Flexible embolic device delivery system

• US 7,651,513 B2
• Filed: 04/03/2003
• Issued: 01/26/2010
• Est. Priority Date: 04/03/2003
• Status: Active Grant

• Current Assignee: Stryker European Operations Holdings, LLC (Stryker Corporation)
• Original Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Inventors: Teoh, Clifford, Porter, Stephen C., Wallace, Michael, Jaeger, Kevin M.
• Primary Examiner(s): Nguyen; Ahntuan T
• Assistant Examiner(s): SONNETT, KATHLEEN C
• Application Number:
  US10/407,295
• Publication Number:
  US 20040199175A1
• Time in Patent Office: 2,490 Days
• Field of Search: 606/113, 606/127, 606191-200, 606/119, 606/108, 623 111- 154, 623/23.72, 128/897, 128/898
• US Class Current: 606/200
• CPC Class Codes: A61B 17/12022 Occluding by internal devices, e.g. balloons or releasable wires plugging an opening in the wall of an organ A61B17/0057; occluders for the cervical canal A61F6/146; vas deferens occluders A61F6/20
• CPC Class Codes: A61B 17/12113 within an aneurysm
• CPC Class Codes: A61B 17/12154 having stretch limiting means
• CPC Class Codes: A61B 2017/00862 elastic or resilient
• CPC Class Codes: A61B 2017/00867 shape memory effect
• CPC Class Codes: A61B 2017/1205 Introduction devices
• CPC Class Codes: A61B 2017/12063 electrolytically detachable

Abstract

The present invention provides an embolic assembly delivery apparatus having superior flexibility characteristics at its distal end, that is, at the point of attachment of the embolic assembly to the delivery apparatus. It also provides a method of using the apparatus to deliver an embolic assembly to a target site in a patient'"'"'s body.

Claims

1. A device for releasing an embolic assembly at a target site in a vessel of a patient, comprising:

a core wire comprising a first electrically-conductive substance that is at least partially fixedly encased in a first non-conductive substance and has a proximal and a distal end, its proximal end being configured to be connected to an electrical signal generator;

a flexible member configured for permanent attachment to the core wire, the flexible member having a proximal and a distal end, its proximal end being coupled to the distal end of the core wire, the flexible member comprising a second wire comprising a second electrically-conductive substance, which may be the same as, or different than, the first electrically-conductive substance, the second wire having a helical coil segment fixedly coupled to the distal end of the core wire and being fixedly encased in the first non-conductive substance, and a straight segment located distal to the helical coil segment, at least a portion of the straight segment comprises a bare comprising an electrolytic detachment site;

an electrically conductive, helically-wound wire fixedly secured to the bare portion of the straight segment, wherein a distal portion of the electrically conductive, helically-wound wire is embedded in a polymeric mass;

an embolic assembly having a proximal and a distal end, its proximal end being embedded in the polymeric mass, the polymeric mass coupling the electrically conductive, helically-wound wire to the proximal end of the embolic assembly; and

wherein the helically wound segment of the second wire comprises a first and a second helically wound portion, the first portion being one of open-pitched or closed-pitched and the second portion being the other of open-pitched or closed-pitch, the first portion being at least partially fixedly encased in the first non-conductive substance and being coupled to the distal end of the core wire, the second portion optionally being partially encased in the first non-conductive substance and distal to the first portion and coupled to the straight segment.

2. The device of claim 1, wherein the electrically conductive, helically-wound wire fixedly secured to the bare portion of the straight segment is, along with the proximal end of the embolic assembly, encased in a non-conductive substance that may be the same as, or different than, the first non-conductive substance.

3. The device of claim 1, wherein the first portion of the helically wound segment is open-pitched and the second portion is closed-pitched.

4. The device of claim 1, wherein the second portion of the helically-wound segment is at least partially surface-coated with a second non-conductive substance, which may be the same as, or different from, the first non-conductive substance.

5. The device of claim 1, wherein:

the core wire comprises stainless steel or nitinol;

the first non-conductive substance comprises a first non-conductive polymer;

the second wire independently comprises stainless steel or nitinol; and

,

the electrically conductive, helically-wound wire fixedly secured to the bare portion of the straight segment comprises a platinum-tungsten alloy.

6. The device of claim 1, further comprising a non-conductive bushing at a distal end of the first non-conductive substance, the bushing having a lumen through which the distal end of the core wire, or the distal end of a flexible member, passes.

7. The device of claim 1, wherein the target site is selected from the group consisting of an aneurysm, an arteriovenous malformation, a fistula, a blood vessel or any other body lumen.

8. The device of claim 1, wherein the first portion of the helically wound segment is closed-pitched and the second portion is open-pitched.

9. The device of claim 1, further comprising a stretch resistant member having a first end and a second end, the first end being fixedly coupled to the distal end of the core wire and the second end being fixedly coupled to the flexible member.

10. A method for releasing an embolic assembly at a target site in a patient'"'"'s body, comprising:

providing a delivery member capable of positioning a core wire in close proximity to a target site, the delivery member comprising a first elongate tube having a proximal end, a distal end and an axial lumen;

providing a core wire slidably disposed within the axial lumen, the wire comprising a first electrically-conductive substance that is at least partially fixedly encased in a first non-conductive substance and has a proximal and a distal end, its proximal end being configured to be connected to an electrical signal generator;

providing a flexible member configured for permanent attachment to the core wire, the flexible member comprising a second wire formed from a second electrically-conductive substance, which may be the same as, or different than, the first electrically-conductive substance, the second wire having a helical coil segment comprising first and second helically wound portions, the first portion being one of open-pitched or closed-pitched and the second portion being the other of open-pitched or closed-pitch, the first portion being at least partially fixedly encased in the first non-conductive substance and being coupled to the distal end of the core wire, the second portion optionally being partially encased in the first non-conductive substance, the second portion being distal to the first portion, the flexible member further comprising a straight segment located distal to the helical coil segment, at least a portion of the straight segment being bare and comprising an electrolytic detachment site;

providing an electrically conductive, helically-wound wire fixedly secured to the bare portion of the straight segment, wherein a distal portion of the electrically conductive, helically-wound wire is embedded in a polymeric mass;

providing an embolic assembly having a proximal and a distal end, its proximal end being embedded in the polymeric mass, the polymeric mass coupling the electrically conductive, helically-wound wire to the proximal end of the embolic assembly; and

,

moving the delivery member to a position in close proximity to the target site;

sliding the core wire through the lumen of the delivery member until the embolic assembly is at or in the target site; and

,

sending an electrical signal to the electrolytic detachment site which results in release of the embolic assembly.

11. The method of claim 10, wherein the first portion of the helically wound segment is open-pitched and the second portion is closed-pitched.

12. The method of claim 10, wherein the second portion of the helically-wound segment is at least partially surface-coated with a second non-conductive substance, which may be the same as, or different from the first non-conductive substance.

13. The method of claim 10, further comprising a stretch resistant member having a first and a second end, the first end being fixedly coupled to the distal end of the core wire and the second end being fixedly coupled to the flexible member.

14. The method of claim 10, further comprising a non-conductive bushing coupled to a distal end of the first non-conductive substance and having a lumen through which the distal end of the core wire, or the distal end of the flexible member, passes.

15. The method of claim 10, wherein the target site is selected from the group consisting of an aneurysm, an arteriovenous malformation, a fistula, a blood vessel or any other body lumen.

16. The method of claim 10, wherein the first portion of the helically wound segment is closed-pitched and the second portion is open-pitched.