U.S. patent application number 12/606874 was filed with the patent office on 2010-02-25 for stent with improved resistance to migration.
This patent application is currently assigned to Boston Scientific Scimed, Inc.. Invention is credited to John Spiridigliozzi, Ilya Yampolsky.
Application Number | 20100049291 12/606874 |
Document ID | / |
Family ID | 34193828 |
Filed Date | 2010-02-25 |
United States Patent
Application |
20100049291 |
Kind Code |
A1 |
Yampolsky; Ilya ; et
al. |
February 25, 2010 |
STENT WITH IMPROVED RESISTANCE TO MIGRATION
Abstract
A modular mating stent is adapted to resist migration within a
receiving stent. The modular mating stent has a substantially
self-expandable first section of predetermined compressibility that
is adapted to permit the first section to conform to the shape of a
body lumen surrounding the first section. The modular mating stent
also has a balloon-expandable second section that is less
compressible than the first section, which is adapted to firmly
engage a surface of the receiving stent surrounding the second
section.
Inventors: |
Yampolsky; Ilya; (Roxbury,
MA) ; Spiridigliozzi; John; (Sharon, MA) |
Correspondence
Address: |
BROOKS, CAMERON & HUEBSCH, PLLC
1221 NICOLLET AVENUE, SUITE 500
MINNEAPOLIS
MN
55403
US
|
Assignee: |
Boston Scientific Scimed,
Inc.
Maple Grove
MN
|
Family ID: |
34193828 |
Appl. No.: |
12/606874 |
Filed: |
October 27, 2009 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10643261 |
Aug 20, 2003 |
7628806 |
|
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12606874 |
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Current U.S.
Class: |
623/1.2 ;
623/1.23; 623/1.39 |
Current CPC
Class: |
A61F 2220/0033 20130101;
A61F 2/89 20130101; A61F 2220/005 20130101; A61F 2250/0042
20130101; A61F 2/848 20130101; A61F 2220/0075 20130101; A61F
2220/0058 20130101; A61F 2/07 20130101; A61F 2002/067 20130101 |
Class at
Publication: |
623/1.2 ;
623/1.39; 623/1.23 |
International
Class: |
A61F 2/82 20060101
A61F002/82 |
Claims
1. A modular mating stent adapted to resist migration within a
receiving stent, comprising: a substantially self-expandable first
section of predetermined compressibility adapted to permit said
section to conform to the shape of a body lumen surrounding said
section; and a balloon-expandable second section less compressible
than said first section adapted to firmly engage a surface of the
receiving stent surrounding the second section.
2. The modular mating stent of claim 1 wherein the
balloon-expandable second section is configured to be deployed at
least partially within the receiving stent and to firmly engage the
surrounding receiving stent to resist migration and leakage.
3. The modular mating stent of claim 2 wherein the
balloon-expandable second section has a predetermined
compressibility when expanded that is less compressible than that
of an aperture of the receiving stent into which the second section
has been deployed.
4. The modular mating stent of claim 1 wherein the self-expandable
first section is comprised of a tubular member, the tubular member
defining a plurality of openings.
5. The modular mating stent of claim 4 wherein the self-expandable
first section is at least partially constructed from at least one
strand of braided stent material.
6. The modular mating stent of claim 4 wherein the self-expandable
first section is at least partially constructed of a shape memory
material.
7. The modular mating stent of claim 6 wherein the shape memory
material is nitinol.
8. The modular mating stent of claim 1 wherein the
balloon-expandable second section is comprised of a tubular member,
the tubular member defining a plurality of openings.
9. The modular mating stent of claim 8 wherein the balloon
expandable second section is at least partially constructed of
stainless steel.
10. The modular mating stent of claim 8 wherein the balloon
expandable second is comprised of a cut tube of stent material
comprising a plurality of interconnected members defining a
plurality of cell spaces.
11. The modular mating stent of claim 8 wherein the balloon
expandable second section is comprised of a cut sheet of stent
material formed into a tubular shape, the tubular shape comprising
a plurality of interconnected members defining a plurality of cell
spaces.
12. The modular mating stent of claim 8 wherein the balloon
expandable second section comprises at least one vessel engagement
member, the at least one vessel engagement member selected from the
group consisting of hooks, barbs, T-fasteners, bumps, ridges, and
combinations thereof.
