US20060085061A1 - Extendible stent apparatus and method for deploying the same - Google Patents

Abstract

An imageable extendable stent apparatus for insertion into a bifurcating vessel or a vessel opening. The stent apparatus comprises a main stent and a flared stent, which may used individually or in combination with each other. The flared stent may be interlocked with the main stent to provide stent coverage over the entire region of a bifurcation. The main stent of the apparatus may be deployed at the bifurcation point of a vessel, allowing unimpeded future access to the side branch of the bifurcated vessel. The flared stent may be employed at vessel openings. Also disclosed and claimed are methods for implanting the extendable stent apparatus into the bifurcation point or the ostium of a subject vessel.

Description

BACKGROUND
• A type of endoprosthesis device, commonly referred to as a stent, is placed or implanted within a vein, artery or other tubular body organ for treating occlusions, stenoses, or aneurysms of the vessel. These stent devices are implanted within tubular vessels to reinforce collapsing, partially occluded, weakened, or abnormally dilated segments of the vessel wall. Stents have been used to treat dissections in blood vessel walls caused by balloon angioplasty of the coronary arteries as well as peripheral arteries and to improve angioplasty results by preventing elastic recoil and remodeling of the vessel wall.
• Stents also have been successfully implanted in the urinary tract, the bile duct, the esophagus and the tracheo-bronchial tree to reinforce those body organs. Two randomized multicenter trials have recently shown a lower restenosis rate in stent treated coronary arteries compared with balloon angioplasty alone (Serruys P W et. al. New England Journal of Medicine 331: 489-495, 1994, Fischman D L et. al. New England Journal of Medicine 331: 496-501, 1994).
• One of the drawbacks of conventional stents is that they are produced in a straight tubular configuration. The use of such stents to treat disease at or near a branch or bifurcation of a vessel runs the risk of compromising the degree of patency of the primary vessel and/or its branches or bifurcation and also limits the ability to insert a second stent into the side branch if the angioplasty result is suboptimal. This may occur as a result of several mechanisms such as displacing diseased tissue or plaque shifting, vessel spasm, dissection with or without intimal flaps, thrombosis, and embolism.
• The risk of branch compromise is increased in two anatomical situations. First the side branch can be compromised when there is a stenosis in the origin of the side branch. Second, when there is an eccentric lesion at the bifurcation site, asymmetric expansion can cause either plaque shifting or dissection at the side branch origin. There are reports of attempting to solve this problem by inserting a balloon into the side branch through the stent struts; however, this technique carries the risk of balloon entrapment and other major complications (Nakamura, S. et al., Catheterization and Cardiovascular Diagnosis 34: 353-361 (1995)). Moreover, adequate dilatation of the side branch is limited by elastic recoil of the origin of the side branch. In addition, the stent may pose a limitation to blood flow and may limit access to the side branch. The term “stent jail” is often used to describe this concept. In this regard, the tubular slotted hinged design of the Palmaz-Schatz intracoronary stent, in particular, is felt to be unfavorable for lesions with a large side branch and it is believed to pose a higher risk of side branch vessel entrapment where the stent prevents or limits access to the side branch. Id.
• One common procedure for implanting the endoprosthesis or stent is to first open the region of the vessel with a balloon catheter and then place the stent in a position that bridges the treated portion of the vessel in order to prevent elastic recoil and restenosis of that segment. The angioplasty of the bifurcation lesion has traditionally been performed using the kissing balloon technique where two guidewires and two balloons are inserted, one into the main branch and the other into the side branch. Stent placement in this situation will require the removal of the guidewire from the side branch and reinsertion of the guidewire via the stent struts and insertion of a balloon through the struts of the stent. The removal of the guidewire poses the risk of occlusion of the side branch during the deployment of the stent in the main branch.
