Endovascular stent apparatus and method

• US 4,856,516 A
• Filed: 01/09/1989
• Issued: 08/15/1989
• Est. Priority Date: 01/09/1989
• Status: Expired due to Term

• Current Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Hillstead, Richard A.
• Primary Examiner(s): Frinks, Ronald L.
• Application Number:
  US07/295,129
• Time in Patent Office: 218 Days
• Field of Search: 623/1, 623/12, 128/343, 128/344, 128/334 R, 604/8, 604/96, 604/104
• US Class Current: 606/194
• CPC Class Codes: A61F 2/88 the wire-like elements formed as helical or spiral coils forming a net-like or mesh-like structure A61F2/90

Abstract

A stent for reinforcing a vessel wall is constructed from a single elongated wire. The wire is first bent into a series of tight bends. The wire is then further bent into a sequence of loops that are connected by half hitch junctions and interconnections which are either aligned or spiral around a circumference of the stent. The completed stent forms a cylindrical form which can be expanded from a initial diameter to a larger implanted diameter by application of a radially outward force from a balloon catheter or the like.

Claims

1. A stent for reinforcing a vessel within a subject comprising a cylindrical support dimensioned to fit within an interior of said vessel constructed from an elongated wire bent to define a series of relatively tightly spaced convolutions or bends, said wire also bent in the form of a plurality of loops spaced along an axial dimension of the stent and connected by a series of half hitch junctions where each of the plurality of loops includes a number of said regularly spaced convolutions around its circumference, said stent being radially expandable from a first outer diameter which fits within said vessel to a second increased diameter which contacts an inner wall surface of said vessel to reinforce said inner wall.

2. The stent of claim 1 wherein the wire is tantalum.

3. The stent of claim 1 wherein an inner diameter of the stent is dimensioned to frictionally engage a non-inflated balloon catheter and be carried by the non-inflated balloon catheter into a blood vessel.

4. The stent of claim 1 wherein the plurality of loops are regularly spaced along the length of the stent and are interconnected by lengths of convoluted wire that are aligned along the length of the stent to form a relatively straight backbone to said stent.

5. The stent of claim 4 wherein gaps are left along the length of the stent to accommodate branches in the vessel so that the stent does not block off fluid flow through the branch.

6. The stent of claim 1 wherein the plurality of loops are regularly spaced along the length of the stent and are interconnected by lengths of convoluted wire that are offset around the diameter of the stent to define a backbone having a relatively wide pitch that spirals about the stent.

7. A method of fabricating a generally cylindrical stent for insertion into a body vessel comprising the steps of:

(a) bending an elongated wire in a series of relatively tight convolutions or bends;

(b) providing a cylindrical mandrel of a dimension smaller than an inner diameter of the vessel into which the stent is to be inserted;

(c) wrapping the elongated wire around the mandrel to form a series of loop segments and interconnecting said loop segments by half hitch junctions and wire portions that connect successive loop segments along an axial dimension of the cylindrical mandrel; and

(d) removing the elongated wire from the mandrel to define a throughpassage for fluid passage through the stent in a region occupied by the cylindrical mandrel.

8. The method of claim 7 wherein the series of loops are connected by a sequence of wire portions that are radially spaced around the circumference of the stent.

9. The method of claim 7 wherein the series of loops are connected by a sequence of wire portions that align along the length of the stent to form a relatively straight backbone to the stent.

10. The method of claim 7 wherein subsequent to the removal of the stent from the mandrel one or more loops are removed from the stent to accommodate branching vessels and allow unimpeded fluid flow to said branching vessels after the stent is positioned within the vessel.