Apparatus and method for non-invasive and minimally-invasive sensing of venous oxygen saturation and pH levels

• US 20060224053A1
• Filed: 03/30/2005
• Published: 10/05/2006
• Est. Priority Date: 03/30/2005
• Status: Abandoned Application

• Current Assignee: Skyline Medical Inc.
• Original Assignee: Skyline Medical Inc.
• Inventors: Khuri-Yakub, Butrus T., Black, John F., Kim, Daniel Hwan
• Application Number:
  US11/095,091
• Publication Number:
  US 20060224053A1
• Time in Patent Office: Days
• US Class Current: 600/310
• CPC Class Codes: A61B 5/0048 Detecting, measuring or recording by applying mechanical forces or stimuli A61B5/021, A61B5/4884 and A61B9/00 take precedence
• CPC Class Codes: A61B 5/0261 using optical means, e.g. infrared light
• CPC Class Codes: A61B 5/029 Measuring or recording blood output from the heart, e.g. minute volume A61B8/065 takes precedence
• CPC Class Codes: A61B 5/14551 for measuring blood gases
• CPC Class Codes: A61B 5/413 Monitoring transplanted tissue or organ, e.g. for possible rejection reactions after a transplant
• CPC Class Codes: A61B 8/08 Detecting organic movements or changes, e.g. tumours, cysts, swellings A61B8/02 - A61B8/06 take precedence

Abstract

Medical diagnostic apparatus and methods are disclosed. Ultrasound radiation pressure selectively modulates a target area within a body. One or more pulses of radiation containing temporally correlated groups of photons are generated. The photons are characterized by two or more different wavelengths that are selected to have specific interaction with a target chromophore. The two or more different wavelengths are also selected to have substantially similar scattering cross-sections and anisotropy parameters in the target and its surroundings. The pulses of radiation are injected into the body proximate the target area being modulated by the radiation pressure field. Photon groups at each of the different wavelengths that are backscattered from the target area are detected in temporal coincidence. Time-gated background-free amplification of the return signal is used to exclude photons which could not by virtue of their arrival time have interacted with the radiation-pressure-modulated target. Photon groups are selected with a modulation component at the modulation frequency of the radiation pressure modulation field, or at a harmonic of the modulation frequency. From the arrival rate of the detected temporally correlated photon pairs or multiplets, chemical information about the target area, such as an oxygenation or pH level can be inferred. Cardiac output may be computed from measurements of venous and/or arterial oxygenation using this technique.

Claims

1. An apparatus, comprising:

an ultrasound transducer configured to provide an ultrasound radiation pressure field to modulate a target area within a body at a modulation frequency;

an optical source configured to generate one or more pulses of radiation containing temporally correlated groups of photons, wherein the photons in each group are characterized by two or more different wavelengths, the two or more different wavelengths being selected to have specific interaction with a target chromophore, and wherein the two or more different wavelengths being selected to have substantially similar scattering cross-sections and anisotropy parameters in the target and its surroundings;

launch optics configured to transmit the pulses of radiation from the optical source to the target area being modulated by the radiation pressure field and to inject the pulses of radiation into the body in proximity to the target area;

an optical detector configured to detect in temporal coincidence photon groups at each of the different wavelengths that are backscattered from the target area, the optical detector using time-gated amplification or time-gated background-free amplification of the return signal so as to exclude photons which could not by virtue of their arrival time have interacted with the radiation-pressure-modulated target; and

a filter coupled to the optical detector, the filter being configured to select those detected photon groups with a modulation component at the same frequency as the modulation frequency of the radiation pressure modulation field, or at a harmonic of the modulation frequency.

2. The apparatus of claim 1 where the ultrasound transducer and launch optics are contained in a catheter.

3. The apparatus of claim 1 wherein the launch optics include one or more optical fibers coupled between the optical source and a handpiece.

4. The apparatus of claim 3 wherein the handpiece includes detection optics coupled to the optical detector by one or more optical fibers, the detection optics and optical fibers being adapted to relay optical signals, including the temporally coincident photon groups, from the target through the handpiece to optical detector.

5. The apparatus of claim 1 wherein the ultrasound transducer is of a design such that the output energy may be focused, such as the phased-array type.

