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AU716753B2 - Stent having a multiplicity of closed circular structures - Google Patents
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AU716753B2 - Stent having a multiplicity of closed circular structures - Google Patents

Stent having a multiplicity of closed circular structures Download PDF

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Publication number
AU716753B2
AU716753B2 AU30209/95A AU3020995A AU716753B2 AU 716753 B2 AU716753 B2 AU 716753B2 AU 30209/95 A AU30209/95 A AU 30209/95A AU 3020995 A AU3020995 A AU 3020995A AU 716753 B2 AU716753 B2 AU 716753B2
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AU
Australia
Prior art keywords
stent
rings
longitudinals
deployment
ovals
Prior art date
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Expired
Application number
AU30209/95A
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AU3020995A (en
Inventor
David R. Fischell
Robert E. Fischell
Tim A. Fischell
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Filing date
Publication date
Priority to US08/202,128 priority Critical patent/US5643312A/en
Priority to EP97202628A priority patent/EP0821920B2/en
Priority to DK95301035T priority patent/DK0669114T3/en
Priority to EP95301035A priority patent/EP0669114B1/en
Priority to DK97202628T priority patent/DK0821920T4/en
Priority to CA002142939A priority patent/CA2142939C/en
Priority to AU30209/95A priority patent/AU716753B2/en
Application filed by Individual filed Critical Individual
Priority to JP24236195A priority patent/JPH0956823A/en
Publication of AU3020995A publication Critical patent/AU3020995A/en
Application granted granted Critical
Publication of AU716753B2 publication Critical patent/AU716753B2/en
Priority to GR20000400647T priority patent/GR3032951T3/en
Anticipated expiration legal-status Critical
Expired legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/844Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents folded prior to deployment
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/90Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/90Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
    • A61F2/91Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/90Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
    • A61F2/91Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes
    • A61F2/915Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2002/825Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents having longitudinal struts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/90Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
    • A61F2/91Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes
    • A61F2/915Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
    • A61F2002/91533Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other characterised by the phase between adjacent bands
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/82Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/90Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
    • A61F2/91Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes
    • A61F2/915Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheets or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
    • A61F2002/9155Adjacent bands being connected to each other
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2210/00Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2210/0014Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof using shape memory or superelastic materials, e.g. nitinol
    • A61F2210/0019Particular material properties of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof using shape memory or superelastic materials, e.g. nitinol operated at only one temperature whilst inside or touching the human body, e.g. constrained in a non-operative shape during surgery, another temperature only occurring before the operation

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Transplantation (AREA)
  • Vascular Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Optics & Photonics (AREA)
  • Physics & Mathematics (AREA)
  • Media Introduction/Drainage Providing Device (AREA)

Description

1
AUSTRALIA
PATENTS ACT 1990 COMPLE T E SPECIFICATION FOR A STANDARD PATENT
ORIGINAL
*90* S S *5
S
S
S
*5 S
S.
S S 5*5* 0 *5S* 55 S S S. S
S
5* Names of Applicants: Actual Inventors: ROBERT E. FISCHELL, TIM A. FISCHELL Robert E. FISCHELL, Tim A. FISCHELL DAVID R. FISCHELL and David R. FISCHELL and Address for Service: Invention Title: SHELSTON WATERS 60 Margaret Street SYDNEY NSW 2000 "STENT HAVING A MULTIPLICITY OF CLOSED CIRCULAR STRUCTURES" The following statement is a full description of this invention, including the best method of performing it known to us:la STENT HAVING A MULTIPLICITY OF CLOSED CIRCULAR
STRUCTURES
FIELD OF THE INVENTION This invention is in the field of stents for maintaining patency of any one of a multiplicity of vessels of the human body.
