Systems and methods for deploying a portion of a stent using an auger-style device

• US 9,655,756 B2
• Filed: 12/13/2013
• Issued: 05/23/2017
• Est. Priority Date: 12/21/2012
• Status: Active Grant

• Current Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Inventors: LeBlanc, Johnny, Havel, William J., Vad, Siddharth
• Primary Examiner(s): Szpira, Julie A
• Application Number:
  US14/105,921
• Publication Number:
  US 20140180384A1
• Time in Patent Office: 1,257 Days
• CPC Class Codes: A61F 2/844 folded prior to deployment
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• 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 2210/0014 using shape memory or superelastic materials, e.g. nitinol

Abstract

The present embodiments provide systems and methods for deploying at least a portion of a stent. In one embodiment, the system comprises a cannula having an outer surface, and an auger having a plurality of turns coupled to the outer surface of the cannula. A stent has a portion dimensioned to be disposed within a valley of the auger. Rotation of the cannula and the auger advances the portion of the stent in a predetermined longitudinal direction.

Claims

1. A system for deploying at least a portion of a stent, the system comprising:

a cannula having an outer surface;

an auger having proximal and distal ends and a plurality of turns disposed therebetween, where the auger is coupled to the outer surface of the cannula;

a stent having a portion dimensioned to be disposed within a valley of the auger, where rotation of the cannula and the auger advances the portion of the stent in a predetermined longitudinal direction;

an enclosure encircling the auger, where the enclosure has a first end having a first outside dimeter and a second end having a second outside diameter, where the first outside diameter is larger than the second outside diameter,

where the first end of the enclosure is proximal to the second end of the enclosure, and

where the enclosure comprises a plurality of struts separated by a plurality of slots, where the portion of the stent extends through one of the plurality of slots in a delivery state.

2. The system of claim 1 where each of the plurality of struts and each of the plurality of slots are generally parallel to each other in a direction running along a longitudinal axis of the apparatus.

3. The system of claim 1 where at least one of the plurality of slots has proximal and distal regions and a width at the proximal region is greater than a width at the distal region.

4. The system of claim 3 where the stent comprises a widened securement region, where the widened securement region comprises a width that is less than a width of the proximal region of the slot and greater than a width at the distal region of the slot.

5. The system of claim 4 where the stent further comprises a proximal extension disposed adjacent to the widened securement region, where a width of the proximal extension is less than the width of the distal region of the slot.

6. The system of claim 1 where the enclosure is circumferentially rotatable relative to the cannula.

7. The system of claim 1 further comprising a distal stop member coupled to the cannula and positioned adjacent to a distal end of the enclosure, where the distal stop member allows the enclosure to rotate relative to the cannula, but prevents the enclosure from sliding distally over the cannula.

8. A system for deploying at least a portion of a stent, the system comprising:

a cannula having an outer surface;

an auger having proximal and distal ends and a plurality of turns disposed therebetween, where the auger is coupled to the outer surface of the cannula;

a stent having a portion dimensioned to be disposed within a valley of the auger, where rotation of the cannula and the auger advances the portion of the stent in a predetermined longitudinal direction,

an enclosure encircling the auger, and

an atraumatic tip coupled to the cannula, where at least a portion of the atraumatic tip is disposed beneath the enclosure, and where the enclosure can rotate circumferentially relative to the atraumatic tip and the cannula.

9. A system for deploying at least a portion of a stent, the system comprising:

a cannula having an outer surface;

an auger having proximal and distal ends and a plurality of turns disposed therebetween, where the auger is coupled to the outer surface of the cannula;

a stent having a portion dimensioned to be disposed within a valley of the auger, where rotation of the cannula and the auger advances the portion of the stent in a predetermined longitudinal direction; and

an enclosure encircling the auger, where the enclosure comprises a plurality of struts separated by a plurality of slots, and where the portion of the stent extends through one of the plurality of slots in a delivery state.

10. The system of claim 9 where at least one of the plurality of slots has proximal and distal regions and a width at the proximal region is greater than a width at the distal region.

11. The system of claim 10 where the stent comprises a widened securement region, where the widened securement region comprises a width that is less than a width of the proximal region of the slot and greater than a width at the distal region of the slot.

12. The system of claim 11 where the stent further comprises a proximal extension disposed adjacent to the widened securement region, where a width of the proximal extension is less than the width of the distal region of the slot.

13. The system of claim 9 where the enclosure is circumferentially rotatable relative to the cannula.