Retaining cage to permit resheathing of a tavi aortic-first transapical system

• US 10,524,909 B2
• Filed: 03/06/2013
• Issued: 01/07/2020
• Est. Priority Date: 10/12/2012
• Status: Active Grant

• Current Assignee: St. Jude Medical Cardiology Division Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: St. Jude Medical Cardiology Division Incorporated (Abbott Laboratories Incorporated)
• Inventors: Glazier, Valerie J.
• Primary Examiner(s): Schwiker, Katherine H
• Application Number:
  US13/787,056
• Publication Number:
  US 20140107758A1
• Time in Patent Office: 2,498 Days
• Field of Search: 623 111, 623 112, 623 119, 606108-110, 606113, 606194, 606198, 604104-107
• CPC Class Codes: A61F 2/2436 Deployment by retracting a sheath
• CPC Class Codes: A61F 2/9661 the proximal portion of the stent or stent-graft is released first
• CPC Class Codes: A61F 2002/9534 for repositioning of stents
• CPC Class Codes: A61F 2002/9665 with additional retaining means

Abstract

A delivery device for an implantable medical device includes an inner shaft extending in a longitudinal direction and an outer shaft surrounding at least a longitudinal portion of the inner shaft. The outer shaft is slidable relative to the inner shaft in the longitudinal direction. A sheath surrounds a longitudinal portion of the outer shaft, the sheath having an outer diameter and being slidable in the longitudinal direction between a first position enclosing the medical device and a second position exposing the medical device to permit full functionality of the medical device. A retaining cage is coupled to the outer shaft, the retaining cage being configured and arrange to collapse the medical device during resheathing.

Claims

1. A medical device implantation system comprising:

(a) a shaft extending in longitudinal directions;

(b) a medical device including a self-expanding stent disposed over an outer surface of the shaft and surrounding the shaft, the stent being expandable in radially outward directions transverse to the longitudinal directions;

(c) a sheath surrounding the shaft, the sheath being slidable relative to the shaft in a first longitudinal direction from a closed position in which the sheath surrounds the stent to an open position in which the sheath is longitudinally offset from the stent and in a second longitudinal direction from the open position towards the closed position;

(d) a cage including a plurality of fingers, each finger having a first end attached to the shaft and extending in the second longitudinal direction from the first end to a second end, each finger having an engagement section extending radially outwardly of the stent over at least a portion of the stent adjacent the first end of the finger when the stent is in a collapsed condition, the engagement section of each finger being movable away from the shaft during expansion of the stent and being movable toward the shaft responsive to movement of the sheath relative to the shaft in the second longitudinal direction so that the stent can be collapsed by moving the sheath in the second longitudinal direction;

(e) a distal cap slidable relative to the shaft and having indentations for receiving the second ends of the plurality of fingers; and

(f) an inner core disposed within the shaft and translatable relative thereto, the distal cap being coupled to the inner core, the inner core being movable from an initial position at which the distal cap directly abuts a free end of the shaft and the second ends of the plurality of fingers are received in the indentations of the distal cap, to a release position at which the distal cap is spaced from the free end of the shaft and the second ends of the plurality of fingers are withdrawn from the indentations,

wherein in an intermediate configuration of the system, the sheath is in the open position, the distal cap directly abuts the free end of the shaft, the first ends of the plurality of fingers are attached to the shaft, the second ends of the plurality of fingers are received in the indentations of the distal cap, and the stent is in an expanded condition.

2. A system as claimed in claim 1 wherein the shaft has a trailing end and a leading end, the first longitudinal direction is a rearward direction toward the trailing end of the shaft, and the second longitudinal direction is a forward direction toward the leading end of the shaft.

3. A system as claimed in claim 2 wherein the second ends are remote from the first ends and wherein the second ends of the plurality of fingers are free from the shaft when the stent is in a fully-expanded condition so that when the stent is in the fully-expanded condition and engaged with the body of a subject, the plurality of fingers can be disengaged from the stent by retracting the shaft rearwardly relative the body of the subject.

4. A system as claimed in claim 1 wherein the plurality of fingers are formed of a shape-memory alloy capable of expanding when the sheath is retracted.

5. A system as claimed in claim 4 wherein the plurality of fingers are formed of nitinol.

6. A system as claimed in claim 1 wherein the plurality of fingers are interwoven with the stent when the sheath is in the open position.

7. A system as claimed in claim 1 further comprising a handle coupled to the shaft and the sheath, the handle being capable of actuating the shaft and the sheath independently.

