In the drawings:
Corresponding reference characters indicate corresponding parts throughout the several views of the drawings.
Referring to the drawings and more specifically to
The endovascular graft 10 includes an elongate circumferential intermediate layer 26 which has a first transverse edge 28 and a second transverse edge 30, as shown in
The endovascular graft 10 includes an elongate circumferential outer layer 34 which has a first transverse edge 36 and a second transverse edge 38, as shown in
The intermediate and outer layers 26, 34, and annular portion 43 define a cuff 45 which is circumferentially secured to the tubular structure 12. The annular portion 43 defines an inner layer 46 of the cuff 45. The inner and outer chambers 32, 42 define an interior cavity 47 of the cuff 45. The interior cavity 47 is bifurcated by the intermediate layer 26. Consequently, the interior cavity 47 includes the inner and outer chambers 32, 42.
The annular portion 43 has a flexibility for radial displacement relative to the adjoining portions of the wall 22. This flexibility provides for variation in the volume of the inner chamber 32, as shown in
The endovascular graft 10 has a port 49 which extends through the annular portion 43. The port 49 provides communication between the inner chamber 32 and a conduit 51. The conduit 51 extends to a location which is external to the cuff 45 and tubular structure 12.
The endovascular graft 10 has a port 53 which extends through the outer layer 34. The port 53 provides communication between the outer chamber 42 and a conduit 55 which is located externally of the cuff 45 and tubular structure 12.
The endovascular graft 10 has an expansion substance 57 within the outer chamber 42. The expansion substance 57 within the outer chamber 42 provides support to the tubular structure 12 and seals the endovascular graft 10 against the interior surface 59 of the vessel 61 in which the graft is deployed, as shown in
The inner chamber 32 of the completely formed endovascular graft 10 is substantially empty, as shown in
The formation of the endovascular graft 10, including the substantially empty inner chamber 32 and the expansion substance 57 in the outer chamber 42, is provided by a method which includes inserting the expansion substance 57 into the outer chamber 42, as shown in
An expansion substance 63 is inserted into the inner chamber 32 to provide resistance to luminal intrusion of the annular portion 43 or inner layer 46 which may result from the insertion of the expansion substance 57 into the outer chamber 42, as shown in
After the insertions of the expansion substances 57, 63 into the outer and inner chambers 42, 32, the expansion substance 57 is stiffened. The stiffening may be provided by the expansion substance 57 being a polymer which may be cured to increase the stiffness thereof. The stiffening of the expansion substance 57, which is such a polymer, is provided by curing the polymer following the insertion thereof into the outer chamber 42.
After the expansion substance 57 in the outer chamber 42 has been stiffened, the expansion substance 63 which is within the inner chamber 32 is removed therefrom, as shown in
The first end 18 of the tubular structure 12 defines an upstream end through which the fluid, typically blood, enters the lumen 24. A cuff 45 may be located longitudinally relative to the tubular structure 12 such that the cuff is adjacent to the upstream or first end 18. The second end 20 of the tubular structure 12 defines a downstream end through which the fluid which is within the lumen 24 exits therefrom. The cuff 45 may be located longitudinally relative to the tubular structure 12 such that the cuff is adjacent to the downstream or second end 20.
The ports 49, 53 may be located relative to the tubular structure 12 such that insertion of the endovascular graft 10 through an ipsilateral location on the body of the patient provides for the ports to have a contralateral position relative to the body of the patient. Consequently, the conduits 51, 55 may extend through a section of the body of the patient which is different from the section thereof through which the endovascular graft 10 is inserted.
While the invention has been described by reference to certain preferred embodiments, it should be understood that numerous changes could be made within the spirit and scope of the inventive concept described. Accordingly, it is intended that the invention not be limited to the disclosed embodiments, but that it have the full scope permitted by the language of the following claims.