Self-aligning radiopaque ring

Abstract

An intravascular device configured to be recaptured within a guide catheter has a ring located at the distal end of a delivery catheter. The ring has an outer diameter greater than that of the delivery catheter and a sloped guide surface near the outer edge of the ring to urge the ring and delivery catheter toward a radially centered position within the guide catheter.

Description

BACKGROUND OF THE DISCLOSURE

Intravascular medical procedures allow the performance of therapeutic treatments in a variety of locations within a patient's body while requiring only relatively small access incisions. An intravascular procedure may, for example, eliminate the need for open-heart surgery, reducing risks, costs, and time associated with an open-heart procedure. The intravascular procedure also enables faster recovery times with lower associated costs and risks of complication. An example of an intravascular procedure that significantly reduces procedure and recovery time and cost over conventional open surgery is a heart valve replacement or repair procedure. An artificial valve is guided to the heart through the patient's vasculature. For example, a catheter is inserted into the patient's vasculature and directed to the inferior vena cava. The catheter is then urged through the inferior vena cava toward the heart by applying force longitudinally to the catheter. Upon entering the heart from the inferior vena cava, the catheter enters the right atrium. In a procedure to repair a mitral valve using a mitral clip, the left atrium must be reached for the catheter to access the mitral valve of the heart. The catheter may reach the left atrium through a puncture in the intra-atrial septum. To do so, the distal end of the catheter may be deflected by one or more wires positioned inside the catheter. Precise control of the distal end of the catheter allows for smaller punctures in the intra-atrial septum, more reliable and faster positioning of a mitral clip on the mitral valve, and other improvements in the procedures.

The mitral clip needs to be placed precisely relative to the mitral valve. Once in place, the mitral clip is difficult to move or replace, so an accurate initial placement during the procedure is preferred. Imaging of the mitral clip and the catheter that delivers the mitral clip to the mitral valve in the heart is needed. Additionally, the ability to recapture a partially deployed mitral clip is desirable in the event that the distal end of the catheter and moves relative to the mitral valve and compromises the precise positioning of the mitral clip.

The recapture of the mitral clip requires the collapse of one or more moveable arms of the mitral clip. The one or more moveable arms move toward the axis of a catheter steerable guide catheter (“SGC”) and the mitral clip may be retracted or recaptured into the tip of the SGC to allow replacement and/or redeployment of the mitral clip. In some instances, the one or more moveable arms of the mitral clip may contact the tip or other portion of the exterior of the SGC and limit or prevent recapture. A more reliable recapture device and/or method may reduce complications and potential harm to the patient.

BRIEF SUMMARY OF THE DISCLOSURE

This summary is provided to introduce a selection of concepts that are further described below in the detailed description. This summary is not intended to identify specific features of the claimed subject matter, nor is it intended to be used as an aid in limiting the scope of the claimed subject matter.

In a first embodiment, a device for aligning components of an intravascular system includes a head and a body with a longitudinal axis extending therethrough. The body is connected proximally to the head and has a body radius. The head has a face with a face radius. A face radius to body radius ratio is in a range of 1.20 to 1.75. The head has a guide surface positioned longitudinally between the face and the body. The guide surface extends distally radially outward and forms an angle with the longitudinal axis in a range of 100° to 160°.

In another embodiment, an intravascular system includes a delivery catheter and a ring. The delivery catheter has a distal end and a proximal end. The delivery catheter also has an inner surface defining a lumen and an outer surface. The ring is affixed to the distal end of the delivery catheter and at least a part of the ring is positioned within the lumen. The ring includes a head having a face at a distal end of the ring and a body connected to the head and positioned proximally of the head with a longitudinal axis extending through the head and body. The face has a face radius and the body has a body radius. A face radius to body radius ratio is in a range of 1.20 to 1.75. The head has a guide surface positioned longitudinally between the face and the body. The guide surface extends distally radially outward and forms an angle with the longitudinal axis in a range of 100° to 160°.

In yet another embodiment, an intravascular system includes a delivery catheter, a ring, a connection arm, and a medical device. The delivery catheter has a distal end and a proximal end. The delivery catheter also has an inner surface defining a lumen and an outer surface. The ring is affixed to the distal end of the delivery catheter and at least a part of the ring is positioned within the lumen. The ring includes a head having a face at a distal end of the ring and a body connected to the head and positioned proximally of the head with a longitudinal axis extending through the head and body. The face has a face radius and the body has a body radius. The face radius is greater than a radius of the outer surface of the delivery catheter. A face radius to body radius ratio is in a range of 1.20 to 1.75. The head has a guide surface positioned longitudinally between the face and the body. The guide surface extends distally radially outward and forms an angle with the longitudinal axis in a range of 100° to 160°. The connection arm has a distal end and proximal end and the connection arm is connected to the ring at the proximal end and extends distally from the face of the ring. The medical device is connected to the distal end of the connection arm.

