Retrievable stent system

Patent metadata

Field	Value
Publication number	US-11596535-B2
Application number	US-202016863161-A
Country	US
Kind code	B2
Filing date	Apr 30, 2020
Priority date	Mar 28, 2017
Publication date	Mar 7, 2023
Grant date	Mar 7, 2023

Abstract

A system for treating a body lumen including a first stent configured to be positioned in a body lumen and a second stent configured to be positioned in the lumen of the first stent prior to removing the first stent from the body lumen. The first stent includes a liner disposed radially inward of the tubular scaffold of the first stent to permit tissue ingrowth within a tissue ingrowth region defined between the liner and the tubular scaffold. The retrieval stent is configured to be expanded within the previously implanted first stent to cause tissue to recede from the tissue ingrowth region to facilitate removal of the first stent from the body lumen.

First claim

What is claimed is:

1. A method of treating a body lumen, the method comprising:
advancing a retrieval stent into the lumen of an implanted stent disposed along an inner surface of the body lumen, wherein a portion of tissue defining the inner surface of the body lumen has grown into the implanted stent, and wherein the implanted stent includes:
a liner disposed within the lumen of the implanted stent, wherein the liner is configured to be radially spaced from a medial region of the implanted stent to define a tissue ingrowth region along a portion of the implanted stent;

deploying the retrieval stent within the lumen of the implanted stent, wherein an outer surface of the retrieval stent exerts an outward radial force along the ingrown tissue region of the implanted stent, and wherein the retrieval stent causes the ingrown tissue to recede.

2. The method of claim 1 , wherein the outer surface of the retrieval stent is defined by a polymeric covering.

3. The method of claim 2 , wherein the retrieval stent includes a radially expandable scaffold and the polymeric covering extends across interstices of the radially expandable scaffold.

4. The method of claim 3 , wherein the radially expandable scaffold is self-expandable.

5. The method of claim 4 , wherein the radially expandable scaffold includes a first end region and a second end region, wherein the tissue ingrowth region extends between the first end region and the second end region.

6. The method of claim 5 , wherein the liner is in direct contact with the first and second end regions, thereby preventing tissue ingrowth along the first and second end regions.

7. The method of claim 5 , wherein the liner extends from the first end region to the second end region.

8. The method of claim 5 , wherein the medial region has a diameter, and the first and second end regions have a diameter greater than the diameter of the medial region.

9. The method of claim 5 , wherein a first end portion of the liner forms an outer layer disposed radially outward of an outer surface of the first end region, and a second end portion of the liner forms an outer layer disposed radially outward of an outer surface of the second end region.

10. The method of claim 1 , wherein deploying the retrieval stent within the lumen of the implanted stent includes placing the retrieval stent through the lumen of the implanted stent such that the retrieval stent spans an entire length of the tissue ingrowth region.

11. The method of claim 1 , further comprising:
extracting the implanted stent with the retrieval stent from the body lumen.

12. The method of claim 11 , wherein extracting the implanted stent with the retrieval stent includes radially constraining a proximal end of the implanted stent.

13. The method of claim 12 , wherein radially constraining the proximal end of the implanted stent includes grasping the proximal end of the implanted stent with a retrieval device.

14. The method of claim 11 , wherein the step of extracting the implanted stent is performed within 2 weeks or less after deploying the retrieval stent within the lumen of the implanted stent.

15. The method of claim 11 , wherein the step of extracting the implanted stent is performed between 7 days and 14 days after deploying the retrieval stent within the lumen of the implanted stent.

16. The method of claim 1 , wherein deploying the retrieval stent within the lumen of the implanted stent pushes a medial region of the liner radially outward toward the implanted stent.

17. The method of claim 1 , wherein the tissue ingrowth region includes at least two circumferential tissue ingrowth regions spaced-apart longitudinally along the medial region of the implanted stent.

18. A system for treating a body lumen, comprising:
a first stent including:
a first tubular scaffold, the first tubular scaffold including an inner surface, an outer surface, a first end region, a second end region, a medial region extending between the first end region and the second end region, and a lumen extending from the first end region to the second end region; and
a liner disposed within the lumen of the first tubular scaffold, wherein first regions of the inner surface of the first tubular scaffold are in direct contact with first portions of the liner, thereby preventing tissue ingrowth, and second regions of the inner surface of the first tubular scaffold are spaced-apart from the liner thereby defining tissue ingrowth regions; and

a second stent including:
a second tubular scaffold and a covering disposed on the second tubular scaffold;

wherein the second stent is configured to be positioned within the first stent such that expansion of the second stent causes the tissue ingrowth to recede.

19. The system of claim 18 , wherein the first portions of the liner are secured to the inner surface of the first tubular scaffold at a plurality of spaced-apart discrete attachment points.

20. The system of claim 19 , wherein regions of the liner between the plurality of spaced-apart discrete attachment points are radially spaced from the inner surface of the first tubular scaffold, creating the tissue ingrowth regions.

Assignees

• Boston Scient Scimed Inc

Inventors

• Folan Martyn G
• Keating Thomas M

Classifications

• A61F2250/0063

  Nested prosthetic parts · CPC title

• A61F2/852 Primary

  Two or more distinct overlapping stents · CPC title

• A61F2210/0076

  multilayered, e.g. laminated structures · CPC title

• A61F2/04 Primary

  Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts (A61F2/18, A61F2/20 take precedence; instruments specially adapted for placement or removal of stents or stent-grafts A61F2/95) · CPC title

• A61F2220/0025

  Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements · CPC title