6. The apparatus of claim 1 wherein the ultrasound transducer operates at fundamental frequencies in the range 2-50 MHz, and preferably from 2-15 MHz.

7. The apparatus of claim 6 wherein the ultrasound transducer operates at fundamental frequencies in the range 2-15 MHz.

8. The apparatus of claim 1 wherein the radiation pressure modulation is occurring at frequencies between 50 Hz and 750 kHz.

9. The apparatus of claim 1 wherein the optical source is configured to deliver the temporally correlated groups of photons at a repetition rate of between about 100 kHz and about 500 MHz.

10. The apparatus of claim 9 wherein the repetition rate is between about 1 MHz and about 250 MHZ.

11. The apparatus of claim 9 wherein the repetition rate is between about 10 MHz and about 200 MHz.

12. The apparatus of claim 1 wherein the optical source is configured to deliver the temporally correlated groups of photons with a pulse width between about 1 picosecond and about 1 nanosecond.

13. The apparatus of claim 12 wherein the pulse width is between about 1 picosecond and about 100 picoseconds.

14. The apparatus of claim 13 wherein the pulse width is between about 5 picoseconds and about 50 picoseconds.

15. The apparatus of claim 1 wherein wavelengths of the temporally correlated pairs of photons fall in the range between 650 and 1175 nm.

16. The apparatus of claim 1 wherein wavelengths of the temporally correlated groups of photons lie in a range between about 650 and about 930 nm.

17. The apparatus of claim 1 wherein wavelengths of the temporally correlated groups of photons lie in the range between about 1020 and about 1150 nm.

18. The apparatus of claim 1 wherein the optical source is configured to generate the temporally correlated groups of photons by Spontaneous Parametric Downconversion (SPDC).

19. The apparatus of claim 1 wherein the optical source includes an optical parametric oscillator pumped by a master laser.

20. The apparatus of claim 1 wherein the optical source includes a fiber Optical Parametric Amplifier.

21. The apparatus of claim 1 wherein the optical detector is configured to perform the time-gated background free amplification of returning photon pairs by upconverting a signal in a fiber Optical Parametric Amplifier (OPA).

22. The apparatus of claim 21 wherein where the fiber OPA is pumped by the same master oscillator as that creating the source of the temporally correlated photon pairs.

23. The apparatus of claim 21 wherein the fiber OPA is pumped by a second pump source slaved temporally to the master oscillator creating the injected source of the temporally correlated photon pairs.

24. The apparatus of claim 1 wherein the time-gated background free amplification of the returning photon groups is performed by upconverting the signal in an optical mixer where it is mixed with a second frequency from the master oscillator or a second slaved oscillator.

25. The apparatus of claim 1 wherein where the wavelengths are selected to provide information about the oxygenation level of the blood by targeting oxy and deoxyhemoglobin.

26. The apparatus of claim 1 wherein where the wavelengths are selected to provide information about the pH level of the blood by targeting met-hemoglobin.

27. The apparatus of claim 1 wherein the ultrasound transducer, launch optics and optical detector (or collecting optics coupled to the optical detector) are configured to be placed on the dermis over the internal jugular vein on the left or right side of the neck.

28. The apparatus of claim 1 wherein the ultrasound transducer, launch optics and optical detector (or collecting optics coupled to the optical detector) are configured to be placed on the dermis simultaneously on the left and right side of the neck over the internal jugular veins.

29. The apparatus of claim 1 wherein the ultrasound transducer, launch optics and optical detector (or collecting optics coupled to the optical detector) are configured to be placed trans-tracheally into the left bronchus of a patient in order to simultaneously probe the patient'"'"'s left pulmonary artery and descending thoracic aorta.

30. The apparatus of claim 1 wherein the ultrasound transducer, launch optics and optical detector (or collecting optics coupled to the optical detector) are configured to be placed trans-esophageally so as to be in close proximity to a patient'"'"'s right pulmonary artery.

31. The apparatus of claim 1 wherein the ultrasound transducer, launch optics and optical detector (or collecting optics coupled to the optical detector) are configured to be placed in direct contact with the pulmonary artery and/or aorta by being inserted on a catheter through an intercostal space using an endoscope.

