CONTINUOUS NONINVASIVE GLUCOSE MONITORING IN DIABETIC, NON-DIABETIC, AND CRITICALLY ILL PATIENTS WITH OCT

• US 20070232872A1
• Filed: 03/13/2007
• Published: 10/04/2007
• Est. Priority Date: 03/16/2006
• Status: Abandoned Application

• Current Assignee: Board of Regents of the University of Texas System (University of Texas System)
• Original Assignee: Board of Regents of the University of Texas System (University of Texas System)
• Inventors: Motamedi, Massoud, Esenaliev, Rinat, Prough, Donald
• Application Number:
  US11/685,574
• Publication Number:
  US 20070232872A1
• Time in Patent Office: Days
• US Class Current: 600/316
• CPC Class Codes: A61B 5/0066 Optical coherence imaging
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/412 Detecting or monitoring sepsis

Abstract

New optical coherence tomography (OCT) techniques are disclosed which are designed to improve OCT glucose concentration measure accuracy and are capable of being performed on a continuous basis. New multi-wavelength optical coherence tomography (OCT) techniques are also disclosed and designed to reduce artifacts do to water. New optical coherence tomography (OCT) techniques are also disclosed for determining local profusion rates, local analyte transport rates and tissue analyte transport rates as a measure of tissue health, disease progression and state and tissue transplantation effectiveness.

Claims

1. A method comprising the steps of:

generating radiation;

directing a first portion of radiation onto a plurality of locations of an area of a tissue site to generate back-scattered radiation corresponding to a plurality of 1-D OCT signals on a continuous or periodic basis,

directing a second portion of the radiation to a reflector to generate reference radiation on a continuous or periodic basis,

combining a portion of the back-scattered radiation and the reference radiation to form a combined radiation on a continuous or periodic basis,

forwarding the combined radiation to a detector to produce a plurality of optical coherence tomography signals on a continuous or periodic basis, and

calculating a glucose concentration using a composite slope of the optical coherence tomography signals on a continuous or periodic basis,

where the number of the plurality of signals is sufficient to improve the signal-to-noise ratio of a composite OCT signal improving the OCT derived glucose concentration.

2. The method of claim 1, wherein the area is of tissue is between about 200μ

×

200μ and

about 2000μ

×

2000μ

.

3. The method of claim 1, wherein a distance between pairs of locations in the area is between about 500 nm and 20 mm.

4. The method of claim 3, wherein the distance is between about 1 μ

m and about 10 mm.

5. The method of claim 1, wherein each scan is an in-depth scan.

6. The method of claim 1, wherein each scan is at a set penetration depth.

7. The method of claim 1, wherein each scan has a variable penetration depth.

8. The method of claim 1, wherein the area is regular or irregular.

9. The method of claim 1, wherein the plurality of locations comprises the entire area.

10. The method of claim 1, wherein the plurality of locations comprises a random selection of locations within the area.

11. The method of claim 1, wherein the plurality of locations comprises a patterned selection of locations within the area.

12. The method of claim 1, wherein the plurality of locations comprises a random selection of contiguous sub-areas within the area.

13. The method of claim 1, wherein the plurality of locations comprises a patterned selection of contiguous sub-areas within the area.

14. The method of claim 1, further comprising the step of:

detecting Doppler data, and

determining local blood profusion rates in the tissue.

15. The method of claim 5, further comprising the step of:

constructing 2-D images of each location.

16. The method of claim 15, further comprising the step of:

constructing a 3-D image of the area from the 2-D images at each location.

