LUMINAL IMPLANT FOR THE CORRECTION OF OCCLUSIONS
20180055669 ยท 2018-03-01
Inventors
- Huseyin Fertac BILGE (Dublin, CA, US)
- Xiao-Yan GONG (Laguna Niguel, CA, US)
- Michael Williamson (Clayton, CA, US)
Cpc classification
A61F2210/008
HUMAN NECESSITIES
A61F2/915
HUMAN NECESSITIES
A61F2002/91583
HUMAN NECESSITIES
International classification
Abstract
Apparatus, systems, and methods for a medical implant with improved durability and strength. An implant structure having a mesh, wherein struts of the mesh vary in width as a function of length, where one or more segments are defined by one or more corresponding equations that define strut width. Connecting elements may be optionally included and may further optionally vary in width and shape. Strut tapering functions may be one or more segments of piecewise linear equations. Implant mesh structures may be symmetric, asymmetric, or may vary in segments along the length and/or circumference of the mesh. The mesh may be of a self-expanding or balloon expandable material suitable for medical use.
Claims
1. An intraluminal stent having a central longitudinal axis, the intraluminal stent comprising: a closed structural cell having a cell longitudinal axis parallel to the central longitudinal axis and further having a deployment configuration, the closed structural cell comprising: a strut having a length, a first end, and a second end and positioned so as to form at least a portion of a perimeter of the closed structural cell; wherein a width of the strut tapers from the first end and the second end towards a point along the strut length; and wherein when in the deployment configuration, an angle greater than 45 degrees is formed between the cell longitudinal axis and the strut.
2. The intraluminal stent of claim 1, wherein the strut has a strut longitudinal axis parallel to the length of the strut, and wherein the width of the strut is measured from an outer surface of the strut to the strut longitudinal axis.
3. The intraluminal stent of claim 1, wherein the closed structural cell perimeter is entirely enclosed by the strut and one additional strut.
4. The intraluminal stent of claim 1, wherein the closed structural cell perimeter is entirely enclosed by the strut and two additional struts.
5. The intraluminal stent of claim 1, wherein the closed structural cell perimeter is entirely enclosed by the strut and three additional struts.
6. The intraluminal stent of claim 1, wherein the width of the strut tapers according to a linear relationship between the width and a distance from a point along the length of the strut where the width is narrowest to a point along the strut where the width is widest.
7. The intraluminal stent of claim 1, comprising an additional closed structural cell that is connected to the structural cell by a linking connection.
8. The intraluminal stent of claim 7, wherein a width of the linking connection tapers along at least a portion of a length of the linking connection.
9. The intraluminal stent of claim 8, wherein the width of the linking connection tapers according to either a piecewise linear function in relation to the length of the linking connection, a polynomial function in relation to the length of the linking connection, an exponential function in relation to the length of the linking connection, a logarithmic function in relation to the length of the linking connection, or a root function in relation to the length of the linking connection.
10. The intraluminal stent of claim 7, wherein the linking connection is S-shaped.
11. An intraluminal stent comprising: a closed structural cell comprising: a strut positioned so as to form at least a portion of a perimeter of the closed structural cell, said strut having a width and a length and comprising a plurality of segments, wherein each segment of the plurality of segments taper according to a linear relationship between the width and the length.
12. The intraluminal stent of claim 11, wherein the closed structural cell perimeter is entirely enclosed by the strut and one additional strut.
13. The intraluminal stent of claim 11, wherein the closed structural cell perimeter is entirely enclosed by the strut and two additional struts.
14. The intraluminal stent of claim 11, wherein the closed structural cell perimeter is entirely enclosed by the strut and three additional struts.
15. The intraluminal stent of claim 11, comprising an additional closed structural cell directly connected to the closed structural cell by a linking connection.
16. The intraluminal stent of claim 15, wherein a width of the linking connection tapers along at least a portion of a length of the linking connection.
17. The intraluminal stent of claim 15, wherein the closed structural cell and the additional closed structural cell are offset relative to one another.
