Method and apparatus for the monitoring of clinical states

• US 20060004270A1
• Filed: 06/23/2005
• Published: 01/05/2006
• Est. Priority Date: 06/23/2004
• Status: Active Grant

• Current Assignee: Cybiocare, Inc., Onsens Incorporated
• Original Assignee: Cybiocare, Inc.
• Inventors: Nolet, Dany, Bedard, Michel
• Granted Patent: US 7,623,988 B2
• Time in Patent Office: Days
• US Class Current: 600/316
• CPC Class Codes: A61B 5/01 Measuring temperature of body parts ; Diagnostic temperature sensing, e.g. for malignant or inflamed tissue clinical contact thermometers G01K13/20
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters

Abstract

A method and apparatus to monitor clinical states, for example hypoglycaemia, hyperglycaemia or an ischemic state, and to detect if a user if affected by such a state. In one embodiment, the method and apparatus use a correlation between one or more non-invasive physical measurements of the body of the subject and a reference value of blood-glucose of the subject to compute an estimation parameter value, and comparing that estimation parameter value with a critical parameter value indicative of the presence of a clinical state, for example hypoglycaemia, hyperglycaemia. In another embodiment, the algorithm estimates chromophore concentrations and the scattering coefficient in order to compute a level of oxygen saturation and detect the presence of an ischemic state.

Claims

1. A method for detecting a clinical state in a subject, comprising:

acquiring a reference value of blood-glucose of the subject;

correlating one or more non-invasive physical measurements of the body of the subject with the reference value of blood-glucose of the subject;

measuring the one or more non-invasive physical measurements of the body of the subject;

computing an estimation parameter value representative of a variation in glucose value using the measured one or more non-invasive physical measurements and the correlation between the one or more non-invasive physical measurements of the body of the subject with the reference value of blood-glucose of the subject;

comparing the estimation parameter value with a critical parameter value, wherein the critical parameter value is indicative of a clinical state; and

indicating that a clinical state is detected if the estimation parameter value has reached the critical parameter value.

2. A method according to claim 1, wherein if a clinical state is not detected the method returns to measuring the one or more non-invasive physical measurements of the body of the subject.

3. A method according to claim 1, wherein before returning to measuring the one or more non-invasive physical measurements of the body of the subject, the method verifies if a new reference value of blood-glucose of the subject is available, if so the method returns to acquiring a reference value of blood-glucose of the subject.

4. A method according to claim 1, wherein the one or more non-invasive physical measurements of the body of the subject is the reflectance of light in the skin of the subject and wherein measuring the one or more non-invasive physical measurements of the body of the subject includes:

propagating at least one probing light beam into the skin of the subject from a propagation point; and

measuring reflectance values of the at least one probing light beam from at least two distances from the propagation point.

5. A method according to claim 4, wherein the blood-glucose value of the subject is acquired from a conventional blood-glucose monitor.

6. A method according to claim 4, wherein the clinical state is one of a hypoglycemic state and hyperglycemic state.

7. A method according to claim 4, wherein the at least one probing light beam has a wavelength between 500 nm and 1000 nm.

8. A method according to claim 4, wherein the correlation between the reflectance of light in the skin of the subject with the reference value of blood-glucose of the subject includes a reflectance mathematical model.

9. A method according to claim 4, wherein the correlation between the reflectance of light in the skin of the subject with the reference value of blood-glucose of the subject includes a chromophore concentration estimation mathematical model.

10. A method according to claim 4, wherein the correlation between the reflectance of light in the skin of the subject with the reference value of blood-glucose of the subject includes a scattering coefficient estimation mathematical model.

11. A method according to claim 4, further comprising measuring a temperature of the skin of the subject and wherein the correlation between the reflectance of light in the skin of the subject with the reference value of blood-glucose of the subject includes a skin temperature correction factor.

12. A method for detecting a clinical state in a subject, comprising:

acquiring a reference value of blood-glucose of the subject;

correlating at least two parameters of skin of the body of the subject with the reference value of blood-glucose of the subject;

propagating at least two probing light beams into the skin from at least one propagation point;

measuring reflectance values of the at least two probing light beams from at least two distances from the at least one propagation point;

estimating values representative of the at least two parameters of skin of the body of the subject using the measured reflectance values and a mathematical skin parameter estimation model;

computing an estimation parameter value representative of a variation in glucose value using the estimated values of the at least two parameters of skin of the body of the subject and the correlation between the at least two parameters of skin of the body of the subject with the reference value of blood-glucose of the subject;

comparing the estimation parameter value with a critical parameter value, wherein the critical parameter value is indicative of a clinical state; and

indicating that a clinical state is detected if the estimation parameter value has reached the critical parameter value.

13. A method according to claim 12, wherein if a clinical state is not detected the method returns to measuring reflectance values of the at least two probing light beams from at least two distances from the at least one propagation point.