5 BACKGROUND OF THE INVENTION In the last decade, many different designs of stents have been used to maintain patency of arteries and other vessels of the human body. In all such devices, hoop strength is an *important characteristic. Specifically, the stent must have enough hoop strength to resist the "elastic recoil exerted by the vessel into which the stent is placed. The Mass stent described in 10 the U.S. Patent No. 4,553,545 and the Dotter stent described in U.S. Patent No. 4,503, 569 are each open helical coils. The Palmaz stent described in the U.S. Patent No. 4,733,665 is of the "chinese finger" design. The Gianturco-Rubin stent currently sold by Cook, Inc. is another stent design which like the stents of Mass, Dotter and Palmaz does not have any closed circular member to optimize hoop strength.
The ideal arterial stent utilizes a minimum wire size of the stent elements to minimize thrombosis at the stent site after implantation. The ideal arterial stent also posses sufficient hoop strength to resist elastic recoil of the artery. Although the optimum design for maximizing hoop strength is a closed circular structure, no prior art stent has been described which has a small diameter when percutaneously inserted into a vessel and which expands into -2the form of multiplicity of closed circular structures rings) when expanded outward against the vessel wall.
BRIEF SUMMARY OF THE PRESENT INVENTION It is an object of the present invention to overcome or ameliorate at least one of the disadvantages of the prior art, or to provide a useful alternative.
A first aspect of the invention provides a post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally S 10 common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced apart from each other; and a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings and at least one longitudinal being adapted to maintain an essentially unchanged shape in the absence of the multiplicity of 15 generally circular rings, and at least one of said longitudinals having an undulating shape 0 o' for enhancing longitudinal flexibility of said post-deployment stent structure.
A second aspect of the invention provides an initial structure that is capable of being formed into a pre-deployment stent structure which in turn is capable of being deployed into a post-deployment stent structure for placement within a vessel of the human body, the initial structure comprising: a multiplicity of flat ovals, the plane of each oval being generally parallel to the plane of all other ovals, the ovals having a common longitudinal axis which is 2a perpendicular to the plane of each oval and which longitudinal axis passes through the geometric center of the ovals; and a multiplicity of longitudinals which are fixedly attached to the ovals, the longitudinals being positioned onto the ovals so as to be generally parallel to the longitudinal axis of the ovals, at least one of the longitudinals having an undulating shape and being spaced apart from all other longitudinals.
A third aspect of the invention provides a pre-deployment stent structure which is capable of being deployed into a post-deployment stent structure for placement within a vessel of the human body, the pre-deployment structure being formed from an initial 10 structure which consists of a multiplicity of flat ovals, the plane of each oval of said initial structure being generally parallel to the plane of all other ovals, the ovals also having a minor axis and a major axis and a minor axis dimension and a major axis dimension; the ovals having a common longitudinal axis which is perpendicular to the plane of each oval and which longitudinal axis passes through the geometric center of 15 the ovals; and a multiplicity of longitudinals at least one of which is fixedly attached to at least two of the ovals, the longitudinals and ovals being formed from a single metallic structure; and -3the pre-deployment stent structure being formed by folding the ovals each oval's minor axis is nested relation each with respect to the other, the pre-deployment stent structure being adapted to form a post-deployment stent structure having a multiplicity of generally circular rings that are formed from the ovals, at least two of the circular rings being joined together by at least one of the longitudinals, and at least one of the longitudinals having an undulating shape to enhance longitudinal flexibility.
A fourth aspect of the invention provides a post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring 10 being generally parallel to the plane of each adjacent ring, the rings having a generally •common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings and at least one longitudinal being 15 spaced apart from all other longitudinals and at least one longitudinal having an undulating shape so as to enhance the longitudinal flexibility of the post-deployment stent structure.
A fifth aspect of the invention provides a post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and 3aa multiplicity of structure forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings and at least one longitudinal being adapted to maintain an essentially unchanged shape in the absence of any externally applied force and at least one longitudinal having an undulating shape so as to enhance the longitudinal flexibility of the post-deployment stent structure.
A sixth aspect of the invention provides a post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally 10 common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings, the longitudinals being of unitary 0. construction with the generally circular rings from a single piece of thin-walled metal 0* 0 15 tubing and at least one longitudinal having an undulating shape for enhancing 0 longitudinal flexibility.
