Stent delivery and guidewire systems

• US 20070027522A1
• Filed: 05/22/2006
• Published: 02/01/2007
• Est. Priority Date: 06/14/2005
• Status: Abandoned Application

• Current Assignee: Biosensors International Group, Ltd.
• Original Assignee: Biosensors International Group, Ltd.
• Inventors: Pandya, Sudip, Chang, Jean
• Application Number:
  US11/439,378
• Publication Number:
  US 20070027522A1
• Time in Patent Office: Days
• US Class Current: 623/1.110
• CPC Class Codes: A61F 2/013 Distal protection devices, i.e. devices placed distally in combination with another endovascular procedure, e.g. angioplasty or stenting
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61F 2/97 the outer sleeve being splittable
• CPC Class Codes: A61F 2002/018 made from tubes or sheets of material, e.g. by etching or laser-cutting
• CPC Class Codes: A61F 2002/9665 with additional retaining means
• CPC Class Codes: A61F 2230/0067 conical

Abstract

Medical device and methods for delivery or implantation of prostheses within hollow body organs and vessels or other luminal anatomy are disclosed. The subject technologies may be used in the treatment of atherosclerosis in stenting procedures.

Claims

1. A stenting system comprising:

a self-expanding stent;

a corewire including a distal stent-receiving region, a solid raised feature on the corewire sized to abut at least a portion of the stent, and an inner sleeve and an outer sleeve set over the corewire;

wherein the corewire has a reduced distal diameter section;

wherein the inner sleeve has a proximal end located along the reduced diameter section; and

wherein the outer sleeve is adapted to restrain the stent in a compressed state.

2. The system of claim 1, wherein the distal end of the inner sleeve abuts the stent together with the raised feature.

3. The system of claim 1, wherein the distal end of the inner sleeve is proximal to the raised feature, and the raised feature is sized to abut the stent for delivery alone.

4. The system of claim 1, wherein the proximal diameter of the corewire is between about 0.009 and about 0.018 inches.

5. The system of claim 1, wherein a maximum outer diameter of the system is between about 0.018 and about 0.026 inches.

6. The system of claim 1, wherein the first and second sleeves are splittable.

7. The system of claim 6, wherein first and second sleeves are splittable up to at least about 10 cm of a distal end of each member.

8. The system of claim 6, wherein the first and second sleeves spittable along a full length of each member.

9. The system of claim 6, wherein at least a distal end of the inner sleeve is not splittable.

10. The system of claim 1, wherein the inner sleeve is pre-split.

11. The system of claim 10, wherein at least a distal end of the inner sleeve is not pre-split.

12. The system of claim 1, further comprising a filter operatively attached to the corewire at a location distal to the stent-receiving section.

13. The system of claim 11, wherein the filter comprises superelastic shape memory alloy material.

20. A method of stenting comprising:

positioning a system according to claim 1 or 14 relative to a treatment site;

delivering a stent with the system;

removing the inner and outer sleeves from the corewire; and

performing a subsequent medical procedure act with the corewire.

21. The method of claim 20, wherein the subsequent medical procedure act comprises advancing a balloon catheter over the corewire.

22. The method of claim 20, wherein the subsequent medical procedure act comprises advancing a balloon catheter over the corewire to locate a balloon across the treatment site.

23. The method of claim 22, wherein the advancing of the balloon catheter is accomplished without advancing the corewire.

24. The method of claim 22, wherein the advancing of the balloon catheter to the treatment site requires advancing the corewire.

25. The method of claim 20, wherein the removing act comprises splitting at least one of the sleeves.

26. The method of claim 20, further comprising delivering a filter with the system.

27. The method of claim 26, wherein removing the outer sleeve deploys the stent.

28. The method of claim 27, wherein the filter is deployed prior to deployment of the stent.

29. The method of claim 27, wherein the filter is deployed concurrently with deployment of the stent.

30. The method of claim 27, wherein the filter is deployed subsequent to deployment of the stent.

14. A stenting system comprising:

a self-expanding stent; and

a corewire including a distal stent-receiving region bordered by a proximal raised feature sized to abut at least a portion of the stent, and an inner sleeve and an outer sleeve set over the corewire;

wherein the inner and outer sleeves can be opened.

15. The system of claim 14, wherein at least one of the inner and outer sleeves are splittable.

16. The system of claim 15, wherein the inner member is pre-split.

17. A self-expanding stent delivery system comprising:

a corewire comprising a constant diameter distal section upon which a stent is received and a solid raised feature on the corewire sized to abut at least a portion of a received stent,

a filter mechanism attached to the distal section of the corewire; and

an outer sleeve set over the corewire wherein the outer sleeve is adapted to hold a stent and a filter in reduced states.

18. The system of claim 17, wherein the stent and the filter mechanism are self-expanding.

19. The system of claim 17, wherein the filter mechanism is positioned distally of the stent.