18. The intraluminal stent of claim 11, wherein the width of the strut is configured so that the strut provides the closed structural cell with a maximum relative flexibility at the narrowest width of the strut and a maximum stiffness at a point of the widest width of the strut.
19. The intraluminal stent of claim 11, wherein the closed structural cell is positioned to receive an axial force transmitted by a lumen into which the intraluminal stent is deployed at the point of the widest width of the strut.
20. The intraluminal stent of claim 11, comprising a nickel titanium alloy, wherein the nickel titanium alloy is substantially in an austenitic phase at a temperature between 15 degrees Celsius to 37 degrees Celsius.
Description
BRIEF DESCRIPTION OF THE FIGURES
[0025]
[0026]
[0027]
[0028]
[0029]
[0030]
[0031]
DETAILED DESCRIPTION
[0032] In some embodiments of the present invention, individual struts may have a tapered shape where the strut is widest at its two endpoints and narrowest at a point in between, such as at its midpoint by way of one example. Tapering, in some embodiments is in accordance with any mathematical function, including polynomial functions, exponential functions, logarithmic functions, root functions, and any combination thereof. The width profile of the strut taper may be described by a plurality of segments; each segment being defined by a function along each segment. The segments may be equal in length or unequal in length and the width of the strut may or may not be symmetric about the midpoint of the strut. Individual struts may have width tapering different from other individual struts in the plurality. Struts may vary in width profiles based on zones along the length of the stent, based on locations within the stent mesh, based on structural variations of individual cells, bridge geometry, and the like. In several embodiments of the present invention, the plurality of segments are described by linear functions and the strut segments are comprised of piecewise linear tapering segments.
[0033] Referring to
[0034] Closed cell 104 is shown as one example of how a plurality of individual struts may be used to create a structural unit. In the example of
[0035] Referring now to
[0036] In the example of
[0037] Referring now to
[0038] In the example of
[0039] Referring now to
[0040] In the example of
[0041] In many of the embodiments of the present invention, a subset of the plurality struts forming the mesh-like structure are interconnected in a manner that forms a closed structural cell (cell), wherein the mesh-like structure is comprised, at least in part, of a plurality of cells which may also be interconnected with a plurality of other adjacent cells. In this fashion, one or more types of structural cell units may be linked or directly joined together to form the complete mesh of a stent. The mesh structure may have structural symmetry or asymmetry depending on the desired mechanical characteristics of the stent, e.g. fatigue resistance, axial or radial stiffness, torsional stiffness, flexibility in bending, and the like.
[0042] Referring now to
[0043] In
[0044] In the example of
[0045]
[0046] In
[0047] In the example of
[0048]
[0049] In
[0050] In the example of
[0051]
[0052] Referring now to
[0053] In some embodiments of the present invention there is provided a tubular, mesh-like stent structure comprised of a plurality of interconnected struts. Struts are oriented so as to have a circumferential and an axial direction describing the position of each of the plurality of struts forming the mesh-like tubular structure of the stent. The orientation of struts, individual strut geometries, the thickness of struts (distance between the surfaces forming the inner diameter and outer diameter of the mesh from a center point of its diameter), the geometry of the intersections between struts and unit cells, bridge geometry, materials of composition, and thermomechanical properties such as material state of phase and residual strain all form a complex set of factors that will influence both the design and the optimized performance of a stent mesh for a particular application.
[0054] In some embodiments, the stent structure may be comprised of balloon expandable materials known in the art such as alloys of cobalt-chromium, alloys of stainless steel, or any other material that will remain patent and apposed to the luminal wall of a vessel upon the application of a dilating strain from the inflation of a catheter-based balloon.
[0055] In some embodiments, the stent structure may be comprised of self-expanding materials known in the art such as nickel-titanium or any other material that exhibits shape memorysuperelastic behavior capable of remaining patent and apposed to the luminal wall of a vessel at body temperature.
