Process and system for simultaneously simulating arterial and non-arterial blood oxygen values for pulse oximetry

• US 6,141,572 A
• Filed: 02/18/1999
• Issued: 10/31/2000
• Est. Priority Date: 02/18/1999
• Status: Expired due to Term

• Current Assignee: BTI Holdings, Inc., Fluke Corporation (Fortive Corp.)
• Original Assignee: Biotek Instruments, Inc. (Agilent Technologies, Inc.), BTI Holdings, Inc., Lionheart Technologies, Inc.
• Inventors: Haas, Peter
• Primary Examiner(s): WINAKUR, ERIC FRANK
• Application Number:
  US09/252,013
• Time in Patent Office: 621 Days
• Field of Search: 600/310, 600/322, 600/323, 600/331, 600/336, 250/252.1
• US Class Current: 600/331
• CPC Class Codes: A61B 2560/0233 Optical standards
• CPC Class Codes: A61B 5/1495 Calibrating or testing of in-vivo probes

Abstract

A problem in pulse oximetry is discriminating between arterial and non-arterial oxygen. Non-arterial oxygen can become detectable by an oximeter when a patient moves, obscuring the oximeter'"'"'s measurement of arterial oxygen at critical times. Recent advances in pulse oximetry have made it possible to make the discrimination between arterial and non-arterial blood oxygen values. To allow manufacturers, hospitals, and medical researchers to evaluate the new oximetry technology, and evaluate oximeters which use it, new simulation technology is presented which can simulate simultaneous arterial and non-arterial blood oxygen on demand, with precision as to oxygen value, waveform amplitude, and waveform frequency. This invention provides the required simulation by double amplitude modulating the red and infra-red oximeter pulses.

Claims

1. A method, for simultaneous simulation of arterial and non-arterial tissue oxygenation which is to be monitored by a pulse oximeter that provides red and infra-red light flashes, comprising:

a) taking as inputs;

     1) the oximeter'"'"'s light flashes;

     2) a first waveform representative of fluctuating arterial attenuation of an optical path through tissue; and

     3) a second waveform representative of fluctuating non-arterial attenuation of an optical path through tissue, and

b) combining said light flashes, said first waveform and said second waveform such that the result is pulses which are amplitude modulated by both said first and second waveforms, whereby said pulse amplitude modulated pulses can be applied to an oximeter for interpretation as attenuations of its light flashes by arterial and non-arterial oxygenated tissue.

2. The method of claim 1, wherein said first waveform includes red and infra-red components and the method further includes varying the percent ratio of the red component to the infra-red component to thereby simulate the arterial attenuation at various blood oxygen levels.

3. The method of claim 1, wherein said second waveform includes red and infra-red components and the method further includes varying the percent ratio of the red component to the infra-red component to thereby simulate the non-arterial attenuation at various blood oxygen levels.

4. A method, for simultaneous simulation of arterial and non-arterial tissue oxygenation which is to be monitored by a pulse oximeter that provides red and infra-red light flashes, comprising:

a) taking as inputs;

     1) an electrical analogue of the oximeter'"'"'s light flashes;

     2) a first waveform representative of fluctuating arterial attenuation of an optical path through tissue; and

     3) a second waveform representative of fluctuating non-arterial attenuation of an optical path through tissue, and

b) combining said electrical analogue, said first waveform and said second waveform such that the result is pulses which are amplitude modulated by both said first and second waveforms, whereby said pulse amplitude modulated pulses can be applied to an oximeter for interpretation as attenuations of its light flashes by arterial and non-arterial oxygenated tissue.

5. The method of claim 4, wherein said first waveform includes red and infra-red components and the method further includes varying the percent ratio of the red component to the infra-red component to thereby simulate the arterial attenuation at various blood oxygen levels.

6. The method of claim 4, wherein said second waveform includes red and infra-red components and the method further includes varying the percent ratio of the red component to the infra-red component to thereby simulate the non-arterial attenuation at various blood oxygen levels.

