IP Library › Granted Patent US 10,500,072
Granted Patent B2
US 10,500,072 · App. 15/640,208 · Granted Dec 10, 2019

Method of treating vascular bifurcations

Inventors: H. Richard Davis (Coral Springs, FL); Aaron Kaplan (Norwich, VT)
Assignee: POSEIDON MEDICAL INC.
A61F2/82A61F2/915A61F2002/821A61F2002/91525A61F2002/91575A61F2220/0008A61F2220/0016A61F2230/0013
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Quick Facts
Patent No.
US 10,500,072
App. No.
15/640,208
Granted
Dec 10, 2019
Kind
B2
Abstract

A prosthesis is disclosed for placement across an ostium opening from a main body lumen to a branch body lumen. The prosthesis comprises a radially expansible support, at least two axially elongate longitudinal members, at least one of which can be fronds, extending from an end of the support, and a circumferential member connected to at least one axially elongate longitudinal member and unconnected to at least one other axially elongate longitudinal member.

Claims (31)

1. A method of treating a bifurcation between a first body lumen and a second body lumen, comprising:

advancing a prosthesis to the bifurcation, the prosthesis comprising a radially expansible support, a transition portion having a first end coupled with the support, a circumferential member spaced axially from the radially expansible support, wherein the transition portion comprises a plurality of second ends, at least one of the second ends coupled with the circumferential member via a single filament, and one or more of the second ends not coupled with the circumferential member;

deploying the support in the first body lumen;

positioning the first end of the transition portion on a first body lumen side of an ostium opening; and

deploying the circumferential member in the second body lumen at a distance from the bifurcation, wherein the one or more of the second ends not coupled with the circumferential member is positioned on a second body lumen side of the ostium opening.

2. The method of claim 1 , wherein the one or more of the second ends not coupled with the circumferential member is positioned at a proximal second body lumen location.

3. The method of claim 1 , wherein the one or more of the second ends not coupled with the circumferential member is positioned at a distal second body lumen location.

4. The method of claim 1 , wherein the one or more of the second ends not coupled with the circumferential member is positioned at a proximal second body lumen location and at a distal second body lumen location.

5. The method of claim 1 , wherein deploying the circumferential member in the second body lumen comprises engaging the circumferential member with a second body vessel wall.

6. The method of claim 5 , further comprising expanding the support and the transition portion.

7. The method of claim 1 , further comprising transferring force applied to the support or the transition portion to the circumferential member via the single filament.

8. The method of claim 1 , further comprising deploying a second device in the second body lumen.

9. The method of claim 8 , wherein deploying the second device comprises deploying the second device within the circumferential member.

10. The method of claim 9 , further comprising advancing the second device in the second body lumen and pushing the one or more of the second ends not coupled to the circumferential member to a distal second body lumen location.

11. The method of claim 10 , further comprising expanding the second device.

12. The method of claim 11 , wherein expanding the second device comprises entrapping the circumferential member between the second device and a second body vessel wall.

13. The method of claim 11 , wherein expanding the second device comprises entrapping the one or more of the second ends not coupled with the circumferential member between the second device and a second body vessel wall.

14. The method of claim 1 , wherein at least a portion of the prosthesis decreases in mass over time.

15. The method of claim 14 , wherein the circumferential member is bioabsorbable.

16. The method of claim 14 , wherein the circumferential member is bioerodable.

17. The method of claim 14 , wherein the circumferential member is biodegradable.

18. The method of claim 14 , wherein a polymer matrix on a surface of the prosthesis decreases in mass over time.

19. The method of claim 14 , wherein any one or combination of the support and the transition portion decreases in mass over time.

20. The method of claim 14 , wherein a proximal or distal portion of the prosthesis including the circumferential member decreases in mass over time.

21. A method of treating a bifurcation between a first body lumen and a second body lumen, comprising:

providing a prosthesis comprising a radially expansible support, a transition portion having a first end coupled with the support, a circumferential member spaced axially from the radially expansible support, wherein the transition portion comprises a plurality of second ends, at least one of the second ends coupled with the circumferential member via a single filament, and one or more of the second ends not coupled with the circumferential member;

transluminally navigating the prosthesis to a treatment site;

deploying the support in the first body lumen;

positioning the first end of the transition portion on a first body lumen side of an ostium opening;

deploying the circumferential member in the second body lumen at a distance from the bifurcation; and

positioning the one or more of the second ends not coupled with the circumferential member on a second body lumen side of the ostium opening.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2019
From: TRYTON MEDICAL, INC.
To: POSEIDON MEDICAL INC.
Reel/Frame 050881/0312 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2018
From: DAVIS, H. RICHARD; KAPLAN, AARON
To: TRYTON MEDICAL, INC.
Reel/Frame 045697/0150 →
Continuity (3)
Continuation 13989539
Provisional Application 61417170 · Nov 24, 2010
Related Publication 20170360583A1 · Dec 21, 2017