Implanted pulse generators with reduced power consumption via signal strength/duration characteristics, and associated systems and methods
Implanted pulse generators with reduced power consumption via signal strength-duration characteristics, and associated systems and methods are disclosed. A representative method for treating a patient in accordance with the disclosed technology includes receiving an input corresponding to an available voltage for an implanted medical device and identifying a signal delivery parameter value of an electrical signal based on a correlation between values of the signal delivery parameter and signal deliver amplitudes. The signal deliver parameter can include at least one of pulse width or duty cycle. The method can further include delivering an electrical therapy signal to the patient at the identified signal delivery parameter value using a voltage within a margin of the available voltage.
1. A method for treating pain in a patient, comprising:
establishing a patient-specific correlation between amplitudes and pulse widths by identifying at least one pulse width/amplitude pair that produces a detectable result in the patient, wherein identifying the at least one pulse width/amplitude pair is based at least in part on (i) producing pain relief without producing paresthesia in the patient with a signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair, and/or (ii) producing an evoked potential in the patient with the signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair;
receiving at least one input corresponding to either a target therapy amplitude or a target therapy pulse width; and
updating the other of the target therapy amplitude or the target therapy pulse width according to the patient-specific correlation.
2. The method of claim 1 wherein identifying the at least one pulse width/amplitude pair is based at least in part on producing pain relief without producing paresthesia in the patient with the signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair.
3. The method of claim 1 wherein identifying the at least one pulse width/amplitude pair is based at least in part on producing an evoked potential in the patient with the signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair.
4. The method of claim 1 wherein establishing the patient-specific correlation includes using the at least one pulse width/amplitude pair to determine which of a plurality of pre-established pulse width/amplitude correlations applies to the patient.
5. The method of claim 4 wherein the at least one pulse width/amplitude pair is one of multiple pulse width/amplitude pairs used to determine which of the plurality of pre-established pulse width/amplitude correlations applies to the patient.
6. The method of claim 4 wherein establishing the pre-established pulse width/amplitude correlations includes using data from other patients.
7. The method of claim 1 wherein establishing the patient-specific correlation between amplitudes and pulse widths further comprises applying a correction factor to the at least one pulse width/amplitude pair that produces a detectable result in the patient.
8. The method of claim 7 wherein the correction factor is patient-specific.
9. A method for treating pain in a patient, comprising:
programming a pulse generator to:
establish a patient-specific correlation between amplitudes and pulse widths by identifying at least one pulse width/amplitude pair that produces a detectable result in the patient, wherein identifying the at least one pulse width/amplitude pair is based at least in part on (i) producing pain relief without producing paresthesia in the patient with a signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair, and/or (ii) producing an evoked potential in the patient with the signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair;
receive at least one input corresponding to either a target therapy amplitude or a target therapy pulse width; and
update the other of the target therapy amplitude or the target therapy pulse width according to the patient-specific correlation.
10. The method of claim 9 wherein identifying the at least one pulse width/amplitude pair is based at least in part on producing pain relief without producing paresthesia in the patient with the signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair.
11. The method of claim 9 wherein identifying the at least one pulse width/amplitude pair is based at least in part on producing an evoked potential in the patient with the signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair.
12. The method of claim 9 wherein establishing the patient-specific correlation includes using the at least one pulse width/amplitude pair to determine which of a plurality of pre-established pulse width/amplitude correlations applies to the patient.
13. The method of claim 12 wherein the at least one pulse width/amplitude pair is one of multiple pulse width/amplitude pairs used to determine which of the plurality of pre-established pulse width/amplitude correlations applies to the patient.
14. The method of claim 12 wherein establishing the pre-established pulse width/amplitude correlations includes using data from other patients.
15. The method of claim 9 wherein establishing the patient-specific correlation between amplitudes and pulse widths further comprises applying a correction factor to the at least one pulse width/amplitude pair that produces a detectable result in the patient.
16. The method of claim 15 wherein the correction factor is patient-specific.
17. A system for treating pain in a patient, comprising:
means for establishing a patient-specific correlation between amplitudes and pulse widths by identifying at least one pulse width/amplitude pair that produces a detectable result in the patient, wherein identifying the at least one pulse width/amplitude pair is based at least in part on (i) producing pain relief without producing paresthesia in the patient with a signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair, and/or (ii) producing an evoked potential in the patient with the signal having the pulse width and the amplitude of the at least one pulse width/amplitude pair;
means for receiving at least one input corresponding to either a target therapy amplitude or a target therapy pulse width; and
means for updating the other of the target therapy amplitude or the target therapy pulse width according to the patient-specific correlation.
18. The system of claim 17 wherein identifying the at least one pulse width/amplitude pair is based at least in part on producing pain relief without producing paresthesia in the patient with the signal having the pulse width and amplitude of the at least one pulse width/amplitude pair.
19. The system of claim 17 wherein identifying the at least one pulse width/amplitude pair is based at least in part on producing an evoked potential in the patient with the signal having the pulse width and amplitude of the at least one pulse width/amplitude pair.
20. The system of claim 17 wherein establishing the patient-specific correlation includes using the at least one pulse width/amplitude pair to determine which of a plurality of pre-established pulse width/amplitude correlations applies to the patient.
21. The system of claim 20 wherein the at least one pulse width/amplitude pair is one of multiple pulse width/amplitude pairs used to determine which of the plurality of pre-established pulse width/amplitude correlations applies to the patient.
22. The system of claim 20 wherein establishing the pre-established pulse width/amplitude correlations includes using data from other patients.
23. The system of claim 17 wherein establishing the patient-specific correlation between amplitudes and pulse widths further comprises applying a correction factor to the at least one pulse width/amplitude pair that produces a detectable result in the patient.
24. The system of claim 23 wherein the correction factor is patient-specific.