MEDICAL IMPLANTS FOR ENHANCING THE HEALING RESPONSE AND THE EFFECTIVE LONGEVITY OF BLOOD VESSELS AND ANASTOMOSES AND METHODS OF USE THEREOF

1 . A method of establishing an anastomosis, the method comprising:

connecting a blood vessel and an artery, thereby forming an anastomosis therebetween; and

wrapping an outer surface of the blood vessel with a first tubular support, whereby the first tubular support exerts a radially-inward force on the blood vessel.

2 . The method according to claim 1 , wherein wrapping the outer surface of the blood vessel includes covering both a portion of the blood vessel and the anastomosis with the first tubular support.

3 . The method according to claim 1 , further comprising positioning an end of the artery through an opening defined in a side of the first tubular support, the blood vessel being a vein.

4 . The method according to claim 3 , wherein the end of the artery is positioned through the opening prior to connecting the vein and the artery and prior to wrapping the outer surface of the vein with the first tubular support.

5 . The method according to claim 4 , further comprising wrapping an outer surface of the artery with a second tubular support.

6 . The method according to claim 5 , further comprising connecting an end of the second tubular support with the side of the first tubular support.

7 . The method according to claim 1 , further comprising:

positioning a segment of the blood vessel and a segment of the artery in parallel relation to one another; and

wrapping the first tubular support around an outer surface of the segment of the artery as the first tubular support is wrapped around the outer surface of the blood vessel.

8 . The method according to claim 1 , further comprising:

ligating side branches from the blood vessel at a plurality of ligation sites; and

aligning the ligation sites with respective cells defined in the first tubular support.

9 . The method according to claim 1 , wherein wrapping the first tubular support includes transitioning the first tubular support from a substantially planar configuration to a cylindrical configuration, in which a pair of longitudinal edges of the first tubular support are disposed adjacent one another.

10 . The method according to claim 1 , wherein wrapping the first tubular support includes helically winding the first tubular support around the outer surface of the blood vessel.

11 . A medical implant for providing external support to an arteriovenous fistula or coronary artery bypass graft, the medical implant comprising:

a main tubular body configured to transition between an opened configuration and a closed configuration, in which the main tubular body defines a longitudinally-extending main passageway therethrough configured to receive a first blood vessel, the main tubular body being resiliently biased toward the closed configuration, the main tubular body including:

a proximal end portion defining an opening in communication with the main passageway;

a distal end portion defining an opening in communication with the main passageway; and

an intermediate portion disposed between the proximal end portion and the distal end portion, wherein the intermediate portion defines a side opening in communication with the main passageway and configured to receive and support a second blood vessel therein.

12 . The medical implant according to claim 11 , wherein the main tubular body has a pair of longitudinal edges configured to be disposed adjacent one another when the main tubular body is in the closed configuration.

13 . The medical implant according to claim 12 , wherein the pair of longitudinal edges together define a seam that extends along a length of the main tubular body, the seam and the side opening being disposed in opposing relation to one another.

14 . The medical implant according to claim 11 , wherein the side opening has a circular shape.

15 . The medical implant according to claim 11 , wherein the distal end portion of the main tubular body has a distal edge extending at a non-perpendicular angle relative to a longitudinal axis of the main tubular body.

16 . The medical implant according to claim 11 , further comprising:

a branching tubular body configured to transition between an opened configuration and a closed configuration, in which the branching tubular body defines a longitudinally-extending branching passageway therethrough, the branching passageway is in communication with the main passageway and is configured to receive and support the second blood vessel, the branching tubular body being resiliently biased toward the closed configuration, the branching tubular body including:

a branching proximal end portion defining an opening in communication with the branching passageway; and

a branching distal end portion defining an opening in communication with the branching passageway.

17 . The medical implant according to claim 16 , wherein the main tubular body and the branching tubular body are fabricated from a mesh that defines a plurality of discrete cells, each of the discrete cells having a smaller diameter than the side opening.

18 . The medical implant according to claim 16 , wherein the main tubular body and the branching tubular body are fabricated from a shape memory material.

19 . A method of establishing an arteriovenous fistula graft, the method comprising:

wrapping an outer surface of a vein with a tubular support;

positioning an end of an artery through an opening defined in a side of the tubular support; and

connecting the end of the artery to a side of the vein, thereby forming a fluid connection therebetween.

20 . The method according to claim 19 , wherein the tubular support defines a longitudinally-extending passageway, the passageway having an inner diameter that approximates an outer diameter of the vein or artery, whereby the tubular support exerts a radially-inward force on the vein or artery.

21 . The method according to claim 19 , wherein wrapping the outer surface of the vein with the tubular support includes:

transitioning the tubular support from a substantially planar configuration to a cylindrical configuration, in which a pair of longitudinal edges of the tubular support are disposed adjacent one another; or

helically winding the tubular support around the outer surface of the vein.