Novel Pain Management System, Method & Device Using Analytics Driven Random Electrical Stimuli

Abstract

Systems, methods, and devices for treating chronic pains effectively are disclosed. The system is based on the use of randomly generated non-pulsed waveform between a frequency of 5 Hz to 2 KHz. The waveforms generated have characteristics which are pre-defined or based on the input and feedback provided by the patient and/or by the clinician, at the same time conforming to certain safety rules and precautions ensuring patient safety. This disclosure also describes a novel approach of implementing a secure memory stick which can be used to exchange data securely between one device and another device where device could be the device mentioned earlier, an off-line server, or a PC.

What is claimed is: 
     
         1 . A tangible, non-transitory computer-readable media comprising instructions stored therein, wherein the instructions, when executed by one or more processing elements, cause a computing system to perform functions comprising:
 generating one or more random electrical stimulation signals in a frequency range between about 5 Hz and about 2 KHz, wherein an individual electrical stimulation signal is based on a plurality of waveforms selected from a library of non-pulsed waveforms; and   applying the one or more random electrical stimulation signals to a patient.   
     
     
         2 . The tangible, non-transitory computer-readable media of  claim 1 , wherein each waveform of the plurality of non-pulsed waveforms has a rise time greater than about 10 microseconds. 
     
     
         3 . The tangible, non-transitory computer-readable media of  claim 1 , wherein the functions further comprise:
 controlling an individual waveform to have a randomized RMS voltage between a configurable lower RMS voltage and a configurable upper RMS voltage.   
     
     
         4 . The tangible, non-transitory computer-readable media of  claim 3 , wherein the functions further comprise:
 setting at least one of the lower RMS voltage and the upper RMS voltage of the random waveform for the patient based at least in part on an analysis of a plurality of quantitative pain metrics for the patient.   
     
     
         5 . The tangible, non-transitory computer-readable media of  claim 3 , wherein the functions further comprise:
 setting the upper RMS voltage and lower RMS voltage to define a range of RMS voltage levels expected to be effective for treating a chronic pain symptom for the patient.   
     
     
         6 . The tangible, non-transitory computer-readable media of  claim 1 , wherein the functions further comprise:
 controlling at least one of the one or more random electrical stimulation signals to limit RMS current applied to the patient, wherein the RMS current applied to the patient is less than or equal to a configurable maximum RMS current limit.   
     
     
         7 . The tangible, non-transitory computer-readable media of  claim 1 , wherein the functions further comprise:
 receiving one or more of an upper RMS voltage level setting, a lower RMS voltage level setting, and a maximum RMS current level setting for one of the waveforms;   determining whether any of the received upper RMS voltage level setting, lower RMS voltage level setting, and maximum RMS current level setting would, if implemented, either (i) increase a likelihood that the electrical stimulation signal will cause the patient to experience pain or discomfort or (ii) reduce a likelihood that the electrical stimulation signal will be effective for treating a chronic pain symptom for the patient; and   in response to determining that at least one of the received upper RMS voltage level setting, lower RMS voltage level setting, and maximum RMS current level setting would, if implemented, increase a likelihood that the electrical stimulation signal will cause the patient to experience pain or discomfort or reduce the likelihood that the electrical stimulation signal will be effective for treating a chronic pain symptom for the patient, overriding at least one of the received upper RMS voltage level setting, lower RMS voltage level setting, or maximum RMS current level setting with a corresponding different setting determined by the system to one or both (i) not increase a likelihood that the electrical stimulation signal will cause the patient to experience pain or discomfort or (i) not reduce the likelihood that the electrical stimulation signal will be effective for treating a chronic pain symptom for the patient.   
     
     
         8 . The tangible, non-transitory computer-readable media of  claim 1 , wherein the functions further comprise generating the plurality of non-pulsed waveforms, wherein generating the plurality of non-pulsed waveforms comprises, for an individual waveform:
 determining one or more waveform attributes for the waveform, the waveform attributes comprising (i) a random number of segments for the waveform, (ii) a random positive peak voltage for the waveform, (iii) a random location in the waveform for the positive peak voltage, (iv) a random negative peak voltage for the waveform, (v) a random location in the waveform for the negative peak voltage, (vi) a random location in the waveform for each waveform segment, and (vii) a random slope for each waveform segment; and   generating the waveform according to the one or more determined waveform attributes.   
     
