IP Library Granted Patent US 9,468,548
Granted Patent B2
US 9,468,548 · App. 13/639,100 · Granted Oct 18, 2016

Systems and methods for delivering a stent to a body lumen

Inventors: David Slattery (Co Galway, IE); Michael Gilmore (Co Galway, IE); Aemon Curley (Co Galway, IE); Damian Kelly (Co Galway, IE)
Assignee: CAPPELLA, INC.
A61F2/97A61F2/958A61F2002/9583
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Quick Facts
Patent No.
US 9,468,548
App. No.
13/639,100
Granted
Oct 18, 2016
Kind
B2
Abstract

A stent delivery system configured to deliver a stent to a target region of a body lumen may include a catheter; a stent associated with the catheter, the stent having a first region and a second region; a balloon associated with the catheter, the balloon having a first balloon portion associated with the catheter proximate the first region of the stent and a second balloon portion associated with the catheter proximate the second region of the stent; and a sheath about the stent and the balloon, the sheath maintaining the stent in an undeployed configuration for delivery to a target region of a body lumen. The sheath may comprise a first sheath region configured to split at a first pressure thereby permitting the first region of the stent to assume a deployed configuration, a second sheath region configured to split at a second pressure thereby permitting the second region of the stent to assume a deployed configuration, the second pressure being greater than the first pressure and the first pressure being insufficient to cause the second region of the sheath to split, a split-stopping structure between the first and second sheath regions, the split-stopping structure being configured to prevent a split from propagating from the first sheath region to the second sheath region at the first pressure.

Claims (39)

1. Method for delivering a stent to a target region of a body lumen, the method comprising:

positioning a stent delivery system at the target region of the body lumen, the delivery system comprising a stent associated with a balloon catheter and a sheath maintaining the stent in an undeployed configuration;

inflating a first balloon portion to a first pressure so as to cause the sheath to split at a first region of the sheath, the first balloon portion being proximate a first region of the stent, said splitting of the first region of the sheath permitting the first region of the stent to expand to a deployed configuration;

preventing propagation of the split from the first region of the sheath to a second region of the sheath at the first pressure with a split-stopping structure of the sheath, said split-stopping structure being between the first and second regions of the sheath; and

inflating a second balloon portion to a second pressure so as to cause the sheath to split at the second region of the sheath until the split at the second region of the sheath reaches the split-stopping structure of the sheath, the second pressure being greater than the first pressure and the first pressure being insufficient to cause the second region of the sheath to split, the second balloon portion being proximate a second region of the stent, said splitting of the second region of the sheath permitting the second region of the stent to expand to a deployed configuration.

2. The method of claim 1 , wherein the step of inflating the first balloon portion causes a proximal end of the sheath to split.

3. The method of claim 2 , wherein the proximal end of the sheath splits along a pre-formed slit.

4. The method of claim 1 , wherein the step of inflating the first balloon portion causes a distal end of the sheath to split.

5. The method of claim 4 , wherein the distal end of the sheath splits along a pre-formed slit.

6. The method of claim 1 , wherein said first balloon portion has at least one of greater compliance and greater diameter relative to the second balloon portion.

7. The method of claim 6 , wherein the first and second balloon portions comprise separate balloons.

8. The method of claim 7 , wherein the first balloon portion and the second balloon portion each has its own inflating assembly.

9. The method of claim 6 , wherein the first balloon portion and the second balloon portion comprise a single balloon structure.

10. The method of claim 1 , further comprising removing the catheter and the sheath from the body lumen.

11. A stent delivery system configured to deliver a stent to a target region of a body lumen, the system comprising:

a catheter, the catheter including a balloon at its distal end;

a stent associated with the catheter about the balloon, the stent having a first region and a second region; and

a sheath about the stent and the balloon, the sheath maintaining the stent in an undeployed configuration for delivery to a target region of a body lumen, the sheath comprising

a first sheath region configured to split at a first pressure thereby permitting the first region of the stent to assume a deployed configuration,

a second sheath region configured to split at a second pressure thereby permitting the second region of the stent to assume a deployed configuration, the second pressure being greater than the first pressure and the first pressure being insufficient to cause the second region of the sheath to split, and

a split-stopping structure between the first and second sheath regions, the split-stopping structure being configured to prevent a split from propagating from the first sheath region to the second sheath region at the first pressure, the split-stopping structure comprising a region having a modified orientation of polymer molecules relative to the first and second sheath regions.