A seventh aspect of the invention provides a post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and 3b a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings and at least one longitudinal having an undulating shape so as to enhance the longitudinal flexibility of post-deployment stent structure.
An eighth aspect of the invention provides a pre-deployment stent structure generally in the form of a cylindrical tube, the structure consisting of at least one longitudinal having an undulating shape, the longitudinal being fixedly attached to a multiplicity of ovals that have been folded around their minor axes in nested relation each with respect to the other, the longitudinals being of unitary construction with the ovals from a single piece of thin-walled metal tubing.
S- A ninth aspect of the invention provides a stent structure for maintaining patency of a vessel of a human body, the stent structure having a longitudinal axis and S: comprising first structures forming longitudinals, the first structures being fixedly *So o 3cattached to second structures around the longitudinal axis, wherein at least two longitudinals have an undulating shape so as to enhance longitudinal flexibility.
A tenth aspect of the invention provides a pre-deployment balloon expandable stent structure adapted for percutaneous delivery to the curved coronary arteries, the predeployment balloon expandable stent structure being characterized by the stent structure being generally in the form of a thin-walled metal tube having a longitudinal axis, the stent structure having a multiplicity of closed perimeter cells, each cell having one or more undulating sections, each undulating section having a generally curved shape and having a first end point and a second end point wherein a line drawn from the first end 10 point to the second end point is generally parallel to the stent's longitudinal axis.
9*.
An eleventh aspect of the invention provides a balloon expandable coronary stent, the coronary stent being characterized by: a stent in the form of a thin-walled metal tube capable of being mounted o oS on an expandable balloon for percutaneous delivery of the stent into a coronary artery, 15 the stent having a plurality of zig-zag segments, the zig-zag segments capable of being S* expanded by the balloon; and, a plurality of longitudinally undulating sections of a generally curved shape positioned between and connecting the zig-zag segments, wherein the plurality of longitudinally undulating sections can expand and contract in length while being passed through a curved coronary artery.
A twelfth aspect of the invention provides an expandable stent that can be used in an artery or any other vessel of the human body which, when expanded, forms a multiplicity of generally circular rings whose closed structure optimizes hoop strength -3dso as to minimize elastic recoil of the vessel into which the stent is inserted.
Furthermore, the structure of the stent is initially in the form of folded ellipses or ovals which can be formed to a small diameter for percutaneous insertion by means of a stent delivery catheter. The ovals are joined to each other by either a straight or undulating shaped wires which are called "longitudinals" which serve to space the deployed rings within the vessel. Straight longitudinals are used in straight vessels and undulating longitudinals can be employed in either straight or highly curved vessels such as some coronary arteries.
Advantageously a preferred embodiment of the invention provides a stent having a maximum hoop strength by the employment of closed, generally circular structures which are in fact rings.
Preferably the rings are initially in the form of ovals that can be folded to fit onto a cylindrical structure at a distal portion of a stent delivery catheter.
Preferably the fully deployed rings are spaced apart by means of longitudinals which are either straight of undulating wires that are placed to be generally parallel to the longitudinal axis of the vessel into which the stent is deployed.
C• C °•Preferably the pre-deployment stent structure is formed as a single piece out of a metal tube having a smaller inside diameter as compared to the outside diameter of an 00 expandable balloon onto which the pre-deployment stent is mounted.
Unless the context clearly requires otherwise, throughout the description and the claims, the words 'comprise', 'comprising', and the like are to be construed in an inclusive as opposed to an exclusive or exhaustive sense; that is to say, in the sense of "including, but not limited to".
1821o0-oo.Dmoc/LEC 3e- These and other advantages of this invention will become apparent from the detailed description of the invention and the associated drawings provided herein.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a side view of the stent after it has been deployed; in its post-deployment form.