13. The modular mating stent of claim 1 wherein the balloon
expandable second section comprises at least one distally extending
member and the self-expandable first section comprises at least one
proximally extending member, the at least one proximally extending
member and the at least one distally extending member being engaged
to each other.
14. The modular mating stent of claim 13 further comprising at
least one crimping member, the at least one crimping member
disposed about the at least one proximally extending member and the
at least one distally extending member.
15. The modular mating stent of claim 14 wherein the at least one
crimping member is at least partially constructed of a radiopaque
material.
16. The modular mating stent of claim 1 further comprising at least
one layer of graft material, the at least one layer of graft
material at least partially disposed about and/or within the
modular mating stent to define a fluid passageway therethrough.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] Not Applicable
STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH
[0002] Not Applicable
BACKGROUND OF THE INVENTION
[0003] 1. Field of the Invention
[0004] The present invention relates to a stent for use in body
lumens. More specifically, the present invention relates to a stent
that is sufficiently flexible to facilitate its deployment and
conformance to a tortuous lumen, and sufficiently rigid to resist
migration, once the stent is deployed.
[0005] 2. Description of the Related Art
[0006] Stents, grafts, stent-grafts, vena cava filters and similar
implantable medical devices, collectively referred to hereinafter
as stents, are radially expandable endoprostheses which are
typically intravascular implants capable of being implanted
transluminally and enlarged radially after being introduced
percutaneously. Stents may be implanted in a variety of body lumens
or vessels such as within the vascular system, urinary tracts, bile
ducts, etc. Stents may be used to reinforce body vessels and to
prevent restenosis following angioplasty in the vascular system.
They may be self-expanding, mechanically expandable or hybrid
expandable.
[0007] Stents are generally tubular devices for insertion into body
lumens. However, it should be noted that stents may be provided in
a wide variety of sizes and shapes. Balloon expandable stents
require mounting over a balloon, positioning, and inflation of the
balloon to expand the stent radially outward. Self-expanding stents
expand into place when unconstrained, without requiring assistance
from a balloon. A self-expanding stent is biased so as to expand
upon release from the delivery catheter. Some stents may be
characterized as hybrid stents which have some characteristics of
both self-expandable and balloon expandable stents.
[0008] Stents may be constructed from a variety of materials such
as stainless steel, Elgiloy, nickel, titanium, nitinol, shape
memory polymers, etc. Stents may also be formed in a variety of
manners as well. For example a stent may be formed by etching or
cutting the stent pattern from a tube or section of stent material;
a sheet of stent material may be cut or etched according to a
desired stent pattern whereupon the sheet may be rolled or
otherwise formed into the desired substantially tubular, bifurcated
or other shape of the stent; one or more wires or ribbons of stent
material may be woven, braided or otherwise formed into a desired
shape and pattern.
[0009] Some examples of stents or stent components that may be
braided are described in U.S. Pat. No. 5,061,275, U.S. Pat. No.
4,655,771, U.S. Pat. No. 6,146,403, U.S. Pat. No. 5,836,966, U.S.
Pat. No. 642,308, as well as in U.S. application Ser. No.
10/063,315 to Eder et al., filed Apr. 10, 2002.
[0010] Typically, a stent is implanted in a blood vessel or other
body lumen at the site of a stenosis or aneurysm by so-called
"minimally invasive techniques" in which the stent is compressed
radially inwards and is delivered by a catheter to the site where
it is required through the patient's skin or by a "cut down"
technique in which the blood vessel concerned is exposed by minor
surgical means. When the stent is positioned at the correct
location, the catheter is withdrawn and the stent is caused or
allowed to expand to a predetermined diameter in the vessel.
[0011] Some stents have been developed specifically to address the
problems that arise in the treatment of stenoses at or near the
site of a bifurcation of a body lumen are known in the art.
Further, single bifurcated stents and grafts have been developed in
order to treat such conditions at the site of a branch of a body
lumen. A bifurcated stent and/or graft typically is configured in a
"pant" design which comprises a tubular body or trunk and two
tubular legs, however other configurations are also known wherein
the stent includes a plurality of separate and/or inter-connectable
portions which may be delivered to various positions at or around
the bifurcation using a single or multiple catheters.