• Prior art patents refer to the construction and design of both the stent as well as the apparatus for positioning the stent within the vessel. One representative patent to Chaudhury, U.S. Pat. No. 4,140,126, discloses a technique for positioning an elongated cylindrical stent at a region of an aneurysm to avoid catastrophic failure of the blood vessel wall. The '126 patent discloses a cylinder that expands to its implanted configuration after insertion with the aid of a catheter. Dotter, U.S. Pat. No. 4,503,569, discloses a spring stent which expands to an implanted configuration with a change in temperature. The spring stent is implanted in a coiled orientation and is then heated to cause the spring to expand. Palmaz, U.S. Pat. No. 4,733,665, discloses a number of stent configurations for implantation with the aid of a catheter. The catheter includes a mechanism for mounting and retaining the vascular prosthesis or stent, preferably on an inflatable portion of the catheter. The stents are implanted while imaged on a monitor. Once the stent is properly positioned, the catheter is expanded and the stent separated from the catheter body. The catheter can then be withdrawn from the subject, leaving the stent in place within the blood vessel. Palmaz, U.S. Pat. No. 4,739,762, discloses an expandable intraluminal graft. Schjeldahl et. al., U.S. Pat. No. 4,413,989, discloses a variety of balloon catheter constructions. Maginot, U.S. Pat. No. 5,456,712 and Maginot, U.S. Pat. No. 5,304,220 disclose graft and stent assembly and method of implantation where a stent is used to reinforce a graft surgically inserted into a blood vessel in order to bypass an occlusion. However, none of these patents relate to the treatment of bifurcation lesions, or disclose a bifurcating stent apparatus and method for deploying the same.
• Taheri, U.S. Pat. No. 4,872,874, Piplani et. al., U.S. Pat. No. 5,489,295, and Marin et al., U.S. Pat. No. 5,507,769, disclose bifurcating graft material which may be implanted with stents. However, there is no mention of bifurcation of the stent, and the stent is used only to anchor the graft into the vessel wall. It does not reinforce the vessel wall, nor does it prevent restenosis after angioplasty.
• MacGregor, U.S. Pat. No. 4,994,071, discloses a hinged bifurcating stent. In the 071' patent, in contrast to the present invention, there is a main stent with two additional stents attached at one end, creating a single unit with a bifurcation. The two additional stents are permanently attached and cannot be removed from the main stent. Thus, this invention may not be used in non-bifurcation vessels. In addition, studies with hinge-containing stents have shown that there is a high incidence of restenosis (tissue growth) at the hinge point that may cause narrowing or total occlusion of the vessel and thus compromise blood flow. Furthermore, this design has a relatively large size which makes insertion into the vessel difficult. Also, by having the two additional stents connected to the main stent, tracking into a wide-angle side branch may be difficult and may carry the risk of dissection of the vessel wall. Furthermore, once the device of the '071 patent is implanted, it is impossible to exchange the side branch stent should the need for a different stent size arise.
• In general, when treating a bifurcation lesion using commercially available stents, great care should be taken to cover the origin of the branch because if left uncovered, this area is prone to restenosis. In order to cover the branch origin, conventional stents must either protrude into the lumen of the main artery or vessel from the branch (which may causes thrombosis [clotting of blood], again compromising blood flow), or they must be placed entirely within the branch, and will generally not cover the origin of the bifurcation. Another frequent complication experienced with the stenting of bifurcations include narrowing or occlusion of the origin of a side branch spanned by a stent placed in the main branch. Lastly, placement of a stent into a main vessel where the stent partially or completely extends across the opening of a branch may make future access into such branch vessels difficult if not impossible.
• In addition, conventional stent technology is inadequate as a means of treating ostial lesions. Ostial lesions are lesions at the origin of a vessel. For example, ostial lesions may form in renal arteries, which are side branches extending from the aorta. Ostial lesions are prone to restenosis due to elastic recoil of the main vessel, such as the aorta. Therefore, the stent cover must include the thickness of the wall of the main vessel. This is extremely difficult to accomplish without protrusion of the stent into the main vessel.
• Lastly, conventional stents are difficult to visualize during and after deployment. While some prior art balloon catheters are “marked” at the proximal and distal ends of the balloon with imageable patches, no FDA-approved stents are currently available which are themselves imageable through currently known imaging procedures used when inserting the stents into a vessel.
• Accordingly, there is a need for an improved stent apparatus and method for deploying the same which 1) may be used to effectively treat bifurcation lesions which reduces the risk of restenosis or occlusion of the side branch and which completely covers bifurcation lesions with the stent apparatus, 2) may be used to treat lesions in one branch of a bifurcation while preserving access to the other branch for future treatment, 3) may be used to treat ostial lesions, 4) allows for differential sizing of the stents in a bifurcated stent apparatus even after the main stent is implanted, and which 5) may be readily visualized by current or future visualization techniques.
