IP Library Granted Patent US 9,060,745
Granted Patent B2
US 9,060,745 · App. 13/591,455 · Granted Jun 23, 2015

System and method for detecting fluid responsiveness of a patient

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Quick Facts
Patent No.
US 9,060,745
App. No.
13/591,455
Granted
Jun 23, 2015
Kind
B2
Abstract

A system is configured to determine a fluid responsiveness index of a patient from a physiological signal. The system may include a sensor configured to be secured to an anatomical portion of the patient, and a monitor operatively connected to the sensor. The sensor is configured to sense a physiological characteristic of the patient. The monitor is configured to receive a physiological signal from the sensor. The monitor may include an index-determining module configured to determine the fluid responsiveness index through formation of a ratio of one or both of amplitude or frequency modulation of the physiological signal to baseline modulation of the physiological signal.

Claims (28)

1. A system for determining a fluid responsiveness index of a patient from a physiological signal, the system comprising:

a sensor configured to be secured to an anatomical portion of the patient, wherein the sensor is configured to sense a physiological characteristic of the patient; and

a monitor operatively connected to the sensor, the monitor configured to receive a physiological signal from the sensor, the monitor comprising an index-determining module configured to determine the fluid responsiveness index through formation of a ratio of one or both of amplitude modulation or frequency modulation of the physiological signal with respect to baseline modulation of the physiological signal.

2. The system of claim 1 , wherein the monitor further comprises a normalization module configured to normalize the fluid responsiveness index.

3. The system of claim 2 , wherein the normalization module is configured to normalize the fluid responsiveness index to correct for changes in one or both of vascular tone or motion artifacts.

4. The system of claim 2 , wherein the normalization module is configured to normalize the fluid responsiveness index based on one or more of a relative amplitude ratio of the physiological signal, a width of at least one primary peak of the physiological signal, a time difference between the at least one primary peak and at least one trailing peak, or a pleth modulation ratio of the physiological signal.

5. The system of claim 1 , wherein the index-determining module determines the fluid responsiveness index by applying a calibration coefficient or constant to the ratio.

6. The system of claim 1 , wherein the physiological signal comprises a photoplethysmogram (PPG) signal, wherein the sensor comprises a PPG sensor, and wherein the monitor comprises a PPG monitor.

7. The system of claim 1 , wherein the sensor comprises a pulse oximetry sensor, and wherein the monitor comprises a pulse oximetry monitor.

8. The system of claim 1 , further comprising a fluid delivery device operatively connected to the monitor, wherein the monitor determines whether or not to administer fluid to a patient from the fluid delivery device based on the fluid responsiveness index.

9. A method for determining a fluid responsiveness index of a patient from a physiological signal, the method comprising:

securing a sensor to an anatomical portion of the patient;

sensing a physiological characteristic of the patient with the sensor;

receiving a physiological signal from the sensor at a monitor comprising an index-determining module; and

determining the fluid responsiveness index with the index-determining module, wherein the determining the fluid responsiveness index operation comprises forming a ratio of one or both of amplitude modulation or frequency modulation of the physiological signal with respect to baseline modulation of the physiological signal.

10. The method of claim 9 , further comprising normalizing the fluid responsiveness index with a normalization module, the normalizing operation comprises correcting for changes in one or both of vascular tone or motion artifacts.

11. The method of claim 10 , wherein the normalizing operation comprises normalizing the fluid responsiveness index based on one or more of a relative amplitude ratio of the physiological signal, a width of at least one primary peak of the physiological signal, a time difference between the at least one primary peak and at least one trailing peak, or a pleth modulation ratio of the physiological signal.

12. The method of claim 9 , further comprising applying a calibration coefficient or constant to the ratio.

13. The method of claim 9 , wherein the physiological signal comprises a photoplethysmogram (PPG) signal, wherein the sensor comprises a PPG sensor, and wherein the monitor comprises a PPG monitor.

14. The method of claim 9 , further comprising determining whether or not to administer fluid to a patient from a fluid delivery device based on the fluid responsiveness index.

15. A tangible and non-transitory computer readable medium that includes one or more sets of instructions configured to direct a computer to:

receive a physiological signal from a sensor secured to an anatomical portion of a patient; and

determine a fluid responsiveness index of a patient by forming a ratio of one or both of amplitude modulation or frequency modulation of the physiological signal with respect to baseline modulation of the physiological signal.

16. The tangible and non-transitory computer readable medium of claim 15 , further configured to direct the computer to normalize the fluid responsiveness index with a normalization module by correcting for changes in one or both of vascular tone or motion artifacts.

17. The tangible and non-transitory computer readable medium of claim 16 , further configured to direct the computer to normalize the fluid responsiveness index based on one or more of a relative amplitude ratio of the physiological signal, a width of at least one primary peak of the physiological signal, a time difference between the at least one primary peak and at least one trailing peak, or a pleth modulation ratio of the physiological signal.

18. The tangible and non-transitory computer readable medium of claim 15 , further configured to direct the computer to apply a calibration coefficient or constant to the ratio.

19. The tangible and non-transitory computer readable medium of claim 15 , wherein the physiological signal comprises a photoplethysmogram (PPG) signal.

20. The tangible and non-transitory computer readable medium of claim 15 , further configured to direct the computer to determine whether or not to administer fluid to a patient from a fluid delivery device based on the fluid responsiveness index.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2012
From: NELLCOR PURITAN BENNETT LLC
To: COVIDIEN LP
Reel/Frame 029432/0260 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2012
From: SU, MARK; WATSON, JAMES NICHOLAS; ADDISON, PAUL STANLEY
To: NELLCOR PURITAN BENNETT LLC
Reel/Frame 028827/0622 →