Neurostimulation therapy manipulation

• US 7,933,655 B2
• Filed: 04/13/2007
• Issued: 04/26/2011
• Est. Priority Date: 10/31/2002
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: North, Richard B., Sieracki, Jeffrey M.
• Primary Examiner(s): Getzow; Scott M
• Application Number:
  US11/735,140
• Publication Number:
  US 20070265678A1
• Time in Patent Office: 1,474 Days
• Field of Search: 607 43- 63
• US Class Current: 607/46
• CPC Class Codes: A61N 1/36071 Pain
• CPC Class Codes: A61N 1/37247 User interfaces, e.g. input or presentation means

Abstract

A user, such as a clinician or the patient, uses a control device to manipulate at least one neurostimulation parameter. A mapping system uses a calibrated map to map the directional output of the control device to values of at least one stimulation parameter to allow the user to intuitively control the value of the parameter. In some embodiments, where a stimulation device is used to deliver spinal cord stimulation (SCS) therapy for example, the user manipulates a parameter to effect the location and/or strength of paresthesia experienced by the patient. In exemplary embodiments, the parameter values are combinations of electrodes, and the mapping system selects electrode combinations based on the output of the control device such that a direction of movement of paresthesia experienced by the patient corresponds to a direction of manipulation of a directional controller of the control device. The mapping system may calibrate the map based on patient paresthesia information received from a user.

Claims

1. A method comprising:

calibrating a map that maps directional information to combinations of electrodes from a set of electrodes coupled to a stimulation device, wherein the calibrated map comprises amplitude scale factors associated with at least some of the electrode combinations;

receiving directional information from a directional controller that reflects manipulation of the directional controller by a user;

selecting an electrode combination based on the received directional information and the calibrated map; and

controlling the stimulation device to deliver electrical stimulation to a patient via the selected electrode combination and based on one of the amplitude scale factors that is associated with the selected electrode combination.

2. The method of claim 1, wherein calibrating the map comprises calibrating the map such that a direction of movement of paresthesia resulting from application of electrical stimulation via the selected electrode combination reflects the direction of the manipulation of the directional controller.

3. The method of claim 1, wherein calibrating a map comprises:

receiving outputs from the directional controller that reflect manipulation of the directional controller to a plurality of predetermined locations;

receiving information that reflects paresthesia experienced by the patient when the directional controller is located at each of the locations; and

adapting a fixed map based on the outputs and the paresthesia information.

4. The method of claim 3, wherein the paresthesia information comprises at least one of an amplitude level associated with a stimulation perception threshold or an outline of a paresthesia region on a body diagram.

5. The method of claim 3, wherein adapting a fixed map comprises applying Euclidian transforms to the fixed map based on the outputs and the paresthesia information.

6. The method of claim 3, further comprising determining the amplitude scale factors based on the paresthesia information.

7. The method of claim 1, wherein the user manipulates the directional controller to test a plurality of electrode combinations by application of electrical stimulation by the stimulation device via the electrode combinations.

8. The method of claim 7, wherein calibrating a map comprises:

receiving paresthesia and directional information during the testing; and

continually calibrating the map based on the paresthesia and directional information.

9. The method of claim 7, further comprising:

identifying one of the tested electrode combinations based on input received from the user; and

recalibrating the map such that a center position of a manipulation range of the directional controller corresponds to the identified electrode combination.

10. The method of claim 1, wherein the user is one of a clinician and the Patient.

11. A mapping system comprising:

an input circuit that receives directional information from a directional controller, the directional information reflecting manipulation of the directional controller by a user;

a memory that stores a map that maps the directional information to combinations of electrodes from a set of electrodes coupled to a stimulation device;

a telemetry circuit; and

a processor that calibrates the map, wherein the calibrated map comprises amplitude scale factors associated with at least some of the electrode combinations, selects an electrode combination based on the received directional information and the calibrated map, and controls the stimulation device via the telemetry circuit to deliver electrical stimulation to a patient via the selected electrode combination and based on one of the amplitude scale factors that is associated with the selected electrode combination.

12. The system of claim 11, wherein the processor calibrates the map such that a direction of movement of paresthesia resulting from application of electrical stimulation via the selected electrode combination reflects the direction of the manipulation of the directional controller.

13. The system of claim 11, wherein the processor receives outputs from the directional controller that reflect manipulation of the directional controller to a plurality of predetermined locations, receives information that reflects paresthesia experienced by the patient when the directional controller is located at each of the locations, and adapts a fixed map based on the outputs and the paresthesia information.

14. The system of claim 13, wherein the paresthesia information comprises at least one of an amplitude level associated with a stimulation perception threshold or an outline of a paresthesia region on a body diagram.

15. The system of claim 13, wherein the processor applies Euclidian transforms to the fixed map based on the outputs and the paresthesia information.

16. The system of claim 13, wherein the processor determines the amplitude scale factors based on the paresthesia information.

17. The system of claim 11, wherein input circuit receives directional information that reflects movement of the directional controller by the user to test a plurality of electrode combinations, and the processor controls the stimulation device via the telemetry circuit to apply electrical stimulation via the electrode combinations.

18. The system of claim 17, wherein the processor receives paresthesia and directional information during the testing, and continually calibrates the map based on the paresthesia and directional information.

19. The system of claim 17, wherein the processor identifies one of the tested electrode combinations based on input received from the user, and recalibrates the map such that a center position of a manipulation range of the directional controller corresponds to the identified electrode combination.

20. A computer-readable medium comprising instructions that cause a programmable processor to:

calibrate a map that maps directional information to combinations of electrodes from a set of electrodes coupled to a stimulation device, wherein the calibrated map comprises amplitude scale factors associated with at least some of the electrode combinations;

receive directional information from a directional controller that reflects manipulation of the directional controller by a user;

select an electrode combination based on the received directional information and the calibrated map; and

control the stimulation device to deliver electrical stimulation to a patient via the selected electrode combination and based on one of the amplitude scale factors that is associated with the selected electrode combination.

21. The computer-readable medium of claim 20, wherein the instructions that cause a programmable processor to calibrate the map comprise instructions that cause a programmable processor to calibrate the map such that a direction of movement of paresthesia resulting from application of electrical stimulation via the selected electrode combination reflects the direction of the manipulation of the directional controller.

22. The computer-readable medium of claim 20, wherein the instructions that cause a programmable processor to calibrate the map comprise instructions that cause a programmable processor to:

receive outputs from the directional controller that reflect manipulation of the directional controller to a plurality of predetermined locations;

receive information that reflects paresthesia experienced by the patient when the directional controller is located at each of the locations; and

adapt a fixed map based on the outputs and the paresthesia information.

23. The computer-readable medium of claim 22, further comprising instructions that cause a programmable processor to determine the amplitude scale factors based on the paresthesia information.