Additional features of embodiments of the disclosure will be set forth in the description which follows. The features of such embodiments may be realized by means of the instruments and combinations particularly pointed out in the appended claims. These and other features will become more fully apparent from the following description and appended claims, or may be learned by the practice of such exemplary embodiments as set forth hereinafter.

BRIEF DESCRIPTION OF THE DRAWINGS

In order to describe the manner in which the above-recited and other features of the disclosure can be obtained, a more particular description will be rendered by reference to specific embodiments thereof which are illustrated in the appended drawings. For better understanding, the like elements have been designated by like reference numbers throughout the various accompanying figures. While some of the drawings may be schematic or exaggerated representations of concepts, at least some of the drawings may be drawn to scale. Understanding that the drawings depict some example embodiments, the embodiments will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:

FIG. 1 depicts an embodiment of a heart valve repair clip connected to a distal end of a delivery catheter system, according to the present disclosure;

FIG. 2 depicts the heart valve repair clip and delivery catheter system of FIG. 1 during a partial recapture of the heart valve repair clip, according to the present disclosure;

FIG. 3 is a side cross-sectional view of an embodiment of a conventional ring and delivery catheter system;

FIG. 4 is a side cross-sectional view of an embodiment of a ring and delivery catheter system, according to the present disclosure;

FIG. 5 is a distal perspective view of another embodiment of a radiopaque ring, according to the present disclosure;

FIG. 6 is a proximal perspective view of yet another embodiment of a radiopaque ring, according to the present disclosure;

FIG. 7 is a side view of an embodiment of a radiopaque ring, according to the present disclosure;

FIG. 8 is a side cross-sectional view of the radiopaque ring of FIG. 7;

FIG. 9 is a distal end view of a further embodiment of a radiopaque ring, according to the present disclosure;

FIG. 10 is a proximal end view of the radiopaque ring of FIG. 9; and

FIG. 11 is a side cross-sectional view of a radiopaque ring having a connection arm connected thereto, according to at least one embodiment described herein.

DETAILED DESCRIPTION

One or more specific embodiments of the present disclosure will be described below. In an effort to provide a concise description of these embodiments, some features of an actual embodiment may be described in the specification. It should be appreciated that in the development of any such actual embodiment, as in any engineering or design project, numerous embodiment-specific decisions will be made to achieve the developers' specific goals, such as compliance with system-related and business-related constraints, which may vary from one embodiment to another. It should further be appreciated that such a development effort might be complex and time consuming, but would nevertheless be a routine undertaking of design, fabrication, and manufacture for those of ordinary skill having the benefit of this disclosure.

One or more embodiments of the present disclosure may generally relate to manufacturing and using delivery catheter systems or other steerable catheters. A delivery catheter system may allow a medical professional to deliver an intravascular or other medical device to a target location in a patient's body. While the present disclosure will describe delivery catheter systems and applications thereof in relation to transvascular procedures in the heart, it should be understood that the devices, systems, and method described herein may be applicable to other bodily lumens and/or cavities. Additionally, elements described in relation to any embodiment depicted and/or described herein may be combinable with elements described in relation to any other embodiment depicted and/or described herein. For example, any element described in relation to an embodiment depicted in FIG. 4 may be combinable an embodiment described in FIG. 9.

A steerable guide catheter (“SGC”) may be directed through a patient's vasculature and provide a steerable conduit through which a delivery catheter may pass. The delivery catheter may convey a medical device, such as a mitral valve repair clip, to a location in the patient's body. The delivery catheter may include one or more control wires extending through the delivery catheter to the medical device to control one or more moveable member thereon. The control wires may be directed through a ring having a plurality of passages therethrough. The ring may be positioned on a distal end of the delivery catheter and between the delivery catheter and the medical device. In some embodiments, the ring may be made of or include a radiopaque material to improve imaging of the ring and, hence, positioning of the ring in the patient's body.

The ring may have one or more features that facilitate and/or ease recapture of the medical device into the SGC. In some embodiments, the ring may have an outer diameter (“OD”) greater than an OD of the delivery catheter. In other embodiments, the ring may have a sloped and/or curved surface adjacent an outer surface to guide the movement of the ring relative to the SGC. In yet other embodiments, the ring may have an OD greater than a width of the medical device. The ring may thereby allow for the medical device to be recaptured into the SGC by self-aligning within the SGC and substantially preventing the medical device contacting a distal tip of the SGC.