32. The apparatus of claim 1 further comprising a display coupled to the filter wherein the display is configured to present an output of the filter in a manner interpretable by a user of the apparatus.

33. A method for detecting oxygen saturation and/or pH of blood in an identified physiological target area in a non-invasive or minimally invasive manner using the apparatus of claim 1, the method comprising the steps of:

placing the launch optics of the apparatus such that a light emitting aperture of the launch optics is placed in proximity to a blood vessel;

using radiation pressure from the ultrasound transducer to mechanically modulate a target area within the blood vessel;

using the optical source to generate one or more pulses of radiation containing temporally correlated groups of photons, wherein the photons in each group are characterized by two or more different wavelengths, the two or more different wavelengths being selected to have specific interaction with a target chromophore, and wherein the two or more different wavelengths being selected to have substantially similar scattering cross-sections and anisotropy parameters in the target and its surroundings;

transmitting the pulses of radiation from the optical source to the target area being modulated by the radiation pressure field and injecting the pulses of radiation into the body in close proximity to the target area;

detecting photon groups backscattered from the target area with the optical detector,

said detection occurring using time-gated or time-gated background-free amplification of the return signal so as to exclude photons which could not by virtue of their arrival time have interacted with the radiation-pressure-modulated target,

said detection occurring in a manner so as to detect two or more photons at each of the different injected wavelengths in temporal coincidence such that detected photons of the two or more different wavelengths have traveled substantially the same pathlength in tissue of the target area;

filtering the detected photon groups with the filter so as to detect those photon groups having a modulation component characterized by the same frequency as the radiation pressure modulation field, or a harmonic of said radiation pressure modulation frequency; and

inferring from the arrival rate of the detected temporally correlated photon pairs an oxygenation level or pH of the target area.

34. The method of claim 33, further comprising the step of displaying results of the aforementioned process in a manner readily interpretable.

35. The method according to claim 33 wherein the target area is a fetal oxygen exchange system, including the placenta, placental vasculature, fetal heart and major fetal blood vessels.

36. The method of claim 33 wherein the target area is a neonatal cardiovascular system.

37. The method of claim 33 wherein the physiological target area is an external or internal jugular vein, located transdermally close to the clavicle.

38. The method of claim 33 wherein the physiological target area is a pulmonary artery.

39. The method of claim 33, wherein the oxygenation level is a venous or arterial blood oxygenation level, wherein the method further comprises inferring a cardiac output from the blood oxygenation level using the Fick principle.

40. A method for obtaining diagnostic information about a patient using the apparatus of claim 1, comprising the steps of:

locating a target tissue within the patient'"'"'s body by ultrasound imaging with the transducer;

placing the launch optics of the apparatus such that a light emitting aperture of the launch optics is placed in proximity to target tissue;

using radiation pressure from the ultrasound transducer to mechanically modulate a target area within the target tissue;

using the optical source to generate one or more pulses of radiation containing temporally correlated groups of photons, wherein the photons in each group are characterized by two or more different wavelengths, the two or more different wavelengths being selected to have specific interaction with a target chromophore, and wherein the two or more different wavelengths being selected to have substantially similar scattering cross-sections and anisotropy parameters in the target and its surroundings;

transmitting the pulses of radiation from the optical source to the target area being modulated by the radiation pressure field and injecting the pulses of radiation into the body in close proximity to the target area;

detecting photon groups backscattered from the target area with the optical detector,

said detection occurring using time-gated or time-gated background-free amplification of the return signal so as to exclude photons which could not by virtue of their arrival time have interacted with the radiation-pressure-modulated target,

said detection occurring in a manner so as to detect two or more photons at each of the different injected wavelengths in temporal coincidence such that detected photons of the two or more different wavelengths have traveled substantially the same pathlength in tissue of the target area;

filtering the detected photon groups with the filter so as to detect those photon groups having a modulation component characterized by the same frequency as the radiation pressure modulation field, or a harmonic of said radiation pressure modulation frequency; and

inferring from the arrival rate of the detected temporally correlated photon pairs diagnostic information about the patient.