WO1997040781A1 - Intravascular stent - Google Patents

Intravascular stent Download PDF

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Publication number
WO1997040781A1
WO1997040781A1 PCT/US1997/006610 US9706610W WO9740781A1 WO 1997040781 A1 WO1997040781 A1 WO 1997040781A1 US 9706610 W US9706610 W US 9706610W WO 9740781 A1 WO9740781 A1 WO 9740781A1
Authority
WO
WIPO (PCT)
Prior art keywords
expansion
stent
strut
ofthe
column
Prior art date
Application number
PCT/US1997/006610
Other languages
French (fr)
Inventor
G. David Jang
Original Assignee
Jang G David
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US08/824,865 external-priority patent/US6152957A/en
Application filed by Jang G David filed Critical Jang G David
Priority to JP53898097A priority Critical patent/JP4223552B2/en
Priority to AU26782/97A priority patent/AU2678297A/en
Priority to EP97918755A priority patent/EP0900059B1/en
Priority to DE69734389T priority patent/DE69734389T2/en
Priority to CA002252882A priority patent/CA2252882C/en
Priority to EP97922481A priority patent/EP0902666B1/en
Priority to AU31158/97A priority patent/AU3115897A/en
Priority to DE1997627670 priority patent/DE69727670T2/en
Priority to PCT/US1997/007006 priority patent/WO1997040784A1/en
Priority to DE69735133T priority patent/DE69735133T2/en
Priority to CA002263397A priority patent/CA2263397C/en
Priority to JP53903197A priority patent/JP4636634B2/en
Priority to ES97922481T priority patent/ES2216145T3/en
Priority to JP1997539074A priority patent/JP4012251B6/en
Priority to AU28135/97A priority patent/AU728242B2/en
Priority to PCT/US1997/006907 priority patent/WO1997040783A2/en
Priority to CA002252596A priority patent/CA2252596C/en
Priority to AT97922481T priority patent/ATE259627T1/en
Priority to EP97926382A priority patent/EP0927006B1/en
Publication of WO1997040781A1 publication Critical patent/WO1997040781A1/en
Priority to JP2007260043A priority patent/JP4749403B2/en

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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
    • A61F2/86Stents 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 sheet material 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 sheet material 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 sheet material 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
    • A61F2/86Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
    • A61F2/89Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
    • 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
    • A61F2/95Instruments specially adapted for placement or removal of stents or stent-grafts
    • A61F2/958Inflatable balloons for placing stents or stent-grafts
    • 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 sheet material 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 sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
    • A61F2002/91525Stents 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 sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other within the whole structure different bands showing different meander characteristics, e.g. frequency or amplitude
    • 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 sheet material 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 sheet material 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 sheet material 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 sheet material 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 sheet material 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
    • A61F2002/91558Adjacent bands being connected to each other connected peak to peak
    • 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
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0002Two-dimensional shapes, e.g. cross-sections
    • A61F2230/0004Rounded shapes, e.g. with rounded corners
    • A61F2230/0013Horseshoe-shaped, e.g. crescent-shaped, C-shaped, U-shaped
    • 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
    • A61F2230/00Geometry of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2230/0002Two-dimensional shapes, e.g. cross-sections
    • A61F2230/0028Shapes in the form of latin or greek characters
    • A61F2230/0054V-shaped
    • 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
    • A61F2250/00Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
    • A61F2250/0014Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis
    • A61F2250/0018Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof having different values of a given property or geometrical feature, e.g. mechanical property or material property, at different locations within the same prosthesis differing in elasticity, stiffness or compressibility

Definitions

  • This invention relates to intravascular stents, and more particularly to an intravascular stent which provides easy introduction through tortuous sections of vessels
  • Angioplasty either coronary or general vascular
  • Balloon catheter dependent angioplasty has consistently proven to be the most reliable and practical interventional procedure
  • Other ancillary technologies such as laser based treatment, or directional or rotational arthrectomy, have proven to be either of limited effectiveness or dependent on balloon angioplasty for completion ofthe intended procedure
  • Restenosis following balloon-based angioplasty is the most serious drawback and is especially prevalent in the coronary artery system
  • Many regimens have been designed to combat restenosis, with limited success, including laser based treatment and directional or rotational arthrectomy Intravascular stenting, however, noticeably reduces the restenosis rate following
  • the intravascular stent functions as scaffolding for the lumen of a vessel
  • the scaffolding ofthe vessel walls by the stent serve to (a) prevent elastic recoil ofthe dilated vessel wall, (b) eliminate residual stenosis ofthe vessel, a common occurrence in balloon angioplasty procedures, (c) maintain the diameter ofthe stented vessel segment slightly larger than the native unobstructed vessel segments proximal and distal the stented segment and (d) as indicated by the latest clinical data, lower the restenosis rate Following an angioplasty procedure, the restenosis rate of stented vessels has proven significantly lower than for unstented or otherwise treated vessels, treatments include drug therapy and other methods mentioned previously
  • vessel stenting Another benefit of vessel stenting is the potential reduction of emergency bypass surgery arising from angioplasty procedures Stenting has proven to be effective in some cases for treating impending closure of a vessel during angioplasty Stenting can also control and stabilize an unstable local intimal tear of a vessel caused by normal conduct during an angioplasty procedure In some cases, an incomplete or less than optimal dilatation of a vessel lesion with balloon angioplasty can successfully be opened up with a stent implant
  • anticoagulation techniques have since been developed and are becoming simpler and more effective Better and easier to use regimens are continuously being introduced, including simple outpatient anticoagulation treatments, resulting in reduced hospital stays for stent patients 0781 PO7US97/06610
  • the unexpanded tubular members ofthe Palmaz Patent are overly rigid so that practical application is limited to short lengths Even with implementation ofthe multilink design with flexible connector members connecting a series of tubular members, longer stents can not navigate tortuous blood vessels Furthermore, the rigidity ofthe unexpanded stent increases the risk of damaging vessels during insertion Foreshortening ofthe stent during insertion complicates accurate placement ofthe stent and reduces the area that can be covered by the expanded stent There is, further, no method of programming the stent diameter along its longitudinal axis to achieve a tapered expanded stent, and no method of reenforcement of stent ends or other regions is provided for.
  • WO 96/03092 Another example of a conventional stent patent is WO 96/03092, the Brun patent The stent described in the Brun patent is formed of a tube having a patterned shape, which has first and second meander patterns The even and odd first meander patterns are 180 degrees out of phase, with the odd patterns occurring between every two even patterns The second meander patterns run perpendicular to the first meander patterns, along the axis ofthe tube
  • Adjacent first meander patterns are connected by second meander patterns to form a generally uniform distributed pattern
  • the symmetrical arrangement with first and second meander patterns having sharp right angled bends allows for catching and snagging on the vessel wall during delivery
  • the large convolutions in the second meander pattern are not fully straightened out during expansion reducing rigidity and structural strength ofthe expanded stent
  • no method of programming the stent diameter along its longitudinal axis to achieve a tapering stent design and no method of reenforcement of stent ends or other regions is provided for
  • These and other conventional stent designs suffer in varying degrees from a variety of drawbacks including (a) inability to negotiate bends in vessels due to columnar rigidity ofthe unexpanded stent, (b) lack of structural strength, radial and axial lateral, ofthe unexpanded stent, ⁇ significant foreshortening ofthe stent during expansion, (d) limited stent length, (e) constant expanded stent diameter
  • a stent with sufficient longitudinal flexibility in the unexpanded state there is a need for a stent with sufficient longitudinal flexibility in the unexpanded state to allow for navigation through tortuous vessels
  • a stent that is structurally strong in the unexpanded state such that risk of damage or distortion during delivery is minimal
  • a stent that is configured to expand to variable diameters along its length such that a taper can be achieved in the expanded stent to match the natural taper ofthe target vessel
  • Another object ofthe invention is to provide a stent which prevents recoil ofthe vessel following angioplasty
  • a further object ofthe invention is to provide a stent that maintains a larger vessel lumen compared to the results obtained only with balloon angioplasty.
  • Yet another object ofthe invention is to provide a stent that reduces foreshortening of a stent length when expanded.
  • Another object ofthe invention is to provide a stent with increased flexibility when delivered to a selected site in a vessel.
  • Another object ofthe invention is to provide a chain mesh stent that reduces vessel "hang up" in a tortuous vessel or a vessel with curvature.
  • a first expansion strut pair includes a first expansion strut positioned adjacent to a second expansion strut.
  • a joining strut ofthe first expansion strut pair couples the first and second expansion struts at a distal end ofthe first expansion strut pair.
  • a plurality ofthe first expansion strut pair form a first expansion column.
  • a second expansion strut pair includes a first expansion strut positioned adjacent to a second expansion strut.
  • a joining strut ofthe second expansion strut pair couples the first and second expansion struts ofthe second expansion strut pair at a proximal end ofthe second expansion strut pair.
  • a plurality ofthe second expansion strut pair form a second expansion column.
  • a first connecting strut includes a first connecting strut proximal head section and a first connecting strut distal tail section.
  • the head section is coupled to the distal end of the first expansion strut pair in the first expansion column
  • the tail section is coupled to the proximal end ofthe second expansion strut pair ofthe second expansion column.
  • a plurality ofthe first connecting strut form a first connecting strut column that couples the first expansion column to the second expansion column.
  • the tail section extends in a first lateral direction relative to a longitudinal axis of the head section to form a first slant angle.
  • a third expansion strut pair includes a first expansion strut positioned adjacent to a second expansion strut A third joining strut ofthe third expansion strut pair couples the first and second expansion struts at a proximal end ofthe third expansion strut pair.
  • a plurality ofthe third expansion strut pair form a third expansion column
  • the first expansion strut ofthe first expansion strut pair in the first expansion column have a longitudinal axis that is parallel to and offset from a longitudinal axis ofthe first expansion strut ofthe second expansion strut pair in the second expansion column
  • the second expansion strut ofthe third expansion strut pair in the third expansion column has a longitudinal axis that is parallel to and offset from a longitudinal axis ofthe first expansion strut ofthe second expansion strut pair ofthe second expansion column
  • a second connecting strut includes a proximal head section and a distal tail section The head section is coupled to the distal end ofthe second expansion strut pair in the second expansion column
  • the tail section is coupled to the proximal end ofthe third expansion strut pair ofthe third expansion column
  • a plurality ofthe second connecting strut form a second connecting strut column that couples the second expansion column to the third expansion column.
  • the tail section extends in a second lateral direction relative to a longitudinal axis ofthe head section to form a second slant angle that extends in an opposite direction from the first lateral direction
  • a ratio of a number of expansion struts in an expansion strut column to a number of connecting struts in a connecting strut column is 2 to 1
  • the first slant angle reduces a fore shortening ofthe stent between the first and second expansion columns when the stent is in an expanded state.