FIG. 1 depicts a valve repair system 100 according to at least one embodiment described herein. It should be understood that while the present description may disclosure features and elements in relation to a valve repair system 100, the features and elements described herein may be applicable to other intravascular devices and/or systems having other medical devices included therein. The valve repair system 100 may include a mitral clip 102, a delivery catheter 104 to which the mitral valve 102 is connected, and an SGC 106 through which the delivery catheter 104 may extend. The delivery catheter 104 may have a ring 108 located at a distal end thereof. In some embodiments, the ring 108 may have an OD that is larger than that of the delivery catheter 104. In other embodiments, the ring 108 may have an OD that is smaller than that of an SGC tip 110. The ring 108 may be configured to self-align concentrically within the SGC tip 110 and/or SGC 106. The ring 108 may be configured to align the mitral clip 102 with the SGC tip 110 and/or SGC 106 to facilitate recapture of the mitral clip 102.

FIG. 2 is a schematic representation depicting the collapse of the moveable arms 109 of the mitral clip 102 prior to recapture of the mitral clip 102 within the SGC tip 110 and/or SGC 106. The moveable arms 109 may be drawn inward from the expanded state depicted in FIG. 1 to the collapsed state depicted in FIG. 2. The one or more control wires 111 may apply a force to the moveable arms 109 to move the moveable arms 109 between the expanded state and the collapsed state. As shown in FIG. 2, the mitral clip 102 may have a lateral dimension greater than that of the delivery catheter 104 and/or the ring 108. The moveable arms 109 may, therefore, catch on the SGC tip 110 and/or SGC 106. The ring 108 may be configured to provide a reliable and robust alignment of the ring 108 and/or mitral clip 102 coaxially with and/or radially within the SGC 106. As used herein, “aligned coaxially” should be understood to mean sharing a common axis with another element, and, particularly in the present description, sharing a common longitudinal axis with another element. As used herein, “aligned radially within” should be understood to mean the first element (e.g., the ring 108) substantially centered within a transverse cross-section of the second element (e.g., the SGC 106). Aligning a first element coaxially with or radially within a second element may include the first element longitudinally overlapping the second element but need not be so limited.

The ring 108 may be made of or include a radiopaque material to facilitate imaging of the ring 108 during an intravascular procedure. In at least one embodiment, the radiopaque ring 108 may be made of or include stainless steel. The stainless steel is visible during imaging, biocompatible, and weldable for connecting the ring 108 to a compression coil of the delivery catheter 104. In other embodiments, the ring 108 may include titanium, tungsten, barium sulfate, zirconium oxide, or combinations thereof. In yet other embodiments, the ring 108 may be made of or include a radiopaque polymer or a radiopaque material embedded in a polymer body.

FIG. 3 illustrates an embodiment of a conventional ring 212 in a conventional delivery catheter 204. The conventional ring 212 and conventional delivery catheter 204 may have substantially similar ODs, such that the conventional ring 212 is simply an extension of the conventional delivery catheter 204 that is guided through the SGC 206. However, the SGC 206 may be steered by a medical professional through tortuous vasculature in the patient's body and/or through a cavity in the patient's body. For example, the distal portion of the SGC 206 may have a radius of curvature one the scale of millimeters. The conventional delivery catheter 204 may include a resilient material. The resilient material may cause the conventional delivery catheter 204 to extend from the SGC 206 in a direction non-coaxial with the distal portion of the SGC 206. In such examples, retracting the conventional delivery catheter 204 into the SGC 206 may, similarly, move the conventional delivery catheter 204 in a direction non-coaxial with the distal portion of the SGC 206. The conventional delivery catheter 204 may not be centered within the SGC 206, causing the mitral clip 202 to contact and/or catch on the distal end of the SGC 206 inhibiting or substantially preventing recapture of the mitral clip 202 within the SGC 206.

FIG. 4 illustrates an embodiment of the ring 108 of FIG. 1 having an OD greater than that of the delivery catheter 104. The delivery catheter 104 may have an OD that is substantially similar to or smaller than the ID of the SGC 106 to allow the delivery catheter 104 to move freely within the SGC 106. The delivery catheter 104 may have an OD that is substantially similar to the ID of the SGC 106 to encourage the delivery catheter 104 to remain coaxial with the SGC 106 during the procedure, thereby providing greater control over the placement of the delivery catheter 104. The delivery catheter 104 may exit the distal portion of the SGC 106 more reliably and centered radially within the SGC 106. The delivery catheter 104 may also reenter the SGC 106 coaxially with the ring 108 centered radially relative to the SGC 106 and SGC tip 110.