[0012] Some examples of bifurcated stents are shown in U.S. Pat.
No. 5,723,004; U.S. Pat. No. 4,994,071 and U.S. Pat. No.
5,755,735.
[0013] In some stents, the compressible and flexible properties
that assist in stent delivery may also result in a stent that has a
tendency to migrate from its originally deployed position. It is
thus desirable to provide a stent configuration that resists
migration following deployment, particularly where the site of the
desired deployment is within or adjacent to a vessel
bifurcation.
[0014] All US patents, applications and all other published
documents mentioned anywhere in this application are incorporated
herein by reference in their entirety.
[0015] Without limiting the scope of the invention a brief summary
of some of the claimed embodiments of the invention is set forth
below. Additional details of the summarized embodiments of the
invention and/or additional embodiments of the invention may be
found in the Detailed Description of the Invention below.
[0016] A brief abstract of the technical disclosure in the
specification is provided as well only for the purposes of
complying with 37 C.F.R. 1.72. The abstract is not intended to be
used for interpreting the scope of the claims.
SUMMARY OF THE INVENTION
[0017] The present invention is embodied in a variety of forms. For
example in at least one embodiment of the invention a stent is
provided that is adapted both to resist migration within a body
lumen and to conform to a tortuous installation path or installed
location. The stent includes a first section, typically
self-expandable, of predetermined compressibility adapted to permit
the section to conform to the shape of the body lumen through which
it is transmitted or surrounding the section when deployed. The
stent also includes a second section which is balloon-expandable
and which is less compressible than the first section. The second
section is adapted to firmly engage that part of the body lumen
surrounding the second section when it is deployed, or to engage
the inner surface of another stent with which it is mated or
assembled upon deployment.
[0018] In some embodiments the stent is a bifurcated stent. The
stent comprises a trunk region and at least one leg region or
branch extending therefrom. In at least one embodiment the trunk
defines an opening which defines a first flow path therethrough and
one or more branches adjacent thereto, wherein each branch defines
additional flow paths.
[0019] Where the stent is bifurcated, the trunk region of the stent
includes a proximal section and a distal section, wherein the
branch(es) extend from the distal section. This distal section of
the trunk region, as well as at least a portion of each branch, is
constructed from braided strands of material. In some embodiments
this braided portion of the stent is self-expandable. The proximal
section of the trunk region comprises a solid, tubular geometry
with cellular openings to provide a rigid construction within a
section of the trunk region of the stent to assist in resisting
migration of the stent-graft. In some embodiments the proximal
section of the trunk region is balloon expandable.
[0020] In at least one embodiment, a modular mating stent is
provided that is adapted to resist migration within a receiving
stent. The modular mating stent includes a substantially
self-expandable first section of predetermined compressibility
adapted to permit the section to conform to the shape of a body
lumen surrounding the section. The modular mating stent further
includes a balloon-expandable second section less compressible than
the first section adapted to firmly engage that part, i.e. the
inner surface, of the receiving stent surrounding the second
section when the two are assembled in a male-female
relationship.
[0021] These and other embodiments which characterize the invention
are pointed out with particularity in the claims annexed hereto and
forming a part hereof. However, for a better understanding of the
invention, its advantages and objectives obtained by its use,
reference should be made to the drawings which form a further part
hereof and the accompanying descriptive matter, in which there is
illustrated and described embodiments of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
[0022] A detailed description of the invention is hereafter
described with specific reference being made to the drawings.
[0023] FIG. 1 is a perspective view of an embodiment of the
invention comprising a bifurcated stent.
[0024] FIG. 2 is a perspective view of an embodiment of the
invention comprising a crimping member that engages the two
sections of differential compressibility in the trunk region of the
stent of FIG. 1.
[0025] FIG. 3 is a perspective view of an embodiment of the
invention comprising a modular mating stent adapted to be received
within and assembled with a receiving stent in accordance with
another embodiment of the present invention.
DETAILED DESCRIPTION OF THE INVENTION
[0026] While this invention may be embodied in many different
forms, there are described in detail herein specific preferred
embodiments of the invention. This description is an
exemplification of the principles of the invention and is not
intended to limit the invention to the particular embodiments
illustrated.
[0027] For the purposes of this disclosure, like reference numerals
in the figures shall refer to like features unless otherwise
indicated.
