Non-Invasive Patient Monitoring Using Near Infrared Spectrophotometry

• US 20110046459A1
• Filed: 06/29/2010
• Published: 02/24/2011
• Est. Priority Date: 06/15/2009
• Status: Abandoned Application

• Current Assignee: O2 Medtech, Inc.
• Original Assignee: O2 Medtech, Inc.
• Inventors: YU, Zengpin, NEFF, Thomas P., ZHANG, Wei, WANG, Shih-Ping
• Application Number:
  US12/826,218
• Publication Number:
  US 20110046459A1
• Time in Patent Office: Days
• US Class Current: 600/310
• CPC Class Codes: A61B 5/14553 specially adapted for cerebral tissue

Abstract

Methods, systems, and related computer program products for non-invasive spectrophotometric monitoring of an optical property of a medium are described. Respective light portions are propagated through respective at least partially non-overlapping subregions of the medium during each of a calibration interval and a subsequent monitoring interval. Detections of the light portions acquired during the calibration interval are processed to compute at least one algorithm compensation that causes a first result related to the optical property for the first subregion to be substantially equal to a second result related to the optical property for the second subregion. Subsequently, detections of respective light portions acquired during the monitoring interval are processed in conjunction with the at least one algorithm compensation to compute a monitoring result for the optical property. Advantages can include a reduction in the number of sources/detectors required and/or an obviation of symmetry requirements in source/detector layout.

Claims

1. A method for non-invasive spectrophotometric monitoring of an optical property of a medium, comprising:

securing each of a first optical source, a second optical source, a first optical detector, and a second optical detector to a surface of the medium;

during each of a calibration interval and a monitoring interval, said monitoring interval being subsequent to said calibration interval, propagating a first portion of light from the first optical source through the medium to the first optical detector, a second portion of light from the second optical source through the medium to the first optical detector, a third portion of light from the first optical source through the medium to the second optical detector, and a fourth portion of light from the second optical through the medium to the second optical detector;

processing detections of said first, second, third, and fourth light portions acquired during said calibration time interval to compute at least one algorithm compensation that causes a first result related to said optical property based on said first and second detected light portions to be substantially equal to a second result related to said optical property based on said third and fourth detected light portions; and

processing detections of said first, second, third, and fourth light portions acquired during said monitoring interval in conjunction with said at least one algorithm compensation to compute a monitoring result for the optical property of the medium.

2. The method of claim 1, said first and second light portions corresponding to a first subregion of the medium, said third and fourth light portions corresponding to a second subregion of the medium that is at least partially non-overlapping with said first subregion, wherein said computing said at least one algorithm compensation comprises:

(i) computing at least one error factor associated with at least one non-ideality of said optical sources and/or detectors to which a difference in said first and second results would be attributable if the optical property was known to be spatially homogenous throughout said first and second subregions during said calibration interval; and

(ii) determining at least one compensation factor associated with said at least one error factor that causes said first and second results to be substantially equal for said calibration interval.

3. The method of claim 2, wherein said at least one compensation factor remains fixed throughout said monitoring interval.

4. The method of claim 2, wherein said at least one non-ideality is associated with one or more of intensity of the optical sources, sensitivity of the optical detectors, coupling efficiency of light from the optical sources into the medium, and coupling efficiency of light from the medium to said optical detectors.

5. The method of claim 4, wherein said first and second optical sources modulate said light portions according to a phase modulated spectrophotometry (PMS) modulation pattern, and wherein said at least one non-ideality is further associated with an error in detected phase differences between corresponding light portions.

6. The method of claim 4, wherein said monitoring result for the optical property of the medium comprises (i) a first monitoring result applicable to said first subregion and based on said detected first and second light portions, and (b) a second monitoring result applicable to said second subregion and based on said detected third and fourth light portions, wherein said first and second monitoring results are computed in a manner that is substantially independent of said at least one non-ideality while requiring only said two optical sources and said two optical detectors.

