Occlusion device

• US 9,687,242 B2
• Filed: 04/03/2009
• Issued: 06/27/2017
• Est. Priority Date: 04/03/2008
• Status: Active Grant

• Current Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Inventors: Clausen, Jacob Lund, Hendriksen, Per, Christiansen, Frank K.
• Primary Examiner(s): WEISBERG, AMY REGINA
• Application Number:
  US12/936,110
• Publication Number:
  US 20110054512A1
• Time in Patent Office: 3,007 Days
• Field of Search: 606200, 623 113, 623 123- 126, 623 13- 131
• CPC Class Codes: A61B 17/12022 Occluding by internal devices, e.g. balloons or releasable wires plugging an opening in the wall of an organ A61B17/0057; occluders for the cervical canal A61F6/146; vas deferens occluders A61F6/20
• CPC Class Codes: A61B 17/1204 temporary occlusion
• CPC Class Codes: A61B 17/12109 in a blood vessel
• CPC Class Codes: A61B 17/12172 having a pre-set deployed three-dimensional shape methods of manufacturing A61B2017/00526
• CPC Class Codes: A61B 17/12177 comprising additional materials, e.g. thrombogenic, having filaments, having fibers or being coated
• CPC Class Codes: A61B 17/1219 expandable in contact with liquids
• CPC Class Codes: A61B 2017/1205 Introduction devices

Abstract

An occlusion device (30) includes at least one self-expanding frame (42, 44) and graft material (46). Occlusion occurs by constricting the graft material (46) at a substantially central point or at an end of the device. The constriction is sized such that a guide wire (34) is able to pass therethrough. A valve mechanism (50) includes a screen (52) made from a resilient material and which includes a closable opening (54). The valve mechanism (50) allows a guide wire to pass through the occlusion device (30) while an effective physical barrier is maintained after removal of the guide wire (34).

Claims

1. An occlusion device for occluding a vessel having an internal wall, the occlusion device comprising:

a frame consisting of a proximal frame and a distal frame for anchoring the device against the internal wall of the vessel to be occluded, the proximal frame being disposed at a proximal end of the occlusion device, the distal frame being at a distal end of the occlusion device, the device having a longitudinal axis therethrough, the proximal frame being longitudinally spaced apart from the distal frame, each of the proximal frame and the distal frame having a tubular metal construction comprising a plurality of struts, each of the proximal frame and the distal frame including a portion for contacting the internal wall of a vessel to be occluded;

at least one occlusion membrane attached to the distal frame at a proximal end of the distal frame and to the proximal frame at a distal end of the proximal frame, the occlusion membrane having a proximal first portion and a distal first portion extending longitudinally for contacting the internal wall of the vessel to be occluded, and a proximal second portion distally adjoining the proximal first portion and a distal second portion proximally adjoining the distal first portion, the proximal and distal second portions directed away from the internal wall of the vessel and toward the longitudinal axis, the occlusion membrane being attached to the frame at least at the proximal and distal first portions, the at least one occlusion membrane radially surrounding at least the proximal end of the distal frame and the distal end of the proximal frame with the proximal and distal first portions, wherein expanding the device within a vessel causes the occlusion membrane to form a physical barrier within a vessel to be occluded, the occlusion membrane having an hourglass shape between the proximal end of the distal frame and the distal end of the proximal frame when expanded; and

a barrier located longitudinally between the distal end of the proximal frame and the proximal end of the distal frame, the barrier extending from the occlusion membrane across a lumen of the device and comprising a closable opening for receiving a guidewire, the barrier comprising a valve biased closed and arranged to not allow blood flow therethrough, the valve comprising leaves which are biased to a closed configuration, the barrier being deformed or relaxed to the closed configuration such that the leaves overlap to form a static screen across the lumen of the device upon removal of the guidewire.

2. The occlusion device of claim 1 wherein the occlusion membrane forms at least one substantially conical portion in the expanded state.

3. The occlusion device of claim 1 wherein the device is bidirectional and wherein the occlusion membrane forms two substantially conical portions in the expanded state.

4. The occlusion device of claim 1 wherein the occlusion membrane is graft material.

5. The occlusion device of claim 1 wherein the occlusion membrane is not fabricated from a bioabsorbable material.

6. The occlusion device of claim 1 wherein the barrier is made of silicone, polyurethane, expanded PTFE, a plastic material, or graft material.

7. The occlusion device of claim 1 wherein the occlusion membrane is attached to the frame internally.

8. The occlusion device of claim 1 wherein the frames are self-expanding.