Method and apparatus for extracting optimum holter ECG reading

• US 8,560,054 B2
• Filed: 05/08/2007
• Issued: 10/15/2013
• Est. Priority Date: 05/08/2006
• Status: Active Grant

• Current Assignee: AMPS, LLC
• Original Assignee: AMPS, LLC
• Inventors: Badilini, Fabio F.
• Primary Examiner(s): Layno, Carl H
• Assistant Examiner(s): Stice, Paula J
• Application Number:
  US11/745,744
• Publication Number:
  US 20070265538A1
• Time in Patent Office: 2,352 Days
• Field of Search: 600/500, 600/509, 600/515, 600/523, 600/485, 600/517, 607/4, 607/5, 607/9
• US Class Current: 600/509
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle
• CPC Class Codes: A61B 5/352 Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval
• CPC Class Codes: A61B 5/7207 of noise induced by motion artifacts

Abstract

The present invention is for a method and apparatus for extracting optimum ECG data from within a optimum timeperiod. The method and apparatus require setting a timeperiod in which to extract ECG data, setting thresholds for noise, determining a segment with stable heart rate, and to measure the ECG data of the time period. Once the parameters are set and the data is collected, optimum data according to the parameters set by the user are extracted for use and analysis, such that the ECGs that are free from noise and have a stable heart rate are retrieved from the desired timeperiod window. The invention can be used in a software program, may be programmable into a Holter monitors, or as well as applicability in other related monitoring devices.

Claims

1. A method for operating an electrocardiography (ECG) machine having a CPU, a memory, a display, and a software program in said memory for operating said ECG machine to identify and display low hysteresis optimum electrocardiography (ECG) heart rates by said electrocardiograph machine comprising the steps of:

providing said electrocardiograph (ECG) machine to receive and record electrocardiograph signals from a patient who is continuously monitored by said ECG machine for one or more transient conditions of the electrical activity of the heart for an extended period of time;

operating the ECG machine to record ECG signals generated by the patient'"'"'s heart, said ECG signals occurring over an extended period of time and including at least one window of time, said window of time including a expected extraction time for an instantaneous and stable heart rate processing the ECG signals to calculate the heart rate for heart beats that occur during the window and to determine the average heart rate for an observation period preceding each heart beat during the window; and

displaying a stable heart rate occurring during said window wherein said displayed stable heart rate is one of the heart rates in the windows that is closest in magnitude to its corresponding average heart rate; and

wherein said displayed stable heart rate indicates a low hysteresis optimum electrocardiography (ECG) heart rate.

2. The method of claim 1 wherein one can predict, or actually know from blood-sample data at what times drug reactivity or absorption should occur and the predetermined time points correspond to one of the group comprising:

(a) a predicted or actually known from blood-sample data showing there is a heightened level of drug interaction with or drug absorption by the patient;

(b) a predicted or actually known blood-sample data showing there is a minimal level of drug interaction with or drug absorption by the patient;

(c) a predicted or actually known blood sample data showing there is a predetermined level of drug interaction with or drug absorption by the patient; and

(d) any combination thereof.

3. The method of claim 1 wherein the ECG signals are recorded by a portable monitor having continuous or extended recording capabilities.

4. The method of claim 1 wherein the window is a first predetermined time and the observation period is a second predetermined time prior to each heart beat.

5. The method of claim 4 wherein the window is two minutes and the observation period is one minute prior to each heart beat.

6. The method of claim 1 wherein the average heart rate is the running average of the heat beats occurring during the observation period preceding each heart beat.

7. A method for operating a machine with a central processing unit (CPU), a memory, a display, and a software program for operating said machine to identify and display low hysteresis electrocardiography (ECG) heart rates recorded by an ECG machine coupled to a patient for an extended period of time, comprising the steps of:

said machine providing at least one window of time, said window of time including a expected extraction time for an instantaneous and low hysteresis heart rate, said expected extraction time corresponding to a predetermined time point when drug reactivity or absorption should occur;

said machine recording in said memory said ECG signals including ECG signals inside and outside of said window;

said machine processing the ECG signals to determine instantaneous heart rates for heart beats in said window and average heart rates for heart beats occurring during observation periods preceding each heart beat and storing said heart rates;

said machine processing the ECG signals to compare each instantaneous heart rate during the window to the average heart rate of the heart beats during the observation period preceding each heart beat; and

said machine displaying an instantaneous heart rate closest to the average heart rate during the corresponding preceding observation period.

8. The method of claim 7 wherein the predetermined time points correspond to one of the group comprising:

(a) where from a predicted or actually known from blood-sample data there is a heightened level of drug interaction with or drug absorption by the patient;

(b) where from a predicted or actually known from blood-sample data there is a minimal level of drug interaction with or drug absorption by the patient;

(c) where from a predicted or actually known from blood-sample data there is a predetermined level of drug interaction with or drug absorption by the patient; and

(d) any combination thereof; and

wherein said displayed stable heart rate indicates a low hysteresis optimum electrocardiography (ECG) heart rate.

9. The method of claim 7 wherein the window is a first predetermined time and the observation period is a second predetermined time prior to each heart beat.

10. The method of claim 9 wherein the window is two minutes and the observation period is one minute prior to each heart beat.

11. The method of claim 7 wherein the average heart rate is the running average of the heat beats occurring during the observation period preceding each heart beat.

12. A method for operating a machine with a central processing unit (CPU), a memory, a display, and a software program for operating said machine to identify and display a stable, low hysteresis electrocardiography (ECG) heart rates recorded by an ECG machine coupled to a patient, comprising the steps of:

storing ECG data recorded over an extended duration of time;

setting at least one expected ECG data extraction time during the extended duration of time;

providing a window of time beginning before the expected extraction time and terminating after the expected extraction time;

calculating an instantaneous heart rate for heart beats occurring during the window;

calculating an average heart rate for heart beats occurring prior to each heart beat in said window;

at the expected ECG data extraction time, comparing the average heart rate during a preceding observation period to the instantaneous heart rate; and

extracting an instantaneous heart rate within the window that is closest in magnitude to the average heart rate over a corresponding preceding observation period;

displaying said extracted instantaneous heart rate,

wherein said displayed instantaneous heart rate indicates a stable, low hysteresis electrocardiography (ECG) heart rate recorded by said ECG machine.

13. The method of claim 12 wherein the window is a first predetermined time and the observation period is a second predetermined time prior to each heart beat.

14. The method of claim 13 wherein the window is two minutes and the observation period is one minute prior to each heart beat.

15. The method of claim 12 wherein the average heart rate is the running average of the heat beats occurring during the observation period preceding each heart beat.