FIG. 2 is a transverse cross section at section 2-2 of FIG. 1 illustrating how the longitudinals are joined to the rings.
FIG. 3 is a cross section at section 3-3 of FIG. 2 showing the joining of a single ring to the longitudinals.
FIG. 4 is a side view of the stent prior to being mounted onto a stent delivery catheter; in the form of an initial structure.
18210-O.Doc/LEC 4 FIG. 5 is a transverse cross section at section 5-5 of FIG. 4 illustrating how the longitudinals are joined to the ovals.
FIG. 6 is a side view of a pre-deployment form of the stent structure in which the ovals have been folded into a small diameter cylinder that is placed around a deflated balloon situated near 5 the distal end of a stent delivery catheter.
o FIG. 7 is a partial side view of a pre-deployment stent structure showing only two of a multiplicity of folded ovals formed around an expandable balloon in which the ovals are folded in an alternative manner as compared with FIG. 6.
FIG. 8 is a side view of a post-deployment stent structure which utilizes two undulating 10 longitudinals on opposite sides of the stent for improved placement in curved vessels.
FIG. 9 is a side view of a stent as etched out of a small diameter metal cylinder as a single piece of metal.
DETAILED DESCRIPTION OF THE DRAWINGS FIG. I is a side view of the cylindrical stent 1 of the present invention shown in its postdeployment configuration. The stent I has a multiplicity of rings 2 which are spaced apart by four wires called longitudinals. As seen in FIGS. I and 2, at the top of the stent is longitudinal 5 4T, at the bottom is longitudinal 4B, at the left side is longitudinal 4L and at the right side is longitudinal 4R. Although FIGS. I and 2 show 7 rings and 4 longitudinals, it is apparent that the stent can be made longer by adding rings or increasing the separation between rings. In a similar manner, the stent can be made shorter by reducing the number of rings or decreasing the spacing between rings. Also variable spacing of the rings is envisioned for accomplishing a variety of purposes including increased hoop strength at a particular section of the stent. Also, a lit is envisioned that the two or more longitudinals could be utilized for this stent design with a maximum number being 32.
o9 FIGS. 2 and 3 illustrate the joining of the longitudinals to the rings. Specifically the 10 longitudinals can be placed into cutouts in the form of notches 5 located on the outside perimeter of the ring 2. The longitudinals can then be spot welded, adhesively bonded or joined by any variety of means to the rings 2. It is also envisioned that the longitudinals could 9 be placed on the inside perimeter of the ring 2, or holes could be mechanically or laser drilled -through the ring 2 for placement therethrough of the longitudinals.
0 FIGS. 4 and 5 illustrate a stent 1' shown in one particular form in which it could be fabricated; in an initial structure form. Specifically, FIGS. 4 and 5 show that this initial form of the stent 1' is a multiplicity of parallel ellipses or ovals 2' each oval having the same minor axis dimension m and major axis dimension M. The oval's minor axis passes through the center of the longitudinals 4L and 4R. The oval's major axis passes through the center of the longitudinals 4T and 4B. It is important to note that, if it is desired to have a final 6 outside diameter D (as seen in FIG. 2) of the ring 2 after it is fully deployed, then it can be shown that D is given by the equation D 2 1/2 (m2+ M 2 To place the stent design of FIGS. 4 and 5 onto a balloon that is mounted near the distal end of a stent delivery catheter, it is necessary to fold the ovals 2' around that balloon.
Specifically, the pre-deployment cylindrical stent 1" can be formed onto an expandable balloon 6 as shown in FIG. 6 by folding the ovals 2' about the dotted line F (which is the minor axis of the oval as shown in FIG. 5. Specifically, as seen in FIG. 4, the top and bottom of the ovals 2' could be held stationery while the side longitudinals 4R and 4L are pushed to the left which results in the pre-deployment structure which is shown as the stent 1" 10 in FIG. 6. An optimum design has the folded ovals 2" as shown in FIG. 6 with the stent 1" being a cylinder whose outside diameter is equal in size to the minor axis dimension m. When the balloon 6 of FIG. 6 is expanded, the pre-deployment stent 1" structure forms the postdeployment stent I structure having circular rings 2 as shown in FIGS. 1 and 2.