SUMMARY OF THE INVENTION
• The present invention concerns a novel extendable stent apparatuses and method for deploying the same. More particularly, the invention concerns a stent apparatus comprising an extendable stent which is suitable for treating bifurcation lesions, and which may also be used to treat lesions at the origin of a blood vessel or other organ. As used herein, the term “vessel” means any tubular tissue, and is not limited to vessels of the vascular system. Devices constructed in accordance with the invention include, singularly or in combination, a flared stent comprising a compressible flared portion at its proximal end, which flared portion may comprise hooks, compressible mesh or any other means of creating such a flared portion at the proximal end of the stent, and a main stent comprising at least one substantially circular opening located between its proximal and distal ends. For ease of visualization, both the flared stent and the main stent may be comprised of materials which are imageable, or the stents of the invention may be “marked” at the ends with an imageable substance and the main stent may also be marked at any opening. At least one flared stent may be extended through at least one opening of the main stent into at least one branch vessel for treating bifurcated or branched lesions, or the stents of the invention may be inserted individually for the treatment of ostial lesions, or lesions near bifurcations requiring a stent in either the main or the branch vessel with unobstructed access to the unstented vessel in the bifurcation. The methods of the invention comprises a two-step process used to deploy both the main and the flared stent in a bifurcated vessel, or to deploy the main stent only within a bifurcated vessel.
• The stent apparatus of the invention may be constructed from any non-immunoreactive material that allows the apparatus to be expanded from an initial shape to a shape which conforms to the shape of the vessel or vessels into which the apparatus is inserted, including but not limited to any of the materials disclosed in the prior art stents, which are incorporated herein by reference. It is hypothesized that the stent apparatuses of the invention may further be constructed of a substance which is observable by imaging methods including but not limited to magnetic resonance, ultrasound, radio-opaque or contrast-dye, or may be marked at certain points including but not limited to the ends and around any opening or flared portion in a stent of the invention, with a material which is discernable by imaging methods as described above.
• A stent constructed in accordance with the invention is suitable for implantation into any vessel in the body, including but not limited to vessels in the cardiac system, the peripheral vascular system, the carotid and intracranial vessels, the venous system, the renal system, the biliary system, the gastrointestinal system, the tracheobronchial system, the biliary system and the genitourinary system.
• The stents of the invention are deployed utilizing a set of guidewires and catheters, which are then withdrawn from the subject following deployment of the stents. The stents of the invention may be self-expanding to conform to the shape of the subject vessel, or they may be expanded utilizing balloon catheters, or by any method currently known or developed in the future which is effective for expanding the stents of the invention. The flared stent of the invention is constructed such that the flared portion is confined along the wall of the flared stent by a sheath running parallel to the longitudinal axis of the flared stent until deployment, during which the sheath is removed and the flared portion is expanded into a configuration extending radially, at least in part, from the longitudinal axis of the flared stent.
• Thus, it is an object of the present invention to provide a double-stent apparatus which makes it possible to completely cover the origin of a bifurcation lesion with a stent apparatus.
• Another object of the invention is to provide a single-stent apparatus and method for deploying the same which may be used to treat only one branch of a bifurcation lesion but which will facilitate future treatment of the corresponding branch.
• Yet another object of the invention is to provide a single-stent apparatus which is effective in treating ostial lesions.
• A further object of the invention is to provide a method for insertion of the extendable double-stent apparatus into both the main and branch vessels of a bifurcation lesion.
• Additionally, it is an object of the invention to provide a stent apparatus which is imageable during and after insertion.
• These objects and other object advantages and features of the invention will become better understood from the detailed description of the invention and the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a schematic depiction of the double-stent apparatus of the present invention in which both the main stent and the flared stent are fully dilated.
• FIG. 2 is a schematic depiction of the main stent of the apparatus of the invention as deployed, without placement of the flared stent.