17. A method comprising the steps of:

generating first radiation having a first wavelength;

directing a first portion of first radiation onto a plurality of locations of an area of a tissue site to generate first back-scattered radiation corresponding to a plurality of 1-D OCT signals on a continuous or periodic basis,

directing a second portion of the first radiation to a reflector to generate first reference radiation on a continuous or periodic basis,

combining a portion of the first back-scattered radiation and the first reference radiation to form a first combined radiation on a continuous or periodic basis,

forwarding the first combined radiation to a detector to produce a plurality of first optical coherence tomography signals on a continuous or periodic basis,

generating second radiation having a second wavelength;

directing a second portion of second radiation onto a plurality of locations of an area of a tissue site to generate second back-scattered radiation corresponding to a plurality of 1-D OCT signals on a continuous or periodic basis,

directing a second portion of the second radiation to a reflector to generate second reference radiation on a continuous or periodic basis,

combining a portion of the second back-scattered radiation and the second reference radiation to form a second combined radiation on a continuous or periodic basis,

forwarding the second combined radiation to a detector to produce a plurality of second optical coherence tomography signals on a continuous or periodic basis, and

calculating a glucose concentration using data from a first composite OCT signal and a second OCT signal on a continuous or periodic basis,

where the number of the plurality of signals is sufficient to improve the signal-to-noise ratio of a composite OCT signal improving the OCT derived glucose concentration, where the first radiation is adapted to produce a high contrast OCT signal, where the second radiation is adapted to produce a water signal, and where data from the second radiation is used to reduce water artifacts during the calculating glucose concentration step.

18. The method of claim 17, where in the first wavelength is between about 700 nm and about 1300 nm and the second wavelength is between about 1300 nm and about 2000 nm.

19. A method comprising the steps of:

generating radiation having a first wavelength and a second wavelength;

directing a first portion of radiation onto a plurality of locations of an area of a tissue site to generate back-scattered radiation corresponding to a plurality of 1-D OCT signals on a continuous or periodic basis,

directing a second portion of the radiation to a reflector to generate first reference radiation on a continuous or periodic basis,

combining a portion of the back-scattered radiation and the reference radiation to form a first combined radiation on a continuous or periodic basis,

forwarding the combined radiation to a detector to produce a plurality of optical coherence tomography signals on a continuous or periodic basis,

calculating a glucose concentration using data from a first composite OCT signal and a second OCT signal on a continuous or periodic basis,

where the number of the plurality of signals is sufficient to improve the signal-to-noise ratio of a composite OCT signal improving the OCT derived glucose concentration, where the first radiation is adapted to produce a high contrast OCT signal, where the second radiation is adapted to produce a water signal, and where data from the second radiation is used to reduce water artifacts during the calculating glucose concentration step.

20. The method of claim 19, where in the first wavelength is between about 700 nm and about 1300 nm and the second wavelength is between about 1300 nm and about 2000 nm.

21. A method comprising the steps of:

2 generating radiation;

directing a first portion of radiation onto a plurality of locations of an area of a tissue site to generate back-scattered radiation corresponding to a plurality of 1-D OCT signals,

directing a second portion of the radiation to a reflector to generate first reference radiation,

combining a portion of the back-scattered radiation and the reference radiation to form a first combined radiation,

forwarding the combined radiation to a detector to produce a plurality of optical coherence tomography signals,

calculating a glucose concentration at each of a plurality of tissue depths using data from a first composite OCT signal, and

determining a tissue depth that generates a best OCT glucose concentration value,

where the number of the plurality of signals is sufficient to improve the signal-to-noise ratio of a composite OCT signal improving the OCT derived glucose concentration.

22. A method comprising the steps of:

generating radiation;

directing a first portion of radiation onto a plurality of locations of an area of a tissue site to generate back-scattered radiation corresponding to a plurality of 1-D OCT signals,

directing a second portion of the radiation to a reflector to generate first reference radiation,

combining a portion of the back-scattered radiation and the reference radiation to form a first combined radiation,

forwarding the combined radiation to a detector to produce a plurality of optical coherence tomography signals,

calculating analyte transport rates in the tissue or at the plurality of locations within the tissue area using data from a first composite OCT signal, and

determining a tissue depth that generates a best OCT glucose concentration value,

where the number of the plurality of signals is sufficient to improve the signal-to-noise ratio of a composite OCT signal improving the OCT derived glucose concentration.