The delivery catheter 104 may have an OD that is smaller than the ID of the SGC 106 to allow the delivery catheter 104 to move within the SGC 106 when the SGC 106 and delivery catheter 104 are moved through tortuous portions of the patient's vasculature. During movement through the tortuous portions of the patient's vasculature, the body of the delivery catheter 104 may contact the SGC 106. The friction therebetween may adversely affect the movement of the delivery catheter 104 within the SGC 106; limiting or substantially preventing deployment of the delivery catheter 140 from the SGC 106. A delivery catheter 104 having a smaller OD than the ID of the SGC 106 may provide more reliable control over longitudinal movement and rotational movement of the delivery catheter 104 within the SGC 106. The ring 108 of FIG. 4 allows the delivery catheter 104 and mitral clip 102 (or other medical device) to align coaxially and/or radially within the SGC 106 irrespective of the relative size of the delivery catheter 104 and SGC 106.

The delivery catheter 104 may define a lumen extending therethrough. At least a portion of the ring 108 may be positioned within the lumen of the delivery catheter 104 to connect the ring 108 to the delivery catheter. In some embodiments, the delivery catheter may contain a plurality of control wires that extend through the delivery catheter and into and/or through channels in the ring 108.

FIG. 5 is a perspective view of an embodiment of a ring 308 according to the present disclosure. The ring 308 may have a major channel 314 that extends through at least a longitudinal portion of the ring 308. In at least one embodiment, the major channel 314 may extend through the entire longitudinal length of the ring 308. The major channel 314 may have a substantially circular transverse cross-section (e.g., be cylindrical). In other embodiments, the major channel 314 may have a transverse cross-section having another shape, such as square, octagonal, other polygonal, elliptical, irregular, or combinations thereof. In some embodiments, the major channel 314 may have a constant transverse cross-section along the length of the major channel 314.

The major channel 314 may have one or more mirror channels 316 spaced about the major channel 314. In some embodiments, the one or more mirror channels 316 may overlap at least a portion of the major channel 314, as shown in FIG. 5. In other embodiments, the one or more mirror channels 316 may extend through a portion of the longitudinal length of the ring 308 without overlapping any portion of the major channel 314. In some embodiments, the one or more mirror channels 316 may have a substantially circular transverse cross-section (e.g., be cylindrical). In other embodiments, the one or more mirror channels 316 may have a transverse cross-section having another shape, such as square, octagonal, other polygonal, elliptical, irregular, or combinations thereof. In some embodiments, the one or more mirror channels 316 may have a constant transverse cross-section along the length of the one or more mirror channels 316.

The ring 308 may have a distal face 318 and a proximal base 320 at opposing longitudinal ends of a body 322. It should be understood that the terms “distal” and “proximal” are used herein as relative to a medical professional operating a heart valve repair system similar to that described herein. In other applications, the face 318 and the base 320 may be oriented in a different relative direction to an operator. The face 318 may be substantially flat or may have a curved surface. The face 318 may be convex relative to the body 322, concave relative to the body 322, have another curve, or combinations thereof. The face 318 may be configured to complimentarily mate with a desired medical device or other interface component. The base 320 may extend away from the body 322 in a direction opposite that of the face 322. The base 320 may have one or more connection points 324 thereon to allow fixation of the ring 308 to a delivery catheter or other elongated member that provides communication between the ring 308 and a control system or operator outside the patient's body. In some embodiments, the ring 308 may have a single connection point 324. In other embodiments, the ring 308 may have a plurality of connection points 324. The plurality of connection points 324 may be distributed symmetrically about the base 320 such that any application of force to the connection points 324 may be applied to the ring 308 symmetrically.

FIG. 6 illustrates a rear perspective view of an embodiment of a ring 408, according to the present disclosure. In some embodiments, the mirror channels 416 of the ring 408 may substantially divide the base 420 into a plurality of posts 426. The plurality of posts 426 may be connected to the body 422. In some embodiments, the plurality of posts 426 may connect laterally to one another. In other embodiments, the plurality of posts 426 may not be connected to one another (e.g., the major channel 414 and plurality of mirror channels 416 connect laterally to one another). In some embodiments, at least one of the posts 426 may have an extension 428 extending proximally therefrom. In embodiments having a plurality of extensions 428, the extensions may substantially radially oppose one another. As shown in FIG. 6, the plurality of extensions 428 may be space around and on opposite sides of the major channel 414. In at least one embodiment, one of the extensions 428 may have a connection point 424 thereon.

