Systems and methods for bilateral stimulation of left and right branches of the dorsal genital nerves to treat urologic dysfunctions

• US 20080132969A1
• Filed: 10/31/2007
• Published: 06/05/2008
• Est. Priority Date: 02/12/2004
• Status: Abandoned Application

• Current Assignee: Medtronic Urinary Solutions, Inc. (Medtronic Plc)
• Original Assignee: NDI Medical, Inc. (Medtronic Plc)
• Inventors: Zmina, Therese M., Lechman, Tina E., Sakai, Jonathan L., Grill, Julie, Strother, Robert B., Bennett, Maria E., Mrva, Joseph J., Thrope, Geoffrey B.
• Application Number:
  US11/981,113
• Publication Number:
  US 20080132969A1
• Time in Patent Office: Days
• US Class Current: 607/41
• CPC Class Codes: A61N 1/0521 Genital electrodes
• CPC Class Codes: A61N 1/0558 Anchoring or fixation means therefor
• CPC Class Codes: A61N 1/36007 of urogenital or gastrointestinal organs, e.g. for incontinence control
• CPC Class Codes: A61N 1/36017 with leads or electrodes penetrating the skin
• CPC Class Codes: A61N 1/36107 Sexual dysfunction stimulating genital organs A61N1/36007
• CPC Class Codes: A61N 1/372 Arrangements in connection with the implantation of stimulators

Abstract

Systems and methods treat urologic dysfunctions by implanting a lead and electrode in a tissue region affecting urologic function, and coupling the lead to an external pulse generator. If desired results are achieved, the external pulse generator is removed and an implantable pulse generator is implanted in an anterior pelvic region remote from the electrode. Bilateral stimulation of the left and/or right branches of the dorsal genital nerves using a single lead implanted in adipose or other tissue in the region at or near the pubic symphysis is able to treat urologic dysfunctions.

Claims

1. A cable pair adapted to be electrically coupled to provide a touch proof connection comprising:

a first elongated cable adapted for implantation in tissue, the first cable including a proximal portion and a distal portion, the proximal portion including an IS-1 connector to be coupled to an implantable electrode lead, and the distal portion including a first touch proof connector,

the first touch proof connector comprising a threaded socket housing, a socket within the threaded socket housing, a wire element shim within the socket, and coupling means to secure the socket within the threaded-socket housing, the socket adapted to receive a contact pin from a second elongated cable to provide a touch proof connection,

the first cable encapsulating a wire element that electrically couples the IS-1 connector to the first touch proof connector,

the second cable including a proximal portion and a distal portion, the proximal portion including a touch proof plug adapted for electrical connection to an external pulse generator, and the distal portion including a second touch proof connector,

the second touch proof connector comprising a threaded pin housing, a connection pin within the threaded pin housing adapted to electrically couple to the socket within the threaded socket housing, and coupling means to secure the connection pin within the threaded pin housing, and

the second cable encapsulating a wire element that electrically couples the touch proof plug to the second touch proof connector.

2. A system for treating urologic dysfunctions comprising:

a lead comprising a proximal portion and a distal portion, the distal portion including at least one stimulation electrode, an Array of expandable anchoring structure, and a first and second visual marker,

the stimulation electrode being sized and configured to be implanted at or near a nerve at a target site between the pubic symphysis and the clitoris of a female or the base of the penis of a male,

the first visual marker adapted to indicate that the stimulation electrode has been exposed out of a distal end of an introducing sleeve without deploying the array of expandable anchoring structure,

the second visual marker adapted to indicate that the introducing sleeve has been withdrawn sufficient to deploy the array of expandable anchoring structure at the target site, and

an implantable pulse generator adapted to couple to the lead and convey electrical stimulation waveforms through the lead, the implantable pulse generator sized and configured to be implanted in an anterior pelvic region remote from the at least one stimulation electrode.

3. A system according to claim 2

wherein the stimulation electrode and the array of expandable anchoring structure are sized and configured to be implanted in adipose tissue.

4. A method of using the system defined in claim 2 to treat urologic dysfunctions.

5. A method for treating a urologic dysfunction comprising:

providing a first implantable lead comprising a proximal portion and a distal portion, the proximal portion including an implantable lead connector, the distal portion including at least one stimulation electrode,

providing an external pulse generator,

providing a percutaneous extension cable comprising a proximal portion and a distal portion, the proximal portion including a proximal extension cable connector, the distal portion including a distal extension cable connector,

creating a first incision near-midline over the pubic symphysis,

inserting the distal portion of the lead through the first incision,

positioning the at least one stimulation electrode at a target site between the pubic symphysis and the clitoris of a female or the base of the penis of a male,

creating a second incision remote from the first incision,

tunneling the proximal portion of the first implantable lead between the first incision and the second incision,

creating a third incision remote from the first incision and second incision,

tunneling the percutaneous extension cable between the second incision and the third incision,

coupling the implantable lead connector to the proximal extension cable connector and implanting the connection below the skin surface at the second incision,

coupling the distal extension cable connector to the external pulse generator, and

operating the external pulse generator for a predetermined amount of time to convey electrical stimulation waveforms to the at least one stimulation electrode to treat the urologic dysfunction.

