SLIDING RESTRAINT STENT DELIVERY SYSTEMS

• US 20090281611A1
• Filed: 05/13/2009
• Published: 11/12/2009
• Est. Priority Date: 03/02/2004
• Status: Abandoned Application

• Current Assignee: Biosensors International Group, Ltd.
• Original Assignee: CardioMind, Inc. (Biosensors International Group, Ltd.)
• Inventors: Chang, Jean C., De Beer, Nicholas C., Nikolchev, Julian, Ton, Dai T., George, William R., Becking, Frank
• Application Number:
  US12/465,484
• Publication Number:
  US 20090281611A1
• Time in Patent Office: Days
• US Class Current: 623/1.110
• 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 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61F 2002/9665 with additional retaining means

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. For such purposes, a self-expanding stent may be deployed in connection with an angioplasty procedure with a sliding restraint based delivery system adapted for simplified use. In the system, the sliding restraint is sized, in coordination with a fixed sleeve accepting a core wire to actuate the restraint to effect an anchoring function with the sleeve so that the stent is not inadvertently advanced during deployment.

Claims

1. A stenting method comprising:

selecting a stent delivery system from a plurality of such systems,

wherein each of the systems comprises a self-expanding stent and a delivery guide, the delivery guide comprising an inner member, an outer sleeve, a stent stop fixed in position relative to the outer sleeve and a distal restraint having a length slidingly disposed over the stent to hold the stent in a collapsed configuration until withdrawal of the restraint to deploy the stent,

locating the delivery system so the stent is at a treatment site, and

actuating the inner member to withdraw the restraint to release the stent for deployment at the treatment site without axial movement of the stop,

wherein a non-selected system would produce axial movement of the stop during stent deployment.

2. The method of claim 1, wherein the delivery system does not”

increase in diameter after releasing the stent.

3. The method of claim 1, wherein the treatment site is a lesion in a blood vessel or graft.

4. The method of claim 3, wherein the blood vessel or graft is in the coronary vasculature.

5. The method of claim 4, wherein the selected delivery guide has an exposed length of restraint that between about a length of the stent and about 5 cm long.

6. The method of claim 5, wherein the selected delivery guide has an exposed length of restraint that between about 5 cm and about 10 long.

7. The method of claim 5, wherein the selected delivery guide has an exposed length of restraint that between about 10 cm and about 20 cm long.

8. The method of claim 4, wherein in locating the stent, a distal end of the sleeve or an extension therefrom is located up to about 30 cm distal of the ostium.

9. The method of claim 8, wherein in locating the stent, a distal end of the sleeve or an extension therefrom is located up to about 20 cm distal of the ostium.

10. The method of claim 6, wherein in’

locating the stent, a distal end of the sleeve or an extension therefrom is located up to about 10 cm distal of the ostium.

11. The method of claim 1, wherein the selecting is between only two stent delivery systems.

12. The method of claim 1, further comprising providing the plurality of stent delivery systems.

13. The method of claim 1, further comprising advancing the delivery system through a catheter lumen having a proximal hemostatic valve, and closing the valve onto the sleeve prior to the withdrawing of the inner member.

14. The method of claim 1, wherein the treatment site is within neurovasculature.

15. The method of claim 1, wherein the treatment site is within an organ selected from the kidney and liver.

16. The method of claim 1, wherein the treatment site is within reproductive anatomy.

17. The method of claim 16, wherein the reproductive anatomy is selected from vasculature, vasdeferens and fallopian tubes.

18. The method of claim 1, wherein the treatment site is distal to tortuous anatomy, the tortuous anatomy having a diameter of less than about 3 mm over a length of at least about 5 cm.

19. The method of claim 18, wherein the diameter is less than about 2.5 mm.

20. The method of claim 19, wherein the diameter is less than about 2.0 mm.

21. The method of claim 18, wherein the length is at least 10 cm.

22. The method of claim 21, wherein the length is at least 15 cm.

23. A stenting system comprising:

a self-expanding stent;

a delivery guide member comprising an inner member, an outer sleeve, a stent stop fixed in position relative to the outer sleeve, and a distal restraint having a length slidingly disposed over the stent to hold the stent in a collapsed configuration until release,

wherein withdrawal of the inner member within the sleeve and withdrawal of the restraint or a connection to the restraint from outside of the sleeve to inside of the sleeve releases the stent, and

wherein the delivery system does not increase in diameter during or after releasing the stent.

24. The system of claim 23, wherein the delivery guide is adapted to release the stent without axial movement of the stop.

25. The system of claim 23, wherein the restraint is has an exposed length, the length adapted to avoid stiction with apposing anatomy.

26. The system of claim 23, wherein the restraint has a lubricious outer coating.

27. The system of claim 23, wherein the sleeve is adapted to grip apposing anatomy.

28. The system of claim 27, wherein the sleeve has no lubricous coating on at least a distal end.

29. The system of claim 23, further comprising a connector member between the restraint and inner member.

30. The system of claim 24, wherein the delivery guide is adapted to release the stent without axial movement of the stop when releasing the stent at a target site within a coronary artery.

31. The system of claim 23, further comprising a removable handle for actuating the inner member.

32. The system of claim 23, further comprising an atraumatic distal tip.

33. The system of claim 32, wherein a proximal end of the atraumatic distal tip abuts the stent.