Method and apparatus for prolapse repair
View Patent ↗A pelvic implant having a central support portion, and a plurality of extension members, is provided. The extension members can be positioned or extend from the central support portion in opposing pairs. The extension members are generally attached to the central support portion at respective junctions (e.g., via rivets), and sheaths or covers can be employed to cover at least a length or portion of the extension members. Further, one or more spanning members can extend from a first of the opposed and paired extensions to the opposing extension, e.g., under or across the central portion and the respective junctions to provide additional tensile strength for the implant during deployment or implantation.
1. A surgical implant to provide support within the pelvic region of a patient, comprising:
a support portion;
a plurality of extension portions operatively extending from the support portion at support junctions, with the plurality of extension portions positioned in opposing pairs; and
at least one spanning member operatively extending from a first of the extension portions, across the support portion, to an opposing second of the extension portions to assist in increasing the strength of the implant.
2. The implant of claim 1 , wherein the implant is selected from a group consisting of: a urethral support, a rectal support, and a vaginal prolapse support.
3. The implant of claim 1 , wherein the support junctions include a rivet.
4. The implant of claim 3 , wherein the rivet is a polymeric rivet.
5. The implant of claim 1 , wherein the support portion comprises biologic material and the extension portions comprise synthetic mesh material.
6. The implant of claim 1 , wherein the at least one spanning member is a polymeric material.
7. The implant of claim 6 , wherein the polymeric material is a low density polyethylene material.
8. The implant of claim 1 , further including a plurality of sheaths, with each sheath covering a portion of a respective extension portion.
9. The implant of claim 8 , wherein a first end of the at least one spanning member extends from a first sheath and a second end of the at least one spanning member is bonded to a second opposing sheath.
10. A surgical implant to provide support within the pelvic region of a patient, comprising:
a support portion;
first and second extension members operatively extending from the support portion at respective first and second support junctions, with the first and second extension members being positioned in opposition to one another with the support portion disposed there between; and
at least one spanning member operatively extending from the first extension member, under the support portion and the first and second support junctions, to the second extension member to assist in increasing the strength of the implant.
11. The implant of claim 10 , wherein the implant is selected from a group consisting of: a urethral support, a rectal support, and a vaginal prolapse support.
12. The implant of claim 10 , wherein at least one of the first and second support junctions includes a rivet.
13. The implant of claim 12 , wherein the rivet is a polymeric rivet.
14. The implant of claim 10 , wherein the support portion comprises biologic material and the extension members comprise synthetic mesh material.
15. The implant of claim 10 , wherein the at least one spanning member comprises a low density polyethylene material.
16. The implant of claim 10 , further including a first sheath covering a portion of the first extension member, and a second sheath covering a portion of the second extension member.
17. The implant of claim 10 , wherein a first end of the at least one spanning member extends from the first sheath and a second end of the at least one spanning member is bonded to the opposing second sheath.
18. The implant of claim 17 , wherein the second end of the at least one spanning member is heat bonded to the opposing second sheath.
19. The implant of claim 17 , wherein the second end of the at least one spanning member is heat bonded to an interior surface of the opposing sheath.
20. A method of implanting and deploying an implant in the pelvic region of a patient, comprising:
providing an implant having a central support portion and at least first and second extension members operatively extending from the central support portion in opposition to one another, the first and second extension members covered at least partially by first and second sheaths, with the implant further having at least one spanning member operatively extending from the first sheath, under the central support portion, to the second sheath to assist in increasing the strength of the implant;
introducing the implant within the pelvic region of the patient with one or more introducer tools;
securing the implant to tissue within the pelvic region of the patient;
cutting a portion of the second sheath and a portion of the spanning member extending from the second sheath; and
removing the first sheath with a portion of the spanning member extending therefrom.