Stent

• US 8,764,847 B2
• Filed: 09/16/2009
• Issued: 07/01/2014
• Est. Priority Date: 09/16/2008
• Status: Expired due to Fees

• Current Assignee: C.R. Bard, Inc. (Becton, Dickinson & Co)
• Original Assignee: C.R. Bard, Inc. (Becton, Dickinson & Co)
• Inventors: Knapp, Tracey
• Primary Examiner(s): STEWART, ALVIN J
• Application Number:
  US13/119,412
• Publication Number:
  US 20110230950A1
• Time in Patent Office: 1,749 Days
• Field of Search: 623 2364- 2376, 623/1.11, 623/1.15, 604/8
• US Class Current: 623/23.66
• CPC Class Codes: A61F 2/04 Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts A61F2/18, A61F2/20 take precedence; devices, other than stent-grafts, providing patency to, or preventing collapsing of, tubular structures of the body other than stent-grafts, e.g. stents A61F2/82; instruments specially adapted for placement or removal of stents or stent-grafts A61F2/95
• CPC Class Codes: A61F 2002/048 Ureters
• CPC Class Codes: A61F 2250/0018 differing in elasticity, stiffness or compressibility
• CPC Class Codes: A61F 2250/0036 differing in thickness
• CPC Class Codes: A61M 27/008 pre-shaped, for use in the urethral or ureteral tract

Abstract

A stent is deployed within a body passageway. The stent is configured to curl a varying degree upon itself as the stent is inserted into the passageway depending on the size of the passageway. In this way a single size stent may be employed in different size passageways. The stent may have a generally rectangular shape or other shape. The stent may be made of one or more materials. For example, a spine of the stent may be made of a material different than a material used for the outer edges of the stent. The edges of the stent curl towards the spine during insertion into the passageway without any further manipulation of the stent or by application of any additional mechanical means. The stent may have a varying thickness and/or width along the longitudinal axis of the stent.

Claims

1. A stent for insertion into a lumen of a patient, comprising:

a proximal portion;

a distal portion; and

a body portion disposed between the proximal and distal portions and having an upper surface and a lower surface, the entire body portion being substantially planar when the body portion is in a delivery state and having lateral edge portions and a center portion, the lateral edge portions being adapted to curl towards the center portion so that a width of the body portion decreases as the body portion is inserted into the lumen.

2. The stent of claim 1, wherein the body portion comprises at least one of silicone, polyurethane, a polyethylene blend, stainless steel, a metal, a metal alloy, and Nitinol materials.

3. The stent of claim 1, wherein the body portion has a curvature when viewed in a cross-section perpendicular to a length of the body portion in the delivery state.

4. The stent of claim 1, wherein at least one of the proximal portion and the distal portion comprises a retention curve.

5. The stent of claim 1 further comprising a guide portion configured to facilitate deployment of the stent within the lumen.

6. The stent of claim 5, wherein the guide portions is configured to receive a push catheter.

7. The stent of claim 1, wherein the proximal portion is tapered to facilitate deployment of the stent within the lumen.

8. The stent of claim 1, wherein at least one of the lateral edge portions comprises a curve.

9. The stent of claim 1, wherein the body portion comprises at least one aperture.

10. The stent of claim 1, wherein the body portion comprises at least two materials, the first material being more rigid than the second material.

11. The stent of claim 1, wherein the body portion has a first thickness, the proximal portion has a second thickness, and the distal portion has a third thickness, and wherein the first thickness is different from at least one of the second and the third thickness.

12. The stent of claim 1, wherein a first portion of the body portion comprises a first width, wherein a second portion of the body portion comprises a second width, and wherein the first width is different from the second width.

13. The stent of claim 1, wherein the distal portion comprises at least one aperture.

14. The stent of claim 1 further comprising a medication layer positioned over at least one of the upper surface and the lower surface so as to dissolve within the lumen.