  • a stent assembly in another embodiment, includes a balloon and an expandable stent positioned at an exterior ofthe balloon
  • the stent includes a first expansion strut A plurality ofthe first expansion struts form a first expansion column A plurality of second expansion struts form a second expansion column A plurality ofthe first connecting struts form a first connecting strut column
  • Each of a first expansion strut ofthe first expansion column is coupled to a second expansion strut ofthe second expansion column
  • the first connecting strut includes a proximal section coupled to a distal section and at least a portion ofthe first connecting strut includes a first linear section and a first slant angle
  • Fig 1 A is a side elevation view ofthe pre-expansion mode of an embodiment ofthe stent ofthe present invention
  • Fig IB is a cross sectional view of an embodiment ofthe stent ofthe present invention
  • Fig IC is a longitudinal cross sectional view of an embodiment of the stent ofthe present invention
  • Fig 2 A is a scale drawing ofthe strut pattern of an embodiment ofthe stent ofthe present invention
  • Fig 2B is an expanded view of a section ofthe pattern of Figure 2 A
  • Fig 3 A is a schematic illustration of a the pre-expansion mode of an embodiment ofthe stent ofthe present invention
  • Fig 3B is a schematic illustration ofthe post-expansion mode of an embodiment ofthe stent ofthe present invention
  • Fig 4 A is a scale drawing including dimensions of an embodiment ofthe stent ofthe present invention
  • Fig 4B is an enlarged section ofthe scale drawing of Figure 4A
  • Fig 5 is a scale drawing of an embodiment ofthe stent of the present invention with a tapered diameter in its post-expansion mode
  • Fig 6A is a scale drawing of an embodiment ofthe stent ofthe present invention with reenforcment expansion columns
  • Fig 6B is a perspective view ofthe embodiment of Figure 6 A
  • Fig 7A is a scale drawing of an embodiment ofthe stent ofthe present invention including relief notches at strut joints to increase flexibility ofthe joints
  • Fig 7B is an enlarged region ofthe embodiment of Figure 7A
  • Fig. 7C is an enlarged view of a single connecting strut joining two expansion strut pairs in accordance with the embodiment of Figure 7 A.
  • Fig. 8 A is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
  • Fig. 8B is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
  • Fig. 8C is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
  • Fig. 8D is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
  • Fig. 8E is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
  • Fig. 9 is a delivery balloon catheter, illustrating a method of deliver of a stent in accord with the present invention.
  • FIG. 1 A An elongate hollow tubular stent 10 in an unexpanded state is shown.
  • a proximal end 12 and a distal end 14 define a longitudinal length 16 of stent 10.
  • the longitudinal length 16 ofthe stent 10 can be as long as 100 mm or longer.
  • a proximal opening 18 and a distal opening 20 connect to an inner lumen 22 of stent 10.
  • Stent 10 can be a single piece, without any seams or welding joints or may include multiple pieces.
  • Stent 10 is constructed of two to fifty or more expansion columns or rings 24 connected together by interspersed connecting strut columns 26.
  • the first column on the proximal end 12 and the last column on the distal end 14 of stent 10 are expansion columns 24.
  • Expansion columns 24 are formed from a series of expansion struts 28, and joining struts 30.
  • Expansion struts 28 are thin elongate members arranged so that they extend at least in part in the direction ofthe longitudinal axis of stent
  • expansion struts 28 When an outward external force is applied to stent 10 from the inside by an expansion balloon or other means, expansion struts 28 are reoriented such that they extend in a more circumferential direction, i.e along the surface of cylindrical stent 10 and perpendicular to its longitudinal axis Reorientation of expansion struts 28 causes stent 10 to have an expanded circumference and diameter.
  • expansion struts 28 of unexpanded stent 10 are seen to extend substantially parallel to the longitudinal axis of stent 10.
  • Expansion struts 28 are joined together by joining struts 30 to form a plurality of expansion strut pairs 32. Expansion strut pairs have a closed end 34 and an open end 36. Additional joining struts 30 join together expansion struts 28 of adjacent expansion strut pairs 32, such that expansion struts 28 are joined alternately at their proximal and distal ends to adjacent expansion struts 28 to form expansion columns 24.
  • Each expansion column 24 contains a plurality, typically eight to twenty, twenty to sixty, or larger of expansion struts 28
  • Connecting struts 38 connect adjacent expansion columns 24 forming a series of interspersed connecting strut columns 26 each extending around the circumference of stent 10. Each connecting strut 38 joins a pair of expansion struts 28 in an expansion column 24 to an adjacent pair of expansion struts 28 in an adjacent expansion column 24.
  • the ratio of expansion struts 28 in an expansion column 24 to connecting struts 38 in a connecting strut column 26 is two to one; however, this ratio in general can be x to 1 where x is greater or less than two
  • this ratio in general can be x to 1 where x is greater or less than two
  • the stent 10 of Figure IA begins with an expansion column 24 on the proximal end 12 and ends with an expansion column 24 on the distal end 14, if there are n expansion columns 24 with m expansion struts 28 per column, there will be m-1 connecting strut columns 26, and n(m-l)/2 connecting struts 38
  • Asymmetrical cell spaces 40 are cell spaces which have no geometrical symmetry i.e. no rotation, reflection, combination rotation and reflection or other symmetry.
  • Asymmetrical cell spaces 40 in Figure 1 A are surrounded by a first expansion strut pair 32 in a first expansion column 24, a first connecting strut 38, a second expansion strut pair 32 in an adjacent expansion column 24, a first joining strut 30, a second connecting strut 38, and a second joining strut 30.
  • expansion strut pairs 32 of asymmetrical cell space 40 may be circumferentially offset i.e. have longitudinal axes that are not collinear and have their open ends 36 facing each other.
  • the space between two expansion struts of an expansion strut pair 32 is known as a loop slot 42.
  • FIG. IB shows inner lumen 22, radius 44 and stent wall 46 of stent 10.
  • Stent wall 46 consists of stent struts including expansion struts 28, connecting struts 38 and joining struts 30.
  • Figure IC shows, proximal end 12, distal end 14, longitudinal length 16, inner lumen 22, and stent wall 46 of stent 10.
  • Inner lumen 22 is surrounded by stent wall 46 which forms the cylindrical surface of stent 10.
  • joining struts 30 of stent 10 are seen to extend at an angle to the expansion struts 28, forming a narrow angle 48 with one expansion strut 28 in an expansion strut pair 32 and a wide angle 50 with the other expansion strut 28 of an expansion strut pair 32.
  • Narrow angle 48 is less than ninety degrees
  • wide angle 50 is greater than ninety degrees.
  • Joining struts 30 extend both longitudinally along the longitudinal axis of stent 10 and circumferentially, along the surface of the stent 10 perpendicular its longitudinal axis.
  • Expansion strut spacing 52 between adjacent expansion struts 28 in a given expansion column 24 are uniform in stent 10 of Figures 2 A and 2B; however, non-uniform spacings can also be used Expansion strut spacings 52 can be varied, for example, spacings 52 between adjacent expansion struts 28 in an expansion column 24 can alternate between a narrow and a wide spacing Additionally, spacings 52 in a single expansion column 24 can differ from other spacings 52 in other columns 24
  • loop slots 42 need not be the same among loop slots of a single or multiple expansion columns 24
  • the shape a loop slots 42 can be altered by changing the orientation or physical dimensions ofthe expansion struts 28 and/or joining struts 30 which connect expansion struts 28 of expansion strut pairs 32 defining the boundaries of loop slots 42
  • Connecting struts 38 couple adjacent expansion columns 24, by connecting the distal end of an expansion strut pair in one expansion column 24 to the proximal end of an adjacent expansion strut pair 32 in a second expansion column 24
  • Connecting struts 38 of Figures 2 A and 2B are formed from two linear sections, a first linear section 54 being joined at its distal end to a second linear section 56 at its proximal end to form a first slant angle 58
  • the first linear section 54 of a connecting strut 38 is joined to expansion strut 28 at the point where joining strut 30 makes narrow angle 48 with expansion strut 28
  • First linear section 54 extends substantially collinear to joining strut 30 continuing the line of joining strut 30 into the space between expansion columns 24
  • the distal end ofthe first linear section 54 is joined to the proximal end ofthe second linear section 56 forming slant angle 58
  • Second linear section 56 extends substantially parallel to expansion struts 28 connecting at its distal end to joining strut 30 in an adjacent expansion column 24
  • the distal end of second linear section 56 attaches to expansion strut 28 at the point where joining strut 30 makes narrow angle 48 with expansion strut 28
  • joining strut 30 can have a second slant angle with a width that can be the same or different from the width ofthe first slant angle
  • Figures 2 A and 2B show connecting struts 38 and joining struts 30 slanted relative to the longitudinal axis
  • Figure 3 A and 3B show a schematic illustration of a stent design according to the present invention in an unexpanded and expanded state respectively
  • the design is depicted as a flat projection, as if stent 10 were cut lengthwise parallel to its longitudinal axis and flattened out
  • the connecting struts 38 consist of first and second linear sections 54 and 56 forming slant angle 58 at pivot point 60
  • An asymmetrical cell space 40 is formed by expansion strut pairs 32, connecting struts 38 and joining struts 30
  • Multiple interlocking asymmetrical cell spaces 40 make up the design pattern
  • the expansion strut pairs 32 spread apart at their open ends 36, shortening the length of expansion struts 28 along the longitudinal axis ofthe cylindrical stent
  • the longitudinal shortening of expansion struts 28 during expansion is countered by the longitudinal lengthening of connecting struts 38
  • the widening of slant angle 58 during expansion straightens connecting struts 38 and lengthens the distance between the coupled expansion strut pairs 32.
  • the lengthening ofthe distance between coupled expansion strut pairs 32 substantially compensates for the longitudinal shortening of expansion struts 28.
  • the stent has substantially constant unexpanded and expanded longitudinal lengths.
  • each expansion column 24 becomes circumferentially stretched, enlarging the space between struts.
  • the interlinking of expansion columns 24 by connecting struts 38 that have been straightened through the expansion process gives the stent 10 a high radial support strength.
  • the entire stent 10 when expanded is unitized into a continuous chain mesh of stretched expansion columns 24 and connecting strut columns 26 forming an asymmetrical interlocking cell geometry which resists collapse both axially and radially When the stent is expanded it has increased rigidity and fatigue tolerance.
  • efficient bending and straightening of connecting struts 38 at pivot points 60 allows increased longitudinal flexibility ofthe stent.
  • connecting struts 38 are forced to bend in their tangent plane.
  • the tangent plane of a specific connecting strut 38 refers to the plane substantially tangent to the cylindrical surface ofthe stent at that connecting strut 38.