     
         9 . The tangible, non-transitory computer-readable media of  claim 8 , wherein an individual waveform has a randomized RMS voltage between a configurable lower RMS voltage and a configurable upper RMS voltage, and wherein the system further comprises:
 one or more communication interfaces configured to transfer system configuration parameters comprising one or more of the waveform attributes, the upper RMS voltage, and the lower RMS voltage used during a therapy session between the system and a database configured for storing system configuration parameters.   
     
     
         10 . The tangible, non-transitory computer-readable media of  claim 9 , wherein an initial set of system configuration parameters for use during an initial therapy session for the patient is based on a clinician's assessment of one or more of the patient's symptoms and an initial set of quantitative pain metrics provided by the patient, and wherein one or more subsequent sets of system configuration parameters for use during one or more subsequent therapy sessions for the patient are based on the clinician's observations of therapy results and one or more subsequent sets of quantitative pain metrics provided by the patient. 
     
     
         11 . The tangible, non-transitory computer-readable media of  claim 9 , wherein the one or more communication interfaces is configured to connect the system to one or both of a secure dongle or a secure cloud-based computing system. 
     
     
         12 . The tangible, non-transitory computer-readable media of  claim 1 , wherein an individual non-pulsed waveform comprises (i) a positive peak voltage that is limited to a maximum positive peak voltage, and (ii) a negative peak voltage that is limited to a maximum negative peak voltage. 
     
     
         13 . The tangible, non-transitory computer-readable media of  claim 1 , wherein applying the one or more random electrical stimulation signals to a patient comprises applying the one or more random electrical stimulation signals to a patient via circuity configured to generate and apply electrical stimulation signals to the patient via one or more sets of electrodes. 
     
     
         14 . The tangible, non-transitory computer-readable media of  claim 13 , wherein the circuity configured to generate and apply electrical stimulation signals to a patient via one or more sets of electrodes comprises:
 waveform generation circuitry configured to generate the plurality of non-pulsed waveforms;   signal generation circuitry configured to generate one or more random electrical stimulation signals based on the plurality of non-pulsed waveforms; and   therapy application circuitry configured to receive at least one of the one or more random electrical stimulation signals from the signal generation circuitry, condition the random electrical stimulation signals for application to the patient, and apply the conditioned random electrical stimulation signals to the patient.   
     
     
         15 . A computer-implemented method comprising:
 generating one or more random electrical stimulation signals in a frequency range between about 5 Hz and about 2 KHz, wherein an individual electrical stimulation signal is based on a plurality of waveforms selected from a library of non-pulsed waveforms; and   applying the one or more random electrical stimulation signals to a patient.   
     
     
         16 . The method of  claim 15 , wherein each waveform of the plurality of non-pulsed waveforms has a rise time greater than about 10 microseconds. 
     
     
         17 . The method of  claim 15 , wherein the method further comprises:
 controlling an individual waveform to have a randomized RMS voltage between a configurable lower RMS voltage and a configurable upper RMS voltage.   
     
     
         18 . The method of  claim 17 , wherein the method further comprises:
 setting at least one of the lower RMS voltage and the upper RMS voltage of the random waveform for the patient based at least in part on an analysis of a plurality of quantitative pain metrics for the patient.   
     
     
         19 . The method of  claim 18 , wherein the method further comprises setting the upper RMS voltage and lower RMS voltage to define a range of RMS voltage levels expected to be effective for treating a chronic pain symptom for the patient. 
     
     
         20 . The method of  claim 15 , wherein the method further comprises:
 controlling at least one of the one or more random electrical stimulation signals to limit RMS current applied to the patient, wherein the RMS current applied to the patient is less than or equal to a configurable maximum RMS current limit.