Devices and methods for heart rate measurement and wrist-watch incorporating same

• US 7,379,770 B2
• Filed: 06/16/2003
• Issued: 05/27/2008
• Est. Priority Date: 05/13/2003
• Status: Active Grant

• Current Assignee: Dayton Technologies Limited
• Original Assignee: Dayton Technologies Limited
• Inventors: Szeto, Chi Cheong
• Primary Examiner(s): Getzow; Scott M.
• Application Number:
  US10/461,353
• Publication Number:
  US 20040228217A1
• Time in Patent Office: 1,807 Days
• Field of Search: 600/508, 600/509, 600519-521, 600/523
• US Class Current: 600/519
• CPC Class Codes: A61B 5/02438 with portable devices, e.g. worn by the patient
• CPC Class Codes: A61B 5/02455 provided with high/low alarm devices
• CPC Class Codes: A61B 5/35 by template matching
• CPC Class Codes: A61B 5/681 Wristwatch-type devices
• CPC Class Codes: G04B 47/00 Time-pieces combined with other articles which do not interfere with the running or the time-keeping of the time-piece clockwork cases for special purposes G04B37/12; clocks with magnifying glass built in the face G04B39/00; time-pieces in which parts or cases produce special effects, e.g. aesthetic effects, G04B45/00, particularly with inscriptions or pictures moved by hand G04B45/003, with specially shaped cases or parts G04B45/0069; combination of writing or drawing implements with devices for indicating time B43K29/087; combined with cameras, projectors, or photographic printing apparatus G03B29/00

Abstract

A method and device for heart rate measurement uses a stream of signals containing ECG signals to select a reference QRS complex according to a set of predetermined criteria and obtain electrical signal characteristics of the reference QRS complex. A first QRS complex is detected from the stream of signals and characterized in relation to the reference QRS in the time domain such that the first QRS complex meets another set of predetermined criteria, and satisfies a level of similarity with the reference QRS complex. An instantaneous heart rate of a subject is evaluated based on the first and the reference QRS complexes when the first and the second QRS complexes are sufficiently similar.

Claims

1. A method of measuring the heart rate of a human being from a stream of incoming ECG signals, the method including the steps of:

selecting and then characterising a reference QRS complex from said stream of incoming ECG signals;

wherein said reference QRS complex is selected by adopting a local amplitude maximum as the R peak of said reference QRS complex, said local amplitude maximum being present within a predetermined time window and said predetermined time window being a time window within which at least one QRS complex must occur among said stream of incoming ECG signals under normal conditions, and said reference QRS complex is characterised by taking amplitude-time samples of said reference QRS complex;

seeking a first QRS complex from said stream of incoming ECG signals and characterising said first QRS complex by taking amplitude-time samples of said QRS complex for comparison of waveform similarity with said reference QRS complex, said first QRS complex being selected from said incoming ECG signals upon satisfying a first set of criteria of;

i. satisfying a threshold level of waveform similarity with said reference QRS complex,

ii. having an amplitude peak within a prescribed range of time from said reference QRS, and

iii. having its peak amplitude within a prescribed range of the peak amplitude of said reference QRS; and

evaluating a reference heart-rate from said first QRS complex and said reference QRS complex.

2. A method according to claim 1, wherein seeking of said first QRS complex is by the following steps:

seeking a local amplitude maximum in a predetermined time window, said predetermined time window being immediately adjacent said reference QRS complex and being a time window within which a next possible QRS complex may present,

adopting said local amplitude maximum as the R peak of said first QRS complex, and then

comparing waveform similarity between said reference QRS complex and said first QRS complex.

3. A method according to claim 2, wherein the method further comprises additional steps of:

seeking a confirmatory QRS complex after said first QRS complex has been identified, said confirmatory QRS complex satisfying a second set of criteria of;

i. satisfying a threshold level of waveform similarity with either said reference QRS complex or said first QRS complex,

ii. having an amplitude peak occurring within a prescribed range of time from either said reference QRS complex or said first QRS complex, and

iii. having its peak amplitude within a prescribed range the peak amplitude of either said reference QRS complex or said first QRS complex;

evaluating a confirmatory heart-rate from said confirmatory QRS complex, and

confirming a heart-rate for output if the confirmatory heart-rate is within a prescribed range from said reference heart-rate evaluated from said first QRS complex and said reference QRS complex.

