Side branch stent with split proximal end

• US 20050049680A1
• Filed: 09/03/2003
• Published: 03/03/2005
• Est. Priority Date: 09/03/2003
• Status: Abandoned Application

• Current Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Original Assignee: Cordis Corporation (Cardinal Health, Inc.)
• Inventors: Fischell, David R., Burgermeister, Robert, Fischell, Tim A., Grishaber, Randy-David Burce
• Application Number:
  US10/654,118
• Publication Number:
  US 20050049680A1
• Time in Patent Office: Days
• US Class Current: 623/1.150
• CPC Class Codes: A61F 2/848 having means for fixation to the vessel wall, e.g. barbs
• CPC Class Codes: A61F 2/856 Single tubular stent with a side portal passage
• CPC Class Codes: A61F 2/91 made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
• CPC Class Codes: A61F 2/915 with bands having a meander structure, adjacent bands being connected to each other
• CPC Class Codes: A61F 2/954 for placing stents or stent-grafts in a bifurcation
• CPC Class Codes: A61F 2002/821 Ostial stents
• CPC Class Codes: A61F 2002/91525 within the whole structure different bands showing different meander characteristics, e.g. frequency or amplitude
• CPC Class Codes: A61F 2002/91533 characterised by the phase between adjacent bands
• CPC Class Codes: A61F 2002/91558 connected peak to peak
• CPC Class Codes: A61F 2250/006 modular

Abstract

The method for use of the present invention stent and stent delivery system is to insert a first guidewire into the branch vessel and advance the stent delivery system until the marker at the distal end of the split proximal end is aligned with the downstream edge of the sidebranch ostium. The balloon is then inflated to deliver the stent into the sidebranch. If the two zone balloon is being used as a stent delivery system, the initial inflation will cause the split proximal end to flare apart. If the stent is delivered on a standard balloon angioplasty catheter, then a second balloon of larger diameter would be used to post-dilate the proximal end of the split end stent. A stent is then advanced into the main branch and deployed, further spreading the split proximal and of the split end sidebranch stent outward against the wall of the main branch. A guidewire is then placed through the main branch stent and the opening into the sidebranch is enlarged using balloon inflation. The final result is a double layer of metal at the ostium of the sidebranch where additional anti-restenosis drug elution is desirable.

Claims

1. A stent for implantation into a vessel of a human body, the stent being in the form of a longitudinal axis, a proximal end and a distal end, the stent having a distal section comprising a plurality of circumferential sets of strut members, each set of strut members being longitudinally separated each from the other and each set of strut members forming a cylindrical portion of the stent, the stent also having a proximal section comprising at least three spokes, each spoke connected to the proximal-most circumferential set of strut members of the distal section of the stent.

2. The stent of claim 1 wherein the stent is self-expanding.

3. The stent of claim 1 wherein the stent is balloon expandable.

4. The stent of claim 1 wherein each spoke is only attached to the proximal-most circumferential set of strut members of the distal section of the stent.

5. The stent of claim 1 wherein each spoke is connected to adjacent spokes by strut members, the strut members collectively forming a circumferential set of strut members at the proximal end of the stent.

6. The stent of claim 1 where each circumferential set of strut members comprises a plurality of connected curved sections, and the number of spokes is equal to the number of curved sections in the proximal-most circumferential set of strut members of the distal section of the stent.

7. The stent of claim 1 where each circumferential set of strut members comprises a multiplicity of connected curved sections and the number of spokes is less than the number of curved sections in the proximal-most circumferential set of strut members of the distal section of the stent.

8. The stent of claim 1 where each circumferential set of strut members comprises a multiplicity of connected curved sections and the number of spokes is more than the number of curved sections in the proximal-most circumferential set of strut members of the distal section of the stent.

9. The stent of claim 1 further comprising a stent delivery system having three radiopaque markers for positioning the stent at the ostium of a side branch vessel.

10. A stent for implantation into a vessel of a human body, the stent having a longitudinal axis, a proximal end and a distal end, the stent having a cylindrical distal section and a split proximal section designed to be flared outward with respect to the cylindrical distal section.

11. The stent of claim 10 where at least some portion of the split proximal section includes a radiopaque material to enhance the radiopacity of the split proximal section.

12. The stent of claim 11 where the radiopaque material is coated onto the exterior surface of some portion of the split proximal section.

13. The stent of claim 11 where the radiopaque material is inserted into one or more holes in the split proximal section.

14. The stent of claim 11 where the radiopaque material includes gold, platinum, tantalum, iridium, palladium or tungsten, or alloys thereof.

15. The stent of claim 13 where the split proximal section further comprises individual spokes, with each spoke having a radiopaque insert.

16. The stent of claim 13 where the split proximal section further comprises individual spokes with every other spoke having a radiopaque insert.

17. The stent of claim 13 where the split proximal section further comprises individual spokes with less than half of the spokes having a radiopaque insert.