The stent is an alternative embodiment for a pre-deployment structure of the stent of the present invention as it is placed onto a balloon. Specifically, FIG. 7 shows 2 folded rings 2." of a multiple ring stent The stent being formed by holding the top and bottom of the stent 1' of FIG. 4 stationery while pushing the longitudinal 4R to the left and pushing the longitudinal 4L to the right. Like the stent 1" of FIG. 6, when mounted onto a balloon, the stent has a cylindrical shape with a diameter equal to the dimension m.
7 FIGS. I to 7 inclusive illustrate stents that employ longitudinals that are formed from generally straight wires. FIG. 8 shows an alternative embodiment of a stent 10 that has two undulating longitudinals. Specifically, the left side longitudinal 14L (shown as dotted lines) and the right side longitudinal 14R are each undulating shaped longitudinals. A stent such as stent 10 could have two or more undulating longitudinals. Such a stent would bend more easily during insertion into a vessel and would be more readily adaptable for placement in curved S" "vessels such as some coronary arteries.
Typically, the rings and longitudinals of the stents would be made of the same material.
Typical metals used for such a stent would be stainless steel, tantulum, titanium, or a shape 10 memory metal such as Nitinol. If Nitinol is used, the stent would be heat treated into the shape at body temperature having circular rings 2 as shown in FIGS. 1 and 2. The rings could then be distorted into ovals as shown in FIGS. 4 and 5 and then mounted onto a stent delivery catheter which does not employ a balloon but is of the more general shape described in the previously cited U.S. Patent No. 4,553,545 by C.T. Dotter. Such a design would 15 provide the desired stent structure having a multiplicity of generally circular rings instead of the Dotter design of a helical spring which inherently has a lesser hoop strength as compared to the present invention.
It should be understood that once the ovals are folded onto a stent delivery catheter, when they fully deploy, they do not form perfectly circular rings as shown in FIG. 2, but rather they are of a generally circular shape. Such comparatively small deviations from an exactly circular 8 shape do not appreciably decrease hoop strength because they are in fact closed structures that are almost exactly circular.
It should also be understood that at least part of the end rings of the stent could be fabricated from or coated with a radiopaque metal such as tantalum or gold to provide a fluoroscopic indication of the stent position within a vessel. However, the other rings and the longitudinals could be made -from a much less dense metal which would provide less obscuration of the central region within the stent. For example, the stent rings and longitudinals could all be fabricated from titanium or a titanium alloy except the end rings which could be formed from gold which is then plated with titanium. Thus, the entire outside surface of the stent would be titanium, which is known to be a comparatively non-thrombogenic metal while the gold in the end rings provides an improved fluoroscopic image of the stent extremities.
The dimensions of stent rings are typically 0.1 to 0.3 mm thick, with a width of 0.1 to 0.5 mm and an outside diameter D between 2.0 and 30.0 mm depending on the luminal diameter of the vessel into which it is inserted. The length of the stent could be between 1 and 10 cm. The wire diameter for the longitudinals would typically be between 0.05 and 0.5 mm.
Although the designs of FIGS. I through 7 inclusive illustrate separate longitudinals attached to a multiplicity of rings, this invention also contemplates an initial stent structure which is chemically etched from thin-walled tubing having an oval transverse cross section. Thus the oval and longitudinals would be formed from a single piece of metal thus precluding the need 9 for attaching the longitudinals to the rings. In a similar manner laser or EDM machining could be used to form the stent from a thin-walled tube.