4. A method according to claim 3, further comprising the steps of:

incrementing said threshold level of waveform similarity if said confirmatory heart-rate is outside said prescribed range of the reference heart-rate evaluated from said reference QRS complex and said first QRS complex,

seeking a new first QRS complex satisfying said first set of criteria with said incremented threshold level and substituting said new first QRS complex for said first QRS complex,

evaluating a new reference heart-rate from said new first QRS complex and said reference QRS,

seeking a new confirmatory QRS complex satisfying said second set of criteria,

evaluating a new confirmatory heart-rate from said new confirmatory QRS complex, and

confirming a heart-rate for output if the confirmatory heart-rate is within a prescribed range from said new reference heart-rate evaluated from said new first QRS complex and said reference QRS complex.

5. A method according to claim 2, wherein the range of variation between said confirmatory heart-rate and said reference heart-rate is 12.5%.

6. A method according to claim 5, wherein said predetermined time window within which at least one QRS must occur under normal conditions is 1.6 seconds.

7. A method according to claim 6, wherein the peak amplitude of said reference QRS complex must occur within said predetermined time window from the beginning of receipt of said stream of ECG signals.

8. A method according to claim 6, wherein the peak amplitude of said reference QRS complex must occur within a time range of 0.25 seconds to 1.5 seconds from the peak amplitude of said reference QRS complex.

9. A method according to claim 8, wherein the peak amplitudes of said reference QRS complex and said first QRS complex is between 40% and 250%.

10. A method according to claim 1, wherein said reference QRS complex is characterised by taking amplitude-time characteristics of said reference QRS complex in a prescribed time span sufficient to characterise said reference QRS complex, said amplitude-time characteristics of said reference QRS complex being for forming a reference matching template.

11. A method according to claim 10, wherein said prescribed time span is at least 90 ms, and preferably 100 ms.

12. A method according to claim 11, wherein the amplitude peak of said local amplitude maximum occurring within said predetermined time window is assumed to be the peak of an R spike of a QRS complex.

13. A method according to claim 10, wherein waveform similarity between said reference QRS complex and said first QRS complex is evaluated by template matching between said reference QRS complex and said first QRS complex, said template matching being performed by comparing said first QRS complex with reference to a reference template, said reference template being formed from amplitude-time characteristics of said reference QRS complex.

14. A method according to claim 13, wherein the degree of waveform similarity between said reference QRS complex and said first QRS complex is measured with reference to a reference benchmark, said reference benchmark being self-correlation or auto-correlation of said reference QRS complex.

15. A method according to claim 14, wherein said reference benchmark is TMC_ref, wherein TMC_ref=Σ

<sub>i−

1</sub>T(i)×

T(i), n is the number of samples and T(i) is the i^th sample value of the reference QRS complex.

16. A method according to claim 15, wherein the degree of waveform similarity is measured by comparing a template matching coefficient TMC with TMC_ref, wherein TMC=Σ

<sub>i−

1</sub> T(i)×

S(i), wherein T(i) is the the i^th sample value of the reference QRS complex and S(i) is the sample value of the signal being evaluated.

17. A method according to claim 10, wherein amplitude-time samples of said stream of incoming ECG signals are taken serially at regular intervals, and waveform similarity is performed continuously and progressively with said incoming data samples until a set of data samples satisfying said first set of criteria is found within said predetermined time window.

18. An apparatus for measuring the heart-rate of a human being, the apparatus comprising:

means for receiving, sampling and storing a stream of incoming ECG signals,

means for detecting a local amplitude maximum from stored samples of said stream of incoming ECG signals within a predetermined time window,

means for forming a reference QRS template using said local amplitude maximum as an R peak of said reference QRS complex,

means for seeking a first QRS complex from said stream of incoming ECG signals, said first QRS complex satisfying a first set of criteria of;

i. satisfying a threshold level of waveform similarity with said reference QRS complex,

ii. having an amplitude peak occurring within a prescribed range of time from said reference QRS, and

iii. having its peak amplitude occurring within a prescribed range of the peak amplitude of said reference QRS; and

means for evaluating a reference heart-rate from said first QRS complex and said reference QRS complex.

19. An apparatus according to claim 18, further comprising a means for seeking a confirmatory QRS complex from said stored sample of said stream of ECG signals, means for evaluating a confirmatory heart-rate from said confirmatory QRS complex, and means to reinitialise seeking of a new reference QRS if said confirmatory heart-rate exceeds a normal range of said reference heart-rate.

20. A wrist watch comprising an apparatus according to claim 18, said wrist watch further comprising:

an amplifier for amplifying incoming ECG signals,

a QRS filter for band-filtering said ECT signals,

an analogue-to-digital converter for converting the band-filtered ECG signals into digital data, and

a visual display unit for displaying heart-rate information obtained from said ECG signals.