Reducing data acquisition, power and processing for photoplethysmography and other applications

• US 7,881,790 B1
• Filed: 11/30/2007
• Issued: 02/01/2011
• Est. Priority Date: 07/19/2004
• Status: Expired due to Fees

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories)
• Inventors: Turcott, Robert G.
• Primary Examiner(s): Layno; Carl H
• Assistant Examiner(s): GHAND, JENNIFER LEIGH-STEWAR
• Application Number:
  US11/948,231
• Time in Patent Office: 1,159 Days
• Field of Search: 600/483, 600/513, 600/529, 607/6, 607/17, 607/20
• US Class Current: 607/17
• CPC Class Codes: A61B 2560/0209 adapted for power saving
• CPC Class Codes: A61B 5/14551 for measuring blood gases
• CPC Class Codes: A61B 5/1459 invasive, e.g. introduced into the body by a catheter A61B5/1464 takes precedence
• CPC Class Codes: A61N 1/3621 for treating or preventing abnormally high heart rate

Abstract

Hemodynamic signals, such as photoplethysmography (PPG) signals, pressure signals, and impedance signals, are sampled once per cyclical body cycle to reduce the amount of data, processing and/or power required to analyze the hemodynamic signals.

Claims

1. A method for reducing the amount of data required to analyze a hemodynamic signal, comprising:

(a) for a window of time that spans at least two respiratory cycles, producing only one sample of the hemodynamic signal per respiratory cycle, at a substantially same instant in each respiratory cycle, to thereby produce a plurality of samples for the window; and

(b) analyzing the hemodynamic signal based on the plurality of samples,

wherein each said sample is indicative of an amplitude of the hemodynamic signal at a single moment in one of the respiratory cycles.

2. The method of claim 1, wherein step (a) comprises sampling the hemodynamic signal in response to a specific respiratory event.

3. The method of claim 2, wherein the sampling of the hemodynamic signal in step (a) occurs a fixed delay after the specific respiratory event.

4. The method of claim 1, wherein step (a) comprises sampling the hemodynamic signal in response to one of the following respiratory events:

expiration; and

inspiration.

5. The method of claim 4, wherein the sampling of the hemodynamic signal in step (a) occurs a fixed delay after the specific respiratory event.

6. A method for reducing the amount of data required to analyze a hemodynamic signal, comprising:

(a) for each of a plurality of windows of time, producing only one sample of the hemodynamic signal per respiratory cycle, at a substantially same instant in each respiratory cycle, to thereby produce a plurality of samples for each window, wherein each window spans at least two respiratory cycles;

(b) for each of the plurality of windows, averaging the plurality of samples, to thereby produce an average value for each window; and

(c) analyzing the hemodynamic signal based on the average values,

wherein each said sample is indicative of an amplitude of the hemodynamic signal at a single moment in one of the respiratory cycles.

7. The method of claim 6, wherein step (a) comprises sampling the hemodynamic signal in response to a specific respiratory event.

8. The method of claim 7, wherein the sampling of the hemodynamic signal in step (a) occurs a fixed delay after the specific respiratory event.

9. The method of claim 6, wherein step (a) comprises sampling the hemodynamic signal in response to one of the following respiratory events:

expiration; and

inspiration.

10. The method of claim 9, wherein the sampling of the hemodynamic signal in step (a) occurs a fixed delay after the specific respiratory event.

11. A method for reducing the amount of data required to analyze a photoplethysmography (PPG) hemodynamic signal, comprising:

(a) for each of a plurality of windows of time, producing only one sample of the PPG signal per respiratory cycle, at a substantially same instant in each respiratory cycle, to thereby produce a plurality of samples for each window, wherein each window spans at least two respiratory cycles, and wherein each said sample is indicative of an amplitude of the PPG signal at a single moment in one of the respiratory cycles;

(b) for each of the plurality of windows, averaging the plurality of samples, to thereby produce an average value for each window; and

(c) analyzing the PPG signal based on the average values.

12. The method of claim 11, wherein the PPG signal is produced using a device that is not implanted in a patient.

13. The method of claim 11, wherein the PPG signal is produced using a device that is implanted in a patient.

14. The method of claim 13, wherein the PPG signal is produced using a light source and a light detector that are implanted in the patient.

15. The method of claim 11, wherein the PPG signal is produced by:

transmitting light from a light source;

receiving, at a light detector, a portion of the light transmitted from the light source; and

producing the PPG signal based on the received portion of light.

16. The method of claim 11, wherein the PPG signal is produced using a light source and a light detector, and wherein the light source is only pulsed once per respiratory cycle, thereby reducing power consumption.

17. The method claim 11, wherein the window of the PPG signal spans one of the following:

a predetermined time interval;

a predetermined number of cardiac cycles; and

a predetermined number of respiratory cycles.

18. The method of claim 11, wherein in step (a), during the sampling of the PPG signal only once per respiratory cycle, the respiratory cycles that are sampled within each window need not be consecutive respiratory cycles.