Methods and apparatus for non-invasive determination of patient's blood conditions

• US 7,758,505 B2
• Filed: 11/27/2006
• Issued: 07/20/2010
• Est. Priority Date: 04/03/2006
• Status: Active Grant

• Current Assignee: Elfi-Tech Ltd
• Original Assignee: Elfi-Tech Ltd
• Inventors: Shvartsman, Leonid, Fine, Ilya
• Primary Examiner(s): Nasser; Robert L
• Application Number:
  US11/604,401
• Publication Number:
  US 20070232940A1
• Time in Patent Office: 1,331 Days
• Field of Search: None
• US Class Current: 600/368
• CPC Class Codes: A61B 5/0053 by applying pressure, e.g. compression, indentation, palpation, grasping, gauging
• CPC Class Codes: A61B 5/14535 for measuring haematocrit
• CPC Class Codes: A61B 5/14546 for measuring analytes not otherwise provided for, e.g. ions, cytochromes
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: A61B 5/6826 Finger
• CPC Class Codes: A61B 5/6838 Clamps or clips
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Abstract

A method and apparatus are presented for non-invasive determination of blood clotting related and blood circulation related parameters of a mammal. At least one stimulus ST is non-invasively induced in a blood containing medium in the mammal for a preset period of time t_ST. This at least one stimulus is selected to cause at least one of the following to occur: (a) inducing at least two of three Virchow'"'"'s triad elements including abnormalities of blood flow; abnormalities of blood constituents and abnormalities of the blood vessel wall, and (b) inducing a change in red blood cell (RBC) aggregation or local blood viscosity. Measurements are non-invasively performed at a measurement location in the mammal by applying an external field thereto for a preset time period t_m, a response of the measurement location to the applied field is detected, and measured data indicative thereof generated. At least a portion of the measured data and stimulus related data are processed so as to determine a relation between a time function of the at least one stimulus ST(t) and a time function of the measured data OR(t). This relation is indicative of at least one blood circulation and blood coagulation related parameter of the mammal.

Claims

1. A non-invasive method for determination of blood clotting and blood circulation related parameters of a mammal, the method comprising:

(i) non-invasively inducing at least two stimuli ST in a blood containing medium in the mammal for a preset period of time t_ST, said at least two stimuli being selected to cause at least one of the following to occur;

(a) inducing at least two of three Virchow'"'"'s triad elements including an abnormality of blood flow, an abnormality of blood constituents, and an abnormality of the blood vessel wall, and (b) inducing a change in red blood cell (RBC) aggregation or local blood viscosity;

(ii) performing non-invasive measurements at a measurement location in the blood containing medium in the mammal by applying an external field thereto for a preset time period t_m, detecting a response of the measurement location to the applied field, and generating measured data indicative thereof; and

(iii) processing, with a processor, at least a portion of the measured data and processing stimuli related data so as to determine an output data indicative of a relation between a time function of said at least two stimuli ST(t) and a time function of the measured data OR(t), said relation being a predetermined mathematical manipulation between the time function of said at least two stimuli ST(t) and the time function of the measured data OR(t), said output data being indicative of at least one blood circulation and blood clotting related parameter of the mammal.

2. The method according to claim 1, wherein said at least two induced Virchow'"'"'s triad elements are the abnormality of blood flow, and the abnormality of the blood vessel wall.

3. The method according to claim 1, wherein the abnormality of blood flow comprises at least one of the following:

an abnormality of blood rheology, an abnormality of turbulence at bifurcations, and an abnormality of turbulence at a stenotic region.

4. The method according to claim 1, wherein the abnormality of the blood vessel wall comprises at least one of the following:

an abnormality of the endothelium, an abnormality of a blood vessel wall thickness, an abnormality of blood vessel wall rigidity, an abnormality of blood vessel wall integrity, an abnormality of blood vessel wall roughness, and an abnormality of plaque concentration.

5. The method according to claim 1, wherein said at least two stimuli are induced in the blood containing medium in the mammal in the vicinity of the measurement location.

6. The method according to claim 1, wherein said inducing of the change in RBC aggregation or local blood viscosity comprises applying an over systolic pressure to the blood containing medium in the mammal to create a stasis state at the measurement location.

7. The method according to claim 1, wherein said inducing of the at least two stimuli includes application of a mechanical pressure of a preset time dependence ST(t)=P(t) to the mammal to at least one of a location different from the measurement location and a location in the vicinity of the measurement location.

8. The method according to claim 1, wherein said non-invasive measurements are optical measurements, the external field being in the form of electromagnetic radiation of at least one predetermined wavelength range, and the response being in the form of electromagnetic radiation of said at least one wavelength range indicative of scattering, reflective, and absorbing properties of the blood containing medium in the mammal at the measurement location.

9. The method according to claim 1, comprising controlling said inducing of the at least two stimuli such that the at least two stimuli vary with time according to a predetermined function for a time period not exceeding said certain time t_ST.

10. The method according to claim 1, wherein said at least one blood circulation and blood clotting related parameter is indicative of at least one of the following:

a condition of thrombosis, a risk of bleeding, and a prothrombin time.

11. The method according to claim 1, wherein said measurement of the time dependence of the response is carried out for at least two different wavelengths of the applied electromagnetic field, the measured data being indicative of the response as the function of time and wavelength;

and said relation between the time functions of at least two stimuli and the response being a function of wavelength of the applied field and the time parameter t_ST and time delay t_d.

