Vascular plug having composite construction

• US 9,655,602 B2
• Filed: 12/15/2011
• Issued: 05/23/2017
• Est. Priority Date: 12/14/2000
• Status: Expired due to Term

• Current Assignee: Cardinal Health Switzerland 515 GmbH (Cardinal Health, Inc.)
• Original Assignee: Cardinal Health Switzerland 515 GmbH (Cardinal Health, Inc.)
• Inventors: Olsen, Phil, Hartridge, Tellis, Shively, Adam, Ginn, Richard, Palermo, Thomas
• Primary Examiner(s): Woo, Julian W
• Application Number:
  US13/326,763
• Publication Number:
  US 20120101520A1
• Time in Patent Office: 1,986 Days
• Field of Search: 606151, 606213, 606215, 606232, 424422-425, 424443, 623 2372, 623 2375, 623 2376
• CPC Class Codes: A61B 17/0057 Implements for plugging an opening in the wall of a hollow or tubular organ, e.g. for sealing a vessel puncture or closing a cardiac septal defect sutures A61B17/04; closing rectum or urethra near body surface A61F2/0009
• 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 17/12109 in a blood vessel
• CPC Class Codes: A61B 17/12159 Solid plugs; being solid before insertion
• CPC Class Codes: A61B 17/12163 having a string of elements connected to each other
• CPC Class Codes: A61B 17/12172 having a pre-set deployed three-dimensional shape methods of manufacturing A61B2017/00526
• CPC Class Codes: A61B 17/1219 expandable in contact with liquids
• CPC Class Codes: A61B 2017/00004 (bio)absorbable, (bio)resorbable or resorptive
• CPC Class Codes: A61B 2017/00654 entirely comprised between the two sides of the opening
• CPC Class Codes: A61B 2017/00778 Operations on blood vessels A61B2017/22097, A61B2017/320741 take precedence
• CPC Class Codes: A61B 2017/00898 expandable upon contact with fluid

Abstract

This invention relates to apparatus and methods used to seal a vascular puncture site, particularly sites of punctures that are the result of catheterization or other interventional procedures. The sealing device includes a sealing member and a tether. The sealing member occupies a space in an incision, puncture, or other wound and sealing the space that it occupies, to prevent further blood flow. The tether is attached to the sealing member, and provides the user with the ability to withdraw the sealing member if necessary. The sealing device further includes a restraining member associated with the sealing member. The restraining member provides the ability to more securely restrain the sealing member to prevent it from migrating from the deployment location within a tissue tract. The restraining member also provides an additional capability of manipulating the sealing member after deployment.

Claims

1. A device for substantially sealing a wound that extends through tissue to an opening in a body lumen comprising:

a porous restraining member comprising a first bioabsorbable material and defining an interior space therein, a sealing member comprising a second bioabsorbable material at least partially located within the interior space of said restraining member and a tether attached at a first end to said sealing member such that a withdrawal tension on the tether causes a radial expansion of the sealing member within the restraining member, said interior space of said restraining member being expandable to accommodate said sealing member said sealing member being configured to expand when disposed within the body lumen as a result of being exposed to tissue and said restraining member being configured to expose the sealing member to tissue when deployed.

2. The device of claim 1, wherein said first bioabsorbable material is the same as said second bioabsorbable material.

3. The device of claim 1, wherein said first bioabsorbable material is selected from the group consisting of polyglycolic acid, polylactide, polyglycol-lactide acid, collagen, and hydrogel.

4. The device of claim 1, wherein said restraining member comprises a material having a knit, braided or woven construction.

5. The device of claim 1, wherein said restraining member is a tubular fabric member and said sealing member is a coiled foam pad enclosed by said tubular fabric member.

6. The device of claim 5, wherein said coiled form pad comprises a hydrogel.

7. A method for substantially sealing a wound that extends through tissue to an opening in a body lumen, comprising:

providing a sealing device comprising a hydrogel material, and deploying the sealing device in the wound, wherein said sealing device comprises a porous restraining member comprising a first bioabsorbable material and defining an interior space therein a sealing member comprising a second bioabsorbable material at least partially located within the interior space of said restraining member and a tether attached at a first end to said sealing member such that a withdrawal tension on the tether causes a radial expansion of the sealing member within the restraining member, said interior space of said restraining member being expandable to accommodate said sealing member, said sealing member being configured to expand when disposed within the body lumen as a result of being exposed to tissue.

8. The method of claim 7, wherein said first bioabsorbable material is selected from the group consisting of polyglycolic acid, polylactide, polyglycol-lactide acid, collagen, and hydrogel.

9. The method of claim 7, wherein said restraining member comprises a material having a knit, braided or woven construction.

10. The method of claim 9, wherein said restraining member is a tubular fabric member and said sealing member is a coiled foam pad enclosed by said tubular fabric member.

11. The method of claim 10, wherein said coiled form pad comprises a hydrogel.

12. A device for substantially sealing a wound that extends through tissue to an opening in a body lumen comprising:

a sealing member, at least a portion of which having a first radial dimension for delivery of said sealing member into the wound and a second radial dimension upon delivery into said wound as a result of being exposed to fluid flow associated with said wound, the second radial dimension being larger than the first radial dimension, and wherein said sealing member comprises a hydrogel;

a restraining member comprising a first bioabsorbable material and defining an interior space therein, said sealing member being located at least partially within the interior space of said restraining member; and

a tether attached at a first end to said sealing member such that a withdrawal tension on the tether causes a radial expansion of the sealing member within the restraining member.

13. The device of claim 12, wherein said first bioabsorbable material is selected from the group consisting of polyglycolic acid, polylactide, polyglycol-lactide acid, collagen, and hydrogel.