FIG. 7 illustrates a side view of another embodiment of a ring 508 according to the present disclosure. The ring 508 may have a face 518 with a face edge 530 that defines a face radius 532. The face radius 532 may be measured from a longitudinal axis 534 of the ring 508 to a radial outermost point of the face 518 and face edge 530. The face edge 530 may, in some embodiments, be a curved edge. In other embodiments, the face edge 530 may be a beveled edge. In yet other embodiments, the face 518 may not have a face edge 530, and the face 518 may extend substantially flat to the radial outermost point of the ring 508. The face radius 532 may be greater than a body radius 536. The body radius 536 may be measured from the longitudinal axis 534 to the radial outermost point of the body 522. In some embodiments, the body radius 536 may be configured to substantially match an inner radius of a delivery catheter (e.g., the delivery catheter 104 described in relation to FIG. 1 and FIG. 2). In other embodiments, the body radius 522 may be larger than the inner radius of the delivery catheter. In some embodiments, the body 522 may include one or more engagement features to engage with an inner surface of the delivery catheter.

The face radius 532 and the body radius 536 may have a face-to-body ratio in a range having upper and lower values including any of 1.20, 1.25, 1.30, 1.35, 1.40, 1.45, 1.50, 1.55, 1.60, 1.65, 1.70, 1.75, or any value therebetween. For example, the face radius 532 and the body radius 536 may have a face-to-body ratio in a range of 1.20 to 1.75. In another example, the face radius 532 and the body radius 536 may have a face-to-body ratio in a range of 1.30 to 1.70. In yet another example, the face radius 532 and the body radius 536 may have a face-to-body ratio in a range 1.40 to 1.60. In at least one example, the face radius 532 and the body radius 536 may have a face-to-body ratio of 1.50.

The base 520 of the ring 508 may define a base radius 538 measured from the longitudinal axis 534 to a radial outermost point of the plurality of posts 526. In some embodiments, the base radius 538 may be the same or less than an inner diameter of a compression coil or other inner support member (e.g., hypotube) of the delivery catheter. The base radius 538 may also be larger than the inner diameter of a compression coil or other inner support member of the delivery catheter to provide a compression fit between the base 520 and the compression coil or other inner support member. The face radius 532 and the base radius 538 may have a face-to-base ratio in a range having upper and lower values including any of 1.60, 1.65, 1.70, 1.75, 1.80, 1.85, 1.90, 1.95, 2.00, 2.05, 2.10, 2.15, 2.20, 2.25, 2.30, or any value therebetween. For example, the face radius 532 and the base radius 538 may have a face-to-base ratio in a range of 1.60 to 2.30. In another example, the face radius 532 and the base radius 538 may have a face-to-base ratio in a range of 1.65 to 2.00. In yet another example, the face radius 532 and the base radius 538 may have a face-to-base ratio in a range 1.70 to 1.80. In at least one example, the face radius 532 and the base radius 538 may have a face-to-base ratio of 1.75.

The base 520 and the plurality of posts 526 therein may include a radial notch 540. In some embodiments, the notch 540 may include an inclined distal surface and a substantially transverse proximal surface as depicted in FIG. 7. In other embodiments, the notch 540 may include an inclined distal surface and an inclined proximal surface. In yet other embodiments, the notch 540 may include a substantially transverse distal surface and a substantially transverse proximal surface. The notch 540 may have a radial depth that is in a range having upper and lower values of 10% of the base radius 538, 15%, 20%, 25%, 30%, 35%, 40% of the base radius 538, or any value therebetween. For example, the notch 540 may have a radial depth in a range of 10% to 40% of the base radius 538. In another example, the notch 540 may have a radial depth in a range of 20% to 30% of the base radius 538. In at least one example, the notch 540 may have a radial depth of 25% of the base radius 538.

The ring 508 may have an angle 542 between the body 522 and a portion of a head 544 at or near the distal end of the ring 508. The angle 542 may define a guide surface 546 located longitudinally and/or laterally between the head 544 and the body 522. The angle 542 may be measured between the outer surface of the body 522 and the guide surface 546. The angle 542 may be an obtuse angle where the guide surface 546 slopes radially and distally (i.e., toward the face 518 of the head 544). The guide surface 546 may have an angle such that longitudinal movement of the ring 508 relative to SGC and/or SGC tip (such as SGC 106 and SGC tip 110 described in relation to FIG. 1 and FIG. 2) may convert at least a portion of a longitudinal compression force between the ring 508 and SGC and/or SGC tip to a transverse force. For example, the guide surface 546 may contact and/or interact with a distal edge of the SGC and/or SGC tip at apply a compressive force thereto. The compressive force may be applied between the guide surface 546 and the distal edge of the SGC and/or SGC tip at an angle to the longitudinal axis 534 of the ring 508, urging the ring 508 toward a radially centered position within the SGC and/or SGC tip.

