ANASTOMOSIS STENT

• US 20110118765A1
• Filed: 11/11/2010
• Published: 05/19/2011
• Est. Priority Date: 11/18/2009
• Status: Abandoned Application

• Current Assignee: Wilson-Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Wilson-Cook Medical Incorporated (Cook Group Incorporated)
• Inventors: Aguirre, Andres F.
• Application Number:
  US12/944,236
• Publication Number:
  US 20110118765A1
• Time in Patent Office: Days
• US Class Current: 606/153
• CPC Class Codes: A61B 17/1114 of the digestive tract, e.g. bowels or oesophagus
• CPC Class Codes: A61B 2017/00278 Transorgan operations, e.g. transgastric
• CPC Class Codes: A61B 2017/00818 Treatment of the gastro-intestinal system
• CPC Class Codes: A61B 2017/00867 shape memory effect for prostheses A61F2210/0014
• CPC Class Codes: A61B 2017/1139 Side-to-side connections, e.g. shunt or X-connections

Abstract

A stent made of single nitinol wire or other biocompatible material having shape memory properties may be configured to define a flower-like configuration generally providing a proximal plane and a distal plane, each generally centered around a generally cylindrical passage and configured for maintaining patency of an anastomosis or other opening. The wire or other biocompatible material may include a shroud or other covering and may also include one or more loops configured to allow relatively secure engagement of sutures. Methods of deployment are also provided.

Claims

1. A medical stent device, comprising:

a biocompatible shape memory material formed as a continuous unitary wire structure including a first plurality of arches defining a first plane, a second plurality of arches defining a second plane spaced apart from the first plane, and a third plurality of arches connecting the first and second plurality of arches;

wherein the third plurality of arches is generally transverse relative to the first and second plurality of arches, and apical portions of the third plurality of arches define a generally cylindrical opening around which the first, second, and third pluralities of arches are generally centered.

2. The device of claim 1, further comprising a multiband ligator cap.

3. The device of claim 1, comprising a deployment configuration wherein apical portions of the first plurality of arches, opposite the third plurality of arches, are unconstrained within a generally cylindrical space having a second diameter that is less than a first diameter defined by the apical portions of the second plurality of arches when said apical portions of the first plurality of arches are maximally separated from each other.

4. The device of claim 3, wherein the biocompatible shape memory material comprises a pre-set shape configured with the apical portions of the first plurality of arches maximally separated from each other.

5. The device of claim 3, wherein the first diameter defined by the first plurality of arches when said apical portions of the first plurality of arches are maximally separated from each other is less than a third diameter defined by the second plurality of arches when said apical portions of the second plurality of arches are maximally separated from each other.

6. The device of claim 4, wherein the first plane is formed when the apical portions of the first plurality of arches are maximally separated from each other, and the first plane comprises a curved plane.

7. The device of claim 1, further comprising a covering across an inner portion of at least one of the first plurality of arches, one of the second plurality of arches, or any combination thereof.

8. The device of claim 7, wherein the covering comprises a biocompatible fabric.

9. The device of claim 1, further comprising a covering between adjacent ones of the first plurality of arches, adjacent ones of the second plurality of arches, or any combination thereof.

10. The device of claim 1, wherein the first plurality of arches includes at least three arches.

11. The device of claim 1, further comprising a circumferential constraining structure configured to constrain at least one of the plurality of arches in a diameter less than a maximally expanded diameter.

12. The device of claim 11, wherein the circumferential constraining structure comprises a suture in mechanical communication with apical portions of at least one plurality of arches.

13. The device of claim 11, wherein the circumferential constraining structure comprises a tubular structure in mechanical communication with apical portions of at least one plurality of arches.

14. The device of claim 1, wherein the first plane comprises a curved plane.

15. A method for deploying a medical stent device, the method comprising the steps of:

providing a medical stent device according to claim 1;

disposing at least a proximal portion of the medical stent device within a generally cylindrical delivery device such that the first plurality of arches is circumferentially constrained together to present a radial profile smaller than when the arches are allowed to separate from one another;

circumferentially constraining the second plurality of arches;

directing the generally cylindrical delivery device and medical stent device adjacent a target site comprising an aperture therethrough;

directing the second plurality of arches to one face of the aperture, said aperture having a diameter less than an expanded diameter of each of the first and second plurality of arches'"'"' apices and a thickness of about the same as a longitudinal thickness of the generally cylindrical opening; and

releasing the constraint of one of the first or second plurality of arches, allowing the arches to deploy.

16. A medical stent device, comprising:

a biocompatible shape memory material formed as a continuous unitary wire structure including a plurality of alternating first arches and second arches, and having a first, non-deployed configuration and a second, deployed configuration;

wherein, the first, non-deployed configuration includes the first plurality of arches having their apices all drawn in proximity to each other, thereby forming a generally columnar first low profile and the second plurality of arches having their apices all drawn in proximity to each other, thereby forming a generally columnar second low profile;

wherein, the second, deployed configuration includes the first plurality of arches having their apices spread apart each other, the first arches'"'"' apices thereby forming a generally columnar first expanded profile having an outside diameter greater than the first low profile, and the second plurality of arches having their apices spread apart each other, the second arches'"'"' apices thereby forming a generally columnar second expanded profile having an outside diameter greater than the second low profile;

wherein, in the second deployed configuration, the first plurality of arches defines a first plane, the second plurality of arches defines a second plane that is spaced apart from the first plane; and

wherein apices of a third plurality of arches connect the first and second plurality of arches, the apical portions of the third plurality of arches define a generally cylindrical opening around which the first, second, and third pluralities of arches are generally centered, and the apical portions of the third plurality of arches are generally transverse relative to the first and second plurality of arches in the second, deployed configuration.

17. The device of claim 16, wherein the first plane comprises a curved plane.

18. The device of claim 16, wherein the second plane comprises a curved plane having a different contour than the first plane.

19. The device of claim 16, wherein the generally cylindrical opening defined by the apical portions of the third plurality of arches is configured to maintain open patency of an anastomosis.

20. The device of claim 16, wherein the first, non-deployed configuration is configured for substantially atraumatic passage through at least a portion of an anastomosis.