7. The method of claim 6, wherein said at least one error factor and said at least one compensation factor are each computed in a manner that accommodates spatial asymmetries among the optical sources and optical detectors, whereby said computing said first and second monitoring results is substantially independent of said at least one non-ideality while not requiring spatial symmetry among the optical sources and optical detectors.

8. The method of claim 1, wherein said optical sources and detectors are positioned on a wearable patch secured to the surface of the medium, said wearable patch being generally elongate and having first and second ends and a center region therebetween, wherein said first and second optical detectors are positioned near said first and second ends, respectively, and wherein said first and second optical sources are positioned near said center region.

9. The method of claim 8, wherein said optical sources and detectors are asymmetrically positioned such that (a) a difference in distances to said first and second optical sources as respectively measured from said first optical detector is not equal to (b) a difference in distances to said second and first optical sources as respectively measured from said second optical detector.

10. The method of claim 8, wherein said medium comprises at least a portion of a cerebral volume of a patient, wherein said wearable patch is secured to the forehead of the patient, and wherein said first and second subregions correspond to opposing brain hemispheres of the patient.

11. A method for non-invasive spectrophotometric monitoring of an optical property of a medium, comprising:

securing each of a first optical source, a second optical source, a first optical detector, and a second optical detector to a surface of the medium, each being secured at a different one of a first location, a second location, a third location, and a fourth location on said surface, wherein said first and second optical sources are secured at either (i) said first and fourth locations, respectively, or (ii) said second and third locations, respectively;

during each of a calibration interval and a monitoring interval, said monitoring interval being subsequent to said calibration interval, propagating a first portion of light through the medium between said first and second locations, a second portion of light through the medium between said first and third locations, a third portion of light through the medium between said second and fourth locations, and a fourth portion of light through the medium between said third and fourth locations;

processing detections of said first, second, third, and fourth light portions acquired during said calibration time interval to compute at least one algorithm compensation that causes a first result related to said optical property based on said first and second detected light portions to be substantially equal to a second result related to said optical property based on said third and fourth detected light portions; and

processing detections of said first, second, third, and fourth light portions acquired during said monitoring interval in conjunction with said at least one algorithm compensation to compute a monitoring result for the optical property of the medium.

12. The method of claim 11, said first and second light portions corresponding to a first subregion of the medium, said third and fourth light portions corresponding to a second subregion of the medium that is at least partially non-overlapping with said first subregion, wherein said computing said at least one algorithm compensation comprises:

(i) computing at least one error factor associated with at least one non-ideality of said optical sources and/or detectors to which a difference in said first and second results would be attributable if the optical property was known to be spatially homogenous throughout said first and second subregions during said calibration interval; and

(ii) determining at least one compensation factor associated with said at least one error factor that causes said first and second results to be substantially equal for said calibration interval.

13. The method of claim 12, wherein said at least one compensation factor remains fixed throughout said monitoring interval.

14. The method of claim 12, wherein said at least one non-ideality is associated with one or more of intensity of the optical sources, sensitivity of the optical detectors, coupling efficiency of light from the optical sources into the medium, and coupling efficiency of light from the medium to said optical detectors.

15. The method of claim 14, wherein said first and second optical sources modulate said light portions according to a phase modulated spectrophotometry (PMS) modulation pattern, and wherein said at least one non-ideality is further associated with an error in detected phase differences between corresponding light portions.

16. The method of claim 14, wherein said monitoring result for the optical property of the medium comprises (i) a first monitoring result applicable to said first subregion and based on said detected first and second light portions, and (b) a second monitoring result applicable to said second subregion and based on said detected third and fourth light portions, wherein said first and second monitoring results are computed in a manner that is substantially independent of said at least one non-ideality while requiring only said two optical sources and said two optical detectors.

17. The method of claim 16, wherein said at least one error factor and said at least one compensation factor are each computed in a manner that accommodates spatial asymmetries among the optical sources and optical detectors, whereby said computing said first and second monitoring results is substantially independent of said at least one non-ideality while not requiring spatial symmetry among the optical sources and optical detectors.

