Endolumenal vascular prosthesis with neointima inhibiting polymeric sleeve
View Patent ↗The present invention is related to a low profile endolumenal prosthesis. The prosthesis comprises a radially expandable tubular wire support and an expanded PTFE membrane. The density, wall thickness and intranodal distance of the ePTFE are selected to inhibit the formation and nourishment of a viable neointima on the inner surface of the prosthesis, through the ePTFE membrane.
1. An endolumenal prosthesis having a lumenal surface and an ablumenal surface, comprising:
a tubular wire support with proximal and distal ends and a central lumen extending therebetween, the wire support comprising at least two axially adjacent tubular segments, each segment comprising a series of proximal and distal bends connected by a length of wire, wherein the wire support is radially compressible into a first, reduced cross sectional configuration for translumenal navigation to a treatment site in a body lumen and self expandable to a second, enlarged cross sectional configuration for deployment at the treatment site in the body lumen; and
a uniform porous tubular ePTFE sheath on the wire support, the tubular sheath having a sheath proximal end region and a sheath distal end region, wherein the sheath is porous and configured to inhibit sufficient cellular ingrowth through the wall of the sheath that would permit the formation of a viable neointimal layer on the lumenal surface of the sheath at the sheath proximal and distal end regions without a coating on the sheath that would inhibit cellular ingrowth,
wherein the sheath is formed from a single ply of ePTFE and wherein a wall thickness of the sheath is the thickness of the single ply of ePTFE.
2. The endolumenal prosthesis of claim 1 , wherein the ePTFE sheath wall thickness is no greater than about 0.2 mm.
3. The endolumenal prosthesis of claim 2 , wherein the ePTFE sheath wall thickness is about 0.1 mm.
4. The endolumenal prosthesis of claim 2 , comprising at least three segments.
5. The endolumenal prosthesis of claim 2 , comprising at least five segments.
6. The endolumenal prosthesis of claim 2 , wherein each segment comprises from about 4 proximal bends to about 12 proximal bends.
7. The endolumenal prosthesis of claim 2 , wherein at least the first and second axially adjacent tubular segments are joined by at least one folded link extending therebetween.
8. The endolumenal prosthesis of claim 7 , wherein the first tubular segment includes two side-by-side legs with a first apex thereon and the folded link is formed by folding around the first apex around a second apex formed on the second tubular segment.
9. The endolumenal prosthesis of claim 1 , wherein the ePTFE sheath wall thickness is within the range of from about 0.05 mm to about 0.15 mm.
10. The endolumenal prosthesis of claim 9 , wherein the ePTFE sheath has a density within the range of from about 1.1 to about 1.5 grams per milliliter.
11. The endolumenal prosthesis of claim 9 , wherein the ePTFE sheath has a plurality of nodes, and the average distance between nodes is within the range of from about 6 microns to about 80 microns.
12. The endolumenal prosthesis of claim 9 , wherein the ePTFE sheath has a density of at least about 0.75 grams per milliliter.
13. The endolumenal prosthesis of claim 12 , wherein the ePTFE sheath has a plurality of nodes, and the average distance between nodes is within the range of from about 6 microns to about 80 microns.
14. The endolumenal prosthesis of claim 1 , wherein the ePTFE sheath has a density of at least about 0.5 grams per milliliter.
15. The endolumenal prosthesis of claim 1 , wherein the ePTFE sheath has a plurality of nodes, and the average distance between nodes is within the range of from about 6 microns to about 80 microns.
16. The endolumenal prosthesis of claim 1 , wherein the ePTFE sheath has a water entry pressure in the range of from about 10 psi to about 24 psi.
17. A bifurcated endolumenal prosthesis having a lumenal surface and an ablumenal surface, comprising:
a proximal wire support section having a proximal end, a distal end and a central lumen extending therethrough, the proximal support section comprising at least two axially adjacent tubular segments comprising a series of distal and proximal bends connected by struts;
a first wire branch section at the distal end of the proximal support;
a second wire branch section at the distal end of the proximal support; and
a uniform porous membrane carried by the wire support section, the membrane having a membrane proximal end region and membrane distal end regions and configured to inhibit cellular growth through the membrane that would be sufficient to enable the formation of a thin, viable neointimal layer on the lumenal surface of the membrane at least at the membrane proximal and distal end regions without a coating on the membrane that would inhibit cellular ingrowth, the membrane consists of and has a thickness of a single ply of ePTFE.