In some embodiments of the ring 508, the guide surface 546 may be substantially flat in longitudinal cross-section. In other embodiments, the guide surface 546 may be at least partially curved in longitudinal cross-section. The guide surface 546 may be concave and/or convex relative to the head 544. In yet other embodiments, the guide surface 546 may be a combination of curved portions and flat portions in longitudinal cross-section. The angle 542 of the guide surface 546 relative to the longitudinal axis 534 of the ring 508 may be within a range having upper and lower values including any of 100°, 110°, 120°, 130°, 140°, 150°, 160°, or any value therebetween. For example, the angle 542 of the guide surface 546 may be in a range of 100° to 160°. In another example, the angle 542 of the guide surface 546 may be in a range of 110° to 140°. In yet another example, the angle 542 of the guide surface 546 may be 120°.

FIG. 8 shows a longitudinal cross-section of the ring 508 of FIG. 7. The longitudinal cross-section shows the major channel 514 of the ring 508. As described herein, the major channel 514 may have a number of shapes in transverse cross-section, and while the size of the major channel 514 may be described in relation to a radius from the longitudinal axis 534 or diameter, the measurement of a radius should not be understood to limit the structure of part or the entire length of the major channel 514. In some embodiments, the major channel 514 may have a constant profile and/or radius in transverse cross-section along a longitudinal length thereof. In other embodiments, the major channel 514 may have a plurality of shapes and/or radii in transverse cross-section along a longitudinal length thereof. For example, the major channel 514 may have a distal radius 548, an intermediate radius 550, and a proximal radius 552. In some embodiments, the distal radius 548 may be greater than the intermediate radius 550. In other embodiments, the intermediate radius 550 may be less than the proximal radius 552. In yet other embodiments, the proximal radius 552 may be less than the distal radius 548 and the intermediate radius 550 may be less than the distal radius 548 and the proximal radius 552.

The major channel 514 may be configured to receive and substantially retain at least part of a connection arm therein. The connection arm and connection to the major channel 514 of the ring 508 will be described in more detail in relation to FIG. 11. Referring again to FIG. 8, the distal radius 548 of the major channel 514 may be configured to receive at least part of a connection arm. In some embodiments, the distal radius 548 may be configured to provide an interference fit with at least part of a connection arm. Similarly, the major channel 514 may have a distal portion 554 with a longitudinal length to receive at least part of a connection arm and retain the connection arm with substantial movement of the connection arm relative to the ring 508.

FIG. 9 is a distal view of an embodiment of a ring 608 according to the present disclosure. The ring 608 may have a major channel 614 and a plurality of mirror channels 616. The face 618 of the ring 608 may include a visual indicator 656. In the depicted embodiment, the visual indicator 656 is a cross. In other embodiments, the visual indicator 656 may be a circle, a dot, a square, or any other identifiable shape that may render the face 618 of the ring 608 asymmetrical. As described herein, the major channel 614 and plurality of mirror channels 616 may be distributed symmetrically about the longitudinal axis 634 of the ring 608. The ring 608 may otherwise exhibit one or more rotational symmetries (e.g., 180°, 120°, 90°, etc.). The visual indicator 656 may allow an operator to identify a particular orientation irrespective of other rotational symmetries of the ring 608. In some embodiments, the visual indicator 656 may be a recessed portion of the face 618. For example, the visual indicator 656 may be milled, stamped, or otherwise imprinted into the face 618 of the ring 608. In other embodiments, the visual indicator 656 may be a raised portion of the face 618. For example, the visual indicator 656 may be created on the face 618 by application of material thereto.

The distal view of FIG. 9 illustrates differences in a distal radius 648 and an intermediate radius 650 of the major channel 614. The transition between the distal radius 648 and the intermediate radius 650 in the major channel 614 may create a ledge 658 against which a connection arm may contact. The ledge 658 may be substantially annular. In some embodiments, the mirror channels 616 may overlap with at least a portion of the major channel 614, such as in a distal portion of the major channel 614, and may overlap with at least part of the ledge 658.

A mirror channel 616 may have a mirror channel radius 660. In some embodiments, a mirror channel 616 may have a constant mirror channel radius 660 along the full longitudinal length of the mirror channel 616. In other embodiments, the mirror channel radius 660 may change over the longitudinal length of the mirror channel 616. In some embodiments, all of the mirror channels 616 may have substantially the same mirror channel radius 660. In other embodiments, at least one of the mirror channels 616 may have a different mirror channel radius 660. The mirror channels 616 may be positioned a mirror channel distance 662 away from the major channel 614 in a transverse direction. For example, each mirror channel 616 may have a mirror longitudinal axis 664 that extends in the longitudinal direction and substantially parallel to the longitudinal axis 634 of the ring 608 and/or major channel 634. In some embodiments, the mirror longitudinal axis 664 of each mirror channel 616 may be an equal distance from the longitudinal axis 634 of the ring 608 and/or major channel 634. In other embodiments, the mirror longitudinal axis 664 of at least one mirror channel 616 may be a different distance from the longitudinal axis 634 of the ring 608 and/or major channel 634 as the mirror longitudinal axis 664 of another mirror channel 616.

