Implantable tissue connector
An implantable tissue connector comprises a conduit and at least one bulge extending outwardly from the conduit's outer surface in a circumferential direction. At least one blocking ring loosely fitting over the outer surface with a clearance between the outer surface and the blocking ring is provided for mounting tubular living tissue within the clearance. The blocking ring has an inner diameter which is sized relative to an outer diameter of the bulge to prevent the blocking ring from slipping over the bulge when living tissue is mounted within the clearance. During implantation, the conduit is inserted into the tubular part of living tissue and over the bulge. Then, the blocking ring is pushed over the free end of the living tissue against the bulge. The living tissue is secured to the conduit with a self-enhancing effect when the tissue tends to be pulled off of the conduit.
1. An implantable tissue connector adapted so as to be connectable to a tubular part of living tissue within a patient's body, comprising:
a conduit having at least a first end and a second end and further having an outer surface with at least one bulge extending outwardly from the conduit's outer surface in a circumferential direction of the conduit about at least a part of the conduit's circumference,
at least one blocking ring arranged on the conduit on a first side of the bulge and loosely fitting over the outer surface of the conduit with a clearance between the outer surface of the conduit and the blocking ring for mounting tubular living tissue within the clearance, said blocking ring having an inner cross sectional diameter which is smaller than or substantially identical to an outer cross sectional diameter of the at least one bulge so as to prevent the blocking ring from slipping over the bulge when living tissue axially extending over the bulge from a second side of the bulge opposite the first side is mounted within the clearance, and
at least one flexible sleeve arranged on the conduit on the first side of the bulge and adapted to axially extend and closely fit around at least part of said outer surface of the conduit, wherein said flexible sleeve is adapted to extend over the bulge,
wherein the implantable tissue connector is adapted for the living tissue to be pulled over the conduit's outer surface from the second side of the bulge over and beyond the bulge and said flexible sleeve arranged on the conduit on the first side of the bulge is adapted to extend over the bulge including the living tissue pulled over and beyond the bulge so as to cover the living tissue, wherein the blocking ring is adapted to be advanced from the first side of the bulge over the sleeve covering the living tissue pulled beyond the bulge, such that the living tissue is located intermediate the conduit's outer surface and the sleeve which is in contact with the bulge.
2. The tissue connector of claim 1 , wherein the blocking ring is adapted to be pushed over the flexible sleeve against the bulge.
3. The tissue connector of claim 2 , wherein the at least one flexible sleeve is located proximately to said first end of the conduit.
4. The tissue connector of claim 3 , wherein the conduit has at least two of said flexible sleeves, and the at least two flexible sleeves are each located proximately to one of said at least first and second ends of the conduit.
5. The tissue connector of claim 2 , wherein said second end of the conduit is adapted for connecting the tissue connector to at least one of the following items: an implantable reservoir, an implantable pump, an implantable motor, an implantable medical device, a biological transplant.
6. The tissue connector of claim 2 , wherein between the first and second ends of the conduit or connected to the second end of the conduit, there is provided at least one of the following items: a reservoir, a pump, a motor, a medical device.
7. The tissue connector of claim 6 , wherein the reservoir is artificial or a biological transplant or made from tissue material of a patient into whom the reservoir is to be implanted.
8. The tissue connector of claim 1 , wherein the blocking ring is made from a material that has a friction coefficient in relation to living human mucosa tissue that is higher than a friction coefficient which the conduit's outer surface has in relation to living human serosa tissue.
9. The tissue connector of claim 1 , wherein the at least one bulge is located proximately to said first end of the conduit.
10. The tissue connector of claim 1 , wherein said at least one bulge comprises at least two bulges, and wherein the conduit has at least two of said bulges with the at least one blocking ring being located intermediate said at least two bulges.
11. The tissue connector of claim 10 , wherein the at least one blocking ring located intermediate said at least two bulges comprises two blocking rings, each of said two blocking rings being located proximate one of said at least first and second ends of the conduit.
12. The tissue connector of claim 11 , wherein the at least two bulges are each located proximate one of said at least first and second ends of the conduit.
13. The tissue connector of claim 1 , wherein—depending upon the intended use—the clearance is in the range of one of the following ranges: 0.1 to 0.4 mm, 0.4 to 0.8 mm, 0.8 to 1.3 mm, 1.3 to 2 mm, 2 to 3 mm, 3 to 4 mm, 4 to 5 mm, over 5 mm.
14. The tissue connector of claim 1 , wherein the flexible sleeve is made from a biocompatible material, which preferably comprises at least one polymer selected from the following group of polymers comprising: polytetrafluoroethylene, silicone, polyurethane, expanded polytetrafluoroethylene (ePTFE).
15. The tissue connector of claim 1 , wherein the conduit is less flexible than the flexible sleeve at least in a radial direction so as to provide support to the flexible sleeve against radial forces.