# US 11,439,503 B2 · Implantable valve prosthesis > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 11,439,503 B2 - Document ID: US11439503B2 - Status: Granted - Kind: B2 - Application number: 16/644,664 - Filed: 2018-09-06 - Published: 2020-12-24 - Granted: 2022-09-13 - Earliest claimed: 2017-09-13 - Assignees: Universitaetsklinikum Hamburg-Eppendorf - Applicants: Universitaetsklinikum Hamburg-Eppendorf - Inventors: Yalin Yildirim; Simon Pecha; Hermann Reichenspurner - Web page: https://patentgrep.com/patent/US11439503B2 ## CPC - A61F 2/2418: {Scaffolds therefor, e.g. support stents} - A61F 2/06: Blood vessels - A61F 2/07: Stent-grafts - A61F 2/2412: {with soft flexible valve members, e.g. tissue valves shaped like natural valves} - A61F 2/2475: {Venous valves} - A61F 2/2476: {Valves implantable in the body not otherwise provided for} - A61F 2002/065: {Y-shaped blood vessels} - A61F 2002/068: {Modifying the blood flow model, e.g. by diffuser or deflector} - A61F 2250/006: modular - A61F 2250/0062: Kits of prosthetic parts to be assembled in various combinations for forming different prostheses - A61F: FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS (dental prosthetics A61C) ## Abstract An implantable valve prosthesis for preventing blood reflux from a cardiac atrium into a vein opening into the atrium, with a generally tubular stent (2), also a flexible tube (3) that can be closed by collapsing the tube (3) and which is arranged at least in a partial area of a second end section (9) of the stent (2) on the outer peripheral surface. The second end opening (11) of the flexible tube (3) is open in the pressureless state. As a result of this valve design, during a physiological flow out of the pulmonary vein in the direction of the left atrium or out of the caval vein in the direction of the right atrium, there is no rise or an only insubstantial rise in the resistance to flow. ## Claims ### Claim 1 An implantable valve prosthesis (1) adapted for preventing blood reflux from a cardiac atrium into a vein opening into the atrium, comprising a generally tubular stent (2) which may be branched or unbranched and which comprises at least a first end section (4) with a first end opening (6) and a second end section (5) with a second end opening (7), and a flexible elastic tube (3) which may be branched or unbranched and which has at least a first end section (8) with a first end opening (10) and a second end section (9) with a second end opening (11) and which is disposed at least in a sub-region of the second end section (9) of the stent (2) on the outer peripheral surface thereof in a manner such that the second end section (9) of the flexible elastic tube (3) with its second end opening (11) protrudes beyond the second end opening (7) of the stent (2), wherein the flexible elastic tube (3) widens in cross-section towards its second end opening (11) such that the second end opening (11) is wider than the first end opening (10), wherein the second end opening (11) of the flexible elastic tube (3) is open in the unpressurized state with no pressure difference between the interior of the tube and the exterior of the tube, and wherein the second end opening (11) of the flexible elastic tube (3) is adapted to collapse under pressurized conditions which arise under physiological conditions in a cardiac atrium during systole so that the tube wall of the flexible elastic tube (3) is drawn or pressed towards the interior of the flexible elastic tube (3) and regions of the inner wall of the flexible elastic tube (3) lie on one another and reversibly close the flexible elastic tube (3). ### Claim 2 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, further comprising at least one wire- or ligature-shaped stabilization element (12) fastened to the stent (2) or integrally formed with the stent (2), wherein the stabilization element (12) protrudes beyond the second end opening (7) of the stent (2) and supports the portion of the tube (3) which protrudes beyond the second end opening (7) of the stent (2) from inside in a manner such that the second end opening (11) of the tube (3) is open in the unpressurized state and cannot gain ingress into the second end opening (7) of the stent (2) when pressure is applied. ### Claim 3 (depends on 2) The implantable valve prosthesis (1) as claimed in claim 2, wherein at least two wire- or ligature-shaped stabilization elements (12) which are opposite each other and which support the tube (3) from inside are present. ### Claim 4 (depends on 2) An implantable valve prosthesis (60), comprising a first and a second implantable valve prosthesis (1) as claimed in claim 2, wherein the first and second implantable valve prostheses (1) are disposed opposite one another in a manner such that their second tube end openings (11) are facing each other, the second tube end openings (11) of the first and second implantable valve prostheses (1) are spaced from each other, the first and second implantable valve prostheses (1) respectively have a wire- or ligature-shaped stabilization element (12) fastened to the stent (2) or integrally formed with the stent (2) which extends beyond the tube end openings (11) of the first and second implantable valve prostheses (1), and the first and second implantable valve prostheses (1) are connected together by means of the at least one wire- or ligature-shaped stabilization element (12). ### Claim 5 (depends on 4) The implantable valve prosthesis (60) as in claim 4, wherein the implantable valve prosthesis (1) is adapted for preventing blood reflux from the right cardiac atrium into a caval vein. ### Claim 6 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the stent (2) and the tube (3) are unbranched and generally configured as a hollow cylinder. ### Claim 7 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the tube (3) consists of body tissue. ### Claim 8 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the stent (2) is covered by the tube (3) in the region of its entire outer peripheral surface. ### Claim 9 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the second end section (9) of the tube (3) has an annular reinforcing element (23) fastened to the outside of the tube, the internal cross section of which element (23) corresponding to at least the internal cross section of the second end opening (7) of the stent (2). ### Claim 10 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the implantable valve prosthesis (1) is configured in a manner such that a coaptation length L of at least 1 cm is produced. ### Claim 11 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein at least one of the stent (2) and the tube (3) are branched and generally Y-shaped in configuration. ### Claim 12 (depends on 1) The implantable valve prosthesis (1, 60) as claimed in claim 1, wherein the implantable valve prosthesis (1, 60) has a fastening element (61) for extravasal fastening of the implantable valve prosthesis (1, 60). ### Claim 13 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the tube (3) consists of human or animal body tissue. ### Claim 14 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the implantable valve prosthesis (1) is configured in a manner such that a coaptation length L of at least 1.2 cm is produced. ### Claim 15 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the implantable valve prosthesis (1) is configured in a manner such that a coaptation length L of at least 1.3 cm is produced. ### Claim 16 (depends on 1) The implantable valve prosthesis (1) as claimed in claim 1, wherein the implantable valve prosthesis (1) is configured in a manner such that a coaptation length L of at least 1.5 cm is produced.