  • connecting struts 38 The width of connecting struts 38 is typically two to four, or more times the thickness, which makes connecting struts 38 relatively inflexible when bending in their tangent plane
  • pivot points 60 in connecting struts 38 provide connecting struts 38 a flexible joint about which to more easily bend increasing longitudinal flexibility ofthe stent
  • stent 10 has a length 16 of 33.25 mm and an uncrimped and unexpanded circumference 88 of 5.26 mm.
  • Fifteen expansion columns 24 are interspersed with connecting strut columns 26.
  • Each expansion column 24 consists of twelve expansion struts 28 joined alternately at their proximal and distal ends by joining struts 30 forming six expansion strut pairs 32
  • Expansion struts 28 are aligned parallel to the longitudinal axis of cylindrical stent 10.
  • Joining struts 30 form a narrow angle 48 and a wide angle 50 with the respective expansion struts 28 of expansion strut pairs 32.
  • Adjacent expansion columns 24 employ alternating circumferential slant directions of joining struts 30.
  • expansion strut width 62 is .20 mm
  • expansion strut length 64 is 1.51 mm
  • connecting strut width 66 is .13 mm.
  • connecting struts 38 consist of a slanted first linear section 54 joined to a second linear section 56 at a slant angle 58.
  • First linear section 54 is slightly longer than second linear section 56 and is attached at its proximal end to an expansion strut 28 in an expansion column 24. The attachment ofthe proximal end of first linear section 54 to expansion strut 28 is at the point where joining strut 30 makes narrow angle 48 with expansion strut 28.
  • First linear section 54 extends substantially collinear to joining strut 30 attaching at its distal end to the proximal end of second linear section 56 to form slant angle 58.
  • Second linear section 56 extends substantially collinear to expansion struts 28, attaching at its distal end to an expansion strut 28 in an adjacent expansion column 24. The attachment occurs at the point where expansion strut 28 forms narrow angle 48 with joining strut 30.
  • Joining struts 30 and connecting strut first linear sections 54 slant in alternating circumferential directions from column to adjacent column.
  • connecting struts 38 and expansion struts 28 at the point where narrow angle 48 is formed aids smooth delivery of stent 10 by streamlining the surface ofthe unexpanded stent and minimizing possible catching points. Bare delivery of stent 10 to the target lesion in a vessel will thus result in minimal snagging or catching as it is navigated through turns and curvatures in the vessel. Stent 10 behaves like a flexible, tubular sled as it is moved forward or backward in the vessel on the delivery catheter, sliding through tortuous vessels and over irregular bumps caused by atherosclerotic plaques inside the vessel lumen.
  • Stent 10 of Figures 4A and 4B has an internal diameter of up to 5.0 mm, while maintaining an acceptable radial strength and fatigue tolerance.
  • the crimped stent outer diameter can be as small as 1.0 mm or less depending on the condition ofthe underlying delivery balloon profile; A small crimped outer diameter is especially important if stent delivery is to be attempted without predilation ofthe target site.
  • the surface ofthe crimped stent is smooth allowing for no snagging ofthe stent struts during either forward or backward movement through a vessel.
  • Figure 5 shows a second embodiment ofthe present invention in which the stent 10 in its expanded form has a gradual taper from proximal end 12 to distal end 14.
  • the shaded segments 72, 74, 76, 78, 80, 82 and 84 of expansion struts 28 represent regions of expansion struts 28 to be removed. Removal ofthe shaded segments 72, 74, 76, 78, 80, 82 and 84 provides stent 10 with a gradual taper when expanded with distal end 14 having a smaller expanded diameter than proximal end 12.
  • the degree of shortening ofthe expanded diameter ofthe stent 10 at a given expansion column 24 will be proportional to the length ofthe removed segment 72, 74, 76, 78, 80, 82, or 84 at that expansion column 24.
  • the shortened expansion struts 28 will have a shortened component along the circumference ofthe stent resulting in a shortened circumference and diameter.
  • the tapered diameter portion can be positioned anywhere along the length of stent 10, and the tapering can be made more or less gradual by removing appropriately larger or smaller portions ofthe expansion struts 28 in a given expansion column 24 Tapering is especially important in long stents, longer than 12 mm, since tapering of blood vessels is more pronounced over longer lengths.
  • a long stent with a uniform stent diameter can only be matched to the target vessel diameter over a short region. If the proximal vessel size is matched with the stent diameter, the expanded distal end ofthe stent will be too large for the natural vessel and may cause an intimal dissection ofthe distal vessel by stent expansion. On the other hand, if the distal vessel size is matched with the stent diameter, the proximal end ofthe expanded stent will be too small to set inside the vessel lumen. It is therefore desirable to have a stent with a tapered expanded diameter.
  • Another way achieve a tapered expanded stent is to change the stiffness ofthe stent struts, expansion struts, connecting struts or joining struts such that the stiffness ofthe struts varies along the length ofthe stent.
  • the stiffness ofthe struts can be changed by altering length, width or thickness, adding additional stiffening material, using a chemical or mechanical means to alter the physical properties ofthe stent material, or applying one or a series of elastic elements about the stent.
  • a matching tapered balloon catheter would ideally be made for delivery and deployment ofthe tapered diameter stent.
  • the method of using a tapered matching balloon catheter with a tapered diameter stent is within the scope ofthe present invention.
  • a tapered balloon to expand a non-tapered stent will also achieve a tapered expanded stent; however, since no metal is removed from the stent, the stent is tapered as a result of incomplete expansion. The stent will therefore have increased metal fraction at the tapered end resulting in increased risk of acute thrombosis. Metal fraction is the proportion ofthe surface ofthe expanded stent covered by the stent strut material. Shortening the expansion struts as shown in Figure 5 allows for a tapered expanded stent with substantially constant metal fraction along its length.
  • a third embodiment ofthe present invention shown in Figures 6 A and 6B has multiple reenforcement expansion columns 86 placed along the length ofthe stent 10.
  • the Reenforcement columns 86 are placed along the stent length to provide additional localized radial strength and rigidity to stent 10. Additional strength and rigidity are especially important at the ends ofthe stent to prevent deformation ofthe stent both during delivery and after placement. During delivery the stent ends can catch on the vessel wall possibly deforming the unexpanded stent and altering its expansion characteristics. After the stent has been placed it is important that the stent ends are rigid so that they set firmly against the vessel wall; otherwise, during a subsequent catheter procedure, the catheter or guidewire can catch on the stent ends pulling the stent away from the vessel wall and possibly damaging and/or blocking the vessel.
  • the specific variation ofthe third embodiment of stent 10 depicted in Figures 6 A and 6B has a length 16 of 20.70 mm and an uncrimped and unexpanded circumference 88 of 5.26 mm.
  • the stent 10 consists of six expansion columns 24 and three reenforcement expansion columns 86, each consisting respectively of twelve expansion struts 28 or reenforcement expansion struts 90.
  • the reenforcement expansion columns 86 are positioned one at either end, and one along the length ofthe stent 10.
  • the expansion strut width 62 is .15 mm
  • reenforcement expansion strut width 92 is .20 mm
  • the connecting strut width 66 is .10 mm.
  • the narrow angle 48 formed by joining strut 30 and expansion strut 28 is 75 degrees
  • the narrow angle 94 formed by reenforcement joining strut 96 and reenforcement expansion strut 90 is 60 degrees.
  • reenforcement expansion columns 86 such as providing reenforcement expansion columns 86 only on the ends of the stent, only on one end, or at multiple locations throughout the length ofthe stent can also be used and fall within the scope ofthe present invention.
  • a taper can also be programmed into the reenforced stent 10 by shortening expansion struts 28 and reenforcement expansion struts 90 in appropriate expansion columns 24 and 86.
  • a relief notch is a notch where metal has been removed from a strut, usually at a joint where multiple struts are connected. Relief notches increase flexibility of a strut or joint by creating a thinned, narrow region along the strut or joint. Relief notch 98 is formed at the joint formed between first linear section 54 of connecting strut 38 and expansion strut 28.
  • Relief notch 100 is formed at the joint between second linear section 56 of connecting strut 38 and expansion strut 28
  • the positioning of the relief notches gives added flexibility to the unexpanded stent Relief notches can be placed at other joints and can be included in any ofthe previously mentioned embodiments
  • Figures 8 A, 8B, 8C, 8D and 8E illustrates some examples of alternate connecting strut designs which can be used in any ofthe previously discussed embodiments
  • Figure 8 A shows a rounded loop connecting strut 38 which joins two circumferentially offset expansion strut pairs 32 in adjacent expansion columns Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30
  • Joining struts 30 are slanted such as to form a narrow angle 48 and a wide angle 50 with the expansion struts 28 they connect
  • the rounded loop connecting strut 38 connects expansion struts 28 at the point where narrow angle is formed between expansion strut 28 and joining strut 30
  • Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30 Joining struts 30 are at right angles to the expansion struts 28 they connect The rounded loop connecting strut 38 connects to expansion struts 28 at the same point as joining struts 30 The rounded connecting strut 38 has a first radius of curvature 106 and a second radius of curvature 108 such that it connects circumferentially offset expansion strut pairs 32
  • connecting strut 38 joins two circumferentially offset expansion strut pairs 32 in adjacent expansion columns Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30 Joining struts 30 are slanted such as to form a narrow angle 48 and a wide angle 50 with the expansion struts 28 they connect The connecting strut 38 connects expansion struts 28 at the point where narrow angle 48 is formed between expansion strut 28 and joining strut 30.
  • the connecting strut 38 is made up of three linear sections 110, 112, and 114 forming two slant angles 116 and 118.
  • the proximal end of section 1 10 is attached to expansion strut 28 at the point where joining strut 30 forms narrow angle 48 with expansion strut 28.
  • Section 110 extends substantially collinear to joining strut 30 and is attached at its distal end to section 112 forming slant angle 116.
  • Section 112 extends at an angle to section 110 such that section 112 is substantially parallel to expansion struts 28 and is connected at its distal end to the proximal end of section 114 forming slant angle 118.
  • Section 114 extends at an angle such that it is substantially collinear to joining strut 30 ofthe adjacent expansion strut pair 32.
  • Section 1 14 attaches at its distal end to expansion strut 28 ofthe adjacent expansion strut pair 32, at the point where joining strut 30 forms narrow angle 48 with expansion strut 28.
  • a connecting strut 38 joins two circumferentially offset expansion strut pairs 32 in adjacent expansion columns. Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30. Joining struts 30 are at right angles to the expansion struts 28 they connect. The connecting strut 38 connects to expansion struts 28 at the same point as joining struts 30.
  • the connecting struts 38 of Figures 8D and 8E are made up of multiple connecting strut sections connected end to end to form a jagged connecting strut 38 with multiple slant angles, coupling expansion strut pair 32 to adjacent expansion strut pair 32.