14. A method according to claim 12, wherein before returning to measuring reflectance values of the at least two probing light beams from at least two distances from the at least one propagation point, the method verifies if a new reference value of blood-glucose of the subject is available, if so the method returns to acquiring a reference value of blood-glucose of the subject.

15. A method according to claim 12, wherein the at least two parameters of skin of the body of the subject is selected from a group including chromophore concentrations, a scattering coefficient and the temperature of the skin.

16. A method according to claim 12, wherein the blood-glucose value of the subject is obtained from a conventional blood-glucose monitor.

17. A method according to claim 12, wherein the clinical state is one of a hypoglycemic state and a hyperglycemic state.

18. A method according to claim 12, wherein the at least one probing light beam has a wavelength between 500 nm and 1000 nm.

19. A method according to claim 12, further comprising measuring a temperature of the skin of the subject and wherein the mathematical skin parameter estimation model includes a skin temperature correction factor.

20. A method for computing an estimate of a value representative of at least one parameter of skin selected from a group including chromophore concentrations and a scattering coefficient, comprising:

propagating at least two probing light beams into the skin from at least one propagation point;

measuring reflectance values of the at least two probing light beams from at least two distances from the at least one propagation point;

computing estimates of the at least one parameter of skin of the body of the subject using a reflectance mathematical model; and

outputting the estimate of the value representative of the at least one selected parameters of skin.

21. A method according to claim 20, wherein the at least one parameter of skin includes oxyhemoglobin (HbO2) and deoxyhemoglobin (Hb) chromophore concentrations and further comprising:

comparing the estimates of a ratio of oxyhemoglobin (HbO2) and deoxyhemoglobin (Hb) chromophore concentrations with a critical parameter value, wherein the critical parameter value is indicative of an ischemic state; and

indicating that a clinical state is detected if the estimation parameter value has reached the critical parameter value.

22. A method according to claim 21, wherein if an ischemic state is not detected the method returns to propagating at least two probing light beams into the skin from at least one propagation point.

23. A method according to claim 20, further comprising measuring a temperature of the skin of the subject and wherein the reflectance mathematical model includes a skin temperature correction factor.

24. An apparatus for detecting a clinical state in a subject, comprising:

an input for acquiring a reference value of blood-glucose of the subject;

a measurement mechanism for measuring one or more non-invasive physical measurements of the body of the subject;

a display;

a microcontroller in operatively connected to the input, the measurement mechanism and the display, wherein the microcontroller comprises an algorithm for;

computing an estimation parameter value representative of a variation in glucose value using the measured one or more non-invasive physical measurements and a correlation between the one or more non-invasive physical measurements of the body of the subject with the reference value of blood-glucose of the subject;

comparing the estimation parameter value with a critical parameter value, wherein the critical parameter value is indicative of a clinical state; and

indicating on the display that a clinical state has been detected if the estimation parameter value has reached the critical parameter value.

25. An apparatus according to claim 24, wherein the one or more non-invasive physical measurements of the body of the subject is the reflectance of light in the skin of the subject and wherein the measurement mechanism includes:

an emitter for propagating at least one probing light beam into the skin of the subject from a propagation point; and

a receiver for measuring reflectance values of the at least one probing light beam from at least two distances from the propagation point.

26. An apparatus according to claim 25, wherein the at least one probing light beam has a wavelength between 500 nm and 1000 nm.

27. An apparatus according to claim 25, further comprising a temperature sensor for measuring the temperature of the skin of the subject and wherein the computing of the estimation parameter value representative of a variation in glucose value includes a skin temperature correction factor.

28. An apparatus for computing an estimate of a value representative of at least one parameter of skin selected from a group including chromophore concentrations and a scattering coefficient, comprising:

emitter for propagating at least two probing light beams into the skin from at least one propagation point;

at least two receivers for measuring reflectance values of the at least two probing light beams from at least two distances from the at least one propagation point;

a display;

a microcontroller in operatively connected to the receivers and the display, wherein the microcontroller comprises an algorithm for;

computing estimates of the at least one parameter of skin of the body of the subject using a reflectance mathematical model; and

outputting to the display the estimate of the value representative of the at least one selected parameters of skin.

29. An apparatus according to claim 28, further comprising a temperature sensor for measuring the temperature of the skin of the subject and wherein the reflectance mathematical model includes a skin temperature correction factor.

30. An apparatus according to claim 28, wherein the at least one parameter of skin includes oxyhemoglobin (HbO2) and deoxyhemoglobin (Hb) chromophore concentrations and wherein the algorithm further comprises:

comparing the estimates of a ratio of oxyhemoglobin (HbO2) and deoxyhemoglobin (Hb) chromophore concentrations with a critical parameter value, wherein the critical parameter value is indicative of an ischemic state; and

indicating on the display that a clinical state has been detected if the estimation parameter value has reached the critical parameter value.