Non-Invasive Total Hemoglobin Measurement by Spectral Optical Coherence Tomography

• US 20090247853A1
• Filed: 03/30/2009
• Published: 10/01/2009
• Est. Priority Date: 03/31/2008
• Status: Abandoned Application

• Current Assignee: Covidien LP (Medtronic Plc)
• Original Assignee: Nellcor Puritan Bennett LLC (Medtronic Plc)
• Inventors: Debreczeny, Martin
• Application Number:
  US12/413,670
• Publication Number:
  US 20090247853A1
• Time in Patent Office: Days
• US Class Current: 600/328
• CPC Class Codes: A61B 5/0059 using light, e.g. diagnosis by transillumination, diascopy, fluorescence A61B5/0093, A61B5/1455, A61B5/02416 and A61B5/0261 take precedence
• CPC Class Codes: A61B 5/0066 Optical coherence imaging
• CPC Class Codes: A61B 5/14535 for measuring haematocrit
• CPC Class Codes: G01N 2021/1782 In-depth resolution
• CPC Class Codes: G01N 21/359 using near infrared light
• CPC Class Codes: G01N 21/4795 spatially resolved investigating of object in scattering medium in vivo A61B

Abstract

Spectral Optical Coherence Tomography (“SOCT”) utilizes Optical Coherence Tomography (“OCT”) to depth-target two or more optical measurements within a blood vessel. OCT achieves depth resolution by the use of optical interferometry. As the path length of the reference arm of the interferometer is varied, the penetration depth at which maximum interference occurs (zero phase difference) in the sample is correspondingly increased. Depth resolution in the range of 10 μm to 100 μm enables measurements that may be made within more narrow spectral regions (in the range of 1 to 50 nm) in multiple regions of the visible and near infrared spectrum. In one embodiment the light source is configured for three spectral regions centered at 805 nm, 980 nm, and 1050 nm. By comparing the OCT signal at these different spectral positions, the absorption due to tissue and blood analytes may be measured.

Claims

1. A method for determining total hemoglobin in vivo, the method comprising the steps of:

(a) positioning a sensor of a sample arm of an interferometer on the skin of a subject over a vasculature area;

(b) positioning a reference arm of the interferometer in a first position to achieve maximum interference with the sample arm that corresponds to a first depth within the vasculature area;

(c) emitting light a first time from a first light source having three spectral regions;

(d) measuring the light returned from the sample arm and the reference arm;

(e) storing the measured light as a first measurement;

(f) positioning the reference arm of the interferometer in a second position to achieve maximum interference with the sample arm that corresponds to a second depth within the vasculature area;

(g) emitting light a second time from the light source having three spectral regions;

(h) measuring the light returned from the sample arm and the reference arm;

(i) storing the measured light as a second measurement; and

(j) combining the first measurement and the second measurement to determine a relative concentration of hemoglobin.

2. The method according to claim 1 wherein said emitting light steps (c) and (g) further comprise the steps of:

emitting light in a first spectral region centered on 805 nm wavelength;

emitting light in a second spectral region centered on 980 nm wavelength; and

emitting light in a third spectral region centered on 1050 nm wavelength.

3. The method according to claim 1 further comprising the step of:

displaying the relative concentration of hemoglobin on a display device.

4. The method according to claim 1 further comprising the step of:

combining the first measurement and the second measurement to determine a relative concentration of water.

5. The method according to claim 4 further comprising the step of:

displaying the relative concentration of water on a display device.

6. The method according to claim 1 wherein said combining step (j) is independent of the oxygen saturation of the hemoglobin.

7. The method according to claim 1 wherein said measuring steps (d) and (h) further comprise the steps of:

capturing the light returned from the sample arm and the reference arm with a photo detector;

processing the output of the photo detector with a digital signal processor.

8. A system for determining total hemoglobin in vivo, the system comprising:

an interferometer, the interferometer further comprising;

a sample arm having a sensor that is positioned on the skin of a subject over a vasculature area;

a reference arm moved to a first position to achieve maximum interference with the sample arm that corresponds to a first depth within the vasculature area;

a light source capable of emitting light in three spectral regions;

a beam splitter/combiner capable of splitting and combining the emitted light;

a photo detector capable of capturing light returned from the sample arm and the reference arm; and

a digital signal processor capable of processing the output of the photo detector;

wherein light is emitted a first time from the light source with the reference arm in a first position to achieve maximum interference with the sample arm that corresponds to a first depth within the vasculature area, and light is emitted a second time from the light source with the reference arm in a second position to achieve maximum interference with the sample arm that corresponds to a second depth within the vasculature area, wherein a first measurement from the first light emission and a second measurement from the second light emission processed by the digital signal processor are combined to determine the relative concentration of hemoglobin.

9. The system according to claim 8 wherein said light source further comprises:

a first diode capable of emitting light in a first spectral region centered on 805 nm wavelength;

a second diode capable of emitting light in a second spectral region centered on 980 nm wavelength; and

a third diode capable of emitting light in a third spectral region centered on 1050 nm wavelength.

10. The system according to claim 8 wherein said first further comprising:

a display device capable of displaying the relative concentration of hemoglobin.

11. The system according to claim 8 wherein the first and second measurements are combined by the digital signal processor to determine a relative concentration of water.

12. A method of estimating total hemoglobin in a patient'"'"'s blood comprising:

transmitting light into skin of the patient;

measuring first intensities of at least three different wavelengths of light reflected from a first depth in the skin;

measuring second intensities of at least three different wavelengths of light reflected from a second depth in the skin; and

estimating the total hemoglobin in the patient'"'"'s blood based on a comparison of the first intensities to the second intensities.

13. The method of claim 12 wherein the at least three different wavelengths include at least one wavelength selected based on its absorption by water in the skin.

14. The method of claim 12 wherein the at least three different wavelengths include two wavelengths that can be compared to determine the oxygen saturation of the patients blood.

15. The method of claim 12 wherein the at least three different wavelengths include a first wavelength of about 805 nm, a second wavelength of about 980 nm, and a third wavelength of about 1050 nm.