• FIG. 3 is a schematic depiction of the flared stent of the apparatus as deployed, without the main stent.
• FIG. 4 is a schematic depiction of the main stent of the apparatus deployed within a subject vessel.
• FIG. 5 is a schematic depiction of the double-stent bifurcating stent apparatus, where the main stent is deployed and showing the placement of the flared stent apparatus prior to full deployment of the flared stent.
• FIG. 6 is a schematic depiction of the method of the invention.
• FIG. 6adepicts initial placement of the main stent of the bifurcating stent apparatus into the vessel, along with the insertion of guidewire and stabilizing catheter for placement of the flared stent into the branch vessel of the subject.
• FIG. 6bis a schematic depiction of the step of inflating the main stent of the invention.
• FIG. 6cis a schematic depiction of the deployment of the flared stent over the side branch guidewire, through an opening in the main stent and into the branch vessel of the subject.
• FIG. 6dis a schematic depiction of the removal of the protective sheath of the flared stent, allowing for full expansion of the flared portion prior to placement and deployment.
• FIG. 6eis a schematic depiction of the fully extended flared stent positioned into the branch by the catheter, but prior to full deployment.
• FIG. 6fis a schematic depiction of the fully dilated main stent and the fully positioned flared stent, where the flared stent is being dilated by inflation of the balloon.
• FIG. 6gis a schematic depiction of the fully dilated bifurcating double stent of the invention, positioned into the bifurcation in a subject vessel.
• The rectilinear matrices shown in the drawings are intended to show the shapes of the surfaces only, and do not illustrate the actual surface patterns or appearances of the stent apparatuses of the invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
• The bifurcating double-stent apparatus10 of the present invention comprises a generally cylindricalmain stent12 and a generally cylindrical flaredstent15, which are shown as fully dilated in a subjectmain vessel8 and asubject branch vessel7, as illustrated inFIG. 1.
• Themain stent12 contains at least one generallycircular opening16 located between theproximal end26 and thedistal end28 of the main stent12 (FIG. 2), which opening is positioned over the opening48 of a branch vessel in avessel bifurcation50, as shown inFIG. 2. The ends of thestent12 and the opening are imaged during imaging procedures by placingmarkers56 around the edges of theopening16 in themain stent12 and at theproximal end26 anddistal end28 of the main stent, as illustrated inFIG. 4.
• The flaredstent apparatus15 of the present invention comprises a generally cylindrical flared stent comprising aproximal end30 and adistal end32, as shown inFIG. 3. Theproximal end30 comprises a flared portion, illustrated here asextended loops18, which flared portion, when dilated, is positioned within thelumen58 of the main vessel8 (FIG. 3). The ends of the flaredstent15 and the flaredportion18 are imaged during imaging procedures by placingmarkers56 around the flaredportion18 and at theproximal end30 anddistal end32 of the flared stent, as illustrated inFIG. 5.
• As shown in the embodiment of the invention illustrated inFIG. 4, aguidewire20 is inserted into thevessel8 prior to insertion of themain stent12, and is used to guide themain stent12 into position within thevessel8. Prior to insertion and dilation, themain stent12 is disposed around the distal end of acatheter48 which may include aninflatable balloon24. The main stent/catheter apparatus is then threaded onto themain guidewire20 and into thevessel8. Themain stent12 is dilated by inflation of theballoon24 until it expands the walls of thevessel8, and is thus affixed into place.
• As shown in the embodiment of the invention illustrated inFIG. 5, prior to insertion of the flaredstent15, aguidewire36 and a stabilizingcatheter44 are inserted through theopening16 in themain stent12, and into a branch vessel. The stabilizingcatheter44 is used to place the opening in themain stent12 over theopening16 in the bifurcation. Theguidewire36 is used to guide the flaredstent15 into position within a vessel. During insertion and prior to dilation, the flaredstent15 is disposed around the distal end of a branch catheter54 which may include aninflatable balloon25, and the flaredportion18 of the flaredstent15 is held in a compressed position by aprotective sheath34.
• In the bifurcating double-stent apparatus10 of the invention, once themain stent12 is dilated and the stabilizingcatheter44 is removed, the flaredstent15 is inserted over the branch guidewire36 and through theopening16 of themain stent12 substantially as shown inFIG. 5, and affixed in place by the expansion of the flaredportion18 positioned at theproximal end30 of the flared stent, as shown inFIGS. 1 and 5. The angle at which the flaredstent15 is affixed depends upon the vessel structure into which the bifurcatingstent apparatus10 is inserted (FIG. 1).