[0028] In at least one embodiment of the invention, such as for
example the embodiment depicted in FIG. 1, there is shown a
bifurcated stent 20 adapted to resist migration within a body
lumen. Stent 20 includes a trunk region 22 at least one leg region
or branches, such as branches 26 and 24, extending therefrom.
[0029] The trunk region 22 of stent 20 includes a first or proximal
section 30 and a second or distal section 28. The branches 24 and
26 define separate flow paths which branch from the single flow
path defined by the trunk region 22.
[0030] At least a portion of each branch 24 and 26, as well as the
distal section 28 of the trunk region 22, share a common
predetermined compressibility (or flexibility) adapted to permit
the branches 24 and 26 and section 28 to conform to the shape of
the body lumens surrounding them at their deployment site and to
easily advanced through the tortuous confines of body lumen(s). In
at least one embodiment the branches 24 and 26 as well as the
section 28 are substantially self-expandable.
[0031] The proximal section 30 of the trunk region 22 is adapted to
firmly engage that part of the body lumen surrounding the section
30 at its deployment site adjacent to the bifurcation of a vessel.
The section 30 is deployed by mechanical or balloon expansion and
is firmly seated within the vessel to resist stent migration. The
section 30 likewise has a predetermined compressibility, but which
is less compressible than that of the distal section 28 or the
branches 24 and 26. In some embodiments section 30 is constructed
from material having a substantially solid, tubular geometry with
cellular openings, which may be obtained from a laser cut tube or
sheet which formed into a tube.
[0032] In some embodiments, the distal section 28 and the branches
24 and 26 are integrally formed of one or more strands 31 of
material that are interwoven or braided to form the respective
portions of the stent 20.
[0033] The sections 28 and 30 may be bonded, welded, or otherwise
engaged together to form the trunk region 22. In at least one
embodiment, one or more distal members 33 of the proximal section
30 and one or more proximal members 35 of the distal section 28 are
engaged together by at least one crimping members 32 (better seen
in FIG. 2). A crimping member 32 comprises a tubular member or band
37 that is disposed about an overlapping portion of one or more
distal members 33 and one or more proximal members 35. Once
properly disposed, the crimping member is crimped or otherwise
compressed in order to frictionally engage and retain the
respective portions of members 33 and 35 contained therein.
[0034] In at least one embodiment, during delivery of the stent 20,
when stent 20 is positioned at the correct location, distal section
28 of the trunk 22 and branches 24 and 26 are caused or allowed to
self-expand to a predetermined diameter within the vessel(s). Even
after the branches 24 and 26 and/or the section 28 are fully
expanded, the location of stent 20 may be adjusted before final
placement and fixation. Once properly positioned, the proximal
section 30 of the trunk 22 is expanded to a predetermined diameter
in the vessel via a balloon or other mechanical expansion mechanism
such as are known.
[0035] Because of the greater rigidity of the proximal section 30,
one the proximal section of the trunk 22 is fully expanded the
stent 20 will remain fixed in its final position.
[0036] As indicated above, when the proximal section 30 is
expanded, it is less compressible than the distal section 28 and
delivers a substantial radial resistance to force, preventing stent
20 from working its way away from its originally deployed
position.
[0037] In the embodiment shown in FIG. 1 the distal section 28 and
branches 24 and 26 are formed of a conventional material to provide
the section 28 and branches 24 and 26 with self-expanding
characteristics. Suitable materials include, but are not limited to
one or more shape-memory metals such as nitinol, one or more shape
memory polymers, etc. The proximal section 30 is typically formed
of any of a variety of materials that provide or can be made to
provide greater rigidity or compression resistance than that of the
distal section 28. Such materials may include but are not limited
to stainless steel, nitinol, etc.
[0038] During balloon expansion of the proximal section 30, the
material or materials of which the section 30 is constructed
undergoes plastic deformation to better set the shape induced by
the balloon expansion. The tendency of the more rigid section 30,
to resist migration may be further enhanced by the inclusion of one
or more vessel engagement members 39, a vessel engagement member
may be comprised of one or more hooks, barbs, T-fasteners, and/or
other external surface features to assist in firmly engaging the
surrounding body lumen.