15. The stent of claim 1, wherein the body portion forms a C-shaped cross-section when in a deployed state.

16. The stent of claim 1, wherein the body portion forms a tubular shape when in a deployed state.

17. The stent of claim 1, wherein the body portion forms a spiral shape such that at least one of the lateral edge portions overlaps the other lateral edge portion when in a deployed state.

18. A self-deploying stent for placement in a lumen of a patient, the stent comprising:

a body member comprising a pliant material and being movable between a first cross-sectional shape when in a delivery state and a second cross-sectional shape when in a deployed state, the first cross-sectional shape being adapted to have an overall width greater than the second cross-sectional shape and greater than an inside diameter of the lumen, and the body member having lateral edge portions and a center portion, the lateral edge portions being adapted to curl towards the center portion when the body member is moved from the first cross-sectional shape to the second cross-sectional shape while the stent is being inserted into the lumen, the entire body member being substantially planar when the body member is in the first cross-sectional shape.

19. The stent of claim 18, wherein the stent is in the delivery state when the stent is outside the lumen.

20. The stent of claim 18, wherein the stent is in the deployed state when the stent is inside the lumen.

21. A self-deploying stent for placement in a lumen of a patient, the stent comprising:

a body member being adapted to be movable between a first cross-sectional shape and a second cross-sectional shape so that when a first portion of the body member is disposed inside the lumen and a second portion of the body member is disposed outside the lumen the first portion has the second cross-sectional shape and the second portion has the first cross-sectional shape, the first cross-sectional shape being adapted to have an overall width greater than an inside diameter of the lumen, and wherein the first portion comprises lateral edge portions and a center portion, the lateral edge portions being adapted to curl towards the center portion when the first portion is dispose inside the lumen so that a width of the first portion decreases as the first portion is inserted into the lumen, the entire body member being substantially planar when the body member is in the first cross-sectional shape.

22. The stent of claim 21, wherein the body member comprises a transition region disposed between the first portion and the second portion at least when the stent is being inserted into the lumen, the transition region moving along a length of the stent as the stent is inserted into the lumen but being generally aligned with the opening.

23. A method of using a stent, the method comprising:

aligning a stent having an overall width that is greater than a width of a lumen of a patient with an opening into the lumen;

pushing a portion of the stent through the opening and into the lumen, the portion having lateral edge portions and a center portion, the entire portion being substantially planar before the stent enters the opening; and

as the stent is entering the opening, curling the lateral edge portions towards the center portion of the stent so that a width of the portion decreases before the entire stent is inserted into the lumen.

24. The method of claim 23 further comprising removing the stent from the lumen, wherein the curled lateral edge portions of the stent reverts to a width greater than the width of the lumen when removed from the lumen.

25. A stent for insertion into a lumen of a patient, comprising:

a proximal portion;

a distal portion; and

a body portion disposed between the proximal and distal portions and having an upper surface and a lower surface, the body portion having lateral edge portions and a center portion, the lateral edge portions being adapted to curl towards the center portion so that a width of the body portion decreases as the body portion is inserted into the lumen, wherein the body portion has a first thickness, the proximal portion has a second thickness, and the distal portion has a third thickness, and wherein the first thickness is different from at least one of the second and the third thickness.

26. A stent for insertion into a lumen of a patient, comprising:

a proximal portion;

a distal portion; and

a body portion disposed between the proximal and distal portions and having an upper surface and a lower surface, the body portion having lateral edge portions and a center portion, the lateral edge portions being adapted to curl towards the center portion so that a width of the body portion decreases as the body portion is inserted into the lumen, wherein a first portion of the body portion comprises a first width, wherein a second portion of the body portion comprises a second width, and wherein the first width is different from the second width.

27. A stent for insertion into a lumen of a patient, comprising:

a proximal portion;

a distal portion; and

a body portion disposed between the proximal and distal portions and having an upper surface and a lower surface, the body portion having lateral edge portions and a center portion, the lateral edge portions being adapted to curl towards the center portion so that a width of the body portion decreases as the body portion is inserted into the lumen, wherein the body portion forms a spiral shape such that at least one of the lateral edge portions overlaps the other lateral edge portion when in a deployed state.