US2012111489A1PendingUtilityA1

Self-sealing vascular graft

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Assignee: WEINBERG STEVENPriority: Nov 14, 2005Filed: Jan 13, 2012Published: May 10, 2012
Est. expiryNov 14, 2025(expired)· nominal 20-yr term from priority
Inventors:Steven Weinberg
A61M 2039/0072A61M 39/0208
43
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Claims

Abstract

The present invention relates to a segmental self-sealing graft for implantation in a patient including a base tubing element, a tubular access element overlying the base tubing, and a strand-like compression element wound over the access element so as to provide radially inward compression, and a method of making same.

Claims

exact text as granted — not AI-modified
1 . A method of making a self-sealing vascular graft comprising:
 providing a base tubing element of biocompatible material,   adhering at least one tubular access element of biocompatible material to the exterior surface of said base tubing element over substantially the entire length of said access element by compression molding or liquid injection molding technique so that said base tubing element and said access element do not delaminate when punctured, wherein said access element is a homogeneous continuous structure over substantially the entire length of said access element,   providing a compression element of a biocompatible material over the exterior surface of said at least one tubular access element, said compression element providing radially inward compression about said access element sufficient to increase the self-sealing ability of said access element without causing said base tubing element to collapse, wherein said compression element is a homogeneous continuous structure over substantially the entire length of said access element.   
     
     
         2 . The method of  claim 1 , wherein said biocompatible material for said base tubing element is polyurethane or polyester. 
     
     
         3 . The method of  claim 1 , wherein said biocompatible material for said base tubing element is expanded polytetrafluoroethylene. 
     
     
         4 . The method of  claim 1 , wherein said access element is comprised of two access elements, wherein one of said two access element is adapted for removal of untreated blood and the other access element is adapted for the return of filtered blood. 
     
     
         5 . The method of  claim 1 , wherein said biocompatible material for said access element is selected from the group consisting of a gum silicone elastomer, liquid silicone elastomer, polyether based polyurethane, polycarbonate based polyurethane, polyurethane and urethane. 
     
     
         6 . The method of  claim 1 , wherein said biocompatible material for said access element is a platinum-cured gum silicone elastomer. 
     
     
         7 . The method of  claim 1 , wherein said access element has a wall thickness of about 0.3 mm to about 1.5 mm. 
     
     
         8 . The method of  claim 1 , wherein said access element has a wall thickness of about 0.5 mm to about 1.0 mm. 
     
     
         9 . The method of  claim 1 , wherein said biocompatible material for said compression element is selected from the group consisting of a platinum cured silicone gum elastomer, liquid silicone elastomer, polyether based polyurethane, polycarbonate based polyurethane, polyurethane, and urethane. 
     
     
         10 . The method of  claim 1 , wherein said compression element has a durometer hardness of about 20 to about 35 Shore A. 
     
     
         11 . The method of  claim 1 , wherein the wall thickness of said compression element is from about 0.25 mm to about 0.55 mm. 
     
     
         12 . The method of  claim 1 , wherein the exterior surface of said compression element is microporous or textured. 
     
     
         13 . The method of  claim 1 , wherein said biocompatible material for said base tubing element is expanded polytetrafluorethylene; said biocompatible material for said access element is a platinum-cured gum silicone elastomer; and said biocompatible material for said compression element is a platinum cured silicone gum elastomer. 
     
     
         14 . The method of  claim 13 , wherein said access element has a wall thickness of about 0.33 mm to about 1.5 mm; and said compression element has a wall thickness of about 0.25 mm to about 0.55 mm, wherein the exterior surface of said compression element is microporous or textured.

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