7. A method for sensing and modulating the red and infra-red signals of a pulse oximeter to simultaneously simulate arterial and non-arterial oxygen, by dual modulation of the red and infra-red signals, comprising:

sensing red and infra-red signals of the pulse oximeter;

modulating the signals to provide a simulated arterial oxygen value, blood pressure wave form, blood pressure wave shape, wave frequency, and wave amplitude;

also modulating the signals to provide a non-arterial oxygen value, motion wave form, wave shape, wave frequency, and wave amplitude, to thereby form double modulated signals; and

conveying the double modulated signals to an oximeter photo diode input.

8. The method of claim 7, wherein said step of modulating the signals to provide a simulated arterial oxygen value includes varying the percent ratio of red to infra-red signals so as to simulate any desired arterial oxygen value.

9. The method of claim 7, wherein said step of also modulating the signals to provide a non-arterial oxygen value includes varying the percent ratio of red to infra-red signals so as to simulate any desired non-arterial oxygen value.

10. A method for simultaneous simulation of arterial and non-arterial tissue oxygenation which is to be monitored by a pulse oximeter that operates on the principle of differential absorbance of two light frequencies by blood oxygen, comprising:

a) sensing oximeter signals used for generating the two different light frequencies, and creating electrical analogues thereof;

b) modulating said electrical analogues to simulate a non-arterial oxygen value, motion wave form, wave shape, wave frequency, and wave amplitude;

c) additionally modulating said analogues to simulate an arterial oxygen value, blood pressure wave form, blood pressure wave shape, wave frequency, and wave amplitude to form doubly modulated analogous; and

d) applying the doubly modulated analogues to a current driver to drive a photo diode input of the oximeter, such that both arterial and non-arterial behavior of living tissue is simulated.

11. The method of claim 10, wherein step (b) includes modulating the electrical analogues to simulate various non-arterial oxygen values within a range of from 0 to 100%.

12. The method of claim 10, wherein step (c) includes additionally modulating the analogues to simulate various arterial oxygen values within a range of from 0 to 100%.

13. A method for creating pulse oximetry simulation signals, comprising:

taking as inputs;

(a) red and infra-red LED drive pulse analogs of a pulse oximeter;

(b) red and infra-red attenuation factors which establish the simulated bulk attenuation of tissue;

(c) red and infra-red arterial modulation waveforms whose ratios and absolute amplitudes determine oxygen value and signal strength, and whose fundamental frequency determines simulated heartbeats/minute; and

(d) red and infra-red motion modulation waveforms whose ratios and absolute amplitudes determine oxygen value and signal strength of the motion, and whose fundamental frequency determines simulated motion waves/minute;

combining inputs (a), (b), (c), and (d) so as to form output red and infra-red pulses, which are pulse amplitude modulated versions of the red and infra-red drive pulse analogs, by;

(1) using the pulse timing of the red and infra-red LED drive pulse analogs as the output red and infra-red pulse timing;

(2) setting the output red and infra-red pulses unmodulated amplitude level by the red and infra-red attenuation factors, respectively;

(3) amplitude modulating the output red and infra-red pulses amplitude by the red and infra-red plethysmographic waves, respectively;

(4) amplitude modulating the output red and infra-red pulses amplitude by the red and infra-red motion waves, respectively;

in order to impress, upon the original drive pulse analogs, appropriate attenuations and modulations to physiologically simulate both arterial and motion characteristics which can be read by the pulse oximeter in a predetermined way.

14. The method of claim 13, further comprising, before said step of combining, varying the ratio of said red and infra-red arterial modulation waveforms to thereby simulate different oxygen values within a range of from 0 to 100%.

15. The method of claim 13, further comprising, before said step of combining, varying the ratio of said red and infra-red motion modulation waveforms to thereby simulate different non-arterial oxygen values within a range of from 0 to 100%.