FIG. 10 illustrates a proximal view of the ring 608 of FIG. 9. As described herein, the plurality of mirror channels 616 extending longitudinally through the base 620 may define a plurality of post 626. The posts 626 may be further divided from one another by the major channel 614 located centrally to the posts 626. At least one of the posts 626 may have an extension 628 extending proximally therefrom. As shown in FIG. 10, an extension 628 may have a substantially constant lateral thickness irrespective of radial distance from the longitudinal axis 634 (i.e., having substantially parallel lateral surfaces). In other embodiments, the extension 628 may have other shapes in transverse cross-section. For example, the extension 628 may have non-parallel lateral surfaces and may taper toward the longitudinal axis 634, similar to the lateral surfaces of the posts 626, as illustrated in FIG. 10. In another example, the extension 628 may have non-parallel lateral surfaces and the extension may taper away the longitudinal axis 634.

As described herein, the extension 628 may have one or more connection points thereon to connect a wire thereto to limit or substantially prevent movement of the ring 608 relative to a delivery catheter. The extension 628 may also be configured to allow connection to a delivery catheter by a weld connection or other bonding of the extension material to a portion of the delivery catheter. For example, an extension 628 or other proximal portion of the ring 608 may be adhered to a body of the delivery catheter or to a support member of the delivery catheter, such as a compression coil. In at least one embodiment, the extension 628 may be laser welded to the compression coil of a delivery catheter. In other embodiments, an adhesive material may be applied between at least part of the ring 608 and the delivery catheter.

FIG. 11 illustrates a side cross-sectional view of an embodiment of a ring 708 having a connection arm 766 extending distally therefrom. The connection arm 766 may have a distal end 768 configured to retain and/or grip a medical device (e.g., a mitral clip) and a proximal end 770 configured to connect to the ring 708. In some embodiments, the proximal end 770 may be configured to fit in the major channel 714 with an interference fit therein. The interference fit between the distal radius 748 of the major channel 714 and the OD 772 of the connection arm 766 may be sufficient to limit or substantially prevent movement of the connection arm 766 relative to the ring 708. In other embodiments, additional reinforcement of the connection therebetween may be provided by an adhesive material between the ring 708 and the connection arm 766. In yet other embodiments, the connection between the ring 708 and the connection arm 766 may include welding, brazing, or otherwise bonding the material of the connection arm 766 to the material of the ring 708.

A medical device may be retained on the connection arm 766 by a wire or other elongate member extending through the major channel 714 and the connection arm 766 to the medical device. The connection arm 766 may have an ID 774 defining a central bore 776 extending therethrough. The central bore 776 may be coaxial with the longitudinal axis 734 of the ring 708 and/or major channel 714. The ID 774 of the connection arm 766 may be substantially the same as the intermediate radius 750. In some embodiments, the central bore 776 and major channel 714 may provide a channel having a substantially continuous inner surface.

The articles “a,” “an,” and “the” are intended to mean that there are one or more of the elements in the preceding descriptions. The terms “comprising,” “including,” and “having” are intended to be inclusive and mean that there may be additional elements other than the listed elements. Additionally, it should be understood that references to “one embodiment” or “an embodiment” of the present disclosure are not intended to be interpreted as excluding the existence of additional embodiments that also incorporate the recited features. Numbers, percentages, ratios, or other values stated herein are intended to include that value, and also other values that are “about” or “approximately” the stated value, as would be appreciated by one of ordinary skill in the art encompassed by embodiments of the present disclosure. A stated value should therefore be interpreted broadly enough to encompass values that are at least close enough to the stated value to perform a desired function or achieve a desired result. The stated values include at least the variation to be expected in a suitable manufacturing or production process, and may include values that are within 5%, within 1%, within 0.1%, or within 0.01% of a stated value.

A person having ordinary skill in the art should realize in view of the present disclosure that equivalent constructions do not depart from the spirit and scope of the present disclosure, and that various changes, substitutions, and alterations may be made to embodiments disclosed herein without departing from the spirit and scope of the present disclosure. Equivalent constructions, including functional “means-plus-function” clauses are intended to cover the structures described herein as performing the recited function, including both structural equivalents that operate in the same manner, and equivalent structures that provide the same function. It is the express intention of the applicant not to invoke means-plus-function or other functional claiming for any claim except for those in which the words ‘means for’ appear together with an associated function. Each addition, deletion, and modification to the embodiments that falls within the meaning and scope of the claims is to be embraced by the claims.

