Pelvic implants and related methods
Described are surgical implants that include a central support portion adapted to be positioned to support pelvic tissue, between mesh end portions adapted to be passed through body tissue, wherein edges of the end portions exhibit extensions that are resistant to deformation.
1. A surgical implant comprising an open pore elongate strip, the strip comprising
two edges comprising edge extensions, and
reinforcement comprising lines of heat treated strip adjacent to the edges and not including the edges, the reinforcement causing an increase in the force required to pull the strip through tissue,
wherein the implant is adapted to be implanted in contact with body tissue, the implant comprising:
a central support portion,
the open pore elongate strip comprising open pore mesh having opposed mesh edges and formed of strands arranged to define mesh pores, strand ends extending outwardly of the opposed mesh edges as edge extensions; and
melted strands of mesh adjacent to un-melted edge extensions.
2. A surgical implant comprising an open pore elongate strip comprising two opposing surfaces and edges having edge extensions, the edge extensions coated with a stiffening material that increases stiffness of the edge extensions, the strip comprising un-coated area on at least one surface between the coated edge extensions of the at least one surface.
3. The surgical implant of claim 2 , wherein the coating comprises a biodegradable polymer.
4. A surgical implant according to claim 2 , adapted to be implanted in contact with body tissue, the implant comprising:
the open pore elongate strip comprising resilient open pore mesh having opposed mesh side edges and formed of strands arranged to define mesh pores adapted to enable tissue ingrowth therethrough, the elongate strip exhibiting strand ends extending outwardly of the opposed mesh side edges; and
a coating of stiffening material applied to the outwardly extending strand ends to stiffen the outwardly extending strand ends to resist deformation when placed in contact with tissue,
wherein the stiffening material comprises a soluble material selected from the group consisting of mannitol, dextrose, sorbose, sucrose, sodium chloride, potassium chloride, and sodium carbonate.
5. The implant of claim 4 wherein the stiffening material comprises a soluble material selected from the group consisting of dextrose, sorbose, sodium chloride, potassium chloride, and sodium carbonate.
6. A method of preparing an implant, the method comprising:
providing an open pore elongate strip comprising edges,
heat treating material of the strip along a line adjacent to an edge to cause edge extensions to be stiffened and thereby increase the force required to pull the strip through tissue, wherein
the open pore elongate strip comprises a mesh and the edge extensions comprise severed mesh strand, and
the method comprises thermally treating mesh adjacent the edge extensions without melting the edge extensions.
7. A method of preparing an implantable sling, the method comprising:
providing an open mesh pore elongate strip comprising two opposing surfaces, edges and edge extensions,
coating edge extensions with stiffening material to increase stiffness of the extensions, while leaving uncoated area on at least one surface between the coated edge extensions of the at least one surface.
8. The implant of claim 7 , wherein the stiffening material comprises a soluble material selected from the group consisting of mannitol, dextrose, sorbose, sucrose, sodium chloride, potassium chloride, and sodium carbonate.
9. The implant of claim 7 wherein the stiffening material comprises a soluble material selected from the group consisting of dextrose, sorbose, sodium chloride, potassium chloride, and sodium carbonate.
10. A method of preparing an implant, the method comprising:
providing a sheet of open pore mesh material,
reinforcing a portion of the open pore mesh material with reinforcement selected from the group consisting of: a reinforcing weave, a reinforcing elongate strand, a strip of adhesive, and melted mesh material, to produce a reinforced portion, and
after reinforcing, cutting the material to produce an elongate mesh strip having edges with reinforced edge extensions, wherein cut edges include edge extensions of severed mesh strands adjacent to the reinforcement.
11. The method of claim 10 , wherein the reinforcement comprises a length of melted mesh material aligned with open pores of the open pore mesh material.
12. A surgical implant comprising an open pore elongate strip comprising edges having edge extensions, the edge extensions coated with a stiffening material that increases stiffness of the edge extensions, the stiffening material selected from the group consisting of mannitol, dextrose, sorbose, sucrose, sodium chloride, potassium chloride, and sodium carbonate.
13. The implant of claim 12 wherein the stiffening material comprises a soluble material selected from the group consisting of dextrose, sorbose, sodium chloride, potassium chloride, and sodium carbonate.