It is further anticipated that a pre-deployment stent structure 20 as shown in FIG. 9 could be formed from a thin-walled cylindrical tube whose inside diameter is slightly smaller than the outside diameter of the balloon 6 shown in FIG. 6. A pattern such as that shown in either 2. ""FIG. 6 or FIG. 7 could be photoetched onto a thin-walled metal cylinder. The one piece $structure 20 shown in FIG: 9 has folded ovals 22 and longitudinals 23T, 24B, 24R and (not shown) 24L. This pre-deployment stent structure 20 could then be mounted onto the expandable balloon; the stent having sufficient elastic recoil to firmly grasp down onto the o 10 balloon.
'"Various other modifications, adaptations, and alternative designs are of course possible in light of the above teachings. Therefore, it should be understood at this time that within the scope of the appended claims, the invention may be practiced otherwise than as specifically described S""herein.

Claims (25)

1. A post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced apart from each other; and a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings and at least one longitudinal being 10 adapted to maintain an essentially unchanged shape in the absence of the multiplicity of generally circular rings, and at least one of said longitudinals having an undulating shape for enhancing longitudinal flexibility of said post-deployment stent structure. *O
2. The stent of claim 1 wherein the rings have a multiplicity of cutouts for the "placement therethrough of the longitudinals forming generally elongated structures that O 15 lie parallel to the common longitudinal axis of the generally circular rings. o. 3. The stent of claim 1 wherein the rings are formed in unitary construction with the longitudinals from a single piece of metal.
4. The stent of claim 3 wherein the single piece of metal is generally in the form of a thin-walled cylinder.
5. The stent of claim 1 wherein the at least one longitudinal is spaced apart from all other longitudinals.
6. The stent of claim 1 wherein each longitudinal is spaced apart from every other longitudinal.
11- 7. The stent of claim 1 wherein at least one of the longitudinals is a linearly directed, elongated structure. 8. The stent of claim 1 wherein all of the longitudinals are of undulating shape so as to enhance longitudinal flexibility. 9. The stent of claim 1 wherein the rings and longitudinals are made from titanium. The stent of claim 1 wherein the multiplicity of circular rings has exactly two end rings which are those rings which have an adjacent ring on only one side and at least one interior ring which has adjacent rings on both sides, at least some portion of the end rings being formed from a metal having a higher density as compared to the density of the metal of the at least one interior ring. 11. The stent of claim 1 wherein the stent is formed from a metal having a shape memory characteristic.
12. An initial structure that is capable of being formed into a pre-deployment stent structure which in turn is capable of being deployed into a post-deployment stent structure for placement within a vessel of the human body, the initial structure comprising: a multiplicity of flat ovals, the plane of each oval being generally parallel 'to the plane of all other ovals, the ovals having a common longitudinal axis which is Sperpendicular to the plane of each oval and which longitudinal axis passes through the geometric center of the ovals; and a multiplicity of longitudinals which are fixedly attached to the ovals, the longitudinals being positioned onto the ovals so as to be generally parallel to the -12- longitudinal axis of the ovals, at least one of the longitudinals having an undulating shape and being spaced apart from all other longitudinals.
13. The initial structure of claim 12 wherein the ovals and the longitudinals are unitary.
14. A pre-deployment stent structure which is capable of being deployed into a post- deployment stent structure for placement within a vessel of the human body, the pre- deployment structure being formed from an initial structure which consists of a multiplicity of flat ovals, the plane of each oval of said initial structure being generally parallel to the plane of all other ovals, the ovals also having a minor axis and a major axis and a minor axis dimension and a major axis dimension; the ovals having a common longitudinal axis which is perpendicular to the plane of each oval and which longitudinal axis passes through the geometric center of the ovals; and a multiplicity of longitudinals at least one of which is fixedly attached to at least two of the ovals, the longitudinals and *o :ovals being formed from a single metallic structure; and the pre-deployment stent structure being formed by folding the ovals each oval's minor axis in nested relation each with respect to the other, the pre-deployment stent structure being adapted to form a post-deployment stent structure having a multiplicity of generally circular rings that are formed from the ovals, at least two of the circular rings being joined together by at least one of the longitudinals, and at least one of the longitudinals having an undulating shape to enhance longitudinal flexibility. The pre-deployment stent structure of claim 14 wherein the ovals are folded around an expandable balloon located near the distal end of a stent delivery catheter. -13
16. The pre-deployment stent structure of claim 14 wherein the ovals are folded around the oval's minor axis to form a pre-deployment structure of a generally cylindrical shape that can be mounted onto a stent delivery catheter.