• The inventive two-stage method for implanting the novel bifurcating double-stent apparatus10 begins with insertion of themain guidewire20 into the subjectmain vessel8 and across thebifurcation50. Once themain guidewire20 is in position in themain vessel8, themain stent12 is mounted around a catheter48 (which may also comprise a balloon24), and thecatheter48 andstent12 are inserted into themain vessel8. Thestent12 is positioned so that theopening16 is directly over thebifurcation point50 in the subject vessel (FIG. 6a). In order to aid such positioning, a side branch guidewire36 and a stabilizing catheter44 (as depicted inFIGS. 5 and 6) are also inserted through theopening16 of themain stent12 and into the branch vessel7 (FIG. 6a).
• In an alternative embodiment of the method of the invention, themain stent12, thecatheters44 and48 and the side branch guidewire36 may be assembled in advance of insertion (with the stabilizingcatheter44 and the side branch guidewire positioned through theopening16 of the main stent) into the subject, and then inserted into thebifurcation point50 in themain vessel8 simultaneously, after which the side branch guidewire36 and the stabilizingcatheter44 are threaded into thebranch vessel7 in order to properly align theopening16 in the main stent12 (FIG. 6a).
• To affix themain stent12 in the desired position within thevessel8, thestent12 may be dilated by inflating theballoon24 until themain stent12 is in contact with the walls of the vessel8 (FIG. 6b). Once themain stent12 is dilated, thecatheters44 and48 are withdrawn, leaving the fully positionedmain stent12 and themain guidewire20 in the main subject vessel, and the side branch guidewire36 in the subject branch vessel (FIG. 6c).
• In the second stage of the method of deploying the bifurcating double-stent of the invention, the flared stent catheter54, containing the compressed flaredstent15 in aprotective sheath34 and which may further contain aballoon25 disposed around the flared stent catheter54 and inside the compressed flaredstent15, is inserted into thesubject branch vessel7 around the side branch guidewire36 as shown inFIG. 6c. The compressed flaredstent15 is initially positioned so that the compressedproximal end30 of the flared stent extends into thelumen42 of themain stent12 to facilitate full expansion of the flaredportion18 after withdrawal of theprotective sheath34, prior to the final positioning of the flaredstent15 into the branch of the bifurcation (FIG. 6c). Thedistal end32 of the flared stent is initially positioned within the branch vessel7 (FIG. 6c). After theproximal end30 of the compressed flared stent is properly placed within thelumen42 of the main stent, theprotective sheath34 is withdrawn from thevessel8, and the flaredportion18 of the flaredstent15 is decompressed to extend radially, at least in part, to the longitudinal axis of the flaredstent15, as shown inFIG. 6d. After the flaredportion18 of the flaredstent15 is in its flared configuration (as shown inFIG. 6d), the flaredstent15 is advanced into theside branch7 at itsproximal end30 until at least a portion of flaredportion18 of the flaredsheath15 contacts at least a portion of an edge of theopening16 of themain stent12, as shown inFIG. 6e. In this example, aballoon25 is inflated in order to dilate the flaredstent15 to bring the walls of the flaredstent15 into contact with the walls of thebranch vessel7, as shown inFIG. 6f. All remaining catheters and guidewires are then withdrawn from the subject, leaving the fully deployed bifurcating double-stent apparatus of theinvention10, comprising themain stent12 with at least oneopening16, and the flaredstent15 positioned through theopening16 into thebranch vessel7, as shown inFIG. 6g.
• When treating ostial lesions, the flaredstent15 alone is used, and is positioned utilizing catheters and guidewires as described above, except that a stabilizing catheter is not used, and the flaredportion18 of the flared stent is positioned at the ostium of a vessel, instead of into a side branch through the anopening16 in a main branch. After the flaredstent15 is positioned near the ostium of a subject vessel, theprotective sheath34 is retracted in order to allow the flared portion to fully expanded and the flaredstent15 is further advanced with the proximal end of the catheter until the unfolded hooks18 are in contact with the walls of the subject vessel.
• All the stents of the invention may be deployed using the methods of the invention without resort to a balloon catheter. For example, a self-expanding compressed stent contained within a protective sheath could be self-dilated by retraction of a protective sheath. Other methods of dilation of the stents of the invention may exist, or may become available in the future, and such methods are contemplated as being within the scope of this invention. While this example used self-unfolding loops to demonstrate one means of creating a flared portion, any other means of creating a flare, such as but not limited to creating a roll in the stent material which is then compressed, is contemplated as within the scope of this invention.
• It is the intent that the invention include all modifications and alterations from the disclosed embodiments that fall within the scope of the claims of the invention.

