Technique for determining optimum treatment parameters

• US 9,061,145 B2
• Filed: 09/13/2013
• Issued: 06/23/2015
• Est. Priority Date: 09/17/2012
• Status: Active Grant

• Current Assignee: Donald A. Rhodes
• Original Assignee: Donald A. Rhodes
• Inventors: Rhodes, Donald A.
• Primary Examiner(s): Stice, Paula J
• Application Number:
  US13/987,897
• Publication Number:
  US 20150080984A1
• Time in Patent Office: 648 Days
• Field of Search: 607/46, 607/67, 607149-150, 607/145
• US Class Current: 1/1
• CPC Class Codes: A61B 5/4035 Evaluating the autonomic nervous system
• CPC Class Codes: A61B 5/4836 Diagnosis combined with treatment in closed-loop systems or methods A61B5/0036 takes precedence
• CPC Class Codes: A61N 1/323 Interference currents, i.e. treatment by several currents summed in the body
• CPC Class Codes: A61N 1/36031 using physiological parameters for adjustment
• CPC Class Codes: A61N 1/36034 specified by the stimulation parameters
• CPC Class Codes: G16H 20/30 relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
• CPC Class Codes: G16H 40/63 for local operation

Abstract

A diagnostic device in an electrical interferential treatment regime applies different pulse frequencies in one selection of electrode placement and determines the change of blood flow in response to the change in pulse frequency in an attempt to determine an optimum or workable set of parameters. The device includes electronic storage to record a series of tests and their results and a communication link. The communication link enables a professional caregiver to determine whether the parameter determinations, made at a location remote from the professional'"'"'s office, such as at the residence of the patient, were conducted and were conducted correctly. The communication link also enables the professional to determine whether the treatments were conducted and conducted correctly.

Claims

1. A method to facilitate home use including determining and applying treatment parameters for an electrical interferential treatment regimen conducted on a patient residing at a first location, comprising

externally applying pairs of electrodes, respectively, at selected placements to opposite limbs of a patient situated at said first location and delivering a series of trial electrical interferential treatments to the patient produced by at least one electronic device at said first location through the electrodes, and, for a pair of electrode placements, each electrical interferential treatment comprises electrical interferential treatment parameters of at least one beat frequency;

measuring at least one biological function responsive to autonomic nervous system activity of the patient caused by each electrical interferential treatment parameter delivered and calculating a numerical value indicative of the at least one measured biological function for each treatment parameter delivered;

comparing each said numerical value to a predetermined numerical value indicative of a desired biological function;

determining whether each said numerical value is in excess of said predetermined numerical value and identifying at least one of said electrical interferential treatment parameters that produced a numerical value in excess of said predetermined numerical value;

storing data, in said at least one electronic device, of said numerical values, said treatment parameters of said series of trial electrical interferential treatments and said treatment parameters of said at least one identified electrical interferential treatment;

electronically transmitting said stored data to at least one other electronic device situated at a second location away from the immediate vicinity of the first location,

selecting from said stored data said treatment parameters of said identified electrical interferential treatment that produced said numerical value in excess of the predetermined value and applying the selected parameters through the electrodes to the patient in a subsequent selected treatment regimen; and

viewing, at said first and second locations, said stored data of said numerical values, said treatment parameters of said series of trial electrical interferential treatments and said treatment parameters of said identified electrical interferential treatment that produced said numerical value in excess of the predetermined value and determining from said stored data whether said treatment parameters of said identified electrical interferential treatment produced a numerical value in excess of the predetermined value.

2. The method of claim 1 wherein the first location comprises a residence of the patient and the second location comprises a professional office.

3. The method of claim 1 wherein the step of storing data further includes storing the time and date of the application of each said series of trial treatment parameters and said treatment parameters of said identified electrical interferential treatment that produced said numerical value in excess of the predetermined value.

