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 incis
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.
대표청구항▼
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 parti
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.
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