System and method for in-vivo hematocrit measurement using impedance and pressure plethysmography

• US 6,128,518 A
• Filed: 07/23/1998
• Issued: 10/03/2000
• Est. Priority Date: 10/04/1990
• Status: Expired due to Fees

• Current Assignee: Microcor, Inc.
• Original Assignee: Microcor, Inc.
• Inventors: Yang, Ke-shieng, Kaminsky, Allan L., Neese, Jon, Billings, Robert Gail, Clark, Justin S.
• Primary Examiner(s): Gilbert, Samuel G.
• Assistant Examiner(s): CARTER, RYAN CHRISTOPHER
• Application Number:
  US09/121,000
• Time in Patent Office: 803 Days
• Field of Search: 600/345, 600/363, 600/506-507, 600/547
• US Class Current: 600/345
• CPC Class Codes: A61B 5/0537 Measuring body composition by impedance, e.g. tissue hydration or fat content
• CPC Class Codes: A61B 5/14535 for measuring haematocrit
• CPC Class Codes: A61B 5/4869 Determining body composition
• CPC Class Codes: H04B 10/2519 using Bragg gratings

Abstract

The hematocrit of blood (i.e., the percentage of whole blood volume occupied by red blood cells) perfusing a finger is determined by stimulating the finger with two current frequencies, one relatively high (e.g., 10 MHZ) and the other relatively low (e.g., 100 KHz). Voltages induced in the finger in response to the two current frequencies are then captured and separated into baseline and pulsatile components. The hematocrit is determined as a function of the ratio of the high frequency pulsatile component to the low frequency pulsatile component, multiplied by the ratio of the square of the low frequency baseline component to the square of the high frequency baseline component. The signal-to-noise ratio of the captured voltages can be enhanced by the application of external pressure to the finger, such as by applying a pressure cuff to the finger.

Claims

1. A method of measuring the hematocrit of blood perfusing a living body part, the method comprising:

driving first and second alternating currents of different frequencies between separate points on the body part;

monitoring first and second signals induced in the body part by the respective first and second currents;

generating first and second pulsatile signals and first and second baseline signals from the respective first and second induced signals; and

determining the hematocrit of the blood from the first and second pulsatile signals and the first and second baseline signals.

2. The method of claim 1, wherein driving the alternating currents comprises driving the first and second alternating currents at frequencies of 100 KHz and 10 MHz, respectively, between separate points on the body part.

3. The method of claim 1, further comprising applying an external bias pressure to the body part proximate the separate points between which the currents are driven to enhance a signal-to-noise ratio of the first and second induced signals.

4. The method of claim 3, wherein applying the external bias pressure comprises applying the pressure using one of a chamber and a cuff.

5. The method of claim 3, further comprising regulating the application of the external bias pressure to the body part in accordance with at least one of the pulsatile and baseline signals.

6. The method of claim 1, wherein driving the currents comprises driving the currents between electrodes positioned on an external surface of the body part.

7. The method of claim 1, wherein the act of monitoring the first and second induced signals comprises monitoring first and second induced voltages.

8. The method of claim 1, wherein generating the pulsatile and baseline signals comprises separating pulsatile components of the induced signals from baseline components of the induced signals.

9. The method of claim 1, wherein determining the hematocrit includes effectively determining the ratio of:

the product of the second pulsatile signal and the square of the first baseline signal to the product of the first pulsatile signal and the square of the second baseline signal.

10. The method of claim 1, wherein determining the hematocrit includes determining the hematocrit from the pulsatile signals, the baseline signals, and a constant, wherein the method further comprises effectively calibrating the constant under predetermined calibration conditions in accordance with the ratio of:

the product of the first pulsatile signal and the square of the second baseline signal to the product of the second pulsatile signal and the square of the first baseline signal.

11. The method of claim 10, wherein effectively calibrating includes driving the first and second alternating currents through a resistor network having parallel fixed and variable resistance paths.

12. The method of claim 11, wherein driving the currents through the resistor network includes varying resistance of the variable resistance path in accordance with an artificial arterial impedance pulse signal.

13. The method of claim 12, wherein the variable resistance path includes a photoresistor, wherein varying the resistance of the variable resistance path comprises varying resistance of the photoresistor by driving a light emitting diode proximate the photoresistor with the artificial arterial impedance pulse signal.

14. The method of claim 1, further comprising:

measuring a change in a volume of the blood over time; and

filtering noise from the induced signals using a template derived from the measured change.

15. The method of claim 14, wherein measuring the change in the volume of the blood over time includes reading a pressure transducer coupled to one of a pressurized chamber and cuff positioned proximate the body part.

16. A system for measuring the hematocrit of blood perfusing a living body part, the system comprising:

circuitry for driving first and second alternating currents of different frequencies between separate points on the body part;

circuitry for monitoring first and second signals induced in the body part by the respective first and second currents;

circuitry coupled to the monitoring circuitry for generating first and second pulsatile signals and first and second baseline signals from the respective first and second induced signals; and

circuitry coupled to the generating circuitry for determining the hematocrit of the blood from the first and second pulsatile signals and the first and second baseline signals.

17. The system of claim 16, further comprising an external bias pressure device for applying an external bias pressure to the body part.

18. The system of claim 17, wherein the external bias pressure device comprises one of a chamber and a cuff.

19. The system of claim 17, further comprising an apparatus coupled to the external bias pressure device and the determining circuitry for regulating the application of the external bias pressure to the body part in accordance with at least one of the pulsatile and baseline signals.

20. The system of claim 16, wherein the driving circuitry includes electrodes positioned on an external surface of the body part.

21. The system of claim 17, wherein the electrodes are integrated into the external bias pressure device.

22. The system of claim 16, wherein the monitoring circuitry includes:

electrodes positioned on an external surface of the body part; and

circuitry coupled to the electrodes for monitoring first and second voltages induced between the electrodes by the first and second currents.

23. The system of claim 16, wherein the generating circuitry includes circuitry for separating the pulsatile components of the induced signals from the baseline components of the induced signals.

24. The system of claim 16, wherein the determining circuitry includes circuitry for effectively determining the ratio of:

the product of the second pulsatile signal and the square of the first baseline signal to the product of the first pulsatile signal and the square of the second baseline signal.

25. The system of claim 16, wherein the determining circuitry includes:

circuitry for determining the hematocrit from the pulsatile signals, the baseline signals, and a constant; and

circuitry for effectively calibrating the constant under predetermined calibration conditions in accordance with the ratio of;

the product of the first pulsatile signal and the square of the second baseline signal to the product of the second pulsatile signal and the square of the first baseline signal.

26. The system of claim 25, wherein the calibrating circuitry includes a resistor network having parallel fixed and variable resistance paths.

27. The system of claim 26, wherein the calibrating circuitry further includes circuitry for varying a resistance of the variable resistance path in accordance with an artificial arterial impedance pulse signal.

28. The system of claim 27, wherein the variable resistance path of the resistor network includes a photoresistor and a light emitting diode proximate the photoresistor, wherein the varying circuitry comprises circuitry for varying a resistance of the photoresistor by driving the light emitting diode with the artificial arterial impedance pulse signal.

29. The system of claim 16, further comprising:

an apparatus for measuring a change in the volume of the blood over time; and

circuitry coupled to the measuring apparatus for filtering noise from the induced signals using a template derived from the measured change.

30. The system of claim 29, wherein the measuring apparatus includes:

a pressure transducer; and

at least one of a chamber and a cuff positioned on the body part and coupled to the pressure transducer.