  • the connecting strut of Figure 8D is made up of three connecting strut sections 120, 122, and 124 with two slant angles 126 and 128, while the connecting strut of Figure 8E consists of four connecting strut sections 130, 132, 134, and 136 with three slant angles 138, 140 and 142.
  • connecting strut section 134 can be modified by replacing connecting strut section 136 by the dotted connecting strut section 144 to give another possible geometry of connecting struts 38.
  • connecting struts and joining struts consistent with the present invention; the above examples are not intended to be an exhaustive list.
  • the stent ofthe present invention is ideally suited for application in coronary vessels although versatility in the stent design allows for applications in non-coronary vessels, the aorta, and nonvascular tubular body organs.
  • Typical coronary vascular stents have expanded diameters that range from 2.5 to 5.0 mm.
  • a stent with high radial strength and fatigue tolerance that expands to a 5.0 mm diameter may have unacceptably high stent metal fraction when used in smaller diameter vessels If the stent metal fraction is high, the chances of acute thrombosis and restenosis potential will increase. Even with the same metal fraction a smaller caliber vessel is more likely than a larger one to have a high rate of thrombosis.
  • stents for coronary application for example, small vessels stents for use in vessels with diameters from 2 5 mm to 3 0 mm, and large vessel stents for use in vessels with diameters from 3 0 mm to 5 0 mm
  • small vessels stents for use in vessels with diameters from 2 5 mm to 3 0 mm
  • large vessel stents for use in vessels with diameters from 3 0 mm to 5 0 mm
  • both small vessels and large vessels when treated with the appropriate sized stent will contain stents of similar idealized metal fraction.
  • the stent of the present invention can be made using a CAM-driven laser cutting system to cut the stent pattern from a stainless steel tube
  • the rough-cut stent is preferably electro-polished to remove surface imperfections and sharp edges
  • Other methods of fabricating the stent can also be used such as EDM, photo-electric etching technology, or other methods
  • Any suitable material can be used for the stent including other metals and polymers so long as they provide the essential structural strength, flexibility, biocompatibility and expandability
  • the stent is typically at least partially plated with a radiopaque metal, such as gold, platinum, tantalum or other suitable metal It is preferred to plate only both ends ofthe stent by localized plating; however, the entire stent or other regions can also be plated When plating both ends, one to three or more expansion columns on each end ofthe stent are plated to mark the ends ofthe stent so they can be identified under fluoroscopy during the stenting procedure 781 PC17US97/06610
  • the stent By plating the stent only at the ends, interference ofthe radiopaque plating material with performance characteristics or surface modulation ofthe stent frame is minimized. Additionally the amount of plating material required is reduced, lowering the material cost ofthe stent.
  • the stent is cleaned, typically with detergent, saline and ultrasonic means that are well-known in the art The stents are then inspected for quality control, assembled with the delivery balloon catheter, and properly packaged, labeled, and sterilized.
  • the stent can be marketed as stand alone or as a pre-mounted delivery balloon catheter assembly as shown in Figure 9. Referring to Figure 9, the stent
  • the assembly 150 includes a proximal end adapter 152, a catheter shaft 154, a balloon channel 156, a guidewire channel 158, a balloon 146, and a guidewire 160.
  • Balloon 146 can be tapered, curved, or both tapered and curved from a proximal end to a distal end in the expanded state. Additionally stent 10 can be non-tapered or tapered in the expanded state
  • the guidewire 160 is inserted into the vein or artery and advanced to the target site.
  • the catheter shaft 154 is then forwarded over the guidewire 160 to position the stent 10 and balloon 146 into position at the target site.
  • the balloon 146 is inflated through the balloon channel 156 to expand the stent 10 from a crimped to an expanded state
  • the stent 10 provides the desired scaffolding support to the vessel.
  • the stent ofthe present invention can be made as short as less than 10 mm in length or as long as 100 mm or more If long stents are to be used, however, matching length delivery catheter balloons will typically be needed to expand the stents into their deployed positions. Long stents, depending on the target vessel, may require curved long balloons for deployment Curved balloons which match the natural curve of a blood vessel reduce stress on the blood vessel during stent deployment. This is especially important in many coronary applications which involve stenting in curved coronary vessels The use of such curved balloons is within the scope ofthe present invention

Abstract

A stent assembly includes a balloon and an expandable stent positioned at an exterior of the balloon. The stent includes a first expansion strut. A plurality of the first expansion struts form a first expansion column. A plurality of second expansion struts form a second expansion column. A plurality of the first connecting struts form a first connecting strut column. Each of a first expansion strut of the first expansion column is coupled to a second expansion strut of the second expansion column. The first connecting strut includes a proximal section coupled to a distal section and at least a portion of the first connecting strut includes a first linear section and a first slant angle.

Description

Intravascular Stent
Cross-reference to Related Applications This application claims the benefit of Provisional Patent Application No
60/017,484 filed April 26, 1996, the disclosure of which is incorporated by reference This application is related to U.S Patent Application Serial No , (Attorney Docket No 18461 702), filed March 25, 1997, entitled "Intravascular Stent" and U.S. Patent Application Serial No , (Attorney Docket No 18461 703), filed March 25, 1997, entitled "Intravascular Stent", both having same named inventor G David Jang and incorporated by reference
BACKGROUND OF THE INVENTION Field ofthe Invention
This invention relates to intravascular stents, and more particularly to an intravascular stent which provides easy introduction through tortuous sections of vessels Description ofthe Related Art Angioplasty, either coronary or general vascular, has advanced to become the most effective means for revascularization of stenosed vessels In the early 1980's, angioplasty first became available for clinical practice in the coronary artery, and has since proven an effective alterative to conventional bypass graft surgery Balloon catheter dependent angioplasty has consistently proven to be the most reliable and practical interventional procedure Other ancillary technologies such as laser based treatment, or directional or rotational arthrectomy, have proven to be either of limited effectiveness or dependent on balloon angioplasty for completion ofthe intended procedure Restenosis following balloon-based angioplasty is the most serious drawback and is especially prevalent in the coronary artery system Many regimens have been designed to combat restenosis, with limited success, including laser based treatment and directional or rotational arthrectomy Intravascular stenting, however, noticeably reduces the restenosis rate following angioplasty procedures The procedure for intravascular stent placement typically involves pre-dilation ofthe target vessel using balloon angioplasty, followed by deployment ofthe stent, and expansion ofthe stent such that the dilated vessel walls are supported from the inside
The intravascular stent functions as scaffolding for the lumen of a vessel The scaffolding ofthe vessel walls by the stent serve to (a) prevent elastic recoil ofthe dilated vessel wall, (b) eliminate residual stenosis ofthe vessel, a common occurrence in balloon angioplasty procedures, (c) maintain the diameter ofthe stented vessel segment slightly larger than the native unobstructed vessel segments proximal and distal the stented segment and (d) as indicated by the latest clinical data, lower the restenosis rate Following an angioplasty procedure, the restenosis rate of stented vessels has proven significantly lower than for unstented or otherwise treated vessels, treatments include drug therapy and other methods mentioned previously
Another benefit of vessel stenting is the potential reduction of emergency bypass surgery arising from angioplasty procedures Stenting has proven to be effective in some cases for treating impending closure of a vessel during angioplasty Stenting can also control and stabilize an unstable local intimal tear of a vessel caused by normal conduct during an angioplasty procedure In some cases, an incomplete or less than optimal dilatation of a vessel lesion with balloon angioplasty can successfully be opened up with a stent implant Early in its development, the practice of stenting, especially in coronary arteries, had serious anticoagulation problems However, anticoagulation techniques have since been developed and are becoming simpler and more effective Better and easier to use regimens are continuously being introduced, including simple outpatient anticoagulation treatments, resulting in reduced hospital stays for stent patients 0781 PO7US97/06610
An example of a conventional stent patent is US 5,102,417 (hereafter the Palmaz Patent) The stent described in the Palmaz Patent consists of a series of elongated tubular members having a plurality of slots disposed substantially parallel to the longitudinal axis ofthe tubular members The tubular members are connected by at least one flexible connector member
The unexpanded tubular members ofthe Palmaz Patent are overly rigid so that practical application is limited to short lengths Even with implementation ofthe multilink design with flexible connector members connecting a series of tubular members, longer stents can not navigate tortuous blood vessels Furthermore, the rigidity ofthe unexpanded stent increases the risk of damaging vessels during insertion Foreshortening ofthe stent during insertion complicates accurate placement ofthe stent and reduces the area that can be covered by the expanded stent There is, further, no method of programming the stent diameter along its longitudinal axis to achieve a tapered expanded stent, and no method of reenforcement of stent ends or other regions is provided for.
Another example of a conventional stent patent is WO 96/03092, the Brun patent The stent described in the Brun patent is formed of a tube having a patterned shape, which has first and second meander patterns The even and odd first meander patterns are 180 degrees out of phase, with the odd patterns occurring between every two even patterns The second meander patterns run perpendicular to the first meander patterns, along the axis ofthe tube
Adjacent first meander patterns are connected by second meander patterns to form a generally uniform distributed pattern The symmetrical arrangement with first and second meander patterns having sharp right angled bends allows for catching and snagging on the vessel wall during delivery Furthermore, the large convolutions in the second meander pattern are not fully straightened out during expansion reducing rigidity and structural strength ofthe expanded stent There is, further, no method of programming the stent diameter along its longitudinal axis to achieve a tapering stent design, and no method of reenforcement of stent ends or other regions is provided for These and other conventional stent designs suffer in varying degrees from a variety of drawbacks including (a) inability to negotiate bends in vessels due to columnar rigidity ofthe unexpanded stent, (b) lack of structural strength, radial and axial lateral, ofthe unexpanded stent, © significant foreshortening ofthe stent during expansion, (d) limited stent length, (e) constant expanded stent diameter, (f) poor crimping characteristics, and (g) rough surface modulation of the unexpanded stent
There is a need for a stent with sufficient longitudinal flexibility in the unexpanded state to allow for navigation through tortuous vessels There is a further need for a stent that is structurally strong in the unexpanded state such that risk of damage or distortion during delivery is minimal A further need exists for a stent that maintains substantially the same longitudinal length during expansion to allow greater coverage^ the target site and simplify proper placement ofthe stent Yet a further need exists for a stent design with sufficient longitudinal flexibility that long stents of up to 100 mm can be safely delivered through tortuous vessels There is a need for a stent that is configured to expand to variable diameters along its length, such that a taper can be achieved in the expanded stent to match the natural taper ofthe target vessel A need exists for a stent which, (i) can be crimped tightly on the expansion balloon while maintaining a low profile and flexibility, (ii) has a smooth surface modulation when crimped over a delivery balloon, to prevent catching and snagging ofthe stent on the vessel wall during delivery or (iii) with reenforcment rings on the ends or middle or both to keep the ends ofthe stent securely positioned against the vessel walls ofthe target blood vessel
SUMMARY OF THE INVENTION Accordingly an object ofthe present invention is to provide a scaffold for an interior lumen of a vessel
Another object ofthe invention is to provide a stent which prevents recoil ofthe vessel following angioplasty A further object ofthe invention is to provide a stent that maintains a larger vessel lumen compared to the results obtained only with balloon angioplasty.
