CARDIAC OUTPUT MONITOR WITH COMPENSATION FOR TISSUE PERFUSION

• US 20100099992A1
• Filed: 10/06/2009
• Published: 04/22/2010
• Est. Priority Date: 10/07/2008
• Status: Active Grant

• Current Assignee: The Alfred E. Mann Institute For Biomedical Engineering At The University Of Southern California (University of Southern California)
• Original Assignee: Alfred E MANN Institute For Biomedical Engineering At The University of Southern California, Southern California
• Inventors: Eskovitz, Alan J., Rubinstein, Eduardo H., Holschneider, Daniel P., Maarek, Jean-Michel I.
• Granted Patent: US 8,249,697 B2
• Time in Patent Office: Days
• US Class Current: 600/454
• CPC Class Codes: A61B 2560/0223 of calibration, e.g. protocols for calibrating sensors
• CPC Class Codes: A61B 5/0261 using optical means, e.g. infrared light
• CPC Class Codes: A61B 5/0275 using tracers, e.g. dye dilution
• CPC Class Codes: A61B 5/029 Measuring or recording blood output from the heart, e.g. minute volume A61B8/065 takes precedence

Abstract

A non-invasive system and method for determination of cardiac output and blood volume of a patient includes compensating for a change in the fluorescence of an indicator circulating in the bloodstream of a tissue or organ that is caused by a variation of the blood content at the site of the measurement.

Claims

1. A system for determining a physical parameter of the cardiovascular system of a subject comprising:

a. an illumination system configured to provide an electromagnetic radiation to a detection area to excite an indicator administrated to the cardiovascular system to fluoresce, and to provide said electromagnetic radiation to said detection area for a Doppler flowmetry measurement;

b. a detection system configured to detect the intensity of the indicator fluorescence emerging from the detection area, and to detect the intensity and the frequency distribution of electromagnetic radiation reflected from the detection area; and

c. a computing system configured to compute a parameter of the cardiovascular system by using the indicator fluorescence intensity, to compute a Doppler flowmetry parameter of the detection area by using the reflected electromagnetic radiation intensity and its frequency distribution, and to compensate the cardiovascular system computation for a variation of the blood content of the detection area by using the computed Doppler flowmetry parameter.

2. The system of claim 1, wherein the illumination system is configured to provide an electromagnetic radiation with a wavelength within the range of 400 nm to 1,000 nm.

3. The system of claim 1, wherein the illumination system is configured to provide electromagnetic radiation at least one wavelength to cause the indicator to fluoresce and for the Doppler flowmetry measurement.

4. The system of claim 1, wherein the illumination system is configured to provide electromagnetic radiation at a plurality of wavelengths to cause the indicator to fluoresce and for the Doppler flowmetry measurement.

5. The system of claim 1, wherein the indicator is capable of fluorescing with a wavelength within the range of 400 nm to 1,000 nm.

6. The system of claim 1, wherein the illumination system is configured to provide a modulated electromagnetic radiation during detection of the indictor fluorescence intensity.

7. The system of claim 6, wherein the illumination system is configured to modulate the electromagnetic radiation intensity at a selected frequency, and the detection system comprises at least one demodulating system for enhancing the detection of the indicator fluorescence only at the selected modulation frequency.

8. The system of claim 6, wherein the system is further configured to carry out the Doppler flowmetry measurements when the electromagnetic radiation provided by the illumination system is not modulated.

9. The system of claim 1, wherein the system is further configured for a calibration of the system to determine the indicator concentration by using a minimally invasive calibration technique.

10. The system of claim 1, wherein the system is further configured for a calibration of the system to determine the indicator concentration by using a noninvasive calibration technique.

11. The system of claim 1, wherein the computing system is further configured to compute the cardiac output of the subject in absolute units of volume over time by:

a. converting the indicator fluorescence intensity detected over a period of time to a measured indicator concentration using a known calibration curve and

b. computing the cardiac output of the subject in absolute units over the period of time based on the measured indicator concentration.

12. The system of claim 1, wherein the computing system is further configured to compute the blood volume of the subject in absolute units of volume over time by:

a. converting the fluorescence intensity detected over a period of time to a measured indicator concentration using a known calibration curve and

b. computing the blood volume by back extrapolating a slow phase of the indicator concentration curve to determine the blood volume.

13. A method of measuring a physical parameter of the cardiovascular system of a subject comprising:

a. administering to the cardiovascular system of a subject a detectable amount of at least one indicator;

b. providing an electromagnetic radiation to a detection area by using an illumination system to excite the indicator present at the detection area to fluoresce;

c. detecting the indicator fluorescence intensity emitted from the detection area by using a detection system;

d. detecting the intensity and the frequency distribution of the reflected electromagnetic radiation from the detection area for a Doppler flowmetry measurement by using said detection system,

e. computing at least one physical parameter of the cardiovascular system using the detected indicator fluorescence intensity, and

f. compensating the physical parameter of the cardiovascular system for variations of the blood content of the detection area by using the Doppler flowmetry measurement.

14. The method of claim 13, wherein the electromagnetic radiation is provided at a wavelength varying within the range of 400 nm to 1,000 nm.

15. The method of claim 13, wherein the electromagnetic radiation is provided at least one wavelength to cause the indicator to fluoresce and for the Doppler flowmetry measurement.

16. The method of claim 13, wherein the electromagnetic radiation is provided at a plurality of wavelengths to cause the indicator to fluoresce and for the Doppler flowmetry measurement.

17. The method of claim 13, wherein the indicator is capable of fluorescing at a wavelength varying within the range of 400 nm to 1,000 nm.

18. The method of claim 13, wherein the provided electromagnetic radiation is modulated during the detection of the indicator fluorescence intensity.

19. The method of claim 18, wherein the method further comprises carrying out the Doppler flowmetry measurement when the electromagnetic radiation is not modulated.

20. The method of claim 13 further comprising converting the detected indicator fluorescence intensity over the time period to a measured indicator concentration using a known calibration curve and determining the cardiac output of the subject in absolute units over the time period based on the measured indicator concentration.

21. The method of claim 13 further comprising removing a blood sample containing indicator from the subject, determining the indicator concentration in the removed blood sample, and computing the at least one physical parameter of the cardiovascular system using the determined indicator concentration.

22. The method of claim 13, wherein the physical parameter of the cardiovascular system is cardiac output and wherein the method further comprises detecting the indicator fluorescence intensity over a time period, forming an indicator fluorescence intensity curve for the time period, and wherein the computing of the cardiac output comprises at least one of curve fitting to a model equation or numerical integration.

23. The method of claim 13, wherein the physical parameter of the cardiovascular system is blood volume and wherein the method further comprises detecting the indicator fluorescence intensity over a time period, forming an indicator fluorescence intensity curve for the time period, converting the fluorescence intensity curve to the indicator concentration curve by using a calibration method and wherein the computing of the blood volume comprises back extrapolating a slow phase of the indictor concentration curve to determine the blood volume.