The terms “approximately,” “about,” and “substantially” as used herein represent an amount close to the stated amount that still performs a desired function or achieves a desired result. For example, the terms “approximately,” “about,” and “substantially” may refer to an amount that is within less than 5% of, within less than 1% of, within less than 0.1% of, and within less than 0.01% of a stated amount. Further, it should be understood that any directions or reference frames in the preceding description are merely relative directions or movements. For example, any references to “up” and “down” or “above” or “below” are merely descriptive of the relative position or movement of the related elements.

The present disclosure may be embodied in other specific forms without departing from its spirit or characteristics. The described embodiments are to be considered as illustrative and not restrictive. The scope of the disclosure is, therefore, indicated by the appended claims rather than by the foregoing description. Changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope.

Claims

1. An intravascular system, the system comprising: a delivery catheter having a distal end and a proximal end, the delivery catheter having an inner surface defining a lumen and an outer surface; anda ring affixed to the distal end of the delivery catheter and at least a part of the ring being positioned within the lumen, the ring including: a head having a face at a distal end of the ring, the face having a face radius,a body connected to the head and positioned proximally of the head, the body having a body radius wherein a ratio of the face radius to the body radius is in a range of 1.20 to 1.75,a longitudinal axis extending through the head and body, anda guide surface positioned longitudinally between the face and the body, the guide surface extending distally radially outward and forming an angle with the longitudinal axis in a range of 100° to 160°.

2. The system of claim 1, wherein the catheter further comprised a support member extending longitudinally therethrough, the ring being welded to the support member.

3. The system of claim 1, wherein a radius of the head is greater than a radius of the outer surface of the delivery catheter.

4. The system of claim 3, wherein the guide surface extends from a radial outermost point of the head to the outer surface of the delivery catheter.

5. The system of claim 4, further comprising a major channel extending longitudinally from the distal end of the ring through the head and body, the major channel having a distal radius that is greater than a proximal radius of the major channel.

6. The system of claim 4, further comprising a base connected to the body and positioned proximally of the body, the base having a base radius wherein a ratio of the face radius to the base radius is in a range of 1.60 to 2.30.

7. The system of claim 6, wherein the base further comprises a plurality of extensions that extend proximally from the base and have one or more connection points to facilitate connecting the ring to the delivery catheter.

8. The system of claim 6, wherein the base is positioned within the lumen and an adhesive material is positioned between at least a portion of the base and delivery catheter.

9. The system of claim 1, further comprising a guide catheter positioned circumferentially about the delivery catheter, the guide catheter having an inner radius that is less than or equal to the face radius.

10. An intravascular system, the system comprising: a delivery catheter having a distal end and a proximal end, the delivery catheter having an inner surface defining a lumen and an outer surface;a ring affixed to the distal end of the delivery catheter and at least a part of the ring being positioned within the lumen, the ring including: a head having a face at a distal end of the ring, the face having a face radius, wherein the face radius is greater than a radius of the outer surface of the delivery catheter;a body connected to the head and positioned proximally of the head, the body having a body radius wherein a ratio of the face radius to the body radius is in a range of 1.20 to 1.75;a longitudinal axis extending through the head and body; anda guide surface positioned longitudinally between the face and the body, the guide surface extending distally radially outward and forming an angle with the longitudinal axis in a range of 100° to 160°;a connection arm having a distal end and proximal end, the connection arm connected to the ring at the proximal end and extending distally from the face of the ring; anda medical device connected to the distal end of the connection arm.

11. The system of claim 10, the medical device being a heart valve repair clip.

12. The system of claim 10, further comprising a steerable guide catheter positioned circumferentially about the delivery catheter, the guide surface of the ring being configured to contact a distal end of the steerable guide catheter.

13. The system of claim 10, wherein the medical device has an expanded state and a collapsed state, wherein the collapsed state defines an outer radius not greater than the face radius.

14. The system of claim 10, wherein at least part of the guide surface is convex in transverse cross-section.

15. The system of claim 10, further comprising a major channel and a plurality of mirror channels extending longitudinally from the distal end to the base, the plurality of mirror channels communicating with the major channel in the head and being separated from the major channel in the base.

16. The system of claim 15, wherein the plurality of mirror channels are distributed radially about the major channel.

17. The system of claim 15, wherein the major channel extends longitudinally from the distal end of the device through the head and body and the plurality mirror channels extend longitudinally from the distal end of the device through the head and body, a radius of the major channel overlapping a radius of one of the plurality of mirror channels.

18. The system of claim 17, wherein the plurality of mirror channel equidistantly spaced around the major channel.

19. The system of claim 17, wherein one of the plurality of mirror channels and the major channel have coincident openings.

20. The system of claim 10, further comprising further comprising a plurality of posts and a plurality of connection points formed in the body.