4. The method of claim 3 wherein the step of electronically transmitting transmits said stored data and time and date of said series of trial treatment parameters and said treatment parameters of said identified electrical interferential treatment that produced said numerical value in excess of the predetermined value to said at least one electronic device and to said at least one other electronic device;

whereby

said stored data corresponding to said numerical value that is in excess of said predetermined value is viewed at both said electronic devices for determining from said stored data whether said treatment parameters of said identified electrical interferential treatment produced said numerical value in excess of the predetermined value.

5. The method of claim 4 wherein the first location comprises a residence of the patient and the second location comprises a professional office.

6. The method of claim 1 wherein the step of measuring of at least one biological function comprises measuring finger temperature.

7. The method of claim 6 further comprising determining whether the applied selected treatment parameters produce at least a one degree Fahrenheit increase in finger temperature in less than four minutes thereby constituting an effective treatment regimen.

8. The method of claim 6 further comprising equalizing the patient'"'"'s initial finger temperature to ambient temperature by

measuring the patient'"'"'s finger temperature prior to delivering the series of trial electrical interferential treatments and, when the rate of change of finger temperature falls below a predetermined value, commencing delivering the series of trial electrical interferential treatments through the electrodes.

9. The method of claim 8 wherein the predetermined value of the rate of change is at least one degree Fahrenheit per minute.

10. A system configured for use including determining and applying treatment parameters for an electrical interferential treatment regimen conducted on a patient situated at a first location, comprising:

pairs of electrodes adapted for external temporary attachment, respectively, to opposite limbs of a patient situated at said first location and at least one electronic device at said first location for delivering a series of trial electrical interferential treatments to the patient through the electrodes, and, for a pair of electrode placements, each electrical interferential treatment comprises electrical interferential treatment parameters of at least one beat frequency;

a sensor configured to measure at least one biological function responsive to autonomic nervous system activity of the patient caused by each electrical interferential treatment parameter delivered;

said at least one electronic device responsive to said sensor and adapted to calculate a numerical value indicative of the at least one measured biological function;

said at least one electronic device further adapted to compare said numerical value to a predetermined numerical value indicative of a desired biological function;

said at least one electronic device further adapted to determine whether said numerical value is in excess of said predetermined numerical value;

said at least one electronic device further adapted to store data of said numerical values, said treatment parameters of said series of trial electrical interferential treatments and said treatment parameters of said at least one electrical interferential treatment that corresponds to a numerical value that is in excess of said predetermined numerical value;

said at least one electronic device further adapted to electronically transmit said stored data of said numerical values, said treatment parameters of said series of trial electrical interferential treatments and said treatment parameters of said at least one electrical interferential treatment that corresponds to a numerical value that is in excess of said predetermined numerical value to at least one other electronic device situated at a second location away from the immediate vicinity of the first location;

said at least one electronic device further adapted to select said treatment parameters of the at least one electrical interferential treatment that produced said numerical value in excess of the predetermined value and apply the selected treatment parameters through the electrodes to the patient in a subsequent selected treatment regimen; and

said at least one electronic device and said at least one other electronic device are adapted for viewing said numerical values, said treatment parameters of said series of trial electrical interferential treatments and said treatment parameters of said identified electrical interferential treatment that produced said numerical value in excess of the predetermined value and determining from said stored data whether said treatment parameters of said identified electrical interferential treatment produced a numerical value in excess of the predetermined value.

11. The system of claim 10 wherein said first location comprises a residence of the patient and the second location comprises a professional office.

12. The system of claim 10 wherein the sensor comprises a finger temperature sensor.

13. The system of claim 12 wherein said finger temperature sensor is adapted to measure a patient'"'"'s finger temperature prior to delivering the series of trial electrical interferential treatments and, said at least one electronic device, in response to a measured rate of change of finger temperature falling below a predetermined value, is adapted to deliver said series of trial electrical interferential treatment parameters through the electrodes.

14. The system of claim 13 wherein the predetermined value of said rate of change is at least one degree Fahrenheit per minute.

15. The system of claim 14 wherein the first location comprises a residence of the patient and the second location comprises a professional office.