18. The method of claim 11, wherein said optical sources and detectors are positioned on a wearable patch secured to the surface of the medium, said wearable patch being generally elongate and having first and second ends and a center region therebetween, wherein said first and fourth locations are positioned near said first and second ends, respectively, and wherein said second and third locations are positioned near said center region.

19. The method of claim 18, wherein said first, second, third, and fourth locations are asymmetrically positioned such that (a) a difference in distances to said second and third locations as respectively measured from said first location is not equal to (b) a difference in distances to said third and second locations as respectively measured from said fourth location.

20. The method of claim 18, wherein said medium comprises at least a portion of a cerebral volume of a patient, wherein said wearable patch is secured to the forehead of the patient, and wherein said first and second subregions correspond to opposing brain hemispheres of the patient.

21. An apparatus for non-invasive spectrophotometric monitoring of an optical property of a tissue volume of a patient, comprising:

a probe patch wearable on a surface of the tissue volume of the patient during each of a calibration interval and a monitoring interval, the probe patch comprising a first optical source, a second optical source, a first optical detector, and a second optical detector each positioned at a different one of a first location, a second location, a third location, and a fourth location on a surface-facing side of the probe patch, wherein said first and second optical sources are secured at either (i) said first and fourth locations, respectively, or (ii) said second and third locations, respectively, said probe patch being configured to propagate a first portion of light through the medium between said first and second locations, a second portion of light through the medium between said first and third locations, a third portion of light through the medium between said second and fourth locations, and a fourth portion of light through the medium between said third and fourth locations;

a calibration processor configured to process detections of said first, second, third, and fourth light portions acquired during said calibration time interval and to determine therefrom at least one algorithm compensation that causes a first result related to said optical property based on said first and second detected light portions to be substantially equal to a second result related to said optical property based on said third and fourth detected light portions;

a monitoring processor configured to process detections of said first, second, third, and fourth light portions acquired during said monitoring interval in conjunction with said at least one algorithm compensation to compute a monitoring result for the optical property of the medium; and

a display device coupled to said monitoring processor for displaying said monitoring result during said monitoring session.

22. The apparatus of claim 21, said first and second light portions corresponding to a first subregion of the tissue volume, said third and fourth light portions corresponding to a second subregion of the tissue volume that is at least partially non-overlapping with said first subregion, wherein said monitoring result for the optical property of the medium includes (i) a first monitoring result applicable to said first subregion and based on said detected first and second light portions, and (b) a second monitoring result applicable to said second subregion and based on said detected third and fourth light portions

23. The apparatus of claim 22, wherein said first, second, third, and fourth locations are asymmetrically positioned on said probe patch such that (a) a difference in distances to said second and third locations as respectively measured from said first location is not equal to (b) a difference in distances to said third and second locations as respectively measured from said fourth location.

24. The apparatus of claim 22, said probe patch being generally elongate and having first and second ends and a center region therebetween, wherein said first and fourth locations are positioned near said first and second ends, respectively, and wherein said second and third locations are positioned near said center region.

25. The apparatus of claim 24, wherein said probe patch is configured for securing to the forehead of a patient, and wherein said first and second subregions correspond to opposing brain hemispheres of the patient.

26. The apparatus of claim 22, wherein said first location is positioned relatively near to said second and third locations, wherein said fourth location is positioned relatively far from said second and third locations such that said first subregion has a relatively shallow penetration depth and said second subregion has a relatively deep penetration depth, wherein said monitoring processor is configured to:

compute a near SO₂ result corresponding to said first subregion based on said detected first and second light portions;

compute a far SO₂ result corresponding to said second subregion based on said detected third and fourth light portions; and

compute a deep SO₂ result based on a weighted difference between said near and far SO₂ results;

and wherein said display device is configured to selectively display color-coded time traces corresponding to said near, far, and deep SO₂ results.