12. The method according to claim 11, wherein said at least two different wavelengths of the applied electromagnetic field are in a visible-NIR range.

13. The method according to claim 1, wherein the measured optical response OR, includes at least one of optical transmission T, optical reflection R, and optical scattering of the medium.

14. The method according to claim 1, wherein said at least portion of the measured data to be processed includes the measured data indicative of the response measured from a predetermined moment of time t_d with respect to the end of inducing said at least two stimuli.

15. The method according to claim 14, wherein said predetermined moment of time t_d is selected to satisfy one of the following conditions:

it precedes the completeness of the inducing of said at least two stimuli, it substantially coincides with the completeness of the inducing of said at least two stimuli, and it occurs after the completeness of said inducing of the at least two stimuli.

16. The method according to claim 15, wherein while said external field is applied to the measurement location, the response from the measurement location is fixed a certain time t_d after the application of the external field to form said portion of the measured data.

17. The method according to claim 15, wherein said portion of the measured data is indicative of the response detected with a certain time delay t_d from the completeness of the inducing of said at least two stimuli.

18. The method according to claim 15, wherein said time delay t_d is selected to satisfy one of the following conditions:

the time delay t_d is negative, said measured data portion corresponding to the measurements starting before said inducing of at least two stimuli is completed;

the time delay t_d is substantially zero, said measured data portion corresponding to the measurements starting substantially when said inducing of the at least two stimuli is complete; and

the time delay t_d is positive, said measured data portion corresponding to the measurements starting after the inducing of said at least two stimuli is complete.

19. The method according to claim 15, wherein the measured data includes said data portion and data indicative of the detected response before performing said inducing of the at least two stimuli.

20. The method according to claim 1, wherein the output data is indicative of at least one blood parameter selected from:

a blood viscosity, a blood rheological property, a blood density, RBC aggregation rate, prothrombin time, a blood clotting parameter, a plasma protein parameter, an erythrocyte sedimentation rate, a fibrin concentration, a fibrinogen concentration, and a drug concentration or concentration of certain product of drug metabolism.

21. An apparatus for use in non-invasive determination of blood clotting related and blood circulation related parameters in a mammal, the apparatus comprising:

(a) a measurement unit configured and operable for applying an external field to a measurement location in a blood containing medium of the mammal, detecting a response from the measurement location to the applied field, and generating measured data indicative thereof;

(b) a stimulus inducing device configured and operable to induce at least two stimuli in the blood containing medium in the mammal, said at least two stimuli being of a kind causing at least one of the following to occur;

(i) inducing at least two of three Virchow'"'"'s triad elements in the medium including an abnormality of blood flow;

an abnormality of blood constituents, and an abnormality of the blood vessel wall; and

(ii) inducing a change in the RBC aggregation;

(c) a control unit configured for selectively operating said stimulus inducing device to maintain each of said at least two stimuli for a preset period of time t_ST, for operating the measurement unit to perform measurements and generate the measured, said control unit being preprogrammed to process and analyze the measured data to determine a time function of at least a portion of the measured data and a time function of said at least two stimuli and determine a relation being a predetermined mathematical manipulation between the time variations of said at least two stimuli and the time function of the response, at least portion of the measured data, said mathematical manipulation being indicative of the blood clotting related and blood circulation related parameters in the mammal.

22. The apparatus according to claim 21, wherein the measurement unit is an optical unit comprising a source of electromagnetic radiation of at least one predetermined wavelength range, and an electromagnetic radiation detector for detecting said response and generating said measured data.

23. The apparatus according to claim 21, wherein said stimulus inducing device is configured and operable to induce an abnormality of blood flow, and an abnormality of the blood vessel wall.

24. The apparatus according to claim 23, wherein said stimulus inducing device is configured and operable to induce the abnormality of blood flow by inducing a change in red blood cell (RBC) aggregation.

25. The apparatus according to claim 21, wherein said stimulus inducing device is configured and operable to apply at least one of the following to a location on the mammal:

electromagnetic radiation of predetermined wavelength and power, and pressure of a predetermined profile.

26. The apparatus according to claim 21, wherein the control unit operates to create said portion of the measured data corresponding to the measured data indicative of the response measured from a predetermined moment of time t_d with respect to the completeness of the application of said at least two stimuli.

27. An apparatus according to claim 26, wherein said predetermined moment of time t_d is selected to satisfy one of the following condition:

it precedes the completeness of the application of said at least two stimuli, it substantially coincides with the completeness of the application of said at least two stimuli, and it occurs after the completeness of the application of the at least two stimuli.

28. The apparatus according to claim 21, wherein the control unit operates to control the operation of the stimulus inducing device to apply the stimulus during certain time t_ST such that the stimulus varies with time according to a predetermined function for a time period t not exceeding said certain time t_ST.

29. The apparatus according to claim 28, wherein the control unit operates to create said portion of the measured data corresponding to the measured data indicative of the response measured from a predetermined moment of time t_d with respect to the completeness of the application of said at least two stimuli and continuing for the time period t larger than t_d.

30. The apparatus according to claim 29, wherein said measurement unit is configured for generating the electromagnetic radiation of at least two different wavelengths, the control unit operating to determine the light response as a function of time and wavelength and determine said relation between the time functions of at least two stimuli and the response in the form of a function of wavelength of the applied radiation and the time parameters t_ST and t_d.

31. The apparatus according claim 22, wherein said stimulus inducing device comprises said source of the electromagnetic radiation.