Yet another object ofthe invention is to provide a stent that reduces foreshortening of a stent length when expanded.
Another object ofthe invention is to provide a stent with increased flexibility when delivered to a selected site in a vessel.
A further object ofthe invention is to provide a stent with a low profile when crimped over a delivery balloon of a stent assembly. Yet a further object ofthe invention is to provide a stent with reduced tupeling ofthe vessel wall.
Another object ofthe invention is to provide a chain mesh stent that reduces vessel "hang up" in a tortuous vessel or a vessel with curvature.
These and other objects ofthe invention are achieved in a stent in a non- expanded state. A first expansion strut pair includes a first expansion strut positioned adjacent to a second expansion strut. A joining strut ofthe first expansion strut pair couples the first and second expansion struts at a distal end ofthe first expansion strut pair. A plurality ofthe first expansion strut pair form a first expansion column. A second expansion strut pair includes a first expansion strut positioned adjacent to a second expansion strut. A joining strut ofthe second expansion strut pair couples the first and second expansion struts ofthe second expansion strut pair at a proximal end ofthe second expansion strut pair. A plurality ofthe second expansion strut pair form a second expansion column. A first connecting strut includes a first connecting strut proximal head section and a first connecting strut distal tail section. The head section is coupled to the distal end of the first expansion strut pair in the first expansion column, and the tail section is coupled to the proximal end ofthe second expansion strut pair ofthe second expansion column. A plurality ofthe first connecting strut form a first connecting strut column that couples the first expansion column to the second expansion column. The tail section extends in a first lateral direction relative to a longitudinal axis of the head section to form a first slant angle. A third expansion strut pair includes a first expansion strut positioned adjacent to a second expansion strut A third joining strut ofthe third expansion strut pair couples the first and second expansion struts at a proximal end ofthe third expansion strut pair. A plurality ofthe third expansion strut pair form a third expansion column The first expansion strut ofthe first expansion strut pair in the first expansion column have a longitudinal axis that is parallel to and offset from a longitudinal axis ofthe first expansion strut ofthe second expansion strut pair in the second expansion column The second expansion strut ofthe third expansion strut pair in the third expansion column has a longitudinal axis that is parallel to and offset from a longitudinal axis ofthe first expansion strut ofthe second expansion strut pair ofthe second expansion column A second connecting strut includes a proximal head section and a distal tail section The head section is coupled to the distal end ofthe second expansion strut pair in the second expansion column The tail section is coupled to the proximal end ofthe third expansion strut pair ofthe third expansion column A plurality ofthe second connecting strut form a second connecting strut column that couples the second expansion column to the third expansion column. The tail section extends in a second lateral direction relative to a longitudinal axis ofthe head section to form a second slant angle that extends in an opposite direction from the first lateral direction A ratio of a number of expansion struts in an expansion strut column to a number of connecting struts in a connecting strut column is 2 to 1 The first slant angle reduces a fore shortening ofthe stent between the first and second expansion columns when the stent is in an expanded state. In another embodiment, a stent assembly includes a balloon and an expandable stent positioned at an exterior ofthe balloon The stent includes a first expansion strut A plurality ofthe first expansion struts form a first expansion column A plurality of second expansion struts form a second expansion column A plurality ofthe first connecting struts form a first connecting strut column Each of a first expansion strut ofthe first expansion column is coupled to a second expansion strut ofthe second expansion column The first connecting strut includes a proximal section coupled to a distal section and at least a portion ofthe first connecting strut includes a first linear section and a first slant angle
BRIEF DESCRIPTION OF THE DRAWINGS
Fig 1 A is a side elevation view ofthe pre-expansion mode of an embodiment ofthe stent ofthe present invention,
Fig IB is a cross sectional view of an embodiment ofthe stent ofthe present invention; Fig IC is a longitudinal cross sectional view of an embodiment of the stent ofthe present invention,
Fig 2 A is a scale drawing ofthe strut pattern of an embodiment ofthe stent ofthe present invention
Fig 2B is an expanded view of a section ofthe pattern of Figure 2 A Fig 3 A is a schematic illustration of a the pre-expansion mode of an embodiment ofthe stent ofthe present invention
Fig 3B is a schematic illustration ofthe post-expansion mode of an embodiment ofthe stent ofthe present invention
Fig 4 A is a scale drawing including dimensions of an embodiment ofthe stent ofthe present invention
Fig 4B is an enlarged section ofthe scale drawing of Figure 4A Fig 5 is a scale drawing of an embodiment ofthe stent of the present invention with a tapered diameter in its post-expansion mode
Fig 6A is a scale drawing of an embodiment ofthe stent ofthe present invention with reenforcment expansion columns
Fig 6B is a perspective view ofthe embodiment of Figure 6 A Fig 7A is a scale drawing of an embodiment ofthe stent ofthe present invention including relief notches at strut joints to increase flexibility ofthe joints Fig 7B is an enlarged region ofthe embodiment of Figure 7A Fig. 7C is an enlarged view of a single connecting strut joining two expansion strut pairs in accordance with the embodiment of Figure 7 A.
Fig. 8 A is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention. Fig. 8B is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
Fig. 8C is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
Fig. 8D is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
Fig. 8E is a drawing of an alternate geometry of connecting struts and joining struts in accord with the present invention.
Fig. 9 is a delivery balloon catheter, illustrating a method of deliver of a stent in accord with the present invention.
DETAILED DESCRIPTION A first embodiment ofthe present invention is shown in Figures 1 A, IB, IC, 2 A and 2B. Referring to Figure 1 A, an elongate hollow tubular stent 10 in an unexpanded state is shown. A proximal end 12 and a distal end 14 define a longitudinal length 16 of stent 10. The longitudinal length 16 ofthe stent 10 can be as long as 100 mm or longer. A proximal opening 18 and a distal opening 20 connect to an inner lumen 22 of stent 10. Stent 10 can be a single piece, without any seams or welding joints or may include multiple pieces.
Stent 10 is constructed of two to fifty or more expansion columns or rings 24 connected together by interspersed connecting strut columns 26. The first column on the proximal end 12 and the last column on the distal end 14 of stent 10 are expansion columns 24.
Expansion columns 24 are formed from a series of expansion struts 28, and joining struts 30. Expansion struts 28 are thin elongate members arranged so that they extend at least in part in the direction ofthe longitudinal axis of stent
10. When an outward external force is applied to stent 10 from the inside by an expansion balloon or other means, expansion struts 28 are reoriented such that they extend in a more circumferential direction, i.e along the surface of cylindrical stent 10 and perpendicular to its longitudinal axis Reorientation of expansion struts 28 causes stent 10 to have an expanded circumference and diameter. In Figure IA, expansion struts 28 of unexpanded stent 10 are seen to extend substantially parallel to the longitudinal axis of stent 10.
Expansion struts 28 are joined together by joining struts 30 to form a plurality of expansion strut pairs 32. Expansion strut pairs have a closed end 34 and an open end 36. Additional joining struts 30 join together expansion struts 28 of adjacent expansion strut pairs 32, such that expansion struts 28 are joined alternately at their proximal and distal ends to adjacent expansion struts 28 to form expansion columns 24. Each expansion column 24 contains a plurality, typically eight to twenty, twenty to sixty, or larger of expansion struts 28
Connecting struts 38 connect adjacent expansion columns 24 forming a series of interspersed connecting strut columns 26 each extending around the circumference of stent 10. Each connecting strut 38 joins a pair of expansion struts 28 in an expansion column 24 to an adjacent pair of expansion struts 28 in an adjacent expansion column 24. For stent 10 of Figure 1 A, the ratio of expansion struts 28 in an expansion column 24 to connecting struts 38 in a connecting strut column 26 is two to one; however, this ratio in general can be x to 1 where x is greater or less than two Furthermore, since the stent 10 of Figure IA begins with an expansion column 24 on the proximal end 12 and ends with an expansion column 24 on the distal end 14, if there are n expansion columns 24 with m expansion struts 28 per column, there will be m-1 connecting strut columns 26, and n(m-l)/2 connecting struts 38
The reduced number of connecting struts 38 in each connecting strut column 26, as compared to expansion struts 28 in each expansion column 24, allows stent 10 to be longitudinally flexibility Longitudinal flexibility can be further increased by using a narrow width connecting strut, providing additional flexibility and suppleness to the stent as it is navigated around turns in a natural blood vessel At least a portion ofthe open spaces between struts in stent 10 form asymmetrical cell spaces 40. A cell space is an empty region on the surface of stent 10, completed surrounded by one or a combination of stent struts, including expansion struts 28, connecting struts 38, or joining struts 30. Asymmetrical cell spaces 40 are cell spaces which have no geometrical symmetry i.e. no rotation, reflection, combination rotation and reflection or other symmetry.
Asymmetrical cell spaces 40 in Figure 1 A are surrounded by a first expansion strut pair 32 in a first expansion column 24, a first connecting strut 38, a second expansion strut pair 32 in an adjacent expansion column 24, a first joining strut 30, a second connecting strut 38, and a second joining strut 30. Furthermore, expansion strut pairs 32 of asymmetrical cell space 40 may be circumferentially offset i.e. have longitudinal axes that are not collinear and have their open ends 36 facing each other. The space between two expansion struts of an expansion strut pair 32 is known as a loop slot 42.
Figure IB shows inner lumen 22, radius 44 and stent wall 46 of stent 10. Stent wall 46 consists of stent struts including expansion struts 28, connecting struts 38 and joining struts 30.
Figure IC shows, proximal end 12, distal end 14, longitudinal length 16, inner lumen 22, and stent wall 46 of stent 10. Inner lumen 22 is surrounded by stent wall 46 which forms the cylindrical surface of stent 10.