17. The pre-deployment stent structure of claim 14 wherein one side of the ovals is folded in one direction and the opposite side of the ovals is folded in the opposite direction to form a pre-deployment structure of a generally cylindrical shape.
18. The pre-deployment stent structure of claim 14 wherein the outer diameter of the generally cylindrical pre-deployment stent structure is approximately the same as the minor axis dimension of the oval.
19. The pre-deployment stent structure of claim 16 wherein the stent structure formed from the single metallic structure, is a cylinder that is smaller in its inside :diameter compared to the outside diameter of an expandable balloon located at a distal portion of a stent delivery catheter onto which the stent structure is mounted. .20. A post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings and at least one longitudinal being spaced apart from all other longitudinals and at least one longitudinal having an 14- undulating shape so as to enhance the longitudinal flexibility of the post-deployment stent structure.
21. A post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings and at least one longitudinal being adapted to maintain an essentially unchanged shape in the absence of any externally applied force and at least one longitudinal having an undulating shape so as to enhance f e the longitudinal flexibility of the post-deployment stent structure. :22. A post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and a multiplicity of structures forming longitudinals, at least one longitudinal being fixedly attached to at least two of the rings, the longitudinals being of unitary construction with the generally circular rings from a single piece of thin-walled metal tubing and at least one longitudinal having an undulating shape for enhancing longitudinal flexibility.
23. A post-deployment stent structure for maintaining patency of a vessel of a human body comprising: a multiplicity of closed, generally circular rings, the plane of each ring being generally parallel to the plane of each adjacent ring, the rings having a generally common longitudinal axis which is perpendicular to the plane of each ring, at least two of the rings being spaced from each other; and a multiplicity of structure forming longitudinals, at least one longitudinal 10 being fixedly attached to at least two of the rings and at least one longitudinal having an undulating shape so as to enhance the longitudinal flexibility of post-deployment stent structure.
24. A pre-deployment stent structure generally in the form of a cylindrical tube, the structure consisting of at least one longitudinal having an undulating shape, the 15 longitudinal being fixedly attached to a multiplicity of ovals that have been folded around their minor axes in nested relation each with respect to the other, the longitudinals being of unitary construction with the ovals from a single piece of thin- walled metal tubing. The pre-deployment stent structure of claim 24 wherein a multiplicity of the longitudinals each has an undulating structure.
26. A stent structure for maintaining patency of a vessel of a human body, the stent structure having a longitudinal axis and comprising first structures forming longitudinals, the first structures being fixedly attached to second structures around the -16- longitudinal axis, wherein at least two longitudinals have an undulating shape so as to enhance longitudinal flexibility.
27. A pre-deployment balloon expandable stent structure adapted for percutaneous delivery to the curved coronary arteries, the pre-deployment balloon expandable stent structure being characterized by the stent structure being generally in the form of a thin- walled metal tube having a longitudinal axis, the stent structure having a multiplicity of closed perimeter cells, each cell having one or more undulating sections, each undulating section having a generally curved shape and having a first end point and a second end point wherein a line drawn from the first end point to the second end point is generally 10 parallel to the stent's longitudinal axis. e o 28. The stent of Claim 27 wherein the line drawn from the first end point to the second end point of the generally curved shape remains generally parallel to the longitudinal axis of the stent as the stent is expanded into its post-deployment state. 0 S: 29. The stent of Claim 27 wherein each cell has at least one circumferentially 0 15 adjacent cell which shares one undulating section. "30. The stent of Claim 27 wherein the undulating section of each closed perimeter cell comprises a shaped curve.
