Stent and catheter assembly and method for treating bifurcations

• US 8,029,558 B2
• Filed: 07/07/2006
• Issued: 10/04/2011
• Est. Priority Date: 07/07/2006
• Status: Expired due to Fees

• Current Assignee: Abbott Cardiovascular Systems Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Cardiovascular Systems Incorporated (Abbott Laboratories Incorporated)
• Inventors: Cox, Daniel L., Wrolstad, David K., Pacetti, Stephen Dirk, Barbod, Leonard D., Ta, Diem Uyen, Hearn, Brenna K., Armstrong, Kenneth Kay, Kent, Darrin J., Wu, Caroline, Delgado, Jessie, Hatten, Thomas Ray
• Primary Examiner(s): Sweet; Thomas J
• Assistant Examiner(s): Straszheim; Rebecca
• Application Number:
  US11/483,300
• Publication Number:
  US 20080009932A1
• Time in Patent Office: 1,915 Days
• Field of Search: 623/1.15, 623/1.16, 623/1.2, 623/1.34, 623/1.35, 623/1.42, 623/1.46, 623 217- 219
• US Class Current: 623/1.35
• 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 2/958 Inflatable balloons for placing stents or stent-grafts
• CPC Class Codes: A61F 2002/067 modular
• 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 2002/91575 connected peak to trough
• CPC Class Codes: A61F 2250/006 modular

Abstract

An improved stent design and stent delivery catheter assembly for repairing a main vessel and a side branch vessel forming a bifurcation. The stent includes rings aligned along a common longitudinal axis and connected by links, where the stent has one or more portals for aligning with and partially expanding into the opening to the side branch vessel. The stent is implanted at a bifurcation so that the main stent section is in the main vessel, and the portal section covers at least a portion of the opening to the side branch vessel. A second stent can be implanted in the side branch vessel and abut the expanded central section to provide full coverage of the bifurcated area in the main vessel and the side branch vessel. Radiopaque markers on the stent and on the tip of the delivery catheter assist in aligning the portal section with the opening to the side branch vessel.

Claims

1. A stent for treating a bifurcated vessel having a main vessel and a side branch vessel, comprising:

cylindrical body having a proximal end, a distal end, and a plurality of rings;

each ring having a delivered diameter, an implanted diameter and a plurality of peaks and a plurality of valleys, the peaks and the valleys being connected by bar arms;

each ring being attached to an adjacent ring by more than one undulating link;

a portal section comprised of one or more rings of the plurality of rings; and

at least some of the bar arms connecting the peaks and the valleys of the one or more rings in the portal section have a length that is relatively longer than the bar arms connecting the peaks and the valleys of rings in a distal section of the stent, wherein at least a portion of a ring of said portal section is nested within a ring in said distal section of the stent such that spaces between adjacent said relatively longer bar arms of said ring of said portal section are circumferentially aligned with spaces between adjacent bar arms of said ring of said distal section so that upon stent expansion the portal section will extend into the side branch vessel.

2. The stent of claim 1, wherein two undulating links connect a portal ring to the adjacent ring distal to the portal ring.

3. The stent of claim 2, wherein the two undulating links comprise undulating portions that point in a direction away from a portal area and transverse to a longitudinal axis of the stent.

4. The stent of claim 1, wherein at least two undulating links connect adjacent rings.

5. The stent of claim 1, wherein three undulating links connect adjacent rings except that two links connect a portal ring to the adjacent ring distal to the portal ring.

6. The stent of claim 1, wherein at least some of the bar arms in the one or more rings of the portal section have a width that is less than a width of the bar arms in the rings not in the portal section.

7. The stent of claim 1, wherein the stent includes a proximal end ring, each of the peaks and the valleys of the proximal end ring having a radius that is greater than a radius of each of the peaks and the valleys of all of the other rings of the stent to improve stent retention and reduce flaring.

8. The stent of claim 1, wherein the stent is formed from a metal.

9. The stent of claim 8, wherein the metal is taken from the group of metals including stainless steel, titanium, nickel-titanium, cobalt-chromium, cobalt-chromium-vanadium, cobalt-chromium-tungsten, tungsten, gold, silver, platinum, and platinum-vanadium.

10. The stent of claim 1, wherein the stent is coated with at least one layer containing a drug.

11. The stent of claim 1, wherein the stent is coated with a therapeutic agent.

12. The stent of claim 1, wherein the stent is coated with a primer material which adheres to the stent, the primer material being coated with a drug or therapeutic agent or a layer containing a drug or therapeutic agent.

13. The stent of claim 1, wherein the relatively longer bar arms connecting the peaks and the valleys of the one or more rings in the portal section are configured to move the undulating links in the portal section closer to the side branch vessel when the stent is expanded to the implanted diameter.

14. The stent of claim 1, wherein the undulating links in the portal section are substantially longer than the undulating links not in the portal section so that as the stent is expanded, the portal section will extend further into the side branch vessel.

15. The stent of claim 1, wherein the rings and undulating links have a constant radial thickness.

16. The stent of claim 1, wherein the rings and undulating links have variable radial thickness to vary the flexibility of the stent.

17. The stent of claim 1, wherein at least some of the bar arms connecting the peaks and the valleys of the rings in a proximal section have a length that is relatively longer than the bar arms connecting the peaks and the valleys of rings in the distal section of the stent.

18. The stent of claim 1, wherein the location of the portal section on the stent can vary by increasing or decreasing the number of rings in a proximal section and/or the distal section.

19. The stent of claim 1, wherein a proximal section has a proximal end ring having peaks and valleys connected by bar arms, each of the peaks, the valleys and the bar arms of the proximal end ring having width greater than a width of the peaks, the valleys and the bar arms respectively of all of the other rings of the stent.

20. The stent of claim 1, wherein the stent is formed from a bioabsorbable polymer.

21. The stent of claim 1, wherein the stent is coated with a primer material which adheres to the stent, a drug or therapeutic agent being embedded in the primer.