16. The method of claim 13, wherein the step of taking (d) as an input includes taking red motion modulation waveforms which are continuous waves, and infra-red motion modulation waveforms which are continuous, to simulate shivering.

17. The method of claim 13, wherein the step of taking (d) as an input includes taking a single red motion modulation waveform, and a single infra-red motion modulation waveform, to simulate a bumped probe event.

18. An apparatus for simultaneous simulation of arterial and non-arterial tissue oxygenation which is to be monitored by a pulse oximeter that provides red and infra-red light flashes, the apparatus comprising:

first means for converting the red and infra-red light flashes of the pulse oximeter into electrical signals;

means for generating a first waveform representative of fluctuating arterial attenuation of an optical path through tissue;

means for generating a second waveform representative of fluctuating non-arterial attenuation of an optical path through tissue;

means for combining said electrical signals with said first and second waveforms so as to form pulses which are amplitude modulated by both said first and second waveforms; and

means for converting said pulses to converted light flashes and for transmitting the converted light flashes to the pulse oximeter for detection so that the pulse oximeter responds to the converted light flashes as it would to light flashes modulated by living tissue.

19. The apparatus of claim 18, wherein said first waveform includes red and infra-red components, and said means for generating a first waveform includes means for varying the ratio of the red component to the infra-red component to thereby simulate the arterial attenuation at various blood oxygen levels.

20. The apparatus of claim 18, wherein said second waveform includes red and infra-red components, and said means for generating a second waveform includes means for varying the ratio of the red component to the infra-red component to thereby simulate the non-arterial attenuation at various blood oxygen levels.

21. An apparatus for simultaneous simulation of arterial and non-arterial tissue oxygenation which is to be monitored by a pulse oximeter that provides red and infra-red light flashes, the apparatus comprising:

first means for receiving electrical signals from the pulse oximeter;

means for generating a first waveform representative of fluctuating arterial attenuation of an optical path through tissue;

means for generating a second waveform representative of fluctuating non-arterial attenuation of an optical path through tissue;

means for combining said electrical signals with said first and second waveforms so as to form pulses which are amplitude modulated by both said first and second waveforms; and

means for transmitting the pulses to the pulse oximeter for detection.

22. The apparatus of claim 21, wherein said first waveform includes red and infra-red components, and said means for generating a first waveform includes means for varying the ratio of the red component to the infra-red component to thereby simulate the arterial attenuation at various blood oxygen levels.

23. The apparatus of claim 21, wherein said second waveform includes red and infra-red components, and said means for generating a second waveform includes means for varying the ratio of the red component to the infra-red component to thereby simulate the non-arterial attenuation at various blood oxygen levels.

24. An apparatus for simultaneous simulation of arterial and non-arterial tissue oxygenation which is to be monitored by a pulse oximeter that provides red and infra-red LED drive signals, the apparatus comprising:

a first circuit which converts the red and infra-red LED drive signals of the pulse oximeter into analogous electrical signals;

circuit elements which generate first waveforms representative of fluctuating red and infra-red arterial attenuation of an optical path through tissue;

other circuit elements which generate second waveforms representative of fluctuating red and infra-red non-arterial attenuation of an optical path through tissue;

a summation amplifier connected to said circuit elements and to said other circuit elements so as to combine said electrical signals with said waveforms so as to form pulses which are amplitude modulated by both said first waveform and said second waveform; and

a second circuit, connected to said summation amplifier, which transmits said combined signals to the pulse oximeter for detection so that the pulse oximeter responds to the converted light flashes as it would to light flashes modulated by living tissue.