[0039] As stated above, the stent 20 may be a stent-graft, wherein
the stent 20 is provided with a graft lining or covering to provide
fluid pathways from the unbifurcated end to the bifurcated end.
[0040] As mentioned above, an alternative to the balloon-expandable
stainless steel proximal section 30 is a balloon-expandable, and
thus more rigid, proximal section 30 constructed of nitinol but
annealed (i.e., heat treated above the temperature necessary to
effect shape-memory retention). Annealing the nitinol transforms
its material properties from a shape memory alloy capable of
re-expansion to a more rigid structure, conducive to fixation
through alternative means such as balloon expansion.
[0041] FIG. 2 is a detail view of crimping member 32 represented in
FIG. 1 that secures the two sections of differential
compressibility (i.e. section 28 and section 30) together. The
exemplary configuration illustrates two braided members 35 of
distal section 28 secured to one or more members 33 of the proximal
section 30 via crimping member 32. In some embodiments crimping
member 32 and/or other portions of the stent may be at least
partially constructed of one or more radiopaque materials.
[0042] As indicated above, stent 20 is not limited to the use of
crimping members 32 as a securing mechanism between the first and
second sections 30 and 38 of the trunk region 22. For example,
first section 30 and second section 28 may be secured together via
welds, chemical or adhesive bonds, direct mechanical engagement
(i.e. hooks, etc.) of the members 33 and 35, and any combinations
thereof. Furthermore, the proximal section 30 and distal section 28
may not be connected at all if their relative positions are
maintained in some other way, such as by securing section 28 and
section 30 each to the inside of a graft, sleeve or other device
via sutures or other securement mechanisms such as sutures.
[0043] In at least on embodiment, the invention is also directed to
a system comprising a modular mating stent 40 and receiving stent
42, an example of which is shown in FIG. 3.
[0044] The modular mating stent 40 includes a first section 44 of
predetermined compressibility adapted to permit section 44 to
conform to the shape of a body lumen surrounding section 44. The
modular mating stent 40 further includes a second section 46 less
compressible than first section 44 and adapted to firmly engage
that part of receiving stent 42 surrounding second section 46, i.e.
the inner surface of stent 42 in the area where stent 40 is
received during in vivo deployment and assembly. A graft 48 covers
modular mating stent 40 and receiving stent 42, at least in part,
defining a fluid passageway.
[0045] The configuration and deployment of this embodiment of the
present invention are essentially the same as those of the
balloon-expandable embodiment of stent 20 described previously with
reference to FIG. 1. First section 44 is constructed from braided
strands of a shape memory alloy capable of re-expansion, while
second section 46 is constructed from a non-shape memory alloy in a
tubular geometry with cellular openings. Therefore, placement and
fixation are achieved through alternative means such as balloon
expansion. A notable difference from stent 20, however, is that
mating stent 40 is deployed at least partially within receiving
stent 42 as opposed to a body lumen, as represented in FIG. 3. The
previously described principles of section 30 of stent 20 firmly
engaging the surrounding body lumen apply to second section 46 of
modular mating stent 40 firmly engaging the surrounding receiving
stent 42 to resist migration and leakage.
[0046] The above disclosure is intended to be illustrative and not
exhaustive. This description will suggest many variations and
alternatives to one of ordinary skill in this art. All these
alternatives and variations are intended to be included within the
scope of the claims where the term "comprising" means "including,
but not limited to". Those familiar with the art may recognize
other equivalents to the specific embodiments described herein
which equivalents are also intended to be encompassed by the
claims.
[0047] Further, the particular features presented in the dependent
claims can be combined with each other in other manners within the
scope of the invention such that the invention should be recognized
as also specifically directed to other embodiments having any other
possible combination of the features of the dependent claims. For
instance, for purposes of claim publication, any dependent claim
which follows should be taken as alternatively written in a
multiple dependent form from all prior claims which possess all
antecedents referenced in such dependent claim if such multiple
dependent format is an accepted format within the jurisdiction
(e.g. each claim depending directly from claim 1 should be
alternatively taken as depending from all previous claims). In
jurisdictions where multiple dependent claim formats are
restricted, the following dependent claims should each be also
taken as alternatively written in each singly dependent claim
format which creates a dependency from a prior
antecedent-possessing claim other than the specific claim listed in
such dependent claim below.
* * * * *