12. The system of claim 11 , wherein the balloon has a first balloon portion proximate the first region of the stent and a second balloon portion proximate the second region of the stent.

13. The system of claim 12 , wherein the first balloon portion is configured to inflate at the first pressure and the second balloon portion is configured to inflate at the second pressure, the second pressure being greater than the first pressure.

14. The system of claim 12 , wherein said first balloon portion has at least one of greater compliance and greater diameter relative to the second balloon portion.

15. The system of claim 14 , wherein the first and second balloon portions comprise separate balloons.

16. The system of claim 15 , wherein the first balloon portion and the second balloon portion each has its own inflating assembly.

17. The system of claim 14 , wherein the first balloon portion and the second balloon portion comprise a single balloon.

18. The system of claim 12 , wherein the first sheath region comprises a proximal end of the sheath configured to split distally when the first balloon portion is inflated to the first pressure until the split reaches the split-stopping structure of the sheath.

19. The system of claim 18 , wherein the second sheath region comprises a distal end of the sheath configured to split proximally when the second balloon portion is inflated to the second pressure at least until the split reaches the split-stopping structure of the sheath.

20. The system of claim 12 , wherein the first sheath region comprises a distal end of the sheath being configured to split proximally when the first balloon portion is inflated until the split reaches the split-stopping structure of the sheath.

21. The system of claim 20 , wherein the second sheath region comprises a proximal end of the sheath configured to split distally when the second balloon portion is inflated to the second pressure at least until the split reaches the split-stopping structure of the sheath.

22. The system of claim 11 , wherein the split-stopping structure comprises a pre-formed aperture in the sheath.

23. The system of claim 11 , wherein the split-stopping structure comprises a circumferential band having a thickened cross-section.

24. The system of claim 11 , wherein the catheter and the sheath are configured to be removed from a patient's cardiovascular system after the stent achieves a deployed configuration.

25. The system of claim 11 , wherein the difference between the second pressure and the first pressure is a measurable difference.

26. The system of claim 25 , wherein the difference between the second pressure and the first pressure is at least 1 atmosphere.

27. The system of claim 11 , wherein the first pressure is about 3 to 4 atmospheres, and the second pressure is about 8 to 10 atmospheres.

28. The system of claim 11 , wherein at least one of the first region of the sheath and the second region of the sheath has a pre-formed slit.

29. The system of claim 11 , wherein a deployed configuration of the stent comprises the first region of the stent having a flared geometry and the second region of the stent having a substantially cylindrical geometry.

Assignments (8)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME PREVIOUSLY RECORDED AT REEL: 046597 FRAME: 0185. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Sep 10, 2018
From: CAPPELLA, INC.
To: MERIT MEDICAL IRELAND LIMITED
Reel/Frame 047044/0988 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 9, 2018
From: CAPPELLA, INC.
To: MERIT MEDICAL IRELAND LIMITED INCORPORATED
Reel/Frame 046597/0185 →
SECURITY INTEREST Recorded Jul 21, 2017
From: CAPPELLA INC.
To: ACT VENTURE CAPITAL LIMITED; PIERRE HOCHULI
Reel/Frame 043069/0894 →
PARTIAL RELEASE Recorded Jul 16, 2014
From: KREOS CAPITAL III (UK) LIMITED; SILICON VALLEY BANK
To: CAPPELLA, INC.
Reel/Frame 033332/0104 →
LICENSE Recorded Jun 24, 2014
From: CAPPELLA, INC.
To: CAPPELLA PEEL AWAY INC.
Reel/Frame 033166/0930 →
LICENSE Recorded May 14, 2014
From: CAPPELLA, INC.
To: CAPPELLA PEEL AWAY INC.
Reel/Frame 032887/0941 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2013
From: SLATTERY, DAVID; GILMORE, MICHAEL; CURLEY, AEMON; KELLY, DAMIAN
To: CAPPELLA, INC.
Reel/Frame 030452/0185 →
SECOND AMENDMENT TO IPSA Recorded Mar 25, 2013
From: CAPPELLA, INC.; KREOS CAPITAL III (UK) LIMITED
To: SILICON VALLEY BANK
Reel/Frame 030081/0320 →
Continuity (2)
Provisional Application 61320690 · Apr 2, 2010
Related Publication 20130226279A1 · Aug 29, 2013