Stent with a crush-resistant zone

US9259336B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9259336-B2
Application numberUS-81053307-A
CountryUS
Kind codeB2
Filing dateJun 6, 2007
Priority dateJun 6, 2006
Publication dateFeb 16, 2016
Grant dateFeb 16, 2016

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

An endoluminal prosthesis system for a branched body lumen comprises a branch vessel prosthesis. The branch vessel prosthesis is deployable within a branch vessel body lumen and comprises a stent having a generally tubular body portion, a flareable proximal end portion, and a coupling portion disposed intermediate the body portion and the flareable portion. The coupling portion is preferably more crush-resistant than the body portion.

First claim

Opening claim text (preview).

What is claimed is: 1. An endoluminal prosthesis system for a branched body lumen, the system comprising: a branch vessel prosthesis deployable within a branch vessel body lumen and comprising a stent having a generally tubular body portion, a flareable proximal end portion, and a coupling portion disposed intermediate the body portion and the flareable portion, wherein the coupling portion is more crush-resistant than the body portion. 2. The system of claim 1 , wherein: the body portion has a stent configuration comprising at least one body stent ring including a plurality of interconnected body struts; and the flareable end portion has a stent configuration comprising at least one flare stent ring including a plurality of interconnected flare struts. 3. The system according to claim 2 , wherein the coupling portion has a stent configuration comprising at least one coupling stent ring disposed between a flare stent ring and a body stent ring, the at least one coupling stent ring including a plurality of interconnected coupling struts. 4. The system according to claim 3 , wherein the coupling portion comprises a plurality of coupling stent rings. 5. The system according to claim 3 , wherein the coupling struts are thicker than the body struts. 6. The system according to claim 5 , wherein the coupling struts are at least one of: circumferentially thicker than the body struts; and radially thicker than the body struts. 7. The system according to claim 5 , wherein the coupling struts are one of at least 10% thicker, at least 20% thicker, and at least 25% thicker than the body struts. 8. The system according to claim 3 , wherein the coupling struts are thicker than the flare struts. 9. The system according to claim 2 , wherein: the body portion comprises a plurality of longitudinally-interconnected body stent rings; the coupling portion comprises a plurality of longitudinally-interconnected coupling stent rings; and the interconnection frequency between the coupling stent rings is greater than the interconnection frequency between the body stent rings adjacent the coupling portion. 10. The system according to claim 2 , wherein: the body portion comprises a plurality of body stent rings, each having an axial dimension; the flareable end portion comprises a plurality of flare stent rings, each having an axial dimension; and the axial dimension of each of the flare stent rings is greater than the axial dimension of each of at least two body stent rings adjacent the flareable end portion. 11. The system according to claim 10 , wherein the axial dimension of each of the flare stent rings is one of at least 10% greater, at least 20% greater, and at least 40% greater than the axial dimension of each of at least two body stent rings adjacent the flareable end portion. 12. The system according to claim 10 , wherein the axial dimension of the flare stent rings increases proximally with the flareable stent configuration. 13. The system according to claim 12 , wherein the axial dimension of the proximal-most flare stent ring is one of at least 10%, at least 20%, and at least 25% greater than the axial dimension of the distal-most flare stent ring. 14. The system according to claim 2 , wherein: the body portion comprises a plurality of body stent rings that are interconnected by a plurality of body connector struts; the flareable end portion comprises a plurality of flare stent rings that are interconnected by a plurality of flare connector struts; and the flare connector struts are thicker than the body connector struts. 15. The system according to claim 14 , wherein each of the flare connector struts are at least one of: circumferentially thicker than the body connector struts; and radially thicker than the body connector struts. 16. The system according to claim 14 , wherein the flare connector struts are one of at least 10% thicker, at least 20% thicker, and at least 25% thicker than the body connector struts. 17. The system according to claim 1 , further comprising: a main vessel prosthesis deployable within a main vessel body lumen and having a main prosthesis lumen and a fenestration for providing fluid communication between the main prosthesis lumen and the branch vessel body lumen; wherein the coupling portion of the branch vessel prosthesis is sized and configured to engage the fenestration. 18. The system according to claim 17 , further comprising a reinforcing member at least partially surrounding the perimeter of the fenestration and configured to engage the coupling portion of the stent. 19. The system according to claim 1 , wherein the branch vessel prosthesis further comprises a graft. 20. The system according to claim 1 , further comprising: a main vessel prosthesis deployable within a main vessel body lumen and having a main prosthesis lumen and a fenestration for providing fluid communication between the main prosthesis lumen and the branch vessel body lumen; and a reinforcing member at least partially surrounding the perimeter of the fenestration and configured to engage the coupling portion of the stent; wherein: the body portion has a stent configuration comprising a plurality of longitudinally-interconnected body stent rings, each of the body stent rings including a plurality of interconnected body struts and having an axial dimension; the flareable end portion has a stent configuration comprising a plurality of longitudinally-interconnected flare stent rings, each of the flare stent rings including a plurality of interconnected flare struts and having an axial dimension; the coupling portion has a stent configuration comprising a plurality of longitudinally-interconnected coupling stent rings disposed between a flare stent ring and a body stent ring, each of the coupling stent rings including a plurality of interconnected coupling struts; the interconnection frequency between the coupling stent rings is greater than the interconnection frequency between the body stent rings adjacent the coupling portion; the coupling struts are thicker than the body struts; the coupling struts are thicker than the flare struts; the axial dimension of each of the flare stent rings is greater than the axial dimension of each of at least two body stent rings adjacent the flareable end portion; the axial dimension of the flare stent rings increases proximally with the flareable stent configuration; the body stent rings are interconnected by a plurality of body connector struts; the flare stent rings are interconnected by a plurality of flare connector struts; and the flare connector struts are thicker than the body connector struts.

Assignees

Inventors

Classifications

  • Stents in the form of a rolled-up sheet expanding after insertion into the vessel {, e.g. with a spiral shape in cross-section} · CPC title

  • Force-limiting means · CPC title

  • the stent being loosely attached to the graft material, e.g. by stitching · CPC title

  • connected peak to peak · CPC title

  • Y-shaped blood vessels · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US9259336B2 cover?
An endoluminal prosthesis system for a branched body lumen comprises a branch vessel prosthesis. The branch vessel prosthesis is deployable within a branch vessel body lumen and comprises a stent having a generally tubular body portion, a flareable proximal end portion, and a coupling portion disposed intermediate the body portion and the flareable portion. The coupling portion is preferably mo…
Who is the assignee on this patent?
Schaeffer Darin G, Boatman Scott E, Dittman Jay A, and 2 more
What technology area does this patent fall under?
Primary CPC classification A61F2/86. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Feb 16 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).