Multi-purpose FES system

• US 7,187,976 B2
• Filed: 01/17/2003
• Issued: 03/06/2007
• Est. Priority Date: 01/21/2002
• Status: Expired due to Fees

• Current Assignee: Neopraxis Pty., Ltd.
• Original Assignee: Neopraxis Pty., Ltd.
• Inventors: Barriskill, Andrew, Milijasevic, Zoran, Duncan, Michael, Bruinsma, Ian
• Primary Examiner(s): LAYNO, CARL HERNANDZ
• Application Number:
  US10/346,072
• Publication Number:
  US 20030181956A1
• Time in Patent Office: 1,509 Days
• Field of Search: 607 39- 41, 607/48, 607/49, 607/60
• US Class Current: 607/43
• CPC Class Codes: A61N 1/36003 of motor muscles, e.g. for walking assistance

Abstract

A multi-purpose FES system includes a multi-function, implantable stimulator for stimulating different sites in a patient'"'"'s body. The stimulator includes a control unit and a receiving device. The stimulator further has a plurality of bundles of electric leads connected to the control unit, each lead terminating in at least one electrode to provide a plurality of discrete groups of electrodes associated with each site. Each group of electrodes is operable to stimulate its associated site in the patient'"'"'s body, under the action of stimulation signals from the control unit, the control unit receiving signals from the receiving device. A transmitter is arranged externally of the patient'"'"'s body for supplying signals transcutaneously to the receiving device of the stimulator. A controller is in communication with the transmitter via a communications interface unit.

Claims

1. A multi-purpose Functional Electrical Stimulation (FES) system comprising:

a multi-function, implantable stimulator configured to stimulate at least one lower extremity site and at least one spinal cord site in a patient'"'"'s body, the stimulator comprising;

a control unit;

a receiving device configured to send signals to the control unit;

a plurality of bundles of electric leads connected to the control unit, each lead terminating in at least one electrode to provide a plurality of discrete groups of electrodes associated with each of the different sites, each group of electrodes being operable to stimulate its associated site in the patient'"'"'s body, under the action of stimulation signals from the control unit; and

a housing defining at least one suture opening for suturing the housing in position;

a transmitter, arranged externally of the patient'"'"'s body, configured to supply signals transcutaneously to the receiving device; and

a controller in communication with the transmitter via a communications interface unit.

2. The system of claim 1 in which the stimulator is configured to effect stimulation in at least four sites of the patient'"'"'s body.

3. The system of claim 2 in which the at least four sites include a posterior and anterior right lower extremity, a posterior and anterior left lower extremity, a posterior, sacral region of a spinal cord of the patient and at a conus of the patient'"'"'s spinal cord.

4. The system of claim 1 in which the stimulator is implanted, in use, in a substantially central location in the patient'"'"'s body, the stimulator being connected to the sites in the patient'"'"'s body to be stimulated via the electrodes and their associated leads to deliver the appropriate stimulation to the desired sites by dedicated, application specific electrodes.

5. The system of claim 1 in which the electrodes are configured to be implanted in the patient'"'"'s body by a surgical, subcutaneous tunneling technique to reduce the number and size of the incisions to be made to the patient'"'"'s body.

6. The system of claim 1 in which the receiving device of the stimulator is in the form of an antenna.

7. The system of claim 6 in which the device is RF operable and is in the form of an RF receiver coil.

8. The system of claim 7 in which the transmitter is in the form of an RF transmitter coil arranged, in use, externally of the patient'"'"'s body in register with the receiver coil so that RF signals are transmitted transcutaneously to the stimulator, in use.

9. The system of claim 8 in which the transmitter coil is removably arranged with respect to the stimulator.

10. The system of claim 9 in which the stimulator includes a retaining means for removably retaining the transmitter coil in position relative to the stimulator.

11. The system of claim 10 in which the retaining means is in the form of a magnet which cooperates with a complementary magnet carried by the transmitter coil so that the transmitter coil is held in position relative to the stimulator by magnetic attraction.

12. The system of claim 11 in which the controller communicates with the transmitter via an implant interface of the communications interface unit using a dedicated, RF transmission protocol.

13. The system of claim 12 in which the protocol also incorporates reception telemetry for receiving data from the stimulator.