8. A system as claimed in claim 1 wherein the medical device is a prosthetic heart valve.

9. A system as claimed in claim 1 wherein the system is sized for transapical delivery.

10. The system as claimed in claim 1 wherein the distal cap in the initial position encloses an open end of the sheath.

11. A medical device implantation system comprising:

(a) a shaft extending in longitudinal directions;

(b) a medical device including a self-expanding stent disposed over an outer surface of the shaft and surrounding the shaft, the stent being expandable in radially outward directions transverse to the longitudinal directions;

(c) a sheath surrounding the shaft, the sheath being slidable relative to the shaft in a first longitudinal direction from a closed position in which the sheath surrounds the stent to an open position in which the sheath is longitudinally offset from the stent and in a second longitudinal direction from the open position towards the closed position;

(d) a retaining cage coupled to the shaft, the retaining cage being configured and arranged to collapse the stent by moving the sheath relative to the shaft in the second longitudinal direction from the open position to the closed position, the retaining cage including a plurality of fingers, each finger having a first end attached to the shaft and extending in the second longitudinal direction from the first end to a second end;

(e) an inner core disposed within the shaft and translatable relative thereto; and

(f) a distal cap having indentations for receiving the second ends of the plurality of fingers, the distal cap being coupled to the inner core, the inner core being movable from an initial position at which the distal cap directly abuts a free end of the shaft and the second ends of the plurality of fingers are received in the indentations of the distal cap, to a release position at which the distal cap is spaced from the free end of the shaft and the second ends of the plurality of fingers are withdrawn from the indentations,

wherein in an intermediate configuration of the system, the sheath is in the open position, the distal cap directly abuts the free end of the shaft, the first ends of the plurality of fingers are attached to the shaft, the second ends of the plurality of fingers are received in the indentations of the distal cap, and the stent is in an expanded condition.

12. A system as claimed in claim 11 wherein the shaft has a trailing end and a leading end, the first longitudinal direction is a rearward direction toward the trailing end of the shaft, and the second longitudinal direction is a forward direction toward the leading end of the shaft.

13. A system as claimed in claim 11 wherein the system is sized for transapical delivery of a heart valve.

14. A method of delivering an implantable medical device, comprising:

(a) advancing a delivery system to a target location in the body of a subject, the delivery system including a delivery apparatus having (i) a shaft extending in first and second longitudinal directions, (ii) a medical device including a self-expanding stent in a collapsed condition surrounding the shaft, (iii) a cage including longitudinally-extending fingers having first ends attached to the shaft, engagement sections disposed outwardly of the stent, and second ends, (iv) a sheath in a closed position in which the sheath surrounds the stent and the fingers, (v) an inner core disposed within the shaft and translatable relative thereto, and (vi) a cap coupled to the inner core, the cap having a plurality of indentations and the second ends of the fingers being disposed in the indentations of the cap when the inner core is in an initial position at which the cap directly abuts a free end of the shaft;

(b) moving the sheath relative to the shaft in the first longitudinal direction from the closed position to an open position in which the sheath is longitudinally offset from the stent; and

(c) expanding the stent until the stent is at least partially engaged with the body of the subject when the distal cap directly abuts the free end of the shaft, the first ends of the fingers are attached to the shaft and the second ends of the fingers are received in the indentations of the distal;

the engagement sections of the fingers are displaced radially outwardly by the expanding of the stent; and

(d) moving the inner core to a release position at which the cap is spaced from the free end of the shaft and the second ends of the fingers are withdrawn from the indentations of the cap; and

(e) releasing the medical device from the cage and withdrawing the delivery apparatus from the body of the subject,

wherein the step of expanding the stent occurs before the step of moving the inner core.

15. The method of claim 14, further comprising evaluating positioning or functionality of the medical device after the expanding the stent step and prior to releasing the medical device from the cage.

16. The method of claim 15 further comprising a step of displacing the engagement sections of the fingers radially inwardly to at least partially collapse the stent.

17. The method of claim 16 wherein the step of displacing the engagement sections of the fingers radially inwardly includes moving the sheath relative to the shaft in the second longitudinal direction.

18. The method of claim 16, wherein, prior to the expanding the stent step, the fingers have sections extending through openings in the stent and the step of releasing the medical device from the cage includes untwining the fingers from the stent.

19. The method of claim 14, wherein the step of releasing the medical device from the cage comprises moving the shaft and the fingers in the first longitudinal direction relative to the body of the subject.

20. The method of claim 14, wherein the medical device is a prosthetic aortic valve and the target location is at or adjacent the native aortic valve.

21. The method of claim 20 wherein the advancing step includes advancing the delivery system through the left ventricle to the target location, and wherein the step of moving the sheath relative to the shaft in the first longitudinal direction includes moving the sheath from the target location toward the left ventricle.