Referring now to Figures 2A and 2B, joining struts 30 of stent 10 are seen to extend at an angle to the expansion struts 28, forming a narrow angle 48 with one expansion strut 28 in an expansion strut pair 32 and a wide angle 50 with the other expansion strut 28 of an expansion strut pair 32. Narrow angle 48 is less than ninety degrees, while wide angle 50 is greater than ninety degrees. Joining struts 30 extend both longitudinally along the longitudinal axis of stent 10 and circumferentially, along the surface of the stent 10 perpendicular its longitudinal axis. Expansion strut spacing 52 between adjacent expansion struts 28 in a given expansion column 24 are uniform in stent 10 of Figures 2 A and 2B; however, non-uniform spacings can also be used Expansion strut spacings 52 can be varied, for example, spacings 52 between adjacent expansion struts 28 in an expansion column 24 can alternate between a narrow and a wide spacing Additionally, spacings 52 in a single expansion column 24 can differ from other spacings 52 in other columns 24
It is noted that varying expansion strut spacings 52 which form the loop slots 42 results in variable loop slot widths. Furthermore, the longitudinal axis of the loop slots 42 need not be collinear or even parallel with the longitudinal axis of loop slots 42 of an adjacent expansion column 24 Figures 2A and 2B show an arrangement of expansion struts 28 such that collinear, parallel adjacent loop slots 42 are formed, but non-collinear and non-parallel loop slots 42 can also be used
Additionally the shape of loop slots 42 need not be the same among loop slots of a single or multiple expansion columns 24 The shape a loop slots 42 can be altered by changing the orientation or physical dimensions ofthe expansion struts 28 and/or joining struts 30 which connect expansion struts 28 of expansion strut pairs 32 defining the boundaries of loop slots 42
Connecting struts 38 couple adjacent expansion columns 24, by connecting the distal end of an expansion strut pair in one expansion column 24 to the proximal end of an adjacent expansion strut pair 32 in a second expansion column 24 Connecting struts 38 of Figures 2 A and 2B are formed from two linear sections, a first linear section 54 being joined at its distal end to a second linear section 56 at its proximal end to form a first slant angle 58
The first linear section 54 of a connecting strut 38 is joined to expansion strut 28 at the point where joining strut 30 makes narrow angle 48 with expansion strut 28 First linear section 54 extends substantially collinear to joining strut 30 continuing the line of joining strut 30 into the space between expansion columns 24 The distal end ofthe first linear section 54 is joined to the proximal end ofthe second linear section 56 forming slant angle 58 Second linear section 56 extends substantially parallel to expansion struts 28 connecting at its distal end to joining strut 30 in an adjacent expansion column 24 The distal end of second linear section 56 attaches to expansion strut 28 at the point where joining strut 30 makes narrow angle 48 with expansion strut 28 Further, joining strut 30 can have a second slant angle with a width that can be the same or different from the width ofthe first slant angle Figures 2 A and 2B show connecting struts 38 and joining struts 30 slanted relative to the longitudinal axis of stent 10, with the circumferential direction ofthe slanted struts alternating from column to adjacent column Circumferential direction refers to the handedness with which the slanted struts wind about the surface ofthe stent 10 The circumferential direction ofthe slant of connecting strut first linear sections 54 in a connecting strut column 26 is opposite the circumferential direction ofthe slant of connecting strut first linear sections 54 in an adjacent connecting strut column 26 Similarly, the circumferential direction ofthe slant of joining struts 30 in an expansion column 24 is opposite the circumferential direction ofthe slant of joining struts 30 in an adjacent expansion column 24 Alternating circumferential slant directions of connecting struts 38 and joining struts 30 prevents axial warping of stent 10 during deliver and expansion Other non-alternating slant direction patterns can also be used for connecting struts 38 or joining struts 30 or both
Figure 3 A and 3B show a schematic illustration of a stent design according to the present invention in an unexpanded and expanded state respectively The design is depicted as a flat projection, as if stent 10 were cut lengthwise parallel to its longitudinal axis and flattened out The connecting struts 38 consist of first and second linear sections 54 and 56 forming slant angle 58 at pivot point 60 An asymmetrical cell space 40 is formed by expansion strut pairs 32, connecting struts 38 and joining struts 30 Multiple interlocking asymmetrical cell spaces 40 make up the design pattern
As the stent is expanded, see Figure 3B, the expansion strut pairs 32 spread apart at their open ends 36, shortening the length of expansion struts 28 along the longitudinal axis ofthe cylindrical stent The longitudinal shortening of expansion struts 28 during expansion is countered by the longitudinal lengthening of connecting struts 38 The widening of slant angle 58 during expansion straightens connecting struts 38 and lengthens the distance between the coupled expansion strut pairs 32. The lengthening ofthe distance between coupled expansion strut pairs 32 substantially compensates for the longitudinal shortening of expansion struts 28. Thus, the stent has substantially constant unexpanded and expanded longitudinal lengths.
When the stent is expanded, each expansion column 24 becomes circumferentially stretched, enlarging the space between struts. The interlinking of expansion columns 24 by connecting struts 38 that have been straightened through the expansion process gives the stent 10 a high radial support strength. The entire stent 10 when expanded is unitized into a continuous chain mesh of stretched expansion columns 24 and connecting strut columns 26 forming an asymmetrical interlocking cell geometry which resists collapse both axially and radially When the stent is expanded it has increased rigidity and fatigue tolerance. In addition, efficient bending and straightening of connecting struts 38 at pivot points 60 allows increased longitudinal flexibility ofthe stent. For the stent to bend longitudinally, at least some of connecting struts 38 are forced to bend in their tangent plane. The tangent plane of a specific connecting strut 38 refers to the plane substantially tangent to the cylindrical surface ofthe stent at that connecting strut 38. The width of connecting struts 38 is typically two to four, or more times the thickness, which makes connecting struts 38 relatively inflexible when bending in their tangent plane However, pivot points 60 in connecting struts 38 provide connecting struts 38 a flexible joint about which to more easily bend increasing longitudinal flexibility ofthe stent Referring to Figures 4A and 4B, a variation ofthe first embodiment of stent 10 ofthe present invention is shown In this variation, stent 10 has a length 16 of 33.25 mm and an uncrimped and unexpanded circumference 88 of 5.26 mm. Fifteen expansion columns 24 are interspersed with connecting strut columns 26. Each expansion column 24 consists of twelve expansion struts 28 joined alternately at their proximal and distal ends by joining struts 30 forming six expansion strut pairs 32 Expansion struts 28 are aligned parallel to the longitudinal axis of cylindrical stent 10. Joining struts 30 form a narrow angle 48 and a wide angle 50 with the respective expansion struts 28 of expansion strut pairs 32. Adjacent expansion columns 24 employ alternating circumferential slant directions of joining struts 30. In this variation ofthe first embodiment, expansion strut width 62 is .20 mm, expansion strut length 64 is 1.51 mm, and connecting strut width 66 is .13 mm. Distance 68 from the outer edge of a first expansion strut 28 to the outer edge of a second adjacent expansion strut 28 in the same expansion column 24 is .64 mm, leaving a loop slot width 70 of .24 mm. In this variation ofthe first embodiment, connecting struts 38 consist of a slanted first linear section 54 joined to a second linear section 56 at a slant angle 58. First linear section 54 is slightly longer than second linear section 56 and is attached at its proximal end to an expansion strut 28 in an expansion column 24. The attachment ofthe proximal end of first linear section 54 to expansion strut 28 is at the point where joining strut 30 makes narrow angle 48 with expansion strut 28. First linear section 54 extends substantially collinear to joining strut 30 attaching at its distal end to the proximal end of second linear section 56 to form slant angle 58. Second linear section 56 extends substantially collinear to expansion struts 28, attaching at its distal end to an expansion strut 28 in an adjacent expansion column 24. The attachment occurs at the point where expansion strut 28 forms narrow angle 48 with joining strut 30. Joining struts 30 and connecting strut first linear sections 54 slant in alternating circumferential directions from column to adjacent column.
The joining of connecting struts 38 and expansion struts 28 at the point where narrow angle 48 is formed aids smooth delivery of stent 10 by streamlining the surface ofthe unexpanded stent and minimizing possible catching points. Bare delivery of stent 10 to the target lesion in a vessel will thus result in minimal snagging or catching as it is navigated through turns and curvatures in the vessel. Stent 10 behaves like a flexible, tubular sled as it is moved forward or backward in the vessel on the delivery catheter, sliding through tortuous vessels and over irregular bumps caused by atherosclerotic plaques inside the vessel lumen.
When fully expanded Stent 10 of Figures 4A and 4B has an internal diameter of up to 5.0 mm, while maintaining an acceptable radial strength and fatigue tolerance. The crimped stent outer diameter can be as small as 1.0 mm or less depending on the condition ofthe underlying delivery balloon profile; A small crimped outer diameter is especially important if stent delivery is to be attempted without predilation ofthe target site. When the stent is optimally crimped over the delivery balloon, the surface ofthe crimped stent is smooth allowing for no snagging ofthe stent struts during either forward or backward movement through a vessel.
Figure 5 shows a second embodiment ofthe present invention in which the stent 10 in its expanded form has a gradual taper from proximal end 12 to distal end 14. The shaded segments 72, 74, 76, 78, 80, 82 and 84 of expansion struts 28 represent regions of expansion struts 28 to be removed. Removal ofthe shaded segments 72, 74, 76, 78, 80, 82 and 84 provides stent 10 with a gradual taper when expanded with distal end 14 having a smaller expanded diameter than proximal end 12. The degree of shortening ofthe expanded diameter ofthe stent 10 at a given expansion column 24 will be proportional to the length ofthe removed segment 72, 74, 76, 78, 80, 82, or 84 at that expansion column 24. In the expanded stent 10 the shortened expansion struts 28 will have a shortened component along the circumference ofthe stent resulting in a shortened circumference and diameter. The tapered diameter portion can be positioned anywhere along the length of stent 10, and the tapering can be made more or less gradual by removing appropriately larger or smaller portions ofthe expansion struts 28 in a given expansion column 24 Tapering is especially important in long stents, longer than 12 mm, since tapering of blood vessels is more pronounced over longer lengths. A long stent with a uniform stent diameter can only be matched to the target vessel diameter over a short region. If the proximal vessel size is matched with the stent diameter, the expanded distal end ofthe stent will be too large for the natural vessel and may cause an intimal dissection ofthe distal vessel by stent expansion. On the other hand, if the distal vessel size is matched with the stent diameter, the proximal end ofthe expanded stent will be too small to set inside the vessel lumen. It is therefore desirable to have a stent with a tapered expanded diameter. Another way achieve a tapered expanded stent is to change the stiffness ofthe stent struts, expansion struts, connecting struts or joining struts such that the stiffness ofthe struts varies along the length ofthe stent. The stiffness ofthe struts can be changed by altering length, width or thickness, adding additional stiffening material, using a chemical or mechanical means to alter the physical properties ofthe stent material, or applying one or a series of elastic elements about the stent.
Along with the use of a tapered diameter stent, a matching tapered balloon catheter would ideally be made for delivery and deployment ofthe tapered diameter stent. The method of using a tapered matching balloon catheter with a tapered diameter stent is within the scope ofthe present invention.
