Indirect-release electrolytic implant delivery systems

• US 7,862,602 B2
• Filed: 12/20/2005
• Issued: 01/04/2011
• Est. Priority Date: 11/02/2005
• Status: Active Grant

• Current Assignee: Biosensors International Group, Ltd.
• Original Assignee: Biosensors International Group, Ltd.
• Inventors: Licata, David, Pandya, Sudip R.
• Primary Examiner(s): Ho; (Jackie) Tan-Uyen T
• Assistant Examiner(s): Dornbusch; Dianne
• Application Number:
  US11/314,151
• Publication Number:
  US 20070100415A1
• Time in Patent Office: 1,841 Days
• Field of Search: 606/108, 606/191, 606/194, 606/192, 606/198, 623/1.11, 623/1.12, 623/1.23, 295/08, 295/15, 295/16, 724/02, 72/64, 72/65, 723/71
• US Class Current: 623/1.11
• CPC Class Codes: A61F 2/88 the wire-like elements formed as helical or spiral coils forming a net-like or mesh-like structure A61F2/90
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61F 2/9522 Means for mounting a stent or stent-graft onto or into a placement instrument
• CPC Class Codes: A61F 2002/9505 having retaining means other than an outer sleeve, e.g. male-female connector between stent and instrument
• CPC Class Codes: A61F 2002/9511 the retaining means being filaments or wires
• CPC Class Codes: A61F 2250/0071 breakable or frangible

Abstract

Medical devices 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 or be used in variety of other procedures. The systems may employ a self expanding stent restrained by one or more members released by an electrolytically erodable latch. Such release means do not connect directly to the implant, though one or more portions may contact it.

Claims

1. A method of loading a self-expanding stent onto a delivery guide, the method comprising:

providing a closed cell, self-expanding stent having a near end, a far end, a radially expanded configuration when unconstrained, and a compressed and lengthened configuration when radially constrained;

placing the stent in at least one sleeve member to radially constrain the stent in said compressed and lengthened configuration;

twisting the stent while the stent is in the sleeve member by rotating at least one end of the stent relative to the other;

releasably securing the twisted stent to the delivery guide so that it can radially expand when released, wherein the stent is twisted prior to securing an end of the stent to the delivery guide; and

removing the at least one sleeve member from over the stent to leave the stent on the delivery guide prior to deployment.

2. The method of claim 1, further comprising compressing the stent prior to placing the stent into the at least one sleeve member.

3. The method of claim 2, wherein the twisting is done from only one end.

4. The method of claim 3, further comprising holding the stent end not being twisted stationary relative to the delivery guide.

5. The method of claim 1, wherein the stent is placed on the delivery guide prior to being twisted.

6. The method of claim 5, wherein placing the stent comprises seating the ends of the stent on the delivery guide.

7. The method of claim 1, wherein the twisting is done from both ends.

8. The method of claim 1, wherein placing the stent in at least one sleeve member comprises placing the stent in a plurality of sleeve members that hold the stent.

9. The method of claim 8, wherein the stent is twisted by rotating one sleeve member relative to another.

10. The method of claim 8, further comprising bulging the stent by axially manipulating one sleeve member relative to another.

11. The method of claim 1, wherein the twisting comprises twisting the stent a plurality of twists.

12. The method of claim 1, wherein the stent is compressed within the sleeve member(s) to within about 33% of a final diameter of the stent.

13. The method of claim 12, wherein the stent is compressed to within about 25% of a final diameter of the stent prior to said twisting the stent.

14. The method of claim 12, wherein the stent is compressed to within about 10% of a final diameter of the stent prior to said twisting the stent.

15. The method of claim 1, wherein removing the at least one sleeve member is performed in the operating room prior to using the delivery guide to deliver the stent.

16. The method of claim 1, wherein removing the at least one sleeve member is performed during fabrication of a stent delivery system.

17. The method of claim 1, wherein each closed cell comprises a plurality of struts including a first pair of axially adjacent and interconnected struts and a second pair of axially adjacent and interconnected struts, one strut of the first pair being directly connected to one strut of the second pair through a strut junction.

18. The method of claim 1, wherein each closed cell consists of four interconnected struts.

19. The method of claim 1, wherein twisting the stent further compresses the stent.

20. The method of claim 1, wherein securing the ends of the stent comprises seating projections on the end(s) of the stent with seat features on the delivery guide to prevent rotation thereof.

21. The method of claim 20, wherein twisting the stent comprises rotating one of the seat features and securing comprises securing the rotated seat feature to prevent rotation thereof.

22. The method of claim 20, wherein twisting the stent comprises rotating both seat features and securing comprises securing the seat features to prevent rotation thereof.

23. The method of claim 1, wherein the sleeve the at least one sleeve member is removed after the stent is releasably secured to the delivery guide.