Claims (22)

1. An extending double-stent apparatus for placement in a bifurcating vessel comprising a first generally cylindrical stent having sides extending between first and second opposing ends and at least one opening being defined in a side; and a second generally cylindrical stent adapted to extend through one of said side openings of said first stent, said first and second stents each being constructed from a material which allows said stents to be expanded to conform to the shape of the subject vessel.

2. The stent apparatus ofclaim 1 wherein said second cylindrical stent additionally comprises a proximal end and an opposing distal end, wherein the proximal end additionally comprises a flared portion, which flared portion is in contact with the edges of said first stent side opening.

3. The stent apparatus ofclaim 1 wherein the stent apparatus is comprised of a biologically acceptable material.

4. The stent apparatus ofclaim 1 wherein the stents comprise a self-expanding material.

5. The stent apparatus ofclaim 1 wherein the stents comprise a balloon-expandable material.

6. The stent apparatus ofclaim 1 wherein at least a portion of the stents are imageable during and after insertion.

7. A generally cylindrical stent apparatus comprising a proximal end and a distal end, wherein the proximal end further comprises a flared portion for anchoring said stent apparatus into place within a vessel.

8. The stent apparatus ofclaim 7 wherein the flared portion is expandable from a compressed position to a configuration extending radially, at least in part, to the longitudinal axis of the stent apparatus.

9. The stent apparatus ofclaim 7 wherein the stent apparatus is comprised of a biologically acceptable material.

10. The stent apparatus ofclaim 7 wherein the stent comprises a self-expanding material.

11. The stent apparatus ofclaim 7 wherein the stents comprise a balloon-expandable material.

12. The stent apparatus ofclaim 7 wherein at least a portion of the stent is imageable during and after insertion.

13. A generally cylindrical stent apparatus having sides extending between first and second opposing ends and at least one opening being defined in a stent side.

14. The stent apparatus ofclaim 13 wherein the stent apparatus is comprised of a biologically acceptable material.

15. The stent apparatus ofclaim 13 wherein the stent comprises a self-expanding material.

16. The stent apparatus ofclaim 13 wherein at least a portion of the stents are imageable during and after insertion.

17. A method for deploying a stent apparatus into a bifurcated vessel comprising the steps of

routing a first guidewire into the main vessel of a subject bifurcating vessel and extending the guidewire beyond the bifurcation point;

inserting a first generally cylindrical stent apparatus comprising at least one side opening into an area of bifurcation of the main vessel;

aligning a side opening of the first stent apparatus with the bifurcation point of the bifurcated vessel by inserting a second guidewire and a stabilizing catheter into the first stent apparatus and into a subject branch vessel by passing the second guidewire and the stabilizing catheter through a side opening of the first stent apparatus and into the subject branch vessel; and

expanding the first cylindrical stent apparatus into contact with the walls of the main vessel.

18. The method ofclaim 17 further comprising

inserting along the second guidewire and into the stabilizing catheter of the branch vessel a second generally cylindrical stent apparatus, comprising a distal end and an opposed proximal end and further comprising a flared portion at the proximal end, positioned so that the flared portion is within a lumen of a subject branch vessel and contacts at least part of the edge of a side opening of the first stent apparatus;

withdrawing the stabilizing catheter from the subject vessel; and

expanding the second cylindrical stent apparatus at least into contact with the walls of the subject branch vessel.

19. The method ofclaim 17 wherein the step of expanding the first cylindrical stent apparatus is performed by balloon catheterization.

20. The method ofclaim 18 wherein the steps of expanding the first and second cylindrical stent apparatuses is performed by balloon catheterization.

21. A method for deploying a flared stent apparatus into the ostium of a vessel comprising:

inserting a guidewire through the ostium of a vessel and into the vessel,

inserting around the guidewire a generally cylindrical flared stent apparatus, the flared stent apparatus comprising a distal end and an opposed proximal end and further comprising a flared portion at the proximal end;

positioning the flared portion so that the flared portion is within the ostium of the vessel and contacts at least part of the ostium of said vessel;

dilating the flared stent apparatus at least into contact with the walls of the subject vessel, and

removing the guidewire from the subject.

22. The method ofclaim 21 further comprising the step of dilating the flared stent apparatus by balloon catheterization.

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