25. An apparatus for simultaneous simulation of arterial and non-arterial tissue oxygenation which is to be monitored by a pulse oximeter that provides electrical signals, the apparatus comprising:

an input configured to receive the electrical signals from the pulse oximeter;

a pair of first circuit elements which generate a first waveform representative of fluctuating arterial attenuation of an optical path through tissue;

a pair of second circuit elements which generate a second waveform representative of fluctuating non-arterial attenuation of an optical path through tissue;

a summation circuit element connected to said pair of first circuit elements, to said pair of second circuit elements, and to said input so as to combine said electrical signals with said first and second waveforms so as to form pulses which are amplitude modulated by both said first and second waveforms; and

a circuit, connected to said summation circuit element, which transmits the pulses to the pulse oximeter for detection.

26. A stimulator comprising an arrangement of modulators which, when applied to the electrical analogues of an oximeter'"'"'s red and infra-red LED drive signals, permits simulation of bulk tissue attenuation, tissue motion induced modulation and tissue heartbeat induced modulation, so that the resulting attenuated and modulated analogues, when conveyed to an oximeter'"'"'s photo diode input, are interpreted in a predetermined manner so as to convey motion and arterial blood oxygen values.

27. The stimulator of claim 26, wherein the modulators are arranged so that any one of various arterial blood oxygen values is conveyed.

28. A method for simultaneous simulation of arterial and respiratory tissue oxygenation, comprising:

a) sensing red and infra-red signals of a pulse oximeter;

b) modulating the red and infra-red signals to provide a simulated arterial oxygen value;

c) amplitude modulating, at a respiration frequency, at least one of the red and infra-red signals to provide a respiratory tissue oxygenation value, so that said at least one of the red and infra-red signals is double modulated; and

d) conveying the modulated red and infra-red signals to an oximeter photo diode input.

29. The method of claim 28, wherein step (b) includes modulating the red and infra-red signals so as to provide different simulated arterial oxygen values.

30. The method of claim 28, wherein step (c) consists of amplitude modulating, at a respiration frequency, only said red signal.

31. The method of claim 28, wherein step (c) consists of amplitude modulating, at a respiration frequency, only said infra-red signal.

32. The method of claim 28, wherein step (c) includes amplitude modulating, at a respiration frequency, both said red and infra-red signals by different amounts.

33. The method of claim 28, further comprising, between step (c) and step (d):

(e) modulating said red and infra-red signals to provide a simulated non-arterial oxygen value, so that step (d) includes conveying at least one triple modulated signal to the oximeter photo diode input.

34. The method of claim 33 wherein step (e) includes modulating the red and infra-red signals so as to provide different simulated non-arterial oxygen values.

35. The method of claim 33, wherein step (c) consists of amplitude modulating, at a respiration frequency, only said red signal.

36. The method of claim 33, wherein step (c) consists of amplitude modulating, at a respiration frequency, only said infra-red signal.

37. The method of claim 33, wherein step (c) includes amplitude modulating, at a respiration frequency, both said red and infra-red signals by different amounts.

38. A method for simultaneous simulation of arterial tissue oxygenation and other parameters, comprising:

a) sensing red and infra-red signals of a pulse oximeter;

b) modulating the red and infra-red signals to provide a simulated arterial oxygen value;

c) amplitude modulating, at a predetermined frequency, at least one of the red and infra-red signals to simulate a parameter, so that said at least one of the red and infra-red signals is double modulated;

d) repeating step (c) with a different modulation to simulate an additional parameter;

e) repeating step (d) to simulate additional parameters, as necessary; and

f) conveying the modulated red and infra-red signals to an oximeter photo diode input.

39. The method of claim 38, wherein step (b) includes modulating the red and infra-red signals so as to provide different simulated arterial oxygen values.

40. The method of claim 38, wherein step (c) comprises amplitude modulating, at a respiration frequency, at least one of the red and infra-red signals to provide a respiratory tissue oxygenation value.

41. The method of claim 40, wherein step (c) consists of amplitude modulating, at a respiration frequency, only said red signal.

42. The method of claim 40, wherein step (c) consists of amplitude modulating, at a respiration frequency, only said infra-red signal.

43. The method of claim 40, wherein step (c) includes amplitude modulating, at a respiration frequency, both said red and infra-red signals by different amounts.