31. A balloon expandable coronary stent, the coronary stent being characterized by: a stent in the form of a thin-walled metal tube capable of being mounted on an expandable balloon for percutaneous delivery of the stent into a coronary artery, the stent having a plurality of zig-zag segments, the zig-zag segments capable of being expanded by the balloon; and, -17- a plurality of longitudinally undulating sections of a generally curved shape positioned between and connecting the zig-zag segments, wherein the plurality of longitudinally undulating sections can expand and contract in length while being passed through a curved coronary artery.
32. A post-deployment stent structure for maintaining patency of a vessel of the human body substantially as herein described with reference to Figures 1, 2 and 3 or Figure 8 of the accompanying drawings.
33. An initial structure that is capable of being formed into a pre-deployment stent structure substantially as herein described with reference to Figures 4 and 5 or Figure 9 of the accompanying drawings.
34. A pre-deployment stent structure substantially as herein described with reference to Figures 4 and 5 or Figures 6 and 7 of the accompanying drawings. o.
35. A stent structure for maintaining patency of a vessel of the human body substantially as herein described with reference to the information disclosed in the accompanying drawings.
36. A pre-deployment balloon expandable stent structure adapted for percutaneous delivery to the curved coronary arteries substantially as herein described with reference to the information disclosed in the accompanying drawings.
37. A balloon expandable coronary stent substantially as herein described with reference to the information disclosed in the accompanying drawings. DATED THIS 18th Day of August 1999 ROBERT E. FISCHELL, DAVID R. FISCHELL and TIM A. FISCHELL Attorney: PETER R. HEATHCOTE Fellow Institute of Patent Attorneys of Australia 6 of BALDWIN SHELSTON WATERS
AU30209/95A 1994-02-25 1995-08-23 Stent having a multiplicity of closed circular structures Expired AU716753B2 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
US08/202,128 US5643312A (en) 1994-02-25 1994-02-25 Stent having a multiplicity of closed circular structures
DK95301035T DK0669114T3 (en) 1994-02-25 1995-02-17 Stent with a plurality of closed circular structures
EP95301035A EP0669114B1 (en) 1994-02-25 1995-02-17 Stent having a multiplicity of closed circular structures
DK97202628T DK0821920T4 (en) 1994-02-25 1995-02-17 Stent
EP97202628A EP0821920B2 (en) 1994-02-25 1995-02-17 Stent
CA002142939A CA2142939C (en) 1994-02-25 1995-02-20 Stent having a multiplicity of closed circular structures
AU30209/95A AU716753B2 (en) 1995-08-23 1995-08-23 Stent having a multiplicity of closed circular structures
JP24236195A JPH0956823A (en) 1994-02-25 1995-08-29 Stent with large number of closed circular structures
GR20000400647T GR3032951T3 (en) 1994-02-25 2000-03-10 Stent having a multiplicity of closed circular structures

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AU30209/95A AU716753B2 (en) 1995-08-23 1995-08-23 Stent having a multiplicity of closed circular structures

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AU716753B2 true AU716753B2 (en) 2000-03-02

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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4856516A (en) * 1989-01-09 1989-08-15 Cordis Corporation Endovascular stent apparatus and method
US5290305A (en) * 1991-10-11 1994-03-01 Kanji Inoue Appliance collapsible for insertion into human organs and capable of resilient restoration
US5496365A (en) * 1992-07-02 1996-03-05 Sgro; Jean-Claude Autoexpandable vascular endoprosthesis

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4856516A (en) * 1989-01-09 1989-08-15 Cordis Corporation Endovascular stent apparatus and method
US5290305A (en) * 1991-10-11 1994-03-01 Kanji Inoue Appliance collapsible for insertion into human organs and capable of resilient restoration
US5496365A (en) * 1992-07-02 1996-03-05 Sgro; Jean-Claude Autoexpandable vascular endoprosthesis

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