outer sheath; and
- an anchor guide attached to a distal end of the inner shaft, the anchor guide comprising a proximal section that defines a central axis and a distal section that curves about the central axis in a tapered spiral.
27. The delivery system of claim 26, wherein the tapered spiral of the distal section extends more than 360 degrees.
28. The delivery system of claim 26, further comprising an anchor slidably disposed within the anchor guide.
29. The delivery system of claim 28, wherein the anchor guide is configured to correctly orient the anchor relative to a longitudinal axis of the inner shaft in order to facilitate concentric wrapping of the anchor around the inner shaft as the anchor is deployed from the anchor guide.
30. The delivery system of claim 26, wherein the outer sheath is steerable.
31. The delivery system of claim 26, wherein the distal section transitions continuously from a high pitch, low radius curve at a proximal end to a low pitch, high radius curve at a distal end.
32. The delivery system of claim 26, wherein a distal-most portion of the distal section resides in a plane that is orthogonal to the central axis.
33. The delivery system of claim 26, wherein a curvature of the distal section is configured to match a curvature of an anchor of the prosthesis.
34. The delivery system of claim 26, wherein the inner shaft and the anchor guide are of unitary construction.
35. A delivery system for delivering a prosthesis to a diseased valve, the delivery system comprising:
- an outer sheath;
- an inner shaft within the outer sheath, the inner shaft translatable and rotatable relative to the outer sheath; and
- an anchor guide attached to a distal end of the inner shaft, the anchor guide comprising a proximal section that defines a central axis and a distal section that forms a tapered corkscrew and curves about the central axis, wherein the inner shaft and anchor guide are configured to rotate relative to the outer sheath.
36. The delivery system of claim 35, wherein the distal section extends more than 360 degrees.
37. The delivery system of claim 35, further comprising an anchor slidably disposed within the anchor guide.
38. The delivery system of claim 37, wherein the anchor guide is configured to correctly orient the anchor of the prosthesis relative to the central axis in order to facilitate concentric wrapping of the anchor around the central axis as the anchor is deployed from the anchor guide.
39. The delivery system of claim 35, wherein the outer sheath is steerable.
40. The delivery system of claim 35, wherein the distal section transitions continuously from a high pitch, low radius curve at a proximal end to a low pitch, high radius curve at a distal end.
41. The delivery system of claim 35, wherein a distal-most plane of the distal section is orthogonal to the central axis.
42. The delivery system of claim 35, wherein a curvature of the distal section is configured to match a curvature of an anchor of the prosthesis.
43. The delivery system of claim 35, wherein the inner shaft and the anchor guide are of unitary construction.
44. A delivery system for delivering a prosthesis to a diseased valve, the delivery system comprising:
- an outer sheath;
- an inner shaft within the outer sheath, the inner shaft translatable and rotatable relative to the outer sheath; and
- an anchor guide attached to a distal end of the inner shaft, the anchor guide comprising a proximal section that defines a central axis, a distal section that curves about the central axis, and an intermediate section between the proximal section and the distal section, wherein the intermediate section transitions in a tapered spiral from a first radius of curvature to a second radius of curvature.
45. The delivery system of claim 44, wherein the distal section extends more than 360 degrees.
46. The delivery system of claim 44, wherein the distal section comprises the second radius of curvature.
47. The delivery system of claim 44, wherein the distal section resides in a distal-most plane that is orthogonal to the central axis.
48. The delivery system of claim 44, wherein the distal section has a relatively constant radius of curvature.
49. The delivery system of claim 44, further comprising an anchor slidably disposed within the anchor guide.
50. The delivery system of claim 44, wherein a curvature of the distal section is configured to match a curvature of an anchor of the prosthesis.
51. The delivery system of claim 44, wherein the inner shaft and the anchor guide are of unitary construction.
52. The delivery system of claim 44, wherein the distal section is concentric to the central axis of the proximal section.
53. The delivery system of claim 44, wherein the second radius of curvature is larger than the first radius of curvature.
54. The delivery system of claim 32, wherein the distal-most portion of the distal section extends at least 180 degrees.
Type: Application
Filed: Sep 12, 2022
Publication Date: Sep 7, 2023
Inventors: Claudio ARGENTO (Felton, CA), Andrew BACKUS (Santa Cruz, CA), Alice YANG (Campbell, CA), Ali SALAHIEH (Saratoga, CA), Jasper Ellington ADAMEK-BOWERS (San Francisco, CA), Connor MULCAHY (San Francisco, CA), Ryan William BOYD (Santa Cruz, CA), Nicholas J. SPINELLI (San Carlos, CA), Tom SAUL (Moss Beach, CA)
Application Number: 17/931,408