6. A method according to claim 5 further including

uncoupling the distal extension cable connector from the external pulse generator,

uncoupling the implantable lead connector from the proximal extension cable connector,

providing an implantable pulse generator,

coupling the implantable lead connector to the implantable pulse generator,

implanting the implantable pulse generator and the implantable lead connector below the skin surface at the second incision, and

operating the implantable pulse generator to convey electrical stimulation waveforms to the at least one stimulation electrode to treat the urologic dysfunction.

7. A method according to claim 6 further including

replacing the first implantable lead with a second implantable lead.

8. A method according to claim 5 further including

providing an intermediate extension cable, and

coupling the intermediate extension cable between the distal extension cable connector and the external pulse generator.

9. A method according to claim 5

wherein the external pulse generator comprises a carrier adapted to be worn by a user and a removable and replaceable electronics pod adapted to be coupled to the carrier, the electronics pod containing circuitry and adapted to generate the electrical stimulation waveforms to be delivered through the first implantable lead and to the electrode to stimulate tissue, the electronics pod including a power input bay adapted to receive a disposable power source that can be released and replaced at a prescribed frequency similar to an individual administering a medication regime in pill form.

10. A method according to claim 5 further including

during the positioning step, questioning the patient to describe the stimulation.

11. A method according to claim 5

wherein the distal extension cable connector comprises a touch proof connector.

12. A method according to claim 5

wherein the predetermined amount of time comprises about a two week period.

13. A method according to claim 5

wherein the second incision and the third incision are located in an anterior pelvic region.

14. A method according to claim 5

wherein the stimulation electrode is sized and configured to be implanted in adipose tissue.

15. A method according to claim 5

wherein the stimulation waveforms conveyed to the at least one stimulation electrode affect bilateral stimulation of the left and right branches of the dorsal genital nerves.

16. A method according to claim 5

wherein the urologic dysfunction is selected from the group consisting of urinary incontinence, fecal incontinence, micturition/retention, defecation/constipation, sexual dysfunctions, pelvic floor muscle activity, and pelvic pain.

17. A method according to claim 5

wherein the distal portion of the lead includes flexible anchoring structure comprising an array of expandable shovel-like paddles.

18. A kit of components adapted for use in a surgical field comprising:

a hand-held, disposable test stimulator including a battery sized to keep the test stimulator operational for a predetermined time, the test stimulator adapted to couple to a lead to convey electrical stimulation waveforms through the lead to test the placement of the lead,

a sterile patch electrode adapted to be placed on the skin of an individual and coupled to the test stimulator to serve as a return path for the stimulation waveforms, and

instructions for coupling the test stimulator to the lead and operating the test stimulator to convey electrical stimulation waveforms through the lead to test the placement of the lead.

19. A kit according to claim 18 further including

a connector cable adapted to couple the test stimulator to the lead.

20. A kit according to claim 18

wherein the instructions include implanting the lead in an adipose tissue region at or near a pubic symphysis.

21. A kit according to claim 18

wherein the instructions include coupling the test stimulator to the lead and operating the test stimulator to convey electrical stimulation waveforms through the lead to achieve stimulation of the left and/or right branches of the dorsal genital nerves.

22. A kit of devices used in a surgical procedure to provide a neurostimulation system to treat urologic dysfunctions, the kit comprising:

a needle and a companion introducer sleeve, the needle including a fitting to secure to a hub on the introducer sleeve,

a sterile return electrode adapted to be placed on or in the skin of an individual and coupled to a test stimulator, the return electrode adapted to serve as a return path for stimulation waveforms,

a connector cable adapted to couple the test stimulator to the needle,

a tunneling tool adapted to pass an implantable lead subcutaneously from a first incision to a second incision,

an extension cable adapted to be tunneled subcutaneously from the second incision to a third incision remote from the first incision and second incision, the extension cable adapted to couple to the implantable lead at the second incision and exit the skin at the third incision to couple to a pulse generator, and

instructions for creating the first incision in a region at or near a pubic symphysis, inserting the needle and companion introducer sleeve into the first incision and into adipose tissue at or near the pubic symphysis, coupling the needle to the test stimulator via the connector cable, coupling the return electrode to the test stimulator, placing the return electrode on or in tissue, operating the test stimulator to provide stimulation waveforms, removing the needle from the companion introducer sleeve, inserting the implantable lead into the companion introducer sleeve, removing the companion introducer sleeve, creating a second incision remote from the first incision, tunneling the implantable lead from the first incision to the second incision, creating a third incision remote from the first incision and second incision, tunneling the extension cable from the second incision to the third incision, coupling the extension cable to the implantable lead, coupling the extension cable to the pulse generator, and operating the pulse generator to provide neurostimulation to treat the urologic dysfunction.

23. A kit according to claim 22

wherein the tunneling tool comprises a shaft positioned inside a introducer sleeve 41, the shaft including a handle to aid a physician in delivering the tunneling tool to a desired location.

24. A kit according to claim 22

the tunneling tool including a detachable tip adapted to allow the tunneling tool shaft, after the tunnel has been formed, to be coupled to the implantable lead or the extension cable to pull the implantable lead or the extension cable through the tunnel.

25. A kit according to claim 22

wherein the instructions include operating the pulse generator to provide neurostimulation to the implantable lead treat the urologic dysfunction by stimulating the left and/or right branches of the dorsal genital nerves.