Selective high frequency spinal cord modulation for inhibiting pain, including cephalic and/or total body pain with reduced side effects, and associated systems and methods
Selective high-frequency spinal cord modulation for inhibiting pain with reduced side effects and associated systems and methods are disclosed. In particular embodiments, high-frequency modulation in the range of from about 1.5 KHz to about 100 KHz may be applied to the patient's spinal cord region to address upper extremity pain without creating paresthesia in the patient.
1. A method of treating an upper extremity pain indication, exclusive of upper extremity gain associated with total body pain, comprising:
configuring a signal generator to generate and deliver an upper extremity pain therapy signal to a target location, wherein the target location is a cervical vertebral location between C2-C6, inclusive, via one or more implanted signal delivery devices coupled to the signal generator,
wherein at least a portion of the therapy signal is at a frequency in a frequency range of from 1.5 kHz to 100 kHz, includes pulses with a pulse width in a pulse width range of 10 microseconds to 333 microseconds, and has an amplitude in an amplitude range of 0.1 mA to 20 mA, which at least partially alleviates the upper extremity pain indication, exclusive of upper extremity pain associated with total body pain, without generating paresthesia.
2. The method of claim 1 , wherein the cervical vertebral location is between C3-C5, inclusive.
3. The method of claim 1 , wherein the upper extremity pain indication is selected from the group consisting of: arthritis pain, acromio-clavicular joint pain, myofascial pain in the shoulders or arms, subdeltoid bursitis pain, bicipital tendonitis pain, supraspinatus pain, rotator cuff tear pain, deltoid pain, teres major pain, scapulocostal pain, tennis elbow pain, golfer's elbow pain, anconeus pain, supinator pain, pain due to ulnar nerve entrapment at the elbow, lateral antebrachial cutaneous nerve pain, olecranon bursitis pain, and phantom limb pain.
4. The method of claim 1 , wherein the frequency range is from 3 kHz to 20 kHz.
5. The method of claim 1 , wherein the frequency range is from 5 kHz to 15 kHz.
6. The method of claim 1 , wherein the one or more signal delivery devices include a percutaneous lead having one or more electrodes disposed toward a distal end of the percutaneous lead.
7. A method of treating a non-total body pain upper extremity pain indication, comprising:
applying an electrical therapy signal to a cervical vertebral location of a patient's spinal cord, wherein the cervical vertebral location is between C2-C6, inclusive, wherein at least a portion of the electrical therapy signal (a) is at a frequency in a frequency range of from 1.5 kHz to 100 kHz, (b) includes pulses having a pulse width in a pulse width range of 10 microseconds to 333 microseconds, and (c) is at an amplitude in an amplitude range of 0.1 mA to 20 mA, and wherein the electrical therapy signal treats the upper extremity pain indication without generating paresthesia in the patient.
8. The method of claim 7 , wherein the cervical vertebral location is between C3-C5, inclusive.
9. The method of claim 7 , wherein the upper extremity pain indication is selected from the group consisting of: arthritis pain, acromio-clavicular joint pain, myofascial pain in the shoulders or arms, subdeltoid bursitis pain, bicipital tendonitis pain, supraspinatus pain, rotator cuff tear pain, deltoid pain, teres major pain, scapulocostal pain, tennis elbow pain, golfer's elbow pain, anconeus pain, supinator pain, pain due to ulnar nerve entrapment at the elbow, lateral antebrachial cutaneous nerve pain, olecranon bursitis pain, and phantom limb pain.
10. The method of claim 7 , wherein the frequency range is from 3 kHz to 20 kHz.
11. The method of claim 7 , wherein the frequency range is from 5 kHz to 15 kHz.
12. The method of claim 7 , further comprising programming the signal generator to generate the electrical therapy signal.
13. The method of claim 7 , wherein the electrical therapy signal is applied via one or more implanted signal delivery devices coupled to an implanted signal generator, wherein the signal generator is programmed with instructions that, when executed, treat the upper extremity pain indication by generating the electrical therapy signal and delivering the electrical therapy signal to the cervical vertebral location.
14. The method of claim 13 , wherein the one or more signal delivery devices include a percutaneous lead having one or more electrodes disposed toward a distal end of the percutaneous lead.
15. The method of claim 7 , wherein the frequency range is 1.5 kHz to 50 kHz.
16. The method of claim 7 , wherein the frequency range is 3 kHz to 10 kHz.
17. The method of claim 7 , wherein the frequency is 10 kHz.
18. The method of claim 7 , wherein the portion of the electrical therapy signal is biphasic.
19. The method of claim 7 , wherein the pulse width range is 25 microseconds to 166 microseconds.
20. The method of claim 7 , wherein the pulse width range is 30 microseconds to 35 microseconds.
21. The method of claim 7 , wherein the frequency range is 5 kHz to 15 kHz, the pulse width range is 30 microseconds to 35 microseconds, and the amplitude range is 0.5 mA to 10 mA.
22. An upper extremity pain treatment system for treating a non-total body pain upper extremity pain indication, comprising:
a spinal cord modulation system having
at least one signal delivery device configured to be implanted proximate to a cervical vertebral location of a patient's spinal cord, wherein the cervical vertebral location is between C2-C6, inclusive, and
a signal generator programmed with instructions that, when executed, treat the upper extremity pain indication by generating and delivering a non-paresthesia-generating electrical therapy signal to the cervical vertebral location, via the at least one signal delivery device,
wherein at least a portion of the electrical therapy signal (a) is at a frequency in a frequency range of from 1.5 kHz to 100 kHz, (b) includes pulses having a pulse width in a pulse width range of 10 microseconds to 333 microseconds, and (c) is at an amplitude in an amplitude range of 0.1 mA to 20 mA.
23. The system of claim 22 , wherein the cervical vertebral location is between C3-C5, inclusive.
24. The system of claim 22 , wherein the upper extremity pain indication is selected from the group consisting of: arthritis pain, acromio-clavicular joint pain, myofascial pain in the shoulders or arms, subdeltoid bursitis pain, bicipital tendonitis pain, supraspinatus pain, rotator cuff tear pain, deltoid pain, teres major pain, scapulocostal pain, tennis elbow pain, golfer's elbow pain, anconeus pain, supinator pain, pain due to ulnar nerve entrapment at the elbow, lateral antebrachial cutaneous nerve pain, olecranon bursitis pain, and phantom limb pain.
25. The system of claim 22 , wherein the frequency range is from 3 kHz to 20 kHz.
26. The system of claim 22 , wherein the frequency range is from 5 kHz to 15 kHz.
27. The system of claim 22 , wherein the at least one signal delivery device includes a percutaneous lead having one or more electrodes disposed toward a distal end of the percutaneous lead.
28. The system of claim 22 , wherein the electrical therapy signal includes one or more pulses with a pulse width between 30 microseconds and 35 microseconds.
29. The system of claim 22 , wherein the electrical therapy signal includes one or more pulses with a pulse width between 25 microseconds and 166 microseconds.