18. A prosthetic vascular graft, comprising:
an expandable tubular wire support;
a uniform porous, tubular ePTFE layer carried by the support, the ePTFE layer formed from a single ply of ePTFE and having:
a wall thickness equal to a thickness of the single ply of ePTFE and less than about 0.15 millimeters;
an average density of greater than about 0.75 grams per milliliter; and
an average distance between nodes in the range of between about 6 to about 80 microns;
so that the uniform porous ePTFE layer prevents the formation and nourishment of a viable neointimal layer therethrough along portions of the tubular ePTFE layer's axial length, which are in contact with a vessel wall.
19. An artificial vascular prosthesis comprising an enlargeable support structure having an expanded, uniform porous, polytetrafluoroethylene layer thereon, the layer consisting of a single ply of polytetrafluoroethylene and having a wall thickness equal to the thickness of the single ply of polytetrafluoroethylene and a microstructure consisting of nodes interconnected by fibrils which prevents tissue ingrowth through portions of the layer that contact a vessel wall when the prosthesis is implanted to span an aneurysm, in which either the density is greater than about 1 gram per milliliter or the wall thickness is less than about 0.2 millimeters, or both.
20. A method of treating a patient, comprising:
providing an implantable tubular prosthesis, having a uniform porous ePTFE layer formed from a single ply of ePTFE thereon, the porous ePTFE layer having a wall thickness equal to the thickness of the single ply of ePTFE, a proximal end and a distal end;
positioning the prosthesis across a defect in a vessel such that a contacting portion of a first side of the layer is in contact with the wall of the vessel; thereby inhibiting formation of a viable neointima on a second side of the layer throughout the contacting portion, nourished through the layer;
wherein said inhibiting step is a result of the ePTFE layer having a density of greater than about 0.75 grams per milliliter and a wall thickness of less than 0.2 mm.
21. An endolumenal prosthesis having a lumenal surface and an ablumenal surface, comprising:
a tubular wire support with proximal and distal ends and a central lumen extending therebetween, the wire support comprising at least two axially adjacent tubular segments, each segment comprising a series of proximal and distal bends wherein the wire support is radially compressible into a first, reduced cross sectional configuration for translumenal navigation to a treatment site in a body lumen and self expandable to a second, enlarged cross sectional configuration for deployment at the treatment site in the body lumen; and
a uniform porous, tubular ePTFE sheath on the wire support, the porous, tubular sheath being formed from a single ply of ePTFE and having a wall thickness equal to the thickness of the single ply of ePTFE, the tubular sheath having a proximal end and a distal end and being configured to have a water entry pressure of at least about 10 psi, and wherein the uniform porous tubular sheath is configured to inhibit the formation of a viable neointimal layer on the lumenal surface of the without a coating on the sheath that would inhibit cellular ingrowth.
22. The endolumenal prosthesis of claim 21 , wherein the ePTFE sheath wall thickness is no greater than about 0.2 mm.
23. The endolumenal prosthesis of claim 22 , wherein the ePTFE sheath wall thickness is about 0.1 mm.
24. The endolumenal prosthesis of claim 21 , wherein the ePTFE sheath wall thickness is within the range of from about 0.05 mm to about 0.15 mm.
25. The endolumenal prosthesis of claim 24 , wherein the ePTFE sheath has a density within the range of from about 1.1 to about 1.5 grams per milliliter.
26. The endolumenal prosthesis of claim 24 , wherein the ePTFE sheath has a plurality of nodes, and the average distance between nodes is within the range of from about 6 microns to about 80 microns.
27. The endolumenal prosthesis of claim 24 , wherein the ePTFE sheath has a density of at least about 0.75 grams per milliliter.
28. The endolumenal prosthesis of claim 27 , wherein the ePTFE sheath has a plurality of nodes, and the average distance between nodes is within the range of from about 6 microns to about 80 microns.
29. The endolumenal prosthesis of claim 21 , wherein the ePTFE sheath has a density of at least about 0.5 grams per milliliter.
30. The endolumenal prosthesis of claim 21 , wherein the ePTFE sheath has a plurality of nodes, and the average distance between nodes is within the range of from about 6 microns to about 80 microns.
31. The endolumenal prosthesis of claim 21 , wherein the tubular sheath is further configured to inhibit the formation of a viable neointimal layer on the lumenal surface of the sheath at the distal end.
32. The endolumenal prosthesis of claim 21 , wherein the proximal end comprises a single opening and the distal end comprises two openings, such that the prosthesis is configured for implantation at a vascular bifurcation.