Stent-graft prosthesis with pressure relief channels

Patent metadata

Field	Value
Publication number	US-12370037-B2
Application number	US-202217703562-A
Country	US
Kind code	B2
Filing date	Mar 24, 2022
Priority date	Apr 24, 2018
Publication date	Jul 29, 2025
Grant date	Jul 29, 2025

Abstract

A stent-graft prosthesis for implantation within a body vessel includes a graft material, a frame, and a channel. The graft material includes a proximal end, a distal end, and a graft lumen extending between the proximal and distal ends. The frame is coupled to the graft material. The channel is configured to relieve pressure associated with pulsatile blood flow during implantation of the stent-graft prosthesis within a body vessel. The channel permits blood to flow from an upstream side of the stent-graft prosthesis to a downstream side of the stent-graft prosthesis when the stent-graft prosthesis is in a partially expanded configuration in the body vessel. The channel may be a plurality of channels.

First claim

What is claimed is:

1. A method comprising:
delivering a stent-graft prosthesis to a treatment site of an aneurysm in a vessel such that an upstream portion of the stent-graft is disposed upstream of the aneurysm, the stent-graft prosthesis including graft material and a frame, the graft material defining a central lumen having an upstream end and a downstream end;
partially deploying the stent-graft prosthesis to a partially deployed configuration such that at least a portion of the upstream portion of the stent-graft prosthesis upstream of the aneurysm is radially expanded against an inner wall of the vessel and blood cannot exit the downstream end of the central lumen, wherein the stent-graft prosthesis includes a channel exit downstream of the upstream portion, upstream of the downstream end of the channel lumen, and disposed within the aneurysm such that blood flow within the central lumen exits through the channel exit with the stent-graft prosthesis in the partially deployed configuration;
fully deploying the stent-graft prosthesis such that the upstream portion of the stent-graft prosthesis upstream of the aneurysm is radially expanded against the inner wall of the vessel, a downstream portion of the stent-graft prosthesis is radially expanded against the inner wall of the vessel, the channel exit disposed within the aneurysm is closed such that blood flow from the central lumen is prevented from exiting the central lumen through the channel exit, the downstream end of the central lumen is open, and blood flow through the central lumen exits the central lumen through the downstream end of the central lumen.

2. The method of claim 1 , wherein the stent-graft prosthesis further includes a channel entrance in the upstream portion downstream of the upstream end of the stent-graft prosthesis such that in the partially deployed configuration blood enters the central lumen through the channel entrance.

3. The method of claim 2 , wherein fully deploying the stent-graft prosthesis comprises closing the channel entrance.

4. The method of claim 3 , wherein the channel entrance includes a valve assembly, wherein in the partially deployed configuration the valve assembly is in an open state, wherein closing the channel entrance comprises closing the valve assembly to prevent blood from entering the central lumen through the channel entrance.

5. The method of claim 1 , wherein the channel exit includes a valve assembly, wherein in the partially deployed configuration the valve assembly is in an open state, wherein fully deploying the stent-graft prosthesis includes closing the valve assembly to prevent blood from exiting the central lumen through the channel exit.

6. A method comprising:
delivering a stent-graft prosthesis to a treatment site in a vessel such at an upstream portion of the stent-graft is disposed upstream of the treatment site, the stent-graft prosthesis including graft material and a frame, the graft material defining a central lumen having an upstream end and a downstream end;
partially deploying the stent-graft prosthesis to a partially deployed configuration such that at least a portion of the upstream portion of the stent-graft prosthesis upstream of the treatment site is radially expanded against an inner wall of the vessel and blood cannot exit the downstream end of the central lumen, wherein a channel is formed downstream of the upstream end of the central lumen and between an outer surface of the graft material and an adjacent first segment of the frame to which the graft material is not attached such that the blood flows past the stent-graft outside of the graft material when the stent-graft prosthesis is in a partially expanded configuration, and
fully deploying the stent-graft prosthesis such that the upstream portion of the stent-graft prosthesis upstream of the channel is radially expanded against the inner wall of the vessel to block access to the channel, the downstream end of the central lumen is open, and blood flow through the central lumen exits the central lumen through the downstream end of the central lumen.

7. The method of claim 6 , frame includes a plurality of first segments aligned longitudinally such that the channel is formed between the first segments and the outer surface of the graft material to which the graft material is not attached such that the graft material is spaced from the first segments.

8. The method of claim 6 , wherein fully deploying the stent-graft prosthesis to block access to the channel comprises radially expanding the frame upstream of the channel, wherein the frame upstream of the channel does not include a segment unattached to the graft material that enables blood flow between the outer surface of the graft material and the frame.

9. The method of claim 8 , wherein fully deploying the stent-graft prosthesis comprises blocking an exit from the channel downstream of the upstream portion of the stent-graft prosthesis, wherein the frame downstream of the channel does not include a segment unattached to the graft material that enables blood flow between the outer surface of the graft material and the frame.

Assignees

• Medtronic Vascular Inc

Inventors

• Argentine Jeffery
• Springer Mitchell
• Shipley Adam
• Stiger Mark

Classifications

• A61F2250/0013

  for adjusting fluid pressure · CPC title

• A61F2/2476

  Valves implantable in the body not otherwise provided for · CPC title

• A61F2250/0069

  Sealing means · CPC title

• A61F2230/0023

  triangular · CPC title

• A61F2210/0014

  using shape memory or superelastic materials, e.g. nitinol · CPC title