Using a tapered balloon to expand a non-tapered stent will also achieve a tapered expanded stent; however, since no metal is removed from the stent, the stent is tapered as a result of incomplete expansion. The stent will therefore have increased metal fraction at the tapered end resulting in increased risk of acute thrombosis. Metal fraction is the proportion ofthe surface ofthe expanded stent covered by the stent strut material. Shortening the expansion struts as shown in Figure 5 allows for a tapered expanded stent with substantially constant metal fraction along its length. A third embodiment ofthe present invention shown in Figures 6 A and 6B has multiple reenforcement expansion columns 86 placed along the length ofthe stent 10. The Reenforcement columns 86 are placed along the stent length to provide additional localized radial strength and rigidity to stent 10. Additional strength and rigidity are especially important at the ends ofthe stent to prevent deformation ofthe stent both during delivery and after placement. During delivery the stent ends can catch on the vessel wall possibly deforming the unexpanded stent and altering its expansion characteristics. After the stent has been placed it is important that the stent ends are rigid so that they set firmly against the vessel wall; otherwise, during a subsequent catheter procedure, the catheter or guidewire can catch on the stent ends pulling the stent away from the vessel wall and possibly damaging and/or blocking the vessel.
The specific variation ofthe third embodiment of stent 10 depicted in Figures 6 A and 6B has a length 16 of 20.70 mm and an uncrimped and unexpanded circumference 88 of 5.26 mm. The stent 10 consists of six expansion columns 24 and three reenforcement expansion columns 86, each consisting respectively of twelve expansion struts 28 or reenforcement expansion struts 90. The reenforcement expansion columns 86 are positioned one at either end, and one along the length ofthe stent 10.
The expansion strut width 62 is .15 mm, reenforcement expansion strut width 92 is .20 mm, and the connecting strut width 66 is .10 mm. The narrow angle 48 formed by joining strut 30 and expansion strut 28 is 75 degrees, and the narrow angle 94 formed by reenforcement joining strut 96 and reenforcement expansion strut 90 is 60 degrees.
Other arrangements of reenforcement expansion columns 86, such as providing reenforcement expansion columns 86 only on the ends of the stent, only on one end, or at multiple locations throughout the length ofthe stent can also be used and fall within the scope ofthe present invention. A taper can also be programmed into the reenforced stent 10 by shortening expansion struts 28 and reenforcement expansion struts 90 in appropriate expansion columns 24 and 86. A fourth embodiment ofthe present invention, shown in the Figures 7 A,
7B and 7C, is similar to the third embodiment but has the added feature of relief notches 98 and 100. A relief notch is a notch where metal has been removed from a strut, usually at a joint where multiple struts are connected. Relief notches increase flexibility of a strut or joint by creating a thinned, narrow region along the strut or joint. Relief notch 98 is formed at the joint formed between first linear section 54 of connecting strut 38 and expansion strut 28. Relief notch 100 is formed at the joint between second linear section 56 of connecting strut 38 and expansion strut 28 The positioning of the relief notches gives added flexibility to the unexpanded stent Relief notches can be placed at other joints and can be included in any ofthe previously mentioned embodiments Figures 8 A, 8B, 8C, 8D and 8E illustrates some examples of alternate connecting strut designs which can be used in any ofthe previously discussed embodiments Figure 8 A shows a rounded loop connecting strut 38 which joins two circumferentially offset expansion strut pairs 32 in adjacent expansion columns Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30 Joining struts 30 are slanted such as to form a narrow angle 48 and a wide angle 50 with the expansion struts 28 they connect The rounded loop connecting strut 38 connects expansion struts 28 at the point where narrow angle is formed between expansion strut 28 and joining strut 30 The slopes of the rounded connecting strut 38 at its proximal end 102 and distal end 104 substantially match the slopes of the joining struts 30 connecting the pairs of expansion struts 28 The rounded loop connecting strut 38 thus blends smoothly into the joining struts 30 Additionally the rounded loop connecting strut 38 has a first radius of curvature 106 and a second radius of curvature 108
In the design of Figure 8B a rounded loop connecting strut 38 joins two circumferentially offset expansion strut pairs 32 in adjacent expansion columns
Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30 Joining struts 30 are at right angles to the expansion struts 28 they connect The rounded loop connecting strut 38 connects to expansion struts 28 at the same point as joining struts 30 The rounded connecting strut 38 has a first radius of curvature 106 and a second radius of curvature 108 such that it connects circumferentially offset expansion strut pairs 32
In the design of Figure 8C connecting strut 38 joins two circumferentially offset expansion strut pairs 32 in adjacent expansion columns Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30 Joining struts 30 are slanted such as to form a narrow angle 48 and a wide angle 50 with the expansion struts 28 they connect The connecting strut 38 connects expansion struts 28 at the point where narrow angle 48 is formed between expansion strut 28 and joining strut 30.
The connecting strut 38 is made up of three linear sections 110, 112, and 114 forming two slant angles 116 and 118. The proximal end of section 1 10 is attached to expansion strut 28 at the point where joining strut 30 forms narrow angle 48 with expansion strut 28. Section 110 extends substantially collinear to joining strut 30 and is attached at its distal end to section 112 forming slant angle 116. Section 112 extends at an angle to section 110 such that section 112 is substantially parallel to expansion struts 28 and is connected at its distal end to the proximal end of section 114 forming slant angle 118. Section 114 extends at an angle such that it is substantially collinear to joining strut 30 ofthe adjacent expansion strut pair 32. Section 1 14 attaches at its distal end to expansion strut 28 ofthe adjacent expansion strut pair 32, at the point where joining strut 30 forms narrow angle 48 with expansion strut 28. In the design of Figures 8D and 8E a connecting strut 38 joins two circumferentially offset expansion strut pairs 32 in adjacent expansion columns. Expansion struts 28 in each expansion strut pair 32 are joined by a joining strut 30. Joining struts 30 are at right angles to the expansion struts 28 they connect. The connecting strut 38 connects to expansion struts 28 at the same point as joining struts 30.
The connecting struts 38 of Figures 8D and 8E are made up of multiple connecting strut sections connected end to end to form a jagged connecting strut 38 with multiple slant angles, coupling expansion strut pair 32 to adjacent expansion strut pair 32. The connecting strut of Figure 8D is made up of three connecting strut sections 120, 122, and 124 with two slant angles 126 and 128, while the connecting strut of Figure 8E consists of four connecting strut sections 130, 132, 134, and 136 with three slant angles 138, 140 and 142. In addition, the connecting strut section 134 can be modified by replacing connecting strut section 136 by the dotted connecting strut section 144 to give another possible geometry of connecting struts 38. One skilled in the art will recognize that there are many possible arrangements of connecting struts and joining struts consistent with the present invention; the above examples are not intended to be an exhaustive list.
The stent ofthe present invention is ideally suited for application in coronary vessels although versatility in the stent design allows for applications in non-coronary vessels, the aorta, and nonvascular tubular body organs.
Typical coronary vascular stents have expanded diameters that range from 2.5 to 5.0 mm. However, a stent with high radial strength and fatigue tolerance that expands to a 5.0 mm diameter may have unacceptably high stent metal fraction when used in smaller diameter vessels If the stent metal fraction is high, the chances of acute thrombosis and restenosis potential will increase. Even with the same metal fraction a smaller caliber vessel is more likely than a larger one to have a high rate of thrombosis. It is, therefore, preferred to have at least two different categories of stents for coronary application, for example, small vessels stents for use in vessels with diameters from 2 5 mm to 3 0 mm, and large vessel stents for use in vessels with diameters from 3 0 mm to 5 0 mm Thus, both small vessels and large vessels when treated with the appropriate sized stent will contain stents of similar idealized metal fraction.
The stent of the present invention can be made using a CAM-driven laser cutting system to cut the stent pattern from a stainless steel tube The rough-cut stent is preferably electro-polished to remove surface imperfections and sharp edges Other methods of fabricating the stent can also be used such as EDM, photo-electric etching technology, or other methods Any suitable material can be used for the stent including other metals and polymers so long as they provide the essential structural strength, flexibility, biocompatibility and expandability
The stent is typically at least partially plated with a radiopaque metal, such as gold, platinum, tantalum or other suitable metal It is preferred to plate only both ends ofthe stent by localized plating; however, the entire stent or other regions can also be plated When plating both ends, one to three or more expansion columns on each end ofthe stent are plated to mark the ends ofthe stent so they can be identified under fluoroscopy during the stenting procedure 781 PC17US97/06610
By plating the stent only at the ends, interference ofthe radiopaque plating material with performance characteristics or surface modulation ofthe stent frame is minimized. Additionally the amount of plating material required is reduced, lowering the material cost ofthe stent. After plating, the stent is cleaned, typically with detergent, saline and ultrasonic means that are well-known in the art The stents are then inspected for quality control, assembled with the delivery balloon catheter, and properly packaged, labeled, and sterilized.