14. The system of claim 13 in which the controller is in the form of a hand-held programmable device and the communications interface unit is a custom designed, dedicated communications interface unit.

15. The system of claim 12 in which the interface unit includes a peripherals interface for enabling the controller to communicate with peripheral devices.

16. The system of claim 15 in which the peripherals interface includes a microphone interface for enabling the patient to issue voice commands to the controller via a microphone connected to the microphone interface.

17. The system of claim 15 in which the peripherals interface includes a remote control interface.

18. The system of claim 15 in which the peripherals interface includes a sensor pack peripherals interface for effecting communication with sensor packs, each sensor pack being provided to sense orientation of the patient'"'"'s torso and extremities when exercising of the patient'"'"'s extremities is to be performed or when the patient wishes to execute a standing, stepping or sitting operation.

19. The system of claim 18 in which the controller receives data regarding the positioning of the patient'"'"'s extremities via the sensor packs and the sensor pack peripherals interface.

20. The system of claim 1 which further includes an external skin surface stimulating device which effects external stimulation, as opposed to subcutaneous stimulation, of certain of the patient'"'"'s muscles.

21. A multi-purpose Functional Electrical Stimulation (FES) system comprising:

a multi-function, implantable stimulator configured to stimulate at least one lower extremity site and at least one spinal cord site in a patient'"'"'s body, the stimulator comprising;

a control unit;

a receiving device configured to send signals to the control unit;

a plurality of bundles of electric leads connected to the control unit, each lead terminating in at least one electrode to provide a plurality of discrete groups of electrodes associated with each of the different sites, each group of electrodes being operable to stimulate its associated site in the patient'"'"'s body, under the action of stimulation signals from the control unit;

a transmitter, arranged externally of the patient'"'"'s body, configured to supply signals transcutaneously to the receiving device; and

a controller in communication with the transmitter via a communications interface unit,

wherein the electrodes are configured to be implanted in the patient'"'"'s body by a surgical, subcutaneous tunneling technique.

22. The system of claim 21, wherein the stimulator further comprises:

a housing of a bio-compatible material, said housing defining at least one suture opening for suturing the housing in position.

23. The system of claim 21 in which the stimulator is configured to effect stimulation in at least four sites of the patient'"'"'s body.

24. The system of claim 21 in which the stimulator is implanted, in use, in a substantially central location in the patient'"'"'s body, the stimulator being connected to the sites in the patient'"'"'s body to be stimulated via the electrodes and their associated leads to deliver the appropriate stimulation to the desired sites by dedicated, application specific electrodes.

25. The system of claim 21 in which the transmitter is in the form of an RF transmitter coil arranged, in use, externally of the patient'"'"'s body in register with the receiver coil so that RF signals are transmitted transcutaneously to the stimulator, in use.

26. A multi-purpose Functional Electrical Stimulation (FES) system comprising:

a multi-function, implantable stimulator configured to stimulate at least four different sites in a patient'"'"'s body including a posterior and anterior right lower extremity, a posterior and anterior left lower extremity, a posterior, sacral region of a spinal cord of the patient and at a conus of the patient'"'"'s spinal cord, the stimulator comprising;

a control unit;

a plurality of bundles of electric leads connected to the control unit, each lead terminating in at least one electrode to provide a plurality of discrete groups of electrodes associated with each of the at least different sites, each group of electrodes being operable to stimulate its associated site in the patient'"'"'s body, under the action of stimulation signals from the control unit; and

an external controller in communication with the control unit via a transcutaneous communications link.

27. The system of claim 26 in which the stimulator is implanted, in use, in a substantially central location in the patient'"'"'s body, the stimulator being connected to the sites in the patient'"'"'s body to be stimulated via the electrodes and their associated leads to deliver the appropriate stimulation to the desired sites by dedicated, application specific electrodes.

28. The system of claim 26 in which the electrodes are configured to be implanted in the patient'"'"'s body by a surgical, subcutaneous tunneling technique to reduce the number and size of the incisions to be made to the patient'"'"'s body.

29. The system of claim 26 which further includes an external skin surface stimulating device which effects external stimulation, as opposed to subcutaneous stimulation, of certain of the patient'"'"'s muscles.

30. The system of claim 26, wherein the stimulator further comprises:

a housing of a bio-compatible material, said housing defining at least one suture opening for suturing the housing in position.