[0056] In embodiments where the stent is comprised of nickel-titanium, the material will have a transition temperature where the material is substantially in the austenite phase when unrestrained, the transition temperature being in a range of temperatures at or below nominal body temperature (37 degrees C.), with one preferred range being about 0 degrees C. to about 30 degrees C.
[0057] The embodiments of the present invention are particularly advantageous for use in catheter-based systems and medical procedures where the desire to provide minimally invasive procedures to deliver robust implantable structures to treat complex conditions of the body is coupled with patient quality of life based on clinical outcomes and the unmet needs of providing implants with high strength and fatigue resistance.
[0058] Referring now to
[0059] In
[0060] As has been described herein, treatment of venous stenosis is better served by having a stent design that directly addresses the unique requirements and differences in the vein as opposed to using a stent designed and optimized for arterial use where loading conditions and tissue behavior are different than the vein. The higher radial strength offered by the present invention, in combination with the improvement in load distribution offered by the linear tapering of strut shapes of the present invention offers a combination of advantages. Nonetheless, embodiments of the present invention may be used in arterial, cardiac, and other physiologic applications where patency of a lumen and fatigue resistance are useful.
[0061] From the foregoing, it will be appreciated that, although specific embodiments of the invention have been described herein for the purpose of illustration, various modifications may be made without deviating from the spirit and scope of the invention. Accordingly, the present invention is not limited except as by the appended claims.
[0062] All patents, patent applications, publications, scientific articles, web sites, and other documents and materials referenced or mentioned herein are indicative of the levels of skill of those skilled in the art to which the invention pertains, and each such referenced document and material is hereby incorporated by reference to the same extent as if it had been incorporated by reference in its entirety individually or set forth herein in its entirety. Additionally, all claims in this application, and all priority applications, including but not limited to original claims, are hereby incorporated in their entirety into, and form a part of, the written description of the invention. Applicant reserves the right to physically incorporate into this specification any and all materials and information from any such patents, applications, publications, scientific articles, web sites, electronically available information, and other referenced materials or documents. Applicant reserves the right to physically incorporate into any part of this document, including any part of the written description, the claims referred to above including but not limited to any original claims.
[0063] The specific methods and compositions described herein are representative of preferred embodiments and are exemplary and not intended as limitations on the scope of the invention. Other objects, aspects, and embodiments will occur to those skilled in the art upon consideration of this specification, and are encompassed within the spirit of the invention as defined by the scope of the claims. It will be readily apparent to one skilled in the art that varying substitutions and modifications may be made to the invention disclosed herein without departing from the scope and spirit of the invention. The invention illustratively described herein suitably may be practiced in the absence of any element or elements, or limitation or limitations, which is not specifically disclosed herein as essential. Thus, for example, in each instance herein, in embodiments or examples of the present invention, any of the terms comprising, consisting essentially of, and consisting of may be replaced with either of the other two terms in the specification. Also, the terms comprising, including, containing, etc. are to be read expansively and without limitation. The methods and processes illustratively described herein suitably may be practiced in differing orders of steps, and that they are not necessarily restricted to the orders of steps indicated herein or in the claims. It is also that as used herein and in the appended claims, the singular forms a, an, and the include plural reference unless the context clearly dictates otherwise. Thus, for example, a reference to a host cell includes a plurality (for example, a culture or population) of such host cells, and so forth. Under no circumstances may the patent be interpreted to be limited to the specific examples or embodiments or methods specifically disclosed herein. Under no circumstances may the patent be interpreted to be limited by any statement made by any Examiner or any other official or employee of the Patent and Trademark Office unless such statement is specifically and without qualification or reservation expressly adopted in a responsive writing by Applicants.
[0064] The terms and expressions that have been employed are used as terms of description and not of limitation, and there is no intent in the use of such terms and expressions to exclude any equivalent of the features reported and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention as claimed. Thus, it will be understood that although the present invention has been specifically disclosed by embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims. Other embodiments are within the following claims.