The stent can be marketed as stand alone or as a pre-mounted delivery balloon catheter assembly as shown in Figure 9. Referring to Figure 9, the stent
10 is crimped over a folded balloon 146 at the distal end 148 of a delivery balloon catheter assembly 150. The assembly 150 includes a proximal end adapter 152, a catheter shaft 154, a balloon channel 156, a guidewire channel 158, a balloon 146, and a guidewire 160. Balloon 146 can be tapered, curved, or both tapered and curved from a proximal end to a distal end in the expanded state. Additionally stent 10 can be non-tapered or tapered in the expanded state
Typically the guidewire 160 is inserted into the vein or artery and advanced to the target site. The catheter shaft 154 is then forwarded over the guidewire 160 to position the stent 10 and balloon 146 into position at the target site. Once in position the balloon 146 is inflated through the balloon channel 156 to expand the stent 10 from a crimped to an expanded state In the expanded state, the stent 10 provides the desired scaffolding support to the vessel. Once the stent 10 has been expanded, the balloon 146 is deflated and the catheter shaft 154, balloon 146, and guidewire 160 are withdrawn from the patient The stent ofthe present invention can be made as short as less than 10 mm in length or as long as 100 mm or more If long stents are to be used, however, matching length delivery catheter balloons will typically be needed to expand the stents into their deployed positions. Long stents, depending on the target vessel, may require curved long balloons for deployment Curved balloons which match the natural curve of a blood vessel reduce stress on the blood vessel during stent deployment. This is especially important in many coronary applications which involve stenting in curved coronary vessels The use of such curved balloons is within the scope ofthe present invention
The foregoing description of a preferred embodiment ofthe invention has been presented for purposes of illustration and description It is not intended to be exhaustive or to limit the invention to the precise forms disclosed Obviously, many modifications and variations will be apparent to practitioners skilled in this art It is intended that the scope ofthe invention be defined by the following claims and their equivalents
What is claimed is

Claims

1. A stent in a non-expanded state, comprising: a first expansion strut pair including a first expansion strut positioned adjacent to a second expansion strut and a joining strut ofthe first expansion strut pair that couples the first and second expansion struts at a distal end ofthe first expansion strut pair, a plurality ofthe first expansion strut pair forming a first expansion column; a second expansion strut pair including a first expansion strut positioned adjacent to a second expansion strut and a joining strut ofthe second expansion strut pair that couples the first and second expansion struts ofthe second expansion strut pair at a proximal end of the second expansion strut pair, a plurality ofthe second expansion strut pair forming a second expansion column; a first connecting strut including a first connecting strut proximal head section and first connecting strut distal tail section, the head section being coupled to the distal end ofthe first expansion strut pair in the first expansion column and the tail section being coupled to the proximal end ofthe second expansion strut pair of the second expansion column, a plurality ofthe first connecting strut forming a first connecting strut column that couples the first expansion column to the second expansion column, the tail section extending in a first lateral direction relative to a longitudinal axis ofthe head section to form a first slant angle; a third expansion strut pair including a first expansion strut positioned adjacent to a second expansion strut and a third joining strut ofthe third expansion strut pair that couples the first and expansion struts at a proximal end ofthe third expansion strut pair, a plurality ofthe third expansion strut pair forming a third expansion column, the first expansion strut ofthe first expansion strut pair in the first expansion column having a longitudinal axis that is parallel to and offset from a longitudinal axis ofthe first expansion strut ofthe second expansion strut pair in the second expansion column, and the second expansion strut ofthe third expansion strut pair in the third expansion column having a longitudinal axis that is parallel to and offset from a longitudinal axis ofthe first expansion strut ofthe second expansion strut pair ofthe second expansion column; a second connecting strut including a proximal head section and a distal tail section, the head section being coupled to the distal end ofthe second expansion strut pair in the second expansion column and the tail section being coupled to the proximal end ofthe third expansion strut pair ofthe third expansion column, a plurality ofthe second connecting strut forming a second connecting strut column that couples the second expansion column to the third expansion column, wherein the tail section extends in a second lateral direction relative to a longitudinal axis ofthe head section to form a second slant angle that extends in an opposite direction from the first lateral direction; and wherein a ratio of a number of expansion struts in an expansion strut column to a number of connecting struts in a connecting strut column is 2 to 1 and the first slant angle reduces a fore shortening ofthe stent between the first and second expansion columns when the stent is in an expanded state.
2. The stent of claim 1, wherein the stent includes m first and second expansion columns, n expansion struts per column and n (m-l)/2 connecting struts.
3. The stent of claim 1 , wherein the first and second expansion columns are each unbroken, continuous structures.
4. The stent of claim 1, wherein each ofthe first slant angles is directed in a first circumferential direction.
5. The stent of claim 1, wherein the first connecting strut includes a third slant angle.
6. The stent of claim 1, wherein a width of a portion ofthe first connecting struts is equal to or less than a width of a portion ofthe first expansion struts.
7. The stent of claim 1, wherein a width of a portion ofthe first connecting struts is larger than a width of a portion ofthe first expansion struts.
8. The stent of claim 1, wherein a width of a portion ofthe second expansion struts is substantially the same as a width of a portion ofthe first expansion struts.
9. The stent of claim 1, further comprising: a reenforcement expansion column made of a plurality of reenforcement expansion struts, wherein each reenforcement expansion strut has a width that is greater than a width of an expansion strut in the first or second expansion columns.
10. The stent of claim 1, wherein the stent has a proximal end with a first reenforcement expansion column and a distal end with a second reenforcement expansion column.
1 1. The stent of claim 1, wherein at least a portion ofthe first connecting struts have a first radius of curvature.
12. The stent of claim 11, wherein the portion ofthe first connecting struts with the first radius of curvature have a second radius of curvature.
13. The stent of claim 1 , wherein at least a portion of the first connecting struts have first linear sections coupled to joining struts of first expansion strut pairs and second linear sections coupled to joining struts of second expansion strut pairs. 14 The stent of claim 1, wherein at least a portion ofthe first connecting struts have first linear sections coupled to joining struts of first expansion strut pairs, second linear sections coupled to joining struts of second expansion strut pairs and third linear sections coupling the first and second linear sections
15 The stent of claim 1 , wherein at least a portion of the first connecting struts have first linear sections coupled to joining struts of first expansion strut pairs, second linear sections coupled to joining struts of second expansion strut pairs, third and fourth linear sections coupling the first and second linear sections
16 The stent of claim 1, wherein the stent further includes a radiopaque marker
17 The stent of claim 1 , wherein the stent includes an electroplated material
18 The stent of claim 1 , wherein in an expanded state the stent has a tapered diameter
19 A stent assembly, comprising a balloon, and an expandable stent positioned at an exterior ofthe balloon, the stent including, a first expansion strut, a plurality ofthe first expansion strut forming a first expansion column, a second expansion strut, a plurality ofthe second expansion strut forming a second expansion column; and a first connecting strut, a plurality ofthe first connecting strut forming a first connecting strut column, each of a first connecting strut connecting a first expansion strut ofthe first expansion column to a second expansion strut ofthe second expansion column, the first connecting strut including a proximal section coupled to a distal section and at least a portion ofthe first connecting strut including a first linear section and a first slant angle
20 The assembly of claim 19, wherein the balloon has a tapered geometry
21 The assembly of claim 19, wherein a proximal end and a distal end of the connecting strut are circumferentially offset from each another when the stent is in a non-expanded state
22 The assembly of claim 19, wherein a proximal end and a distal end ofthe connecting strut are circumferentially offset from each another when the stent is in an expanded state
23 The assembly of claim 19, wherein a ratio of a number of expansion struts in an expansion strut column to a number of connecting struts in an connecting strut column is 2 to 1
24 The assembly of claim 19, wherein the connecting strut has a geometry which provides for a reduction of a fore shortening ofthe stent between the first and second expansion columns when the stent is in an expanded state
25 The assembly of claim 19, wherein the stent includes m first and second expansion columns, n expansion struts per column and n (m-l)/2 connecting struts 26 The stent of claim 19, wherein the first and second expansion columns are each unbroken, continuous structures
27 The stent of claim 19, wherein each first connecting strut first slant angle is directed in a first circumferential direction
28 The stent of claim 19, wherein the first connecting strut includes a second slant angle
29 The stent of claim 19, wherein the first expansion strut ofthe first expansion column is longitudinally offset from a corresponding second expansion strut ofthe second expansion column
30 The stent of claim 1, wherein the stent has a tapered diameter in an expanded state
31 The stent of claim 1 , wherein the stent has a tapered geometry extending from a proximal end to a distal end in an expanded state
32 The stent assembly of claim 19, wherein the balloon is tapered in an expanded state
33 The stent assembly of claim 32, wherein the balloon in an expanded state is curved along a longitudinal axis from a proximal end to a distal end
34 The stent assembly of claim 32, wherein the balloon is tapered in an expanded state and the stent has a non-tapered geometry in an expanded state 35 The stent assembly of claim 32, wherein the balloon and the stent are both tapered in an expanded state
36 The stent assembly of claim 33, wherein the stent is non-tapered in an expanded state
37 The stent assembly of claim 33, wherein the stent is tapered in an expanded state
38 The stent of claim 1, wherein the stent includes an electroplated material at a stent proximal end and at a stent distal end
39 A stent in a non-expanded state, comprising a first column expansion strut pair, a plurality ofthe first column expansion strut pair forming a first expansion column, a second column expansion strut pair, a plurality ofthe second column expansion strut pair forming a second expansion column, and a first connecting strut a plurality of first connecting struts forming a first connecting strut column, the plurality of first connecting struts coupling the first expansion column to the second expansion column, and wherein the first expansion column, the second expansion column, and the first connecting strut column provide a low profile when crimped over a balloon
PCT/US1997/006610 1996-04-26 1997-04-24 Intravascular stent WO1997040781A1 (en)

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JP53898097A JP4223552B2 (en) 1996-04-26 1997-04-24 Intravascular stent
AU26782/97A AU2678297A (en) 1996-04-26 1997-04-24 Intravascular stent
EP97918755A EP0900059B1 (en) 1996-04-26 1997-04-24 Intravascular stent
DE69734389T DE69734389T2 (en) 1996-04-26 1997-04-24 INTRAVASCULAR STENT
CA002252882A CA2252882C (en) 1996-04-26 1997-04-24 Intravascular stent
EP97926382A EP0927006B1 (en) 1996-04-26 1997-04-25 Intravascular stent
PCT/US1997/007006 WO1997040784A1 (en) 1996-04-26 1997-04-25 Intravascular stent
ES97922481T ES2216145T3 (en) 1996-04-26 1997-04-25 INTRAVASCULAR PROTESIS.
DE1997627670 DE69727670T2 (en) 1996-04-26 1997-04-25 INTRAVASCULAR STENT
EP97922481A EP0902666B1 (en) 1996-04-26 1997-04-25 Intravascular stent
DE69735133T DE69735133T2 (en) 1996-04-26 1997-04-25 INTRAVASCULAR STENT
CA002263397A CA2263397C (en) 1996-04-26 1997-04-25 Intravascular stent
JP53903197A JP4636634B2 (en) 1996-04-26 1997-04-25 Intravascular stent
AU31158/97A AU3115897A (en) 1996-04-26 1997-04-25 Intravascular stent
JP1997539074A JP4012251B6 (en) 1996-04-26 1997-04-25 Intravascular stent
AU28135/97A AU728242B2 (en) 1996-04-26 1997-04-25 Intravascular stent
PCT/US1997/006907 WO1997040783A2 (en) 1996-04-26 1997-04-25 Intravascular stent
CA002252596A CA2252596C (en) 1996-04-26 1997-04-25 Intravascular stent
AT97922481T ATE259627T1 (en) 1996-04-26 1997-04-25 INTRAVASCULAR STENT
JP2007260043A JP4749403B2 (en) 1996-04-26 2007-10-03 Intravascular stent

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US1748496P 1996-04-26 1996-04-26
US60/017,484 1996-04-26
US08/824,865 1997-03-25
US08/824,866 1997-03-25
US08/824,865 US6152957A (en) 1996-04-26 1997-03-25 Intravascular stent
US08/824,866 US5954743A (en) 1996-04-26 1997-03-25 Intravascular stent
US08/824,142 1997-03-25
US08/824,142 US6241760B1 (en) 1996-04-26 1997-03-25 Intravascular stent

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PCT/US1997/006610 WO1997040781A1 (en) 1996-04-26 1997-04-24 Intravascular stent
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US9445926B2 (en) 1996-04-26 2016-09-20 Boston Scientific Scimed, Inc. Intravascular stent
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